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 |
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Task1_train_34000 | Here’s a variant located on Chromosome 2. What is the predicted biological effect — harmless or disease-causing? | Benign | ACGTCACATCTAAAAGCTTCAATTCGAACATCTCTTTCTTTAACCAGAATCCTAGCCTACAAGCTCTTATATTTTTTTACTCTTCCACTTTTTCTTCATCTCTAAGACCTTTGTTTTGAACCATTAGCTTTTTTTAAGATCATGATAACTGCGTCCTGGCTTTTCTTCCTTCCTTATCTAGTCTGGTTTGTTTCTATTAATTCTTGTAGTTCCTTGGGACCCATAATTCCATGTACTCTTCAGCCAGATCCCAACCTAGATCAGTGCTATGTTTTCTGCTGCCAGTATAACCAGATGTGCAATGCTGCAGAGCATCAAAC... | ACGTCACATCTAAAAGCTTCAATTCGAACATCTCTTTCTTTAACCAGAATCCTAGCCTACAAGCTCTTATATTTTTTTACTCTTCCACTTTTTCTTCATCTCTAAGACCTTTGTTTTGAACCATTAGCTTTTTTTAAGATCATGATAACTGCGTCCTGGCTTTTCTTCCTTCCTTATCTAGTCTGGTTTGTTTCTATTAATTCTTGTAGTTCCTTGGGACCCATAATTCCATGTACTCTTCAGCCAGATCCCAACCTAGATCAGTGCTATGTTTTCTGCTGCCAGTATAACCAGATGTGCAATGCTGCAGAGCATCAAAC... |
Task1_train_34001 | Given this variant on Chromosome 2, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGAGATTACAGGCATGTGCCAACACTCCCGGCTAATTTTGCATTTTTAGCAGAGATGGGGTTTCACCATGTTGGTCAGGCTGGCCTCGAACTCCTGATCTCAGGTGATCCGCCCGCTCTGGCCTCCCAAAGTACTGGGATTACAGGTGTGAGCCACCGCGCCCACCAGGAACCTAAATCTTGTGGACAGGTCCAGCGAATTCCTTTGAATTCATTTTTAGAATTTTCCTATATCTTCAACAACATTCAGTATATTTTAAATTCTTACCAGGCAAAA... | CTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGAGATTACAGGCATGTGCCAACACTCCCGGCTAATTTTGCATTTTTAGCAGAGATGGGGTTTCACCATGTTGGTCAGGCTGGCCTCGAACTCCTGATCTCAGGTGATCCGCCCGCTCTGGCCTCCCAAAGTACTGGGATTACAGGTGTGAGCCACCGCGCCCACCAGGAACCTAAATCTTGTGGACAGGTCCAGCGAATTCCTTTGAATTCATTTTTAGAATTTTCCTATATCTTCAACAACATTCAGTATATTTTAAATTCTTACCAGGCAAAA... |
Task1_train_34002 | A change on Chromosome 2 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GCGCAGTCTGGATTTGCGTTGTTCACTGACGATCCTTCTGGCAGAGATTTAGAGCATTGTCTTCAAGGAAACATCAAGGTGAAACCAAGTCCTTTTCAGGAGCCAAGCCCAACGAACAGCAAAGAAGCTACTCTTTACAAGAAGAGTAAACTTTGCAAGAAGTTTAATTCAGGAGTTTTCCAAAACTTTAACCAATCTAATCTCCACGATAAGAAAAAAAAAATGCAGGACTTTGTTAAACCCATAGAATTCTTAATACACAATCTCTACATATACACATTCCATATTAAAGAGAGGAAAGGTGTTAGTAATGGAAATGA... | GCGCAGTCTGGATTTGCGTTGTTCACTGACGATCCTTCTGGCAGAGATTTAGAGCATTGTCTTCAAGGAAACATCAAGGTGAAACCAAGTCCTTTTCAGGAGCCAAGCCCAACGAACAGCAAAGAAGCTACTCTTTACAAGAAGAGTAAACTTTGCAAGAAGTTTAATTCAGGAGTTTTCCAAAACTTTAACCAATCTAATCTCCACGATAAGAAAAAAAAAATGCAGGACTTTGTTAAACCCATAGAATTCTTAATACACAATCTCTACATATACACATTCCATATTAAAGAGAGGAAAGGTGTTAGTAATGGAAATGA... |
Task1_train_34003 | Chromosome 2 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | ATCTTTCAGTTTCACATCTCTTCTTACCCTCTGCCCCATTTAAGGAAGAAAGTTGGGTACTGCTTTGCAAAATTCCATGAAATTTAGCAGGGTTTTTTTTTTTTCCAACACTATAGTTGATCCTATATAGTGCAGTTGAGAATATTGATTCAATATTATGAACAATCTAATTAAGTTAATAAAAACAAAACACAGGCCAGGTGTGGTAGCTCTTGCCTCTAATCTCAACACTTGGAGGGTGAGGTGGGAAGATCAGTTGAGGCCAGAAGTTCAAGACCAGCCTGGGCAACAAAATGAGACCTTGTCTTGACAAAAAATTT... | ATCTTTCAGTTTCACATCTCTTCTTACCCTCTGCCCCATTTAAGGAAGAAAGTTGGGTACTGCTTTGCAAAATTCCATGAAATTTAGCAGGGTTTTTTTTTTTTCCAACACTATAGTTGATCCTATATAGTGCAGTTGAGAATATTGATTCAATATTATGAACAATCTAATTAAGTTAATAAAAACAAAACACAGGCCAGGTGTGGTAGCTCTTGCCTCTAATCTCAACACTTGGAGGGTGAGGTGGGAAGATCAGTTGAGGCCAGAAGTTCAAGACCAGCCTGGGCAACAAAATGAGACCTTGTCTTGACAAAAAATTT... |
Task1_train_34004 | A variant was discovered on Chromosome 2. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | AACTGATGTGACATATATAATCTGTAAGACATTGTGTAACTATTACACCATAATCATCCATGTCAAAGACCTTTTATAAAAATTGACAATACTAGTCTGATAATTTACCAATGCCTCCACATCCTTAAATACTGTTCTAAGAAATAGAATTTTACTGTGGTTTCCTTAATGAAATGATCTTTCCTATTTCAGTGTGAGACATTTCAAATGCTATAATTTATCTTTCTTCACAAGTTAGGTCACAGTCAGTGAACAAGTTCATGCGCTCTCTACCATATTCTCACCCAAAGTTACCATAGTAACACTGAGACAGTTTCATT... | AACTGATGTGACATATATAATCTGTAAGACATTGTGTAACTATTACACCATAATCATCCATGTCAAAGACCTTTTATAAAAATTGACAATACTAGTCTGATAATTTACCAATGCCTCCACATCCTTAAATACTGTTCTAAGAAATAGAATTTTACTGTGGTTTCCTTAATGAAATGATCTTTCCTATTTCAGTGTGAGACATTTCAAATGCTATAATTTATCTTTCTTCACAAGTTAGGTCACAGTCAGTGAACAAGTTCATGCGCTCTCTACCATATTCTCACCCAAAGTTACCATAGTAACACTGAGACAGTTTCATT... |
Task1_train_34005 | A genetic alteration is present on Chromosome 2. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TAGCAGCCTGAGTGGACTGAGACAGTCTGGGAATTCCTCTTCTTTTTTTTTTTTAAGATGGAGTCTCACTGCTGCCCAGGCTAGAGTGCAGTGGCACAATCTTGGCTCACTACAACCTCCACCTCCCAGGTTCAAGGGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACCTGCCACCAGGCCTGGCTAATTTTTTTTTTGCATTTTTAGTAGAGACGGGTTTTGCCATGTTAGCCAGGCTGGTCTCGAATTCCTGACCTCAAGTGATCCGCCCGCCTCTGCCTCCCAAAGTGCTGGGATTACAAGCAT... | TAGCAGCCTGAGTGGACTGAGACAGTCTGGGAATTCCTCTTCTTTTTTTTTTTTAAGATGGAGTCTCACTGCTGCCCAGGCTAGAGTGCAGTGGCACAATCTTGGCTCACTACAACCTCCACCTCCCAGGTTCAAGGGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACCTGCCACCAGGCCTGGCTAATTTTTTTTTTGCATTTTTAGTAGAGACGGGTTTTGCCATGTTAGCCAGGCTGGTCTCGAATTCCTGACCTCAAGTGATCCGCCCGCCTCTGCCTCCCAAAGTGCTGGGATTACAAGCAT... |
Task1_train_34006 | A variant affecting Chromosome 2 has been observed. Determine if it's benign or associated with disease. | Benign | CAGATAAGATCTGATAAGGCCCGATGTTAATACATGAACTTTTAAATATTATTCTCCAGTCTTTTTTTTTTTTTTTTTGAGACAGGGTCTTGCTCTGTTGCCCAGGCTAGAGTGCAGTGGCACTATCTCAGCTCACTGAAGTCTTAATCTCCTGGGCTCAAGCAATCCTCCCACCTCAGCCTCCCAAGTAGCTGGGACCGCAGACATGCACCACCATGCCTGGCTAACTTTTGTATGTTTTTGTAGAGATGGGGTCCCACTATGTTGCTTAGGTTGCTCTCGAACTCCTGGGCTCAAGCAATCCTCTCACCTCAGCCTCT... | CAGATAAGATCTGATAAGGCCCGATGTTAATACATGAACTTTTAAATATTATTCTCCAGTCTTTTTTTTTTTTTTTTTGAGACAGGGTCTTGCTCTGTTGCCCAGGCTAGAGTGCAGTGGCACTATCTCAGCTCACTGAAGTCTTAATCTCCTGGGCTCAAGCAATCCTCCCACCTCAGCCTCCCAAGTAGCTGGGACCGCAGACATGCACCACCATGCCTGGCTAACTTTTGTATGTTTTTGTAGAGATGGGGTCCCACTATGTTGCTTAGGTTGCTCTCGAACTCCTGGGCTCAAGCAATCCTCTCACCTCAGCCTCT... |
Task1_train_34007 | This sequence variant lies on Chromosome 2. Is it clinically significant, and what condition might it cause if any? | Benign | AATGGAACTCTGGAGTTCTACTCACTGGCTTGCTCTCTCAATTTGACAACATATTGTGAAATATCGTACACAAATCAGCTTAAAGAACTCTCATGTACACACCACCAATTACCAAAAGCTTTGAAGCTTGATCCCCGCACTCCTACTGTGTCCCCTTTCTCCTTTCATCTCTCCCCGCTCCCCAGAGATAACCCCTCTCCTGAATTAGGTGTTTATCTTTCCCATTTTTTTCTGTATAATTTTGGGTCTTTATGGTGATAATTCAAACATTAAGCAATGGAAGTCACTTTCGTCTGCTGTTTTTCATACTCTCCCAGAAC... | AATGGAACTCTGGAGTTCTACTCACTGGCTTGCTCTCTCAATTTGACAACATATTGTGAAATATCGTACACAAATCAGCTTAAAGAACTCTCATGTACACACCACCAATTACCAAAAGCTTTGAAGCTTGATCCCCGCACTCCTACTGTGTCCCCTTTCTCCTTTCATCTCTCCCCGCTCCCCAGAGATAACCCCTCTCCTGAATTAGGTGTTTATCTTTCCCATTTTTTTCTGTATAATTTTGGGTCTTTATGGTGATAATTCAAACATTAAGCAATGGAAGTCACTTTCGTCTGCTGTTTTTCATACTCTCCCAGAAC... |
Task1_train_34008 | A genomic variant on Chromosome 2 is under review. What is the biological outcome — benign or pathogenic? | Benign | CCAGCACACGAATGATTTTATAGGTATGATTACAGAGTAGTGGGTTCTCAGAGTAACTAAGATCAGCAGTTCTCATCCCTCCTTTTCAGGGCCATGCCCCACTTAGGTTATGAATAACTTCAGACAGCTGATAACTTAGGCTAACTAAATCTAAAAACCTGTGTAAGTTAAAGTTTCATTCAAATCATAATTCTTGGCAGATGTGACTTAAATGTCTCATTTGTAAAGTTAATCCTATCAGGCTCAAACTATGCAGCACTGACTCTGGCACACATAGGGGTTAAACTAAAACAAAAAACAAAACAAGAAACAAAATATAA... | CCAGCACACGAATGATTTTATAGGTATGATTACAGAGTAGTGGGTTCTCAGAGTAACTAAGATCAGCAGTTCTCATCCCTCCTTTTCAGGGCCATGCCCCACTTAGGTTATGAATAACTTCAGACAGCTGATAACTTAGGCTAACTAAATCTAAAAACCTGTGTAAGTTAAAGTTTCATTCAAATCATAATTCTTGGCAGATGTGACTTAAATGTCTCATTTGTAAAGTTAATCCTATCAGGCTCAAACTATGCAGCACTGACTCTGGCACACATAGGGGTTAAACTAAAACAAAAAACAAAACAAGAAACAAAATATAA... |
Task1_train_34009 | This is a variant located on Chromosome 2. Is this mutation a likely cause of disease or not? | Benign | TAGTGTCAGAAATTAACTAAATTAGAGGACACCCAGGTGACGTCTGCTGGATAATCTGCTGCAGAATTGACTGGTTGGAGGGGAGAAATCCCTACATATTTTGGTGACCAGAGGCCACGAAAGTGTTCTATGTTGTACTGAGAGTAGACAGTATAAAAAAGTTTGGTATTTCCTATATCTCTTAAATTTCATTAACAGGAAAATAGATAAGCTGTGGTATATTCACACAATGGAATATTACTGAGCAATAAAAAATAAGCTACTGGTACTTGCTACAACATGGATAAATCTCTAAATACGATGCTGAAAGAAGCCTTACA... | TAGTGTCAGAAATTAACTAAATTAGAGGACACCCAGGTGACGTCTGCTGGATAATCTGCTGCAGAATTGACTGGTTGGAGGGGAGAAATCCCTACATATTTTGGTGACCAGAGGCCACGAAAGTGTTCTATGTTGTACTGAGAGTAGACAGTATAAAAAAGTTTGGTATTTCCTATATCTCTTAAATTTCATTAACAGGAAAATAGATAAGCTGTGGTATATTCACACAATGGAATATTACTGAGCAATAAAAAATAAGCTACTGGTACTTGCTACAACATGGATAAATCTCTAAATACGATGCTGAAAGAAGCCTTACA... |
Task1_train_34010 | This variant lies on Chromosome 2. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TTTTACCGTCTAAGCCCCCTCCTTGGGATTTTCTTTTCACATGAAACCTGGAGCAGGGGGTTATTTTGGACCTGGCATCTCCATGATGTCCCTGGGGAATTCAACTTTTCATTTGGCCAAGTTTGAGAGTAGGAAGGCGAGAGATTTATTTAGAAATAAGGAGGTAATAAGGGCAGGAAACTAGCAGTGTTTGCATGCAGACTACCAGCATTCTCCCTTTTTATGTAAACATTAATCCAATACAAAACATGTATTTTGTTTGACAAAGTCTTTTATTACCCTTGCTCCAAAAGAGTTGCTGTAATGGAAAGGAGACAAGC... | TTTTACCGTCTAAGCCCCCTCCTTGGGATTTTCTTTTCACATGAAACCTGGAGCAGGGGGTTATTTTGGACCTGGCATCTCCATGATGTCCCTGGGGAATTCAACTTTTCATTTGGCCAAGTTTGAGAGTAGGAAGGCGAGAGATTTATTTAGAAATAAGGAGGTAATAAGGGCAGGAAACTAGCAGTGTTTGCATGCAGACTACCAGCATTCTCCCTTTTTATGTAAACATTAATCCAATACAAAACATGTATTTTGTTTGACAAAGTCTTTTATTACCCTTGCTCCAAAAGAGTTGCTGTAATGGAAAGGAGACAAGC... |
Task1_train_34011 | A variant was discovered on Chromosome 2. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CCAGCCACTGGCCCCTGTAGCCCCGCACAGTCCCTTCCTCCTGGACAAGTTTCAGCAGCAGCTGGAGAGCAAGAAGACAGAGCCCGAGCACCGGCCCATGTCCTCCATCTTCTTTGATGCCGGAAGCAAAGCATCCCTGCCACCGTGCTGTGGCCAGGCCAGCACCCCTCTCTCTTCCATGGGGGGCAGATCCAATACCCAGTGGCCCCCAGATCCACCATTACATTTTGGGCCCACAAAGTGGGCCGTCGGGGATCAGCGCACAGAGTTCTTGGGAGCAGCGCCGTTGGGGCCCCCTGTCTCTCCACCCCATGTCTCCA... | CCAGCCACTGGCCCCTGTAGCCCCGCACAGTCCCTTCCTCCTGGACAAGTTTCAGCAGCAGCTGGAGAGCAAGAAGACAGAGCCCGAGCACCGGCCCATGTCCTCCATCTTCTTTGATGCCGGAAGCAAAGCATCCCTGCCACCGTGCTGTGGCCAGGCCAGCACCCCTCTCTCTTCCATGGGGGGCAGATCCAATACCCAGTGGCCCCCAGATCCACCATTACATTTTGGGCCCACAAAGTGGGCCGTCGGGGATCAGCGCACAGAGTTCTTGGGAGCAGCGCCGTTGGGGCCCCCTGTCTCTCCACCCCATGTCTCCA... |
