ID stringlengths 13 17 | question stringlengths 88 1.13k | answer stringlengths 6 156 | reference_sequence stringlengths 4.1k 4.1k | variant_sequence stringlengths 4.1k 4.1k |
|---|---|---|---|---|
Task1_train_48600 | Located on Chromosome 22, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | CCCACAAGGAGCCTTGGGGGATGTGGACCAGGGCTGGATCATGTGCAGGTGGGCGGTTGACAGGCATGGACTGAGCTGCTGCTGGACCATTCTCCTTGGTGCTGAAGGAAGGCAAAGGAGAAGGGCAGAAAGAAATGAAAGAGCCTTGGCTTTCTAGCTAGAGCAACTTCATCAATGTGAAATAGTCACCTTAAGAACCAGTTAATACAGAAAAGCACTGTACTATAGAAACAGGAAGTACATTCGTGGCTGCCTAGATCCAGGGGTGTGGGAGTTGGGAAAGACAGAGGAGTGACTACTAGTGGGGTTTCTTTGAGGGG... | CCCACAAGGAGCCTTGGGGGATGTGGACCAGGGCTGGATCATGTGCAGGTGGGCGGTTGACAGGCATGGACTGAGCTGCTGCTGGACCATTCTCCTTGGTGCTGAAGGAAGGCAAAGGAGAAGGGCAGAAAGAAATGAAAGAGCCTTGGCTTTCTAGCTAGAGCAACTTCATCAATGTGAAATAGTCACCTTAAGAACCAGTTAATACAGAAAAGCACTGTACTATAGAAACAGGAAGTACATTCGTGGCTGCCTAGATCCAGGGGTGTGGGAGTTGGGAAAGACAGAGGAGTGACTACTAGTGGGGTTTCTTTGAGGGG... |
Task1_train_48601 | A genomic variant on Chromosome 22 is under review. What is the biological outcome — benign or pathogenic? | Benign | ATTGACATAAAGATTGAGCATGTAATACACAAAGTTCCCACATCATTCTCTTCTCTCATCCTACCTTATAATTCCACCTAATATTCACATCTTACATTACTGTGTTATATTTGCTAAAATTAATGGGCAAATATTGATACATTAGTATCTAAAGTCTGTCATTCACATAGTGTTCTTTCTTCCTGTTACACATTTCTATGAATTTTGAAATATTTACTATGTTATGTTTACCATTTCGAACTCATAAGGAATATTCTCACTGCTCCAAAAATTCCCTCTTCTTTACTTATGAATCTCTGTCCTCTTCTCCAGAAATCATG... | ATTGACATAAAGATTGAGCATGTAATACACAAAGTTCCCACATCATTCTCTTCTCTCATCCTACCTTATAATTCCACCTAATATTCACATCTTACATTACTGTGTTATATTTGCTAAAATTAATGGGCAAATATTGATACATTAGTATCTAAAGTCTGTCATTCACATAGTGTTCTTTCTTCCTGTTACACATTTCTATGAATTTTGAAATATTTACTATGTTATGTTTACCATTTCGAACTCATAAGGAATATTCTCACTGCTCCAAAAATTCCCTCTTCTTTACTTATGAATCTCTGTCCTCTTCTCCAGAAATCATG... |
Task1_train_48602 | Assess the clinical impact of this variant found on Chromosome 22. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TCCACCTAATATTCACATCTTACATTACTGTGTTATATTTGCTAAAATTAATGGGCAAATATTGATACATTAGTATCTAAAGTCTGTCATTCACATAGTGTTCTTTCTTCCTGTTACACATTTCTATGAATTTTGAAATATTTACTATGTTATGTTTACCATTTCGAACTCATAAGGAATATTCTCACTGCTCCAAAAATTCCCTCTTCTTTACTTATGAATCTCTGTCCTCTTCTCCAGAAATCATGCCAACTATGGATATTTTTACTGTTCCCTTGGTTTTGCCTTTTCTAGAATGTCATATAGTTGGAGTCATATAT... | TCCACCTAATATTCACATCTTACATTACTGTGTTATATTTGCTAAAATTAATGGGCAAATATTGATACATTAGTATCTAAAGTCTGTCATTCACATAGTGTTCTTTCTTCCTGTTACACATTTCTATGAATTTTGAAATATTTACTATGTTATGTTTACCATTTCGAACTCATAAGGAATATTCTCACTGCTCCAAAAATTCCCTCTTCTTTACTTATGAATCTCTGTCCTCTTCTCCAGAAATCATGCCAACTATGGATATTTTTACTGTTCCCTTGGTTTTGCCTTTTCTAGAATGTCATATAGTTGGAGTCATATAT... |
Task1_train_48603 | A genomic change on Chromosome 22 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TCTTTCTTCCTGTTACACATTTCTATGAATTTTGAAATATTTACTATGTTATGTTTACCATTTCGAACTCATAAGGAATATTCTCACTGCTCCAAAAATTCCCTCTTCTTTACTTATGAATCTCTGTCCTCTTCTCCAGAAATCATGCCAACTATGGATATTTTTACTGTTCCCTTGGTTTTGCCTTTTCTAGAATGTCATATAGTTGGAGTCATATATTAGGTTGGTGCAAAAGTAATTGCGGTTTTCCCATTCTTTAAATGCCAAAAACCACAATTACTTTTGCACCAACCAAATATTATGCAGCTTTTTCAGCTGAA... | TCTTTCTTCCTGTTACACATTTCTATGAATTTTGAAATATTTACTATGTTATGTTTACCATTTCGAACTCATAAGGAATATTCTCACTGCTCCAAAAATTCCCTCTTCTTTACTTATGAATCTCTGTCCTCTTCTCCAGAAATCATGCCAACTATGGATATTTTTACTGTTCCCTTGGTTTTGCCTTTTCTAGAATGTCATATAGTTGGAGTCATATATTAGGTTGGTGCAAAAGTAATTGCGGTTTTCCCATTCTTTAAATGCCAAAAACCACAATTACTTTTGCACCAACCAAATATTATGCAGCTTTTTCAGCTGAA... |
Task1_train_48604 | A variant found on Chromosome 22 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CCCCACTCGCTGTAACTTGCGGTCTACGAAGAGGAAAGTCAGCGGCACCGTGGTGGCAGAGAGGCGGCCTCCATCCCTCAAACTCACAGTCCAGAATCCAAGCTCTGTGGTCAGCTGGATCCTCCCTTTGCGGTGAACAGATTCTCTGCAGACTCCCAGGTCCCATTCTGTGCTTGTTCCCACGTCCACCTCCCAGCAGTGGCGGCCACAGGTAAAGCGAGGGGAGCCCAGGATGCAAACGGACACGTCAAATCTCTCGGCAAGGTCTTGCCGATTCTGTCTGATGCGCCCACTTCGGACGCTCCTGAGGTCGTCAGAAA... | CCCCACTCGCTGTAACTTGCGGTCTACGAAGAGGAAAGTCAGCGGCACCGTGGTGGCAGAGAGGCGGCCTCCATCCCTCAAACTCACAGTCCAGAATCCAAGCTCTGTGGTCAGCTGGATCCTCCCTTTGCGGTGAACAGATTCTCTGCAGACTCCCAGGTCCCATTCTGTGCTTGTTCCCACGTCCACCTCCCAGCAGTGGCGGCCACAGGTAAAGCGAGGGGAGCCCAGGATGCAAACGGACACGTCAAATCTCTCGGCAAGGTCTTGCCGATTCTGTCTGATGCGCCCACTTCGGACGCTCCTGAGGTCGTCAGAAA... |
Task1_train_48605 | Here is a mutation located on Chromosome 22. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CCTCCATCCCTCAAACTCACAGTCCAGAATCCAAGCTCTGTGGTCAGCTGGATCCTCCCTTTGCGGTGAACAGATTCTCTGCAGACTCCCAGGTCCCATTCTGTGCTTGTTCCCACGTCCACCTCCCAGCAGTGGCGGCCACAGGTAAAGCGAGGGGAGCCCAGGATGCAAACGGACACGTCAAATCTCTCGGCAAGGTCTTGCCGATTCTGTCTGATGCGCCCACTTCGGACGCTCCTGAGGTCGTCAGAAATGAGGAGGAAGTTGTTGGCTGTGTTGGCATCCAAGGTCATATCCACTGTGAAAAGGAAAAAAAGTTG... | CCTCCATCCCTCAAACTCACAGTCCAGAATCCAAGCTCTGTGGTCAGCTGGATCCTCCCTTTGCGGTGAACAGATTCTCTGCAGACTCCCAGGTCCCATTCTGTGCTTGTTCCCACGTCCACCTCCCAGCAGTGGCGGCCACAGGTAAAGCGAGGGGAGCCCAGGATGCAAACGGACACGTCAAATCTCTCGGCAAGGTCTTGCCGATTCTGTCTGATGCGCCCACTTCGGACGCTCCTGAGGTCGTCAGAAATGAGGAGGAAGTTGTTGGCTGTGTTGGCATCCAAGGTCATATCCACTGTGAAAAGGAAAAAAAGTTG... |
Task1_train_48606 | Consider a variant on Chromosome 22. Determine its clinical classification and disease relevance. | Benign | CTCCATTCCCAACTCTTCCCAACCCTGGGGTAAGGTTGTTTGTACAATGGGTGCCAATATTCACCGTGCATTAGAATTACCAGGCCCATTTTAATGTTAGAGTCCTGGGAACCTTTGCTAGAGAGAAATTCAAATTCAGTTGCTCTATGTTTTTGCTACTCAGCAAAGTCCCCAAGCCAGTGGGATCAATCCTGAGACTTCCCAGTTCAGCATCTGCATTTTAACAAGATCCCCAGGTAATCTGAGCACACTAAGTTTAGAGAATCCCTTGTCTAACCCATGACATAGACATCGGGTTTTTGTTTGTTTTTGTTTTTGAC... | CTCCATTCCCAACTCTTCCCAACCCTGGGGTAAGGTTGTTTGTACAATGGGTGCCAATATTCACCGTGCATTAGAATTACCAGGCCCATTTTAATGTTAGAGTCCTGGGAACCTTTGCTAGAGAGAAATTCAAATTCAGTTGCTCTATGTTTTTGCTACTCAGCAAAGTCCCCAAGCCAGTGGGATCAATCCTGAGACTTCCCAGTTCAGCATCTGCATTTTAACAAGATCCCCAGGTAATCTGAGCACACTAAGTTTAGAGAATCCCTTGTCTAACCCATGACATAGACATCGGGTTTTTGTTTGTTTTTGTTTTTGAC... |
Task1_train_48607 | Given this context: Chromosome 22 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CTCACCAAAAAATAAAAAAATAAAAAAATAAAAAAAATTACATCCTTCTCCAGCCTTGGAAGTGAATACCAAATTGACTGCCACCACTCTTACACTCCTAGACTGGGGATCCAGGGTGACTGGTTTCCAACTCTGAGGCAGCACTCAGACGGCCTTTGTTGAATTCATTAATTACGAATTTCTCTCATTCATCCCCCCAAGTCATAACCCCCATTTCTAGGCATCTAAGAGGAAAAACACACACACAGGCATGGGCTCACCTCTTCTGCTGGAAGCTCCTCTGTCCTCCAGCTGCTTCCACTGGGCGCTCAGGTCTTGTG... | CTCACCAAAAAATAAAAAAATAAAAAAATAAAAAAAATTACATCCTTCTCCAGCCTTGGAAGTGAATACCAAATTGACTGCCACCACTCTTACACTCCTAGACTGGGGATCCAGGGTGACTGGTTTCCAACTCTGAGGCAGCACTCAGACGGCCTTTGTTGAATTCATTAATTACGAATTTCTCTCATTCATCCCCCCAAGTCATAACCCCCATTTCTAGGCATCTAAGAGGAAAAACACACACACAGGCATGGGCTCACCTCTTCTGCTGGAAGCTCCTCTGTCCTCCAGCTGCTTCCACTGGGCGCTCAGGTCTTGTG... |
Task1_train_48608 | Chromosome 22 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GCCTGCAGTGAGCGGAGATCGCGCCACTGCACTCCAGCCTGGGTGACAGAGCAAGACTCTGTCTCAAAAAAAAAAAAAAAAAGAAAATAGACAGATGCTGAGATGTTTCAGTCACTACTCCTCAGAGCAGGAGTCAAGCAAACAATGGCCCCTGGGCTAATCCAGCCCACAGTCAGTTTCTGAATGGCCCACGAGCCAAGAATGTTTTTTTACATTTTTGCATTGTTAAATAATGGTAAACAATCTAAGTAAGCATAATATTTTGTGAAATGTGAAATTGTAAACTTGTGAAATTGTATGATTCAAATTTCATTGTCTGG... | GCCTGCAGTGAGCGGAGATCGCGCCACTGCACTCCAGCCTGGGTGACAGAGCAAGACTCTGTCTCAAAAAAAAAAAAAAAAAGAAAATAGACAGATGCTGAGATGTTTCAGTCACTACTCCTCAGAGCAGGAGTCAAGCAAACAATGGCCCCTGGGCTAATCCAGCCCACAGTCAGTTTCTGAATGGCCCACGAGCCAAGAATGTTTTTTTACATTTTTGCATTGTTAAATAATGGTAAACAATCTAAGTAAGCATAATATTTTGTGAAATGTGAAATTGTAAACTTGTGAAATTGTATGATTCAAATTTCATTGTCTGG... |
Task1_train_48609 | The following genetic variant occurs on Chromosome 22. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CCTTTCTTTTTTTATATTAGAGAATATAATAGAACTAAGAAATCTCAATCAGGTGTGGCAGCTCACACCTGTAATCTCAGCACTTTGGGAGGCCAAGGCAGGAGGATCACTTGAGCCAGGGGTTCTAGACCAGCCAGGGCAACATGGTGAGACCCCCATCTCTACAAAAAATAGAAAAAGTTCGTTGGGCATGGTGGCATGTGCCTGTGGTCCCAGCTTCTTGGGAGGCTCAGGTGGATCACCTGAGCCCATGTAGTTAACGTTACAGTAAGCCATGATTATGCCACTGCATTCTAGCAGCAGTGGGCGACAGAGACCCA... | CCTTTCTTTTTTTATATTAGAGAATATAATAGAACTAAGAAATCTCAATCAGGTGTGGCAGCTCACACCTGTAATCTCAGCACTTTGGGAGGCCAAGGCAGGAGGATCACTTGAGCCAGGGGTTCTAGACCAGCCAGGGCAACATGGTGAGACCCCCATCTCTACAAAAAATAGAAAAAGTTCGTTGGGCATGGTGGCATGTGCCTGTGGTCCCAGCTTCTTGGGAGGCTCAGGTGGATCACCTGAGCCCATGTAGTTAACGTTACAGTAAGCCATGATTATGCCACTGCATTCTAGCAGCAGTGGGCGACAGAGACCCA... |
Task1_train_48610 | Here is a mutation located on Chromosome 22. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AAAATGATACAATATATATTGTTTCCTTAAAGCAGTCAATACAATGCATAAATTTCTAGAGAAATCAGTAAAAAAAAAAAAAGTTCATAACAAAGGTAGTAACATTAGGAATAAAAGAGGGCTCAACACTGCAGGTTCTTAAAGGCAAAAGTTAGTGAAGCATTGTTTTTGGTTGTGAATCTTGCCCTAAAAACATTATAATTCCACATGATCCTCCCCTTCCTTTTCCTGTTGCAACGATGTGATGAACCAAATTTGCTTATGCAGATGACAATACTCTCAGAAAATGGTGGCAGAGAAATAAAATGAAGGGAATATGG... | AAAATGATACAATATATATTGTTTCCTTAAAGCAGTCAATACAATGCATAAATTTCTAGAGAAATCAGTAAAAAAAAAAAAAGTTCATAACAAAGGTAGTAACATTAGGAATAAAAGAGGGCTCAACACTGCAGGTTCTTAAAGGCAAAAGTTAGTGAAGCATTGTTTTTGGTTGTGAATCTTGCCCTAAAAACATTATAATTCCACATGATCCTCCCCTTCCTTTTCCTGTTGCAACGATGTGATGAACCAAATTTGCTTATGCAGATGACAATACTCTCAGAAAATGGTGGCAGAGAAATAAAATGAAGGGAATATGG... |
Task1_train_48611 | A variant was discovered on Chromosome 22. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | AAGAAACAGAGGCTGTGGGTGGGTAGAGGGTCTTGACTAGGGTAGGGACAGAGGGTGCGTCTTAAGGCTCAGCTAGGGACAGCTTCATCCAGGAAGTAGTCAGCAATTGGGGGCCAAGCTGCAAGGAGGAAGAGGTGGGGAGAGAGAATGGAGAGAGAGGTGTTCAGTGATCAAATGCCTGGCCTGGCCTGTTTCCTCAGGAGACACCCCTGGGAGTCTGGGAGCCTCTCCCCCGGGCTGCTATCCAACAGGGTGCAAGTAATCCCCCCTTACACACACTAAGAACCCAGGGTGAGTGTCAAATTATATGTTAGCTAAGA... | AAGAAACAGAGGCTGTGGGTGGGTAGAGGGTCTTGACTAGGGTAGGGACAGAGGGTGCGTCTTAAGGCTCAGCTAGGGACAGCTTCATCCAGGAAGTAGTCAGCAATTGGGGGCCAAGCTGCAAGGAGGAAGAGGTGGGGAGAGAGAATGGAGAGAGAGGTGTTCAGTGATCAAATGCCTGGCCTGGCCTGTTTCCTCAGGAGACACCCCTGGGAGTCTGGGAGCCTCTCCCCCGGGCTGCTATCCAACAGGGTGCAAGTAATCCCCCCTTACACACACTAAGAACCCAGGGTGAGTGTCAAATTATATGTTAGCTAAGA... |
