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_48800 | Chromosome 22 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GCTCCCTCAGTGCCCCCCTAGCAGCCCCGGCGGTCTTCTCCCCACCTTCAGCCCCCTCCCCGGTCCCCCAGGAAGGGGCCAGACTCCAGCTCAGCACCCAGCGCTTCCTGGTCTTTCCCTTCTGGGCGCCCTCCCGACAGTTCCCTTTAGGGAAGTTGGCCCGCTGCGCGCTCCCACCCCCGGCCGCCGCCTGGACAGAGGCGCGCAATCCGGAGGGCGCAGGCTCCGGCCCGGAGAAGGGGGTGCCGCCGGCGTTCCGATTTCTCAGGAATGGGGAAACAGAGGCACGGTGGATCCGGCGGCGGGGCTGGGTCTGGGGC... | GCTCCCTCAGTGCCCCCCTAGCAGCCCCGGCGGTCTTCTCCCCACCTTCAGCCCCCTCCCCGGTCCCCCAGGAAGGGGCCAGACTCCAGCTCAGCACCCAGCGCTTCCTGGTCTTTCCCTTCTGGGCGCCCTCCCGACAGTTCCCTTTAGGGAAGTTGGCCCGCTGCGCGCTCCCACCCCCGGCCGCCGCCTGGACAGAGGCGCGCAATCCGGAGGGCGCAGGCTCCGGCCCGGAGAAGGGGGTGCCGCCGGCGTTCCGATTTCTCAGGAATGGGGAAACAGAGGCACGGTGGATCCGGCGGCGGGGCTGGGTCTGGGGC... |
Task1_train_48801 | A mutation has occurred on Chromosome 22. What is the medical relevance of this mutation? | Benign | TCTGGGCGCCCTCCCGACAGTTCCCTTTAGGGAAGTTGGCCCGCTGCGCGCTCCCACCCCCGGCCGCCGCCTGGACAGAGGCGCGCAATCCGGAGGGCGCAGGCTCCGGCCCGGAGAAGGGGGTGCCGCCGGCGTTCCGATTTCTCAGGAATGGGGAAACAGAGGCACGGTGGATCCGGCGGCGGGGCTGGGTCTGGGGCTGGACGTTGACCTAGGACCCCGCCCCTGCCCGCCCTGCGCCGCGCCCCTCCCGGGCCGGCCTTGACCGAGCAGCTCCACGCGGGCCCGGGGCTCGTCCACCCGACAGGAGCGGGGGGCTG... | TCTGGGCGCCCTCCCGACAGTTCCCTTTAGGGAAGTTGGCCCGCTGCGCGCTCCCACCCCCGGCCGCCGCCTGGACAGAGGCGCGCAATCCGGAGGGCGCAGGCTCCGGCCCGGAGAAGGGGGTGCCGCCGGCGTTCCGATTTCTCAGGAATGGGGAAACAGAGGCACGGTGGATCCGGCGGCGGGGCTGGGTCTGGGGCTGGACGTTGACCTAGGACCCCGCCCCTGCCCGCCCTGCGCCGCGCCCCTCCCGGGCCGGCCTTGACCGAGCAGCTCCACGCGGGCCCGGGGCTCGTCCACCCGACAGGAGCGGGGGGCTG... |
Task1_train_48802 | A mutation located on Chromosome 22 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GCCCGCTGCGCGCTCCCACCCCCGGCCGCCGCCTGGACAGAGGCGCGCAATCCGGAGGGCGCAGGCTCCGGCCCGGAGAAGGGGGTGCCGCCGGCGTTCCGATTTCTCAGGAATGGGGAAACAGAGGCACGGTGGATCCGGCGGCGGGGCTGGGTCTGGGGCTGGACGTTGACCTAGGACCCCGCCCCTGCCCGCCCTGCGCCGCGCCCCTCCCGGGCCGGCCTTGACCGAGCAGCTCCACGCGGGCCCGGGGCTCGTCCACCCGACAGGAGCGGGGGGCTGCAGCCCACGAGCCCACGAGCCCGCAGCGACGCACCCGG... | GCCCGCTGCGCGCTCCCACCCCCGGCCGCCGCCTGGACAGAGGCGCGCAATCCGGAGGGCGCAGGCTCCGGCCCGGAGAAGGGGGTGCCGCCGGCGTTCCGATTTCTCAGGAATGGGGAAACAGAGGCACGGTGGATCCGGCGGCGGGGCTGGGTCTGGGGCTGGACGTTGACCTAGGACCCCGCCCCTGCCCGCCCTGCGCCGCGCCCCTCCCGGGCCGGCCTTGACCGAGCAGCTCCACGCGGGCCCGGGGCTCGTCCACCCGACAGGAGCGGGGGGCTGCAGCCCACGAGCCCACGAGCCCGCAGCGACGCACCCGG... |
Task1_train_48803 | Chromosome 22 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TTTTCGTCTGGGTTGATGATTTCACACGTTAGCTAGAGTTTTTCAAATTCGTATTTCATGTATCAGGTCTTCTAGCAAGGAAGGATGAATAGATCTCAAGGAATTCAGCTTTGCTGATTATAGCAGCTGTGAGTACCTCTCATGAACTGTTTGAAGGATGAGGGCATAAATTCTAGATGAGGCAACCTCTTTATACCATTCTAGGTTTTAATTCATGTTCCCCAATCCTTTATTAATAGGCCACTTGCATTTTTTTTCATGTCTCTATTTTTTGCTTATTTTGCAATTTGGGGGTATTGTCATCCTGTAAACGGATTGCA... | TTTTCGTCTGGGTTGATGATTTCACACGTTAGCTAGAGTTTTTCAAATTCGTATTTCATGTATCAGGTCTTCTAGCAAGGAAGGATGAATAGATCTCAAGGAATTCAGCTTTGCTGATTATAGCAGCTGTGAGTACCTCTCATGAACTGTTTGAAGGATGAGGGCATAAATTCTAGATGAGGCAACCTCTTTATACCATTCTAGGTTTTAATTCATGTTCCCCAATCCTTTATTAATAGGCCACTTGCATTTTTTTTCATGTCTCTATTTTTTGCTTATTTTGCAATTTGGGGGTATTGTCATCCTGTAAACGGATTGCA... |
Task1_train_48804 | A variant was discovered on Chromosome 22. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TGGTGTGTGCACATGTGCACTGTGTGGTGTGTATGCATGGTGTGTGCACGTGTGCACTGTGTATGCATGGTGTGTGCATGTGTGCACTGTATGCATAGTGTGCACGTGTGCACTGTGTGTGGATGCATGGTAATGTGCACGTGTGCACTGTGTGTGGTGTGTATGCATGGTGTGTGCACGTGTGCACGGTGTGTGGTGTGTATGCATGGTGTGTGCACATGTGCACTGTGTATGCATGGTGTGTGCACGTGTGCACTGTGTATGCATGGTGTGTGCACGTGTGCACTGTGTGGTGTGTATGCATGGTGTGTGCACATGTG... | TGGTGTGTGCACATGTGCACTGTGTGGTGTGTATGCATGGTGTGTGCACGTGTGCACTGTGTATGCATGGTGTGTGCATGTGTGCACTGTATGCATAGTGTGCACGTGTGCACTGTGTGTGGATGCATGGTAATGTGCACGTGTGCACTGTGTGTGGTGTGTATGCATGGTGTGTGCACGTGTGCACGGTGTGTGGTGTGTATGCATGGTGTGTGCACATGTGCACTGTGTATGCATGGTGTGTGCACGTGTGCACTGTGTATGCATGGTGTGTGCACGTGTGCACTGTGTGGTGTGTATGCATGGTGTGTGCACATGTG... |
Task1_train_48805 | A mutation has occurred on Chromosome 22. What is the medical relevance of this mutation? | Benign | GTGAGTGCCTTAAAACCTCTTAGAAGATACTTTTTATTTTCCAACTTAGAATTTGAAATAACCTCAGACTTAGAAAGGTACAGGAACAGTAGGGAGCTCCCACCTGCCTCGCACCCACCTTACCCCTGCATTACCGTTTTTTATCACCAGAGTCAGCGATCAAAACCAGGAAATTAAGGAGAAGATTCTGTCCACACCTAGACTCTTGTTTCCTGGACCTTACAATACTCCAGAGCATATGTTACGTTCAGCTGCATGTTTGTTTTAAAGAACCGTGTCTGCTGGGATTCAGTGAATGTTTTCCTCCATCCTCAGGAAGA... | GTGAGTGCCTTAAAACCTCTTAGAAGATACTTTTTATTTTCCAACTTAGAATTTGAAATAACCTCAGACTTAGAAAGGTACAGGAACAGTAGGGAGCTCCCACCTGCCTCGCACCCACCTTACCCCTGCATTACCGTTTTTTATCACCAGAGTCAGCGATCAAAACCAGGAAATTAAGGAGAAGATTCTGTCCACACCTAGACTCTTGTTTCCTGGACCTTACAATACTCCAGAGCATATGTTACGTTCAGCTGCATGTTTGTTTTAAAGAACCGTGTCTGCTGGGATTCAGTGAATGTTTTCCTCCATCCTCAGGAAGA... |
