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_41900 | Here is a genetic alteration on Chromosome 12. Based on the data, is it a benign variant or a cause of disease? | Benign | GAGTAAAAGAATACAATATTTAAGTATGGCAAAGATAAGAGACACAAGAAATTACTCAGGATCTGAAATGACTGAGCAAGGGAGTTCTTTCTCTGAGATCTTTAAGACTAGTAGTAGTTGGTAATGTCTGATTGAGTGGGAAGAGTATGGACGAAGTGATGTCCAAGTTTCATACTGACTAGATTTCTTTTCACCGCATAATTCCAAAACTAGGTTATACCTTGGAAAAATGAATTTACTTTTAATTTAGAATGATTATTATTCTCTGCTCTTTTTTCTCTCTGTTGTATTCTGGGATTGTTCCTATAGCCACCTACACA... | GAGTAAAAGAATACAATATTTAAGTATGGCAAAGATAAGAGACACAAGAAATTACTCAGGATCTGAAATGACTGAGCAAGGGAGTTCTTTCTCTGAGATCTTTAAGACTAGTAGTAGTTGGTAATGTCTGATTGAGTGGGAAGAGTATGGACGAAGTGATGTCCAAGTTTCATACTGACTAGATTTCTTTTCACCGCATAATTCCAAAACTAGGTTATACCTTGGAAAAATGAATTTACTTTTAATTTAGAATGATTATTATTCTCTGCTCTTTTTTCTCTCTGTTGTATTCTGGGATTGTTCCTATAGCCACCTACACA... |
Task1_train_41901 | This variant lies on Chromosome 12. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CCGAGTAACTGGGATTACAGGCATGCGCCACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCTGCATGTTGGTCAGGCTAGTAGTCGCCAACTCCCGACCTCAGGTGATCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGCCTGGCCCTTGAATTATTCTTTACTCTATAGATGTATTTTTTGGCCGAGTGTGATGACTCTCACCTATAATTCCAGTACTTTGGGAGGCCAAGGCCGGTGGATTTCTTGAGCTCAGGAGTTTGAGACCAGCCTGAGCAACATAGTGA... | CCGAGTAACTGGGATTACAGGCATGCGCCACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCTGCATGTTGGTCAGGCTAGTAGTCGCCAACTCCCGACCTCAGGTGATCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGCCTGGCCCTTGAATTATTCTTTACTCTATAGATGTATTTTTTGGCCGAGTGTGATGACTCTCACCTATAATTCCAGTACTTTGGGAGGCCAAGGCCGGTGGATTTCTTGAGCTCAGGAGTTTGAGACCAGCCTGAGCAACATAGTGA... |
Task1_train_41902 | A variant has been detected on Chromosome 12. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TTCACATTATCACTTCCTATCCTCATCCTTGCAGATATCATAATGGACAAATCAAAACTAGCTCCAGAATGATTCACCTTTATGGCATTGTTGAGCAGTGACCCAGAGCTCCTGAAACAGCCATTGTCCTTCTGCCTCTGGGAGAGCCATATGAGGGCTTGGGTAATGTGTGCTTCATCGATGAAGATGTAGGCTCGAGCTTGGGCAAAAGTCTTCAGAACAAAGGCTGTGAGCCTGACCAGGGAGGAAGCAATCATGATGTTTATGTTGTCAAAATGGTTTTATAACCACTTCACAGCAACAGGCTTCATATGATGTGA... | TTCACATTATCACTTCCTATCCTCATCCTTGCAGATATCATAATGGACAAATCAAAACTAGCTCCAGAATGATTCACCTTTATGGCATTGTTGAGCAGTGACCCAGAGCTCCTGAAACAGCCATTGTCCTTCTGCCTCTGGGAGAGCCATATGAGGGCTTGGGTAATGTGTGCTTCATCGATGAAGATGTAGGCTCGAGCTTGGGCAAAAGTCTTCAGAACAAAGGCTGTGAGCCTGACCAGGGAGGAAGCAATCATGATGTTTATGTTGTCAAAATGGTTTTATAACCACTTCACAGCAACAGGCTTCATATGATGTGA... |
Task1_train_41903 | A change on Chromosome 12 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | AATATGAGGCCAGTTTCCCGAGAGTTTTATTGGCTCCATAAGTCAAGTTTGATTCCTTAAAGGACAGCACACCTCTCCAGTCAAAGCCTTGGTAAAATAACCAGTTTTTCAAATCATGTTCTGTTACAAAATAAAACAGATTCTTATTGCACTGATGGAAATAACTATATTGCCATAACTTAAATATACTCAAAAAGTAAAAAAGATTACTTCAGTCTCTAGGGGACCAAAAACAAGACAACAATTGTTTATGGATGACAAAAAGTTTTATAGTAGCCATAAAGTTACAATTGACAAGAATATCTGTTACCTTTGTGGCA... | AATATGAGGCCAGTTTCCCGAGAGTTTTATTGGCTCCATAAGTCAAGTTTGATTCCTTAAAGGACAGCACACCTCTCCAGTCAAAGCCTTGGTAAAATAACCAGTTTTTCAAATCATGTTCTGTTACAAAATAAAACAGATTCTTATTGCACTGATGGAAATAACTATATTGCCATAACTTAAATATACTCAAAAAGTAAAAAAGATTACTTCAGTCTCTAGGGGACCAAAAACAAGACAACAATTGTTTATGGATGACAAAAAGTTTTATAGTAGCCATAAAGTTACAATTGACAAGAATATCTGTTACCTTTGTGGCA... |
Task1_train_41904 | Chromosome 12 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GTTCTCACCTTCCACCTTTCTCAACTGAATTTTCATTCAATTTCTTTACCTGCAACCTCCACTCTGCTTTCCTACTAGAATGCTAACCTATTAGAATCCAACCTTTGCACCAAAATTAAACAGAAAGAATATAACTCATCATGTGAACATGTTATTAATGTCTGATGAATGAATGATGCAACAAGTGATAGTTTGACCAGAAGTACATATTTATTCAGCAAATATTTTTAGTGTCTATTTTATAGAGACAAATAACTCCATTCCTTCTAAGTAAATGTATAGGACAGAGAATCCACCAAAATATACAGCCTGTATGGTCC... | GTTCTCACCTTCCACCTTTCTCAACTGAATTTTCATTCAATTTCTTTACCTGCAACCTCCACTCTGCTTTCCTACTAGAATGCTAACCTATTAGAATCCAACCTTTGCACCAAAATTAAACAGAAAGAATATAACTCATCATGTGAACATGTTATTAATGTCTGATGAATGAATGATGCAACAAGTGATAGTTTGACCAGAAGTACATATTTATTCAGCAAATATTTTTAGTGTCTATTTTATAGAGACAAATAACTCCATTCCTTCTAAGTAAATGTATAGGACAGAGAATCCACCAAAATATACAGCCTGTATGGTCC... |
Task1_train_41905 | A variant has been detected on Chromosome 12. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CACATCATCCAGGACTTCATCTTTGCAATTTCCTTGTGCCTCCTTCCTCCCTTCACCCCTGGGGGATGTTATGTTGATGTGTGTCAGGCTCAGAAGTTTGTGGAACAGTTCACCTTTATGGCATTGTTGAGCAGTGACCCAGAGCTCCTGAAACAGCCATTGTCCTTCTGCATCTGGGAGAGCCACGTGAGAGATTGGGTAATGTGTGCTTCATCAATGAAGATGTAGGATCGAGCCTGGGCGAAAGTCTTCAGTACAAAAGCTGTGAGCCTAGGGGGAGGAAAAATGCAGTGCTGAGGCTCTTTTCATTGAGCACTTTA... | CACATCATCCAGGACTTCATCTTTGCAATTTCCTTGTGCCTCCTTCCTCCCTTCACCCCTGGGGGATGTTATGTTGATGTGTGTCAGGCTCAGAAGTTTGTGGAACAGTTCACCTTTATGGCATTGTTGAGCAGTGACCCAGAGCTCCTGAAACAGCCATTGTCCTTCTGCATCTGGGAGAGCCACGTGAGAGATTGGGTAATGTGTGCTTCATCAATGAAGATGTAGGATCGAGCCTGGGCGAAAGTCTTCAGTACAAAAGCTGTGAGCCTAGGGGGAGGAAAAATGCAGTGCTGAGGCTCTTTTCATTGAGCACTTTA... |
Task1_train_41906 | Here is a variant on Chromosome 12. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TTTTTGTTTTTTTCGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGTTCTCAAACCCCTGACCTCAAGTCATCCTCCCGCCTCAGCCTCCCAAAATGCTGGGATTACAAATGTGAGCCACCACACCCGGCTAACCCTGCTCTCTTTCTACCTCATCCTGGGACACTCTAAGCTTCTGCAGCTGGGCTTGTCAGTGAGCAGCCACTGGGCTATCCAGGTAAAAGGGCTACGTATGAACCAAGAAAGCCCAGGTATTAGTCCTGTCTGTACCACCTGAGTCACATTAACTTGCTCTCTTGGGCTCAATGTCTTCATCTGT... | TTTTTGTTTTTTTCGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGTTCTCAAACCCCTGACCTCAAGTCATCCTCCCGCCTCAGCCTCCCAAAATGCTGGGATTACAAATGTGAGCCACCACACCCGGCTAACCCTGCTCTCTTTCTACCTCATCCTGGGACACTCTAAGCTTCTGCAGCTGGGCTTGTCAGTGAGCAGCCACTGGGCTATCCAGGTAAAAGGGCTACGTATGAACCAAGAAAGCCCAGGTATTAGTCCTGTCTGTACCACCTGAGTCACATTAACTTGCTCTCTTGGGCTCAATGTCTTCATCTGT... |
Task1_train_41907 | A mutation on Chromosome 12 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | ATGAGAGATATGTGAATCTTAGGAGAGAGGTGGAGATCAAGAAATTGCGCTCAATGTAATCCCAGCACTTTGGGAGGCCGAGAAGGGAGGATCACGAGGTCAGGAGATTGAGACCATCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAAAAAAAAAAAAAAATTAGCCAGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCATGAACCCGGGAGGCAGAGCTTTCAGTGAGCCGAGATCGCAACACTGCACTTCAGCCTGTGCAACAGAGCAAAACTCCGTCTCAAAAAAA... | ATGAGAGATATGTGAATCTTAGGAGAGAGGTGGAGATCAAGAAATTGCGCTCAATGTAATCCCAGCACTTTGGGAGGCCGAGAAGGGAGGATCACGAGGTCAGGAGATTGAGACCATCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAAAAAAAAAAAAAAATTAGCCAGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCATGAACCCGGGAGGCAGAGCTTTCAGTGAGCCGAGATCGCAACACTGCACTTCAGCCTGTGCAACAGAGCAAAACTCCGTCTCAAAAAAA... |