Task1_train_48612 | This alteration occurs on Chromosome 22. Is it associated with a disease or is it a benign variant? | Benign | GGACAGCTTCATCCAGGAAGTAGTCAGCAATTGGGGGCCAAGCTGCAAGGAGGAAGAGGTGGGGAGAGAGAATGGAGAGAGAGGTGTTCAGTGATCAAATGCCTGGCCTGGCCTGTTTCCTCAGGAGACACCCCTGGGAGTCTGGGAGCCTCTCCCCCGGGCTGCTATCCAACAGGGTGCAAGTAATCCCCCCTTACACACACTAAGAACCCAGGGTGAGTGTCAAATTATATGTTAGCTAAGAAATGAAGAGAGGGAGCAGGATTTCTGGTTGACGGTGAGGATATTTATTAAGGGTTTACTGGTACAAGGAGAGGGGC... | GGACAGCTTCATCCAGGAAGTAGTCAGCAATTGGGGGCCAAGCTGCAAGGAGGAAGAGGTGGGGAGAGAGAATGGAGAGAGAGGTGTTCAGTGATCAAATGCCTGGCCTGGCCTGTTTCCTCAGGAGACACCCCTGGGAGTCTGGGAGCCTCTCCCCCGGGCTGCTATCCAACAGGGTGCAAGTAATCCCCCCTTACACACACTAAGAACCCAGGGTGAGTGTCAAATTATATGTTAGCTAAGAAATGAAGAGAGGGAGCAGGATTTCTGGTTGACGGTGAGGATATTTATTAAGGGTTTACTGGTACAAGGAGAGGGGC... |
Task1_train_48613 | A mutation located on Chromosome 22 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GAGGTGTTCAGTGATCAAATGCCTGGCCTGGCCTGTTTCCTCAGGAGACACCCCTGGGAGTCTGGGAGCCTCTCCCCCGGGCTGCTATCCAACAGGGTGCAAGTAATCCCCCCTTACACACACTAAGAACCCAGGGTGAGTGTCAAATTATATGTTAGCTAAGAAATGAAGAGAGGGAGCAGGATTTCTGGTTGACGGTGAGGATATTTATTAAGGGTTTACTGGTACAAGGAGAGGGGCTGGATGATTTGGGGTGGGAGGGGATCTCTGTTCTGGGATCCTGCAGCTCCAGGCCCCCATGGGTGGGGTGAGGGTCAGGG... | GAGGTGTTCAGTGATCAAATGCCTGGCCTGGCCTGTTTCCTCAGGAGACACCCCTGGGAGTCTGGGAGCCTCTCCCCCGGGCTGCTATCCAACAGGGTGCAAGTAATCCCCCCTTACACACACTAAGAACCCAGGGTGAGTGTCAAATTATATGTTAGCTAAGAAATGAAGAGAGGGAGCAGGATTTCTGGTTGACGGTGAGGATATTTATTAAGGGTTTACTGGTACAAGGAGAGGGGCTGGATGATTTGGGGTGGGAGGGGATCTCTGTTCTGGGATCCTGCAGCTCCAGGCCCCCATGGGTGGGGTGAGGGTCAGGG... |
Task1_train_48614 | A mutation on Chromosome 22 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TACACACACTAAGAACCCAGGGTGAGTGTCAAATTATATGTTAGCTAAGAAATGAAGAGAGGGAGCAGGATTTCTGGTTGACGGTGAGGATATTTATTAAGGGTTTACTGGTACAAGGAGAGGGGCTGGATGATTTGGGGTGGGAGGGGATCTCTGTTCTGGGATCCTGCAGCTCCAGGCCCCCATGGGTGGGGTGAGGGTCAGGGACCTAAGAACATTCTTCAGGGGCCACTGTCTTCTCCACAGTGCTCTCTTGTGTGTGACCTTACAGCTGTAGCTGCTGCAGGACCTCCACTGGTCGGGTGTCAGGCTCAGGTCGC... | TACACACACTAAGAACCCAGGGTGAGTGTCAAATTATATGTTAGCTAAGAAATGAAGAGAGGGAGCAGGATTTCTGGTTGACGGTGAGGATATTTATTAAGGGTTTACTGGTACAAGGAGAGGGGCTGGATGATTTGGGGTGGGAGGGGATCTCTGTTCTGGGATCCTGCAGCTCCAGGCCCCCATGGGTGGGGTGAGGGTCAGGGACCTAAGAACATTCTTCAGGGGCCACTGTCTTCTCCACAGTGCTCTCTTGTGTGTGACCTTACAGCTGTAGCTGCTGCAGGACCTCCACTGGTCGGGTGTCAGGCTCAGGTCGC... |
Task1_train_48615 | The following genetic variant occurs on Chromosome 22. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GGAGCAGGATTTCTGGTTGACGGTGAGGATATTTATTAAGGGTTTACTGGTACAAGGAGAGGGGCTGGATGATTTGGGGTGGGAGGGGATCTCTGTTCTGGGATCCTGCAGCTCCAGGCCCCCATGGGTGGGGTGAGGGTCAGGGACCTAAGAACATTCTTCAGGGGCCACTGTCTTCTCCACAGTGCTCTCTTGTGTGTGACCTTACAGCTGTAGCTGCTGCAGGACCTCCACTGGTCGGGTGTCAGGCTCAGGTCGCTTCTGGCTGTGTGCTTGTTGCTCTGTTTGGAGGTCTTGGTGACTTCCGTACCCTGGGTGAC... | GGAGCAGGATTTCTGGTTGACGGTGAGGATATTTATTAAGGGTTTACTGGTACAAGGAGAGGGGCTGGATGATTTGGGGTGGGAGGGGATCTCTGTTCTGGGATCCTGCAGCTCCAGGCCCCCATGGGTGGGGTGAGGGTCAGGGACCTAAGAACATTCTTCAGGGGCCACTGTCTTCTCCACAGTGCTCTCTTGTGTGTGACCTTACAGCTGTAGCTGCTGCAGGACCTCCACTGGTCGGGTGTCAGGCTCAGGTCGCTTCTGGCTGTGTGCTTGTTGCTCTGTTTGGAGGTCTTGGTGACTTCCGTACCCTGGGTGAC... |
Task1_train_48616 | This alteration on Chromosome 22 may affect genome function. Does it lead to a disease or is it benign? | Benign | TCCCACATCAAGGAACTGGAGCCCAAGCTGAAGAAGATTCTACAGATGAACCCAAGGATGCGGAAGTTCCAAGGTAAGGAATCTGTATACCCTGCCCCCTTCCCAAGACCAGACCAGGAAAAATCATCTGTGCAGTTGGCCCCTCATTCCACATGGGGATTAGCTGCTGTCTGGCACCTAAAATTGAGATGCTTCATCATCACATTCTCAGCCCTGACAACACATAGAATCACCTGGTGATGTCAAAAACAAAAACAAACAAAAACCCGATGTCTATGTCATGGGTTAGACAAGGGATTCTCTAAACTTAGTGTGCTCAG... | TCCCACATCAAGGAACTGGAGCCCAAGCTGAAGAAGATTCTACAGATGAACCCAAGGATGCGGAAGTTCCAAGGTAAGGAATCTGTATACCCTGCCCCCTTCCCAAGACCAGACCAGGAAAAATCATCTGTGCAGTTGGCCCCTCATTCCACATGGGGATTAGCTGCTGTCTGGCACCTAAAATTGAGATGCTTCATCATCACATTCTCAGCCCTGACAACACATAGAATCACCTGGTGATGTCAAAAACAAAAACAAACAAAAACCCGATGTCTATGTCATGGGTTAGACAAGGGATTCTCTAAACTTAGTGTGCTCAG... |
Task1_train_48617 | A mutation on Chromosome 22 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GTACTGTCCTGTAGTGTATAACTTTAGGATCTTTATTAGTCGATTTCCTCTAAACTACAGCTAAGCGAAATCCAGAAGTTTAAAGTATAATCTAGTTATCTTTTGTTTTGGAAATGCTTTTCAGCAGCTTATGAAAACACCTTGAGTCTGGGTCAGGTTCGGTGCATTGGCTTGGAGTTTACACCCTCAGCTGGGAGGGGAAAAAGATAACGCCAGCAGCTGAGAAAGAAAAACCTGTTTGAGTAAATACCATAGCTGAACATTTATGTTTCAGAATGAATCTGGATATACACCAAATAACTTTTTTGGTCAGAAAGGAG... | GTACTGTCCTGTAGTGTATAACTTTAGGATCTTTATTAGTCGATTTCCTCTAAACTACAGCTAAGCGAAATCCAGAAGTTTAAAGTATAATCTAGTTATCTTTTGTTTTGGAAATGCTTTTCAGCAGCTTATGAAAACACCTTGAGTCTGGGTCAGGTTCGGTGCATTGGCTTGGAGTTTACACCCTCAGCTGGGAGGGGAAAAAGATAACGCCAGCAGCTGAGAAAGAAAAACCTGTTTGAGTAAATACCATAGCTGAACATTTATGTTTCAGAATGAATCTGGATATACACCAAATAACTTTTTTGGTCAGAAAGGAG... |
Task1_train_48618 | This alteration on Chromosome 22 may affect genome function. Does it lead to a disease or is it benign? | Benign | TATGCAGGTAGGGGAAAACCACTAGAGGGCCTAAGGGATTTCCACTGAGAATGACCAATACAAATACAGACTTAGAGTTGCTTACCCACCTGGTCAGAAGTACATGCCTAGCTCTTGTCCTAGAATCTTTCTTGCCCCAAACAAACAAACAAACATAAACACAGACACACGCAGCATGCATACACTCACATTCAGACACCTCTATTTATCCCTTTAACAGAGTCTGCCTTATTCTGGGTTCCTGAAGGCTTAAGAAAGAAAACTTTCTGCCTAAGCAATTCACAAGGGCTTTACAATTCCAGTGTGTACTGTCTTTCCCT... | TATGCAGGTAGGGGAAAACCACTAGAGGGCCTAAGGGATTTCCACTGAGAATGACCAATACAAATACAGACTTAGAGTTGCTTACCCACCTGGTCAGAAGTACATGCCTAGCTCTTGTCCTAGAATCTTTCTTGCCCCAAACAAACAAACAAACATAAACACAGACACACGCAGCATGCATACACTCACATTCAGACACCTCTATTTATCCCTTTAACAGAGTCTGCCTTATTCTGGGTTCCTGAAGGCTTAAGAAAGAAAACTTTCTGCCTAAGCAATTCACAAGGGCTTTACAATTCCAGTGTGTACTGTCTTTCCCT... |
Task1_train_48619 | A mutation located on Chromosome 22 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TGGAGCCAAATACACTATCAAGACTCAAACCCTGAGCACTTACCCGGGAGAGCACGTTGCCAAGGCCTTGAGAGTTTTGAACAAAATGGTTGGAAATCTGGAAAATAAAGCCCATTATGTCACTGTTAGGATTTTACGTGGATTGTCTTTTCAGGGAAAATGTAGTGTTCCCTATAATTTGACGAATTGTGAAGCTGTTACACCATAAAATATTCAGTGTTTAAAGGTGACCTATCATTTTATAGCCCAATCATAGGGAATCCGAGGCTCAGAGAAGTAAAGTGACTTGCCCAAGGTCACACAGGATGTTATATTTCTTT... | TGGAGCCAAATACACTATCAAGACTCAAACCCTGAGCACTTACCCGGGAGAGCACGTTGCCAAGGCCTTGAGAGTTTTGAACAAAATGGTTGGAAATCTGGAAAATAAAGCCCATTATGTCACTGTTAGGATTTTACGTGGATTGTCTTTTCAGGGAAAATGTAGTGTTCCCTATAATTTGACGAATTGTGAAGCTGTTACACCATAAAATATTCAGTGTTTAAAGGTGACCTATCATTTTATAGCCCAATCATAGGGAATCCGAGGCTCAGAGAAGTAAAGTGACTTGCCCAAGGTCACACAGGATGTTATATTTCTTT... |
Task1_train_48620 | Chromosome 22 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TTTACACTCTACTGAAAGAGCTGATTCACTCAACTGTAAACTTTGCATGGGCAGAAACATGTCTTTTTGGTCTCTTGAGTCTCCAGCATGTGGGGTATCTGTCACAAAGTAGGCAATCAATACATATTTATTTGCAGAATCAAGGGCAGGATGTGGACAAGTGCTGCCACCTATTGGGAGAAACTTTATTTGACTCTAAGGATTTGGACTATGGTTATCACACAAGGACGAAACTTGATACTCTCTCTCATCTAAGTTATCATTAGTTAGACCCTCTATGGTAGCCAGCCTCCAGGATGGCCCGCAGCGATCCCTGTCTG... | TTTACACTCTACTGAAAGAGCTGATTCACTCAACTGTAAACTTTGCATGGGCAGAAACATGTCTTTTTGGTCTCTTGAGTCTCCAGCATGTGGGGTATCTGTCACAAAGTAGGCAATCAATACATATTTATTTGCAGAATCAAGGGCAGGATGTGGACAAGTGCTGCCACCTATTGGGAGAAACTTTATTTGACTCTAAGGATTTGGACTATGGTTATCACACAAGGACGAAACTTGATACTCTCTCTCATCTAAGTTATCATTAGTTAGACCCTCTATGGTAGCCAGCCTCCAGGATGGCCCGCAGCGATCCCTGTCTG... |
Task1_train_48621 | A variant has been detected on Chromosome 22. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TTGTTTTCTAGCAAACAGGAATAGCTTCTATTTCAGTAATTTTAATTTCTCTACCAAGGACACTTCAATCAGTAAGAAAAAATATATTTACGAGTGAAATAAAAACAAGAATTATTTGGAGCACTTTTCAAAATGCAGCATTGTAAGAATAAGTAAACAATATAATTTTTAAAGGACTTCATCTTTTGTTAACCTCTCAAAAAAGTAATGAAATTAGCATTGCTGAGTGTAAATGTTTTTAAAAATGTTTTATAATGTTTTGTTATTGTTCCTCACCACTGTGTGATGAAAAACATTTTATTCTTCTAATGTCAAATAAT... | TTGTTTTCTAGCAAACAGGAATAGCTTCTATTTCAGTAATTTTAATTTCTCTACCAAGGACACTTCAATCAGTAAGAAAAAATATATTTACGAGTGAAATAAAAACAAGAATTATTTGGAGCACTTTTCAAAATGCAGCATTGTAAGAATAAGTAAACAATATAATTTTTAAAGGACTTCATCTTTTGTTAACCTCTCAAAAAAGTAATGAAATTAGCATTGCTGAGTGTAAATGTTTTTAAAAATGTTTTATAATGTTTTGTTATTGTTCCTCACCACTGTGTGATGAAAAACATTTTATTCTTCTAATGTCAAATAAT... |
Task1_train_48622 | A variant found on Chromosome 22 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | TTTATTATTTATTTATGCAAATATTTTTTATTTGCATAAGGAAGCACTGAAAGGACACATAGGAACTAACAAAAGTCATTTCTGGGGATGGGGGTAGCAAAGCGTTGGATGAGAATGGGGCGGGAACGAGGCTTTTCAACATACATCTTTGATTTATTTATTTATTTATTTATTTATTTATTTATTGAGATGGAGTCTCACTTTGTTGCCCAGGCTGGAGTGCAATGGCGCCATCTCAGCTCACTGCAACCTCAGCCTCTCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGTGCACC... | TTTATTATTTATTTATGCAAATATTTTTTATTTGCATAAGGAAGCACTGAAAGGACACATAGGAACTAACAAAAGTCATTTCTGGGGATGGGGGTAGCAAAGCGTTGGATGAGAATGGGGCGGGAACGAGGCTTTTCAACATACATCTTTGATTTATTTATTTATTTATTTATTTATTTATTTATTGAGATGGAGTCTCACTTTGTTGCCCAGGCTGGAGTGCAATGGCGCCATCTCAGCTCACTGCAACCTCAGCCTCTCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGTGCACC... |
Task1_train_48623 | Located on Chromosome 22, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | ACCTATGTAACAAACCTGCACATTCTGCACATGTATCCCAGAACTTAAAATTAAAAAAAAAAAATTCTCCTTTGCTGTCTCCCTTTCCCCAGAAAACTTGGAGCCTATGATTGGAGAATGGTGGCATCACTGTTTGAAAGGAATCTGGGTCCCTAAATGACTACATTAGAATGTGATGTGGGTGAGCTATTATGCTCCCAAGACTATAGGGTTTACTTGCTACTACAGCAGAGCCTATTCCCCCCCTAACTAAATCAGACAGCCTGACACTTCCAAGGGGCACAGCTCCTAAAATGGGGCATCTTTACCTGTTCCCTCTC... | ACCTATGTAACAAACCTGCACATTCTGCACATGTATCCCAGAACTTAAAATTAAAAAAAAAAAATTCTCCTTTGCTGTCTCCCTTTCCCCAGAAAACTTGGAGCCTATGATTGGAGAATGGTGGCATCACTGTTTGAAAGGAATCTGGGTCCCTAAATGACTACATTAGAATGTGATGTGGGTGAGCTATTATGCTCCCAAGACTATAGGGTTTACTTGCTACTACAGCAGAGCCTATTCCCCCCCTAACTAAATCAGACAGCCTGACACTTCCAAGGGGCACAGCTCCTAAAATGGGGCATCTTTACCTGTTCCCTCTC... |
Task1_train_48624 | This mutation on Chromosome 22 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CCCAGAAAACTTGGAGCCTATGATTGGAGAATGGTGGCATCACTGTTTGAAAGGAATCTGGGTCCCTAAATGACTACATTAGAATGTGATGTGGGTGAGCTATTATGCTCCCAAGACTATAGGGTTTACTTGCTACTACAGCAGAGCCTATTCCCCCCCTAACTAAATCAGACAGCCTGACACTTCCAAGGGGCACAGCTCCTAAAATGGGGCATCTTTACCTGTTCCCTCTCTCAGGGTGAGTCCCTCTCTCTCCTGACTCACTCTTCTCAGGGAGTGGAGACCAACGTTCCCTATCCTTCACCTCCCACCCCTGCCCT... | CCCAGAAAACTTGGAGCCTATGATTGGAGAATGGTGGCATCACTGTTTGAAAGGAATCTGGGTCCCTAAATGACTACATTAGAATGTGATGTGGGTGAGCTATTATGCTCCCAAGACTATAGGGTTTACTTGCTACTACAGCAGAGCCTATTCCCCCCCTAACTAAATCAGACAGCCTGACACTTCCAAGGGGCACAGCTCCTAAAATGGGGCATCTTTACCTGTTCCCTCTCTCAGGGTGAGTCCCTCTCTCTCCTGACTCACTCTTCTCAGGGAGTGGAGACCAACGTTCCCTATCCTTCACCTCCCACCCCTGCCCT... |