Task1_train_48806 | This variant lies on Chromosome 22. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TCATTTATGGCTTCTTAGTGTCACTTCCATACATCCTGCCTGCCCTGAGAACACTTAGTGTGGCAAAGTAAGTCATAGGTATTTGCTGCAGGAAAATCAGAAAATTCAAGTCAGATGAAAAGAAAACAGTTAAAAACCCAGGAACTCCCTGGAGAGCGCACCCTGCTGGTGCCTCCACTGCTCGTGCCCCCCCAGCGCCCCCGCAACGTGCCCTGCGTGACTTTCCGCAGCGCCTGTCGGGTGTTTTCCACTCAGCAGCTTGTTGCGAACGTCTCTGCGTCCTGTGGTTTCTCTGTCACGCTAATGATTTTGGAGCCATT... | TCATTTATGGCTTCTTAGTGTCACTTCCATACATCCTGCCTGCCCTGAGAACACTTAGTGTGGCAAAGTAAGTCATAGGTATTTGCTGCAGGAAAATCAGAAAATTCAAGTCAGATGAAAAGAAAACAGTTAAAAACCCAGGAACTCCCTGGAGAGCGCACCCTGCTGGTGCCTCCACTGCTCGTGCCCCCCCAGCGCCCCCGCAACGTGCCCTGCGTGACTTTCCGCAGCGCCTGTCGGGTGTTTTCCACTCAGCAGCTTGTTGCGAACGTCTCTGCGTCCTGTGGTTTCTCTGTCACGCTAATGATTTTGGAGCCATT... |
Task1_train_48807 | This mutation is located on Chromosome 22. Is it associated with a disease or is it a benign polymorphism? | Benign | GAAAATCAGAAAATTCAAGTCAGATGAAAAGAAAACAGTTAAAAACCCAGGAACTCCCTGGAGAGCGCACCCTGCTGGTGCCTCCACTGCTCGTGCCCCCCCAGCGCCCCCGCAACGTGCCCTGCGTGACTTTCCGCAGCGCCTGTCGGGTGTTTTCCACTCAGCAGCTTGTTGCGAACGTCTCTGCGTCCTGTGGTTTCTCTGTCACGCTAATGATTTTGGAGCCATTATTTCATACTTTTACAACAATGTCTGTTGCTGGACGTTTACGTCATAACAGTTTTTCAACTTATAAACTGTGAACACTTGAAGGTAAACTT... | GAAAATCAGAAAATTCAAGTCAGATGAAAAGAAAACAGTTAAAAACCCAGGAACTCCCTGGAGAGCGCACCCTGCTGGTGCCTCCACTGCTCGTGCCCCCCCAGCGCCCCCGCAACGTGCCCTGCGTGACTTTCCGCAGCGCCTGTCGGGTGTTTTCCACTCAGCAGCTTGTTGCGAACGTCTCTGCGTCCTGTGGTTTCTCTGTCACGCTAATGATTTTGGAGCCATTATTTCATACTTTTACAACAATGTCTGTTGCTGGACGTTTACGTCATAACAGTTTTTCAACTTATAAACTGTGAACACTTGAAGGTAAACTT... |
Task1_train_48808 | This alteration occurs on Chromosome 22. Is it associated with a disease or is it a benign variant? | Benign | GCGTGGACCACCTCCCGGTGAAGATCCTGCAGCCAGGTACGCGCGGGGCCGGCGGGGCCGGGGCCGGGGCCAGGGCGGGGACCGGGGGCGCCCCGGGCCGCACCAACCCCGCCCGCGCCTCCCTGCAGCCAAGGCGGACAAGGAGAGCTTCGAGAAGGCGTACCAGGTGGGCGCCGTGCTGGGTAGCGGCGGCTTCGGCACGGTCTACGCGGGTAGCCGCATCGCCGACGGGCTCCCGGTGAGTCGGACCGCCGGGCGGGCCCGGGTTTCTCGCGCGCCTTGCGCCTCGCTTGGCCCGGCCTGACCCCCGCGTCTCCGCA... | GCGTGGACCACCTCCCGGTGAAGATCCTGCAGCCAGGTACGCGCGGGGCCGGCGGGGCCGGGGCCGGGGCCAGGGCGGGGACCGGGGGCGCCCCGGGCCGCACCAACCCCGCCCGCGCCTCCCTGCAGCCAAGGCGGACAAGGAGAGCTTCGAGAAGGCGTACCAGGTGGGCGCCGTGCTGGGTAGCGGCGGCTTCGGCACGGTCTACGCGGGTAGCCGCATCGCCGACGGGCTCCCGGTGAGTCGGACCGCCGGGCGGGCCCGGGTTTCTCGCGCGCCTTGCGCCTCGCTTGGCCCGGCCTGACCCCCGCGTCTCCGCA... |
Task1_train_48809 | This is a variant located on Chromosome 22. Is this mutation a likely cause of disease or not? | Benign | GGATCTGGGGAAGCTGAGACCCTCTGGAGGGGTCCGAGTGGGGCGGGTGCCCCAGTGAAGCTCAGCACCCAAGGATGCACAGACAGGAGAGGTGGACTCCAGCCAGTGTGGGGTGCCCTGGGCAGAAACTGGGGTGATCCTTGACCACCTCGGGCCTGATCAGCTACAGGAAGGGTGGGGTTGCACCCTGCACCCCAGAGCACTGGGGAAGCTCCAGGCAGCTGCCAGGGCCTTGTCTTCAGGGCCAGGGACAGTGGCCATGACCATGAATTGTCTGAGAGGGAGGCTGGGGTCCAGCACCTGGGCCATCCGGGGAAGGG... | GGATCTGGGGAAGCTGAGACCCTCTGGAGGGGTCCGAGTGGGGCGGGTGCCCCAGTGAAGCTCAGCACCCAAGGATGCACAGACAGGAGAGGTGGACTCCAGCCAGTGTGGGGTGCCCTGGGCAGAAACTGGGGTGATCCTTGACCACCTCGGGCCTGATCAGCTACAGGAAGGGTGGGGTTGCACCCTGCACCCCAGAGCACTGGGGAAGCTCCAGGCAGCTGCCAGGGCCTTGTCTTCAGGGCCAGGGACAGTGGCCATGACCATGAATTGTCTGAGAGGGAGGCTGGGGTCCAGCACCTGGGCCATCCGGGGAAGGG... |
Task1_train_48810 | Chromosome 22 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GGATTGCTGCAGGAGGAACTTCGCCTCCCGTGGGGCAAGAGGCATCTCCGTGAGTGGGTCCCAGCCCCTGAATCGCAGTGGGAATCAGGGAGGCGGCAACACCTGCGTGCCGTCATAAAGACCCCCACCATGCCCTCGTAAAGACCCCCATCACACCGTCCTGAAGACCCCCACATACCCTCGTAAAGACCCCATCACACCATCCTAAAGACCCCCACACACACTCGTAAAGACCCCATCACACCATCCTGAAGACCCCACACACCCTCGTAAAGACCCCATCACACCGTCCTAAAGACCCCCACATACCCTCGTAAAGA... | GGATTGCTGCAGGAGGAACTTCGCCTCCCGTGGGGCAAGAGGCATCTCCGTGAGTGGGTCCCAGCCCCTGAATCGCAGTGGGAATCAGGGAGGCGGCAACACCTGCGTGCCGTCATAAAGACCCCCACCATGCCCTCGTAAAGACCCCCATCACACCGTCCTGAAGACCCCCACATACCCTCGTAAAGACCCCATCACACCATCCTAAAGACCCCCACACACACTCGTAAAGACCCCATCACACCATCCTGAAGACCCCACACACCCTCGTAAAGACCCCATCACACCGTCCTAAAGACCCCCACATACCCTCGTAAAGA... |
Task1_train_48811 | A genomic variant on Chromosome 22 is under review. What is the biological outcome — benign or pathogenic? | Benign | CCCGCGGTCACTTTGGCCCCTCGCTCGGCCAGGGAGCTTGGTGCTGTTCACGGCGCTGTTCAAGGTCCTAACTCAAATCCTCCGACCCGCGCCACACCCCAGAGGTATGGGGACAAAGGCGTCACCCGCCAGGTTCTACAGAGGGGACCCCACCATCCACCTGGCCGGCACTCCCACGCCCCCCACCCCGAGACCCCCGTGCCGGGCTGGGACAGGTGCCCCAACCCCGCTCCCCGGCTCCCGCCGGCGCCTCCGTCAGGGGACACCCCGGGCCCCAGCACCGAAGCCTGCCCTGCGCCCCGCTCTGGAGGATGCAGCGG... | CCCGCGGTCACTTTGGCCCCTCGCTCGGCCAGGGAGCTTGGTGCTGTTCACGGCGCTGTTCAAGGTCCTAACTCAAATCCTCCGACCCGCGCCACACCCCAGAGGTATGGGGACAAAGGCGTCACCCGCCAGGTTCTACAGAGGGGACCCCACCATCCACCTGGCCGGCACTCCCACGCCCCCCACCCCGAGACCCCCGTGCCGGGCTGGGACAGGTGCCCCAACCCCGCTCCCCGGCTCCCGCCGGCGCCTCCGTCAGGGGACACCCCGGGCCCCAGCACCGAAGCCTGCCCTGCGCCCCGCTCTGGAGGATGCAGCGG... |
Task1_train_48812 | This alteration on Chromosome 22 may affect genome function. Does it lead to a disease or is it benign? | Benign | TACAGATGTGCCAGCGTGGATGGACCTCACCAACCCCACGTGTGCCAGCGTGGATGGACCTCACGGATCTCATGTGTGTCAGTGTGGACAGACCTCACTGACCCCACGTGTATCAGTGTGGACGGACCTCATGGACCTCATGTGTGCCAGTGTGGATGGATCTCACAGACCTCACATGTATCAGCGTGGACAGACCTCACAGACCTCACATGTGCCAGCGTGGATGGACCTCATGGACCTCATGTGTGTCGGTGTGGACAGACCTCACTGACCCCACGTGTATCAGTGTGGACGGACCTCACGGACCTCATGTGTGCCAG... | TACAGATGTGCCAGCGTGGATGGACCTCACCAACCCCACGTGTGCCAGCGTGGATGGACCTCACGGATCTCATGTGTGTCAGTGTGGACAGACCTCACTGACCCCACGTGTATCAGTGTGGACGGACCTCATGGACCTCATGTGTGCCAGTGTGGATGGATCTCACAGACCTCACATGTATCAGCGTGGACAGACCTCACAGACCTCACATGTGCCAGCGTGGATGGACCTCATGGACCTCATGTGTGTCGGTGTGGACAGACCTCACTGACCCCACGTGTATCAGTGTGGACGGACCTCACGGACCTCATGTGTGCCAG... |