Task1_train_41908 | Here is a variant on Chromosome 12. Please identify whether it is a benign mutation or associated with a disorder. | Benign | AGACATGAAAGCAATTTTGTCCACGTTGTGCCTGAAATCATGCTTACTAATTGAATTTGATTTAAGATCTCCCTCCATGTATCCCATCTGATATTTCAGAAATACCTTGTGAAAGAATACTTACAAGGAAAAATATATTTCTAGCAATTTCACCCTAACAGTTTTCTCCACTGAAGAAAGCATCAGTAGTAATTTCTTTAGTGAATATCATACACCTTGCCCCATGTCCTTCCAAGTGGTAACAATTTCTATCTCTGACTCTGATTTCTCACTGTTTTGTCTTCTCTGTCTTCACTCTTATCTTAAATATTGAAATATCT... | AGACATGAAAGCAATTTTGTCCACGTTGTGCCTGAAATCATGCTTACTAATTGAATTTGATTTAAGATCTCCCTCCATGTATCCCATCTGATATTTCAGAAATACCTTGTGAAAGAATACTTACAAGGAAAAATATATTTCTAGCAATTTCACCCTAACAGTTTTCTCCACTGAAGAAAGCATCAGTAGTAATTTCTTTAGTGAATATCATACACCTTGCCCCATGTCCTTCCAAGTGGTAACAATTTCTATCTCTGACTCTGATTTCTCACTGTTTTGTCTTCTCTGTCTTCACTCTTATCTTAAATATTGAAATATCT... |
Task1_train_41909 | Given this context: Chromosome 12 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GGATGTGTTAGGGGAGCAAGGAGAGATGAATCTGAGGATACTCACTGTCTCCTGACTCCACAGGCAGAGTGTGGGTTCCAGATCTGACGATGACTCCCTTAGCCATGATCTGAAATGAAAAAACAGTGAAGGAAATTTCTTGAGCTGGACACAGTTCTCAGCCTTCTATTCCCCACATGACCCACTTTCAGTTGTCAAGTCTGTGCTGGAGAGAATCAACCTCAAGAAAACTCATGGAATGAAGGACGCACAACAAGAACACAAGGTGGCTGTGTGCAAGTAGTTTATTTTGACATTCCTGAGCCTATTGACCACTTTTG... | GGATGTGTTAGGGGAGCAAGGAGAGATGAATCTGAGGATACTCACTGTCTCCTGACTCCACAGGCAGAGTGTGGGTTCCAGATCTGACGATGACTCCCTTAGCCATGATCTGAAATGAAAAAACAGTGAAGGAAATTTCTTGAGCTGGACACAGTTCTCAGCCTTCTATTCCCCACATGACCCACTTTCAGTTGTCAAGTCTGTGCTGGAGAGAATCAACCTCAAGAAAACTCATGGAATGAAGGACGCACAACAAGAACACAAGGTGGCTGTGTGCAAGTAGTTTATTTTGACATTCCTGAGCCTATTGACCACTTTTG... |
Task1_train_41910 | This genomic variant is located on Chromosome 12. Can you determine its pathogenicity and name any linked disease? | Benign | ACAGACATGAGTCCTGTGGCTCACTGCAGGTAGGAGGTGATGATATAATTCAAACAAAGGGACAGGCTGTATTGGGGTTGAGTTGCAAGGACGGTGTGAGTTCAAGACTCTCCTATTTGTCTCAAACGGATGAGGTGGTGGCAGCATGCTGGGCTCCATCACAGCTTTTCTTTAGTCCTTTGTTCCATTTTCTCATGTAGCCTCTTGGGGCTGCTTGTCTGATTTCTTCCTACTGCCCAACCTTCTAGTCAAACCAAGAACTTCTTTCAACTGGGCTATTGCAAAAGTTCCCTATATTTTATCTCTTCCACCCTTTTAAT... | ACAGACATGAGTCCTGTGGCTCACTGCAGGTAGGAGGTGATGATATAATTCAAACAAAGGGACAGGCTGTATTGGGGTTGAGTTGCAAGGACGGTGTGAGTTCAAGACTCTCCTATTTGTCTCAAACGGATGAGGTGGTGGCAGCATGCTGGGCTCCATCACAGCTTTTCTTTAGTCCTTTGTTCCATTTTCTCATGTAGCCTCTTGGGGCTGCTTGTCTGATTTCTTCCTACTGCCCAACCTTCTAGTCAAACCAAGAACTTCTTTCAACTGGGCTATTGCAAAAGTTCCCTATATTTTATCTCTTCCACCCTTTTAAT... |
Task1_train_41911 | Here is a mutation located on Chromosome 12. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | ACATAGTTTCTTGGAAAGCTAATTCTTATACCATTATGCAATGCTTTTCTTCATTCCTGATAAATTTCCTTGCTTTGAGGTTTGTTCTGTTTGAAATTTGTATAGCTTCTCCTGCTTTCTTTTGTTTGTGCCAGTATGATATAATACATATATATATTCATGATCCATTTACTTTTAATTTGTGTGTCTTTATATTTAAAGTGCATTTCCTGCAGACATCATATAGTTTAATCTCTGATTTTTAATTGGTGCATTTAGATCATTGATATTAAAATGATTATTAATATAGGTGGATTAAATATCTACCATATTTCTTTCTG... | ACATAGTTTCTTGGAAAGCTAATTCTTATACCATTATGCAATGCTTTTCTTCATTCCTGATAAATTTCCTTGCTTTGAGGTTTGTTCTGTTTGAAATTTGTATAGCTTCTCCTGCTTTCTTTTGTTTGTGCCAGTATGATATAATACATATATATATTCATGATCCATTTACTTTTAATTTGTGTGTCTTTATATTTAAAGTGCATTTCCTGCAGACATCATATAGTTTAATCTCTGATTTTTAATTGGTGCATTTAGATCATTGATATTAAAATGATTATTAATATAGGTGGATTAAATATCTACCATATTTCTTTCTG... |
Task1_train_41912 | This alteration occurs on Chromosome 12. Is it associated with a disease or is it a benign variant? | Benign | TATGATTTGAAAGAGTAAAAGATTTACCTAATAAGTCCCTAAATTTACTAATAATAAAGAAAATTGTTTATATATTTAATTGCGTTAAAATTCAGAACTTGTAATCATAAAAAGGACAGTACACATTGACAAGGAAACACAGCAAAGGAAACCAGCCTATGCTGCTGCTGTTGTGAGGATAATTTGGTACACTTACATTAGTTTGGTGTCTTTTCTTTCTCTTTCTTTCTTTCTTTCTTTCTCTTTCTTTCGTTCGTTCGTTCGTTCGTTTCTTTTTGAGACAGAATCTCACTCTATTGCCCAGGCTGGAGTGCAGTGGC... | TATGATTTGAAAGAGTAAAAGATTTACCTAATAAGTCCCTAAATTTACTAATAATAAAGAAAATTGTTTATATATTTAATTGCGTTAAAATTCAGAACTTGTAATCATAAAAAGGACAGTACACATTGACAAGGAAACACAGCAAAGGAAACCAGCCTATGCTGCTGCTGTTGTGAGGATAATTTGGTACACTTACATTAGTTTGGTGTCTTTTCTTTCTCTTTCTTTCTTTCTTTCTTTCTCTTTCTTTCGTTCGTTCGTTCGTTCGTTTCTTTTTGAGACAGAATCTCACTCTATTGCCCAGGCTGGAGTGCAGTGGC... |
Task1_train_41913 | Mutation context: Chromosome 12. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CAATCTGTCGGTCTATTTACACAGTGGATTTTGCCCCTATATCATGCAAAAAAAAAAAAAAAAAAAGAGAGAAGAACTCTCTAAAACAGTGAGATATATAGATAGAGCCAGGTAGAGCTCCTGATTTATGGACTGGTGGTCGGTGCAATAAGGTGTATACCCACTTGTTTTGGTTTTGGAGTGAGAGAGGGGAGTAGTGTGTAGGTCTACTACATAGCTTGGCTATTTCTTGTGCCATTTCTTCTGAAAAGTCATGGTAGCTAACCAAATATCCCGGAGCACAGAGCAAAATGTCAGAAAAAAAACATAAATAAATATAA... | CAATCTGTCGGTCTATTTACACAGTGGATTTTGCCCCTATATCATGCAAAAAAAAAAAAAAAAAAAGAGAGAAGAACTCTCTAAAACAGTGAGATATATAGATAGAGCCAGGTAGAGCTCCTGATTTATGGACTGGTGGTCGGTGCAATAAGGTGTATACCCACTTGTTTTGGTTTTGGAGTGAGAGAGGGGAGTAGTGTGTAGGTCTACTACATAGCTTGGCTATTTCTTGTGCCATTTCTTCTGAAAAGTCATGGTAGCTAACCAAATATCCCGGAGCACAGAGCAAAATGTCAGAAAAAAAACATAAATAAATATAA... |
Task1_train_41914 | A variant on Chromosome 12 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TGGTGTTTTACAATGCTACACTCATCATTTGGAGTATTTCCATTGTGTCTGGCAGCACTCCAGTGGTACTTCATTGACCAGTCTGTCAATATCTACATAATAAAATTATTTCATCCAAGTGGCACATTCTCACTAGTAATAGTTAATAAATATCCCCTCTCAAATCATAACTTGGGAGGTATATGAGAGGTCATTTTATACCTTTTAGCAAACAACTATGTATTTGTACAACTGAAATTACAATTTAGTTATCCTGAATCTTTTCAATTTTTTTTAAATTACAATTTTTCAGCATTGGCCACTCTTGCCCGGATACAGCA... | TGGTGTTTTACAATGCTACACTCATCATTTGGAGTATTTCCATTGTGTCTGGCAGCACTCCAGTGGTACTTCATTGACCAGTCTGTCAATATCTACATAATAAAATTATTTCATCCAAGTGGCACATTCTCACTAGTAATAGTTAATAAATATCCCCTCTCAAATCATAACTTGGGAGGTATATGAGAGGTCATTTTATACCTTTTAGCAAACAACTATGTATTTGTACAACTGAAATTACAATTTAGTTATCCTGAATCTTTTCAATTTTTTTTAAATTACAATTTTTCAGCATTGGCCACTCTTGCCCGGATACAGCA... |
Task1_train_41915 | A sequence alteration has been identified on Chromosome 12. Is it disease-inducing or harmless? | Benign | TTATTTCATTTAAGAGAATGGTCTCCAGCTCCATCCATTTTGCTGCAAAGTCATGATTTCCTTCTTTTTTATACTTGAGTAGTATTTCATGGTGTATACACTCTAAAAGAAAGCATGGTTTCATGTTTTCTTATGCAATAATCCGTTGATGGACACTTAGGACAGTTCCATGACTTTGCTATTGTAAATAGTTCTACAACAAACATTTAAGTGTAGGTGTCTTTTTTTTAATATAATAATTCCTTTCCCTTTGGTTAGATACCCAATAGTGGAATTGCTGGATCAAATGGTAATTCTATTTTTAGTTCTTTGAAAAATTG... | TTATTTCATTTAAGAGAATGGTCTCCAGCTCCATCCATTTTGCTGCAAAGTCATGATTTCCTTCTTTTTTATACTTGAGTAGTATTTCATGGTGTATACACTCTAAAAGAAAGCATGGTTTCATGTTTTCTTATGCAATAATCCGTTGATGGACACTTAGGACAGTTCCATGACTTTGCTATTGTAAATAGTTCTACAACAAACATTTAAGTGTAGGTGTCTTTTTTTTAATATAATAATTCCTTTCCCTTTGGTTAGATACCCAATAGTGGAATTGCTGGATCAAATGGTAATTCTATTTTTAGTTCTTTGAAAAATTG... |
Task1_train_41916 | Assess the clinical impact of this variant found on Chromosome 12. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TTGCATGACTACTTTTAGTTATAAATCTTCAACCTGGCATCTGCCTAGACTAATACAAATTAAGGATATGCATATATGTCTCGAATTAATCTCTATATAATAGAGCTGAGATTTTAGAAAACTATCTTATTTTGCTGGAGTGGAAAGAAAAGCTAATTTATGTAACTGGATATCTTCCGTATGCGTCTGAGTCCACAGAAACAGTAAGTGGACAGCACAGCAAGTTAGAACAACAGAGGACACAAATAAATATGAACATCACTGGGCTGACTCTTCATGTGTGACCCACTATGTACCTGAGCTGTCAGGAAGGGACAAGT... | TTGCATGACTACTTTTAGTTATAAATCTTCAACCTGGCATCTGCCTAGACTAATACAAATTAAGGATATGCATATATGTCTCGAATTAATCTCTATATAATAGAGCTGAGATTTTAGAAAACTATCTTATTTTGCTGGAGTGGAAAGAAAAGCTAATTTATGTAACTGGATATCTTCCGTATGCGTCTGAGTCCACAGAAACAGTAAGTGGACAGCACAGCAAGTTAGAACAACAGAGGACACAAATAAATATGAACATCACTGGGCTGACTCTTCATGTGTGACCCACTATGTACCTGAGCTGTCAGGAAGGGACAAGT... |