Task1_train_48625 | A mutation is present on Chromosome 22. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CATGCAGGATTAGAAATACAGTAGCCCATTGTCACTCACTAGAGGTATTTCCTGCCCTCTTCACATGCACCCAGCTTTGCAAGTGCCACCCTAGCACACGACGTTCCACCAGATCTCACTGTGGCACCGTTAGCATTCTCTCTAAAATAGTTCTCTAAGTTGCTCTCCTTTTTTTCTTTCCACAAATGTGATGGACTCATTCTAATTCAAAATCAGGCCAACATTCTGTTCTTTATTCTATCCTTTCCTTCTGGCTGGGGACCACTCATGTCTAAGACTTCTCTCCTTTTTCTTCCCATCTAGAATCAGGCACTAGCTAA... | CATGCAGGATTAGAAATACAGTAGCCCATTGTCACTCACTAGAGGTATTTCCTGCCCTCTTCACATGCACCCAGCTTTGCAAGTGCCACCCTAGCACACGACGTTCCACCAGATCTCACTGTGGCACCGTTAGCATTCTCTCTAAAATAGTTCTCTAAGTTGCTCTCCTTTTTTTCTTTCCACAAATGTGATGGACTCATTCTAATTCAAAATCAGGCCAACATTCTGTTCTTTATTCTATCCTTTCCTTCTGGCTGGGGACCACTCATGTCTAAGACTTCTCTCCTTTTTCTTCCCATCTAGAATCAGGCACTAGCTAA... |
Task1_train_48626 | Here is a mutation located on Chromosome 22. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TTGAACTCAGGGGGTCGAAGCTGCAGTGAGCTGTGATCGTGCCACTGCACTCCAGCCTGGGTGACAGAGAAAGACCCTGTCTCAAAACAAACAAACAAAACCTCCCTCCACAGGGACACTGCTAGCAGGAAAGATGATGAAGCTTGGAGCTGCTGGAGTCATCACCTGAATCTGAGAATAAAGCTAACAGAGGAGAGCACCACAGACACGTCAAAGGACCAGCTTGAGTTACCTCCCTGGAAGTGACCATGTCTGCAGGTACTGGAAATTTCAATCATGTGAGCCAATAAATTCCCCTCTTCTGGGGAAACACATGGAAA... | TTGAACTCAGGGGGTCGAAGCTGCAGTGAGCTGTGATCGTGCCACTGCACTCCAGCCTGGGTGACAGAGAAAGACCCTGTCTCAAAACAAACAAACAAAACCTCCCTCCACAGGGACACTGCTAGCAGGAAAGATGATGAAGCTTGGAGCTGCTGGAGTCATCACCTGAATCTGAGAATAAAGCTAACAGAGGAGAGCACCACAGACACGTCAAAGGACCAGCTTGAGTTACCTCCCTGGAAGTGACCATGTCTGCAGGTACTGGAAATTTCAATCATGTGAGCCAATAAATTCCCCTCTTCTGGGGAAACACATGGAAA... |
Task1_train_48627 | A mutation located on Chromosome 22 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GGTTGCACATGGGGCCTTTGCATAGCATGGAAACATTGTTTCTTCAGGTTTGATTCTTGTATTTGCAGCTAGGTCATCAAGAAATATTCTGTTCCCCTGGGTCTAGCCCTGTATTTCAGTGGACTTGATTGAAACATTGTTTTAATTTGGAAATAGAGGAACTGTTGCATTACCTGCATGACGATTTGGTCATTACTTACTTGACTTTCTCATTTCCTTTCCCAAATAAACCTGTGCTTCTCAGATTGTTTTGATGGTGATCATACCTTTGAGGACATAGGACTTGCAGCTGGCCGAAGCCAACGAGAGAAAAAACGTTC... | GGTTGCACATGGGGCCTTTGCATAGCATGGAAACATTGTTTCTTCAGGTTTGATTCTTGTATTTGCAGCTAGGTCATCAAGAAATATTCTGTTCCCCTGGGTCTAGCCCTGTATTTCAGTGGACTTGATTGAAACATTGTTTTAATTTGGAAATAGAGGAACTGTTGCATTACCTGCATGACGATTTGGTCATTACTTACTTGACTTTCTCATTTCCTTTCCCAAATAAACCTGTGCTTCTCAGATTGTTTTGATGGTGATCATACCTTTGAGGACATAGGACTTGCAGCTGGCCGAAGCCAACGAGAGAAAAAACGTTC... |
Task1_train_48628 | Given a variant located on Chromosome 22, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AAACCCTGTCTCTATTAAAAATACAAAAAATTAGCCAGGCTGGTAGTGCACACCTGTAGTCCCGTTACTCGGGAGGGTGAGGCAGGAGAATTGCTTGAACTGGGAGATCGCGCCATTGCACTGCAGCCTGGACAACAGACAGAGACCCCGTCTCAAAAAAAAAAAAAAAAAAAAAAAAGACGCCAAAGTGCCATGATAAGGGAGTGTTTCTATAAACATGACAATACATCTTCTCTTAAGGAAATAGCATAGAGTCATCAAAAATAATAGTTATAACAACTGTATAGCAAGATGGAAAATACTTGTATAACATTACATTT... | AAACCCTGTCTCTATTAAAAATACAAAAAATTAGCCAGGCTGGTAGTGCACACCTGTAGTCCCGTTACTCGGGAGGGTGAGGCAGGAGAATTGCTTGAACTGGGAGATCGCGCCATTGCACTGCAGCCTGGACAACAGACAGAGACCCCGTCTCAAAAAAAAAAAAAAAAAAAAAAAAGACGCCAAAGTGCCATGATAAGGGAGTGTTTCTATAAACATGACAATACATCTTCTCTTAAGGAAATAGCATAGAGTCATCAAAAATAATAGTTATAACAACTGTATAGCAAGATGGAAAATACTTGTATAACATTACATTT... |
Task1_train_48629 | A mutation on Chromosome 22 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TCCTGACCTCAGGTGACCCACCCGCCTCGGTGTCCCAAAGTGCTGAGATTACAGGCGTGAGCCACCGTGCCCGGCCTTGTATCCACATACATTTAGAAGAGAGCTGTTTGTGGATGAATGGAATAGTAAGCCATCAGCCTAGGCCTGCATAGGGGTAGTTTGAACTGTGCTCCTGCTAAAAACACACGGCCACCCCCACCCAGGGCTCCAGGCCAGAGTGGACCTTCTGTCTGTCTGTCTGTCTGCTGCCCACATTGTAATAGCCCAGTGGGTTCATTTTGCCCTCTGCCCAGATAGAGTTGATTTATCAAGACAGGGGA... | TCCTGACCTCAGGTGACCCACCCGCCTCGGTGTCCCAAAGTGCTGAGATTACAGGCGTGAGCCACCGTGCCCGGCCTTGTATCCACATACATTTAGAAGAGAGCTGTTTGTGGATGAATGGAATAGTAAGCCATCAGCCTAGGCCTGCATAGGGGTAGTTTGAACTGTGCTCCTGCTAAAAACACACGGCCACCCCCACCCAGGGCTCCAGGCCAGAGTGGACCTTCTGTCTGTCTGTCTGTCTGCTGCCCACATTGTAATAGCCCAGTGGGTTCATTTTGCCCTCTGCCCAGATAGAGTTGATTTATCAAGACAGGGGA... |
Task1_train_48630 | Given this context: Chromosome 22 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GGTAGTTTGAACTGTGCTCCTGCTAAAAACACACGGCCACCCCCACCCAGGGCTCCAGGCCAGAGTGGACCTTCTGTCTGTCTGTCTGTCTGCTGCCCACATTGTAATAGCCCAGTGGGTTCATTTTGCCCTCTGCCCAGATAGAGTTGATTTATCAAGACAGGGGAATTGCAATAAAGAGTTTAATTCATGCAGAGCCAGATGAATGGGAGACTGGAGTTTTATTATTACTCAAGTCGGTTTCTCCAAAAATTCGAGGACTGGGTTTTTTGTTTTGTTTTTTTGTTTTGTTTTTTTAGATGAACTCTTGCTCTGTCACC... | GGTAGTTTGAACTGTGCTCCTGCTAAAAACACACGGCCACCCCCACCCAGGGCTCCAGGCCAGAGTGGACCTTCTGTCTGTCTGTCTGTCTGCTGCCCACATTGTAATAGCCCAGTGGGTTCATTTTGCCCTCTGCCCAGATAGAGTTGATTTATCAAGACAGGGGAATTGCAATAAAGAGTTTAATTCATGCAGAGCCAGATGAATGGGAGACTGGAGTTTTATTATTACTCAAGTCGGTTTCTCCAAAAATTCGAGGACTGGGTTTTTTGTTTTGTTTTTTTGTTTTGTTTTTTTAGATGAACTCTTGCTCTGTCACC... |
Task1_train_48631 | Consider a variant on Chromosome 22. Determine its clinical classification and disease relevance. | Benign | TGTGTAAAAGCTATCCAGGGCATCAAGGATCTTCATGCCTACCAGATGGCCAAATCCAACTCTGGCTTCATGGCTATGGTCAAGAATTTTGTGGCCAAGAGACACATCCCTTTCTGGACGGCTAGAGGGGTGCAGAGAGCCTTTGAGGGCACAACTCTGGCCATGACCAATGGTGCCTGGGTGATGGGTGCTGCTGGGGCTGGCTTCTTACTTATGAAAGACATGAGCAGCTTCCTGCAGAGCTGGAAGCACCTGGAGGATGGGGCAAGGACGGAGACAGCAGAGGAACTGAGAGCACTTGCTAAGAAGCTGGAGCAGGA... | TGTGTAAAAGCTATCCAGGGCATCAAGGATCTTCATGCCTACCAGATGGCCAAATCCAACTCTGGCTTCATGGCTATGGTCAAGAATTTTGTGGCCAAGAGACACATCCCTTTCTGGACGGCTAGAGGGGTGCAGAGAGCCTTTGAGGGCACAACTCTGGCCATGACCAATGGTGCCTGGGTGATGGGTGCTGCTGGGGCTGGCTTCTTACTTATGAAAGACATGAGCAGCTTCCTGCAGAGCTGGAAGCACCTGGAGGATGGGGCAAGGACGGAGACAGCAGAGGAACTGAGAGCACTTGCTAAGAAGCTGGAGCAGGA... |
Task1_train_48632 | A variant on Chromosome 22 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GCAAGCAGGAAGCTCAGGATTTGACTCAAGGCCAGCGTTCCCTTGCCATTACTTTGAAGACTCCATATATTTTGAAAATGCCTGTGGTTCCTGCATTCTCCACTGTAGTATACCTGTGGGATTTTAAACATTTTATTGAAAAAGAATATTTCAACCCTACACCATTGAATAAACTACCATGCACAGAGGATTCCTCCTGCTGCTCATGGGCGCTCTCAGATGGGCAGTGGAGGGGGTTCTTTAGGCGGGCAGGGGAGCAAGACCCTCAGCACTGATCCCTGTGGCCCTTCTGTGTTACCTCTGTCCTCTGCAGGCTGGTC... | GCAAGCAGGAAGCTCAGGATTTGACTCAAGGCCAGCGTTCCCTTGCCATTACTTTGAAGACTCCATATATTTTGAAAATGCCTGTGGTTCCTGCATTCTCCACTGTAGTATACCTGTGGGATTTTAAACATTTTATTGAAAAAGAATATTTCAACCCTACACCATTGAATAAACTACCATGCACAGAGGATTCCTCCTGCTGCTCATGGGCGCTCTCAGATGGGCAGTGGAGGGGGTTCTTTAGGCGGGCAGGGGAGCAAGACCCTCAGCACTGATCCCTGTGGCCCTTCTGTGTTACCTCTGTCCTCTGCAGGCTGGTC... |
Task1_train_48633 | A mutation found on Chromosome 22 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AGAATCACTTGAACCCAGGAGGCGGAGGGTGCAGTGAGCCGATGGTGCTACTTGCACTCCAGCCTGGGCGACAGAGCAAGACTCCGTCAGAAAAAAAAGACTAATGAATGCGATGCCTCCCTTAAAGAAATGAGGAGGAAAAGAAGCTGCACAGAATCAAAGACCCTTCGAGGCCACGACACAGAGGTGAGAAACACAGGGCTCCATGAAGTGAAATCTGAATAGCAGGTGTGAGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTGAATTTGTGAGTGTGTGTGTGGCATATGCAAGGTTTGCCTTTTATTTGGTTGCCAG... | AGAATCACTTGAACCCAGGAGGCGGAGGGTGCAGTGAGCCGATGGTGCTACTTGCACTCCAGCCTGGGCGACAGAGCAAGACTCCGTCAGAAAAAAAAGACTAATGAATGCGATGCCTCCCTTAAAGAAATGAGGAGGAAAAGAAGCTGCACAGAATCAAAGACCCTTCGAGGCCACGACACAGAGGTGAGAAACACAGGGCTCCATGAAGTGAAATCTGAATAGCAGGTGTGAGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTGAATTTGTGAGTGTGTGTGTGGCATATGCAAGGTTTGCCTTTTATTTGGTTGCCAG... |
Task1_train_48634 | This alteration on Chromosome 22 may affect genome function. Does it lead to a disease or is it benign? | Benign | GAATGACTTAAACAAGTCCAGCTTGGCGAGTAGCTAAGTTTATTAGGACTTACACACAGGGCACTCAGCAAGACAGCTCGAGAGATCCAGCCTCCCCCAATGTCTAAACTGCTTTTCAGTTAATTTTCTGGCTCTTTGTCTACTATATATGAGCAACGAGACTTTTACTTGGTTGGTTCTCAGATACTCTCCAGGATGTTTGGATTCTCAGAGACACCTGGTCCTCAGCTGGGCACCATGGAAATGGCTCATTACCCGGCCTTCAGGGTTCAAGCAGGGGACATGCACCCTTAAATAACCTAAAGGGGACCTGTCACACT... | GAATGACTTAAACAAGTCCAGCTTGGCGAGTAGCTAAGTTTATTAGGACTTACACACAGGGCACTCAGCAAGACAGCTCGAGAGATCCAGCCTCCCCCAATGTCTAAACTGCTTTTCAGTTAATTTTCTGGCTCTTTGTCTACTATATATGAGCAACGAGACTTTTACTTGGTTGGTTCTCAGATACTCTCCAGGATGTTTGGATTCTCAGAGACACCTGGTCCTCAGCTGGGCACCATGGAAATGGCTCATTACCCGGCCTTCAGGGTTCAAGCAGGGGACATGCACCCTTAAATAACCTAAAGGGGACCTGTCACACT... |
Task1_train_48635 | Here is a mutation located on Chromosome 22. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CTTGGCGAGTAGCTAAGTTTATTAGGACTTACACACAGGGCACTCAGCAAGACAGCTCGAGAGATCCAGCCTCCCCCAATGTCTAAACTGCTTTTCAGTTAATTTTCTGGCTCTTTGTCTACTATATATGAGCAACGAGACTTTTACTTGGTTGGTTCTCAGATACTCTCCAGGATGTTTGGATTCTCAGAGACACCTGGTCCTCAGCTGGGCACCATGGAAATGGCTCATTACCCGGCCTTCAGGGTTCAAGCAGGGGACATGCACCCTTAAATAACCTAAAGGGGACCTGTCACACTACAACCACCACCACCATCATC... | CTTGGCGAGTAGCTAAGTTTATTAGGACTTACACACAGGGCACTCAGCAAGACAGCTCGAGAGATCCAGCCTCCCCCAATGTCTAAACTGCTTTTCAGTTAATTTTCTGGCTCTTTGTCTACTATATATGAGCAACGAGACTTTTACTTGGTTGGTTCTCAGATACTCTCCAGGATGTTTGGATTCTCAGAGACACCTGGTCCTCAGCTGGGCACCATGGAAATGGCTCATTACCCGGCCTTCAGGGTTCAAGCAGGGGACATGCACCCTTAAATAACCTAAAGGGGACCTGTCACACTACAACCACCACCACCATCATC... |
Task1_train_48636 | Given this context: Chromosome 22 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CCTGTCACACTACAACCACCACCACCATCATCAAGAAGCCACTGGCTGACTCAGATACACCCCCGGGAGGACAAGGGAGAGTGGATGCTGGTAAGACAGGGTGAGAGACCATCACCAGGGAAGGATTCCATTCTTGGAAGGACATCCAACCGGGGGGCGGGTCTTTAGTGGAGCCGCTGTTTCTTCTCCTGTATCCAACAGTTCTAACTGTGGCTTTCTCCATTTTCAGCTCTTTCTTTTCCTGGTCTTCTCATTGCTTGTTCCTACGTGCCTCCCTCTCTTCCTCCCCCAATATACTCTTTAGTCTAGAGTAAACTGCT... | CCTGTCACACTACAACCACCACCACCATCATCAAGAAGCCACTGGCTGACTCAGATACACCCCCGGGAGGACAAGGGAGAGTGGATGCTGGTAAGACAGGGTGAGAGACCATCACCAGGGAAGGATTCCATTCTTGGAAGGACATCCAACCGGGGGGCGGGTCTTTAGTGGAGCCGCTGTTTCTTCTCCTGTATCCAACAGTTCTAACTGTGGCTTTCTCCATTTTCAGCTCTTTCTTTTCCTGGTCTTCTCATTGCTTGTTCCTACGTGCCTCCCTCTCTTCCTCCCCCAATATACTCTTTAGTCTAGAGTAAACTGCT... |
Task1_train_48637 | This variant is present on Chromosome 22. Is the change likely to result in a pathogenic outcome? | Benign | TCCAACAGTTCTAACTGTGGCTTTCTCCATTTTCAGCTCTTTCTTTTCCTGGTCTTCTCATTGCTTGTTCCTACGTGCCTCCCTCTCTTCCTCCCCCAATATACTCTTTAGTCTAGAGTAAACTGCTTCTTTCCATTCCCCACACTCTCCAGTCCCCTCTCCTCCCTTATTCCAGGCCCCAGCATTTCTGCCTTCTCCTTGGCGCACTTGCCATCTTGAGTAACCCCTCCCCTGCTGTGCTCAGCTACAGATGCCAAAGTTCCTAACACTGAGTTCCATAAACTTTACCTCGCCCTCTTTATTCCCCTAAAAAATGTCTG... | TCCAACAGTTCTAACTGTGGCTTTCTCCATTTTCAGCTCTTTCTTTTCCTGGTCTTCTCATTGCTTGTTCCTACGTGCCTCCCTCTCTTCCTCCCCCAATATACTCTTTAGTCTAGAGTAAACTGCTTCTTTCCATTCCCCACACTCTCCAGTCCCCTCTCCTCCCTTATTCCAGGCCCCAGCATTTCTGCCTTCTCCTTGGCGCACTTGCCATCTTGAGTAACCCCTCCCCTGCTGTGCTCAGCTACAGATGCCAAAGTTCCTAACACTGAGTTCCATAAACTTTACCTCGCCCTCTTTATTCCCCTAAAAAATGTCTG... |