Task1_train_48813 | A mutation on Chromosome 22 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GGGCAGCCAGGCCTTGCGTCCAGAAGGCACAAAACTCCAGATGCACAAATAAAGCTGAATTCCCAGCCAGGCACGGCGGCTCATGCCTGTAATCCTAGCACTTTGGGAGGCCGAGGCAGACGGATCGTGAGGTCAGGAGTTTGAGTACAGCCTGGCCAACATGGTAAACCCCGTCTCTACTAAAAATAACAAAAATTAGCTGGGCGTGGTGGCGGGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATCGCTTCAACTCAGGAGGCAGAGGTTGCAGTGAACCAAGATCACACCACTGCACTCTAGCCTG... | GGGCAGCCAGGCCTTGCGTCCAGAAGGCACAAAACTCCAGATGCACAAATAAAGCTGAATTCCCAGCCAGGCACGGCGGCTCATGCCTGTAATCCTAGCACTTTGGGAGGCCGAGGCAGACGGATCGTGAGGTCAGGAGTTTGAGTACAGCCTGGCCAACATGGTAAACCCCGTCTCTACTAAAAATAACAAAAATTAGCTGGGCGTGGTGGCGGGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATCGCTTCAACTCAGGAGGCAGAGGTTGCAGTGAACCAAGATCACACCACTGCACTCTAGCCTG... |
Task1_train_48814 | This genomic variant is located on Chromosome 22. Can you determine its pathogenicity and name any linked disease? | Benign | CCCTGCTGGCTCCTGTATGTGTTCCAGCACCCAGCCCAAGACACAGGCTTAGCGGGGATTTGAAATGCTAGGGAGTGCGCCACTCTCTCCCTTCCCACAGCAAGAACTATCAGTACACTCTGCATCCATGGACAGGCAAGGTCCAGGCTGTCATCAGACTGACAGATCTGACCTAGGAAAATAAAGCTATGTCAATCAAAAATAAGTCGGGGCTGGGCGCAGTGGCTCACACCTGTAATCCCAGCACTCGGGAGGCCAAGGCGGGTGGATCACCTGCGGGTCAGAAGTTCGAGACCAGCCTGACCAACATGGTAAAACCT... | CCCTGCTGGCTCCTGTATGTGTTCCAGCACCCAGCCCAAGACACAGGCTTAGCGGGGATTTGAAATGCTAGGGAGTGCGCCACTCTCTCCCTTCCCACAGCAAGAACTATCAGTACACTCTGCATCCATGGACAGGCAAGGTCCAGGCTGTCATCAGACTGACAGATCTGACCTAGGAAAATAAAGCTATGTCAATCAAAAATAAGTCGGGGCTGGGCGCAGTGGCTCACACCTGTAATCCCAGCACTCGGGAGGCCAAGGCGGGTGGATCACCTGCGGGTCAGAAGTTCGAGACCAGCCTGACCAACATGGTAAAACCT... |
Task1_train_48815 | A mutation found on Chromosome 22 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GAGCGGCGCGGGCGCGTGCGGGCGGCGGCAGCGGCGGTGACGGCAGCCTAGGCCGGGCGAGGGCCATGCTGAGCCTCGCAGCCAAGCTGGTGGCCTTCTTCTGGAGGACGGCGGACACCCCTAGGGAGGAAGCCGGGCAGCTGGAGCCCGAGCTCGCGGAAGGTGGCTCGCGGGAGGCGGCTGGGAGGCGGGTCCCGGGCCCTCGCGTGTCGGCCACGAGGGAGCCGCGCCCATAGGTCTTTGAGTGCAGTGCGGGCCGGCAGGCAACGCTGGGCCCGGCCTTTCCTCATCTCCGCTGGCGGGGATCCCCGTTCGCCTCA... | GAGCGGCGCGGGCGCGTGCGGGCGGCGGCAGCGGCGGTGACGGCAGCCTAGGCCGGGCGAGGGCCATGCTGAGCCTCGCAGCCAAGCTGGTGGCCTTCTTCTGGAGGACGGCGGACACCCCTAGGGAGGAAGCCGGGCAGCTGGAGCCCGAGCTCGCGGAAGGTGGCTCGCGGGAGGCGGCTGGGAGGCGGGTCCCGGGCCCTCGCGTGTCGGCCACGAGGGAGCCGCGCCCATAGGTCTTTGAGTGCAGTGCGGGCCGGCAGGCAACGCTGGGCCCGGCCTTTCCTCATCTCCGCTGGCGGGGATCCCCGTTCGCCTCA... |
Task1_train_48816 | A genomic variant on Chromosome 22 is under review. What is the biological outcome — benign or pathogenic? | Benign | GCTCTGTCACCCAGGCTGGAGTGCAGTGGCACAATTGTAGCTCACTGCAGCCTGGAATTCCTGGGCTTAAGTCATCCCACCTTAGCCTCGTGAGTAGCTGGGACTTCAGGCTCATGCCACCACACCCCAACTAATTCTTTTTTTTTTTTTTTTTTTTTTTAGAGATGGGATCTTACTGTGTTGCCCAGGCTGGTCTCAAACTCCTGGGCTCAAGTGATCTTCCCACCTCAGCCTCACAAAGTGCTAGAAATCTTTACTATGATTCCATGATTCTGCTGGAAAAAAAAATTAATTGAATTTAACTTTTTTTTTCTTTAAAG... | GCTCTGTCACCCAGGCTGGAGTGCAGTGGCACAATTGTAGCTCACTGCAGCCTGGAATTCCTGGGCTTAAGTCATCCCACCTTAGCCTCGTGAGTAGCTGGGACTTCAGGCTCATGCCACCACACCCCAACTAATTCTTTTTTTTTTTTTTTTTTTTTTTAGAGATGGGATCTTACTGTGTTGCCCAGGCTGGTCTCAAACTCCTGGGCTCAAGTGATCTTCCCACCTCAGCCTCACAAAGTGCTAGAAATCTTTACTATGATTCCATGATTCTGCTGGAAAAAAAAATTAATTGAATTTAACTTTTTTTTTCTTTAAAG... |
Task1_train_48817 | Here’s a variant located on Chromosome 22. What is the predicted biological effect — harmless or disease-causing? | Benign | GGGGGAAAAACCTTCATTGTGGTCATCTGTGACGGAAAGTAAGGGCCTGGAGGTCTGGGGAGAGCCGCGTTTTTAAGTTTCTCTGATACTTCTAGGTTGGGTGTTATAAAAGGTACTCCTTTGTGGCGGGTGGATCACCTGAGACCAGGAGTTCGAAACCAGCCTGGCCACCATGGCGAAACCCCGCCTCTACTAAAAATACAAAAATTACTTGGGCCCCTGTAGTCCTAGCTACTCAGGAGGCTGAGGCAGTAGAATCGCTTAAATCCAGGTGACGGAGGGTGCAGTGAGCCAAGATCGCACGACTGCACTCCAGCCTG... | GGGGGAAAAACCTTCATTGTGGTCATCTGTGACGGAAAGTAAGGGCCTGGAGGTCTGGGGAGAGCCGCGTTTTTAAGTTTCTCTGATACTTCTAGGTTGGGTGTTATAAAAGGTACTCCTTTGTGGCGGGTGGATCACCTGAGACCAGGAGTTCGAAACCAGCCTGGCCACCATGGCGAAACCCCGCCTCTACTAAAAATACAAAAATTACTTGGGCCCCTGTAGTCCTAGCTACTCAGGAGGCTGAGGCAGTAGAATCGCTTAAATCCAGGTGACGGAGGGTGCAGTGAGCCAAGATCGCACGACTGCACTCCAGCCTG... |
Task1_train_48818 | With a mutation on Chromosome 22, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GGCGGCTGTCTTTTCCCTGTGTCCTCACGCAGCAGAAGGGATGGGAGAGCTCTCTGTGCTCCCTTGTGTAAGGGCACTAATTCCATTCATGAGGCCCCACCCTCATGACCTAATCACTTGCCAAAGGCCTCAACTCCTCATACCCAGTAACATCACATTGGGGATGAAGTTTCACCATACGAAGCTGGGGGGAACACAAACCTAGTGTATGATATGTGCCTTTATGATAAGTCTCAAAATCAGGTAGTATCAAGCCTCCAACTTTGTTCCTTTTCAAGGTTGTCTGGCTGTTCCAGGTCTTTCTTCTTACATGGATTTTA... | GGCGGCTGTCTTTTCCCTGTGTCCTCACGCAGCAGAAGGGATGGGAGAGCTCTCTGTGCTCCCTTGTGTAAGGGCACTAATTCCATTCATGAGGCCCCACCCTCATGACCTAATCACTTGCCAAAGGCCTCAACTCCTCATACCCAGTAACATCACATTGGGGATGAAGTTTCACCATACGAAGCTGGGGGGAACACAAACCTAGTGTATGATATGTGCCTTTATGATAAGTCTCAAAATCAGGTAGTATCAAGCCTCCAACTTTGTTCCTTTTCAAGGTTGTCTGGCTGTTCCAGGTCTTTCTTCTTACATGGATTTTA... |