Task1_train_41917 | Here is a genetic alteration on Chromosome 12. Based on the data, is it a benign variant or a cause of disease? | Benign | TTTAGTTATAAATCTTCAACCTGGCATCTGCCTAGACTAATACAAATTAAGGATATGCATATATGTCTCGAATTAATCTCTATATAATAGAGCTGAGATTTTAGAAAACTATCTTATTTTGCTGGAGTGGAAAGAAAAGCTAATTTATGTAACTGGATATCTTCCGTATGCGTCTGAGTCCACAGAAACAGTAAGTGGACAGCACAGCAAGTTAGAACAACAGAGGACACAAATAAATATGAACATCACTGGGCTGACTCTTCATGTGTGACCCACTATGTACCTGAGCTGTCAGGAAGGGACAAGTCAATTTGACTGAT... | TTTAGTTATAAATCTTCAACCTGGCATCTGCCTAGACTAATACAAATTAAGGATATGCATATATGTCTCGAATTAATCTCTATATAATAGAGCTGAGATTTTAGAAAACTATCTTATTTTGCTGGAGTGGAAAGAAAAGCTAATTTATGTAACTGGATATCTTCCGTATGCGTCTGAGTCCACAGAAACAGTAAGTGGACAGCACAGCAAGTTAGAACAACAGAGGACACAAATAAATATGAACATCACTGGGCTGACTCTTCATGTGTGACCCACTATGTACCTGAGCTGTCAGGAAGGGACAAGTCAATTTGACTGAT... |
Task1_train_41918 | Assess the clinical impact of this variant found on Chromosome 12. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CTTAGAAATAATTAGGAATCAGGTGACATTCTTCATCATTGTTCAAGCTAAGCATCATTTCATGGATAGTGAGAAGTTAATACTTTGTTAGGAAGCTTTAAGGTATGTGAAAGAATTAAGGAAATGAGGATGAAAACCCAGTTTTTGCAAAATCTGGTGAAAGTCATGAGACGTGAGGCCAGCCAGACTTCCTGAATCGAGTGGGGACTCAGGGAACTTTCCTGTCTTACAAGAGGATTGTAAAACGCACCAATCAGTGCCACGTAAAACGCACCGATCAGCGCTCTGTAAAACGCACCAATCAGCAGGATTCTAAAAGT... | CTTAGAAATAATTAGGAATCAGGTGACATTCTTCATCATTGTTCAAGCTAAGCATCATTTCATGGATAGTGAGAAGTTAATACTTTGTTAGGAAGCTTTAAGGTATGTGAAAGAATTAAGGAAATGAGGATGAAAACCCAGTTTTTGCAAAATCTGGTGAAAGTCATGAGACGTGAGGCCAGCCAGACTTCCTGAATCGAGTGGGGACTCAGGGAACTTTCCTGTCTTACAAGAGGATTGTAAAACGCACCAATCAGTGCCACGTAAAACGCACCGATCAGCGCTCTGTAAAACGCACCAATCAGCAGGATTCTAAAAGT... |
Task1_train_41919 | A variant was discovered on Chromosome 12. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CTCACTCCCGATTCCTTATTATGTGGAAGATGTTAAAATTAACTCAACTCCACAGTTGCTCCTTCTGTTAAGCCTTTCCTGAACTCCTCTACTTAATTAGGTAAAAATTAAGCCGAGAGCTTGGTTAAGCTCTCGGCTGTACTGTACATGCTTCTGCCATAACACCTTATTATACTTACTCCTTAGTTGAGAATTGTATTAGACTTTCAATTTCCTTATGAACAGGGACCATATCACATTGGACATTATATCCTCAGTACTAGGATAACATGACCCCAAACATAAGTTTGTGAAAAATGTATGAGGTTGTTGTTTTTCAT... | CTCACTCCCGATTCCTTATTATGTGGAAGATGTTAAAATTAACTCAACTCCACAGTTGCTCCTTCTGTTAAGCCTTTCCTGAACTCCTCTACTTAATTAGGTAAAAATTAAGCCGAGAGCTTGGTTAAGCTCTCGGCTGTACTGTACATGCTTCTGCCATAACACCTTATTATACTTACTCCTTAGTTGAGAATTGTATTAGACTTTCAATTTCCTTATGAACAGGGACCATATCACATTGGACATTATATCCTCAGTACTAGGATAACATGACCCCAAACATAAGTTTGTGAAAAATGTATGAGGTTGTTGTTTTTCAT... |
Task1_train_41920 | This variant is located on Chromosome 12. Evaluate its biological effect and specify any disease association. | Benign | AAAAAAAAAGATTCCTGCTAGATTGTGTGCAGCAAAATAAAAAGGCTTCCTTTAAAGTAGAATAGCCTGTGAAGAGTGGGTGGAAAGGAAATAGAAGCCTAAAAATAGAAGATATATTTCTAATTCCATCTGTTTCTATTCAGCGATATTTGCATACCTGGCTTAGTTTGTTCTAGATTGAGTGTCTTCATTTTTTTTGTCTTGTATGTTTCGGAATTATAGCATAGCAAAACAGAGTTGAGAAGAGTTCATCTACAAAAGGTATGTTCTTTAGGGAAAGAAATTCTATTCTTACCTCTGGGCCACACATCCCATGATTC... | AAAAAAAAAGATTCCTGCTAGATTGTGTGCAGCAAAATAAAAAGGCTTCCTTTAAAGTAGAATAGCCTGTGAAGAGTGGGTGGAAAGGAAATAGAAGCCTAAAAATAGAAGATATATTTCTAATTCCATCTGTTTCTATTCAGCGATATTTGCATACCTGGCTTAGTTTGTTCTAGATTGAGTGTCTTCATTTTTTTTGTCTTGTATGTTTCGGAATTATAGCATAGCAAAACAGAGTTGAGAAGAGTTCATCTACAAAAGGTATGTTCTTTAGGGAAAGAAATTCTATTCTTACCTCTGGGCCACACATCCCATGATTC... |
Task1_train_41921 | Given a variant located on Chromosome 12, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | ACTATTCCATAAAATCCTAAGCAAGCCTTTGTTTCTTTGCAGTCAGCTTTTCTTCTGCTGATGCTGCCTGTTGCCTCCCTGGAAACATATTTTCCTACTTTTCTTTAATAAATCTGCCTTCCTTTACCTACAGCTGTCTTGGTAAATTCTTTTACCTCAATGCCACCGGCCCAGGTAGCCGTTGCTCACCCACAACATTAGTGTATTAGTCCGTTCTTATGCTGCTACTAAAGATATACCCAAGACTGGGAAATTTATAAAATAAAGACATTTAATTGACTCACAGTTCTGCAGGGTTGGAGAAGCCTCAGGAAACTTAC... | ACTATTCCATAAAATCCTAAGCAAGCCTTTGTTTCTTTGCAGTCAGCTTTTCTTCTGCTGATGCTGCCTGTTGCCTCCCTGGAAACATATTTTCCTACTTTTCTTTAATAAATCTGCCTTCCTTTACCTACAGCTGTCTTGGTAAATTCTTTTACCTCAATGCCACCGGCCCAGGTAGCCGTTGCTCACCCACAACATTAGTGTATTAGTCCGTTCTTATGCTGCTACTAAAGATATACCCAAGACTGGGAAATTTATAAAATAAAGACATTTAATTGACTCACAGTTCTGCAGGGTTGGAGAAGCCTCAGGAAACTTAC... |
Task1_train_41922 | The following genetic variant occurs on Chromosome 12. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TTCCAGGTAATTTATATGTTAACTATCTTGATGTTCTTTATGTTTTCATGGGCTCATATAGTTCTCGAGACTTATCAAATTGTATACTTTATATATGTGCAATTTATTATATGTTAATTATATCTCAACATGTCTGGTAATAAATTCAAAAAGAAATGTATGTAATATTTAACCTCTCTGTTTCTGTCTCTTTATCTGTAAAACGAACATATTAGACCTGCCTTCCACAGTACTTACCATATAGTAAACAATTTGTATTACTTACTAGTATTTGTGTTGGCTGCTCTACAACTAATACAACTTTCTCCCAAATTTAGGGC... | TTCCAGGTAATTTATATGTTAACTATCTTGATGTTCTTTATGTTTTCATGGGCTCATATAGTTCTCGAGACTTATCAAATTGTATACTTTATATATGTGCAATTTATTATATGTTAATTATATCTCAACATGTCTGGTAATAAATTCAAAAAGAAATGTATGTAATATTTAACCTCTCTGTTTCTGTCTCTTTATCTGTAAAACGAACATATTAGACCTGCCTTCCACAGTACTTACCATATAGTAAACAATTTGTATTACTTACTAGTATTTGTGTTGGCTGCTCTACAACTAATACAACTTTCTCCCAAATTTAGGGC... |
Task1_train_41923 | This variant lies on Chromosome 12. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TTTCCTGATACTGTGCATGTATTTCTCCAGATATTCTGATTAAATAAATGTATTTTTCCACTATGTGTCTCATAGTGGAACTTTTCCTCCTTGAAGTTTAGAAGGAAATTGAAAGGTTGCCATTGAGGAAATAAATGACACAGCAGCCAAAAATTGGCTTTTCTGGGCACCACACCACTCTCTAACTAGATAAGCCCTCACTTTTATCTGATTTGGTTTTGGTGGAATAACAATGGTCTTGACCAGGTACATGGACTCCTTTTTCTCTGCTACTCCCTAATAAATACAACTCTAAACTCTGCAAGTAATGAAAGACACAC... | TTTCCTGATACTGTGCATGTATTTCTCCAGATATTCTGATTAAATAAATGTATTTTTCCACTATGTGTCTCATAGTGGAACTTTTCCTCCTTGAAGTTTAGAAGGAAATTGAAAGGTTGCCATTGAGGAAATAAATGACACAGCAGCCAAAAATTGGCTTTTCTGGGCACCACACCACTCTCTAACTAGATAAGCCCTCACTTTTATCTGATTTGGTTTTGGTGGAATAACAATGGTCTTGACCAGGTACATGGACTCCTTTTTCTCTGCTACTCCCTAATAAATACAACTCTAAACTCTGCAAGTAATGAAAGACACAC... |
Task1_train_41924 | A genomic variant on Chromosome 12 is under review. What is the biological outcome — benign or pathogenic? | Benign | GAAAAGCAAAACTGGAAATAACCAAATGTGCATTAACAGTATATGAATATAAAAATATTATGAAGTCAGTTGAATACTACACAGACTTAAAAATATATGAAGTAAATATATGTATAAACATATGGATGATTTCTACAAATATGATATTGACAGAAATAAGCTTTTAGTAAAGTGTTGAAACATTTACGTCTTACCATTTCTTCCTCATTATCTATAGAAAGCAGATCAGAGTTCTTCGAAGCACAGGCCAGCAAACTCTTTCTTCCCAAGTTCTTCTTTCCTTACCAATGTAATAACAACTGTTGGAATATGTAATCCAC... | GAAAAGCAAAACTGGAAATAACCAAATGTGCATTAACAGTATATGAATATAAAAATATTATGAAGTCAGTTGAATACTACACAGACTTAAAAATATATGAAGTAAATATATGTATAAACATATGGATGATTTCTACAAATATGATATTGACAGAAATAAGCTTTTAGTAAAGTGTTGAAACATTTACGTCTTACCATTTCTTCCTCATTATCTATAGAAAGCAGATCAGAGTTCTTCGAAGCACAGGCCAGCAAACTCTTTCTTCCCAAGTTCTTCTTTCCTTACCAATGTAATAACAACTGTTGGAATATGTAATCCAC... |