Task1_train_48638 | A mutation on Chromosome 22 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CCGTCGCCACATTCGGCTAATTTTTTGTATTTTCAGTAGAGAAGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCATGATCAGCCCGTCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCGGTCGCGCCGGGCCTGTGATGTGCAGGGCTTCTGACATGTGTCTCATTCAATGATCACACACAGCCCGGGAGATGGGTACCACTTTCCCATTTGAACACAGAGGAATCCACAAAAGTTAGGGAACTTGCCAGTGTTTTCTATTGCTAGAGCCAGGACTTCTGCTTCAACCTCATGTCTTCAA... | CCGTCGCCACATTCGGCTAATTTTTTGTATTTTCAGTAGAGAAGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCATGATCAGCCCGTCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCGGTCGCGCCGGGCCTGTGATGTGCAGGGCTTCTGACATGTGTCTCATTCAATGATCACACACAGCCCGGGAGATGGGTACCACTTTCCCATTTGAACACAGAGGAATCCACAAAAGTTAGGGAACTTGCCAGTGTTTTCTATTGCTAGAGCCAGGACTTCTGCTTCAACCTCATGTCTTCAA... |
Task1_train_48639 | A mutation is present on Chromosome 22. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CATTCGGCTAATTTTTTGTATTTTCAGTAGAGAAGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCATGATCAGCCCGTCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCGGTCGCGCCGGGCCTGTGATGTGCAGGGCTTCTGACATGTGTCTCATTCAATGATCACACACAGCCCGGGAGATGGGTACCACTTTCCCATTTGAACACAGAGGAATCCACAAAAGTTAGGGAACTTGCCAGTGTTTTCTATTGCTAGAGCCAGGACTTCTGCTTCAACCTCATGTCTTCAATGACTGTGC... | CATTCGGCTAATTTTTTGTATTTTCAGTAGAGAAGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCATGATCAGCCCGTCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCGGTCGCGCCGGGCCTGTGATGTGCAGGGCTTCTGACATGTGTCTCATTCAATGATCACACACAGCCCGGGAGATGGGTACCACTTTCCCATTTGAACACAGAGGAATCCACAAAAGTTAGGGAACTTGCCAGTGTTTTCTATTGCTAGAGCCAGGACTTCTGCTTCAACCTCATGTCTTCAATGACTGTGC... |
Task1_train_48640 | Here’s a variant located on Chromosome 22. What is the predicted biological effect — harmless or disease-causing? | Benign | GACCTGAGATATCACCTTTTCCAGCCCCCTTCTACAGCTGATGAGGAAACTGAGGCTCAGAGGGGTGAAGTCTCATGACCACAAGCAGGGTTGAACTCCTGGACACACCTCAAGCTTCCTTGACCTGTTCCTGGCATCTCCTTTCATTTTTCCTTTCTTCCCAAATTAACCTCTTTCCAACACAGCACTTCAAGTTCCCCTGGAACTTCATCGGTCCATCGGTGTCCCCTGGTCTGGAAGAGCACCGACCACTTGCCAAGGCCCCCACCACTCTGCTGCCATCACAACCACCATCACCACCATTACGAGAAAAACTTGAG... | GACCTGAGATATCACCTTTTCCAGCCCCCTTCTACAGCTGATGAGGAAACTGAGGCTCAGAGGGGTGAAGTCTCATGACCACAAGCAGGGTTGAACTCCTGGACACACCTCAAGCTTCCTTGACCTGTTCCTGGCATCTCCTTTCATTTTTCCTTTCTTCCCAAATTAACCTCTTTCCAACACAGCACTTCAAGTTCCCCTGGAACTTCATCGGTCCATCGGTGTCCCCTGGTCTGGAAGAGCACCGACCACTTGCCAAGGCCCCCACCACTCTGCTGCCATCACAACCACCATCACCACCATTACGAGAAAAACTTGAG... |
Task1_train_48641 | A mutation found on Chromosome 22 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CCAGGCTTCATCATCAGTCAGCAGTTGTAGCAGATTCTCTCTGCTCACTTGGTCCTGGAAATACTTAAGGTAATCCTCAATAAAGATACTGCTCTCTAGTTGGAAAGAAGAAAGGATAAGGTTGGAGGATAGTGTAGGGGAGCATAACAGCCATTGCACATTAGGTGGTTACATGTTAATTTTTCCTGGACAACTGTGATGTGGGACATGTTTGATGGAGTCATCAGTGCTATAGAGGGATTGTGTGCCCCCAAAATTCATATGCTGAAGCCCTAAACTCGAGTGACTATATTTGAAGATTGGGCCTTTAAGGAAGCAAT... | CCAGGCTTCATCATCAGTCAGCAGTTGTAGCAGATTCTCTCTGCTCACTTGGTCCTGGAAATACTTAAGGTAATCCTCAATAAAGATACTGCTCTCTAGTTGGAAAGAAGAAAGGATAAGGTTGGAGGATAGTGTAGGGGAGCATAACAGCCATTGCACATTAGGTGGTTACATGTTAATTTTTCCTGGACAACTGTGATGTGGGACATGTTTGATGGAGTCATCAGTGCTATAGAGGGATTGTGTGCCCCCAAAATTCATATGCTGAAGCCCTAAACTCGAGTGACTATATTTGAAGATTGGGCCTTTAAGGAAGCAAT... |
Task1_train_48642 | A variant has been detected on Chromosome 22. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CAGAACTGGCTGAAGAAATGACAACTGAATAAAGAGGGGTGAAGGGAGCTGTGAACCACAGCAATGCCAAGAGGGCATCCAGCCAGGCAGAGTGGTCTACTAGGCAGAGCCTCAGAGAGGGGAGGAGTTCACCAGGCCCACGTGCCATATGGGATTCATGCCAGCCTTGAGTCTACACCAGTGAAAAAAATCAGAGAGTTCATGACTGAAGCAATATGCCCCAGAAATAATATCTTTGTATTCTGACACTTCAGTGGGTTCCCATTCAATCACCCTACAGGGAAGACTGCCAGTAGACCTGCCCCCCACCCCGTTCAATA... | CAGAACTGGCTGAAGAAATGACAACTGAATAAAGAGGGGTGAAGGGAGCTGTGAACCACAGCAATGCCAAGAGGGCATCCAGCCAGGCAGAGTGGTCTACTAGGCAGAGCCTCAGAGAGGGGAGGAGTTCACCAGGCCCACGTGCCATATGGGATTCATGCCAGCCTTGAGTCTACACCAGTGAAAAAAATCAGAGAGTTCATGACTGAAGCAATATGCCCCAGAAATAATATCTTTGTATTCTGACACTTCAGTGGGTTCCCATTCAATCACCCTACAGGGAAGACTGCCAGTAGACCTGCCCCCCACCCCGTTCAATA... |
Task1_train_48643 | A genetic alteration is present on Chromosome 22. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | CTGGGGCAGTGGCCAGAACCAGTAGCCTTCAGCCAGGTGAAAGGGCATGAGGCATTGGAAGGGAGCAGATGCCAGGCAAAGTGAACTCCTGTCTCTCCGGGGTTTTGTTTTTGTTTGAATTCAAAGTACTCAGAGATAGCCAGACTGCAATGTCTGAGGGCACCCTTACCTTTGACACCACCTGCAAATTTAAGGGGATTTCTAAATCCATCCTTTGATTTTGTAATTCACTGGAAGGACTCACATAACTCACTGAAAACTGCTATTTCACAATTGTGGTTGATCACACGGAAAGAACACAGATTAAAATCAGCCTAAGA... | CTGGGGCAGTGGCCAGAACCAGTAGCCTTCAGCCAGGTGAAAGGGCATGAGGCATTGGAAGGGAGCAGATGCCAGGCAAAGTGAACTCCTGTCTCTCCGGGGTTTTGTTTTTGTTTGAATTCAAAGTACTCAGAGATAGCCAGACTGCAATGTCTGAGGGCACCCTTACCTTTGACACCACCTGCAAATTTAAGGGGATTTCTAAATCCATCCTTTGATTTTGTAATTCACTGGAAGGACTCACATAACTCACTGAAAACTGCTATTTCACAATTGTGGTTGATCACACGGAAAGAACACAGATTAAAATCAGCCTAAGA... |
Task1_train_48644 | The following genetic variant occurs on Chromosome 22. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GGACTCACATAACTCACTGAAAACTGCTATTTCACAATTGTGGTTGATCACACGGAAAGAACACAGATTAAAATCAGCCTAAGAAAGAGACACACGGGGCAGAGTTTGGGAGGGTTTTAAGTGTGAAGCTTCATTGTCCTCAGGACGCTGTGTTCTCCTGTGTGAATGTGGGACAAAACACATGCGGTGTTGCCAACCAGGGAAGCTCACCCAGTTAAGGAAAAATTCCTGTGAATCACATTAAACCAGAAATGAAGCCTTTTTTCAGGATTGTTGTTACAGGGGAGGGAGACTGAGCCCAGCTCCAAATATAGTAAAGA... | GGACTCACATAACTCACTGAAAACTGCTATTTCACAATTGTGGTTGATCACACGGAAAGAACACAGATTAAAATCAGCCTAAGAAAGAGACACACGGGGCAGAGTTTGGGAGGGTTTTAAGTGTGAAGCTTCATTGTCCTCAGGACGCTGTGTTCTCCTGTGTGAATGTGGGACAAAACACATGCGGTGTTGCCAACCAGGGAAGCTCACCCAGTTAAGGAAAAATTCCTGTGAATCACATTAAACCAGAAATGAAGCCTTTTTTCAGGATTGTTGTTACAGGGGAGGGAGACTGAGCCCAGCTCCAAATATAGTAAAGA... |
Task1_train_48645 | With a mutation on Chromosome 22, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | AAGAAAGAGACACACGGGGCAGAGTTTGGGAGGGTTTTAAGTGTGAAGCTTCATTGTCCTCAGGACGCTGTGTTCTCCTGTGTGAATGTGGGACAAAACACATGCGGTGTTGCCAACCAGGGAAGCTCACCCAGTTAAGGAAAAATTCCTGTGAATCACATTAAACCAGAAATGAAGCCTTTTTTCAGGATTGTTGTTACAGGGGAGGGAGACTGAGCCCAGCTCCAAATATAGTAAAGACAGAGGGGGAGTCACAGCCAACACCAGGGTGGGGGCGGGAGATGGAACAGGACTGATAGGAGACACCAGAGTGGGGGGTT... | AAGAAAGAGACACACGGGGCAGAGTTTGGGAGGGTTTTAAGTGTGAAGCTTCATTGTCCTCAGGACGCTGTGTTCTCCTGTGTGAATGTGGGACAAAACACATGCGGTGTTGCCAACCAGGGAAGCTCACCCAGTTAAGGAAAAATTCCTGTGAATCACATTAAACCAGAAATGAAGCCTTTTTTCAGGATTGTTGTTACAGGGGAGGGAGACTGAGCCCAGCTCCAAATATAGTAAAGACAGAGGGGGAGTCACAGCCAACACCAGGGTGGGGGCGGGAGATGGAACAGGACTGATAGGAGACACCAGAGTGGGGGGTT... |
Task1_train_48646 | A mutation on Chromosome 22 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | ACACCAGGGTGGGGGCGGGAGATGGAACAGGACTGATAGGAGACACCAGAGTGGGGGGTTCCTGCTAAATTGGCCTAACAGGATTCTCACTAAAGGCAGGTCAGACACTCACCCATCAATGGTGGGGGTGAAGAGCATAATCAGATAGCAAAGCGTAATCAGACAGCAAGGGGGGAAGACCCTCCCTAAACTGACTTGGGGAGATTCTTGCTGAGCTGGGTGGTGCAGGTCCAGCAAGCAGTGGGTGGCTGTGGAAGGCCAAGGTCGGCGCCTAGTGGAGAAGAGGCTCAGAAGAGCCCAGCTGGAGTTGGTCAAGGAGA... | ACACCAGGGTGGGGGCGGGAGATGGAACAGGACTGATAGGAGACACCAGAGTGGGGGGTTCCTGCTAAATTGGCCTAACAGGATTCTCACTAAAGGCAGGTCAGACACTCACCCATCAATGGTGGGGGTGAAGAGCATAATCAGATAGCAAAGCGTAATCAGACAGCAAGGGGGGAAGACCCTCCCTAAACTGACTTGGGGAGATTCTTGCTGAGCTGGGTGGTGCAGGTCCAGCAAGCAGTGGGTGGCTGTGGAAGGCCAAGGTCGGCGCCTAGTGGAGAAGAGGCTCAGAAGAGCCCAGCTGGAGTTGGTCAAGGAGA... |
Task1_train_48647 | A variant on Chromosome 22 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TGAAGAGCATAATCAGATAGCAAAGCGTAATCAGACAGCAAGGGGGGAAGACCCTCCCTAAACTGACTTGGGGAGATTCTTGCTGAGCTGGGTGGTGCAGGTCCAGCAAGCAGTGGGTGGCTGTGGAAGGCCAAGGTCGGCGCCTAGTGGAGAAGAGGCTCAGAAGAGCCCAGCTGGAGTTGGTCAAGGAGAAAGTCCTTCTTTCTCAACCCATGCCTTAGTGTCCAGAGTATCTGCTGGGGCTGGATCACAAGCTGCCCTCATGGCTGACCTGGAGTCTCCAGCCCCTCCCTGAGGTCTAACCCCTTTAGTCCCCGGGT... | TGAAGAGCATAATCAGATAGCAAAGCGTAATCAGACAGCAAGGGGGGAAGACCCTCCCTAAACTGACTTGGGGAGATTCTTGCTGAGCTGGGTGGTGCAGGTCCAGCAAGCAGTGGGTGGCTGTGGAAGGCCAAGGTCGGCGCCTAGTGGAGAAGAGGCTCAGAAGAGCCCAGCTGGAGTTGGTCAAGGAGAAAGTCCTTCTTTCTCAACCCATGCCTTAGTGTCCAGAGTATCTGCTGGGGCTGGATCACAAGCTGCCCTCATGGCTGACCTGGAGTCTCCAGCCCCTCCCTGAGGTCTAACCCCTTTAGTCCCCGGGT... |
Task1_train_48648 | A mutation has occurred on Chromosome 22. What is the medical relevance of this mutation? | Benign | CTCCCTGTTCTGGGTAAGCCAGAGCTTGGAGTCAGCTCTGGAGGCCACAGGCAGATGGCTACACCCTGGACGCACTCGCAGCCGGCACATCACGCTGCAGGGCACCCTCCAGACCTGGGAAACACTTCAGGACGGGCTCAGGTGCGACGGGCAGGGCGGCCGAGGGGACGCTCAGACCCCTTCTCACCAGGCAGCATTCACAGCAGGAGGTGGTGGTGGCCACAAAGCCTCATCTCATGTGAGGGATGCCAGTTTCACACACACACACACTCTGATCATACGAGGGAGCCCCGCTATGAAACGGAACCCTGGAGGGAATC... | CTCCCTGTTCTGGGTAAGCCAGAGCTTGGAGTCAGCTCTGGAGGCCACAGGCAGATGGCTACACCCTGGACGCACTCGCAGCCGGCACATCACGCTGCAGGGCACCCTCCAGACCTGGGAAACACTTCAGGACGGGCTCAGGTGCGACGGGCAGGGCGGCCGAGGGGACGCTCAGACCCCTTCTCACCAGGCAGCATTCACAGCAGGAGGTGGTGGTGGCCACAAAGCCTCATCTCATGTGAGGGATGCCAGTTTCACACACACACACACTCTGATCATACGAGGGAGCCCCGCTATGAAACGGAACCCTGGAGGGAATC... |
Task1_train_48649 | Chromosome 22 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CAAACAAACAAACAAACAATGAAGTCAGGCCAGGCACAGTGGCTCACGCCTGTAATCCTAGCACTTTGGGAGGCCGATGGAAAGGAGGGTCTGGACAGGCACACCAGCTTCTCCTTTGTCTTTCTGCACCCTGGTCAGAAGACAAGTGAAAGACTGGATGCTGCTTTGATACCAAACCTCCCGAGGTAGTCGGCAGCAATGTTTAAAATCTAGGCTTCATAAAATAGCCCTTCAAAATACAATGATAAATAACTTAAGCAACTAACATTTTATTGAGCACATAATACATGCCAAGTACTTTCTTTATTTTAAGAGATAGG... | CAAACAAACAAACAAACAATGAAGTCAGGCCAGGCACAGTGGCTCACGCCTGTAATCCTAGCACTTTGGGAGGCCGATGGAAAGGAGGGTCTGGACAGGCACACCAGCTTCTCCTTTGTCTTTCTGCACCCTGGTCAGAAGACAAGTGAAAGACTGGATGCTGCTTTGATACCAAACCTCCCGAGGTAGTCGGCAGCAATGTTTAAAATCTAGGCTTCATAAAATAGCCCTTCAAAATACAATGATAAATAACTTAAGCAACTAACATTTTATTGAGCACATAATACATGCCAAGTACTTTCTTTATTTTAAGAGATAGG... |