Task1_train_48819 | A mutation found on Chromosome 22 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GCCGGTGCTGGCACCCTTTACTGCAGAGATGAGCGATTGGGGTATGTGCTCATGAGGGGCAAGGAGAAGAGCAACTCTGAGACTGTCGCCTGGAAAACGGGGACTTTGAGGAGTGGGCTCTCATGCAGAAGGAAGAACAGTAGGGGGCGTGTGGCCTGTGACAGGCGGCTGCCGTCTCCACCCTGACTGGAGACTTGGTGTTTTAGCTTAGATACTTTAAGAAGACTTTTAGATTCTGGGTTGTTTTTTTCCAGGTACTCTGCAGATGTGGACATTTTTTAATCCAGTCTCTAATATTTGAGTGTGATCTCTAAAGCCGC... | GCCGGTGCTGGCACCCTTTACTGCAGAGATGAGCGATTGGGGTATGTGCTCATGAGGGGCAAGGAGAAGAGCAACTCTGAGACTGTCGCCTGGAAAACGGGGACTTTGAGGAGTGGGCTCTCATGCAGAAGGAAGAACAGTAGGGGGCGTGTGGCCTGTGACAGGCGGCTGCCGTCTCCACCCTGACTGGAGACTTGGTGTTTTAGCTTAGATACTTTAAGAAGACTTTTAGATTCTGGGTTGTTTTTTTCCAGGTACTCTGCAGATGTGGACATTTTTTAATCCAGTCTCTAATATTTGAGTGTGATCTCTAAAGCCGC... |
Task1_train_48820 | This alteration on Chromosome 22 may affect genome function. Does it lead to a disease or is it benign? | Benign | GACAGAGCTGGCTGGGGCCCAGGTGGCTGCTCCGCTCCCAGGGACAGATTCAGTCAGGGCTTCAGGGCATCTCTGCGATGCTGGGGCCGGTTGGTCACAGAGTAGAGAGTGGCGAGGCTGACACAGGTGTGGGGGCAGACAGTGGTCTCTGCTGTGGGTGGGCTTCAGAGAAAGCCTCTGGGTTTCTAGGGAGAATGGGCTCCCAGAGGTCAAGCTTTCCCACACCATCTTCCAAAGGGAAGGGCTGCCCTGTCTGAAGAGTCCCGCCCACGTGCAGGATGAGACGTGGAAAATATTGTTGCTTTAACTTAAAAAACAAG... | GACAGAGCTGGCTGGGGCCCAGGTGGCTGCTCCGCTCCCAGGGACAGATTCAGTCAGGGCTTCAGGGCATCTCTGCGATGCTGGGGCCGGTTGGTCACAGAGTAGAGAGTGGCGAGGCTGACACAGGTGTGGGGGCAGACAGTGGTCTCTGCTGTGGGTGGGCTTCAGAGAAAGCCTCTGGGTTTCTAGGGAGAATGGGCTCCCAGAGGTCAAGCTTTCCCACACCATCTTCCAAAGGGAAGGGCTGCCCTGTCTGAAGAGTCCCGCCCACGTGCAGGATGAGACGTGGAAAATATTGTTGCTTTAACTTAAAAAACAAG... |
Task1_train_48821 | A change on Chromosome 22 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | AAGGTGTTGTAGGACTGCTGCATGAGTGCAAAGTTGGGGTGCTCTGCACCCCGCGGGCCCCCAGGGGGCCCCCAGGCCTGGGAGATGAGCTGGCTGCGGAACTTGAGCACGAGGCTGAAGATGCTGTGGATGACGTTCATGACGGGCGCCGCCTTCTCCGTGAGCAGGCCCCTGGGGGGAAGCAGTGCTGCTGGGTGGGCTGAGCCGTGACCACAGGGACGCAGCCGCTGCCCAGGCCTCACCTGAAGACGGCCTTGTGCAGGTACTCTGCGTGCGCACGCTGGATCTCCTCCAGGTCGCCCACGGTGGCCAACCTGGCC... | AAGGTGTTGTAGGACTGCTGCATGAGTGCAAAGTTGGGGTGCTCTGCACCCCGCGGGCCCCCAGGGGGCCCCCAGGCCTGGGAGATGAGCTGGCTGCGGAACTTGAGCACGAGGCTGAAGATGCTGTGGATGACGTTCATGACGGGCGCCGCCTTCTCCGTGAGCAGGCCCCTGGGGGGAAGCAGTGCTGCTGGGTGGGCTGAGCCGTGACCACAGGGACGCAGCCGCTGCCCAGGCCTCACCTGAAGACGGCCTTGTGCAGGTACTCTGCGTGCGCACGCTGGATCTCCTCCAGGTCGCCCACGGTGGCCAACCTGGCC... |
Task1_train_48822 | With a mutation on Chromosome 22, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CGCACGCTGGATCTCCTCCAGGTCGCCCACGGTGGCCAACCTGGCCCTGAACTCGCACCAGGTGACGTGCAGGATCTGGTTGGCGATGTAGCCCTGGATGACCTTCACGAAATGCTGCATCTCGTGCTTGAACAGCTGCAGCTGACGGAACTGCACAGAGCCGGCCATGTGGCTCAGCAGGGCTGGCGGAGGGCAGAAGGCAGAGGGCAGAGGTGAGCGCAGCCTCCAGCCAGGGGTGCGGGGCGCCGGGCTCCAGCGGGGCCTCACCTGTGCGCTTGAGGTGGAAGCAGACGTCCTTGAGCGCCCACATCATGAGCTTC... | CGCACGCTGGATCTCCTCCAGGTCGCCCACGGTGGCCAACCTGGCCCTGAACTCGCACCAGGTGACGTGCAGGATCTGGTTGGCGATGTAGCCCTGGATGACCTTCACGAAATGCTGCATCTCGTGCTTGAACAGCTGCAGCTGACGGAACTGCACAGAGCCGGCCATGTGGCTCAGCAGGGCTGGCGGAGGGCAGAAGGCAGAGGGCAGAGGTGAGCGCAGCCTCCAGCCAGGGGTGCGGGGCGCCGGGCTCCAGCGGGGCCTCACCTGTGCGCTTGAGGTGGAAGCAGACGTCCTTGAGCGCCCACATCATGAGCTTC... |
Task1_train_48823 | Consider this mutation on Chromosome 22. Is this a benign change or a disease-causing variant? | Benign | CCCTACCTCGCCTTCCTCTCCAGCTCCTCCTCCAGGGACTTCAGCCTTCTCTCCCTGTCTCGGAGTTCACGGGCGTAGCTGAAGTCATCATCCAGCTCCTCCTGCCTGGCCGCCTGGCGTCGCTATAAAACACATAGAGCCTGGCCTGTGAAATCAGAACTGACAGGCGTGACCCCGCAGGGACAGGTCCTACCCACCTCCTGGTCCTTCACAAATTGTTCTTTCAGCCTCTGAAACTGCTCACGCTTCCGGGCATCCAAGGCCATCCGTTCTGACATCTGCCGGTCTACATTGGGACAGTAAGGGGCGCACTGTCACAA... | CCCTACCTCGCCTTCCTCTCCAGCTCCTCCTCCAGGGACTTCAGCCTTCTCTCCCTGTCTCGGAGTTCACGGGCGTAGCTGAAGTCATCATCCAGCTCCTCCTGCCTGGCCGCCTGGCGTCGCTATAAAACACATAGAGCCTGGCCTGTGAAATCAGAACTGACAGGCGTGACCCCGCAGGGACAGGTCCTACCCACCTCCTGGTCCTTCACAAATTGTTCTTTCAGCCTCTGAAACTGCTCACGCTTCCGGGCATCCAAGGCCATCCGTTCTGACATCTGCCGGTCTACATTGGGACAGTAAGGGGCGCACTGTCACAA... |
Task1_train_48824 | A mutation on Chromosome 22 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TGTGGGAAGAATTGGGGAGGTGGGTTCTAGGGGACTCCCAAGGAGCGGACAGGCCACCCACGGTCCAGGAGACCCCGGGGGGTTGGACTTGAAGCTCCCAAGCTGGGGCCTCCTGACAACCTTCAAGGACTTGAGGCCACGCCCTCGGACCCCAAACTGCCCCGAGCTCCTCCCTCTGGCCAGTGCACCAAGCCCAGCAGCCCTCGGGACGGAGCAGGTGCCCTGGGTACGGCATGTTGTGTACCACTGCCTCTTGGGCTCACCCACCCACCAGCTCCTCAGCCACTGCCCAGAGCCTGGGACCTTGGCCCCCTGCCCAG... | TGTGGGAAGAATTGGGGAGGTGGGTTCTAGGGGACTCCCAAGGAGCGGACAGGCCACCCACGGTCCAGGAGACCCCGGGGGGTTGGACTTGAAGCTCCCAAGCTGGGGCCTCCTGACAACCTTCAAGGACTTGAGGCCACGCCCTCGGACCCCAAACTGCCCCGAGCTCCTCCCTCTGGCCAGTGCACCAAGCCCAGCAGCCCTCGGGACGGAGCAGGTGCCCTGGGTACGGCATGTTGTGTACCACTGCCTCTTGGGCTCACCCACCCACCAGCTCCTCAGCCACTGCCCAGAGCCTGGGACCTTGGCCCCCTGCCCAG... |