Task1_train_34012 | This variant lies on Chromosome 2. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AGAAAGATCTATTCCAGGTCTACGATGGTTAATTTTACATGTTGACGTCAGTGAGCCATTGGATGGCCAGATCTCTGATTAAATGTTATTTCTGGGTGTTTCTGGAAGAGATTAACATTTGAATTGGTGGACTGAGTAAAGCAGTCTGCCCTCCTCAATGTGGGTGGGATTCATCCACTCCACTGAGGGCCTAAATGGAACAAGGCAGACTGCCAGTTGAACTGGTGCTCTCAATTCAATTGCCTGACTACATGAGGTGATCCGTCAGTCTTCTCCTGACCTTGGACTGGGACTTCCACCATCAGTGCTCCTGGTTCTCA... | AGAAAGATCTATTCCAGGTCTACGATGGTTAATTTTACATGTTGACGTCAGTGAGCCATTGGATGGCCAGATCTCTGATTAAATGTTATTTCTGGGTGTTTCTGGAAGAGATTAACATTTGAATTGGTGGACTGAGTAAAGCAGTCTGCCCTCCTCAATGTGGGTGGGATTCATCCACTCCACTGAGGGCCTAAATGGAACAAGGCAGACTGCCAGTTGAACTGGTGCTCTCAATTCAATTGCCTGACTACATGAGGTGATCCGTCAGTCTTCTCCTGACCTTGGACTGGGACTTCCACCATCAGTGCTCCTGGTTCTCA... |
Task1_train_34013 | A variant was discovered on Chromosome 2. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | AAATACACCCATTATTAGACATAGACTTGAAAACTGGAGAAATCACTAATCCAAAGTAATAAGATTTCAATCCAATTTCACTATTTAAAAATTTCAAACTAAAAGGCTAAAAGCAATTAATACCATTTGGGATATTATGGTAATAATGTAGAAAATGCTTTCAGTTGTTACACTTCTGTTTTCTAGAGACTTTATGAATATTAGAAGACGGTTCCAAGGGAAAACAGTACTGATTCCTTTTTTTTTTTTTTTTTTTTTGAGACAGATTCTCACTATGTTGCCCAGGCTGGAGTCCAGTGGTGCGATCTCGGCTCACTGCA... | AAATACACCCATTATTAGACATAGACTTGAAAACTGGAGAAATCACTAATCCAAAGTAATAAGATTTCAATCCAATTTCACTATTTAAAAATTTCAAACTAAAAGGCTAAAAGCAATTAATACCATTTGGGATATTATGGTAATAATGTAGAAAATGCTTTCAGTTGTTACACTTCTGTTTTCTAGAGACTTTATGAATATTAGAAGACGGTTCCAAGGGAAAACAGTACTGATTCCTTTTTTTTTTTTTTTTTTTTTGAGACAGATTCTCACTATGTTGCCCAGGCTGGAGTCCAGTGGTGCGATCTCGGCTCACTGCA... |
Task1_train_34014 | A change on Chromosome 2 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TGTGGAACTCCTGCTTCCTGTCTGTAATGCGCCATCAGCCCTCCACCTCACAATGCTTCCATTCTGGTTCTCATAGGCCTGCCTTTAACCTCAGCACTGCTATGATCTTCTGGAGCCTTTTAAATCCCCCTCAATACGTGGCATAGGGCTGGGTACGCAGCAGGTGCTTAGTAACTACTTGTGCTCGGCTAATGGATTCTGCTCCTTCCTGCCCCACACCTGGCCTTCTCTTGCCAACCCTGCCAGCTCAGCCATGTGTCTTACTCCGTCTATCAGGCAGCCACCTACTTTGATCTTGTAGCTTGAGGGATGGGGAGTGA... | TGTGGAACTCCTGCTTCCTGTCTGTAATGCGCCATCAGCCCTCCACCTCACAATGCTTCCATTCTGGTTCTCATAGGCCTGCCTTTAACCTCAGCACTGCTATGATCTTCTGGAGCCTTTTAAATCCCCCTCAATACGTGGCATAGGGCTGGGTACGCAGCAGGTGCTTAGTAACTACTTGTGCTCGGCTAATGGATTCTGCTCCTTCCTGCCCCACACCTGGCCTTCTCTTGCCAACCCTGCCAGCTCAGCCATGTGTCTTACTCCGTCTATCAGGCAGCCACCTACTTTGATCTTGTAGCTTGAGGGATGGGGAGTGA... |
Task1_train_34015 | Given this variant on Chromosome 2, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | AGCCCAATGACAGATAAGATCCCAGGTGCTCTCCAGGCTAGGGGAATCCCACCAAGAGTTGCCCAAGAGGAAAACATTTCTCCCCATGTACTCCCCTTAGGTTAAGAAGATGTTATAGGGAAAAATCTTACTGGAAACATTTGCAAATCAGGCAGTCCTTGTTTGATTTCTACGGGAAATAAGACATCTTAAAGGTTTTCCATTTCTCCTGGGGGAAGATATACTCTACGTATAAAAATACTTTCCTCAGGGGCTCTTAGTAGCTTTCCCACACAAAGCAATCTGCCAGTAGCGCTTTACCTGATCTTTGTCAACTAGTG... | AGCCCAATGACAGATAAGATCCCAGGTGCTCTCCAGGCTAGGGGAATCCCACCAAGAGTTGCCCAAGAGGAAAACATTTCTCCCCATGTACTCCCCTTAGGTTAAGAAGATGTTATAGGGAAAAATCTTACTGGAAACATTTGCAAATCAGGCAGTCCTTGTTTGATTTCTACGGGAAATAAGACATCTTAAAGGTTTTCCATTTCTCCTGGGGGAAGATATACTCTACGTATAAAAATACTTTCCTCAGGGGCTCTTAGTAGCTTTCCCACACAAAGCAATCTGCCAGTAGCGCTTTACCTGATCTTTGTCAACTAGTG... |
Task1_train_34016 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GCTAGCTTTTTCTTTTTTTTCCTCTTCAGTTGAACTGAGGAGATAGTTTTTGTTTTTAATGATTGTGCTCTTTTAACTAGACAAAAGGAATTAGATAGTCTTGCCTATTCGAAGTTAAATGAACTTTTGAGGTTGTTAAGGACAAAACTATTAAACTGACATCAATAATACAGAATGGGCTGCTTAGTATCACTTTCCTTATCAGGTACTAGGATTTAATTTAGTTAGGAAACTCACTTAAAGGGAGGACTATAACTGCAGTTGAAAGTGTAATTTTTCCAAGATATAAAATTGTTTAAAGATTGAATATATTCCTGTTA... | GCTAGCTTTTTCTTTTTTTTCCTCTTCAGTTGAACTGAGGAGATAGTTTTTGTTTTTAATGATTGTGCTCTTTTAACTAGACAAAAGGAATTAGATAGTCTTGCCTATTCGAAGTTAAATGAACTTTTGAGGTTGTTAAGGACAAAACTATTAAACTGACATCAATAATACAGAATGGGCTGCTTAGTATCACTTTCCTTATCAGGTACTAGGATTTAATTTAGTTAGGAAACTCACTTAAAGGGAGGACTATAACTGCAGTTGAAAGTGTAATTTTTCCAAGATATAAAATTGTTTAAAGATTGAATATATTCCTGTTA... |
Task1_train_34017 | This variant lies on Chromosome 2. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CTTCAATGGGTTTTCTGTTCATTACAGTTGAATGCTTTCATAACTGATACAGGAGGGACCCTGTGATTGGCAGTTCCACTAGACTGCATGGAGATGGGTGGAGTTATCTAAAAGAACAGAGATAGTGTCCCTAGAAGAAGGGGACAGGAAAGCATCCTGGGTACACAAAAGTCAAGGCTCCAGGATCTGCCCTGGGGGCTATCTCAACACCCCTACACTCTCACCGCACGTATTTGGTCAGCTATGAATATGACCAACTCTCGTCGTTTATCTCTATTCAGTGGAACACAGCAGCACTGTGACCTGCCCACGAGAAGAAG... | CTTCAATGGGTTTTCTGTTCATTACAGTTGAATGCTTTCATAACTGATACAGGAGGGACCCTGTGATTGGCAGTTCCACTAGACTGCATGGAGATGGGTGGAGTTATCTAAAAGAACAGAGATAGTGTCCCTAGAAGAAGGGGACAGGAAAGCATCCTGGGTACACAAAAGTCAAGGCTCCAGGATCTGCCCTGGGGGCTATCTCAACACCCCTACACTCTCACCGCACGTATTTGGTCAGCTATGAATATGACCAACTCTCGTCGTTTATCTCTATTCAGTGGAACACAGCAGCACTGTGACCTGCCCACGAGAAGAAG... |
Task1_train_34018 | A variant on Chromosome 2 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | CTCTCTGGGGGTGTTTACGTATGCCGGTGGGGGAAAGAGACCAACTCTCAAATATTATCTCAAACAGTTGGTTTCACTGTGCTTGCTTGGGTAGCACATATACCAAAATTGGAATGACCCCTGCACAGGGATGAAATGCAAATTCGTGAAGCATACTGTATTTTTCTTAGCACATACCACCTTTGGCAATATTCTTTTTTTTTTTTTGAGAGGGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCAGAGGCGCGATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCACACCATTCTCCTACCTCAGCCTCCCCAGTAG... | CTCTCTGGGGGTGTTTACGTATGCCGGTGGGGGAAAGAGACCAACTCTCAAATATTATCTCAAACAGTTGGTTTCACTGTGCTTGCTTGGGTAGCACATATACCAAAATTGGAATGACCCCTGCACAGGGATGAAATGCAAATTCGTGAAGCATACTGTATTTTTCTTAGCACATACCACCTTTGGCAATATTCTTTTTTTTTTTTTGAGAGGGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCAGAGGCGCGATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCACACCATTCTCCTACCTCAGCCTCCCCAGTAG... |
Task1_train_34019 | A mutation has occurred on Chromosome 2. What is the medical relevance of this mutation? | Benign | TTGTATTTTGCATTCATAAGAATAGATGTTAAATAAACCTTGAAATACAACCTTGGCTCAAACGTTAATGGTCATGGATAAAGTGAATTAAAACTTGTTAGGGGCCAGGTGTGGTGGTTAATGCCTATAATCCCAGCACTTTAGGAAGCTGAGGCAGTTGGATGTCCTGAGGACAGGAGTTCAAGACCAGCCTGGCCAACACAGTGAAACCCTGTTTCTATAAAAAATACAAAAATTAGCTGGGCGTGGTGGCACACACCTGTAGTCCCAACCACTTGGGAGGCTGAGGCATGAGAATTGCTTGAACTTGGGAGGCAGAG... | TTGTATTTTGCATTCATAAGAATAGATGTTAAATAAACCTTGAAATACAACCTTGGCTCAAACGTTAATGGTCATGGATAAAGTGAATTAAAACTTGTTAGGGGCCAGGTGTGGTGGTTAATGCCTATAATCCCAGCACTTTAGGAAGCTGAGGCAGTTGGATGTCCTGAGGACAGGAGTTCAAGACCAGCCTGGCCAACACAGTGAAACCCTGTTTCTATAAAAAATACAAAAATTAGCTGGGCGTGGTGGCACACACCTGTAGTCCCAACCACTTGGGAGGCTGAGGCATGAGAATTGCTTGAACTTGGGAGGCAGAG... |
Task1_train_34020 | A variant affecting Chromosome 2 has been observed. Determine if it's benign or associated with disease. | Benign | TATAGAGTTTCTCTCTGTCGTCCAGGCTGGAGTGCAATGGTGCAATCTCAGCTCACTGCAACCTCCTCCTCTCAGGTTCAAGCAATTCTCCTGCCCACCACCATGCCTGGCTAATTTTTGGGCAGGTACCCACCACCATGCTTGGTTAACTTTTGTATTTTTAGTAGAGACTGGGTTTTGCCATGTTGGCCAGGCTGGTCTCTAACTCCTGACCTCAAGTGATCTACCCACCTTGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACTGTGCCTGGCCTTAATTCTTCCTCCAGTGTGGCTGAGGGAAGCCAAAAG... | TATAGAGTTTCTCTCTGTCGTCCAGGCTGGAGTGCAATGGTGCAATCTCAGCTCACTGCAACCTCCTCCTCTCAGGTTCAAGCAATTCTCCTGCCCACCACCATGCCTGGCTAATTTTTGGGCAGGTACCCACCACCATGCTTGGTTAACTTTTGTATTTTTAGTAGAGACTGGGTTTTGCCATGTTGGCCAGGCTGGTCTCTAACTCCTGACCTCAAGTGATCTACCCACCTTGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACTGTGCCTGGCCTTAATTCTTCCTCCAGTGTGGCTGAGGGAAGCCAAAAG... |
Task1_train_34021 | An alteration has been detected on Chromosome 2. Is it pathogenic, and if so, what disease is involved? | Benign | CACTCTTTTGCATGTGGATATCAAGTTTTTTCAACACCACTTTTTTTTTTTTGTTTGAGACAAAGTTTCGTTCTCCTTGCCCAGGCTGGAGAGTAATGACACAGTCTCTGTTCACTGCAACCTCTGCCTCCCGGGCTCAAGCGATTTTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAAGTGTGTGCCACCATGCCCAGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCTCCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTGCTCTCCTCAGCCTCCCAAAGTGCTGGGATTATAGAT... | CACTCTTTTGCATGTGGATATCAAGTTTTTTCAACACCACTTTTTTTTTTTTGTTTGAGACAAAGTTTCGTTCTCCTTGCCCAGGCTGGAGAGTAATGACACAGTCTCTGTTCACTGCAACCTCTGCCTCCCGGGCTCAAGCGATTTTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAAGTGTGTGCCACCATGCCCAGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCTCCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTGCTCTCCTCAGCCTCCCAAAGTGCTGGGATTATAGAT... |
Task1_train_34022 | Here is a variant on Chromosome 2. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CTTTAAATCTAAAGTGAGTACCTTATAGACAGCATACAGTTGGATCATGTTTTTTTTTTAATCCACTTAGCCACCAACAGAATTATAATTTTTAAGCATTTATCAGAAGTAAAGACATTTAGTAATGATTCCCCCCTTCATTTTATATACCTATTTTCTCTTTATTTTATTTTTTTAACAGAGTCAACCTATTTGATTTCTTGACAAGACCACAATCTGATCCCAAAGATGTGCTCCACAAATCCAGGCAAATGGGTCACCTTTGATGATGATCCTGCTGTTCAATCTTCTCAAAAGTCAAAGAATTTTCCTCTGGAGAA... | CTTTAAATCTAAAGTGAGTACCTTATAGACAGCATACAGTTGGATCATGTTTTTTTTTTAATCCACTTAGCCACCAACAGAATTATAATTTTTAAGCATTTATCAGAAGTAAAGACATTTAGTAATGATTCCCCCCTTCATTTTATATACCTATTTTCTCTTTATTTTATTTTTTTAACAGAGTCAACCTATTTGATTTCTTGACAAGACCACAATCTGATCCCAAAGATGTGCTCCACAAATCCAGGCAAATGGGTCACCTTTGATGATGATCCTGCTGTTCAATCTTCTCAAAAGTCAAAGAATTTTCCTCTGGAGAA... |
Task1_train_34023 | A mutation on Chromosome 2 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CTGTTCATTAGGACTTACTAGCTTCATTGCTAATAACTGTAGAATAGGATTCCTCTTGATCCTTAATGGGATGATCGATATTGAAAACTATTTTATTCAAAGAACTCAGCCCTAATATTAAATGTTAAGTATTGTCAAACTATTGTCCAGAATCAGATTTTTTGACTCCCTGTGAGATCAGGGAAAAAAAGATACAAGTAAAGTCCTTTTCTAACTTTCTAATATAAATTTCTTATATCTAGGGCACTTCAAACTCCAGTGCAAACTTTACTTTTCCTGGTTATCCCATTCATGTACCAGCAGGTGTGACACTACAGACT... | CTGTTCATTAGGACTTACTAGCTTCATTGCTAATAACTGTAGAATAGGATTCCTCTTGATCCTTAATGGGATGATCGATATTGAAAACTATTTTATTCAAAGAACTCAGCCCTAATATTAAATGTTAAGTATTGTCAAACTATTGTCCAGAATCAGATTTTTTGACTCCCTGTGAGATCAGGGAAAAAAAGATACAAGTAAAGTCCTTTTCTAACTTTCTAATATAAATTTCTTATATCTAGGGCACTTCAAACTCCAGTGCAAACTTTACTTTTCCTGGTTATCCCATTCATGTACCAGCAGGTGTGACACTACAGACT... |
Task1_train_34024 | An alteration has been detected on Chromosome 2. Is it pathogenic, and if so, what disease is involved? | Benign | TTAGCCCCACTGAGTTTCTCCAGCATCAAGTGAAGTGTTTTGTTTTCATTAAATGAGCTCACAGTTGGTAAAGATTTGGGTAGGGGGAGGGCAAGACAGGTTCTACAAAAAGCAAAATCTCAAATACCACTAATAATGAAAAGAGAAGGCTTGCTTTCATTATTTTCTAATTAGAGAGTTGAACTTTATAGCTGAGAAAATAAGGCTTTCCTCTTTAAGCGTAATGCCCTTTTTCCAGCAGGCTGCTCCACACGATCCTTTGCTTACAGAGGGGCCCATTCAGCAGAGAACAAGTGCCAGGCAAATAAATGACTAATCAC... | TTAGCCCCACTGAGTTTCTCCAGCATCAAGTGAAGTGTTTTGTTTTCATTAAATGAGCTCACAGTTGGTAAAGATTTGGGTAGGGGGAGGGCAAGACAGGTTCTACAAAAAGCAAAATCTCAAATACCACTAATAATGAAAAGAGAAGGCTTGCTTTCATTATTTTCTAATTAGAGAGTTGAACTTTATAGCTGAGAAAATAAGGCTTTCCTCTTTAAGCGTAATGCCCTTTTTCCAGCAGGCTGCTCCACACGATCCTTTGCTTACAGAGGGGCCCATTCAGCAGAGAACAAGTGCCAGGCAAATAAATGACTAATCAC... |