Task1_train_48650 | This mutation occurs on Chromosome 22. Does this change lead to a known medical condition, or is it benign? | Benign | ATGGAGATCTTGCACTGTCGCCTGGGCTGGAGTCCACAATGGCGCGATCTCGGCTCACTGCAACCTCCACCTCCCAGGTTCAGGCGATTCTCTTGCCTCAGCCTCCCGAGTAGCTGGGATTACCGGCACGTGCCACCATGCCTGGCTAATTTTTTGTATTTTTGGTAGAGACGGGGTTTCGCTACATTGGTCAGGCTGGTCTTGAACTCCTAACCTTGTGATCCGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGCATGAGCTACTGTGACCAGCCATCTCTTTTTTTTTTTGAGACAGGGTCTCACTCTGTTGCC... | ATGGAGATCTTGCACTGTCGCCTGGGCTGGAGTCCACAATGGCGCGATCTCGGCTCACTGCAACCTCCACCTCCCAGGTTCAGGCGATTCTCTTGCCTCAGCCTCCCGAGTAGCTGGGATTACCGGCACGTGCCACCATGCCTGGCTAATTTTTTGTATTTTTGGTAGAGACGGGGTTTCGCTACATTGGTCAGGCTGGTCTTGAACTCCTAACCTTGTGATCCGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGCATGAGCTACTGTGACCAGCCATCTCTTTTTTTTTTTGAGACAGGGTCTCACTCTGTTGCC... |
Task1_train_48651 | Chromosome 22 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GCCAGCAGCACTGCTAAATTGCACCAATCACATGGCTCTCCAGATATTTGCTCCTGAGGGGTGAAATCGCAACCACTTGTGTAATATGGGACAACAGTACATACCTTGCCCACAGCAGTAAAAGCTGCTGATGAAGAGTGTGAACTCAGAGTCAGCCTGTTTGGGCCATTTCCTAGCTCTGTTTTTCACTAGCTTTGTGGACCTTTGGAAACTTGCTCAAACTTGCGGTTTCCTTTTCTGTAAATGTTTCTTCATCGGCTTCCTGGAAAGGGTAAAGGAGGTGGTAGATGGCCAGGGCTCGCCCCAGAGCCTGGGTGTGC... | GCCAGCAGCACTGCTAAATTGCACCAATCACATGGCTCTCCAGATATTTGCTCCTGAGGGGTGAAATCGCAACCACTTGTGTAATATGGGACAACAGTACATACCTTGCCCACAGCAGTAAAAGCTGCTGATGAAGAGTGTGAACTCAGAGTCAGCCTGTTTGGGCCATTTCCTAGCTCTGTTTTTCACTAGCTTTGTGGACCTTTGGAAACTTGCTCAAACTTGCGGTTTCCTTTTCTGTAAATGTTTCTTCATCGGCTTCCTGGAAAGGGTAAAGGAGGTGGTAGATGGCCAGGGCTCGCCCCAGAGCCTGGGTGTGC... |
Task1_train_48652 | A variant has been detected on Chromosome 22. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TCCCCCTCCATGACAGCCTCGGGGGCTGGGAGTGCAGTGACCCATGAGGGACGCCTGTCCTGGCTGTGGGTGAGGAGGGGCGGTTCCCCTGCTGTGTGTCTGCCGTTCTGGGTTGATGGTTCCTGACATGCTCTAGCATGCCATAACCCATGTCCAGCAGAGAGCACTTACATCCTATGTGTGAGGATGTTTTCGTTTGAAAGCCATCCCTCAGCAAGCAGACACCAGAAACCAGAAATCAGGTGCCGTGTCTTCATTCTGCATTTTCTTGAACAACCCAGAGTTCCCAGGAGATAGATGCTTGCCTTGTGGCTGCAAGG... | TCCCCCTCCATGACAGCCTCGGGGGCTGGGAGTGCAGTGACCCATGAGGGACGCCTGTCCTGGCTGTGGGTGAGGAGGGGCGGTTCCCCTGCTGTGTGTCTGCCGTTCTGGGTTGATGGTTCCTGACATGCTCTAGCATGCCATAACCCATGTCCAGCAGAGAGCACTTACATCCTATGTGTGAGGATGTTTTCGTTTGAAAGCCATCCCTCAGCAAGCAGACACCAGAAACCAGAAATCAGGTGCCGTGTCTTCATTCTGCATTTTCTTGAACAACCCAGAGTTCCCAGGAGATAGATGCTTGCCTTGTGGCTGCAAGG... |
Task1_train_48653 | A genomic change on Chromosome 22 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TGGGGGCTTCTCTGTTCCTGCCTCTCTTGTCTCTGTCCCCACCTCCTCCTTCCCTTCCTGTGGGCTTTGGGTGGTAGGGATGTAGGTGGACTGGGCTTTGGGAGCTTTGGGAGTGGGGCCAGCACTTGGAAATTCATTCCCGGGATTCCCTGGAGTGCCCACACCTGGCCCTGCCTGCCAGAGCTCTGCATGGAGCCCAGTGGAGAGAACTGAGTGTGGGGATGCCTGGGACAGGGTGGGCTCACAGAGGGGGTTCCTGCTACCAGGATGGATGGGGTGTCAGGAGGCAGAAGGGCTCCCCAAGGACAAGATACCTGGGC... | TGGGGGCTTCTCTGTTCCTGCCTCTCTTGTCTCTGTCCCCACCTCCTCCTTCCCTTCCTGTGGGCTTTGGGTGGTAGGGATGTAGGTGGACTGGGCTTTGGGAGCTTTGGGAGTGGGGCCAGCACTTGGAAATTCATTCCCGGGATTCCCTGGAGTGCCCACACCTGGCCCTGCCTGCCAGAGCTCTGCATGGAGCCCAGTGGAGAGAACTGAGTGTGGGGATGCCTGGGACAGGGTGGGCTCACAGAGGGGGTTCCTGCTACCAGGATGGATGGGGTGTCAGGAGGCAGAAGGGCTCCCCAAGGACAAGATACCTGGGC... |
Task1_train_48654 | This genomic variant is located on Chromosome 22. Can you determine its pathogenicity and name any linked disease? | Benign | CAACCTATTCACAGGGCTGGGGAGCTGGGGTATACAAAGGCCCCAGCCCCAACTCCTCTCATCATCTGCACTGCTGTGGGTGGGGGGCATCAAGTTAATGATCATAAAACCTCTTCCAAGCATTGAGCATCTGCTACCTGCAACATTGGGACGGGGGGTCTCTATAGGGTGCCACTCTTCCCACCATTTTATAAATGAGGAAAGCGGGCCTCAGGAGACCAAAGATCACCCAGTTCACATGGCTGGCAGGGCACAGAGCCCTGGCTTGCCTCCTACAACTGAGGCACCACACAGGGCAGCTCTGGGTGGGTGCTTAACTT... | CAACCTATTCACAGGGCTGGGGAGCTGGGGTATACAAAGGCCCCAGCCCCAACTCCTCTCATCATCTGCACTGCTGTGGGTGGGGGGCATCAAGTTAATGATCATAAAACCTCTTCCAAGCATTGAGCATCTGCTACCTGCAACATTGGGACGGGGGGTCTCTATAGGGTGCCACTCTTCCCACCATTTTATAAATGAGGAAAGCGGGCCTCAGGAGACCAAAGATCACCCAGTTCACATGGCTGGCAGGGCACAGAGCCCTGGCTTGCCTCCTACAACTGAGGCACCACACAGGGCAGCTCTGGGTGGGTGCTTAACTT... |
Task1_train_48655 | A genomic variant on Chromosome 22 is under review. What is the biological outcome — benign or pathogenic? | Benign | TGTCAAGGTTGGGCCTCACACAGGGGATAAGTGAGGGCTGATCTGCAGCCCATACTCCACACACCCAGCCATGTGCCCTGGTGGGGGCTCAGCCTCTGCCTGGCAGAAGGGGCCCTTTCCTCTCACCTGCACAACGGTGGCTTCCCAGCACAAAGGGCTTAAAGTGTTTGGGAAGTTTACACCCAGGAAGGCTGTGGGCTGGCCTGGCATAGTGGGCTGGCGAGCTGGTGCACTGTCTCTGGTATGCAGGAAAGATAGAGAGGAGAGGGAGGGAGGTGCGAAGTCACTGTTGCTGCTGCTAGAAGGGCCAGAGAGAGCCC... | TGTCAAGGTTGGGCCTCACACAGGGGATAAGTGAGGGCTGATCTGCAGCCCATACTCCACACACCCAGCCATGTGCCCTGGTGGGGGCTCAGCCTCTGCCTGGCAGAAGGGGCCCTTTCCTCTCACCTGCACAACGGTGGCTTCCCAGCACAAAGGGCTTAAAGTGTTTGGGAAGTTTACACCCAGGAAGGCTGTGGGCTGGCCTGGCATAGTGGGCTGGCGAGCTGGTGCACTGTCTCTGGTATGCAGGAAAGATAGAGAGGAGAGGGAGGGAGGTGCGAAGTCACTGTTGCTGCTGCTAGAAGGGCCAGAGAGAGCCC... |
Task1_train_48656 | Mutation context: Chromosome 22. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CTGGCTCTACCGCCCAGGCTGGAGTGCAGTGGCACAATCATGGCTCACTGCAGCCTCAACCTCCTGGGCTCAGGTGACCCTCCCCGCTCAGCCTGACCTTGCCTTTAAAGGCCACTGCATGAGGTGGGGAAGGAGATTTGACTTCCACTTGCCTCGGTGACTTTGTCTGTTAAGCAGAACCATAATACTGGCCCTTCCCCTCCTGTGCTTTGGGCAGTGACTCTCCCTAGCTCATTGGGAACCCTGGTTGCCCAAACAGCTCTCAATCCAACACTAGAGGTGTGGGGGGTCACTGTGGAATGTTGGGGGGCAGGCCCCAG... | CTGGCTCTACCGCCCAGGCTGGAGTGCAGTGGCACAATCATGGCTCACTGCAGCCTCAACCTCCTGGGCTCAGGTGACCCTCCCCGCTCAGCCTGACCTTGCCTTTAAAGGCCACTGCATGAGGTGGGGAAGGAGATTTGACTTCCACTTGCCTCGGTGACTTTGTCTGTTAAGCAGAACCATAATACTGGCCCTTCCCCTCCTGTGCTTTGGGCAGTGACTCTCCCTAGCTCATTGGGAACCCTGGTTGCCCAAACAGCTCTCAATCCAACACTAGAGGTGTGGGGGGTCACTGTGGAATGTTGGGGGGCAGGCCCCAG... |
Task1_train_48657 | Mutation context: Chromosome 22. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CTACAGGCGTGAGCCACCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGAAGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTTGTGATCTGCCTGCCTCGGCCTCCCAAAATGCTAGGATTACAGGCGTGAGCCACCGGCTGTTTTTTGGTTTTCTATCGTTTTATTTTTTTAAAATAGAGATGGGGGCCAGGCGCAGTGGCTCGCACCTGTAATCCCAGCACTTTGGGAGGCCAAAGTAGGAGGATCACTTGAGCTCAGGAGTTCAAAACCAGCCTGGCCAACGTGGTGAAACCCTATCTCTACT... | CTACAGGCGTGAGCCACCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGAAGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTTGTGATCTGCCTGCCTCGGCCTCCCAAAATGCTAGGATTACAGGCGTGAGCCACCGGCTGTTTTTTGGTTTTCTATCGTTTTATTTTTTTAAAATAGAGATGGGGGCCAGGCGCAGTGGCTCGCACCTGTAATCCCAGCACTTTGGGAGGCCAAAGTAGGAGGATCACTTGAGCTCAGGAGTTCAAAACCAGCCTGGCCAACGTGGTGAAACCCTATCTCTACT... |
Task1_train_48658 | This sequence change occurs on Chromosome 22. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CCCCAGCTCAAGTCTCACAGCCTCCAGGCAGCTTGCCTTGACTTGCCCAGTCCACGCTCCCCTCCGGCCCCTTCCCACTGGATCATCCCCACTGCTCCTGGGGTCAGGAGCCAGGTCCTTCACCCCTGTGGCCCCAGCATAGTGCTGGCACATGGTTGGAGCCCAAGGCTTTATTCAGTGGCTCAAAGAATGCAAAGGAAGGGAGTGTCGCACTGGACGGGGCCTTGGCAGACAGGGAGCTGGGAGACAGGAGTCTATGCCACCTCCACTCCTAACCCCCAGTGCCACTATGAGGATGTCTTAACCGCCTCTCTGAGCCT... | CCCCAGCTCAAGTCTCACAGCCTCCAGGCAGCTTGCCTTGACTTGCCCAGTCCACGCTCCCCTCCGGCCCCTTCCCACTGGATCATCCCCACTGCTCCTGGGGTCAGGAGCCAGGTCCTTCACCCCTGTGGCCCCAGCATAGTGCTGGCACATGGTTGGAGCCCAAGGCTTTATTCAGTGGCTCAAAGAATGCAAAGGAAGGGAGTGTCGCACTGGACGGGGCCTTGGCAGACAGGGAGCTGGGAGACAGGAGTCTATGCCACCTCCACTCCTAACCCCCAGTGCCACTATGAGGATGTCTTAACCGCCTCTCTGAGCCT... |
Task1_train_48659 | Given a variant located on Chromosome 22, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TCTTCCTGCTGCAGCACCCAAGTCTCCCCAACCACACCGGTGCCCCCCACCCTCCCATACAGCCACGTCCTTTTTGGCCTTACCGGCTCATCTTCCCTGGGAGGTGGGAGATACGATATTAGGATGGAAGAGACCTGGAGGTCACCTTTAATGGGGGCTTTAGCTTTCATTGTTGGGGGGTTTTATTTTATTTACCTAGCGGCAGAGCCCTTCTTATAAATGAAATATGGAACGCAGAATCAAAGCACATGGTTGAAACTGAGCAAGGGGCCACCTGCTCTGTCTTCCCATCACCACCAAAGTCCCCCTCACCCCCATTC... | TCTTCCTGCTGCAGCACCCAAGTCTCCCCAACCACACCGGTGCCCCCCACCCTCCCATACAGCCACGTCCTTTTTGGCCTTACCGGCTCATCTTCCCTGGGAGGTGGGAGATACGATATTAGGATGGAAGAGACCTGGAGGTCACCTTTAATGGGGGCTTTAGCTTTCATTGTTGGGGGGTTTTATTTTATTTACCTAGCGGCAGAGCCCTTCTTATAAATGAAATATGGAACGCAGAATCAAAGCACATGGTTGAAACTGAGCAAGGGGCCACCTGCTCTGTCTTCCCATCACCACCAAAGTCCCCCTCACCCCCATTC... |
Task1_train_48660 | A variant was discovered on Chromosome 22. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GGCTAGTTCAGGCCCAGCCTACCTGATTGGACAGAGCTTGGTGCCAAACCCCCTCATAGGCTGCTGGTCAGAGCCTGTGGGGGCGTGTGGTCAGGTGCCCAATCAGCTGTGAGCAAGGCCTGTAAGTGCAGGTGCCTGAGGGCTCCCAGGTCAGAGTTAGCTGGGACTGGGGTCACTGTCCTGCTGGGGTGGAATGTTGTTTGAGCCATTGCAACGTGATCTGCCTAGGAAAGATACGTGGAGGGGTCGGGGTAGGGGGTTGAGCCCCTTGCAGGAGGGGGCATGCCAGACCTAATGGGCACGGGACTCTGCCTCTCTGT... | GGCTAGTTCAGGCCCAGCCTACCTGATTGGACAGAGCTTGGTGCCAAACCCCCTCATAGGCTGCTGGTCAGAGCCTGTGGGGGCGTGTGGTCAGGTGCCCAATCAGCTGTGAGCAAGGCCTGTAAGTGCAGGTGCCTGAGGGCTCCCAGGTCAGAGTTAGCTGGGACTGGGGTCACTGTCCTGCTGGGGTGGAATGTTGTTTGAGCCATTGCAACGTGATCTGCCTAGGAAAGATACGTGGAGGGGTCGGGGTAGGGGGTTGAGCCCCTTGCAGGAGGGGGCATGCCAGACCTAATGGGCACGGGACTCTGCCTCTCTGT... |
Task1_train_48661 | Chromosome 22 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CAGGTGTTTGTAAAGGCAGCACCAGGCCGGAGGAGGGCTCTGAGACGAGGAGCTGCCCACCCGGGCCTTAGCACCTTGATAAAGCCTGGAGAGTCGGGGCACTGGGCCGGTGAGAGGGGCATGAGGGGCAGAGAGCACCTGGGGACAGACATCAGTGTCTGAGGGCAGCTGGAGGCCCTGGGGAAACGGAAGTTCAGATGACTTTGGTGGAAGGGACTGAGCAAGGCCCTGGCAGAGCCCTGGGAGGAGGCAGGAAGGGGATCCCAGTGAGGAGGGCAGGTCTTCTCGCAGGATGCCGTATCAGCTGTGGGGAGAGCTAT... | CAGGTGTTTGTAAAGGCAGCACCAGGCCGGAGGAGGGCTCTGAGACGAGGAGCTGCCCACCCGGGCCTTAGCACCTTGATAAAGCCTGGAGAGTCGGGGCACTGGGCCGGTGAGAGGGGCATGAGGGGCAGAGAGCACCTGGGGACAGACATCAGTGTCTGAGGGCAGCTGGAGGCCCTGGGGAAACGGAAGTTCAGATGACTTTGGTGGAAGGGACTGAGCAAGGCCCTGGCAGAGCCCTGGGAGGAGGCAGGAAGGGGATCCCAGTGAGGAGGGCAGGTCTTCTCGCAGGATGCCGTATCAGCTGTGGGGAGAGCTAT... |
Task1_train_48662 | Assess the clinical impact of this variant found on Chromosome 22. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | ATTTTAAAGAGGATTATGTCCACCTCAGGGGTGTTTGTGAGCCCTCAACAAAATGTCCTGTGGGAAAGCACTTTGCAAACTCTGCAACTAAGAGGCAGAACAGTTCACCCAGCACGGCTGGCCCATCCCGACCTGCTCTGAGGTCTGGCAGCATCTACAATGGCCCCCAGGCAGGCACAGCCCTGCCCGGCCCTTAGTCCAGGCTGACTTTCAACATAAGAAAAGCAGGTGACCACCCACGCCTGGAGGGACCCGACCTCACATAGCTCCCTGCCACCTGTCACAGTGCCTGGAGTCACACGAGCAACCACATCCTTGCA... | ATTTTAAAGAGGATTATGTCCACCTCAGGGGTGTTTGTGAGCCCTCAACAAAATGTCCTGTGGGAAAGCACTTTGCAAACTCTGCAACTAAGAGGCAGAACAGTTCACCCAGCACGGCTGGCCCATCCCGACCTGCTCTGAGGTCTGGCAGCATCTACAATGGCCCCCAGGCAGGCACAGCCCTGCCCGGCCCTTAGTCCAGGCTGACTTTCAACATAAGAAAAGCAGGTGACCACCCACGCCTGGAGGGACCCGACCTCACATAGCTCCCTGCCACCTGTCACAGTGCCTGGAGTCACACGAGCAACCACATCCTTGCA... |