Task1_train_48825 | With a mutation on Chromosome 22, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GCGCGTTCCAGGGGAGGGTGGGGGCCTCAGCCACAGCCACTCGGCCTCCTCCCCTGAGGGGCTCTCAGGTACCTCAGGTACCTATGTCCCAAGGCAGCACTGGAGATTGTAGGTCAGAGGTCAGTGACCTTGTTCTCCAGTGCAGCGGCAATCTGCTGCAGGCGGAAGGCCAGCTGCATCTTCTGGGCGGCAGGATCCTCCTCCAAGGCATTGATGATCTGAGGGAGGGTCGCATCAGAGCACACCGGGGGACCGCCCAGCACCCCACCTGCCCCCGCCCCCGGGGGCCTGACCCTACCTCGTCATAGTACTTCTGCGTG... | GCGCGTTCCAGGGGAGGGTGGGGGCCTCAGCCACAGCCACTCGGCCTCCTCCCCTGAGGGGCTCTCAGGTACCTCAGGTACCTATGTCCCAAGGCAGCACTGGAGATTGTAGGTCAGAGGTCAGTGACCTTGTTCTCCAGTGCAGCGGCAATCTGCTGCAGGCGGAAGGCCAGCTGCATCTTCTGGGCGGCAGGATCCTCCTCCAAGGCATTGATGATCTGAGGGAGGGTCGCATCAGAGCACACCGGGGGACCGCCCAGCACCCCACCTGCCCCCGCCCCCGGGGGCCTGACCCTACCTCGTCATAGTACTTCTGCGTG... |
Task1_train_48826 | Assess the clinical impact of this variant found on Chromosome 22. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TCCGTCAGCGTCTTCATGGTGCAGCGCTCGGCACCCACGAAGGCCTCGGCCTCCTGCAGCGTCATCGCCTTGTTCAGATTGGTGCCCTGGGGAGGCGGCAGTGGTCGGGGTGAGGAGGAGGGAACCAGGGACAGGTGGACCAGCTCTCAGCCCAGACCCGAGCAGGACCCAGACACCCGGGGCTGCACCGTCCTCACCCGGGCGTGGATGAGCTTGTTGACCTGCTTCTTGACGCCACCTGTGAAGTTCTCAAAGGTGGGGTCAGGCACGTACTCGAAGGCCCCGGCCTCTGTTCTGAGCAGGGCACGGTGCCCGTCCAT... | TCCGTCAGCGTCTTCATGGTGCAGCGCTCGGCACCCACGAAGGCCTCGGCCTCCTGCAGCGTCATCGCCTTGTTCAGATTGGTGCCCTGGGGAGGCGGCAGTGGTCGGGGTGAGGAGGAGGGAACCAGGGACAGGTGGACCAGCTCTCAGCCCAGACCCGAGCAGGACCCAGACACCCGGGGCTGCACCGTCCTCACCCGGGCGTGGATGAGCTTGTTGACCTGCTTCTTGACGCCACCTGTGAAGTTCTCAAAGGTGGGGTCAGGCACGTACTCGAAGGCCCCGGCCTCTGTTCTGAGCAGGGCACGGTGCCCGTCCAT... |
Task1_train_48827 | This variant lies on Chromosome 22. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CGAAGGCCCCGGCCTCTGTTCTGAGCAGGGCACGGTGCCCGTCCATCTCGATCAGCACCGTGAGGTTGTAGGCCTCTGGCTCCTCAGGCACAGCCGGGGACAGGAAGACGACCTTGGTGTCATTGTGGAACACGTAGTCTGTACCCACCACCTGCAGGCAAGTCCCAGCTGTCAGCCCCCGGGCGCAGACCCCGCCCTTCCTGGGCACGATCCCATGGGCCGGTGCCAGAGCTGAGCCCACGCCAGGACTGACCGTCATGGGCTGCAGGGATTCAGCCTCCCGCGGCGGCTGCCAGGACTGCAGGGGCTCCGCGATGACC... | CGAAGGCCCCGGCCTCTGTTCTGAGCAGGGCACGGTGCCCGTCCATCTCGATCAGCACCGTGAGGTTGTAGGCCTCTGGCTCCTCAGGCACAGCCGGGGACAGGAAGACGACCTTGGTGTCATTGTGGAACACGTAGTCTGTACCCACCACCTGCAGGCAAGTCCCAGCTGTCAGCCCCCGGGCGCAGACCCCGCCCTTCCTGGGCACGATCCCATGGGCCGGTGCCAGAGCTGAGCCCACGCCAGGACTGACCGTCATGGGCTGCAGGGATTCAGCCTCCCGCGGCGGCTGCCAGGACTGCAGGGGCTCCGCGATGACC... |
Task1_train_48828 | A variant on Chromosome 22 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GTCCCAACAGCTCCCAGCATGGGGGAGCCCCCACCTGGCCCGGCCTGGGGCCCAGGACCCCCACCCCAGACCCACCACGCACCTCCCCCTGGGCCCGCCGGCTCATGTTCTGTGGCTGGGCGCTGGTGACGGCCACGCAGGACTTGCTTCGGCTCCACAGCCAGTGGCTGGCCTCCTCGGCCCGCGGACACTCGGCCTTCCGGGTGCATCTGCAGGCGCAGGGGGCGGCCTCAGCCCAGGGTGGAGTCTTGTTCTCCCGGGACAGGACAGTGCGATGTGCCCCCCGACCCAGGCCACGACCTTCCGGGATCCCAGAGGCA... | GTCCCAACAGCTCCCAGCATGGGGGAGCCCCCACCTGGCCCGGCCTGGGGCCCAGGACCCCCACCCCAGACCCACCACGCACCTCCCCCTGGGCCCGCCGGCTCATGTTCTGTGGCTGGGCGCTGGTGACGGCCACGCAGGACTTGCTTCGGCTCCACAGCCAGTGGCTGGCCTCCTCGGCCCGCGGACACTCGGCCTTCCGGGTGCATCTGCAGGCGCAGGGGGCGGCCTCAGCCCAGGGTGGAGTCTTGTTCTCCCGGGACAGGACAGTGCGATGTGCCCCCCGACCCAGGCCACGACCTTCCGGGATCCCAGAGGCA... |
Task1_train_48829 | A variant has been detected on Chromosome 22. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | ACTATATGCAAAATAGCCTCCCATCCCCAGACAAGACGGGGGCTGTGTCAGGAGAGGGTCCCTCCTGTCCTGGGCAGCCTGTTGGGCTGAGGGAAGCATCACACACAGCGCAGGGGGGTCGGGGGCCAACAGATGGGCACCGGGAGGGGCAGACGGTAGACGCACCCACATCAGCAAGGGCTCCCAGCCTGTCCCCGCCCCCGTCCCAGCCTAAGGTCTGCAGAGGCCAGGTGGGACCCAGGAGGAGGCAAGGCTCTGCCTGCGAGGAACCCCTATGGTCAAGGCCATGCTGTGGTTCCAAATGTCGCCTTTACTGCTGA... | ACTATATGCAAAATAGCCTCCCATCCCCAGACAAGACGGGGGCTGTGTCAGGAGAGGGTCCCTCCTGTCCTGGGCAGCCTGTTGGGCTGAGGGAAGCATCACACACAGCGCAGGGGGGTCGGGGGCCAACAGATGGGCACCGGGAGGGGCAGACGGTAGACGCACCCACATCAGCAAGGGCTCCCAGCCTGTCCCCGCCCCCGTCCCAGCCTAAGGTCTGCAGAGGCCAGGTGGGACCCAGGAGGAGGCAAGGCTCTGCCTGCGAGGAACCCCTATGGTCAAGGCCATGCTGTGGTTCCAAATGTCGCCTTTACTGCTGA... |
Task1_train_48830 | A variant has been detected on Chromosome 22. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CAGGACAGAAGGGCCTTGGGTCCCATGCCAGGCAAGGACAGGGCGGGGGGGGGGCGAGGACAGGGCGGGGGGGCGGCGAGGACAGGGTGGGGGGGCGGCGAGGACAGGGCGGGGGGCCCCGAGGACAGGGTGGGGGGGGGCGGCGAGGACGGGGGGGGGGCGGCGAGGACAGGGCGGGGGGCCGCGAGGACAGGGTGGGGGGGGGCGGCGAGGACAGGGTGGGGGGGTGGCGAGGACAGGGTGGGGGGCGGCGAGGACAGGGTGGGGGGGCGGCAAGGAGAGCTGGACACAGCCCAGGTGGGGCTGCAGGAGGGGTGGGC... | CAGGACAGAAGGGCCTTGGGTCCCATGCCAGGCAAGGACAGGGCGGGGGGGGGGCGAGGACAGGGCGGGGGGGCGGCGAGGACAGGGTGGGGGGGCGGCGAGGACAGGGCGGGGGGCCCCGAGGACAGGGTGGGGGGGGGCGGCGAGGACGGGGGGGGGGCGGCGAGGACAGGGCGGGGGGCCGCGAGGACAGGGTGGGGGGGGGCGGCGAGGACAGGGTGGGGGGGTGGCGAGGACAGGGTGGGGGGCGGCGAGGACAGGGTGGGGGGGCGGCAAGGAGAGCTGGACACAGCCCAGGTGGGGCTGCAGGAGGGGTGGGC... |