Task1_train_41925 | Assess the clinical impact of this variant found on Chromosome 12. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CCTGATACTGTGCATTCATTCCTCCAGATACTGTGACTAAATCAATCTATTTTTGTGCTATATTTCTCAGAGTTGGAGATTTAGAAGGGAATTGAGGGGTTGTCATTCAGAAATAGATGACATGGAAGCTACAGATTGGGTTTTCTGGGTACCACACCATTCTTTAACTAGATAAGCCCTCAATTTTTATCCGATTCGGTTTTTGCGGAATAACAGGGGTCCTGGCCAGGTGGTGTAGACTCGTCTCTCTCTGCTACTCCCGACTAAAAACAACTATAAACTCTGGGATTAATGAAAGACAAAAGCAATGGAGAACTCTG... | CCTGATACTGTGCATTCATTCCTCCAGATACTGTGACTAAATCAATCTATTTTTGTGCTATATTTCTCAGAGTTGGAGATTTAGAAGGGAATTGAGGGGTTGTCATTCAGAAATAGATGACATGGAAGCTACAGATTGGGTTTTCTGGGTACCACACCATTCTTTAACTAGATAAGCCCTCAATTTTTATCCGATTCGGTTTTTGCGGAATAACAGGGGTCCTGGCCAGGTGGTGTAGACTCGTCTCTCTCTGCTACTCCCGACTAAAAACAACTATAAACTCTGGGATTAATGAAAGACAAAAGCAATGGAGAACTCTG... |
Task1_train_41926 | A genomic change on Chromosome 12 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CCTCAAAAATTAAGAGTAAAACTACCCATATAACCCAATAATATCACTTCTGGGTATACAGTATATCCAAAAGAATTAAAATTAGTATCTTGAAGAGATATCTGCACTCCCACATCAATGGTAGGATTATCAAGAATAAATAATATTTAAACAACCTAAATGTACACTGACAGATGAACAGATAAAGAAAATGTAGTATGTACATATGATGGAATATTCTTCAGCCTTAAAGAAAGAATATTCTGCCATTCATGACAACATGAATGACCCTTGAGGACATTAAGCTAAATAAAATAAGCCAGTCACAGAAGAACAAATGC... | CCTCAAAAATTAAGAGTAAAACTACCCATATAACCCAATAATATCACTTCTGGGTATACAGTATATCCAAAAGAATTAAAATTAGTATCTTGAAGAGATATCTGCACTCCCACATCAATGGTAGGATTATCAAGAATAAATAATATTTAAACAACCTAAATGTACACTGACAGATGAACAGATAAAGAAAATGTAGTATGTACATATGATGGAATATTCTTCAGCCTTAAAGAAAGAATATTCTGCCATTCATGACAACATGAATGACCCTTGAGGACATTAAGCTAAATAAAATAAGCCAGTCACAGAAGAACAAATGC... |
Task1_train_41927 | This mutation is located on Chromosome 12. Is it associated with a disease or is it a benign polymorphism? | Benign | ATTTTCAGAAAACAAGAAAATAAACAAAAAACAGTTTACCTTTACTTTTGTGAGCTGAACGTCTTCCGTTCTTTCATTTTGAAAAGGGGAATTTTGTCTCTGTGCATGTCACTCTCTCCTCACTCATATCTGAGGGCTGCAGTCAAAGAACACAGCAAGAATCCTTTCGAACAGCATAATTCTTCAGTTGAAATGGGAACATTCATCATGAAGGAATGGAGAGACCTCAATAAGTAATAAGCATGATAGTCAAGAAAAAGTGAAATAAAGTAACCATTTGTCAGGGAATATCAGAAAATATGATTTTGTAGACTTCTCTT... | ATTTTCAGAAAACAAGAAAATAAACAAAAAACAGTTTACCTTTACTTTTGTGAGCTGAACGTCTTCCGTTCTTTCATTTTGAAAAGGGGAATTTTGTCTCTGTGCATGTCACTCTCTCCTCACTCATATCTGAGGGCTGCAGTCAAAGAACACAGCAAGAATCCTTTCGAACAGCATAATTCTTCAGTTGAAATGGGAACATTCATCATGAAGGAATGGAGAGACCTCAATAAGTAATAAGCATGATAGTCAAGAAAAAGTGAAATAAAGTAACCATTTGTCAGGGAATATCAGAAAATATGATTTTGTAGACTTCTCTT... |
Task1_train_41928 | Chromosome 12 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AGGAAGGGACTAAAAACAATTTATCCATGCTTGAGTTTCTGCCCCCTAACTTCTATCTAATTTTCTTTAAAACATACACACCACTTGAGAATATTAATATGAGAAATATGGCATCAAAAACAAGGCTAACAAGGAAACGTCACACCATCAGTTGTCATGTTGCCTCATCTTACCAGCGCCAAAAGGACCTGCTTTCCGATGTGATATACTTGTTTTTCTGTGAGATCATAGAGAAGACCATCCATAGTCATCACATCCTAAAGAGACAGGGAAAAAAAGCCATTATATCAAAATAGCACTCACAGATTTGGAAAAGAAAT... | AGGAAGGGACTAAAAACAATTTATCCATGCTTGAGTTTCTGCCCCCTAACTTCTATCTAATTTTCTTTAAAACATACACACCACTTGAGAATATTAATATGAGAAATATGGCATCAAAAACAAGGCTAACAAGGAAACGTCACACCATCAGTTGTCATGTTGCCTCATCTTACCAGCGCCAAAAGGACCTGCTTTCCGATGTGATATACTTGTTTTTCTGTGAGATCATAGAGAAGACCATCCATAGTCATCACATCCTAAAGAGACAGGGAAAAAAAGCCATTATATCAAAATAGCACTCACAGATTTGGAAAAGAAAT... |
Task1_train_41929 | Consider this mutation on Chromosome 12. Is this a benign change or a disease-causing variant? | Benign | TTTCGTAATTCCGCAAATACTTCTCCAAGGACTTCTTATGATCAAATTCATTCCCACGTCTTGCTTTAAACCATAAACCCACTTCATATACACTAAGGGGAAGGGTTGGGGAGGAAGACCATAGATTTCCATAACATTTATCAGAAGGAAAATTTTTTTGCACTCATGAAAACTATTTTTCCTGGCCTATGTGCTTATAAACTCAAGTGAAGGCCCATTTGCAAATACTAGAACATATCCATTTTAGTCAGCATTGTGCCTAGTACATCTTAGGCATCTATGTGTTTGCTTGGCAAAGGAAAGGGGATGGCAGGACACAC... | TTTCGTAATTCCGCAAATACTTCTCCAAGGACTTCTTATGATCAAATTCATTCCCACGTCTTGCTTTAAACCATAAACCCACTTCATATACACTAAGGGGAAGGGTTGGGGAGGAAGACCATAGATTTCCATAACATTTATCAGAAGGAAAATTTTTTTGCACTCATGAAAACTATTTTTCCTGGCCTATGTGCTTATAAACTCAAGTGAAGGCCCATTTGCAAATACTAGAACATATCCATTTTAGTCAGCATTGTGCCTAGTACATCTTAGGCATCTATGTGTTTGCTTGGCAAAGGAAAGGGGATGGCAGGACACAC... |
Task1_train_41930 | This sequence variant lies on Chromosome 12. Is it clinically significant, and what condition might it cause if any? | Benign | CTAAATCTTTCTACAACCAATGGCTAATGATTGAATAACACAAATCTCCCATTTTTGCAAGAGCAATAACTCCCTTGACATATAACTAATTTGAAGCATAAAGATACATAAAATTTGCCTACATTATTGTAGTCAATCAGTGAATGTATCATTGCACTTTCTTTTGCCACTCTGAATTAAAACACAAATGCTTCATTCTTTAGTTTTCAAGTCCTGATAACTGCTTAAACACTAATTTGTCACAGAGTAAGTGAAATTTAAAGCCACCATTAGTCACACACAGTTTACATGAAAAATTTGAAGTCCATTCTAATGGCCTG... | CTAAATCTTTCTACAACCAATGGCTAATGATTGAATAACACAAATCTCCCATTTTTGCAAGAGCAATAACTCCCTTGACATATAACTAATTTGAAGCATAAAGATACATAAAATTTGCCTACATTATTGTAGTCAATCAGTGAATGTATCATTGCACTTTCTTTTGCCACTCTGAATTAAAACACAAATGCTTCATTCTTTAGTTTTCAAGTCCTGATAACTGCTTAAACACTAATTTGTCACAGAGTAAGTGAAATTTAAAGCCACCATTAGTCACACACAGTTTACATGAAAAATTTGAAGTCCATTCTAATGGCCTG... |
Task1_train_41931 | This alteration on Chromosome 12 may affect genome function. Does it lead to a disease or is it benign? | Benign | GGCAACTGGAACATCACCTATGATAGGACGATCTTGGATATGATCCCTGACCTAGACTTATCATTTCTTTTGTTTTTTTTTTGAGATGGAATTTCGTTCTTGTTGCTCAGGCTGGAGTGCTATTTTGGCTCACCGCAACCTCCATCTCCCAGGTTCAAGTGATTCTCCTGCCTGAGCCTGCCAAGTAGCTGGGATTACAGGCAGGTGCAACCATGCCTGGCTAATTTTGTATTTTTAGTAGATTCCGGGTTTCTCCATGTTGGTCAGGCTGGTCTTGAACTCCCGACCTCAGGCGATCCGTGTGCCTTGGCCTCCCAAAG... | GGCAACTGGAACATCACCTATGATAGGACGATCTTGGATATGATCCCTGACCTAGACTTATCATTTCTTTTGTTTTTTTTTTGAGATGGAATTTCGTTCTTGTTGCTCAGGCTGGAGTGCTATTTTGGCTCACCGCAACCTCCATCTCCCAGGTTCAAGTGATTCTCCTGCCTGAGCCTGCCAAGTAGCTGGGATTACAGGCAGGTGCAACCATGCCTGGCTAATTTTGTATTTTTAGTAGATTCCGGGTTTCTCCATGTTGGTCAGGCTGGTCTTGAACTCCCGACCTCAGGCGATCCGTGTGCCTTGGCCTCCCAAAG... |
Task1_train_41932 | A genetic alteration is present on Chromosome 12. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TTCTCCCAGATGCAAAGAAATTTTCACTTTGGAAGTAATTAGTACAATTAGATTGTAGATATTTAACATTTAGTCAGAGGATAATAATTCTTGTCTTCATTTAAACGGCTAATTAGGGAAGGATATAATACAAATCTAATTAGAAATGACTTTTTTTTAGGCAGGCACATGATAATATTTACTAAGAATTTGCTTTCTTTTCAATTGTTCCTCAGAAGTGAAATATGCCAGGTAAAGATTTGTTATCTTTAGTTTTTTTTTAATGTGACAAATACCCTTGAAGACAATTCATTTCCTGAATCACTGTCTCTTGTATAATA... | TTCTCCCAGATGCAAAGAAATTTTCACTTTGGAAGTAATTAGTACAATTAGATTGTAGATATTTAACATTTAGTCAGAGGATAATAATTCTTGTCTTCATTTAAACGGCTAATTAGGGAAGGATATAATACAAATCTAATTAGAAATGACTTTTTTTTAGGCAGGCACATGATAATATTTACTAAGAATTTGCTTTCTTTTCAATTGTTCCTCAGAAGTGAAATATGCCAGGTAAAGATTTGTTATCTTTAGTTTTTTTTTAATGTGACAAATACCCTTGAAGACAATTCATTTCCTGAATCACTGTCTCTTGTATAATA... |
Task1_train_41933 | This variant is present on Chromosome 12. Is the change likely to result in a pathogenic outcome? | Benign | AATTCAGAAACTTGTTGTTTCCTGTACTTAAAAAATCTAAAAAAGAATTATGTGCTTTTTAATGATAAAGATTAGATATTAAAATTTTCTGTATTCAGCGACATTGGAGGTGATAATGAGAGGTAGCTGGAGACAGTTACATATCAAATTCTTTTGCTTCTTAGGGTTATTTTCTATTCAACTTTGCCTCAGCAACTTGAGTTAAATTTGGTAGTCTATATTATCTGACAATAATACTGATATTGCTGGAATTTTTACAATCAGAACAGAGTTTTACTCAAATTTCTTGCCCTTTAAAGTACATTATGCTGCACCCTTTA... | AATTCAGAAACTTGTTGTTTCCTGTACTTAAAAAATCTAAAAAAGAATTATGTGCTTTTTAATGATAAAGATTAGATATTAAAATTTTCTGTATTCAGCGACATTGGAGGTGATAATGAGAGGTAGCTGGAGACAGTTACATATCAAATTCTTTTGCTTCTTAGGGTTATTTTCTATTCAACTTTGCCTCAGCAACTTGAGTTAAATTTGGTAGTCTATATTATCTGACAATAATACTGATATTGCTGGAATTTTTACAATCAGAACAGAGTTTTACTCAAATTTCTTGCCCTTTAAAGTACATTATGCTGCACCCTTTA... |