Task1_train_34025 | Chromosome 2 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | AGTGAGACCCTGTATAAAAAAAAAAAGATTAAAAGAAATTTAATAAAAGAATTTTGGGGCCTGACCTTAGCCCAGTCATTCATTCATTTAACAAACATTTATTGGGCACCTACATGTGGCAAGCATCGTTCTATGTGCTGGGAATACAGCTGTGAACAAAGCAAAAAAAGCCTTCATGGAGCTAGCATGCTAGTCTTAGGACCTTCTTTGGGAATCCATAAACTTTCCCTGAGAGTGCTTTATGTTTCTTTCTGTTGATGAATGTTGCTTTGCATCACGGGAAGCTTTATTTATCATTAGCTGCCCTGGTGGTTCTCAAT... | AGTGAGACCCTGTATAAAAAAAAAAAGATTAAAAGAAATTTAATAAAAGAATTTTGGGGCCTGACCTTAGCCCAGTCATTCATTCATTTAACAAACATTTATTGGGCACCTACATGTGGCAAGCATCGTTCTATGTGCTGGGAATACAGCTGTGAACAAAGCAAAAAAAGCCTTCATGGAGCTAGCATGCTAGTCTTAGGACCTTCTTTGGGAATCCATAAACTTTCCCTGAGAGTGCTTTATGTTTCTTTCTGTTGATGAATGTTGCTTTGCATCACGGGAAGCTTTATTTATCATTAGCTGCCCTGGTGGTTCTCAAT... |
Task1_train_34026 | This variant is located on Chromosome 2. Evaluate its biological effect and specify any disease association. | Benign | AAAAGAATTTTGGGGCCTGACCTTAGCCCAGTCATTCATTCATTTAACAAACATTTATTGGGCACCTACATGTGGCAAGCATCGTTCTATGTGCTGGGAATACAGCTGTGAACAAAGCAAAAAAAGCCTTCATGGAGCTAGCATGCTAGTCTTAGGACCTTCTTTGGGAATCCATAAACTTTCCCTGAGAGTGCTTTATGTTTCTTTCTGTTGATGAATGTTGCTTTGCATCACGGGAAGCTTTATTTATCATTAGCTGCCCTGGTGGTTCTCAATATAAGCTGTGTTTTAGCATTACCTGGGAAGTCTGTTAAAACTGC... | AAAAGAATTTTGGGGCCTGACCTTAGCCCAGTCATTCATTCATTTAACAAACATTTATTGGGCACCTACATGTGGCAAGCATCGTTCTATGTGCTGGGAATACAGCTGTGAACAAAGCAAAAAAAGCCTTCATGGAGCTAGCATGCTAGTCTTAGGACCTTCTTTGGGAATCCATAAACTTTCCCTGAGAGTGCTTTATGTTTCTTTCTGTTGATGAATGTTGCTTTGCATCACGGGAAGCTTTATTTATCATTAGCTGCCCTGGTGGTTCTCAATATAAGCTGTGTTTTAGCATTACCTGGGAAGTCTGTTAAAACTGC... |
Task1_train_34027 | A mutation on Chromosome 2 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CACAATAAATTTCCAACACATTTTTTTTCCTATGTGGGTGTTATCTAAAAATGTGACACAAGGGAATAGCTGCTCTAGCAGAAGGAGAATTTTTATGATTGGAATCTATCTTTTTTTCTCCTTAAAAGGTATATCATCACTTATAAAATGCATTCAGTCATTTGAAGCAAGGTTAATTATCTGTATTTTAATGACTCTTAAAAATCATACCTTTTCTTCAAAGGTCTCTAGTTATTATTTGTATTACAAAGATAAAAATATGTGAGTATCCTAAACACAATTTCTTTCCTAGAAAAATTATCCCCTTTCAAATGTGTTTT... | CACAATAAATTTCCAACACATTTTTTTTCCTATGTGGGTGTTATCTAAAAATGTGACACAAGGGAATAGCTGCTCTAGCAGAAGGAGAATTTTTATGATTGGAATCTATCTTTTTTTCTCCTTAAAAGGTATATCATCACTTATAAAATGCATTCAGTCATTTGAAGCAAGGTTAATTATCTGTATTTTAATGACTCTTAAAAATCATACCTTTTCTTCAAAGGTCTCTAGTTATTATTTGTATTACAAAGATAAAAATATGTGAGTATCCTAAACACAATTTCTTTCCTAGAAAAATTATCCCCTTTCAAATGTGTTTT... |
Task1_train_34028 | A genomic variant on Chromosome 2 is under review. What is the biological outcome — benign or pathogenic? | Benign | TAAAAAATGTAAAAATAAATAAGTGAAACTAATTTTTAAATGTATTTGTCCTGATACCTCCAAAACAATATTGTCCTAGTATGTAATCAATAAAATAATTATTGAGCTATTTTATGATTTTTTATATGAAGTATTTGGAATCCCATGTGTATTTTACACTTACAGCACATCTAAATTCAGGCTAGCCACGGTTCAAGTGCCCAGTAGCCACATGTGGCTAGCAGCCACTGTGCTAGACAGTAAAGCTCTAGACTCTTTACAAGGACAATTATTTTATTTTGCACTTGATGCTCACAGTATATCAAAATGGTGCCAGGTCA... | TAAAAAATGTAAAAATAAATAAGTGAAACTAATTTTTAAATGTATTTGTCCTGATACCTCCAAAACAATATTGTCCTAGTATGTAATCAATAAAATAATTATTGAGCTATTTTATGATTTTTTATATGAAGTATTTGGAATCCCATGTGTATTTTACACTTACAGCACATCTAAATTCAGGCTAGCCACGGTTCAAGTGCCCAGTAGCCACATGTGGCTAGCAGCCACTGTGCTAGACAGTAAAGCTCTAGACTCTTTACAAGGACAATTATTTTATTTTGCACTTGATGCTCACAGTATATCAAAATGGTGCCAGGTCA... |
Task1_train_34029 | This variant lies on Chromosome 2. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AACTCCACAAGCACACCCTGAGCCCTGCTTACATTCTTGTTGCCTCTGACCTTGGTGATGAAAGTGCCGTACAGAAGTTGGAGCCTTTATCATGGAGCTTAACAAATATACCTGGCCCAGGACGAGTCTGAGAACCTGAAGGAGGATCCAGGGAAAGGTGGAGCAATTGGAGACCCAGCCGTTGCTTCACAGCAGTGAGCTGAGTCAGCATCAGCAACAGAGTGTGCTGAGCTACAAAATGGCTGCCATTTTCCTCTGCCCTCCTGTTTTCCTAGAGTCCTCACTATGGCCCACACTAACTGGAAACACATGAGGAAGGG... | AACTCCACAAGCACACCCTGAGCCCTGCTTACATTCTTGTTGCCTCTGACCTTGGTGATGAAAGTGCCGTACAGAAGTTGGAGCCTTTATCATGGAGCTTAACAAATATACCTGGCCCAGGACGAGTCTGAGAACCTGAAGGAGGATCCAGGGAAAGGTGGAGCAATTGGAGACCCAGCCGTTGCTTCACAGCAGTGAGCTGAGTCAGCATCAGCAACAGAGTGTGCTGAGCTACAAAATGGCTGCCATTTTCCTCTGCCCTCCTGTTTTCCTAGAGTCCTCACTATGGCCCACACTAACTGGAAACACATGAGGAAGGG... |
Task1_train_34030 | Given a variant located on Chromosome 2, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CTTAAGAAAAAAACAAAATGAAACAAAACCAACAACTCAATCCTACTGGTCCCCACTGAATTCCTTCATCCATTTTGCGTTTTTTCTCTTGAAGCAAGTAGTTCATCATCCCAAAGAATATCTGAAATCGTTGCCATCTACCTCTACCTGGCTGCTGGAGCATGAAGCTGTTAGGACTCCTGCTCAGATGAAAATAAGCATGGAAGATATGCTATGGACTGAACTGTGTCCTCTCAAAACTCAATTGTTAAAACTCTAATCCCCACTGTAACTGTATTTGGAAATAGAACTTCTGGTAGGTAATTAAGGTTAAATGAGGT... | CTTAAGAAAAAAACAAAATGAAACAAAACCAACAACTCAATCCTACTGGTCCCCACTGAATTCCTTCATCCATTTTGCGTTTTTTCTCTTGAAGCAAGTAGTTCATCATCCCAAAGAATATCTGAAATCGTTGCCATCTACCTCTACCTGGCTGCTGGAGCATGAAGCTGTTAGGACTCCTGCTCAGATGAAAATAAGCATGGAAGATATGCTATGGACTGAACTGTGTCCTCTCAAAACTCAATTGTTAAAACTCTAATCCCCACTGTAACTGTATTTGGAAATAGAACTTCTGGTAGGTAATTAAGGTTAAATGAGGT... |
Task1_train_34031 | This mutation is located on Chromosome 2. Is it associated with a disease or is it a benign polymorphism? | Benign | GCATGGAAGATATGCTATGGACTGAACTGTGTCCTCTCAAAACTCAATTGTTAAAACTCTAATCCCCACTGTAACTGTATTTGGAAATAGAACTTCTGGTAGGTAATTAAGGTTAAATGAGGTCATAAGTGTAGGGCCCTAAACCTGTTAGGATTATTGCCATTATATAAGATAAGACACCAGAAACTCATTCTTGCTCACTCAAGTCTCTCTTTCTCCTTTCTCTCCACCTCTCTCTCCCTCTCTCTCTCTTTCTCTATCTTCCCCCCCCACCCCCACTTTCTCACTCTCACTCTTGGTACTATTTGAGGACACAGGGA... | GCATGGAAGATATGCTATGGACTGAACTGTGTCCTCTCAAAACTCAATTGTTAAAACTCTAATCCCCACTGTAACTGTATTTGGAAATAGAACTTCTGGTAGGTAATTAAGGTTAAATGAGGTCATAAGTGTAGGGCCCTAAACCTGTTAGGATTATTGCCATTATATAAGATAAGACACCAGAAACTCATTCTTGCTCACTCAAGTCTCTCTTTCTCCTTTCTCTCCACCTCTCTCTCCCTCTCTCTCTCTTTCTCTATCTTCCCCCCCCACCCCCACTTTCTCACTCTCACTCTTGGTACTATTTGAGGACACAGGGA... |
Task1_train_34032 | This variant lies on Chromosome 2. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GTCATGCTTCTATTCTTGCCACCTCTTCCCCTTATCTCAGCTGCAGGTTTCACTATGCAGCATTATTGTTTTTCTTCATTAACCTTAATAGAGGTCTCATGTATTCCCAGGTTATTAGTTTAGTCTGTTAGACCTTCACTCCTTTGAAGTAATGGCTATATTTGCCTCATTTTTAATACGCAGCACCTAAAGTAATGCCAAAATATAGTAGGCTCTGTGTGTGGAAAAAGGTATACAATAAAGTTCAGAGACTTTTCAAAAAATAAGACAGCATCTTGACAGTCCTTGTTCTTCCTAATATTGGGAGGAAGAGAGAATAA... | GTCATGCTTCTATTCTTGCCACCTCTTCCCCTTATCTCAGCTGCAGGTTTCACTATGCAGCATTATTGTTTTTCTTCATTAACCTTAATAGAGGTCTCATGTATTCCCAGGTTATTAGTTTAGTCTGTTAGACCTTCACTCCTTTGAAGTAATGGCTATATTTGCCTCATTTTTAATACGCAGCACCTAAAGTAATGCCAAAATATAGTAGGCTCTGTGTGTGGAAAAAGGTATACAATAAAGTTCAGAGACTTTTCAAAAAATAAGACAGCATCTTGACAGTCCTTGTTCTTCCTAATATTGGGAGGAAGAGAGAATAA... |
Task1_train_34033 | A mutation on Chromosome 2 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CATATAGGATTTACCTTAAAAGGATCACTATTACAGGGGAAAGAGACTGTAGGAGAGGACTGGAAGTGGGAAAACGATGAGGTTGGTTTAATTTTCCAGGTAAAAGATGATGGGGACATGGGCTAGTGGGGTGGGGACGGAAGAGGTGAGAAATCGTTGGATTTAGAGTCTATTTTTAAAATAATTCAGGATTTGTCAATAGGTTGGATATGGTGTGCAAGAGAAAGAAAAGAGTCAAGGACGCCAAATTGAGCTGTGCAGCTGGGTTACTGCAGTGCTGTTTACTGAGATGATAAAACGGTAGGAGGAGTTCGTGTGGT... | CATATAGGATTTACCTTAAAAGGATCACTATTACAGGGGAAAGAGACTGTAGGAGAGGACTGGAAGTGGGAAAACGATGAGGTTGGTTTAATTTTCCAGGTAAAAGATGATGGGGACATGGGCTAGTGGGGTGGGGACGGAAGAGGTGAGAAATCGTTGGATTTAGAGTCTATTTTTAAAATAATTCAGGATTTGTCAATAGGTTGGATATGGTGTGCAAGAGAAAGAAAAGAGTCAAGGACGCCAAATTGAGCTGTGCAGCTGGGTTACTGCAGTGCTGTTTACTGAGATGATAAAACGGTAGGAGGAGTTCGTGTGGT... |
Task1_train_34034 | This mutation is located on Chromosome 2. Is it associated with a disease or is it a benign polymorphism? | Benign | CTCATCTGGAAAATTGACATTTTAAAAAGTCACTATGACTGAAAAACATATTTACCTCATGCTGTAACATTACTCTATCAATCAACAGTGCTCTGATATGTTGTTTTTTCCCATGGAGCTGGAAAACAAAGTAGCAACAAATACTTCAACATTTTCCCTAAATGACTTCAACAATGGATGCCTCTAAATACCTTAATAAGTGGTCAAAAAGGTCCCTGGTTGACTGGTGAGTGGTGGTGGTATTTCCTTTATTCTAAAGACATCAGGCTTATATAAAAATGTTGTCTTAATTTTTATGGCTAACAGTAGAAATATCCCCC... | CTCATCTGGAAAATTGACATTTTAAAAAGTCACTATGACTGAAAAACATATTTACCTCATGCTGTAACATTACTCTATCAATCAACAGTGCTCTGATATGTTGTTTTTTCCCATGGAGCTGGAAAACAAAGTAGCAACAAATACTTCAACATTTTCCCTAAATGACTTCAACAATGGATGCCTCTAAATACCTTAATAAGTGGTCAAAAAGGTCCCTGGTTGACTGGTGAGTGGTGGTGGTATTTCCTTTATTCTAAAGACATCAGGCTTATATAAAAATGTTGTCTTAATTTTTATGGCTAACAGTAGAAATATCCCCC... |
Task1_train_34035 | This alteration occurs on Chromosome 2. Is it associated with a disease or is it a benign variant? | Benign | GGTTGCAGTGAGCCGAGATGGCGCCACTGCACTCCAGCCTGGACGACAAGAGTGAAATTCCATCTCAGAAGAAAAAAAAAGAGTTCTAGTAGACTGGATCAATAGAAATTTTAGTATGATGTAGTTAAAATAATTCAAAATCAAAATGTTGCTACTTACATAGCATAACTGAATTTGGAGCTAGAAAAAGGCAATTTTAAAAGACTATTAATAATAATAGGAGAGATAAATCTACCCATAGACAATTATAACATTTCTGTGCCAAGTCCAGAGCCAACAGAAAACATCAGAATCTTTTAGTCTTATAAAAACTCTGCAAA... | GGTTGCAGTGAGCCGAGATGGCGCCACTGCACTCCAGCCTGGACGACAAGAGTGAAATTCCATCTCAGAAGAAAAAAAAAGAGTTCTAGTAGACTGGATCAATAGAAATTTTAGTATGATGTAGTTAAAATAATTCAAAATCAAAATGTTGCTACTTACATAGCATAACTGAATTTGGAGCTAGAAAAAGGCAATTTTAAAAGACTATTAATAATAATAGGAGAGATAAATCTACCCATAGACAATTATAACATTTCTGTGCCAAGTCCAGAGCCAACAGAAAACATCAGAATCTTTTAGTCTTATAAAAACTCTGCAAA... |
Task1_train_34036 | This sequence change occurs on Chromosome 2. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CCCTCTAGGAATTGCTAAAGAGGGGTGAGGGGCTGAGAAGAAAGGAGAATGGGCAATAAGAGGTCTGGCAGTCTATTTTACAGAACAGCCTGCCTCTGGACATGACAAAGAGAGCCAAGAAACTAAAAAGCCTGCTTCTGCGGATGTTTCTGAACTACTACTTTTGTTTTTTTTAAAGGAAGACAGAAGAGATTTATGAGAGATGAGAGAAAAGAAAGTGTACACTCACTCTGGCACTTCATTAGGTTCAGGAAGGGAGGCAAATAAAGGTACCTAGATTTTGAATGAATCCACTGGTTGTGGCTGAGAAAGCCTGGTAC... | CCCTCTAGGAATTGCTAAAGAGGGGTGAGGGGCTGAGAAGAAAGGAGAATGGGCAATAAGAGGTCTGGCAGTCTATTTTACAGAACAGCCTGCCTCTGGACATGACAAAGAGAGCCAAGAAACTAAAAAGCCTGCTTCTGCGGATGTTTCTGAACTACTACTTTTGTTTTTTTTAAAGGAAGACAGAAGAGATTTATGAGAGATGAGAGAAAAGAAAGTGTACACTCACTCTGGCACTTCATTAGGTTCAGGAAGGGAGGCAAATAAAGGTACCTAGATTTTGAATGAATCCACTGGTTGTGGCTGAGAAAGCCTGGTAC... |