Task1_train_48831 | Assess the clinical impact of this variant found on Chromosome 22. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GGACAGGGTGGGGGGGGGCGGCGAGGACGGGGGGGGGGCGGCGAGGACAGGGCGGGGGGCCGCGAGGACAGGGTGGGGGGGGGCGGCGAGGACAGGGTGGGGGGGTGGCGAGGACAGGGTGGGGGGCGGCGAGGACAGGGTGGGGGGGCGGCAAGGAGAGCTGGACACAGCCCAGGTGGGGCTGCAGGAGGGGTGGGCACTGCTGGAGGCTCAGGCCCCTTGCCCGCCCACAGCCCCTCCTGCTGCCTGCCAGCTCCTGCCGCTCTTGAGGTGCCAGCCCAGAGTGGCCAAGCAGCGCACCTTCTGGAAGTAGCCCCTCT... | GGACAGGGTGGGGGGGGGCGGCGAGGACGGGGGGGGGGCGGCGAGGACAGGGCGGGGGGCCGCGAGGACAGGGTGGGGGGGGGCGGCGAGGACAGGGTGGGGGGGTGGCGAGGACAGGGTGGGGGGCGGCGAGGACAGGGTGGGGGGGCGGCAAGGAGAGCTGGACACAGCCCAGGTGGGGCTGCAGGAGGGGTGGGCACTGCTGGAGGCTCAGGCCCCTTGCCCGCCCACAGCCCCTCCTGCTGCCTGCCAGCTCCTGCCGCTCTTGAGGTGCCAGCCCAGAGTGGCCAAGCAGCGCACCTTCTGGAAGTAGCCCCTCT... |
Task1_train_48832 | A mutation located on Chromosome 22 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | AGCAGGTGTTCCCAGTTGTGTGAGGGTGCTGAGGCCCCCGATGAGCACCGGGGGAGGAGCACTGAGGCCCCAGATGAGCAGTGGGCCTGGAGGAACGCTGAAGCCATCCCCCTTGCTCTTGCAGTGCCCCGTTTGACAGGATCGCAGAGATCAACTTCAACATCGACGCTGACGAGGACAGTGTGAGCAAGCCGGGCTGTGTGGGGTGCCGCCACCCTTTTCCCAGGCAGCTCAGGCCATGCCCATGGCTCGGTCTGTCATGGGCCTGTGCGGTGGGGCTGGGAGAGGCCCCTCTGTGGAGCTCGGAACAGTCGCTTTCC... | AGCAGGTGTTCCCAGTTGTGTGAGGGTGCTGAGGCCCCCGATGAGCACCGGGGGAGGAGCACTGAGGCCCCAGATGAGCAGTGGGCCTGGAGGAACGCTGAAGCCATCCCCCTTGCTCTTGCAGTGCCCCGTTTGACAGGATCGCAGAGATCAACTTCAACATCGACGCTGACGAGGACAGTGTGAGCAAGCCGGGCTGTGTGGGGTGCCGCCACCCTTTTCCCAGGCAGCTCAGGCCATGCCCATGGCTCGGTCTGTCATGGGCCTGTGCGGTGGGGCTGGGAGAGGCCCCTCTGTGGAGCTCGGAACAGTCGCTTTCC... |
Task1_train_48833 | Given a variant located on Chromosome 22, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TGAGAATCCCCCTACCCTCGAAGGCCGCCCTAACAACTTCCCATCCGCTGACCCCTCCAACGCCATCAATCTCCAGCTGTGGTTGTTGAACTCGGAGGTGAGCTCCTCTCACCACTCTCTTGAATAAAGCTTTTCTCACCATTTTAACAAGTCCTCAGAATCATCTTTTCTTAACAAGCTCCTGCCCCACCCAGAATCACGGGGGGCCTGGGGACAAGTTTTCACCTCCTGAGATCCAGTGGGGCAGCCGGGGAAGGGGTGGTGCAGAGGGGGCGTGTGCTTGAGGGTGGGGTCTTGGGTCTGCCCCTACTTGTGGGACC... | TGAGAATCCCCCTACCCTCGAAGGCCGCCCTAACAACTTCCCATCCGCTGACCCCTCCAACGCCATCAATCTCCAGCTGTGGTTGTTGAACTCGGAGGTGAGCTCCTCTCACCACTCTCTTGAATAAAGCTTTTCTCACCATTTTAACAAGTCCTCAGAATCATCTTTTCTTAACAAGCTCCTGCCCCACCCAGAATCACGGGGGGCCTGGGGACAAGTTTTCACCTCCTGAGATCCAGTGGGGCAGCCGGGGAAGGGGTGGTGCAGAGGGGGCGTGTGCTTGAGGGTGGGGTCTTGGGTCTGCCCCTACTTGTGGGACC... |
Task1_train_48834 | A variant on Chromosome 22 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GAGGCTCCTCTGTGATCAGGCAGTGGGCAACACCAAGCCAGGCCTCTTCAGAGAGAATGCTGAGGACGGGGCAGGAGGGTGCCCAGGGAGCCACGCCGTGGCGGAGCCTGACTGTGCTCTGGGCGGCCCACTGCCTGGGGCAGGGGAGACAATCCCATCCTCATGCCTCCTGGGAAAGCAGCACCAGGCACACAGCCAAGCACAAAAGACGCCTTTATTGGTGCCCAGATCTAAAGGGCAGGATGGGCTGGTGTGAAGATGACGTGGAAGATGACAGTGCTTCCCCTCTTCCCCTGGGAGTCAGCCTCTTCCCCTCTGGC... | GAGGCTCCTCTGTGATCAGGCAGTGGGCAACACCAAGCCAGGCCTCTTCAGAGAGAATGCTGAGGACGGGGCAGGAGGGTGCCCAGGGAGCCACGCCGTGGCGGAGCCTGACTGTGCTCTGGGCGGCCCACTGCCTGGGGCAGGGGAGACAATCCCATCCTCATGCCTCCTGGGAAAGCAGCACCAGGCACACAGCCAAGCACAAAAGACGCCTTTATTGGTGCCCAGATCTAAAGGGCAGGATGGGCTGGTGTGAAGATGACGTGGAAGATGACAGTGCTTCCCCTCTTCCCCTGGGAGTCAGCCTCTTCCCCTCTGGC... |
Task1_train_48835 | A sequence alteration has been identified on Chromosome 22. Is it disease-inducing or harmless? | Benign | CTGCCCGCCCTGGGAGGGCTCACCGTCCAGTGGTGGCCGTCGTAACTGCCCTCCAGCACCACCTCAGGCCGTCCACCAAGCCCAGTCATGCGGCGGAAGAGGCCGTAGGAGTTGGCCAGCTGTAGGTGCTCCACGGCACCAAACAGGCGGTGGGCCCCGGTCCAGAGGCGCCCGTGGGTCCCGGGCTCCACGTAGGAGTACGGCACCTGGAGACAGGTGGGAGGTTCTCAGGGCTGCCCTGCCCCCAGCCCATCCCCCAGCCCTGCAGCGCTACCCACCAGGCTAATCAGGAACAAGGCCACGGTCGCAGTGCCCACAAG... | CTGCCCGCCCTGGGAGGGCTCACCGTCCAGTGGTGGCCGTCGTAACTGCCCTCCAGCACCACCTCAGGCCGTCCACCAAGCCCAGTCATGCGGCGGAAGAGGCCGTAGGAGTTGGCCAGCTGTAGGTGCTCCACGGCACCAAACAGGCGGTGGGCCCCGGTCCAGAGGCGCCCGTGGGTCCCGGGCTCCACGTAGGAGTACGGCACCTGGAGACAGGTGGGAGGTTCTCAGGGCTGCCCTGCCCCCAGCCCATCCCCCAGCCCTGCAGCGCTACCCACCAGGCTAATCAGGAACAAGGCCACGGTCGCAGTGCCCACAAG... |
Task1_train_48836 | A mutation found on Chromosome 22 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TGTGGGGCTCCGAGTCAGCAGCAGCATGGATCTGATGCTCCTGGAAACAAGCACAGGCGTCAGGAGCCAGAAGGGAAGGCCCAGGACAGTGCCTGGGCTGCCCCTGCGACTTGAGACCAGCCACCCATCTGAAGGACCCAGCCCACGTTCAGGCTTAACAGGCATTTGCAGCTGCTCACCTGAGCTCAGAACTCCACCTCCACCAAACATCCACACCTGGGCAACCACACCTGTCACTCCTGTCCTCTACCTGGGATCACCAGCCTGTCACCGCACCCTGCCCTGCACCTGCACCTCAGCAAGGTGAACCTCTTGCTGAC... | TGTGGGGCTCCGAGTCAGCAGCAGCATGGATCTGATGCTCCTGGAAACAAGCACAGGCGTCAGGAGCCAGAAGGGAAGGCCCAGGACAGTGCCTGGGCTGCCCCTGCGACTTGAGACCAGCCACCCATCTGAAGGACCCAGCCCACGTTCAGGCTTAACAGGCATTTGCAGCTGCTCACCTGAGCTCAGAACTCCACCTCCACCAAACATCCACACCTGGGCAACCACACCTGTCACTCCTGTCCTCTACCTGGGATCACCAGCCTGTCACCGCACCCTGCCCTGCACCTGCACCTCAGCAAGGTGAACCTCTTGCTGAC... |
Task1_train_48837 | Chromosome 22 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GGTTTCTAAGGGATCCAGGTGCTGGCTGATGCGGTAACTGGAGTAGGGGGCAGGCTGGGCTCAGGGTTCTCCAGGGGCACAGTGAGAGTCTCATCTGGGCAGTCAAGACACTCTCGATGGGCGCAGGGGGTCCAGGAGATCCTAGAAGGTCTAGGTGGGCTGAAATAAGCCTGGCCATAAAGAGAGAAATATGTTTGGATTTTATTTATCCCATTAATTTTTTTTTTCTCTTGACTTGATAACCCTATCCCATGTCTGGTAAACCCAGAGTAAGGAGTCCAAAAGCTGCTGGAGGAGGAGCTATGGGAGCCTCAGTCTCC... | GGTTTCTAAGGGATCCAGGTGCTGGCTGATGCGGTAACTGGAGTAGGGGGCAGGCTGGGCTCAGGGTTCTCCAGGGGCACAGTGAGAGTCTCATCTGGGCAGTCAAGACACTCTCGATGGGCGCAGGGGGTCCAGGAGATCCTAGAAGGTCTAGGTGGGCTGAAATAAGCCTGGCCATAAAGAGAGAAATATGTTTGGATTTTATTTATCCCATTAATTTTTTTTTTCTCTTGACTTGATAACCCTATCCCATGTCTGGTAAACCCAGAGTAAGGAGTCCAAAAGCTGCTGGAGGAGGAGCTATGGGAGCCTCAGTCTCC... |