Task1_train_41934 | This mutation is located on Chromosome 12. Is it associated with a disease or is it a benign polymorphism? | Benign | TAGATATTAAAATTTTCTGTATTCAGCGACATTGGAGGTGATAATGAGAGGTAGCTGGAGACAGTTACATATCAAATTCTTTTGCTTCTTAGGGTTATTTTCTATTCAACTTTGCCTCAGCAACTTGAGTTAAATTTGGTAGTCTATATTATCTGACAATAATACTGATATTGCTGGAATTTTTACAATCAGAACAGAGTTTTACTCAAATTTCTTGCCCTTTAAAGTACATTATGCTGCACCCTTTATGAAATCCACTCAAGTTTTTAAAAAGAATGGTGAACGACTTAGGGAGGAAGAGAGCTGAGCAATGAAAAAAG... | TAGATATTAAAATTTTCTGTATTCAGCGACATTGGAGGTGATAATGAGAGGTAGCTGGAGACAGTTACATATCAAATTCTTTTGCTTCTTAGGGTTATTTTCTATTCAACTTTGCCTCAGCAACTTGAGTTAAATTTGGTAGTCTATATTATCTGACAATAATACTGATATTGCTGGAATTTTTACAATCAGAACAGAGTTTTACTCAAATTTCTTGCCCTTTAAAGTACATTATGCTGCACCCTTTATGAAATCCACTCAAGTTTTTAAAAAGAATGGTGAACGACTTAGGGAGGAAGAGAGCTGAGCAATGAAAAAAG... |
Task1_train_41935 | A variant affecting Chromosome 12 has been observed. Determine if it's benign or associated with disease. | Benign | CCTAGAAAACAAAATCGGTTACTTTTGAACTTGTTAAAATTTCTCTCAGCTTCTGGGATTTTCTTTCATTGGTATTGTTTTGCTTACATTCATAAGCTGACTAGAATATCAAGAAATGACCTGAAAATAATTGTACAACTTAAATTCGAGCTATAGAAGACAGAGAAGGAAAGAAACAGTGGAACTCCTTCCCCAGGTGGATGACTTAATAAGGATAAGGAGGAGAGAAGCTTGCTGGAAACATCAAGGAGAAGGGGTCCTGGATATTCTTACAATGTGAACATGGGTCTCAGATTCTAGAGTCCCAAACACTCAGAAAG... | CCTAGAAAACAAAATCGGTTACTTTTGAACTTGTTAAAATTTCTCTCAGCTTCTGGGATTTTCTTTCATTGGTATTGTTTTGCTTACATTCATAAGCTGACTAGAATATCAAGAAATGACCTGAAAATAATTGTACAACTTAAATTCGAGCTATAGAAGACAGAGAAGGAAAGAAACAGTGGAACTCCTTCCCCAGGTGGATGACTTAATAAGGATAAGGAGGAGAGAAGCTTGCTGGAAACATCAAGGAGAAGGGGTCCTGGATATTCTTACAATGTGAACATGGGTCTCAGATTCTAGAGTCCCAAACACTCAGAAAG... |
Task1_train_41936 | Consider this mutation on Chromosome 12. Is this a benign change or a disease-causing variant? | Benign | AAGAACTTATATTCAGAATGATATGGTCTGGCTGTGTCCCCACCCAAATCTCATCTTGAATTGTAGCTCCCATAATTCCCATGTGTTATGGGAGGGACTCAGTGGGAGATAATTGAATGATGGGGGTGGTTTCCCCCATACTGTTCTCATGGTAGTGAATAAGTCTCATGAAACTTGATGTTTTTATAAGGGGTTTCCCCTTTCGCTTGGCTGTCATTCTCTCTTCACTGCCACCATGTAAGACGTGACTTTTGTCTCTGCCATTATTGTGAGGCCTTTCCAGCCATGTGGAACTGTCAGTCAATTAAACCTCTTTTTCT... | AAGAACTTATATTCAGAATGATATGGTCTGGCTGTGTCCCCACCCAAATCTCATCTTGAATTGTAGCTCCCATAATTCCCATGTGTTATGGGAGGGACTCAGTGGGAGATAATTGAATGATGGGGGTGGTTTCCCCCATACTGTTCTCATGGTAGTGAATAAGTCTCATGAAACTTGATGTTTTTATAAGGGGTTTCCCCTTTCGCTTGGCTGTCATTCTCTCTTCACTGCCACCATGTAAGACGTGACTTTTGTCTCTGCCATTATTGTGAGGCCTTTCCAGCCATGTGGAACTGTCAGTCAATTAAACCTCTTTTTCT... |
Task1_train_41937 | Assess the clinical impact of this variant found on Chromosome 12. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CTTCTTCTTGGATAATCCTGTAACTTCAATCTGAAACCAGAACAGAAATGTGCACCCAACTGTAGATTTTGTGATGTGTTACATTTTCATTGGTTCACCACCCCAATATAGTTCATATTCATTCATTCACCAATTAACTTGTTCATCAAAGTATCATTTTTCAATACCTATTCTATGTGCTATCTTTATGTCTTGGGAGTCTACAGTAAGCAAGATCTATATGATCTCTACTTTTATGGTATTTACATTGTACCAGGTAAGATATATGATAAACAAACAAATCAGATGTGGAGATGATTTATCTTAAGGTTTAGATAATA... | CTTCTTCTTGGATAATCCTGTAACTTCAATCTGAAACCAGAACAGAAATGTGCACCCAACTGTAGATTTTGTGATGTGTTACATTTTCATTGGTTCACCACCCCAATATAGTTCATATTCATTCATTCACCAATTAACTTGTTCATCAAAGTATCATTTTTCAATACCTATTCTATGTGCTATCTTTATGTCTTGGGAGTCTACAGTAAGCAAGATCTATATGATCTCTACTTTTATGGTATTTACATTGTACCAGGTAAGATATATGATAAACAAACAAATCAGATGTGGAGATGATTTATCTTAAGGTTTAGATAATA... |
Task1_train_41938 | This alteration occurs on Chromosome 12. Is it associated with a disease or is it a benign variant? | Benign | GGATAATCCTGTAACTTCAATCTGAAACCAGAACAGAAATGTGCACCCAACTGTAGATTTTGTGATGTGTTACATTTTCATTGGTTCACCACCCCAATATAGTTCATATTCATTCATTCACCAATTAACTTGTTCATCAAAGTATCATTTTTCAATACCTATTCTATGTGCTATCTTTATGTCTTGGGAGTCTACAGTAAGCAAGATCTATATGATCTCTACTTTTATGGTATTTACATTGTACCAGGTAAGATATATGATAAACAAACAAATCAGATGTGGAGATGATTTATCTTAAGGTTTAGATAATATTGTTAAAA... | GGATAATCCTGTAACTTCAATCTGAAACCAGAACAGAAATGTGCACCCAACTGTAGATTTTGTGATGTGTTACATTTTCATTGGTTCACCACCCCAATATAGTTCATATTCATTCATTCACCAATTAACTTGTTCATCAAAGTATCATTTTTCAATACCTATTCTATGTGCTATCTTTATGTCTTGGGAGTCTACAGTAAGCAAGATCTATATGATCTCTACTTTTATGGTATTTACATTGTACCAGGTAAGATATATGATAAACAAACAAATCAGATGTGGAGATGATTTATCTTAAGGTTTAGATAATATTGTTAAAA... |
Task1_train_41939 | This variant lies on Chromosome 12. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ACTGTAGATTTTGTGATGTGTTACATTTTCATTGGTTCACCACCCCAATATAGTTCATATTCATTCATTCACCAATTAACTTGTTCATCAAAGTATCATTTTTCAATACCTATTCTATGTGCTATCTTTATGTCTTGGGAGTCTACAGTAAGCAAGATCTATATGATCTCTACTTTTATGGTATTTACATTGTACCAGGTAAGATATATGATAAACAAACAAATCAGATGTGGAGATGATTTATCTTAAGGTTTAGATAATATTGTTAAAATTGCATAACACCAGAAATTAATACAGTCACACAGAATTTAGCTGTTGAA... | ACTGTAGATTTTGTGATGTGTTACATTTTCATTGGTTCACCACCCCAATATAGTTCATATTCATTCATTCACCAATTAACTTGTTCATCAAAGTATCATTTTTCAATACCTATTCTATGTGCTATCTTTATGTCTTGGGAGTCTACAGTAAGCAAGATCTATATGATCTCTACTTTTATGGTATTTACATTGTACCAGGTAAGATATATGATAAACAAACAAATCAGATGTGGAGATGATTTATCTTAAGGTTTAGATAATATTGTTAAAATTGCATAACACCAGAAATTAATACAGTCACACAGAATTTAGCTGTTGAA... |
Task1_train_41940 | A variant has been detected on Chromosome 12. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GTTAAAATTGCATAACACCAGAAATTAATACAGTCACACAGAATTTAGCTGTTGAACTAGGTTATACATTTTCTTCTTGTAATAGAACTTGCTATTAGTGAATATGTCAACACACTTTCTCTCATTTCATTATTTACACCAAGATTATAATAAAACATATCTTTAAGACATTTCCTATCATTAATATATAGATTTCATAGATGCCATAGTTTCTATACCCTCTTTAGATTGAGCTTCTTTTTAAAGTAAGGAAAATTTGAGCTTTTTGAGGAATTTTAAGGATGGAAGATAAAGGAGGAAATTGACAATTCAGGAGCTCA... | GTTAAAATTGCATAACACCAGAAATTAATACAGTCACACAGAATTTAGCTGTTGAACTAGGTTATACATTTTCTTCTTGTAATAGAACTTGCTATTAGTGAATATGTCAACACACTTTCTCTCATTTCATTATTTACACCAAGATTATAATAAAACATATCTTTAAGACATTTCCTATCATTAATATATAGATTTCATAGATGCCATAGTTTCTATACCCTCTTTAGATTGAGCTTCTTTTTAAAGTAAGGAAAATTTGAGCTTTTTGAGGAATTTTAAGGATGGAAGATAAAGGAGGAAATTGACAATTCAGGAGCTCA... |
Task1_train_41941 | This variant is located on Chromosome 12. Evaluate its biological effect and specify any disease association. | Benign | AAATTAATACAGTCACACAGAATTTAGCTGTTGAACTAGGTTATACATTTTCTTCTTGTAATAGAACTTGCTATTAGTGAATATGTCAACACACTTTCTCTCATTTCATTATTTACACCAAGATTATAATAAAACATATCTTTAAGACATTTCCTATCATTAATATATAGATTTCATAGATGCCATAGTTTCTATACCCTCTTTAGATTGAGCTTCTTTTTAAAGTAAGGAAAATTTGAGCTTTTTGAGGAATTTTAAGGATGGAAGATAAAGGAGGAAATTGACAATTCAGGAGCTCAGAGGTGGCTTAGACAAAAAAC... | AAATTAATACAGTCACACAGAATTTAGCTGTTGAACTAGGTTATACATTTTCTTCTTGTAATAGAACTTGCTATTAGTGAATATGTCAACACACTTTCTCTCATTTCATTATTTACACCAAGATTATAATAAAACATATCTTTAAGACATTTCCTATCATTAATATATAGATTTCATAGATGCCATAGTTTCTATACCCTCTTTAGATTGAGCTTCTTTTTAAAGTAAGGAAAATTTGAGCTTTTTGAGGAATTTTAAGGATGGAAGATAAAGGAGGAAATTGACAATTCAGGAGCTCAGAGGTGGCTTAGACAAAAAAC... |