Task1_train_48663 | A genomic change on Chromosome 22 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AGCCCTCAACAAAATGTCCTGTGGGAAAGCACTTTGCAAACTCTGCAACTAAGAGGCAGAACAGTTCACCCAGCACGGCTGGCCCATCCCGACCTGCTCTGAGGTCTGGCAGCATCTACAATGGCCCCCAGGCAGGCACAGCCCTGCCCGGCCCTTAGTCCAGGCTGACTTTCAACATAAGAAAAGCAGGTGACCACCCACGCCTGGAGGGACCCGACCTCACATAGCTCCCTGCCACCTGTCACAGTGCCTGGAGTCACACGAGCAACCACATCCTTGCATGGGCTAGAAGGCCCTGTGTTTTCCACAGGGGGGGAAGG... | AGCCCTCAACAAAATGTCCTGTGGGAAAGCACTTTGCAAACTCTGCAACTAAGAGGCAGAACAGTTCACCCAGCACGGCTGGCCCATCCCGACCTGCTCTGAGGTCTGGCAGCATCTACAATGGCCCCCAGGCAGGCACAGCCCTGCCCGGCCCTTAGTCCAGGCTGACTTTCAACATAAGAAAAGCAGGTGACCACCCACGCCTGGAGGGACCCGACCTCACATAGCTCCCTGCCACCTGTCACAGTGCCTGGAGTCACACGAGCAACCACATCCTTGCATGGGCTAGAAGGCCCTGTGTTTTCCACAGGGGGGGAAGG... |
Task1_train_48664 | A sequence alteration has been identified on Chromosome 22. Is it disease-inducing or harmless? | Benign | GTTCACCCAGCACGGCTGGCCCATCCCGACCTGCTCTGAGGTCTGGCAGCATCTACAATGGCCCCCAGGCAGGCACAGCCCTGCCCGGCCCTTAGTCCAGGCTGACTTTCAACATAAGAAAAGCAGGTGACCACCCACGCCTGGAGGGACCCGACCTCACATAGCTCCCTGCCACCTGTCACAGTGCCTGGAGTCACACGAGCAACCACATCCTTGCATGGGCTAGAAGGCCCTGTGTTTTCCACAGGGGGGGAAGGGGACAGAAAGGAGGGCACAGGCCCTTGAGGTGGAAGCCCAGAGAGCTGGGCAGGGCAAGGCCA... | GTTCACCCAGCACGGCTGGCCCATCCCGACCTGCTCTGAGGTCTGGCAGCATCTACAATGGCCCCCAGGCAGGCACAGCCCTGCCCGGCCCTTAGTCCAGGCTGACTTTCAACATAAGAAAAGCAGGTGACCACCCACGCCTGGAGGGACCCGACCTCACATAGCTCCCTGCCACCTGTCACAGTGCCTGGAGTCACACGAGCAACCACATCCTTGCATGGGCTAGAAGGCCCTGTGTTTTCCACAGGGGGGGAAGGGGACAGAAAGGAGGGCACAGGCCCTTGAGGTGGAAGCCCAGAGAGCTGGGCAGGGCAAGGCCA... |
Task1_train_48665 | This variant is located on Chromosome 22. Evaluate its biological effect and specify any disease association. | Benign | AACCCCCGGGGGCCCCTACTCCAGCCATAAGACCCAACATGAGCTTCCTTGGGGATTGGGTGGCTGACCTCAGCAGGGGCAGAGCCAGGCTTTGGGTGGCCTAAGCTTATGCAGTTCGAGGTCCCTCTTTAAGAAAACGAATACAAAATGACAAGTACAAAAGTAGATGCAGGGCCTTGCAAAAGCCCAGGCAGTGAGAGACCCTGAAGCTGGACTTCATTCGCTTCCATGAGCAGGAAATTCACCTGCTCTTCCCGTCCAGGAGCACAGGACCTCCAGCATTGACTGCCTGGGCCAAAAGGGTGTAGAGGTTGTTGGGT... | AACCCCCGGGGGCCCCTACTCCAGCCATAAGACCCAACATGAGCTTCCTTGGGGATTGGGTGGCTGACCTCAGCAGGGGCAGAGCCAGGCTTTGGGTGGCCTAAGCTTATGCAGTTCGAGGTCCCTCTTTAAGAAAACGAATACAAAATGACAAGTACAAAAGTAGATGCAGGGCCTTGCAAAAGCCCAGGCAGTGAGAGACCCTGAAGCTGGACTTCATTCGCTTCCATGAGCAGGAAATTCACCTGCTCTTCCCGTCCAGGAGCACAGGACCTCCAGCATTGACTGCCTGGGCCAAAAGGGTGTAGAGGTTGTTGGGT... |
Task1_train_48666 | Chromosome 22 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GCAACCGGCCCCTTCCCCAGCTCTGCATCTCCCACGGTGCTCATCGCCTTTGACTACATGAAATAGCTGACGTGGGACTGTGTATCTCACATACTGCCAGTCTCCCCTGCTGGAGTTCCCCCTCAAGGAAAAGGCACCTTTGTTTTGCTCACTGCGGCATCTCAAGCGCCTAGAAGGGTGCCTCCGTCAACATCTGAGAACAAATGAATGCAGTTCTCAGCGCGGCGCCTGCGTCAAGCAGATGCTCAGGGAAGGCGTGAGCACACAGGCCCTGCCTGACACCCTCCCGCACAAGGGGCAGGGCACGGGCAGGGCCCCAC... | GCAACCGGCCCCTTCCCCAGCTCTGCATCTCCCACGGTGCTCATCGCCTTTGACTACATGAAATAGCTGACGTGGGACTGTGTATCTCACATACTGCCAGTCTCCCCTGCTGGAGTTCCCCCTCAAGGAAAAGGCACCTTTGTTTTGCTCACTGCGGCATCTCAAGCGCCTAGAAGGGTGCCTCCGTCAACATCTGAGAACAAATGAATGCAGTTCTCAGCGCGGCGCCTGCGTCAAGCAGATGCTCAGGGAAGGCGTGAGCACACAGGCCCTGCCTGACACCCTCCCGCACAAGGGGCAGGGCACGGGCAGGGCCCCAC... |
Task1_train_48667 | A mutation is present on Chromosome 22. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CCAGTGGTGGTGATGAGGTGTTTAGTGGCATGGGGGAGCTGGGAGCCCAGAGATCGGGTTCTTTTTTTTTTTTTTTTTTTTGAGATGGAGTCTTGCTCTTGTTGCCCAGGCTGGAGTACAGTGGCGCAATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTTCTGCCTCAGCCTGCCAGGTAGCTGGGACTACAGGTGCGCACCACCACTCCCGGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTAGCCAGGGTGGTCTCGATCTCCTCAGCTCGTGATCCACCAGCCTCGGCCT... | CCAGTGGTGGTGATGAGGTGTTTAGTGGCATGGGGGAGCTGGGAGCCCAGAGATCGGGTTCTTTTTTTTTTTTTTTTTTTTGAGATGGAGTCTTGCTCTTGTTGCCCAGGCTGGAGTACAGTGGCGCAATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTTCTGCCTCAGCCTGCCAGGTAGCTGGGACTACAGGTGCGCACCACCACTCCCGGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTAGCCAGGGTGGTCTCGATCTCCTCAGCTCGTGATCCACCAGCCTCGGCCT... |
Task1_train_48668 | Chromosome 22 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CTCCTATCTTTTTAGGCAGCCAGGGGAGGCCAGGAGTCAAGGTGATAAAGAGCCCAGGTCTTGCCACCTGGCACTCTGGGTTTAGATTTGACCTTGGGCAGGTGAGTTCACCTGTCTGAGCCTCACCTTCCTCCTCTGTGTAATGGGACAGTGTCTGCACTTACCTTATGGGGCTGCATGGAGCCTGCAGTGGTGCTGCAGGAAGAGTGCCTGGCCCTGGCACACAGCACGTGCCCACTAAGGGGGAGCCGGCGTGAGTACTGGGGTACTGGAGTCCCGTCCCTCCAGAAGCCCAGAGGTCACAGACTACAGTGGAAGGA... | CTCCTATCTTTTTAGGCAGCCAGGGGAGGCCAGGAGTCAAGGTGATAAAGAGCCCAGGTCTTGCCACCTGGCACTCTGGGTTTAGATTTGACCTTGGGCAGGTGAGTTCACCTGTCTGAGCCTCACCTTCCTCCTCTGTGTAATGGGACAGTGTCTGCACTTACCTTATGGGGCTGCATGGAGCCTGCAGTGGTGCTGCAGGAAGAGTGCCTGGCCCTGGCACACAGCACGTGCCCACTAAGGGGGAGCCGGCGTGAGTACTGGGGTACTGGAGTCCCGTCCCTCCAGAAGCCCAGAGGTCACAGACTACAGTGGAAGGA... |
Task1_train_48669 | The following genetic variant occurs on Chromosome 22. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TTTACTCTTCACCTAAAGCAGTAGCCAAGGGACATGTACATAGGGGTGCTCAACACCTGCTTGGTGACCGAGGGATTGAGCGGGGTGGAGGGTGACACACCAAGGTCATGGCAACTCTGTCATGAGGCTAGGAGTTGCAAAGAGGGTCACTACTGAGGACAGTTACATTAATCCTTTAGGCCAGTGCTTCTGAAACTATAAGGTGTACAAATCACCAGACAGTTTTGTTAAATGCAGATCCAGAAGCAGTGCATCTGGGCTGGGACCTGAGATTCTGCATTTCTGGCAAACTCCCAGCTACCAGTTTATAAAAGGTTGTC... | TTTACTCTTCACCTAAAGCAGTAGCCAAGGGACATGTACATAGGGGTGCTCAACACCTGCTTGGTGACCGAGGGATTGAGCGGGGTGGAGGGTGACACACCAAGGTCATGGCAACTCTGTCATGAGGCTAGGAGTTGCAAAGAGGGTCACTACTGAGGACAGTTACATTAATCCTTTAGGCCAGTGCTTCTGAAACTATAAGGTGTACAAATCACCAGACAGTTTTGTTAAATGCAGATCCAGAAGCAGTGCATCTGGGCTGGGACCTGAGATTCTGCATTTCTGGCAAACTCCCAGCTACCAGTTTATAAAAGGTTGTC... |
Task1_train_48670 | A variant found on Chromosome 22 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CAGGGTCTCAATTTCAAATTCTTGACCTCAGCTTGAGAGAGGCATCCAAGCCCTTGTCTAATCAGCCTTGGTCAGAGAGGTGGAGTCACTTGGTACAGACAGTGAGACCTGTAGGAGGAGGGTGTGGGGTTTGCCCTAATCACTGGTCCTAAGGGACAAAGAAAGGTAGAATATGAGAGCTGCCTGGACCTCTCCCCTTACCTTGAGCCCCTCTCTTCTCTCTCCAGACACCGGCGGTGGGGGCCGGAGCGCAGGACAGCACTGGGCAAGGCTCCGGGGAGAAAGCGGGTTGTCCCTGGAGCGGCACCGGTCAACACTGA... | CAGGGTCTCAATTTCAAATTCTTGACCTCAGCTTGAGAGAGGCATCCAAGCCCTTGTCTAATCAGCCTTGGTCAGAGAGGTGGAGTCACTTGGTACAGACAGTGAGACCTGTAGGAGGAGGGTGTGGGGTTTGCCCTAATCACTGGTCCTAAGGGACAAAGAAAGGTAGAATATGAGAGCTGCCTGGACCTCTCCCCTTACCTTGAGCCCCTCTCTTCTCTCTCCAGACACCGGCGGTGGGGGCCGGAGCGCAGGACAGCACTGGGCAAGGCTCCGGGGAGAAAGCGGGTTGTCCCTGGAGCGGCACCGGTCAACACTGA... |
Task1_train_48671 | This mutation occurs on Chromosome 22. Does this change lead to a known medical condition, or is it benign? | Benign | TCACTGGTCCTAAGGGACAAAGAAAGGTAGAATATGAGAGCTGCCTGGACCTCTCCCCTTACCTTGAGCCCCTCTCTTCTCTCTCCAGACACCGGCGGTGGGGGCCGGAGCGCAGGACAGCACTGGGCAAGGCTCCGGGGAGAAAGCGGGTTGTCCCTGGAGCGGCACCGGTCAACACTGACCCAGGCTTCCTCCATGACACCACACAGTGGACCTCGAAGCACCACGTCTCAGGCTTCTCCTGCCCAAAGGGACACTGCTCAGGCTGCCTCTACACGTGAAATCCCCAGAGCCTCCTCTCCCCATCGAATCACCCAAAG... | TCACTGGTCCTAAGGGACAAAGAAAGGTAGAATATGAGAGCTGCCTGGACCTCTCCCCTTACCTTGAGCCCCTCTCTTCTCTCTCCAGACACCGGCGGTGGGGGCCGGAGCGCAGGACAGCACTGGGCAAGGCTCCGGGGAGAAAGCGGGTTGTCCCTGGAGCGGCACCGGTCAACACTGACCCAGGCTTCCTCCATGACACCACACAGTGGACCTCGAAGCACCACGTCTCAGGCTTCTCCTGCCCAAAGGGACACTGCTCAGGCTGCCTCTACACGTGAAATCCCCAGAGCCTCCTCTCCCCATCGAATCACCCAAAG... |
Task1_train_48672 | A variant was discovered on Chromosome 22. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GTGCCCAGCGGGACAATCCCAGAGCCTCCAGAACCTCCTCTCCCAATAGAGCCACACGAGACAACCCCAGAACATCCTGCGCCCAGCGGGACAATCCCAGAGCCTCCTCTCCCAATAGAGCTGCACGAGACAACCCCACAACATCCTGTGCCCAGCGGGACAATCCCAGAGCCTCCAGAACCTCCTCTCCCAATAGAGCCACACGAGACAACCCCAGAACATCCTGTGCCCAGCGGGACAATCCCAGAGCCTCCTCTCCCAATAGAGCTACACGAGACAACCCCACAACATCCTGTGCCCAGCGGGACAATCCCAGAGCC... | GTGCCCAGCGGGACAATCCCAGAGCCTCCAGAACCTCCTCTCCCAATAGAGCCACACGAGACAACCCCAGAACATCCTGCGCCCAGCGGGACAATCCCAGAGCCTCCTCTCCCAATAGAGCTGCACGAGACAACCCCACAACATCCTGTGCCCAGCGGGACAATCCCAGAGCCTCCAGAACCTCCTCTCCCAATAGAGCCACACGAGACAACCCCAGAACATCCTGTGCCCAGCGGGACAATCCCAGAGCCTCCTCTCCCAATAGAGCTACACGAGACAACCCCACAACATCCTGTGCCCAGCGGGACAATCCCAGAGCC... |
Task1_train_48673 | Here is a variant on Chromosome 22. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GGGAGATTAAGGCAGAGAATCACTTGAACCCGGGAGATGGAAGTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGGTGACAGAGCGAGACTCCATCTCAAAAAAAAAAAAAAAAAAAAGACACTTGCTTGGACAGTTTATGTTGGCCTCTCTGAAGTTGTCAGGGAGAATGTTTCTTTCTTCTGATCTTGCTCAGAGCTCTTTTGCCAACAGCTAGGATGGCCTGGAGTTTTCAAGGCTAAGCGCTGGGATTCTGTTGGTTAACAGTGATGGGAGGGAAAAAGGAAAAGAAATCCAAAATTTACAATATGGA... | GGGAGATTAAGGCAGAGAATCACTTGAACCCGGGAGATGGAAGTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGGTGACAGAGCGAGACTCCATCTCAAAAAAAAAAAAAAAAAAAAGACACTTGCTTGGACAGTTTATGTTGGCCTCTCTGAAGTTGTCAGGGAGAATGTTTCTTTCTTCTGATCTTGCTCAGAGCTCTTTTGCCAACAGCTAGGATGGCCTGGAGTTTTCAAGGCTAAGCGCTGGGATTCTGTTGGTTAACAGTGATGGGAGGGAAAAAGGAAAAGAAATCCAAAATTTACAATATGGA... |
Task1_train_48674 | A genomic variant on Chromosome 22 is under review. What is the biological outcome — benign or pathogenic? | Benign | GGATGTTCCTGGGGTCTGTTAACCAGGAAGCTCAGGTCGGGCTGCTTCCTTCCCTGGGGTCTGTCTCCAGCCCCTGGCACAGGGCCTGGCACACAGGTGTCGCTCCAAAAGTGCTCATTGTGGGACTGCAGGGGTGAGGACCCACCTGACGTGGCTCTGCTGGTGCCCTAGGCTCTCGGACTCTAACAAGGAGAACGCGCTGCACAGCTACAGCACCCAGAAGGGCCCCCTGAAGGCAGGGGAGCAGCGGGCGGGCTCTGAGGTCATCAGCCGGGGTGGCCCTCGGAAGGCGGACGGGCAGCGTCAGGCCTTGGACTACG... | GGATGTTCCTGGGGTCTGTTAACCAGGAAGCTCAGGTCGGGCTGCTTCCTTCCCTGGGGTCTGTCTCCAGCCCCTGGCACAGGGCCTGGCACACAGGTGTCGCTCCAAAAGTGCTCATTGTGGGACTGCAGGGGTGAGGACCCACCTGACGTGGCTCTGCTGGTGCCCTAGGCTCTCGGACTCTAACAAGGAGAACGCGCTGCACAGCTACAGCACCCAGAAGGGCCCCCTGAAGGCAGGGGAGCAGCGGGCGGGCTCTGAGGTCATCAGCCGGGGTGGCCCTCGGAAGGCGGACGGGCAGCGTCAGGCCTTGGACTACG... |