Task1_train_48838 | This variant is located on Chromosome 22. Evaluate its biological effect and specify any disease association. | Benign | TGCGGTAACTGGAGTAGGGGGCAGGCTGGGCTCAGGGTTCTCCAGGGGCACAGTGAGAGTCTCATCTGGGCAGTCAAGACACTCTCGATGGGCGCAGGGGGTCCAGGAGATCCTAGAAGGTCTAGGTGGGCTGAAATAAGCCTGGCCATAAAGAGAGAAATATGTTTGGATTTTATTTATCCCATTAATTTTTTTTTTCTCTTGACTTGATAACCCTATCCCATGTCTGGTAAACCCAGAGTAAGGAGTCCAAAAGCTGCTGGAGGAGGAGCTATGGGAGCCTCAGTCTCCTCTCTATGCCCCCTCCCTGTGCCCCAGTA... | TGCGGTAACTGGAGTAGGGGGCAGGCTGGGCTCAGGGTTCTCCAGGGGCACAGTGAGAGTCTCATCTGGGCAGTCAAGACACTCTCGATGGGCGCAGGGGGTCCAGGAGATCCTAGAAGGTCTAGGTGGGCTGAAATAAGCCTGGCCATAAAGAGAGAAATATGTTTGGATTTTATTTATCCCATTAATTTTTTTTTTCTCTTGACTTGATAACCCTATCCCATGTCTGGTAAACCCAGAGTAAGGAGTCCAAAAGCTGCTGGAGGAGGAGCTATGGGAGCCTCAGTCTCCTCTCTATGCCCCCTCCCTGTGCCCCAGTA... |
Task1_train_48839 | Here’s a variant located on Chromosome 22. What is the predicted biological effect — harmless or disease-causing? | Benign | GGCGGAGACAGGTGGTGTCAGGGCGTCCTCTCGCCAGGCCGCAGGCCCCGCGGGGCAACAGGACACTGGCCCCTGGCAGGCGGGCGCGGGGCCCTCGGGCTCGATGGGGAGAGGCCGGGGCCGGCGGCGGCGGATGGACGCTGGCTCGGGAGACAGAGCCCGCCGCCCCCGGAAACTGGACCCGCTCCGCCTGGGCGCCGCGGGGAGCGTGTGGGACGCGGTGGACGGGGCCGCCGCCCTGGACGCCCACGCGCGCGGCCTCCCCACAGGACCCCCACTCGCCCAGGAGCCCGCACTCCCGGCGCTGCCCGCTCCCCGCG... | GGCGGAGACAGGTGGTGTCAGGGCGTCCTCTCGCCAGGCCGCAGGCCCCGCGGGGCAACAGGACACTGGCCCCTGGCAGGCGGGCGCGGGGCCCTCGGGCTCGATGGGGAGAGGCCGGGGCCGGCGGCGGCGGATGGACGCTGGCTCGGGAGACAGAGCCCGCCGCCCCCGGAAACTGGACCCGCTCCGCCTGGGCGCCGCGGGGAGCGTGTGGGACGCGGTGGACGGGGCCGCCGCCCTGGACGCCCACGCGCGCGGCCTCCCCACAGGACCCCCACTCGCCCAGGAGCCCGCACTCCCGGCGCTGCCCGCTCCCCGCG... |
Task1_train_48840 | A variant was discovered on Chromosome 22. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | ACCAACCTCAGCCACCACCTCAACCTCATCCCCCACCTCAGCCCCAGCCCCAGCTCCAACCTCAGCTCCAACTTCAACCCCAGCCCCAGCCCCAAGTCCAGCTGCAGCCGCAACTCCAGCCCCAGCCCCAGTCCCAGTCCCAACCCTCACACCCCCATCCCCAGCCCTAACCCCAGTCCCAACCCCAGCCCTAAGCCCAGCTCCAACTCCAGCCCTAACCCCAGCCGCATCCCCAGCCCTAACCCCAGTCCCAACCCCAGCCCTAAGCCCAGCTCCAACTCCAGCCCCAACCCCAGCCGCATCCCCTGCCCCAGCCCCCA... | ACCAACCTCAGCCACCACCTCAACCTCATCCCCCACCTCAGCCCCAGCCCCAGCTCCAACCTCAGCTCCAACTTCAACCCCAGCCCCAGCCCCAAGTCCAGCTGCAGCCGCAACTCCAGCCCCAGCCCCAGTCCCAGTCCCAACCCTCACACCCCCATCCCCAGCCCTAACCCCAGTCCCAACCCCAGCCCTAAGCCCAGCTCCAACTCCAGCCCTAACCCCAGCCGCATCCCCAGCCCTAACCCCAGTCCCAACCCCAGCCCTAAGCCCAGCTCCAACTCCAGCCCCAACCCCAGCCGCATCCCCTGCCCCAGCCCCCA... |
Task1_train_48841 | Here’s a variant located on Chromosome 22. What is the predicted biological effect — harmless or disease-causing? | Benign | GGGCTGCGGTCTCTGCACCATGCACAACTACCTGTTTCTGGCGGGGGGCATCCGTGGCTCCGGTGCCAAGGCCGTCTGCTCCAACGAGGTCTTCTGCTACAACCCTCTGACCAACATCTGGAGCCAGGTTCGGCCCATGCAGCAGGCCCGAGCCCAGCTCAAGCTGGTGGCCCTGGACGGGCTGCTCTATGCCATCGGTGGCGAATGCCTGTACAGCATGGAGTGCTACGACCCGCGAACAGACGCCTGGACCCCACGCGCGCCACTCCCCGCAGGCACCTTCCCTGTGGCCCACGAGGCTGTGGCCTGCCGTGGGGACA... | GGGCTGCGGTCTCTGCACCATGCACAACTACCTGTTTCTGGCGGGGGGCATCCGTGGCTCCGGTGCCAAGGCCGTCTGCTCCAACGAGGTCTTCTGCTACAACCCTCTGACCAACATCTGGAGCCAGGTTCGGCCCATGCAGCAGGCCCGAGCCCAGCTCAAGCTGGTGGCCCTGGACGGGCTGCTCTATGCCATCGGTGGCGAATGCCTGTACAGCATGGAGTGCTACGACCCGCGAACAGACGCCTGGACCCCACGCGCGCCACTCCCCGCAGGCACCTTCCCTGTGGCCCACGAGGCTGTGGCCTGCCGTGGGGACA... |
Task1_train_48842 | Chromosome 22 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CCCACAAGCAAGGATGCCTCCCCAGCCAAAGACACCTGTGTTCCTGGGCAGCCCCAGGTGGCACCCCTTCCTCAGGCCTGAGCTGTGGCAGGAGACTCACCGTCTCTGAGCTTGAGAACTTGCTGGAGATGTGGAAGAAGATCGTGTTCTCGCCTGCAATCATGTAGGAAACTCCATAGCCATCATCTGCTACCTGAGGGCAACAAGAAGGGTGAAGAAGGCATAAATCAAACCTTGAAGATCTGAAAGCCAAGCTGATATTGTACTTGTTCTTCCCACAAGAGTTGCAGGAACGGGCCCCAGCCCTAGACACTGCATTT... | CCCACAAGCAAGGATGCCTCCCCAGCCAAAGACACCTGTGTTCCTGGGCAGCCCCAGGTGGCACCCCTTCCTCAGGCCTGAGCTGTGGCAGGAGACTCACCGTCTCTGAGCTTGAGAACTTGCTGGAGATGTGGAAGAAGATCGTGTTCTCGCCTGCAATCATGTAGGAAACTCCATAGCCATCATCTGCTACCTGAGGGCAACAAGAAGGGTGAAGAAGGCATAAATCAAACCTTGAAGATCTGAAAGCCAAGCTGATATTGTACTTGTTCTTCCCACAAGAGTTGCAGGAACGGGCCCCAGCCCTAGACACTGCATTT... |
Task1_train_48843 | Mutation context: Chromosome 22. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CTCCCTGAAGCCAGTTTGGACTCTACAGGTATCCTGAGACGTGCCCTGTGCCTTCCCGAGGGCTGGGCCAGGCAGTGAGGCCAGCAGGGGAGGAGGAGGCTCAGGCCTCGTCGGGGCTGTACCCACCTGCTGCTTTGTGGTCTCACACCTGCTCTGGGAGCTTCCAACCCACCTGTTTTGGAATGTCCCACTGCAGCCGTGTAGGAGGTGCGAGCGCAGGGTTCGGTTTGCCCAGGCAGTGCCCGGTCTCCGTGTAGCCCAGGTGGAAGCTGTCTGTGCCCAGGACAAACTGCAGGGAGAGGATGAGACTGAGAGGCTGG... | CTCCCTGAAGCCAGTTTGGACTCTACAGGTATCCTGAGACGTGCCCTGTGCCTTCCCGAGGGCTGGGCCAGGCAGTGAGGCCAGCAGGGGAGGAGGAGGCTCAGGCCTCGTCGGGGCTGTACCCACCTGCTGCTTTGTGGTCTCACACCTGCTCTGGGAGCTTCCAACCCACCTGTTTTGGAATGTCCCACTGCAGCCGTGTAGGAGGTGCGAGCGCAGGGTTCGGTTTGCCCAGGCAGTGCCCGGTCTCCGTGTAGCCCAGGTGGAAGCTGTCTGTGCCCAGGACAAACTGCAGGGAGAGGATGAGACTGAGAGGCTGG... |