Task1_train_41942 | This mutation is located on Chromosome 12. Is it associated with a disease or is it a benign polymorphism? | Benign | AGTTTCTATACCCTCTTTAGATTGAGCTTCTTTTTAAAGTAAGGAAAATTTGAGCTTTTTGAGGAATTTTAAGGATGGAAGATAAAGGAGGAAATTGACAATTCAGGAGCTCAGAGGTGGCTTAGACAAAAAACTGAAATATATAACATCAGATCTCAACTTCAAAAAGGTTTTTGTTTAATTCAAAAACTGGAAGAGATGACTTTTCTAATTGCGTATGGAAACTTATAACAGCACTGAAAAGAGCTCATGATCATGTTTCTTCATCCTTTTTATAGAAATGATTTTTTCTAAGCTATTAACATACTATATTAAATATA... | AGTTTCTATACCCTCTTTAGATTGAGCTTCTTTTTAAAGTAAGGAAAATTTGAGCTTTTTGAGGAATTTTAAGGATGGAAGATAAAGGAGGAAATTGACAATTCAGGAGCTCAGAGGTGGCTTAGACAAAAAACTGAAATATATAACATCAGATCTCAACTTCAAAAAGGTTTTTGTTTAATTCAAAAACTGGAAGAGATGACTTTTCTAATTGCGTATGGAAACTTATAACAGCACTGAAAAGAGCTCATGATCATGTTTCTTCATCCTTTTTATAGAAATGATTTTTTCTAAGCTATTAACATACTATATTAAATATA... |
Task1_train_41943 | A genetic alteration is present on Chromosome 12. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GTCATTTTTGTTTAAATAATCAACTAGAAAATATCATAATACAAATAATTGACAATAGAAAAAAATACATATTCAAATAGACCAAAGTTGTTTATATGATTTTTCAAACTATTATAATAGGTGCCATCTAATTTTGGTGTTCTACCTTGTCTCCAACTCAGACACCTGATACAGCTGCATCAAGACTATATTATTGTCATATTTCCCCTAAAATTGTGGAATAGCCAAACTTTTCCTTAGGAGAAGGATTCTGCTTGGATAAGCCTGTAATCTTAACCTGAGACTGGAACAGGGGAATTCATGCAACTGCAGATTTTGTG... | GTCATTTTTGTTTAAATAATCAACTAGAAAATATCATAATACAAATAATTGACAATAGAAAAAAATACATATTCAAATAGACCAAAGTTGTTTATATGATTTTTCAAACTATTATAATAGGTGCCATCTAATTTTGGTGTTCTACCTTGTCTCCAACTCAGACACCTGATACAGCTGCATCAAGACTATATTATTGTCATATTTCCCCTAAAATTGTGGAATAGCCAAACTTTTCCTTAGGAGAAGGATTCTGCTTGGATAAGCCTGTAATCTTAACCTGAGACTGGAACAGGGGAATTCATGCAACTGCAGATTTTGTG... |
Task1_train_41944 | With a mutation on Chromosome 12, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TATCATAATACAAATAATTGACAATAGAAAAAAATACATATTCAAATAGACCAAAGTTGTTTATATGATTTTTCAAACTATTATAATAGGTGCCATCTAATTTTGGTGTTCTACCTTGTCTCCAACTCAGACACCTGATACAGCTGCATCAAGACTATATTATTGTCATATTTCCCCTAAAATTGTGGAATAGCCAAACTTTTCCTTAGGAGAAGGATTCTGCTTGGATAAGCCTGTAATCTTAACCTGAGACTGGAACAGGGGAATTCATGCAACTGCAGATTTTGTGTGAGTTTCCTTTTCACTGGTTTACCACATCA... | TATCATAATACAAATAATTGACAATAGAAAAAAATACATATTCAAATAGACCAAAGTTGTTTATATGATTTTTCAAACTATTATAATAGGTGCCATCTAATTTTGGTGTTCTACCTTGTCTCCAACTCAGACACCTGATACAGCTGCATCAAGACTATATTATTGTCATATTTCCCCTAAAATTGTGGAATAGCCAAACTTTTCCTTAGGAGAAGGATTCTGCTTGGATAAGCCTGTAATCTTAACCTGAGACTGGAACAGGGGAATTCATGCAACTGCAGATTTTGTGTGAGTTTCCTTTTCACTGGTTTACCACATCA... |
Task1_train_41945 | This is a variant located on Chromosome 12. Is this mutation a likely cause of disease or not? | Benign | AAATAGACCAAGGTTGTTTATACGCTTTCTAAAAATATTGTAATAGGCGCCATCTAATTTTGATGTTCTACCTTGTCTCCAATTCAGACACCTGATACAGTTGCATCAAGACTATATTATTGTCATATTTCCCCTAAAATTGTGGAATAGCCAAACTTTTCCTCTGCGGAAGGATTCTGCTTGGATAAGCCTGTAACCTTAACCTGAGAACAGAACAGGGGAATTCATGCAACTGCAGATTTTGTGATGAGTTTCCCTTTCATTGGTTTACCACATCAGCTTACCCATTTTATCCACCCATTTATTTGTTCATTAAAATA... | AAATAGACCAAGGTTGTTTATACGCTTTCTAAAAATATTGTAATAGGCGCCATCTAATTTTGATGTTCTACCTTGTCTCCAATTCAGACACCTGATACAGTTGCATCAAGACTATATTATTGTCATATTTCCCCTAAAATTGTGGAATAGCCAAACTTTTCCTCTGCGGAAGGATTCTGCTTGGATAAGCCTGTAACCTTAACCTGAGAACAGAACAGGGGAATTCATGCAACTGCAGATTTTGTGATGAGTTTCCCTTTCATTGGTTTACCACATCAGCTTACCCATTTTATCCACCCATTTATTTGTTCATTAAAATA... |
Task1_train_41946 | A variant on Chromosome 12 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TATCAGGTATTACGTTAAAAACATTTTAGTAAAGTAGCTGGTTACTAACTCAATTTTTTGAAATGAAATGCCATTTTTATATGATAATCAACTAGAAAATATCATAATACAAATATATAATTCACAATAGAAAAAAATACATACGCAAATAGACCAAAGTCTTTTATATGCTTTTTTAAAATATTGTAATAGTGGCATCTAATTTTGATGTTCTACCTTGTCGCCAATTCAGACACCTGATACAGCTGCATCAAGACTATATTATTGTGATATTTCCCCTAAAATTGTGGAATAGCCAAACTTTTCCTCTGAGGAAGGAT... | TATCAGGTATTACGTTAAAAACATTTTAGTAAAGTAGCTGGTTACTAACTCAATTTTTTGAAATGAAATGCCATTTTTATATGATAATCAACTAGAAAATATCATAATACAAATATATAATTCACAATAGAAAAAAATACATACGCAAATAGACCAAAGTCTTTTATATGCTTTTTTAAAATATTGTAATAGTGGCATCTAATTTTGATGTTCTACCTTGTCGCCAATTCAGACACCTGATACAGCTGCATCAAGACTATATTATTGTGATATTTCCCCTAAAATTGTGGAATAGCCAAACTTTTCCTCTGAGGAAGGAT... |
Task1_train_41947 | A mutation has occurred on Chromosome 12. What is the medical relevance of this mutation? | Benign | ACACAAAAATATAAATAGTATTTTGTGTTTTAAAGAATACAAGGTTAAGTCATTTATATAAAAGAATATCTTTAAAATAAACTCAGTATCTAAGTCTAAAATATATTCAGCTTGATTTGCACATTACCTTTTATCAAGGCAAGAAAATTATAATTATAATCTTTGACAAAATACTAAATTAGTGATCAAAATAATATATGTACATTTTATTTTGTAAAATGCAAATTACTAAAAAAAGATGTTGTATTATCATTAAAACAATCATCAACATCATTGTTATTGATACATGATACCATATAGCCCAGATGTACTTACAATTT... | ACACAAAAATATAAATAGTATTTTGTGTTTTAAAGAATACAAGGTTAAGTCATTTATATAAAAGAATATCTTTAAAATAAACTCAGTATCTAAGTCTAAAATATATTCAGCTTGATTTGCACATTACCTTTTATCAAGGCAAGAAAATTATAATTATAATCTTTGACAAAATACTAAATTAGTGATCAAAATAATATATGTACATTTTATTTTGTAAAATGCAAATTACTAAAAAAAGATGTTGTATTATCATTAAAACAATCATCAACATCATTGTTATTGATACATGATACCATATAGCCCAGATGTACTTACAATTT... |
Task1_train_41948 | Here is a variant on Chromosome 12. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CTCAGTATCTAAGTCTAAAATATATTCAGCTTGATTTGCACATTACCTTTTATCAAGGCAAGAAAATTATAATTATAATCTTTGACAAAATACTAAATTAGTGATCAAAATAATATATGTACATTTTATTTTGTAAAATGCAAATTACTAAAAAAAGATGTTGTATTATCATTAAAACAATCATCAACATCATTGTTATTGATACATGATACCATATAGCCCAGATGTACTTACAATTTCATTTTATGCATATGGGGAGGGGGAAGTACTAATAATTCTAACATCATTTCCGGCTCCAGGGCACAGCTGTGGAGTCATGC... | CTCAGTATCTAAGTCTAAAATATATTCAGCTTGATTTGCACATTACCTTTTATCAAGGCAAGAAAATTATAATTATAATCTTTGACAAAATACTAAATTAGTGATCAAAATAATATATGTACATTTTATTTTGTAAAATGCAAATTACTAAAAAAAGATGTTGTATTATCATTAAAACAATCATCAACATCATTGTTATTGATACATGATACCATATAGCCCAGATGTACTTACAATTTCATTTTATGCATATGGGGAGGGGGAAGTACTAATAATTCTAACATCATTTCCGGCTCCAGGGCACAGCTGTGGAGTCATGC... |
Task1_train_41949 | This variant is found on Chromosome 12. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TGATTTGCACATTACCTTTTATCAAGGCAAGAAAATTATAATTATAATCTTTGACAAAATACTAAATTAGTGATCAAAATAATATATGTACATTTTATTTTGTAAAATGCAAATTACTAAAAAAAGATGTTGTATTATCATTAAAACAATCATCAACATCATTGTTATTGATACATGATACCATATAGCCCAGATGTACTTACAATTTCATTTTATGCATATGGGGAGGGGGAAGTACTAATAATTCTAACATCATTTCCGGCTCCAGGGCACAGCTGTGGAGTCATGCCCTCAACTATAGCTTCATCAAGATTAATTTA... | TGATTTGCACATTACCTTTTATCAAGGCAAGAAAATTATAATTATAATCTTTGACAAAATACTAAATTAGTGATCAAAATAATATATGTACATTTTATTTTGTAAAATGCAAATTACTAAAAAAAGATGTTGTATTATCATTAAAACAATCATCAACATCATTGTTATTGATACATGATACCATATAGCCCAGATGTACTTACAATTTCATTTTATGCATATGGGGAGGGGGAAGTACTAATAATTCTAACATCATTTCCGGCTCCAGGGCACAGCTGTGGAGTCATGCCCTCAACTATAGCTTCATCAAGATTAATTTA... |
Task1_train_41950 | Located on Chromosome 12, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TCCATTCAGGTTTCATTAAAGAAAGGTGAGGAACATAGGGAGGGAGGGAAGTGATCACTGTTAAAATAGGGTCAATGGGATAGAGAGGGCTCTGGGAATAAGAAGCATAGAACCCTGTTTGTTCCCTTGAAACCAAACTCAGTTTCTTAGAAATTATAAGGATTTCTTTTAGTTTCTGTGACTTATTTTCCATTTGTTGTGGTTTTTGTCCTTAAAATTACTGGAATATCAGTAAACAATCTGAAAATAATTTTAGATTTTCAATTTGTGCTGTAGAAGTCAGGGAGGAGCCAGGTGTGGTGGCTCATGCCTGTAATCCC... | TCCATTCAGGTTTCATTAAAGAAAGGTGAGGAACATAGGGAGGGAGGGAAGTGATCACTGTTAAAATAGGGTCAATGGGATAGAGAGGGCTCTGGGAATAAGAAGCATAGAACCCTGTTTGTTCCCTTGAAACCAAACTCAGTTTCTTAGAAATTATAAGGATTTCTTTTAGTTTCTGTGACTTATTTTCCATTTGTTGTGGTTTTTGTCCTTAAAATTACTGGAATATCAGTAAACAATCTGAAAATAATTTTAGATTTTCAATTTGTGCTGTAGAAGTCAGGGAGGAGCCAGGTGTGGTGGCTCATGCCTGTAATCCC... |