Task1_train_34037 | This sequence variant lies on Chromosome 2. Is it clinically significant, and what condition might it cause if any? | Benign | AAAGCCTGGTACTTGTCAAGAACACCAACATATTAACCTTGCCATGAGGATAGGGTCTGACATGTCCCCTCAACCACCTGTCTAACAAACAGTAGGGTTTCTGAGTGATGAGGGTGGTGGTGGTAAAGAGAGGTCTTTTGGAAGAGGAACAGGTCTTTTGTGTGCTGACAGGAAAGCTGTGTCCACCACCAGTGTTCTGGAGATCCCTGTTTATTAGAAACCAGAGAGTGGAGCTGGCAATGGTCTGGGATATGTTCACTCAGCAGGGAGCTGCCCAAGTAGCAGTACTTGGGAATAGCCAGTAGCAGGCAGCAATAGGT... | AAAGCCTGGTACTTGTCAAGAACACCAACATATTAACCTTGCCATGAGGATAGGGTCTGACATGTCCCCTCAACCACCTGTCTAACAAACAGTAGGGTTTCTGAGTGATGAGGGTGGTGGTGGTAAAGAGAGGTCTTTTGGAAGAGGAACAGGTCTTTTGTGTGCTGACAGGAAAGCTGTGTCCACCACCAGTGTTCTGGAGATCCCTGTTTATTAGAAACCAGAGAGTGGAGCTGGCAATGGTCTGGGATATGTTCACTCAGCAGGGAGCTGCCCAAGTAGCAGTACTTGGGAATAGCCAGTAGCAGGCAGCAATAGGT... |
Task1_train_34038 | This sequence change occurs on Chromosome 2. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TGTAGGCTATATGGTATAATCAATTGCTCCTAGGCTACTAACCTATACAGGATGTTACTGTAGGCAACTGTAACACAATGGTATTTGTGTAGTGTTTATCTAAACATACCTAAAATAACACTGTACAAAGGATTAAAAGATGGCACACGTGTGCAGGGCACTGGCCATGAACAGAGCTTGCCAGCCTGGAAGCTGCTGTGGACGTGAGTAGTGAGTGAATGTGAAGGCCTAGGACATTACCATGTACTACTGTACAACTTACAGACACTCTACGGTTAGGCTACACTAAATTTATCTTTAGATATATTTTTTCAATAATA... | TGTAGGCTATATGGTATAATCAATTGCTCCTAGGCTACTAACCTATACAGGATGTTACTGTAGGCAACTGTAACACAATGGTATTTGTGTAGTGTTTATCTAAACATACCTAAAATAACACTGTACAAAGGATTAAAAGATGGCACACGTGTGCAGGGCACTGGCCATGAACAGAGCTTGCCAGCCTGGAAGCTGCTGTGGACGTGAGTAGTGAGTGAATGTGAAGGCCTAGGACATTACCATGTACTACTGTACAACTTACAGACACTCTACGGTTAGGCTACACTAAATTTATCTTTAGATATATTTTTTCAATAATA... |
Task1_train_34039 | A variant on Chromosome 2 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GAAGCAATAGTATAAATATTTCAAAGACAAATCTAAATGTCATCATAACAAAAGTGTGATTTATTTCTGAGATCTTCTTACTCTAGATTTATTTATAAGTTAGTTACGTTAAAATCAGTTTTTCCCAACCAGCATACATAAGGTGTTGTACAAGCTCCCTCAGCTGGTTAAGATATAGAACTACCAAAACACATGTTCCATTAGGTTGACTGCGTCATCCTCTTCAGAAATTTCTGTAACTGCAGCCTGAGATCGAAGAATAGACGTGATGTCATTAGATAATTTGTCAAAGCCATTCTGTGAACATATATTTGCCACTT... | GAAGCAATAGTATAAATATTTCAAAGACAAATCTAAATGTCATCATAACAAAAGTGTGATTTATTTCTGAGATCTTCTTACTCTAGATTTATTTATAAGTTAGTTACGTTAAAATCAGTTTTTCCCAACCAGCATACATAAGGTGTTGTACAAGCTCCCTCAGCTGGTTAAGATATAGAACTACCAAAACACATGTTCCATTAGGTTGACTGCGTCATCCTCTTCAGAAATTTCTGTAACTGCAGCCTGAGATCGAAGAATAGACGTGATGTCATTAGATAATTTGTCAAAGCCATTCTGTGAACATATATTTGCCACTT... |
Task1_train_34040 | A mutation on Chromosome 2 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CCTTGACCAGTGACAGACTTATCTACTATGGCTTTCACTCCCATACTATCAATTCAGTATAGTAAGGCTTCTTAATCTGTACTCCCCTCCTAAGGTAATTTAAATAGTTCACTTGATTAATTATGGGTGACAAGTATCACTTTCTCTTTTGAGATGAAAGCCCTTTAAAATGAGAGAAAAATCCCAAAGAACAATGTCTTCTAATTAATGAATTAAATTTAGTCATAGAAACTTACCTTAAGTAAGCAGTTTTTAAATTTGGTAAGAAAATCTTTTTTCCAATCATCAATTTCTCTAATTTTTTAAAAAGTCCCCACACA... | CCTTGACCAGTGACAGACTTATCTACTATGGCTTTCACTCCCATACTATCAATTCAGTATAGTAAGGCTTCTTAATCTGTACTCCCCTCCTAAGGTAATTTAAATAGTTCACTTGATTAATTATGGGTGACAAGTATCACTTTCTCTTTTGAGATGAAAGCCCTTTAAAATGAGAGAAAAATCCCAAAGAACAATGTCTTCTAATTAATGAATTAAATTTAGTCATAGAAACTTACCTTAAGTAAGCAGTTTTTAAATTTGGTAAGAAAATCTTTTTTCCAATCATCAATTTCTCTAATTTTTTAAAAAGTCCCCACACA... |
Task1_train_34041 | Given this variant on Chromosome 2, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CTACTATGGCTTTCACTCCCATACTATCAATTCAGTATAGTAAGGCTTCTTAATCTGTACTCCCCTCCTAAGGTAATTTAAATAGTTCACTTGATTAATTATGGGTGACAAGTATCACTTTCTCTTTTGAGATGAAAGCCCTTTAAAATGAGAGAAAAATCCCAAAGAACAATGTCTTCTAATTAATGAATTAAATTTAGTCATAGAAACTTACCTTAAGTAAGCAGTTTTTAAATTTGGTAAGAAAATCTTTTTTCCAATCATCAATTTCTCTAATTTTTTAAAAAGTCCCCACACAGGACAACTCTAAGTATATAAAT... | CTACTATGGCTTTCACTCCCATACTATCAATTCAGTATAGTAAGGCTTCTTAATCTGTACTCCCCTCCTAAGGTAATTTAAATAGTTCACTTGATTAATTATGGGTGACAAGTATCACTTTCTCTTTTGAGATGAAAGCCCTTTAAAATGAGAGAAAAATCCCAAAGAACAATGTCTTCTAATTAATGAATTAAATTTAGTCATAGAAACTTACCTTAAGTAAGCAGTTTTTAAATTTGGTAAGAAAATCTTTTTTCCAATCATCAATTTCTCTAATTTTTTAAAAAGTCCCCACACAGGACAACTCTAAGTATATAAAT... |
Task1_train_34042 | A variant has been detected on Chromosome 2. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TAGATCTGAAGGTAACTTGTACTTAAGGAACGAGAACAGTGAGAAATATATGTTTTTAATGGAGTTGATACTATTTCATGTGGTCTTTGGTTTTGAACAGGTGTATTACCTGACTGCTTAACCGATGGCTCTGATGTGGTCAGTGACCTTGAACACGAAGAGATGAAAATCCTGAGGGAAGTTCTTAGGTACCATTCTTTAATTGTTTTTTAAATGAATCATTATTAATATTATATGATCTGTACATATGCTTTTTGCCCAACAAATATGAACTAATAAAATTGCTAAATTCTCTACTGAAAACCATCAAAATGATCTAT... | TAGATCTGAAGGTAACTTGTACTTAAGGAACGAGAACAGTGAGAAATATATGTTTTTAATGGAGTTGATACTATTTCATGTGGTCTTTGGTTTTGAACAGGTGTATTACCTGACTGCTTAACCGATGGCTCTGATGTGGTCAGTGACCTTGAACACGAAGAGATGAAAATCCTGAGGGAAGTTCTTAGGTACCATTCTTTAATTGTTTTTTAAATGAATCATTATTAATATTATATGATCTGTACATATGCTTTTTGCCCAACAAATATGAACTAATAAAATTGCTAAATTCTCTACTGAAAACCATCAAAATGATCTAT... |
Task1_train_34043 | A variant was discovered on Chromosome 2. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GTTACCTTGCTTCTTTGTACCAAGTCAAACCATTTCTTTTTTATATATATGCTACAGATTGTAAGGAGAAATAGCCTCATTTTAATGATATATATGAAAGCTCCTGCTTTAGGTTTGTCTGTGCTCTAGTTTGCTGACCCAAATTAACTTTGTTTTATATACACCTAAGTACATACACTATTTAAATCTTGTGTCTAACATAAATTGAATAAATTTGCTTTGTCTGCTTTCTTATCTAAGTGAAGCTATAGAAAACTTGATCTCAAACCACATATAATTCAGTTGTACACATTAATGGTACACCATAAATGGTAGATCTC... | GTTACCTTGCTTCTTTGTACCAAGTCAAACCATTTCTTTTTTATATATATGCTACAGATTGTAAGGAGAAATAGCCTCATTTTAATGATATATATGAAAGCTCCTGCTTTAGGTTTGTCTGTGCTCTAGTTTGCTGACCCAAATTAACTTTGTTTTATATACACCTAAGTACATACACTATTTAAATCTTGTGTCTAACATAAATTGAATAAATTTGCTTTGTCTGCTTTCTTATCTAAGTGAAGCTATAGAAAACTTGATCTCAAACCACATATAATTCAGTTGTACACATTAATGGTACACCATAAATGGTAGATCTC... |
Task1_train_34044 | Given a variant located on Chromosome 2, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GCTTCTTTGTACCAAGTCAAACCATTTCTTTTTTATATATATGCTACAGATTGTAAGGAGAAATAGCCTCATTTTAATGATATATATGAAAGCTCCTGCTTTAGGTTTGTCTGTGCTCTAGTTTGCTGACCCAAATTAACTTTGTTTTATATACACCTAAGTACATACACTATTTAAATCTTGTGTCTAACATAAATTGAATAAATTTGCTTTGTCTGCTTTCTTATCTAAGTGAAGCTATAGAAAACTTGATCTCAAACCACATATAATTCAGTTGTACACATTAATGGTACACCATAAATGGTAGATCTCAAAAGTAA... | GCTTCTTTGTACCAAGTCAAACCATTTCTTTTTTATATATATGCTACAGATTGTAAGGAGAAATAGCCTCATTTTAATGATATATATGAAAGCTCCTGCTTTAGGTTTGTCTGTGCTCTAGTTTGCTGACCCAAATTAACTTTGTTTTATATACACCTAAGTACATACACTATTTAAATCTTGTGTCTAACATAAATTGAATAAATTTGCTTTGTCTGCTTTCTTATCTAAGTGAAGCTATAGAAAACTTGATCTCAAACCACATATAATTCAGTTGTACACATTAATGGTACACCATAAATGGTAGATCTCAAAAGTAA... |
Task1_train_34045 | Chromosome 2 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CTCATGCATAGCACTGGGTGTTGGTGCAAATACAGAAAACGTTTCTTCATCCACCTGACTAATAGTTACACCTTTTAAAAACAAAATGTAACATATTAAAGTTAACTTGGCTGGGCATAGTGGGTCACATCTGTAATCCCAGCACTCTGGGGGGCTGAGGTGGGAGGATCACTTGAGCTCAGGAGTTCAAGGCCAGCCTGGGCAACATAGGGAGAGCCTGTTACTACAAAAAATAAATTCAAAAATTAGCTGGACCTGGTAGCATGTGCCCACCTACTTGGGACTCACAGTCGGGAGGATCACTTGATCCCAGGGGTCAA... | CTCATGCATAGCACTGGGTGTTGGTGCAAATACAGAAAACGTTTCTTCATCCACCTGACTAATAGTTACACCTTTTAAAAACAAAATGTAACATATTAAAGTTAACTTGGCTGGGCATAGTGGGTCACATCTGTAATCCCAGCACTCTGGGGGGCTGAGGTGGGAGGATCACTTGAGCTCAGGAGTTCAAGGCCAGCCTGGGCAACATAGGGAGAGCCTGTTACTACAAAAAATAAATTCAAAAATTAGCTGGACCTGGTAGCATGTGCCCACCTACTTGGGACTCACAGTCGGGAGGATCACTTGATCCCAGGGGTCAA... |
Task1_train_34046 | Given this variant on Chromosome 2, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GAGGCTAAGGCTGTGATATTCTTGCAAAGGCATATTTGCAAGGTGTATTTATTTATTTCAAATGAATGAAATGGTTACTTAAGTATATGTGTCATTATCCTGAAAGAAAGTATTATTCAGGAAGTATTAAAATATAATAAAGTAGAGGTTCAGAGGATCCAGCAATAAAATTAGGTAATAAAAATTAGTTACGTTAGTTGTCCTATTCCCAGCCTGATTTGGTCTCCACTCACTGTAGTCACGCTGATCTTCTTTTTAAACTCATTAATTTCTTTCCTGCCTCTGGGCTTTCAATGCTTCCCTGACACACCTTGGTTGGC... | GAGGCTAAGGCTGTGATATTCTTGCAAAGGCATATTTGCAAGGTGTATTTATTTATTTCAAATGAATGAAATGGTTACTTAAGTATATGTGTCATTATCCTGAAAGAAAGTATTATTCAGGAAGTATTAAAATATAATAAAGTAGAGGTTCAGAGGATCCAGCAATAAAATTAGGTAATAAAAATTAGTTACGTTAGTTGTCCTATTCCCAGCCTGATTTGGTCTCCACTCACTGTAGTCACGCTGATCTTCTTTTTAAACTCATTAATTTCTTTCCTGCCTCTGGGCTTTCAATGCTTCCCTGACACACCTTGGTTGGC... |
Task1_train_34047 | A mutation found on Chromosome 2 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AGAGTTCCACCAACCATGTTATGGACACGAGGCAATCATCCCAAAGGGGACTGAGCTGAGAGAAGGAGCCTAAGATTTTGACGACCTCATGAAGATACCATACCAGCCCTCAGCTGCCTCTCTTTAGAATACCAGGTAGGTGAGAAAAAATAAATGACTTTTTTAAAGTGACTGTTTTTTGAGTTTCTGTTTTTAGCAGTCAAATGAAGCTCCTGACACCATACATGACCTTAGCAACATGAAGCAACATTATTCATTCATGCAGATAATTATTATTCTGAATCAATGACCAAAATTAGAAACATGAAAACCTTAAGGTG... | AGAGTTCCACCAACCATGTTATGGACACGAGGCAATCATCCCAAAGGGGACTGAGCTGAGAGAAGGAGCCTAAGATTTTGACGACCTCATGAAGATACCATACCAGCCCTCAGCTGCCTCTCTTTAGAATACCAGGTAGGTGAGAAAAAATAAATGACTTTTTTAAAGTGACTGTTTTTTGAGTTTCTGTTTTTAGCAGTCAAATGAAGCTCCTGACACCATACATGACCTTAGCAACATGAAGCAACATTATTCATTCATGCAGATAATTATTATTCTGAATCAATGACCAAAATTAGAAACATGAAAACCTTAAGGTG... |
Task1_train_34048 | A mutation is present on Chromosome 2. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | AGAGGCGGAGAGATTTACATGTCAAAGGGTCAGAGGAAACATTCACCAATGGAAGTTGGCTAAAGTAAATGCTCTGAGAAAAGGAAGGTCTGGGGCCTACAGTTAGGAAGAAACCTGTCTAAAGTTTAGTTAAGCTGAGGGGAATGTTAAGGCCATTTGGTCACCGTAAGCAGTACCACATTTCCTTGCCTCTCCCGGGAGCCAGGTCTCAGTGTCCCCAATAGGGGACACGCACTGACCGGCGGGTGAAGGGACTGATTTTGATTATCATCCTACCAGATAGAGATTATTCCCTCTGCACCCGGGTTAACTGAAACCCG... | AGAGGCGGAGAGATTTACATGTCAAAGGGTCAGAGGAAACATTCACCAATGGAAGTTGGCTAAAGTAAATGCTCTGAGAAAAGGAAGGTCTGGGGCCTACAGTTAGGAAGAAACCTGTCTAAAGTTTAGTTAAGCTGAGGGGAATGTTAAGGCCATTTGGTCACCGTAAGCAGTACCACATTTCCTTGCCTCTCCCGGGAGCCAGGTCTCAGTGTCCCCAATAGGGGACACGCACTGACCGGCGGGTGAAGGGACTGATTTTGATTATCATCCTACCAGATAGAGATTATTCCCTCTGCACCCGGGTTAACTGAAACCCG... |
Task1_train_34049 | A variant on Chromosome 2 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TCCCTTCTTTCCTCCCCTACCCCAGTCAGTCTGTTTTCCACACAACTATGGAGATTCTTTGCAAAAGGAATCATGTAATGTCACTCCTCTATCCTCAGCTCCCTAACAACCCAAAGCCTTTCCCGTCGCTGACCATGCCATGCATATTCTAGGCCCTGATGCCTCTCAGACCCCCTTTCCCATGTCCGTTGACTTGCTCTCTGTTCTTTAGACATGCTCACCTCGCTGTACTTGAGCTCTTGCTCTCATGCTGGTCTTAGGGCTTTTTACTTGCCCTCTCCCTGCCTGGGATCATCTTCACTCAAATGTTGGCTCCTTCA... | TCCCTTCTTTCCTCCCCTACCCCAGTCAGTCTGTTTTCCACACAACTATGGAGATTCTTTGCAAAAGGAATCATGTAATGTCACTCCTCTATCCTCAGCTCCCTAACAACCCAAAGCCTTTCCCGTCGCTGACCATGCCATGCATATTCTAGGCCCTGATGCCTCTCAGACCCCCTTTCCCATGTCCGTTGACTTGCTCTCTGTTCTTTAGACATGCTCACCTCGCTGTACTTGAGCTCTTGCTCTCATGCTGGTCTTAGGGCTTTTTACTTGCCCTCTCCCTGCCTGGGATCATCTTCACTCAAATGTTGGCTCCTTCA... |