Task1_train_48675 | Assess the clinical impact of this variant found on Chromosome 22. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | AAAGCCAAGCCGGTCAAGGCATCCAAGCCCAAAAAGGCCAAACCAGTGAAACCCAAAGCAAAGTCCAGTGCCAAGAGGGCCGGCAAGAAGAAGTGACAATGAAGTCTTTTCTTGCGGACACTCCCTCCTGTCTCCTATTTTCTGTAAATAATTTTCTCCTTTTTTCTCTCTTGATGCTCACCACCACCTTTTGCCCCCTTCTGTTCTGACTTTATAAGAGACAGGATTTGGATTCTTCAGAAATTACAGAATAATTCATTTTTCCTTAACCAGTTGTGCAAGGACAGCAACAACCAATCTAATGATGAGAATGTACTTAT... | AAAGCCAAGCCGGTCAAGGCATCCAAGCCCAAAAAGGCCAAACCAGTGAAACCCAAAGCAAAGTCCAGTGCCAAGAGGGCCGGCAAGAAGAAGTGACAATGAAGTCTTTTCTTGCGGACACTCCCTCCTGTCTCCTATTTTCTGTAAATAATTTTCTCCTTTTTTCTCTCTTGATGCTCACCACCACCTTTTGCCCCCTTCTGTTCTGACTTTATAAGAGACAGGATTTGGATTCTTCAGAAATTACAGAATAATTCATTTTTCCTTAACCAGTTGTGCAAGGACAGCAACAACCAATCTAATGATGAGAATGTACTTAT... |
Task1_train_48676 | This alteration occurs on Chromosome 22. Is it associated with a disease or is it a benign variant? | Benign | AGGCAGGCAGGCGCGCTCGGGCGAGGTAGGAGCGATGTGGCCTGGGAACGCCTGGCGCGCCGCACTCTTCTGGGTGCCCCGCGGCCGCCGCGCACAGTCAGCGCTGGCCCAGCTGCGTGGCATTCTGGAGGGGGAGCTGGAAGGCATCCGCGGAGCTGGCACTTGGAAGAGTGAGCGGGTCATCACGTCCCGTCAGGGGCCGCACATCCGCGTGGACGGCGTCTCCGGAGGTAACGCTCCGTTCCGGGAGTCGTTCCAAGACCTTTCCCGAGCTTGCGCTGGAATGGAGGTCCTGGAGGTGGGGGTGGGCGGCTCCTACA... | AGGCAGGCAGGCGCGCTCGGGCGAGGTAGGAGCGATGTGGCCTGGGAACGCCTGGCGCGCCGCACTCTTCTGGGTGCCCCGCGGCCGCCGCGCACAGTCAGCGCTGGCCCAGCTGCGTGGCATTCTGGAGGGGGAGCTGGAAGGCATCCGCGGAGCTGGCACTTGGAAGAGTGAGCGGGTCATCACGTCCCGTCAGGGGCCGCACATCCGCGTGGACGGCGTCTCCGGAGGTAACGCTCCGTTCCGGGAGTCGTTCCAAGACCTTTCCCGAGCTTGCGCTGGAATGGAGGTCCTGGAGGTGGGGGTGGGCGGCTCCTACA... |
Task1_train_48677 | This variant is present on Chromosome 22. Is the change likely to result in a pathogenic outcome? | Benign | TCTCTATTTCTCAAGGCTTCTATCCCTTGTAGATACTACTTTCAAACTCAGGAAAGTCTCTCTTTTATTATGTTTTTTTTAGGGATGGGGTCTTGCTGTGTTGCCCAGGCTGGTCCTGAACTCCTGAGCTCAAGGGATCCTCCCGACTTGGCCTCTCAAAGTGCTGGGATTACAGGTGTGAACCACTGCACCTGGCTTCAGGAATTTTCTTATTCTTTTGAGACAGGGTCTCACTCCATTGGCCCAGGCTGGAATGTAGTGGTGCCATCTTGGCTCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCTCCCACTTCA... | TCTCTATTTCTCAAGGCTTCTATCCCTTGTAGATACTACTTTCAAACTCAGGAAAGTCTCTCTTTTATTATGTTTTTTTTAGGGATGGGGTCTTGCTGTGTTGCCCAGGCTGGTCCTGAACTCCTGAGCTCAAGGGATCCTCCCGACTTGGCCTCTCAAAGTGCTGGGATTACAGGTGTGAACCACTGCACCTGGCTTCAGGAATTTTCTTATTCTTTTGAGACAGGGTCTCACTCCATTGGCCCAGGCTGGAATGTAGTGGTGCCATCTTGGCTCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCTCCCACTTCA... |
Task1_train_48678 | Assess the clinical impact of this variant found on Chromosome 22. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TTATGTTTTTTTTAGGGATGGGGTCTTGCTGTGTTGCCCAGGCTGGTCCTGAACTCCTGAGCTCAAGGGATCCTCCCGACTTGGCCTCTCAAAGTGCTGGGATTACAGGTGTGAACCACTGCACCTGGCTTCAGGAATTTTCTTATTCTTTTGAGACAGGGTCTCACTCCATTGGCCCAGGCTGGAATGTAGTGGTGCCATCTTGGCTCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCTCCCACTTCAGCCTCCTGAGTAGCTGGAACCAGAGGTGCACGCCACCACACCTAGCTAATTTTGTTTTGTTTTGTTT... | TTATGTTTTTTTTAGGGATGGGGTCTTGCTGTGTTGCCCAGGCTGGTCCTGAACTCCTGAGCTCAAGGGATCCTCCCGACTTGGCCTCTCAAAGTGCTGGGATTACAGGTGTGAACCACTGCACCTGGCTTCAGGAATTTTCTTATTCTTTTGAGACAGGGTCTCACTCCATTGGCCCAGGCTGGAATGTAGTGGTGCCATCTTGGCTCACTGCAACCTCCACCTCCTGGGCTCAAGCCATCCTCCCACTTCAGCCTCCTGAGTAGCTGGAACCAGAGGTGCACGCCACCACACCTAGCTAATTTTGTTTTGTTTTGTTT... |
Task1_train_48679 | Assess the clinical impact of this variant found on Chromosome 22. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | AACGATGGTCCCAGAACATCCCAGGAGGGTGTGACAGCCTCCATCTAGAAGGTTCTATCCTCAGGTCCCCAAGGCATCTGCAGCACACCGTCCTCTGCTGTGGGTCTGTGAAGCAGCCACTCCAGCAGCAGGTGTCCCTATCGTTGGCGTTCTCAGTCATCTCTCTCCCCACTGACCCCCTTCCGTTCCTGTCCCTGTGGTCACCCGCCCAGCTATGGACCTTCGCGCCTAACTATGAGTCCCTCCATACATCACCTATCCCCCACTCACCTGTCTATACTCCATCCCCCGTGTAGCCACGAATCCATCCAGCACCCCCT... | AACGATGGTCCCAGAACATCCCAGGAGGGTGTGACAGCCTCCATCTAGAAGGTTCTATCCTCAGGTCCCCAAGGCATCTGCAGCACACCGTCCTCTGCTGTGGGTCTGTGAAGCAGCCACTCCAGCAGCAGGTGTCCCTATCGTTGGCGTTCTCAGTCATCTCTCTCCCCACTGACCCCCTTCCGTTCCTGTCCCTGTGGTCACCCGCCCAGCTATGGACCTTCGCGCCTAACTATGAGTCCCTCCATACATCACCTATCCCCCACTCACCTGTCTATACTCCATCCCCCGTGTAGCCACGAATCCATCCAGCACCCCCT... |
Task1_train_48680 | Here is a mutation located on Chromosome 22. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AAACCTCTATGTACGGCCACTCAGGAGGGGGCAGCTCCTAGAAGCGCCCCGCTTGCTGCCCCCCAGTCCAACTCACCCGGCCGAAGAACTGCAGGAAGGTGTTGGAAAGTAGCAGGTGCTTCTCTGCTAGGAAGCGATAGCGCCGCTTCTCTTCCAATTCAGCCGCCCGCTGACTCTCAGACACGAAGGCCTGCATCTGTGCGTGCAGCCGGTTCACACTCTCCTGGGGGGGAACGGGAGTTCTGGCTGGGGGCGGTGGGTGTGTCTCATCCCACCCCCCTCGCCCACAGGCGCCAGCTGTTCAAGCCCCCTGTTCTTCC... | AAACCTCTATGTACGGCCACTCAGGAGGGGGCAGCTCCTAGAAGCGCCCCGCTTGCTGCCCCCCAGTCCAACTCACCCGGCCGAAGAACTGCAGGAAGGTGTTGGAAAGTAGCAGGTGCTTCTCTGCTAGGAAGCGATAGCGCCGCTTCTCTTCCAATTCAGCCGCCCGCTGACTCTCAGACACGAAGGCCTGCATCTGTGCGTGCAGCCGGTTCACACTCTCCTGGGGGGGAACGGGAGTTCTGGCTGGGGGCGGTGGGTGTGTCTCATCCCACCCCCCTCGCCCACAGGCGCCAGCTGTTCAAGCCCCCTGTTCTTCC... |
Task1_train_48681 | A genomic change on Chromosome 22 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GAGGGGAGAGAGAGGTGGAGCCAGGACTAGAAGCCACAGTCACGGTGCCTCTCCAGAGTTCCAGGCTTGGTCGGGCTACCCTGGCTGAAGGTGCTGCCGCCTCCACAGTGAAGTCTGGCTCACCAAGGACTGGCTCCTGGCTGCCCTCTGTTCAGGGGACCCCGCTCCCAAACAATGGAGGTCCCTGAGTGGGCCAGCCCACAGAAAGTCCAGAGAAGGGTCCTGTCTAGTCTGGGGATGTCTCCCTGGGCACCAAGGAATGCACCGGGGCAGATGCTGGCTGCCTGGCCACATTCAACGTCTGAAAGTCACCACGGGGC... | GAGGGGAGAGAGAGGTGGAGCCAGGACTAGAAGCCACAGTCACGGTGCCTCTCCAGAGTTCCAGGCTTGGTCGGGCTACCCTGGCTGAAGGTGCTGCCGCCTCCACAGTGAAGTCTGGCTCACCAAGGACTGGCTCCTGGCTGCCCTCTGTTCAGGGGACCCCGCTCCCAAACAATGGAGGTCCCTGAGTGGGCCAGCCCACAGAAAGTCCAGAGAAGGGTCCTGTCTAGTCTGGGGATGTCTCCCTGGGCACCAAGGAATGCACCGGGGCAGATGCTGGCTGCCTGGCCACATTCAACGTCTGAAAGTCACCACGGGGC... |
Task1_train_48682 | This sequence variant lies on Chromosome 22. Is it clinically significant, and what condition might it cause if any? | Benign | GCAACGCTGGGCAGGCGAAAACCAAGGGAGTGGGAATCAGCAGCACTTTGGCCTGGAGGGAGAAGGGAAGCCACGGTGGAGAGACAGCTTGGTGAAAGCAGATGGCGGGGCAGGGCCAGGGCTGGTCCTCAGCCTGTGTCTGCACCCACCCTCCCGGGCAGCTTGGGCCCAACTGCTCCGCCCCCCCAAGATGGAGGGGGAGAGCTGGCCTCTGGCACCCACATGCAGGCCTCTGCCACGAGGAAAGGAAGGAGGCCAGGAAGACGGCTGGGCCCCAACTCTCCTCACAGGTGGCAGGGAGGGAACCTGTTCATTCCAGG... | GCAACGCTGGGCAGGCGAAAACCAAGGGAGTGGGAATCAGCAGCACTTTGGCCTGGAGGGAGAAGGGAAGCCACGGTGGAGAGACAGCTTGGTGAAAGCAGATGGCGGGGCAGGGCCAGGGCTGGTCCTCAGCCTGTGTCTGCACCCACCCTCCCGGGCAGCTTGGGCCCAACTGCTCCGCCCCCCCAAGATGGAGGGGGAGAGCTGGCCTCTGGCACCCACATGCAGGCCTCTGCCACGAGGAAAGGAAGGAGGCCAGGAAGACGGCTGGGCCCCAACTCTCCTCACAGGTGGCAGGGAGGGAACCTGTTCATTCCAGG... |
Task1_train_48683 | This sequence variant lies on Chromosome 22. Is it clinically significant, and what condition might it cause if any? | Benign | GGCCAGCTGACTGGACCTCGGAACACAGTGGCTGTATGTGCTGAGAGTGGCTTCCAGGCCCCAGGGATCCACAGATCCCAGCACCCCGGTGCAGCCAACAACACAGGGTGTCCTGTCTACTGTTGGGTAGCATGGGAAGGGCCTGGCCTCAGGGTGAAGGTTCCCATTGCATGTTTTCCAGGTGCTTCTGCCAGGGGACTGCTGGAGGTGGTTCAGCTCACTACAGTGGCCGTGGCATTGAGTCAGAGATTGGCAAAGGATAAGGCTGTGGGTGCCTCTGCCCAGCTTCTAACTCCAGGGCCTGCCTCAAGAGGGACTTC... | GGCCAGCTGACTGGACCTCGGAACACAGTGGCTGTATGTGCTGAGAGTGGCTTCCAGGCCCCAGGGATCCACAGATCCCAGCACCCCGGTGCAGCCAACAACACAGGGTGTCCTGTCTACTGTTGGGTAGCATGGGAAGGGCCTGGCCTCAGGGTGAAGGTTCCCATTGCATGTTTTCCAGGTGCTTCTGCCAGGGGACTGCTGGAGGTGGTTCAGCTCACTACAGTGGCCGTGGCATTGAGTCAGAGATTGGCAAAGGATAAGGCTGTGGGTGCCTCTGCCCAGCTTCTAACTCCAGGGCCTGCCTCAAGAGGGACTTC... |
Task1_train_48684 | An alteration has been detected on Chromosome 22. Is it pathogenic, and if so, what disease is involved? | Benign | AATGAAAGGGTCACTGATTTCAAATTCTAGGCAACTGGACCCAAGATAAATTGCAAACACATTTAACCTCTTCATGTTACATTATGGCAGAACACTGACCCTTAGGTTTGGTAGGCTAGGAGCGTAGTAAATAGGCCGGGAAATGACTTCATAGATTCGATTCCCATGTCTCTCTCCCCTTTTAGGTGGTTTTTCTCCTCTGTGCCTATGTTACAGTGTACATGATATATGGGAAATTCCGTAAAACTTTTGACAGTGAGAATGACACATTCCGCCTGGAGTTTCTTCTGGTCCCAGTCATTGGCCTTTCCTTCCTTGAA... | AATGAAAGGGTCACTGATTTCAAATTCTAGGCAACTGGACCCAAGATAAATTGCAAACACATTTAACCTCTTCATGTTACATTATGGCAGAACACTGACCCTTAGGTTTGGTAGGCTAGGAGCGTAGTAAATAGGCCGGGAAATGACTTCATAGATTCGATTCCCATGTCTCTCTCCCCTTTTAGGTGGTTTTTCTCCTCTGTGCCTATGTTACAGTGTACATGATATATGGGAAATTCCGTAAAACTTTTGACAGTGAGAATGACACATTCCGCCTGGAGTTTCTTCTGGTCCCAGTCATTGGCCTTTCCTTCCTTGAA... |
Task1_train_48685 | This variant is present on Chromosome 22. Is the change likely to result in a pathogenic outcome? | Benign | GGCTCCTCTCTTGTGCTCCTAGAAGTCAGAGCGCCGAGCAAGCGTGTGGGGGAAGCGGCGGGGTGCTGTTCACCCACTCCCAGATGGCTGGCAGCAGGCACCAGTAAGCAGGGCTAGTGGGCGGGCTCCCCATGCACTCTGAAGCGGTAGATGCAGGTGTACTCGGGGTGGCCCCAGTTAGTCAGGATCCGCAGCTCCACCACCTGGTACGTGGCCATCGTAGGGGCCTGGGTAGAGAAGAAAGGGATTAAGAGCATCAGAGACCTGTGAGGCCTCACTGACAGAGAAGGTGGGAAGGGGAGACAGCCTCGCCTAGGGCC... | GGCTCCTCTCTTGTGCTCCTAGAAGTCAGAGCGCCGAGCAAGCGTGTGGGGGAAGCGGCGGGGTGCTGTTCACCCACTCCCAGATGGCTGGCAGCAGGCACCAGTAAGCAGGGCTAGTGGGCGGGCTCCCCATGCACTCTGAAGCGGTAGATGCAGGTGTACTCGGGGTGGCCCCAGTTAGTCAGGATCCGCAGCTCCACCACCTGGTACGTGGCCATCGTAGGGGCCTGGGTAGAGAAGAAAGGGATTAAGAGCATCAGAGACCTGTGAGGCCTCACTGACAGAGAAGGTGGGAAGGGGAGACAGCCTCGCCTAGGGCC... |
Task1_train_48686 | With a mutation on Chromosome 22, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CTCTGCCCGGACCTGGATTACGGCCAGAGGGATCCTGACTTCTGGGTTCCGTGTTCTTCTGCCTAAGGGGCACATTCTCAAATCCTGGTTCTGCTGGTTTAGGGACTTGGGGAATGAACCCATAGCATCCTCAGGCAGAGCCTCTTTGTGGCTCTGACCATGAGTGGGGAACTCGGGGGGTTAGATTGTCCCAGGCCCAAGAAGGAAGATGGACTTTCTGGGAAACCCCACTTCTTGCCTGGAGTCAGTGGGCCTACCCTGCAGGAGGAAAGCCATCGTGTGTCTGAGAGCCAGGCACGGCTAGACTAGTGTGGCGTTTA... | CTCTGCCCGGACCTGGATTACGGCCAGAGGGATCCTGACTTCTGGGTTCCGTGTTCTTCTGCCTAAGGGGCACATTCTCAAATCCTGGTTCTGCTGGTTTAGGGACTTGGGGAATGAACCCATAGCATCCTCAGGCAGAGCCTCTTTGTGGCTCTGACCATGAGTGGGGAACTCGGGGGGTTAGATTGTCCCAGGCCCAAGAAGGAAGATGGACTTTCTGGGAAACCCCACTTCTTGCCTGGAGTCAGTGGGCCTACCCTGCAGGAGGAAAGCCATCGTGTGTCTGAGAGCCAGGCACGGCTAGACTAGTGTGGCGTTTA... |
Task1_train_48687 | Mutation context: Chromosome 22. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TTGCATTCTCCTAATGGGTTGGGGAGTGGGTTGGCAGAAATACTAGGAGGGTGGGGAATGTACCCCTGGAAAGGCCAGAGTTGGACCCGAGCTGGGAGAGATCACCCCAGCCCGCCTGCCAGCATCCCCTCCTCTTCCTCTCCCCTCAGTCTTCCTGCCTGGGAAGGCAGCAGAAATTCTCAGGGCTGTGGAGGGGTCGGGGAGGCCCAGGGCCATCCTGGGAGCTGTGTTCAGTGGACATGAGCCCCGAGGACTCCCGGGAGGGCTCCCTGCATGGGCCGGTTTCTCTCTTGTGCCTTCAGAAATCCGATGGAGCGGAT... | TTGCATTCTCCTAATGGGTTGGGGAGTGGGTTGGCAGAAATACTAGGAGGGTGGGGAATGTACCCCTGGAAAGGCCAGAGTTGGACCCGAGCTGGGAGAGATCACCCCAGCCCGCCTGCCAGCATCCCCTCCTCTTCCTCTCCCCTCAGTCTTCCTGCCTGGGAAGGCAGCAGAAATTCTCAGGGCTGTGGAGGGGTCGGGGAGGCCCAGGGCCATCCTGGGAGCTGTGTTCAGTGGACATGAGCCCCGAGGACTCCCGGGAGGGCTCCCTGCATGGGCCGGTTTCTCTCTTGTGCCTTCAGAAATCCGATGGAGCGGAT... |