Task1_train_41951 | A mutation on Chromosome 12 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GCCGAGGCGGGTGGATCACAAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCTGTCTCTACTAAAAATAGAAAAAATTAGCTGGGCGCAGTGGCAGGTGCCTGTAGTCCCAGATACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAACTGCATTCCAGCCTGGGCGATAAAGCAAGACTCCGTCTCAAAAAAAAAGAAATATATTATTTACAGAACCAAGATCAAGAAAACTGGCAGGTAGTTAAGTAACAGAGGAGTAATCATGTTGACAGTTGAAGAAAAAGCTCTTCACCAACCAACC... | GCCGAGGCGGGTGGATCACAAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCTGTCTCTACTAAAAATAGAAAAAATTAGCTGGGCGCAGTGGCAGGTGCCTGTAGTCCCAGATACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAACTGCATTCCAGCCTGGGCGATAAAGCAAGACTCCGTCTCAAAAAAAAAGAAATATATTATTTACAGAACCAAGATCAAGAAAACTGGCAGGTAGTTAAGTAACAGAGGAGTAATCATGTTGACAGTTGAAGAAAAAGCTCTTCACCAACCAACC... |
Task1_train_41952 | Chromosome 12 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | AGCCTTTGCAGATTAAAAGAACGAATGAATGAAGGAACAAATGAACGAATGAACGAATGAATGAAAAAAATTAAAAACAGGTTTAAGGATGCTGGTACCATACAGGGAAGAAGGAAAGAAGGGGTGACGGAGCCAATGACACCACTGTATGTATGTGTCTGTATGTATATATATATATATGCATAGCTCAAGAAAACATAACAAAGAGGCCAGAAAAGGAATTCTAATTTTAAAATCTACTGCACTCACTGCAAACTAGGAAAATAAATCCTATTTAATCAATGTTATATATTGTTATATAAAGTGTATTAATTTTTATT... | AGCCTTTGCAGATTAAAAGAACGAATGAATGAAGGAACAAATGAACGAATGAACGAATGAATGAAAAAAATTAAAAACAGGTTTAAGGATGCTGGTACCATACAGGGAAGAAGGAAAGAAGGGGTGACGGAGCCAATGACACCACTGTATGTATGTGTCTGTATGTATATATATATATATGCATAGCTCAAGAAAACATAACAAAGAGGCCAGAAAAGGAATTCTAATTTTAAAATCTACTGCACTCACTGCAAACTAGGAAAATAAATCCTATTTAATCAATGTTATATATTGTTATATAAAGTGTATTAATTTTTATT... |
Task1_train_41953 | A sequence alteration has been identified on Chromosome 12. Is it disease-inducing or harmless? | Benign | ATCGAGACCATCCTGACTAACACAGTGAAACCCCGTCTTTACTAAAAATATAAAAAATTAGCTGGGCGTGTTGGCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGGGAACCCAGGAGGCGGAGCTGGCAGTGAGCCGAGATCGCGCCACTGCACTCTAGCCTGGGTGACAGAGCAAGACTCTGTCACACACACACACACACACACACACACACACACACACACACAAGTTAACTAGAACAGATCCCAAGTGGATATGGCCATTTATCAGAACTGACTTATCATTGTCTCCATGTGGGCTAA... | ATCGAGACCATCCTGACTAACACAGTGAAACCCCGTCTTTACTAAAAATATAAAAAATTAGCTGGGCGTGTTGGCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGGGAACCCAGGAGGCGGAGCTGGCAGTGAGCCGAGATCGCGCCACTGCACTCTAGCCTGGGTGACAGAGCAAGACTCTGTCACACACACACACACACACACACACACACACACACACACACAAGTTAACTAGAACAGATCCCAAGTGGATATGGCCATTTATCAGAACTGACTTATCATTGTCTCCATGTGGGCTAA... |
Task1_train_41954 | Chromosome 12 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | AGAAGCCAGTAGCAAGTATCAGGTCTCCAGGTCACCCACACTTCTGCCTGACTCGGCTACTGCTAATTCAGGGATTCCCATGATCCTACCCCCTCAGATTTGATAATTTGCAAGAACAACTAATAGAACTAAGGAAAATGCTGTATTTACTATTACAGTTTATAATAAGGGATACAAATGAACAGCCAAAAGAGGCTCCTAGAGTCCCAAGTGCAGGAGACTTTGTCCCTGGGGAACTGAGGTGCATAATTCTCTTGACACTGGGATGTGTTCACCAACTTGGATGCTTCCCGATCATCTAGGGGTTTTTATGATGGTCT... | AGAAGCCAGTAGCAAGTATCAGGTCTCCAGGTCACCCACACTTCTGCCTGACTCGGCTACTGCTAATTCAGGGATTCCCATGATCCTACCCCCTCAGATTTGATAATTTGCAAGAACAACTAATAGAACTAAGGAAAATGCTGTATTTACTATTACAGTTTATAATAAGGGATACAAATGAACAGCCAAAAGAGGCTCCTAGAGTCCCAAGTGCAGGAGACTTTGTCCCTGGGGAACTGAGGTGCATAATTCTCTTGACACTGGGATGTGTTCACCAACTTGGATGCTTCCCGATCATCTAGGGGTTTTTATGATGGTCT... |
Task1_train_41955 | Here is a mutation located on Chromosome 12. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CCCTACCCTGGGCTCCAATGATCCGCAGCCCCGCGCATTTCGAAAGCCCGCCCGGCTCGCCGGCGCCTGGGGAGGGCCACGGCGGCGCGCAGCCCGGGCCCCGCACCACGGCCGCCCGCGTGGGTCCCCTCTGCCCTCACCCCCGCTCGGCAACGTGCCCCCATCGCAACCCCGGCCGCCCGGCGCGGGGGCCTGGGACGGGGAAGAACTGGGGAAATGTGGGTTTGGGGGCGTGTTTGGGGGACTCCGGGAGCGTGGGCTTCACAGGCGAGGAGCGGGGCGAGAGGCCTCTCAGGCCGGGGTGCGCCCACCGCCCCGGC... | CCCTACCCTGGGCTCCAATGATCCGCAGCCCCGCGCATTTCGAAAGCCCGCCCGGCTCGCCGGCGCCTGGGGAGGGCCACGGCGGCGCGCAGCCCGGGCCCCGCACCACGGCCGCCCGCGTGGGTCCCCTCTGCCCTCACCCCCGCTCGGCAACGTGCCCCCATCGCAACCCCGGCCGCCCGGCGCGGGGGCCTGGGACGGGGAAGAACTGGGGAAATGTGGGTTTGGGGGCGTGTTTGGGGGACTCCGGGAGCGTGGGCTTCACAGGCGAGGAGCGGGGCGAGAGGCCTCTCAGGCCGGGGTGCGCCCACCGCCCCGGC... |
Task1_train_41956 | A variant was discovered on Chromosome 12. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TCACATGGGCTACAATTGCTACTTCAAATGAAAACCTGGGAAGCCAATGCCCTATTGTGGTTGAAAGTGTACAATTAGCTCCTCATGCAGCCTGACCCCACTGATTTTTCTGATGCATGTGACCTGGAGTGTGCCCTTTCTGAGACCGCCAATGTCTTCTCCACAGCTGGAGATGCCCAAAACTGCACGCAGCACTTCCTGTGGGTGTGGCCTTGCATTCTTAGGACTGCAGGGTACCCGCTGCATGCCAAATGATCCCAGGCTCCAGCCACTCACAGATTCACAACGCTTTTAAAAATACAGCAGTGGAGTATGAGCGG... | TCACATGGGCTACAATTGCTACTTCAAATGAAAACCTGGGAAGCCAATGCCCTATTGTGGTTGAAAGTGTACAATTAGCTCCTCATGCAGCCTGACCCCACTGATTTTTCTGATGCATGTGACCTGGAGTGTGCCCTTTCTGAGACCGCCAATGTCTTCTCCACAGCTGGAGATGCCCAAAACTGCACGCAGCACTTCCTGTGGGTGTGGCCTTGCATTCTTAGGACTGCAGGGTACCCGCTGCATGCCAAATGATCCCAGGCTCCAGCCACTCACAGATTCACAACGCTTTTAAAAATACAGCAGTGGAGTATGAGCGG... |
Task1_train_41957 | A variant found on Chromosome 12 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CAGTGATGTGATTATGCCTCACCAACAAGCAATGGAAAACTTTTATGGGAAAAAGTGTGTAGTATCAATTTCCAACTTTTGGTCAACTGAACTGAAAAGAATCAATGGATGTATTTATCTGAACAGGATTTAATTTGAATGCGCAACTAGCCACAGATTACAGCTCAAAAAAAGTGTATGTACTTAAAAGGAAGCTTATGTGAATTTTTTTGAGCCTGGTGAACATTATGTGTGCTGTACAATATATAAAATAACATCATCATTACATATTAGAAATAAAATGTGAGAAATCAGATGCCTATTAAGACACAAAAATTGAT... | CAGTGATGTGATTATGCCTCACCAACAAGCAATGGAAAACTTTTATGGGAAAAAGTGTGTAGTATCAATTTCCAACTTTTGGTCAACTGAACTGAAAAGAATCAATGGATGTATTTATCTGAACAGGATTTAATTTGAATGCGCAACTAGCCACAGATTACAGCTCAAAAAAAGTGTATGTACTTAAAAGGAAGCTTATGTGAATTTTTTTGAGCCTGGTGAACATTATGTGTGCTGTACAATATATAAAATAACATCATCATTACATATTAGAAATAAAATGTGAGAAATCAGATGCCTATTAAGACACAAAAATTGAT... |
Task1_train_41958 | Here is a mutation located on Chromosome 12. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CATTGAGAAATCATTCGAATATTTACATCAAGTGCACAAAAGAAGTTTAAGCCACAGCCCTTGCCCTTCATGAACTTACAGCTCAGTTGTGGGAAAACAAAATAAACACACGCTTGCCCTTCAAACAATTAAATAACAGGAGGATAAAAGTGAATGTCCACAGGAGTAATCCTGCCAGAGCTGTAGGTGGTTAAGGGCTGGAGGATCTAGTGCAGCTTCTTCGGTCTCTAGAAGAGCCTTCCCAGCAGCAGGGGTGAGTGGAGCTTGAGGTGAACCTGGAGGAGTGGTAGATGGCTGAGGTTTCTCTTAGTGAAAGAGGG... | CATTGAGAAATCATTCGAATATTTACATCAAGTGCACAAAAGAAGTTTAAGCCACAGCCCTTGCCCTTCATGAACTTACAGCTCAGTTGTGGGAAAACAAAATAAACACACGCTTGCCCTTCAAACAATTAAATAACAGGAGGATAAAAGTGAATGTCCACAGGAGTAATCCTGCCAGAGCTGTAGGTGGTTAAGGGCTGGAGGATCTAGTGCAGCTTCTTCGGTCTCTAGAAGAGCCTTCCCAGCAGCAGGGGTGAGTGGAGCTTGAGGTGAACCTGGAGGAGTGGTAGATGGCTGAGGTTTCTCTTAGTGAAAGAGGG... |
Task1_train_41959 | A mutation has occurred on Chromosome 12. What is the medical relevance of this mutation? | Benign | TGAATGGAATGGAATCACTGGGTCATATGACAACTCTGTACTTCACATATTGTGGAACTGCCTGTTTTCCAAAGCAGCTGCACCTATTTGCAATCCCACTATCATTGTATGAAAGTTCCAGTTTTTTCACATCCTTGCCAACACTCATTATTCTCGTTGATTGTAGCCGTCCTGTCGTGTGTGCAGTGTTATTTCATTGTGGTTTTGACTTGCGTTTCCCTGATGTCTCATGATGTTTATTGCTTATGGACTTTTGGCTTAGGGGTCTCTTTCTGGAAATGTCTGTTCAAGTCCTTTGACCATTTTTAAATTGGGTGATT... | TGAATGGAATGGAATCACTGGGTCATATGACAACTCTGTACTTCACATATTGTGGAACTGCCTGTTTTCCAAAGCAGCTGCACCTATTTGCAATCCCACTATCATTGTATGAAAGTTCCAGTTTTTTCACATCCTTGCCAACACTCATTATTCTCGTTGATTGTAGCCGTCCTGTCGTGTGTGCAGTGTTATTTCATTGTGGTTTTGACTTGCGTTTCCCTGATGTCTCATGATGTTTATTGCTTATGGACTTTTGGCTTAGGGGTCTCTTTCTGGAAATGTCTGTTCAAGTCCTTTGACCATTTTTAAATTGGGTGATT... |