Task1_train_34050 | Given this variant on Chromosome 2, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | ATCATCTTCACTCAAATGTTGGCTCCTTCATTCCACCCAGGTGCCTGCTCAAATGTTTCCCTTCTCTGTAGCGGTATCTTCTCTTGAAAAAGAGTATTCTTTAACCTGCTTCAATTTTCCTTCCAGAACTTCTCACTGCATGACGTTATGCTCTATACGTGTTTTTTGCCAGTCTTTCCCACCACAATAAAAGCTGTACCATGTCAGGGTCTTTGCTGTGTCCACTGATATATCCCTACCACCTGGACTGGTACCTGGTACAGTAATAGATGTTTACTGAGTATTTGTGAACAAGCAAGTGAATCATCACTCATGCAGGA... | ATCATCTTCACTCAAATGTTGGCTCCTTCATTCCACCCAGGTGCCTGCTCAAATGTTTCCCTTCTCTGTAGCGGTATCTTCTCTTGAAAAAGAGTATTCTTTAACCTGCTTCAATTTTCCTTCCAGAACTTCTCACTGCATGACGTTATGCTCTATACGTGTTTTTTGCCAGTCTTTCCCACCACAATAAAAGCTGTACCATGTCAGGGTCTTTGCTGTGTCCACTGATATATCCCTACCACCTGGACTGGTACCTGGTACAGTAATAGATGTTTACTGAGTATTTGTGAACAAGCAAGTGAATCATCACTCATGCAGGA... |
Task1_train_34051 | Chromosome 2 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TTAAAGACATGTTTATAAATGTATAGAGACGGTATATATGATCTTATCAAGAAACAAACAAATATAAAATTCATGTGGCTGGGCACGGTGGCTCATGCCTGTAATCCCAGCACTTTGAGAGGCTAAGGCAGGCGGATCATGAGGTCAAGAGGTCGAGACCATCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGTGCATGCCTGCAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCTGAGATTGCACCACTG... | TTAAAGACATGTTTATAAATGTATAGAGACGGTATATATGATCTTATCAAGAAACAAACAAATATAAAATTCATGTGGCTGGGCACGGTGGCTCATGCCTGTAATCCCAGCACTTTGAGAGGCTAAGGCAGGCGGATCATGAGGTCAAGAGGTCGAGACCATCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGTGCATGCCTGCAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCTGAGATTGCACCACTG... |
Task1_train_34052 | This mutation on Chromosome 2 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GGCTGGGCGTGGTGGTTCATGCCTGTAATCCCAGCACTTTAGGAGGCCAAGTGGAAGGACTGCTTGAGCCCAGGAGTTTGAGACCAGCCAGGGCAACATAACCAGACCGTGTCTCTACAAAAAAATTAAAAAATTAGCCAGGCATGGTGGCATGTGCCTGTAGTTCCAGCTACTCAGGAGGCCGAGGTGGGAGGATCACTTGACCCTGGAAGGTTAAGGCTGCAGTGAGCTATGATTGCACTACTGCACTCTAGTCCAGGCAACAGAGCAAGACCCAGTGTCAAGAAATTAAGTAAAAACATATTGAAGAAAAGGGAATG... | GGCTGGGCGTGGTGGTTCATGCCTGTAATCCCAGCACTTTAGGAGGCCAAGTGGAAGGACTGCTTGAGCCCAGGAGTTTGAGACCAGCCAGGGCAACATAACCAGACCGTGTCTCTACAAAAAAATTAAAAAATTAGCCAGGCATGGTGGCATGTGCCTGTAGTTCCAGCTACTCAGGAGGCCGAGGTGGGAGGATCACTTGACCCTGGAAGGTTAAGGCTGCAGTGAGCTATGATTGCACTACTGCACTCTAGTCCAGGCAACAGAGCAAGACCCAGTGTCAAGAAATTAAGTAAAAACATATTGAAGAAAAGGGAATG... |
Task1_train_34053 | A mutation on Chromosome 2 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GGCGTGGTGGTTCATGCCTGTAATCCCAGCACTTTAGGAGGCCAAGTGGAAGGACTGCTTGAGCCCAGGAGTTTGAGACCAGCCAGGGCAACATAACCAGACCGTGTCTCTACAAAAAAATTAAAAAATTAGCCAGGCATGGTGGCATGTGCCTGTAGTTCCAGCTACTCAGGAGGCCGAGGTGGGAGGATCACTTGACCCTGGAAGGTTAAGGCTGCAGTGAGCTATGATTGCACTACTGCACTCTAGTCCAGGCAACAGAGCAAGACCCAGTGTCAAGAAATTAAGTAAAAACATATTGAAGAAAAGGGAATGAATAG... | GGCGTGGTGGTTCATGCCTGTAATCCCAGCACTTTAGGAGGCCAAGTGGAAGGACTGCTTGAGCCCAGGAGTTTGAGACCAGCCAGGGCAACATAACCAGACCGTGTCTCTACAAAAAAATTAAAAAATTAGCCAGGCATGGTGGCATGTGCCTGTAGTTCCAGCTACTCAGGAGGCCGAGGTGGGAGGATCACTTGACCCTGGAAGGTTAAGGCTGCAGTGAGCTATGATTGCACTACTGCACTCTAGTCCAGGCAACAGAGCAAGACCCAGTGTCAAGAAATTAAGTAAAAACATATTGAAGAAAAGGGAATGAATAG... |
Task1_train_34054 | This genomic variant is located on Chromosome 2. Can you determine its pathogenicity and name any linked disease? | Benign | GCTGGAGTGCAATGGCACGATCTTGGCTCACTGTAACCTCTGCCTCCCAGGTTCAAGCGATTTTCCTGCCTCAGCCTCCCAAGTAGCTAGGATTACAGGTGTCCGCCACCACGCCCAGCTAGTTTTTGTATTTTTAGTAGAGACCAGGCTGGTCTTGAACTCCTGACCTCAGGTGATCCACCCGCCTCAGCCTCCCAAAGTGCTGGCATTACAGGCGTGAGCCACCATGCCCAGCCACCACATTTTATCTATCCATCCTTCGATGGACATTTTGGGTTTTTCTACCTTTTGGTATTTTGAGTAATTCTGCCATGAGCAAG... | GCTGGAGTGCAATGGCACGATCTTGGCTCACTGTAACCTCTGCCTCCCAGGTTCAAGCGATTTTCCTGCCTCAGCCTCCCAAGTAGCTAGGATTACAGGTGTCCGCCACCACGCCCAGCTAGTTTTTGTATTTTTAGTAGAGACCAGGCTGGTCTTGAACTCCTGACCTCAGGTGATCCACCCGCCTCAGCCTCCCAAAGTGCTGGCATTACAGGCGTGAGCCACCATGCCCAGCCACCACATTTTATCTATCCATCCTTCGATGGACATTTTGGGTTTTTCTACCTTTTGGTATTTTGAGTAATTCTGCCATGAGCAAG... |
Task1_train_34055 | With a mutation on Chromosome 2, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | AGATCAGATATTGGTATAAGATTATAACCATTAACTAAGGCCACAATAGAAAATGTCTGTATTCATCAACATAGCTTCATGGTTCTCACCATAAAGGTGAGTTTATATGTTGGTTCTCACCATGAGGTGAGTGTGTGTGCACTGAACACAAGTAACTGATGACAATTTAAATCCATAAGCTAAAACACTAATGCTATTTTCAATCTGCTCATATTTTACTATCTACTGATTAAAAAAAAAAGAGTTTGAAAACCAGTGGTCTGGAGATTCAAGATTTTTTCATGATACCTGAGACATTTTACTCTGGATTTAGATATTTG... | AGATCAGATATTGGTATAAGATTATAACCATTAACTAAGGCCACAATAGAAAATGTCTGTATTCATCAACATAGCTTCATGGTTCTCACCATAAAGGTGAGTTTATATGTTGGTTCTCACCATGAGGTGAGTGTGTGTGCACTGAACACAAGTAACTGATGACAATTTAAATCCATAAGCTAAAACACTAATGCTATTTTCAATCTGCTCATATTTTACTATCTACTGATTAAAAAAAAAAGAGTTTGAAAACCAGTGGTCTGGAGATTCAAGATTTTTTCATGATACCTGAGACATTTTACTCTGGATTTAGATATTTG... |
Task1_train_34056 | Chromosome 2 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CTGGATCCTCTTCTTGTTTTTTGAGCGCTTTATGTACCATTTCGATATCTGATTTAGATTTCATGGACTCTTCTTTTTTCTTCTGTTCTCTTATCATCATTTGAAAAGGCTCCGGTACTGTAATTGTGGGCACCCATTCTTTTCGTTTCTTCCTTCTTTTTTCAGCTGCATGGAAGCCAGTATCTTTACAGCGAATATAATCCTCAACACAAAAGTCTGTCCACATATTGTTGATGAGCTCCTTAGCATAGGTCATCATTCTGTTTTTCCTAGGATACTCTTTTTCTAGGTTGGGTAACTCCTCTTCAGAGGAGGACACA... | CTGGATCCTCTTCTTGTTTTTTGAGCGCTTTATGTACCATTTCGATATCTGATTTAGATTTCATGGACTCTTCTTTTTTCTTCTGTTCTCTTATCATCATTTGAAAAGGCTCCGGTACTGTAATTGTGGGCACCCATTCTTTTCGTTTCTTCCTTCTTTTTTCAGCTGCATGGAAGCCAGTATCTTTACAGCGAATATAATCCTCAACACAAAAGTCTGTCCACATATTGTTGATGAGCTCCTTAGCATAGGTCATCATTCTGTTTTTCCTAGGATACTCTTTTTCTAGGTTGGGTAACTCCTCTTCAGAGGAGGACACA... |
Task1_train_34057 | A mutation located on Chromosome 2 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CTGGAGACACATGGTTGGACGAGGACAAAGTTTGCCAGATCAGGGAGGCAGTGAAAAAGGAATAAATAAATCCGAGGCATAGTGCTAGAACATCCATCGCCAGGAAACATGTGGATAAATGTCTGGAGACCTGGTGAGAAGGCTGGGCTGGAGAGCAGATACAGGAGCCACCAATCCACACAGAAGTAGCAGGTGCAGCCTTGGTTATGGACGAGGCTGCCTGGAGGGAGTGTGAGCAACAAGACATGAGAGGACCTGAGAATGGAGATGTTGGAGAACACCAACATTTAAATAAGCAGCGGAAGGAGGACTAATAGGAG... | CTGGAGACACATGGTTGGACGAGGACAAAGTTTGCCAGATCAGGGAGGCAGTGAAAAAGGAATAAATAAATCCGAGGCATAGTGCTAGAACATCCATCGCCAGGAAACATGTGGATAAATGTCTGGAGACCTGGTGAGAAGGCTGGGCTGGAGAGCAGATACAGGAGCCACCAATCCACACAGAAGTAGCAGGTGCAGCCTTGGTTATGGACGAGGCTGCCTGGAGGGAGTGTGAGCAACAAGACATGAGAGGACCTGAGAATGGAGATGTTGGAGAACACCAACATTTAAATAAGCAGCGGAAGGAGGACTAATAGGAG... |
Task1_train_34058 | A change on Chromosome 2 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GACACATATATTGAAATCAGTTGCTGTACACGTAAGATTTTAAAGGCTCTAAAATAAATGTCTTAAAAACATTATTTTCTCCTTTTCTCCATAGCTGAGTGTTTTTATCTGTCACTTAATTATTTTAAAATATAAGAAATAGTCATGGTCTCTCACAGCAAAATAGTTTCTTTTAGCTCCAAGAATATGCCTGATTATTATGATCTACTTTTGCTTGCAACTGTTTATTAAATTACCACTGATAAAGGAATGAATTCTTAAAATCTGTTAAATCTGAAGACAACTCACCAGCCTAGGATCTTTTCGATAGCAACAGTACA... | GACACATATATTGAAATCAGTTGCTGTACACGTAAGATTTTAAAGGCTCTAAAATAAATGTCTTAAAAACATTATTTTCTCCTTTTCTCCATAGCTGAGTGTTTTTATCTGTCACTTAATTATTTTAAAATATAAGAAATAGTCATGGTCTCTCACAGCAAAATAGTTTCTTTTAGCTCCAAGAATATGCCTGATTATTATGATCTACTTTTGCTTGCAACTGTTTATTAAATTACCACTGATAAAGGAATGAATTCTTAAAATCTGTTAAATCTGAAGACAACTCACCAGCCTAGGATCTTTTCGATAGCAACAGTACA... |
Task1_train_34059 | This variant is located on Chromosome 2. Evaluate its biological effect and specify any disease association. | Benign | GAAATCAGTTGCTGTACACGTAAGATTTTAAAGGCTCTAAAATAAATGTCTTAAAAACATTATTTTCTCCTTTTCTCCATAGCTGAGTGTTTTTATCTGTCACTTAATTATTTTAAAATATAAGAAATAGTCATGGTCTCTCACAGCAAAATAGTTTCTTTTAGCTCCAAGAATATGCCTGATTATTATGATCTACTTTTGCTTGCAACTGTTTATTAAATTACCACTGATAAAGGAATGAATTCTTAAAATCTGTTAAATCTGAAGACAACTCACCAGCCTAGGATCTTTTCGATAGCAACAGTACAAAGCTGCGGACA... | GAAATCAGTTGCTGTACACGTAAGATTTTAAAGGCTCTAAAATAAATGTCTTAAAAACATTATTTTCTCCTTTTCTCCATAGCTGAGTGTTTTTATCTGTCACTTAATTATTTTAAAATATAAGAAATAGTCATGGTCTCTCACAGCAAAATAGTTTCTTTTAGCTCCAAGAATATGCCTGATTATTATGATCTACTTTTGCTTGCAACTGTTTATTAAATTACCACTGATAAAGGAATGAATTCTTAAAATCTGTTAAATCTGAAGACAACTCACCAGCCTAGGATCTTTTCGATAGCAACAGTACAAAGCTGCGGACA... |
Task1_train_34060 | A variant on Chromosome 2 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | AAAGCACTCCATTATGTTAACCAAAAACCTATGTGAATTCTTATCAAAAACCTAAGTGAATTATTTTAAAGATATTTTCCCCTGGCATTGAAAAAAGATGCAAGATACCTTCTTCAGATTGTAATTATGTTATCAAAATCCTGGAGGAAAAAAAGTGATAGAATTATGGGTATTTTTCCTTCTAATTTTATTATTCAAATTTCCTATATGAGCGTACATTTTCTAGTTAGAAAAAAATCTTGTTAAAAATAAATTGAGAGGAAGAGGCAATGATGATGCAAAAACATTAGAGAAGATAATTTGAGAGGAAAAAAAATGTG... | AAAGCACTCCATTATGTTAACCAAAAACCTATGTGAATTCTTATCAAAAACCTAAGTGAATTATTTTAAAGATATTTTCCCCTGGCATTGAAAAAAGATGCAAGATACCTTCTTCAGATTGTAATTATGTTATCAAAATCCTGGAGGAAAAAAAGTGATAGAATTATGGGTATTTTTCCTTCTAATTTTATTATTCAAATTTCCTATATGAGCGTACATTTTCTAGTTAGAAAAAAATCTTGTTAAAAATAAATTGAGAGGAAGAGGCAATGATGATGCAAAAACATTAGAGAAGATAATTTGAGAGGAAAAAAAATGTG... |
Task1_train_34061 | This is a variant located on Chromosome 2. Is this mutation a likely cause of disease or not? | Benign | TGATCTTAACCAATATGTCAGTGTTTTTAGATAATTTGGGAATGTTTAGAATACTGCCTGTGGTGCTTTCCCTGATGGCCTGCAATTGATGCCTGTCAGTCAAGTTGTCAAGACACATGAAAAGGAAAATGACTTCAATTTTCCTAAAACATGTAAAATAACAAACCAAGCCTATACATGCACACCAACTGAGTCATTCTCTCTAGTAAATATTTTGAGGTACCTATATTATGAAGCCTAGTGCTGTGAAAATTGAAGAGGTTTTAATATCACAATTTATTTTTCATTTTCTTTCTTACTTGTTCCATAATGTTTGTTAA... | TGATCTTAACCAATATGTCAGTGTTTTTAGATAATTTGGGAATGTTTAGAATACTGCCTGTGGTGCTTTCCCTGATGGCCTGCAATTGATGCCTGTCAGTCAAGTTGTCAAGACACATGAAAAGGAAAATGACTTCAATTTTCCTAAAACATGTAAAATAACAAACCAAGCCTATACATGCACACCAACTGAGTCATTCTCTCTAGTAAATATTTTGAGGTACCTATATTATGAAGCCTAGTGCTGTGAAAATTGAAGAGGTTTTAATATCACAATTTATTTTTCATTTTCTTTCTTACTTGTTCCATAATGTTTGTTAA... |
Task1_train_34062 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CTAACGCATCCTCACCCTCCCCCAACCAGATGTGATGAGGGGAGCAAGCGTCCCCTGAGAAGCGTCTGGGCTCCCTCGGGGCAGCTGCGGTGGGGAGCTCCGGCTCTATCCGCAGGGCTTTCTTTAGTCCCTAGTCAGCGGGAATATTTTTACTGATTGGAAAAATAACCAGTCGTGCTCAGGTGCTCTCCCTCACTGAGATATACTGGCGAGGCTTCCCTGGCCGCAACGCCGCCGTAAGTGCTGCTCCCACGCGCGGTATCCCCGCGTACTGCTCAGTGCCCAACTCCGACGGGCTCTCAAGTGCCGCAACGCCCCGC... | CTAACGCATCCTCACCCTCCCCCAACCAGATGTGATGAGGGGAGCAAGCGTCCCCTGAGAAGCGTCTGGGCTCCCTCGGGGCAGCTGCGGTGGGGAGCTCCGGCTCTATCCGCAGGGCTTTCTTTAGTCCCTAGTCAGCGGGAATATTTTTACTGATTGGAAAAATAACCAGTCGTGCTCAGGTGCTCTCCCTCACTGAGATATACTGGCGAGGCTTCCCTGGCCGCAACGCCGCCGTAAGTGCTGCTCCCACGCGCGGTATCCCCGCGTACTGCTCAGTGCCCAACTCCGACGGGCTCTCAAGTGCCGCAACGCCCCGC... |