Task1_train_48688 | This sequence variant lies on Chromosome 22. Is it clinically significant, and what condition might it cause if any? | Benign | GCCCGCCTGCCAGCATCCCCTCCTCTTCCTCTCCCCTCAGTCTTCCTGCCTGGGAAGGCAGCAGAAATTCTCAGGGCTGTGGAGGGGTCGGGGAGGCCCAGGGCCATCCTGGGAGCTGTGTTCAGTGGACATGAGCCCCGAGGACTCCCGGGAGGGCTCCCTGCATGGGCCGGTTTCTCTCTTGTGCCTTCAGAAATCCGATGGAGCGGATGTATCGAGACACATTCTACGACAACTTTGAAAACGAACCCATCCTCTATGGTCGGAGCTACACTTGGCTGTGCTATGAAGTGAAAATAAAGAGGGGCCGCTCAAATCTC... | GCCCGCCTGCCAGCATCCCCTCCTCTTCCTCTCCCCTCAGTCTTCCTGCCTGGGAAGGCAGCAGAAATTCTCAGGGCTGTGGAGGGGTCGGGGAGGCCCAGGGCCATCCTGGGAGCTGTGTTCAGTGGACATGAGCCCCGAGGACTCCCGGGAGGGCTCCCTGCATGGGCCGGTTTCTCTCTTGTGCCTTCAGAAATCCGATGGAGCGGATGTATCGAGACACATTCTACGACAACTTTGAAAACGAACCCATCCTCTATGGTCGGAGCTACACTTGGCTGTGCTATGAAGTGAAAATAAAGAGGGGCCGCTCAAATCTC... |
Task1_train_48689 | A mutation found on Chromosome 22 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CCCAGCCAATTCTTTTGTATTTTTAGTAGAAACAGGATTTTGCCATGTTGGCCAGGCTGGTTTCGAACTCCTGACCTCAAGTGATCCACCAGCCTTGGCCTCCCAAAGTGCTAGGATTACATGCGTGAGACACCATGCCCCTGGCCTCCTCCCCACATTATTTATTTATTTATTTATTTATTTTGAGACGGAGTCTTGCTCTATCGCCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAAGCTCCGCCTCCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCCCACCAC... | CCCAGCCAATTCTTTTGTATTTTTAGTAGAAACAGGATTTTGCCATGTTGGCCAGGCTGGTTTCGAACTCCTGACCTCAAGTGATCCACCAGCCTTGGCCTCCCAAAGTGCTAGGATTACATGCGTGAGACACCATGCCCCTGGCCTCCTCCCCACATTATTTATTTATTTATTTATTTATTTTGAGACGGAGTCTTGCTCTATCGCCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAAGCTCCGCCTCCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCCCACCAC... |
Task1_train_48690 | Located on Chromosome 22, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | CCCCTGGCCTCCTCCCCACATTATTTATTTATTTATTTATTTATTTTGAGACGGAGTCTTGCTCTATCGCCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAAGCTCCGCCTCCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCCCACCACCATGCCCAGCTAATTTTTTCTTTTTTTCTTTTTTTTTTTTTTTTTAGTAGAGACGGGGTTTCATGGTGTTAGCCAAGATGGTCTCGATCTCCTGACCTCATGATCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGATT... | CCCCTGGCCTCCTCCCCACATTATTTATTTATTTATTTATTTATTTTGAGACGGAGTCTTGCTCTATCGCCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAAGCTCCGCCTCCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCCCACCACCATGCCCAGCTAATTTTTTCTTTTTTTCTTTTTTTTTTTTTTTTTAGTAGAGACGGGGTTTCATGGTGTTAGCCAAGATGGTCTCGATCTCCTGACCTCATGATCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGATT... |
Task1_train_48691 | Mutation context: Chromosome 22. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GGCACCTCCTCTGTAAGATGGGAATGGCCCGTGCGGGCCTAGGGCAGCCTCACATGAGCTCACATCCGCGCAGCACTTAGAAGAGTGGCCTGGGCCTCAGAATTCGGTTCTACCATGATTTAACAATAGTAATATACAGAGGTGAAATGTCAGAAGGAACTGGCTGAAAGGTTAAAATCTATTATTTTGGGGTGAATAGTTTTATTCTCTCTCTCTTTTTTTTTTTTTTTTTTGAGATGGAGTTTCGCTCTTGTAGCCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTACAACCTCCGCCTCCCAGGTTCAAGCG... | GGCACCTCCTCTGTAAGATGGGAATGGCCCGTGCGGGCCTAGGGCAGCCTCACATGAGCTCACATCCGCGCAGCACTTAGAAGAGTGGCCTGGGCCTCAGAATTCGGTTCTACCATGATTTAACAATAGTAATATACAGAGGTGAAATGTCAGAAGGAACTGGCTGAAAGGTTAAAATCTATTATTTTGGGGTGAATAGTTTTATTCTCTCTCTCTTTTTTTTTTTTTTTTTTGAGATGGAGTTTCGCTCTTGTAGCCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTACAACCTCCGCCTCCCAGGTTCAAGCG... |
Task1_train_48692 | Chromosome 22 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CCCAGATCAGGGACCACTGCCCGCTCTGCCCACGGGGCCTCTGCTGCCCCTTCCTGCCTGGTGGCCCTGCTGGGCCTCAGCCTGGCCTCCCCCTGCCCCTGCCCCAGCGCTAGTCTCTCTCCCCTCTGGTTCCTCTGCTGCTCCCACTACCAGCCAGGCTCTTTGCCCTGCTATGTGGTCGCCCCTTTACAGCTTCTGAATGGGCCATCTCCCCCACCTGCCCCAGCCCAGGCCCCCTGCTGAGACTCTCCCCCGAAAGTCACCCCTTTGCTATTGCTCCCCGCCCTGGGATGGTGCTCCCTCTCTGTGCTTCTCGCCAT... | CCCAGATCAGGGACCACTGCCCGCTCTGCCCACGGGGCCTCTGCTGCCCCTTCCTGCCTGGTGGCCCTGCTGGGCCTCAGCCTGGCCTCCCCCTGCCCCTGCCCCAGCGCTAGTCTCTCTCCCCTCTGGTTCCTCTGCTGCTCCCACTACCAGCCAGGCTCTTTGCCCTGCTATGTGGTCGCCCCTTTACAGCTTCTGAATGGGCCATCTCCCCCACCTGCCCCAGCCCAGGCCCCCTGCTGAGACTCTCCCCCGAAAGTCACCCCTTTGCTATTGCTCCCCGCCCTGGGATGGTGCTCCCTCTCTGTGCTTCTCGCCAT... |
Task1_train_48693 | This sequence variant lies on Chromosome 22. Is it clinically significant, and what condition might it cause if any? | Benign | GGGTTTCACCATATTCACCAGGCTGGTCTCGAACTTCTGACCTCAGGTGATCCACCTGCCTCGGCCTCCCAAAGTGTTGGGATTACAGGTGTGAGCCACAGCGCCGGCCTAATTTTAATATTTAATTAATCCAATGTGGCTAACATATTACTTCAACATTAATTAACATAAAATTCTTGACAAGATAATGAAGTTTCTTTTTCTTGTCACACCGAGTCTTTGAAATGAGCTGCGTGGGTCACGTACAGTGGGTGGCTCGCACCTCTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAGATCACCTGAAGTTAGATATTC... | GGGTTTCACCATATTCACCAGGCTGGTCTCGAACTTCTGACCTCAGGTGATCCACCTGCCTCGGCCTCCCAAAGTGTTGGGATTACAGGTGTGAGCCACAGCGCCGGCCTAATTTTAATATTTAATTAATCCAATGTGGCTAACATATTACTTCAACATTAATTAACATAAAATTCTTGACAAGATAATGAAGTTTCTTTTTCTTGTCACACCGAGTCTTTGAAATGAGCTGCGTGGGTCACGTACAGTGGGTGGCTCGCACCTCTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAGATCACCTGAAGTTAGATATTC... |
Task1_train_48694 | With a mutation on Chromosome 22, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GAGATCAAGACCATCCTGGCTAACACGGTGAAACCCCATCTCTATTAAAAATACAAAAAATTAGCCAGGTGTGGTGGCAGGCGCCTGTAGTCCCAGCTATTCAGGAGACTGAGGCAGGAGAATGGCATGAACCTGGGAGGCAGAGCTTGCAGTGAGCCAAGATCGTGCCACTGCACTCCACCTGGGCAACAGAGCGAGACTCCGTCTCAAGAAAAAAAAAAAAAGTGCTTCCTGAGGACCCTCCCAGGATCCCCTCACAGACACAGCTCCCACCAGGAATGATTCAGAACTGTGGGATTTGAGGATCAGGGCCTACCTGA... | GAGATCAAGACCATCCTGGCTAACACGGTGAAACCCCATCTCTATTAAAAATACAAAAAATTAGCCAGGTGTGGTGGCAGGCGCCTGTAGTCCCAGCTATTCAGGAGACTGAGGCAGGAGAATGGCATGAACCTGGGAGGCAGAGCTTGCAGTGAGCCAAGATCGTGCCACTGCACTCCACCTGGGCAACAGAGCGAGACTCCGTCTCAAGAAAAAAAAAAAAAGTGCTTCCTGAGGACCCTCCCAGGATCCCCTCACAGACACAGCTCCCACCAGGAATGATTCAGAACTGTGGGATTTGAGGATCAGGGCCTACCTGA... |
Task1_train_48695 | A genomic variant on Chromosome 22 is under review. What is the biological outcome — benign or pathogenic? | Benign | AGAGCACAGTGCTGGAGGAAGCCCCAGTTTCCACCCCATCACTCCCCAAGGGGAAGGGTTCTGGTATTGGACATGTAGGGGTCGAGAGGCCTGTGGACCTCAAGGAGGGGGTGTCCAACTGCAGCTGGAAAGAGGGATCTGGGACTCAGGCCAGAGGCGTGTGAGCAGCTCAGAGCAGCTCTGAGCCCAGGGGAGCCAGAAAGGCACACCCACAGTTCTCAGGCAGGGGATCCCCACCCAACCCAGGAAGAATAGTGACGAGGTCGGGGCATCCCCATGCAAAGAGCCTCAGCTGTGGGCAGCAGCCGGTGCCCTCCCAG... | AGAGCACAGTGCTGGAGGAAGCCCCAGTTTCCACCCCATCACTCCCCAAGGGGAAGGGTTCTGGTATTGGACATGTAGGGGTCGAGAGGCCTGTGGACCTCAAGGAGGGGGTGTCCAACTGCAGCTGGAAAGAGGGATCTGGGACTCAGGCCAGAGGCGTGTGAGCAGCTCAGAGCAGCTCTGAGCCCAGGGGAGCCAGAAAGGCACACCCACAGTTCTCAGGCAGGGGATCCCCACCCAACCCAGGAAGAATAGTGACGAGGTCGGGGCATCCCCATGCAAAGAGCCTCAGCTGTGGGCAGCAGCCGGTGCCCTCCCAG... |
Task1_train_48696 | Here is a genetic alteration on Chromosome 22. Based on the data, is it a benign variant or a cause of disease? | Benign | CAACATGGTGAAACCCCGTCTGTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGCAGGCATCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACTTGGAAGGCGGAGGTTGCAGTGAGCCAAGATCGGGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCTGTCTCAAAAAACAAAAAAGAGTTGGGTTTGAAAAGTGGCTTGAGCCTGGGGTGACTCAAGAGGACGCTCCCTTCATCTTTGGTTTTCCCCTTTCTGTTGCACAGAAACACGATGGCTCTGTTAACAGCCGAAACATT... | CAACATGGTGAAACCCCGTCTGTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGCAGGCATCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACTTGGAAGGCGGAGGTTGCAGTGAGCCAAGATCGGGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCTGTCTCAAAAAACAAAAAAGAGTTGGGTTTGAAAAGTGGCTTGAGCCTGGGGTGACTCAAGAGGACGCTCCCTTCATCTTTGGTTTTCCCCTTTCTGTTGCACAGAAACACGATGGCTCTGTTAACAGCCGAAACATT... |
Task1_train_48697 | Chromosome 22 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TCCGGAGTGAATCCGAACTACCCCAGGGAGACGGCAGCGAAGAAAATCTTGTTCTTAGGAGAACGCAATCTTCGGACACCAGAAGTTCCTCTATGATGCTATTCTGTGGCAGCCTTGCACTTGAGCCGGATGAAAATTGTAAAAACCCAGGTTGGGCGACAGGACGGCGCGTCTTCCCGGCTCCTTTCCAGAGTTTAGGAGGAGCCATGCAGACTCAGCCGGCCTTTGGGGGTAGGTGGACAGGCCCGGCGCGCCCTCTCGAGGCCCCTTCAACCTCCCGGGGGCAGCAGCGCCGTGTCGGCTATGAATGGGGCCTCTGG... | TCCGGAGTGAATCCGAACTACCCCAGGGAGACGGCAGCGAAGAAAATCTTGTTCTTAGGAGAACGCAATCTTCGGACACCAGAAGTTCCTCTATGATGCTATTCTGTGGCAGCCTTGCACTTGAGCCGGATGAAAATTGTAAAAACCCAGGTTGGGCGACAGGACGGCGCGTCTTCCCGGCTCCTTTCCAGAGTTTAGGAGGAGCCATGCAGACTCAGCCGGCCTTTGGGGGTAGGTGGACAGGCCCGGCGCGCCCTCTCGAGGCCCCTTCAACCTCCCGGGGGCAGCAGCGCCGTGTCGGCTATGAATGGGGCCTCTGG... |
Task1_train_48698 | A genomic change on Chromosome 22 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CCTCCGTTCTCTGAGGCTCTGGGGATACTTGCAGTCAGGCAGATGTAGGGTTGTGACCTAGGTTCTTGTTAGCATCTCATTTCCCTTTTCCAAACCTCAGTTTTCCCATTTGCAAAATGGCGGTGGAAACACCCATAGAAAAATTCTAGAGGGAGCTGGGAAGGGAGGAGCTGGACTGACCTGCATTCTAACGTGACGGATGCTCTCCCAGGGTGACGCCAATCGCTCCTACTCGGACGAGGACCAGAGCTCATCCAACATAGAAGAGTTTGATAAGCTCCAGGAAGGCCTGGACAGCAGCGGAGGTAAACAGGCCCTCG... | CCTCCGTTCTCTGAGGCTCTGGGGATACTTGCAGTCAGGCAGATGTAGGGTTGTGACCTAGGTTCTTGTTAGCATCTCATTTCCCTTTTCCAAACCTCAGTTTTCCCATTTGCAAAATGGCGGTGGAAACACCCATAGAAAAATTCTAGAGGGAGCTGGGAAGGGAGGAGCTGGACTGACCTGCATTCTAACGTGACGGATGCTCTCCCAGGGTGACGCCAATCGCTCCTACTCGGACGAGGACCAGAGCTCATCCAACATAGAAGAGTTTGATAAGCTCCAGGAAGGCCTGGACAGCAGCGGAGGTAAACAGGCCCTCG... |
Task1_train_48699 | This variant is present on Chromosome 22. Is the change likely to result in a pathogenic outcome? | Benign | GAGTGGTGTCCCTGCTTGTCAGGTCTGCTTGTCAGTGCAGCTTCCTGAGGGCTGCTGGGTGAAGATGGATTTGGGGAGGGGGATTGGGTGGAGGAAGTCAGGGAGGAGACTCAGCCTTGGCTTCTGAGACCCCTGAGTAGCAGGGGTCCCTCTGGGGCTAGGCGGGGACTTTAGGCAAGACGTGTGGCTGACCAAGGTTGGCTGTGTCCAGACTGAGGGGGTCACTGGGAGAAGAAACAGAAAGATTCTCTAGCTCAAGACAGGGCCCACTCAGTGGTGGAAGCAGGGCTGTGTGCAACTCCCAGGCTGGTAATGGACCT... | GAGTGGTGTCCCTGCTTGTCAGGTCTGCTTGTCAGTGCAGCTTCCTGAGGGCTGCTGGGTGAAGATGGATTTGGGGAGGGGGATTGGGTGGAGGAAGTCAGGGAGGAGACTCAGCCTTGGCTTCTGAGACCCCTGAGTAGCAGGGGTCCCTCTGGGGCTAGGCGGGGACTTTAGGCAAGACGTGTGGCTGACCAAGGTTGGCTGTGTCCAGACTGAGGGGGTCACTGGGAGAAGAAACAGAAAGATTCTCTAGCTCAAGACAGGGCCCACTCAGTGGTGGAAGCAGGGCTGTGTGCAACTCCCAGGCTGGTAATGGACCT... |
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