Task1_train_48844 | This sequence change occurs on Chromosome 22. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TTTGATAAAGGGGTTCTACCACTAAAAAGCAGTTTAAAACCTCTGCTATGGGCAAGTTGTGTGTAAGTTCCTGGAAGGACAGCTTATGGAGGAGAATTCCAGTAGGCTCTGGCAAGTCAAGTGTGCTTTGGACCGTGGGAAAGGAGAGAAGAGGCATGCCATACAGCCCAGGTGGCTGGGAGACCCAGAGACTCAGAAGGGCCAGTTACATGGGGCAGAGGCAGACTGACTTCCTGAGCTCTAAAAGCAGCAGCCTGGCCTCCATTCTGCTGTCCGGCTCTGCAGAGGGACACAAAGCAAGACACGTTCTAGACAATTCC... | TTTGATAAAGGGGTTCTACCACTAAAAAGCAGTTTAAAACCTCTGCTATGGGCAAGTTGTGTGTAAGTTCCTGGAAGGACAGCTTATGGAGGAGAATTCCAGTAGGCTCTGGCAAGTCAAGTGTGCTTTGGACCGTGGGAAAGGAGAGAAGAGGCATGCCATACAGCCCAGGTGGCTGGGAGACCCAGAGACTCAGAAGGGCCAGTTACATGGGGCAGAGGCAGACTGACTTCCTGAGCTCTAAAAGCAGCAGCCTGGCCTCCATTCTGCTGTCCGGCTCTGCAGAGGGACACAAAGCAAGACACGTTCTAGACAATTCC... |
Task1_train_48845 | 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 | CCAAATTGCTAGGACAAATGCTACCACGCCTGGCTAATTAAAACAAATATTGTTGGCCAGGTGTGGTGGTTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGTGGATCACCTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAATCTTGTCTCTATTAAATAAAAAAAAATTAGCTGGGCATGGCAGCACACACCTGTAGTTCCAGCTACTAGGGAGGCTGAGGCAGGAGAATCCCTGGAACCCGGGAGGCGGAGGTTGCAGTGAGCGGAGATGGTACCACTGCACTCTAGCCTGGGCGACAG... | CCAAATTGCTAGGACAAATGCTACCACGCCTGGCTAATTAAAACAAATATTGTTGGCCAGGTGTGGTGGTTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGTGGATCACCTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAATCTTGTCTCTATTAAATAAAAAAAAATTAGCTGGGCATGGCAGCACACACCTGTAGTTCCAGCTACTAGGGAGGCTGAGGCAGGAGAATCCCTGGAACCCGGGAGGCGGAGGTTGCAGTGAGCGGAGATGGTACCACTGCACTCTAGCCTGGGCGACAG... |
Task1_train_48846 | This variant is present on Chromosome 22. Is the change likely to result in a pathogenic outcome? | Benign | AAAAACAAATCTTTAGAGCTGGGGTCTCACTATGTTGCCCAGGCTGGTCTGAATTCCTGGCCTCAGGCATCCTCTCACCTCAGCCTCCCAAAGCACTGGGAATACAGGAGTGAATCGCCGTGTGCAGCCTAACAGATTTTTTGTTTTTTGAGACAGAGTTTTTCTCTTGTTGCCCAGGCTGGAGTGCAATGGTGCGATCTCGGCTCACTGCAACCACCGCCTCCCAGGTTCAAGTGATTCTCCAGCCTCAGACTCCCAAGTAGCTGGGATTACAGGGATGCACCACTACACCTGGCTAATTTTGTATTTTTAGTAGAGAT... | AAAAACAAATCTTTAGAGCTGGGGTCTCACTATGTTGCCCAGGCTGGTCTGAATTCCTGGCCTCAGGCATCCTCTCACCTCAGCCTCCCAAAGCACTGGGAATACAGGAGTGAATCGCCGTGTGCAGCCTAACAGATTTTTTGTTTTTTGAGACAGAGTTTTTCTCTTGTTGCCCAGGCTGGAGTGCAATGGTGCGATCTCGGCTCACTGCAACCACCGCCTCCCAGGTTCAAGTGATTCTCCAGCCTCAGACTCCCAAGTAGCTGGGATTACAGGGATGCACCACTACACCTGGCTAATTTTGTATTTTTAGTAGAGAT... |
Task1_train_48847 | This variant lies on Chromosome 22. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TTCAAATCCCAGCCCAACCTCTTTCTGGCTGGGTGATCTTGTACAAGTCCTGAACCTCTCTGCACCTCAGTTTCCTCATTCGTACCACAGGGGACCGGCACCAGCACACAGCATTACCCCAGGATTGGACGAATTGTCACATCTGCAAGTCTCCACTGGTGTTATTACGTTATCAGGCACAAACCCCCTCCAGACACCTGAGCCTCCCCCACAGGCTCCCAGTGAGGAGCCATCACATGCCCAGGCCAGCCGAGGGGCCCTCAGGCATGGGGATCTGGGCAATGGCAGCAAGCTGGGCGGGGGGTGCAGCCAGGATGACA... | TTCAAATCCCAGCCCAACCTCTTTCTGGCTGGGTGATCTTGTACAAGTCCTGAACCTCTCTGCACCTCAGTTTCCTCATTCGTACCACAGGGGACCGGCACCAGCACACAGCATTACCCCAGGATTGGACGAATTGTCACATCTGCAAGTCTCCACTGGTGTTATTACGTTATCAGGCACAAACCCCCTCCAGACACCTGAGCCTCCCCCACAGGCTCCCAGTGAGGAGCCATCACATGCCCAGGCCAGCCGAGGGGCCCTCAGGCATGGGGATCTGGGCAATGGCAGCAAGCTGGGCGGGGGGTGCAGCCAGGATGACA... |
Task1_train_48848 | Here’s a variant located on Chromosome 22. What is the predicted biological effect — harmless or disease-causing? | Benign | CCCTGTTTCACAGATGGGGACACAGAGTACCCGACTGTGTAGACAGTGAAGCTGGGGCTGAACCCAGATCTGTCTGATTCCAGGCCCTGTGCCCAGGCATGCCTTTGAGGTGTCTACTGCTGGGTGCCACCCCCAACTGGGCCTGACCCCAAATGCTCTTGAGGGGGGCACCTTACTATTTCCCGCTGAATGTCAGAGGGGCAGGGTGGGTGCCACAGCCCCTCCCCAGGGGCTTCCACCCGCAGCTCACAGTCCAGCAGGCACTTGTTTGCTGGATACTTTATGGGCGGTCTCGAGCTCAGGAGAGGGGTCAGAATGGA... | CCCTGTTTCACAGATGGGGACACAGAGTACCCGACTGTGTAGACAGTGAAGCTGGGGCTGAACCCAGATCTGTCTGATTCCAGGCCCTGTGCCCAGGCATGCCTTTGAGGTGTCTACTGCTGGGTGCCACCCCCAACTGGGCCTGACCCCAAATGCTCTTGAGGGGGGCACCTTACTATTTCCCGCTGAATGTCAGAGGGGCAGGGTGGGTGCCACAGCCCCTCCCCAGGGGCTTCCACCCGCAGCTCACAGTCCAGCAGGCACTTGTTTGCTGGATACTTTATGGGCGGTCTCGAGCTCAGGAGAGGGGTCAGAATGGA... |
Task1_train_48849 | This variant is located on Chromosome 22. Evaluate its biological effect and specify any disease association. | Benign | GTGTCCCCTGTCTCCCGTCCTGGCCTGTGCAGCTATGTTCTGGGTCTGCCCCTACCTCAGTCTGCTCCCATCTGCTCTGCAGGTGACGTCCAGATCCACCCCCAGGGTTGTAGGTGCTGCTGCGGTGGGGGCCAGAGTGGCTGCTGCTGTTGGGGACCCTTCTGTCTGTGGGACCCCTTGAAAAGGAGCAACGCTGGCGCATGCGCCGTAGCATCGGGTCTTTCTAACCCAAAGGTCACGGTAGAGAGTCCAGCGCTTTCTTTCTTTTTTTGTTTGAGACGGAGTCTCGCTCTGTGGCCCGGGCTGGAGTGCAGTGGCGC... | GTGTCCCCTGTCTCCCGTCCTGGCCTGTGCAGCTATGTTCTGGGTCTGCCCCTACCTCAGTCTGCTCCCATCTGCTCTGCAGGTGACGTCCAGATCCACCCCCAGGGTTGTAGGTGCTGCTGCGGTGGGGGCCAGAGTGGCTGCTGCTGTTGGGGACCCTTCTGTCTGTGGGACCCCTTGAAAAGGAGCAACGCTGGCGCATGCGCCGTAGCATCGGGTCTTTCTAACCCAAAGGTCACGGTAGAGAGTCCAGCGCTTTCTTTCTTTTTTTGTTTGAGACGGAGTCTCGCTCTGTGGCCCGGGCTGGAGTGCAGTGGCGC... |
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