Task1_train_34063 | Chromosome 2 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AAAATGTTTGGAACTAGATAGAGGTGGCGGTTACGCATCACTGTGAAGACACTAAGTGCCACTGAATTGTTCACTTTAAAATAGTTAATTTTATGTTATGTGAATTTCACCTCAAAAAAAGTCAAAAGCTACATTTTTAGAGCAATTTCAGAAACAAAAACTTTTAAGCAGGTAGTTTATGTCCTTGGCTACAGGGTAGAGGTTAATCTTCAGGGATATTTCAAAGACATGAATTGACTTATAAAGAATGAGTTTCTGTTAGCATGTGACAGTGAGGATTCTCTAAGGTCAGACTGACTTCCAAATAGCTATATTAAGAA... | AAAATGTTTGGAACTAGATAGAGGTGGCGGTTACGCATCACTGTGAAGACACTAAGTGCCACTGAATTGTTCACTTTAAAATAGTTAATTTTATGTTATGTGAATTTCACCTCAAAAAAAGTCAAAAGCTACATTTTTAGAGCAATTTCAGAAACAAAAACTTTTAAGCAGGTAGTTTATGTCCTTGGCTACAGGGTAGAGGTTAATCTTCAGGGATATTTCAAAGACATGAATTGACTTATAAAGAATGAGTTTCTGTTAGCATGTGACAGTGAGGATTCTCTAAGGTCAGACTGACTTCCAAATAGCTATATTAAGAA... |
Task1_train_34064 | This mutation on Chromosome 2 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | AAACCAGCCTGGGCAACATAGTGAGACCCTGTCTCTGAAAAAAGAAAAAGAAAAGGAATGAACTGTTGACAAATGCAGCAACATGGATAGCTCTCAAGGGCATTATTAGGCTGAGGGAAAAAGCCAGCTTCAAAGGGTTATGTATTGTGTGATTCTATTTATATATAACATTCTTGATGTAACAAATTATAATGATGTAGAATAGATCGAGGATTAGGGTTTAGGGAAGAGTGTGACTATTAAGAGGTAACATGAGGGAGTTTTTTTTGTGTTGATAGAACAGTTCTTATCCTGATTGTAGTGATGGTCACTCTAATCCA... | AAACCAGCCTGGGCAACATAGTGAGACCCTGTCTCTGAAAAAAGAAAAAGAAAAGGAATGAACTGTTGACAAATGCAGCAACATGGATAGCTCTCAAGGGCATTATTAGGCTGAGGGAAAAAGCCAGCTTCAAAGGGTTATGTATTGTGTGATTCTATTTATATATAACATTCTTGATGTAACAAATTATAATGATGTAGAATAGATCGAGGATTAGGGTTTAGGGAAGAGTGTGACTATTAAGAGGTAACATGAGGGAGTTTTTTTTGTGTTGATAGAACAGTTCTTATCCTGATTGTAGTGATGGTCACTCTAATCCA... |
Task1_train_34065 | A variant was discovered on Chromosome 2. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CCAAGCAATAAAATACTCACTGTCTCAAAATTTGGACAGCTCCTTAAAGTTCCTTATGAAGGCATTTTGATTTGCACAAATATGTCATGACATGTTTTAAGATGACTCCTTTATAGCAAGAAATCTATAGTAAATTGCCTTCCTCCTTAATTGAGGTTAGCCACAATTAAGTCTTCCCTTGCCTGGCACAGTGGGTGGTGCCAGCTACCAAGGAGGATCCCATAAGCCCAGGAACTGGGAGACCAGCCTGGGCAACATAGCGAGACCTTGTCCCAGAAAGAGAGGAAAGAAAGGAAAGAAAGGGAAAGAAGGAAAGAAGG... | CCAAGCAATAAAATACTCACTGTCTCAAAATTTGGACAGCTCCTTAAAGTTCCTTATGAAGGCATTTTGATTTGCACAAATATGTCATGACATGTTTTAAGATGACTCCTTTATAGCAAGAAATCTATAGTAAATTGCCTTCCTCCTTAATTGAGGTTAGCCACAATTAAGTCTTCCCTTGCCTGGCACAGTGGGTGGTGCCAGCTACCAAGGAGGATCCCATAAGCCCAGGAACTGGGAGACCAGCCTGGGCAACATAGCGAGACCTTGTCCCAGAAAGAGAGGAAAGAAAGGAAAGAAAGGGAAAGAAGGAAAGAAGG... |
Task1_train_34066 | This mutation is located on Chromosome 2. Is it associated with a disease or is it a benign polymorphism? | Benign | TGTATCCAAGGGGAAAGACGTCTGGGTTCTGGTCCTGACTCTGTTACCCTTGGTGAGTGGTCAGCCTCATTTTACCCAGTCTCACAGGCTGTAAAATGGGGATGGTATAACCCTGACTGTTTCGGTTCCTCGGGGTTATCCTAGGGAGAGATGAAGACGGCCTGGCTGAAAGTCCCTGCATTCTGCCTCAGGAAGGACCTGCATCTCTCACCCCAGCTTTATCCCCCACTGATGAGTACCCTGTGCTTGTGCCCTAGGTACGTACCTGTGGGCATCATGTTCCTTGTTGGAAGCAAGATCGTGGAAATGAAAGACATCAT... | TGTATCCAAGGGGAAAGACGTCTGGGTTCTGGTCCTGACTCTGTTACCCTTGGTGAGTGGTCAGCCTCATTTTACCCAGTCTCACAGGCTGTAAAATGGGGATGGTATAACCCTGACTGTTTCGGTTCCTCGGGGTTATCCTAGGGAGAGATGAAGACGGCCTGGCTGAAAGTCCCTGCATTCTGCCTCAGGAAGGACCTGCATCTCTCACCCCAGCTTTATCCCCCACTGATGAGTACCCTGTGCTTGTGCCCTAGGTACGTACCTGTGGGCATCATGTTCCTTGTTGGAAGCAAGATCGTGGAAATGAAAGACATCAT... |
Task1_train_34067 | Consider a variant on Chromosome 2. Determine its clinical classification and disease relevance. | Benign | TGACAACAGCCAACACTTAGTGTCCATACCATGCCAGGCACTGTCATAGATGTTCTGCCTGCCCTGGCTCATTTTGGCAAAGGAATGGGGGACAAGGGCGGAGAGAGACTTACATCTGCTGTGCATTTTACATTTGAGCTGTATATTACCTTTCAAAAATAATTTTCTGATTAGTTCCTGCCCCACCTGGTGGTTGTGGGAACTAGACGAGCGTCCGTGCGAAGGGCATGCTCTTCTCCAGGGTCACTTCTGAATCAGGCTGGAGCCTGGCATGCCCCATCAGGCAGAGTAGGGAAGGGCCCTCTTGGATTCCAGTGCAA... | TGACAACAGCCAACACTTAGTGTCCATACCATGCCAGGCACTGTCATAGATGTTCTGCCTGCCCTGGCTCATTTTGGCAAAGGAATGGGGGACAAGGGCGGAGAGAGACTTACATCTGCTGTGCATTTTACATTTGAGCTGTATATTACCTTTCAAAAATAATTTTCTGATTAGTTCCTGCCCCACCTGGTGGTTGTGGGAACTAGACGAGCGTCCGTGCGAAGGGCATGCTCTTCTCCAGGGTCACTTCTGAATCAGGCTGGAGCCTGGCATGCCCCATCAGGCAGAGTAGGGAAGGGCCCTCTTGGATTCCAGTGCAA... |
Task1_train_34068 | A sequence alteration has been identified on Chromosome 2. Is it disease-inducing or harmless? | Benign | GAAGCATCTGAAGACACAAAGGCCCAGTCCTATGGGAGAGGGAGCTGCAGGGAGCGGGAGCTGGACATCCCAGGGCCCATGAGTGGGGAGCAGCCCCCACGCCTGGAAGCTGAGGGAGGGCTCATCTCCCCTGTATGGGGGGCAGAAGGGATACCTGCCCCTACTTGCTGGATTGGGACTGACCCTGGCGGCCCCTCTAGAGCCCACCAGCCACAGGCCAGTGATGCCAACAGAGAGCCCGTAGCTGAGAGGTCTGAGCCTGCACTCAGTGGCCTGCCTCCTGCCACCATGGGGTCTGGAGACCTTCTGCTCTCCGGGGA... | GAAGCATCTGAAGACACAAAGGCCCAGTCCTATGGGAGAGGGAGCTGCAGGGAGCGGGAGCTGGACATCCCAGGGCCCATGAGTGGGGAGCAGCCCCCACGCCTGGAAGCTGAGGGAGGGCTCATCTCCCCTGTATGGGGGGCAGAAGGGATACCTGCCCCTACTTGCTGGATTGGGACTGACCCTGGCGGCCCCTCTAGAGCCCACCAGCCACAGGCCAGTGATGCCAACAGAGAGCCCGTAGCTGAGAGGTCTGAGCCTGCACTCAGTGGCCTGCCTCCTGCCACCATGGGGTCTGGAGACCTTCTGCTCTCCGGGGA... |
Task1_train_34069 | Here is a mutation located on Chromosome 2. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GTTTCTGACTTGGTGATTAAAGGCTTTAGGGGTACCCTGAAGAGACTTGGGAAAGGAGTGTCCAGGGCTTTGGGCTCCTGGGGGCTCTGAACCTAAATCCTCTTCAGACCCAAGGGACATGTCAGAACCTTGGAGCCCTGTAGTAGGCAGCACTGTCCCTGGTTAAGGAGAATTCCTTGGGCTTCTCTGACTGCCAGGCAGCTTCTCCTAGTGGGAGTCACATGGGGCAGGGAATCCTACCAGGTTCTGTGACTGCAGGCAAATCACCAGATCTTTCAGGCCCTCAGTATCATTGGGAGGTGACCGGAATGATCTGTTCT... | GTTTCTGACTTGGTGATTAAAGGCTTTAGGGGTACCCTGAAGAGACTTGGGAAAGGAGTGTCCAGGGCTTTGGGCTCCTGGGGGCTCTGAACCTAAATCCTCTTCAGACCCAAGGGACATGTCAGAACCTTGGAGCCCTGTAGTAGGCAGCACTGTCCCTGGTTAAGGAGAATTCCTTGGGCTTCTCTGACTGCCAGGCAGCTTCTCCTAGTGGGAGTCACATGGGGCAGGGAATCCTACCAGGTTCTGTGACTGCAGGCAAATCACCAGATCTTTCAGGCCCTCAGTATCATTGGGAGGTGACCGGAATGATCTGTTCT... |
Task1_train_34070 | A mutation is present on Chromosome 2. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TTCTGACTTGGTGATTAAAGGCTTTAGGGGTACCCTGAAGAGACTTGGGAAAGGAGTGTCCAGGGCTTTGGGCTCCTGGGGGCTCTGAACCTAAATCCTCTTCAGACCCAAGGGACATGTCAGAACCTTGGAGCCCTGTAGTAGGCAGCACTGTCCCTGGTTAAGGAGAATTCCTTGGGCTTCTCTGACTGCCAGGCAGCTTCTCCTAGTGGGAGTCACATGGGGCAGGGAATCCTACCAGGTTCTGTGACTGCAGGCAAATCACCAGATCTTTCAGGCCCTCAGTATCATTGGGAGGTGACCGGAATGATCTGTTCTGC... | TTCTGACTTGGTGATTAAAGGCTTTAGGGGTACCCTGAAGAGACTTGGGAAAGGAGTGTCCAGGGCTTTGGGCTCCTGGGGGCTCTGAACCTAAATCCTCTTCAGACCCAAGGGACATGTCAGAACCTTGGAGCCCTGTAGTAGGCAGCACTGTCCCTGGTTAAGGAGAATTCCTTGGGCTTCTCTGACTGCCAGGCAGCTTCTCCTAGTGGGAGTCACATGGGGCAGGGAATCCTACCAGGTTCTGTGACTGCAGGCAAATCACCAGATCTTTCAGGCCCTCAGTATCATTGGGAGGTGACCGGAATGATCTGTTCTGC... |
Task1_train_34071 | This sequence change occurs on Chromosome 2. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CACTGGTATGCCCAATATTGTGCTGGATGCTGAGTTATTCTAAGAAGAGTCCTTGCCTTTGAGTAGCCTATAATCTAGTAGTAAAATTATTTTTTAAATTGTGTGATATTTATGTTCATTCTAGGTACTATAAAATAGAGTGAAAATGGTTACTTGATTTGATTTGTTGGTTTGGTTTGCAATTAATGCCTAAAGCTCATTCTGTAATTTTTTTGTGTGATCAAGTGACTGAAAGGTACAGCAAAAGTATCCAGGTCTAAAATGCCTTTTTTCTGTATATTATCTGGGCTAAACTTTTCTGTTTTCTCTATTTTTTTATT... | CACTGGTATGCCCAATATTGTGCTGGATGCTGAGTTATTCTAAGAAGAGTCCTTGCCTTTGAGTAGCCTATAATCTAGTAGTAAAATTATTTTTTAAATTGTGTGATATTTATGTTCATTCTAGGTACTATAAAATAGAGTGAAAATGGTTACTTGATTTGATTTGTTGGTTTGGTTTGCAATTAATGCCTAAAGCTCATTCTGTAATTTTTTTGTGTGATCAAGTGACTGAAAGGTACAGCAAAAGTATCCAGGTCTAAAATGCCTTTTTTCTGTATATTATCTGGGCTAAACTTTTCTGTTTTCTCTATTTTTTTATT... |
Task1_train_34072 | This genomic variant is located on Chromosome 2. Can you determine its pathogenicity and name any linked disease? | Benign | GAAACATAAGTGGATCAATTATTGTAGCTTATTATTGCTATCTCCCAACTTCCTATTGTTTTTGAGTTTGGTAAGTGTTACCTCACCAGAATTTAGGAAATTAATTCAAAATCATTAGTTTTTATTGTCTTTTTTCTTTCTTTTGTTTTTTTGGAAGACGGGGGATGCTACACTGGTACTTTATACCTCTTTTTTTCCCTATCTGCCAAAGGATGAAAAACCAACAACAAATTCTATGCTGGACATGTGGATTGGTGAAACTGCTATTCCTTGTACTCCCAGTGTAGCAAAAGGAAAATCAAGAGCAAAAATCAGCTGCA... | GAAACATAAGTGGATCAATTATTGTAGCTTATTATTGCTATCTCCCAACTTCCTATTGTTTTTGAGTTTGGTAAGTGTTACCTCACCAGAATTTAGGAAATTAATTCAAAATCATTAGTTTTTATTGTCTTTTTTCTTTCTTTTGTTTTTTTGGAAGACGGGGGATGCTACACTGGTACTTTATACCTCTTTTTTTCCCTATCTGCCAAAGGATGAAAAACCAACAACAAATTCTATGCTGGACATGTGGATTGGTGAAACTGCTATTCCTTGTACTCCCAGTGTAGCAAAAGGAAAATCAAGAGCAAAAATCAGCTGCA... |
Task1_train_34073 | This variant is located on Chromosome 2. Evaluate its biological effect and specify any disease association. | Benign | AACTAACAGCTCCCAGAGCCTTATTTTCAATTTATTGCCATTTACCTGTCCAGTCTTCAAAATAAGGACCATGAGGACTTACAGACAATGTTTATGGTCATAATAAGCTAAGGTCTTTATCATTCACATTAGACTAAAAGATTAAAAACCAGCAACTGGAAGGTTAACAGGTTGTTAGCACCTCAAAAGCAGCCAGTAAATCCATCCCGGCGCCACTGCATTAACTGGGGGGAACTTAGGAGAGAGAGAGAGACAGAGGGAGAGAGAGAAAGGAGGCGGGAGGGAATGAATGACTGCTGCTTTGTAGAAGCAGTGGGGCT... | AACTAACAGCTCCCAGAGCCTTATTTTCAATTTATTGCCATTTACCTGTCCAGTCTTCAAAATAAGGACCATGAGGACTTACAGACAATGTTTATGGTCATAATAAGCTAAGGTCTTTATCATTCACATTAGACTAAAAGATTAAAAACCAGCAACTGGAAGGTTAACAGGTTGTTAGCACCTCAAAAGCAGCCAGTAAATCCATCCCGGCGCCACTGCATTAACTGGGGGGAACTTAGGAGAGAGAGAGAGACAGAGGGAGAGAGAGAAAGGAGGCGGGAGGGAATGAATGACTGCTGCTTTGTAGAAGCAGTGGGGCT... |
Task1_train_34074 | Located on Chromosome 2, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TGAAACCCCATCTCTACCAAAATAAAAAATAAAAAAATAAAAAGTACAAAAAAATTAGTTAGGTGTGGTGGCACACACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGTGGGGAGGCGGAGGTTGCAGTGAGCTGTGTTTGCACCACAGCACTCCGGGCTGGGTGACAGATTGAGACCCTGTCTCAAAAAAAAAAAAAAAAAAAAAAAAGCCACTGGTTACCAGAAGCTAAGTGATGAACAATACAAGGAACGAAGGAAAGGTAGAAAAAAATAAGCCATGTTTCATGTTTGTCATTCAGGGAAACTTAAAGCGGGATGG... | TGAAACCCCATCTCTACCAAAATAAAAAATAAAAAAATAAAAAGTACAAAAAAATTAGTTAGGTGTGGTGGCACACACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGTGGGGAGGCGGAGGTTGCAGTGAGCTGTGTTTGCACCACAGCACTCCGGGCTGGGTGACAGATTGAGACCCTGTCTCAAAAAAAAAAAAAAAAAAAAAAAAGCCACTGGTTACCAGAAGCTAAGTGATGAACAATACAAGGAACGAAGGAAAGGTAGAAAAAAATAAGCCATGTTTCATGTTTGTCATTCAGGGAAACTTAAAGCGGGATGG... |
Task1_train_34075 | Consider a variant on Chromosome 2. Determine its clinical classification and disease relevance. | Benign | AGTTCCAGTGGGACAAGCACACCACCAATGGAAATATTCCTGCAATAGACTTGAGTTGACCACATACGGTTGAAATTAGCCTAGGCACCCTGTCCTGTTTTGGACCAAAACTCTAGGCAGGAAACTTACAGGGTTTCACTAAGGGGGGCATTGTGGTGCGGGAGAAAGTTCTGCAAGTTCAGGGGGCAGTGCTTCTCCTATTTATGAATTAAAAACCTACCTATCCCCAGCCCCAGACATTAGGATTCAGTTGGCCTGGGATGTAGTTTGGACACTGGTACATTTATTTTAAGGTTATCTAGGTGATCTTAATATGCAGG... | AGTTCCAGTGGGACAAGCACACCACCAATGGAAATATTCCTGCAATAGACTTGAGTTGACCACATACGGTTGAAATTAGCCTAGGCACCCTGTCCTGTTTTGGACCAAAACTCTAGGCAGGAAACTTACAGGGTTTCACTAAGGGGGGCATTGTGGTGCGGGAGAAAGTTCTGCAAGTTCAGGGGGCAGTGCTTCTCCTATTTATGAATTAAAAACCTACCTATCCCCAGCCCCAGACATTAGGATTCAGTTGGCCTGGGATGTAGTTTGGACACTGGTACATTTATTTTAAGGTTATCTAGGTGATCTTAATATGCAGG... |
Task1_train_34076 | A mutation on Chromosome 2 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TGCAGTGAAAGAACACTGACGGGTGTAATGAGGAAAATCTAGTCCTACGATTGCTTTCATCATCTCTGTTGAACTTATCATTGAAAAGGATCAGCTCTAGGATAACGGAGATTTGCCTTGAAGATGAAGAACAACTAATATTTATGGATACTAGTTATGTTTCAGACACTCTTCTAAATACTTCCATGTCTATCTCATTTAATCTTCAGAATGACCTCATTGGATAGGTGTTATTATCCCCGTATTACAGATGAGAAAACTGAGGCACAAAGTAATAACAAACTTGCTCATTTTCACATGGTCAGATTAACGGGTCTCTA... | TGCAGTGAAAGAACACTGACGGGTGTAATGAGGAAAATCTAGTCCTACGATTGCTTTCATCATCTCTGTTGAACTTATCATTGAAAAGGATCAGCTCTAGGATAACGGAGATTTGCCTTGAAGATGAAGAACAACTAATATTTATGGATACTAGTTATGTTTCAGACACTCTTCTAAATACTTCCATGTCTATCTCATTTAATCTTCAGAATGACCTCATTGGATAGGTGTTATTATCCCCGTATTACAGATGAGAAAACTGAGGCACAAAGTAATAACAAACTTGCTCATTTTCACATGGTCAGATTAACGGGTCTCTA... |
Task1_train_34077 | Consider this mutation on Chromosome 2. Is this a benign change or a disease-causing variant? | Benign | ATTTGACTTCCCCTGGGTGGTTATATTGCTGCATCAGGTGCATGGGACCAAAGAGCTCTGGAAACATGTAGCTCTTTTTTAGTGGGATACAGTGACCTCAGTGTCTCCACCTCTCCTGTCACTTTTCTCCAGATTGAAGTCCAGATCGTCTTGCATTTTCTCATTGAGCCTCCTGGCCCCACTGAAGCAGGGTGTGGAGGATCTGGAAGGACCTTAGATCTGTCAGCAGTTTTTCTTTAATCTCCTTCTGCTCTTACTTATTTTGGGGGGCCCTGATCTATATTAGAGTGAGTCTGGCTTTTTCACCAAGAGGATGAGGT... | ATTTGACTTCCCCTGGGTGGTTATATTGCTGCATCAGGTGCATGGGACCAAAGAGCTCTGGAAACATGTAGCTCTTTTTTAGTGGGATACAGTGACCTCAGTGTCTCCACCTCTCCTGTCACTTTTCTCCAGATTGAAGTCCAGATCGTCTTGCATTTTCTCATTGAGCCTCCTGGCCCCACTGAAGCAGGGTGTGGAGGATCTGGAAGGACCTTAGATCTGTCAGCAGTTTTTCTTTAATCTCCTTCTGCTCTTACTTATTTTGGGGGGCCCTGATCTATATTAGAGTGAGTCTGGCTTTTTCACCAAGAGGATGAGGT... |
Task1_train_34078 | This variant is located on Chromosome 2. Evaluate its biological effect and specify any disease association. | Benign | GATTCCCAAGTTCAGCAGCGGACACAAGCTCAGAGCCTGTCAATTTGTCATGTGCTTGTTGCACTCAAAAGCTCAACCTGCCAAGAGCCAGAGGACAGCTTTGAGAGAGAGAAATTAGGAGTGGCTGTTAGCATGGTGAAAGATTTCTAAACATTGTTTAAATTGTAACTTGAATTTAAAAATCAAACATTCACTACTCTTTTTAGGAATACAATATTGCATAAATCACACTGCATCTCCATTCTTATGCAATCTTGTGTATAGTTTGACTAATAAAATAATGGCCGACCAAATTTGTGTCATCTCTGTTTTAAATTTCT... | GATTCCCAAGTTCAGCAGCGGACACAAGCTCAGAGCCTGTCAATTTGTCATGTGCTTGTTGCACTCAAAAGCTCAACCTGCCAAGAGCCAGAGGACAGCTTTGAGAGAGAGAAATTAGGAGTGGCTGTTAGCATGGTGAAAGATTTCTAAACATTGTTTAAATTGTAACTTGAATTTAAAAATCAAACATTCACTACTCTTTTTAGGAATACAATATTGCATAAATCACACTGCATCTCCATTCTTATGCAATCTTGTGTATAGTTTGACTAATAAAATAATGGCCGACCAAATTTGTGTCATCTCTGTTTTAAATTTCT... |
Task1_train_34079 | Given this context: Chromosome 2 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GGAAAAAGAAAACTGGGGAGAACTGACCCAGGGGGAACTGCCTAGTAGGGAGGTGGGTTAGGATTGCCCAATTCTCACTCGAGAGTTCCAGTTGCTGGTACAGACCAGTTGGTCCTGGAGTTGGGGGGTTGAGATTGGGGTGTACTTGTGCAGCGTGGGAGCAAAGAGCGTATGTTTTAGAGAGACATGACATGAATGTTGCCAGTGTAGCCAAAGGATTGCTTTCCCCATAGGTTATCTGTTACTATACAGGAACCATGATAAGATCTAGGTTCCTTTTTTCAAGGCAGTTAGTCAGTTTGGGTAGCATTTTAATGTAC... | GGAAAAAGAAAACTGGGGAGAACTGACCCAGGGGGAACTGCCTAGTAGGGAGGTGGGTTAGGATTGCCCAATTCTCACTCGAGAGTTCCAGTTGCTGGTACAGACCAGTTGGTCCTGGAGTTGGGGGGTTGAGATTGGGGTGTACTTGTGCAGCGTGGGAGCAAAGAGCGTATGTTTTAGAGAGACATGACATGAATGTTGCCAGTGTAGCCAAAGGATTGCTTTCCCCATAGGTTATCTGTTACTATACAGGAACCATGATAAGATCTAGGTTCCTTTTTTCAAGGCAGTTAGTCAGTTTGGGTAGCATTTTAATGTAC... |
Task1_train_34080 | A genomic change on Chromosome 2 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GCGCTGCACTGGCTGCGGCCGTGGGGTGCGGCGGCTTCTGAGTGAAGAGGGGACTTTGCCAGGGATTCACTCCTGTGAGTTTCTTCAGGAGAGCCAGGCTTCCCCTCCTCTGTCCTTAGGGGAAGCTGCCCAGGCTCCAGGGAGAAAGTTGGGAGCAGGCGGGGGACTTGCCAGCAGGGGTTTGTGAGAGAGGCTTCTAGCGATCGAGAGGTCACCAGGTGGGGGTAGGATTGGGGTTCCCCTCTGAACGGTGAGAATAAAGGAGAAAAGACCTCTGGACAATCATCCTTAATCTCGTGACGCCCTCCTCTCCACCCCCG... | GCGCTGCACTGGCTGCGGCCGTGGGGTGCGGCGGCTTCTGAGTGAAGAGGGGACTTTGCCAGGGATTCACTCCTGTGAGTTTCTTCAGGAGAGCCAGGCTTCCCCTCCTCTGTCCTTAGGGGAAGCTGCCCAGGCTCCAGGGAGAAAGTTGGGAGCAGGCGGGGGACTTGCCAGCAGGGGTTTGTGAGAGAGGCTTCTAGCGATCGAGAGGTCACCAGGTGGGGGTAGGATTGGGGTTCCCCTCTGAACGGTGAGAATAAAGGAGAAAAGACCTCTGGACAATCATCCTTAATCTCGTGACGCCCTCCTCTCCACCCCCG... |
Task1_train_34081 | A change on Chromosome 2 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | AGTTTCTTATTTATCCTTCCAATGTTCCTTTATGAAAATATAAGAAGACATGAGTGTAAATTATTTACCTCCTTTTTTACACAAAATGTAGTATAATTCTCTCTCTCTCTACAGTCACACACATACACATACAGTCACACACAAACTCCCACACAAAACTATGTATCTTGCATTTTTGTACTTAGCAGTATATTCTGGAGACTTTTTCATGTCAATACATAAACAGCTACCTCATATGACCTCATGTTTTCTAGAGGTGTATAGTGTCCCATTCTGTAGATGTACCAGTCCCTATAGATGAACACACTGCCTTCAGTTCT... | AGTTTCTTATTTATCCTTCCAATGTTCCTTTATGAAAATATAAGAAGACATGAGTGTAAATTATTTACCTCCTTTTTTACACAAAATGTAGTATAATTCTCTCTCTCTCTACAGTCACACACATACACATACAGTCACACACAAACTCCCACACAAAACTATGTATCTTGCATTTTTGTACTTAGCAGTATATTCTGGAGACTTTTTCATGTCAATACATAAACAGCTACCTCATATGACCTCATGTTTTCTAGAGGTGTATAGTGTCCCATTCTGTAGATGTACCAGTCCCTATAGATGAACACACTGCCTTCAGTTCT... |
Task1_train_34082 | A genetic alteration is present on Chromosome 2. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TTTCTTATTTATCCTTCCAATGTTCCTTTATGAAAATATAAGAAGACATGAGTGTAAATTATTTACCTCCTTTTTTACACAAAATGTAGTATAATTCTCTCTCTCTCTACAGTCACACACATACACATACAGTCACACACAAACTCCCACACAAAACTATGTATCTTGCATTTTTGTACTTAGCAGTATATTCTGGAGACTTTTTCATGTCAATACATAAACAGCTACCTCATATGACCTCATGTTTTCTAGAGGTGTATAGTGTCCCATTCTGTAGATGTACCAGTCCCTATAGATGAACACACTGCCTTCAGTTCTTT... | TTTCTTATTTATCCTTCCAATGTTCCTTTATGAAAATATAAGAAGACATGAGTGTAAATTATTTACCTCCTTTTTTACACAAAATGTAGTATAATTCTCTCTCTCTCTACAGTCACACACATACACATACAGTCACACACAAACTCCCACACAAAACTATGTATCTTGCATTTTTGTACTTAGCAGTATATTCTGGAGACTTTTTCATGTCAATACATAAACAGCTACCTCATATGACCTCATGTTTTCTAGAGGTGTATAGTGTCCCATTCTGTAGATGTACCAGTCCCTATAGATGAACACACTGCCTTCAGTTCTTT... |
Task1_train_34083 | This mutation on Chromosome 2 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TCATGAGGTTTGTCTCAATCACTCACACTGTTAGTAAAAACACTTTTAGGGAATTGAGAAGTAGAAACAGTGAGCTCATTGATTTTTATATCAGAACCATTTTGTGAGATCAATGTTTGCAATGTTCACCTTAGTTGCTAAGGTCATGGGCATACCAGCCCACAAAGATTTGCTCATATGCCATGTTTATCTTGGAACCAATGTTTACCTTGGTATCAGGGTAAAGAGAAATACTCAGATGTAGTTAAAGAAAAGCAATAACTGTGATTACATAAACTTGCGTTTTTTCCTCCCTGAATGGTATCCGGATCATAGGAAAC... | TCATGAGGTTTGTCTCAATCACTCACACTGTTAGTAAAAACACTTTTAGGGAATTGAGAAGTAGAAACAGTGAGCTCATTGATTTTTATATCAGAACCATTTTGTGAGATCAATGTTTGCAATGTTCACCTTAGTTGCTAAGGTCATGGGCATACCAGCCCACAAAGATTTGCTCATATGCCATGTTTATCTTGGAACCAATGTTTACCTTGGTATCAGGGTAAAGAGAAATACTCAGATGTAGTTAAAGAAAAGCAATAACTGTGATTACATAAACTTGCGTTTTTTCCTCCCTGAATGGTATCCGGATCATAGGAAAC... |
Task1_train_34084 | This sequence variant lies on Chromosome 2. Is it clinically significant, and what condition might it cause if any? | Benign | CTTCCATCCTTGGGGTCTTCGTCCTAACCCCATCCCTGGCCATGATGGTGAGTAAGGATGGAAAGAGTTCAACCTGTCTAGTCCTCCTTTAGCAGAAGCATTTTAAAAGGTGATAATTAAGGGCAACCTCCTCAAATTTCCTGTGGGTACCCGTAAAACCTACAAGGCATGGGCAAAGTAGGAACTCTGAACTTTCAACTTTTCTCACTGTTGCTTGGTTTTCTCCAGAACATCCGTTTCAACCATCCTTTGTATGGATCTTTTGGGACTCAAATTATCCATATTGGTGCCTTCCAAGGTATGGTCAGCATCCGAGACAA... | CTTCCATCCTTGGGGTCTTCGTCCTAACCCCATCCCTGGCCATGATGGTGAGTAAGGATGGAAAGAGTTCAACCTGTCTAGTCCTCCTTTAGCAGAAGCATTTTAAAAGGTGATAATTAAGGGCAACCTCCTCAAATTTCCTGTGGGTACCCGTAAAACCTACAAGGCATGGGCAAAGTAGGAACTCTGAACTTTCAACTTTTCTCACTGTTGCTTGGTTTTCTCCAGAACATCCGTTTCAACCATCCTTTGTATGGATCTTTTGGGACTCAAATTATCCATATTGGTGCCTTCCAAGGTATGGTCAGCATCCGAGACAA... |
Task1_train_34085 | This sequence change occurs on Chromosome 2. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | ATCCCTGGCCATGATGGTGAGTAAGGATGGAAAGAGTTCAACCTGTCTAGTCCTCCTTTAGCAGAAGCATTTTAAAAGGTGATAATTAAGGGCAACCTCCTCAAATTTCCTGTGGGTACCCGTAAAACCTACAAGGCATGGGCAAAGTAGGAACTCTGAACTTTCAACTTTTCTCACTGTTGCTTGGTTTTCTCCAGAACATCCGTTTCAACCATCCTTTGTATGGATCTTTTGGGACTCAAATTATCCATATTGGTGCCTTCCAAGGTATGGTCAGCATCCGAGACAACAATATTTTCAGTGAATAGGACGGAATCCTG... | ATCCCTGGCCATGATGGTGAGTAAGGATGGAAAGAGTTCAACCTGTCTAGTCCTCCTTTAGCAGAAGCATTTTAAAAGGTGATAATTAAGGGCAACCTCCTCAAATTTCCTGTGGGTACCCGTAAAACCTACAAGGCATGGGCAAAGTAGGAACTCTGAACTTTCAACTTTTCTCACTGTTGCTTGGTTTTCTCCAGAACATCCGTTTCAACCATCCTTTGTATGGATCTTTTGGGACTCAAATTATCCATATTGGTGCCTTCCAAGGTATGGTCAGCATCCGAGACAACAATATTTTCAGTGAATAGGACGGAATCCTG... |
Task1_train_34086 | A mutation on Chromosome 2 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | AGGATGGAAAGAGTTCAACCTGTCTAGTCCTCCTTTAGCAGAAGCATTTTAAAAGGTGATAATTAAGGGCAACCTCCTCAAATTTCCTGTGGGTACCCGTAAAACCTACAAGGCATGGGCAAAGTAGGAACTCTGAACTTTCAACTTTTCTCACTGTTGCTTGGTTTTCTCCAGAACATCCGTTTCAACCATCCTTTGTATGGATCTTTTGGGACTCAAATTATCCATATTGGTGCCTTCCAAGGTATGGTCAGCATCCGAGACAACAATATTTTCAGTGAATAGGACGGAATCCTGGACTACAAGAATATAAGATGAGA... | AGGATGGAAAGAGTTCAACCTGTCTAGTCCTCCTTTAGCAGAAGCATTTTAAAAGGTGATAATTAAGGGCAACCTCCTCAAATTTCCTGTGGGTACCCGTAAAACCTACAAGGCATGGGCAAAGTAGGAACTCTGAACTTTCAACTTTTCTCACTGTTGCTTGGTTTTCTCCAGAACATCCGTTTCAACCATCCTTTGTATGGATCTTTTGGGACTCAAATTATCCATATTGGTGCCTTCCAAGGTATGGTCAGCATCCGAGACAACAATATTTTCAGTGAATAGGACGGAATCCTGGACTACAAGAATATAAGATGAGA... |
Task1_train_34087 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | ACAGGCTAGTGATTTTCAACTCTGCTCTATGCCATGGAGACTTTTCTTCAAACAAAAATATTCCACGGTAGTCTATGACGTGGAACAGAAGAAGCCAGAACTACTCTGGCTGGAGGAGGGAGATGCAGGCGAACCTTAGGCACAGTCAGACACAGCTGAAGAACTGCTGCTCTACTCCAGGCTGTGAGAGGCCAGAAGACAGGCCCAGGGACTCATGGAGGGGGATGGTCAGTGGCAGACCTAGGGCTAGAATCTGAGTCTAGAGGGCCTGGCCCAAGGTTCCTGACAACCTTGTACATTCAGAGAGCACTCCATAATTT... | ACAGGCTAGTGATTTTCAACTCTGCTCTATGCCATGGAGACTTTTCTTCAAACAAAAATATTCCACGGTAGTCTATGACGTGGAACAGAAGAAGCCAGAACTACTCTGGCTGGAGGAGGGAGATGCAGGCGAACCTTAGGCACAGTCAGACACAGCTGAAGAACTGCTGCTCTACTCCAGGCTGTGAGAGGCCAGAAGACAGGCCCAGGGACTCATGGAGGGGGATGGTCAGTGGCAGACCTAGGGCTAGAATCTGAGTCTAGAGGGCCTGGCCCAAGGTTCCTGACAACCTTGTACATTCAGAGAGCACTCCATAATTT... |
Task1_train_34088 | A variant on Chromosome 2 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GTCCCAGCTACTTTGGAGGCTGAGGCAGGAGAATCAGCCTGAACATGGGAGGCGGAGGTTGCAGTGAGCTGAGATCATGCCACTGCACTCCAACCTGAGTGACAGAGCGAGACTCCATCTCTGGAAAAAAAAAAAAAATTTGTTTAGCCCTTTTGTGCTTTAATTTCCCAATCGATAAAACTAAGATAATAAAAAATTTATATCAGTATTGTGAAGATTAAATGAAATAATATTTGTAAAGTATTTGGCAGAAGACCTAGCAGGTAGTAAGTGCTCAGTAATTATTAGCTGTTTTATAGTGGAAGCTTAATGAAAAAAGT... | GTCCCAGCTACTTTGGAGGCTGAGGCAGGAGAATCAGCCTGAACATGGGAGGCGGAGGTTGCAGTGAGCTGAGATCATGCCACTGCACTCCAACCTGAGTGACAGAGCGAGACTCCATCTCTGGAAAAAAAAAAAAAATTTGTTTAGCCCTTTTGTGCTTTAATTTCCCAATCGATAAAACTAAGATAATAAAAAATTTATATCAGTATTGTGAAGATTAAATGAAATAATATTTGTAAAGTATTTGGCAGAAGACCTAGCAGGTAGTAAGTGCTCAGTAATTATTAGCTGTTTTATAGTGGAAGCTTAATGAAAAAAGT... |
Task1_train_34089 | A change on Chromosome 2 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CCCACCTGTTCCAAAGACTCGTGAACCTTTAGATAAGTCAATGGACACAAACATGGCACGCTCTGAGGAGTGTCCACTTCATGGGCCTGGTGAGTTACTTCCCAGTTACCTAAGAAGGATTTTCACCCCTTCTGCAAAGCGAAGCTGGACAGATTATTCCAGAAATTCAGGTATAACAAGTAGGCAGCTCATGATTAGCTCAGTCCCAAAACTCTATCCCATGAGTGTATTTTCCCCAACAAGGATCTCCCCAAACTGTTTCTCAATACCAGGAAACAACCTCTGAAGAAAAGAAGACCCTTCCAAACAACCAGTTGCAG... | CCCACCTGTTCCAAAGACTCGTGAACCTTTAGATAAGTCAATGGACACAAACATGGCACGCTCTGAGGAGTGTCCACTTCATGGGCCTGGTGAGTTACTTCCCAGTTACCTAAGAAGGATTTTCACCCCTTCTGCAAAGCGAAGCTGGACAGATTATTCCAGAAATTCAGGTATAACAAGTAGGCAGCTCATGATTAGCTCAGTCCCAAAACTCTATCCCATGAGTGTATTTTCCCCAACAAGGATCTCCCCAAACTGTTTCTCAATACCAGGAAACAACCTCTGAAGAAAAGAAGACCCTTCCAAACAACCAGTTGCAG... |
Task1_train_34090 | This alteration on Chromosome 2 may affect genome function. Does it lead to a disease or is it benign? | Benign | TTTTTTCAATCAATCTACTTCAAAGTTTGCTTTGTTTTCAAGTTTCTTGTGAAAAAAATAAAATGTGTAAGAATAATGTTATGATCTAAATACTGAGAAGTAAATCCTCTTTGATGGGGCATACATCTCTGACAACTCCTTGTGCCAGAGAAGAAAACTGTGAGGGAAAACATGATACTTACCAGATTATATCAGACCTATTCAAAGGTGCAATGTCAAAATTGACTACATCCAAGCTAGGCATTTAATCCAAAGTGAAGACAATTAGCAAGTGAAGACATGTGTAAAAGGGCATCACTAAAAATACCTTTTGTCTTATG... | TTTTTTCAATCAATCTACTTCAAAGTTTGCTTTGTTTTCAAGTTTCTTGTGAAAAAAATAAAATGTGTAAGAATAATGTTATGATCTAAATACTGAGAAGTAAATCCTCTTTGATGGGGCATACATCTCTGACAACTCCTTGTGCCAGAGAAGAAAACTGTGAGGGAAAACATGATACTTACCAGATTATATCAGACCTATTCAAAGGTGCAATGTCAAAATTGACTACATCCAAGCTAGGCATTTAATCCAAAGTGAAGACAATTAGCAAGTGAAGACATGTGTAAAAGGGCATCACTAAAAATACCTTTTGTCTTATG... |
Task1_train_34091 | Consider this mutation on Chromosome 2. Is this a benign change or a disease-causing variant? | Benign | TCATTTTCTCTTCCCAGCTTCTTTTTCATTTTTGGTAGATTCTTACTTTATAGAATTAAAGTCTTTTTTTTTTTTAGACAGAGTCTCGTTCTGTCACCCAGGCTGGAGGGCAGTGGCGCTATCTCAGCTCACTGCAACCTCCACCTCCTGAGTTCAAGCGATTCTCCCGCCTCAGCCTCTTGAGCAGCAGCTGGGATTACAGGCGTGTGTTACCACGCCTGGCTAATTTTTGTATTTTTAGCAGTGACAGGGTTTCACCACGCTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTGCCCGCCTCGGCCTCCCA... | TCATTTTCTCTTCCCAGCTTCTTTTTCATTTTTGGTAGATTCTTACTTTATAGAATTAAAGTCTTTTTTTTTTTTAGACAGAGTCTCGTTCTGTCACCCAGGCTGGAGGGCAGTGGCGCTATCTCAGCTCACTGCAACCTCCACCTCCTGAGTTCAAGCGATTCTCCCGCCTCAGCCTCTTGAGCAGCAGCTGGGATTACAGGCGTGTGTTACCACGCCTGGCTAATTTTTGTATTTTTAGCAGTGACAGGGTTTCACCACGCTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTGCCCGCCTCGGCCTCCCA... |
Task1_train_34092 | A genomic change on Chromosome 2 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TGGAGCCCAGGAGGCGGAGGTTACAGTGAGCCAAGATCACATCACTGCACTTTAGCCTGGGCAACATAGTGAGACCCTGCCTCAAAAACAAACAAAAAAAAACACCTAATTTGAATAGGTACTTAACAAAATCATTACAATTATAATCTCAATTGGGTTTAATTTTGTATTTCAAAAATGACTCCCAGGTCCATCATCCAGAAAGATGCTCATGAAAATGTCATGAGACTTACAACAGGAAACAGGACAGAATGATAAAAAATATTTCTTCCTTTTTTTTTTTTTGAGACAGTGTCTCACTCTGCTGCCCAGGCTGAAGT... | TGGAGCCCAGGAGGCGGAGGTTACAGTGAGCCAAGATCACATCACTGCACTTTAGCCTGGGCAACATAGTGAGACCCTGCCTCAAAAACAAACAAAAAAAAACACCTAATTTGAATAGGTACTTAACAAAATCATTACAATTATAATCTCAATTGGGTTTAATTTTGTATTTCAAAAATGACTCCCAGGTCCATCATCCAGAAAGATGCTCATGAAAATGTCATGAGACTTACAACAGGAAACAGGACAGAATGATAAAAAATATTTCTTCCTTTTTTTTTTTTTGAGACAGTGTCTCACTCTGCTGCCCAGGCTGAAGT... |
Task1_train_34093 | Chromosome 2 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TTTTTGAAGGGACAGGGTCTCGCTGTGTTGCCAGAGTTGGTCTTGAACTTCCTGGGCTCAACTGATCCTCCTGCCTCAGCCTTCCAAAATGCTGGTATTACAGGTGTGTGGCACTGCACCTGGCCAGCTTTATTTTAAGGCACTAATAATAAAGGGTATGAAAAAAGCTAGGAATAAGTCAGATCTTTCCAGAAATAAAAGACAATTTTAAAAAACATCAGTTAACCTGTCTGGCCTATTTCAACATCTAAAGAGGATAGAGAATGTAAAAGTTTTCATGCCTACCTGATTCAGCTCTTTTCCATTCTCCCAAACACTTA... | TTTTTGAAGGGACAGGGTCTCGCTGTGTTGCCAGAGTTGGTCTTGAACTTCCTGGGCTCAACTGATCCTCCTGCCTCAGCCTTCCAAAATGCTGGTATTACAGGTGTGTGGCACTGCACCTGGCCAGCTTTATTTTAAGGCACTAATAATAAAGGGTATGAAAAAAGCTAGGAATAAGTCAGATCTTTCCAGAAATAAAAGACAATTTTAAAAAACATCAGTTAACCTGTCTGGCCTATTTCAACATCTAAAGAGGATAGAGAATGTAAAAGTTTTCATGCCTACCTGATTCAGCTCTTTTCCATTCTCCCAAACACTTA... |
Task1_train_34094 | Consider a variant on Chromosome 2. Determine its clinical classification and disease relevance. | Benign | CTGAATAAGGGCCTCTTTTCTTAGAAAGCCCTCTGCATGTGTTTGGGTAACTCCAATGTCCACAGAGGAACCTGCTTTCTCATTCCTCTCTCAAATCACACTTACCTGCTGTCTCCCTTCTTCCCCCAGGCACCGATGAAGACGCCATTATTAGCGTCCTTGCCTACCGCAACACCGCCCAGCGCCAGGAGATCAGGACAGCCTACAAGAGCACCATCGGCAGGGTAGGCCACAGTCTTTCCTGCTCTGTCTGGCTGACTTCGCAGCAACAGGAAGCAGGGCCTCTTCCTGATCTAGGTTCCCGAAGTGACCTTGTGTTT... | CTGAATAAGGGCCTCTTTTCTTAGAAAGCCCTCTGCATGTGTTTGGGTAACTCCAATGTCCACAGAGGAACCTGCTTTCTCATTCCTCTCTCAAATCACACTTACCTGCTGTCTCCCTTCTTCCCCCAGGCACCGATGAAGACGCCATTATTAGCGTCCTTGCCTACCGCAACACCGCCCAGCGCCAGGAGATCAGGACAGCCTACAAGAGCACCATCGGCAGGGTAGGCCACAGTCTTTCCTGCTCTGTCTGGCTGACTTCGCAGCAACAGGAAGCAGGGCCTCTTCCTGATCTAGGTTCCCGAAGTGACCTTGTGTTT... |
Task1_train_34095 | Consider this mutation on Chromosome 2. Is this a benign change or a disease-causing variant? | Benign | ACACCCCATTCCCAGATCTGGGAATGTCCTCCCCTCCATCAGGTCATCTAGTTTCAGGCTCTGTTCCAAGTCCCTCCAAGAAGAAGCTGACCTCCCACCGCCGGGACCCTGCCTTGCCACAGCCTCCCCCGTCCTCCAGCATGCCCTTGGGCTGCCCCACACAGGTCAACACTTGTCTCCTGGCCCTGCTTTCTGCCTCCAAGTTCTCGCTCCTGGACAGCTGTAAGAACCTATTTGCCCAGCAGACACTTTCCTGTTTGTTTATCATAACCATAATTTCCCAATCCCCAATCAAGACATCTCACATAAAACTTTAGGGT... | ACACCCCATTCCCAGATCTGGGAATGTCCTCCCCTCCATCAGGTCATCTAGTTTCAGGCTCTGTTCCAAGTCCCTCCAAGAAGAAGCTGACCTCCCACCGCCGGGACCCTGCCTTGCCACAGCCTCCCCCGTCCTCCAGCATGCCCTTGGGCTGCCCCACACAGGTCAACACTTGTCTCCTGGCCCTGCTTTCTGCCTCCAAGTTCTCGCTCCTGGACAGCTGTAAGAACCTATTTGCCCAGCAGACACTTTCCTGTTTGTTTATCATAACCATAATTTCCCAATCCCCAATCAAGACATCTCACATAAAACTTTAGGGT... |
Task1_train_34096 | This mutation occurs on Chromosome 2. Does this change lead to a known medical condition, or is it benign? | Benign | TTCAAAAACAAAACAACTCACAGAGCTGGTAAAAGGGGAAAATATAATCTTCTGTTTTTTTCCCTCATAGCGATTATTGGAGCCGGAATTGGTGGCACTTCAGCAGCCTATTACCTGCGGCAGAAATTTGGGAAAGATGTGAAGATAGACCTGTTTGAAAGAGAAGAGGTCGGGGGCCGCCTGGCTACCATGATGGTGCAGGGGCAAGAATACGAGGCAGGAGGTTCTGTCATCCATCCTTTAAATCTGCACATGAAACGTTTTGTCAAAGACCTGGGTATGTAATTTTGGTCTTGGAGCTCACCAGATTACTGTGTGAC... | TTCAAAAACAAAACAACTCACAGAGCTGGTAAAAGGGGAAAATATAATCTTCTGTTTTTTTCCCTCATAGCGATTATTGGAGCCGGAATTGGTGGCACTTCAGCAGCCTATTACCTGCGGCAGAAATTTGGGAAAGATGTGAAGATAGACCTGTTTGAAAGAGAAGAGGTCGGGGGCCGCCTGGCTACCATGATGGTGCAGGGGCAAGAATACGAGGCAGGAGGTTCTGTCATCCATCCTTTAAATCTGCACATGAAACGTTTTGTCAAAGACCTGGGTATGTAATTTTGGTCTTGGAGCTCACCAGATTACTGTGTGAC... |
Task1_train_34097 | This alteration on Chromosome 2 may affect genome function. Does it lead to a disease or is it benign? | Benign | CCCGGATTCGGCCCCATGGGGGTGAGTGGCAGGAGTGGTTCTGGCCCAGTGAAGAGTGAAAGTCCACTTGGAGAGGACTAAAAAGATAATGCAAGGGAAGTTATAGAGCAATCCAAGAATCACATTTTCAAAGACCCCATCTATAAAATTAGCTGTCAAAAAGAACACAAAGAAACCCTTTGGGGTTCCATGATCTTGAAGAAGTTATTCCTTCATAATGGCAGTAACTTTGAAGCGTTTTGAATGGAAGAATGTAAAGATGTGTCACATTATGTATAAGTTTCCATGTGGATGGAACCTCAGGCTATGAAAGGCTGGCT... | CCCGGATTCGGCCCCATGGGGGTGAGTGGCAGGAGTGGTTCTGGCCCAGTGAAGAGTGAAAGTCCACTTGGAGAGGACTAAAAAGATAATGCAAGGGAAGTTATAGAGCAATCCAAGAATCACATTTTCAAAGACCCCATCTATAAAATTAGCTGTCAAAAAGAACACAAAGAAACCCTTTGGGGTTCCATGATCTTGAAGAAGTTATTCCTTCATAATGGCAGTAACTTTGAAGCGTTTTGAATGGAAGAATGTAAAGATGTGTCACATTATGTATAAGTTTCCATGTGGATGGAACCTCAGGCTATGAAAGGCTGGCT... |
Task1_train_34098 | A change on Chromosome 2 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CTGGAGTGCAGTGACGTGATCTTGGCTCACTGCAAGCTCTGCCTCCCGGATTCACGCCATTCTCCTGCCTCAGCTTCCCGAGTAGCTGGGACTACAGGCGCCCACCACCACACCTGGCCAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACTGTGTTAGCCAGGATGGTCTGGATCTCCTGACCTCGTGATCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGTGCCTGAACATTATTTATTTTTTTTTGAGACGGAGTTTCGCTCTTGTTGTCCAGGCTGGAGCGCAATGGCATGCGA... | CTGGAGTGCAGTGACGTGATCTTGGCTCACTGCAAGCTCTGCCTCCCGGATTCACGCCATTCTCCTGCCTCAGCTTCCCGAGTAGCTGGGACTACAGGCGCCCACCACCACACCTGGCCAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACTGTGTTAGCCAGGATGGTCTGGATCTCCTGACCTCGTGATCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGTGCCTGAACATTATTTATTTTTTTTTGAGACGGAGTTTCGCTCTTGTTGTCCAGGCTGGAGCGCAATGGCATGCGA... |
Task1_train_34099 | A genetic alteration is present on Chromosome 2. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GGTGGCTCACCATGACAGTGACATGATGACACCTACCTGACAAGGATCAATGAGGATTAAGTGCAAGTAAGATTTTCACCTTGATACTAGCATTTGCAGAAGCATTACTCTTCTTAGATAGTCAGGCTCAAGGTCTAGCTCAGGTCATTTTTTTTTTTTTTTTGAGATGGTGTCTCACTCTGTCACCCAGGCTGGAATGCAGTGGCATAATCTCAGCTCACTGCAACCTCCCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCTTGAGTGAGTAACTGGGACTACAGGTGCCCGCCACCACGCCTGATTTTTAGTA... | GGTGGCTCACCATGACAGTGACATGATGACACCTACCTGACAAGGATCAATGAGGATTAAGTGCAAGTAAGATTTTCACCTTGATACTAGCATTTGCAGAAGCATTACTCTTCTTAGATAGTCAGGCTCAAGGTCTAGCTCAGGTCATTTTTTTTTTTTTTTTGAGATGGTGTCTCACTCTGTCACCCAGGCTGGAATGCAGTGGCATAATCTCAGCTCACTGCAACCTCCCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCTTGAGTGAGTAACTGGGACTACAGGTGCCCGCCACCACGCCTGATTTTTAGTA... |
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