Task1_train_41960 | A mutation has occurred on Chromosome 12. What is the medical relevance of this mutation? | Benign | GGAGTTACTAACAATGAGTATTAAAATCAGAAAGATATGGAAAAATATAGAAAGAAAAATGTATTTTAATGAGTTTGTGATCTGTTTACAAGAAAGCAAACAAATTTTTATTTCACTGAAACTGAGGTTGAGAGATGAGGTCTTAAAACACTTAAAATGAGCAAAGGGTAGTAAATGGAGAGTTAATTTTCAAATAATTTATTTTAAAGTTCAAAAATAGTTTTAGTAATTCTGTGTACTGTGTTAGCTTATTGTTTATCTTACAGTGAAAAAAATACTTCTAGCGCCTTAATAGGTATTCATCAATGATCCTTGTCCTT... | GGAGTTACTAACAATGAGTATTAAAATCAGAAAGATATGGAAAAATATAGAAAGAAAAATGTATTTTAATGAGTTTGTGATCTGTTTACAAGAAAGCAAACAAATTTTTATTTCACTGAAACTGAGGTTGAGAGATGAGGTCTTAAAACACTTAAAATGAGCAAAGGGTAGTAAATGGAGAGTTAATTTTCAAATAATTTATTTTAAAGTTCAAAAATAGTTTTAGTAATTCTGTGTACTGTGTTAGCTTATTGTTTATCTTACAGTGAAAAAAATACTTCTAGCGCCTTAATAGGTATTCATCAATGATCCTTGTCCTT... |
Task1_train_41961 | A genetic alteration is present on Chromosome 12. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | AGGCTGTATCTTACAATTCCCTTACTGCACTGGGTAAGTGTTAACTTAGTTTTTGTTGTTTGCTCTTTTGCTTTAAATATTCTCCAAATTACCATTTATGCAACATGGTTAGGGTTAATACTGCATGGTATTCATTTATCTTGTTTCATGAACTTTCCAGTACTGTACAAGGTCAACAAAGTAATGCCTGTGGTATCCTCATCTCTCACTTTTTTACTCTGTGATTTTAGCACAGTAAGGTACTGCAAAGACCTTCCTTCCAAATGTTCTCCTTGACTTTATTTCTTGGGCCAATTCAGTATCCTCAACATCCTAAGATT... | AGGCTGTATCTTACAATTCCCTTACTGCACTGGGTAAGTGTTAACTTAGTTTTTGTTGTTTGCTCTTTTGCTTTAAATATTCTCCAAATTACCATTTATGCAACATGGTTAGGGTTAATACTGCATGGTATTCATTTATCTTGTTTCATGAACTTTCCAGTACTGTACAAGGTCAACAAAGTAATGCCTGTGGTATCCTCATCTCTCACTTTTTTACTCTGTGATTTTAGCACAGTAAGGTACTGCAAAGACCTTCCTTCCAAATGTTCTCCTTGACTTTATTTCTTGGGCCAATTCAGTATCCTCAACATCCTAAGATT... |
Task1_train_41962 | A genetic alteration is present on Chromosome 12. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TCTTAGGGAGTTTCAAGGGGTCTAGGAATGGGACTGCAGAGAACCAAGTCTACCATTCTGTTATCAGCAACTGTCCAAAGAAGAAAAGACTACTTTAGCAAGCATCTCTCTCTCTTGAGGCATGCTATTATTTTCAGGCTCTTAGGAGCTGGGTTCTCTGTTTTGAATTGCTCTATGCTAAACAGTAACCACCTAATGATTTGACTTCTTGGATGGATTTTCCTAACAAGCAAAGAAGAAGGTAGGTCCACTGCTTGGTAGCATATGAACTGCTTGGCAATGAAACTCCCACCTTTTGTTTTATGCATAAGTCTTAGTGC... | TCTTAGGGAGTTTCAAGGGGTCTAGGAATGGGACTGCAGAGAACCAAGTCTACCATTCTGTTATCAGCAACTGTCCAAAGAAGAAAAGACTACTTTAGCAAGCATCTCTCTCTCTTGAGGCATGCTATTATTTTCAGGCTCTTAGGAGCTGGGTTCTCTGTTTTGAATTGCTCTATGCTAAACAGTAACCACCTAATGATTTGACTTCTTGGATGGATTTTCCTAACAAGCAAAGAAGAAGGTAGGTCCACTGCTTGGTAGCATATGAACTGCTTGGCAATGAAACTCCCACCTTTTGTTTTATGCATAAGTCTTAGTGC... |
Task1_train_41963 | A sequence alteration has been identified on Chromosome 12. Is it disease-inducing or harmless? | Benign | TGTCCTTAAATGTCAGTGTAATAGAATGTGAAAGAATCAAAGCACAGTCTAACTCAGAGAGAGGAGTCCCCAGTCCCCCTCAATGCTAAAACAACTAAGCAAACTAAGACAAAGATGAAATCAAATTGGTTTCAAAGAAAGGATCAGGTCACAAGGACAGAGAAATACTGGGTTATGCCCTTGGTCAGAATTCCTGATAGGGGCCGGACATGATTGCTCACACCTTAATCCCAGCACTTTGGGAGGCTGAGGCTGGAGGACCACTTGAACCCAGGAGCTTAAGACCAGCCTGGGGAATGTAGCAAGATCCCATCTCCATA... | TGTCCTTAAATGTCAGTGTAATAGAATGTGAAAGAATCAAAGCACAGTCTAACTCAGAGAGAGGAGTCCCCAGTCCCCCTCAATGCTAAAACAACTAAGCAAACTAAGACAAAGATGAAATCAAATTGGTTTCAAAGAAAGGATCAGGTCACAAGGACAGAGAAATACTGGGTTATGCCCTTGGTCAGAATTCCTGATAGGGGCCGGACATGATTGCTCACACCTTAATCCCAGCACTTTGGGAGGCTGAGGCTGGAGGACCACTTGAACCCAGGAGCTTAAGACCAGCCTGGGGAATGTAGCAAGATCCCATCTCCATA... |
Task1_train_41964 | A variant was discovered on Chromosome 12. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | ATTAGAGCAAACCATATGTGTACAACTACACGTCTTTCCCCTTTCTCTCCTAGAAAAATAGGAGTTTCTTGATGGCAGTAACTTGCTCATTTATCTCTGAATATTCAAAATATGCTTGGAAAAGAGGCATTAAACAAATGTTCAAAATTCAAAAGGGATGACTTTGCTACAGGATCAAATTTCAATGCATTCCATTCACTTTACATTTTATAATTCTTATTTTATGTAGAGATGGGGTCTCACTATGTTGGCCATGCTGGTCTCAAACTCCTGGCCTCCAGCAATCCTACTGCCTCAGCCTTCCCAAAGTGCTGGCATTA... | ATTAGAGCAAACCATATGTGTACAACTACACGTCTTTCCCCTTTCTCTCCTAGAAAAATAGGAGTTTCTTGATGGCAGTAACTTGCTCATTTATCTCTGAATATTCAAAATATGCTTGGAAAAGAGGCATTAAACAAATGTTCAAAATTCAAAAGGGATGACTTTGCTACAGGATCAAATTTCAATGCATTCCATTCACTTTACATTTTATAATTCTTATTTTATGTAGAGATGGGGTCTCACTATGTTGGCCATGCTGGTCTCAAACTCCTGGCCTCCAGCAATCCTACTGCCTCAGCCTTCCCAAAGTGCTGGCATTA... |
Task1_train_41965 | A variant has been detected on Chromosome 12. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TATTCTTACCACCAGTTATAAATATTTCAAAATATTGATGGAGATACATACTAATTTTTAGCAGAATCTTTAAACTGCCCTTGAAGGTATAAGATCGGTCCTATACCTAAACTTACCTTTGTGTTAGGAAATTCTTGATTTGATTTTAGACTGAATTTGAGTGTCAGAAAGCAATGACGAGATATTGTAGGTTAAAGCTGATAAACCAGGTAGTACATAAAAAAGAAAATAATCTTGAACTGCGAAGGTGAGCTAAGTTGTAATGTTTTGCAACTAGTTTTTTTTCTTTCCTAACACATTAGTGATCATAGTTTTGCAAC... | TATTCTTACCACCAGTTATAAATATTTCAAAATATTGATGGAGATACATACTAATTTTTAGCAGAATCTTTAAACTGCCCTTGAAGGTATAAGATCGGTCCTATACCTAAACTTACCTTTGTGTTAGGAAATTCTTGATTTGATTTTAGACTGAATTTGAGTGTCAGAAAGCAATGACGAGATATTGTAGGTTAAAGCTGATAAACCAGGTAGTACATAAAAAAGAAAATAATCTTGAACTGCGAAGGTGAGCTAAGTTGTAATGTTTTGCAACTAGTTTTTTTTCTTTCCTAACACATTAGTGATCATAGTTTTGCAAC... |
Task1_train_41966 | A mutation on Chromosome 12 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | AGTCACATAAATTGTCTGTTTGTAGAAATTCTTTCTTTTTTTCTTTTTTTGAGATCGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGTGTGAACTTGGCTCACTGCACTACCTCCGCCTCCTGGGTTTAGGCAATTTTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGTGCGTGCCACCATGCCTGGCTAATTTTTGTATTTGTAGTAGAGACGGGGTTTCACCATGCTGGCCAGGCTGGTCTTGAACTCCTGACCTCGTGATCCGTCCTCCTCGGCCTCCCAAAGTGCTGGGATTACAGGGGTGAGCCA... | AGTCACATAAATTGTCTGTTTGTAGAAATTCTTTCTTTTTTTCTTTTTTTGAGATCGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGTGTGAACTTGGCTCACTGCACTACCTCCGCCTCCTGGGTTTAGGCAATTTTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGTGCGTGCCACCATGCCTGGCTAATTTTTGTATTTGTAGTAGAGACGGGGTTTCACCATGCTGGCCAGGCTGGTCTTGAACTCCTGACCTCGTGATCCGTCCTCCTCGGCCTCCCAAAGTGCTGGGATTACAGGGGTGAGCCA... |
Task1_train_41967 | This sequence change occurs on Chromosome 12. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | AGTTCCAAAGAATCCTGGAACCTGGCTATGAATGTTTTCATTTATTATCAAAATCTCACTGTTTTCTTCATATTCTACTATAGTTTTTCATCCTCTACAAACACTAATCTCCTGTGTCTGTGGGGCAGATACTCATTTCACTCGTTTTGCTGCCATGTTTCCAAGGTGACATGTGAGGAGATGAAAGTATTGATAGGTCTCCTCTCCCTGGTCTGTATTTATGGCTAGGACAGAGTGAGCAGATTCTAGACCTCAGTGTGGATGCCAGTTTGAACACTTTTGCAACACTACTGCCCTGAAATGTTGAGAAATGCTGAGAG... | AGTTCCAAAGAATCCTGGAACCTGGCTATGAATGTTTTCATTTATTATCAAAATCTCACTGTTTTCTTCATATTCTACTATAGTTTTTCATCCTCTACAAACACTAATCTCCTGTGTCTGTGGGGCAGATACTCATTTCACTCGTTTTGCTGCCATGTTTCCAAGGTGACATGTGAGGAGATGAAAGTATTGATAGGTCTCCTCTCCCTGGTCTGTATTTATGGCTAGGACAGAGTGAGCAGATTCTAGACCTCAGTGTGGATGCCAGTTTGAACACTTTTGCAACACTACTGCCCTGAAATGTTGAGAAATGCTGAGAG... |
Task1_train_41968 | A variant affecting Chromosome 12 has been observed. Determine if it's benign or associated with disease. | Benign | TTTTATCCACATCATTTAACGGAATCCCAGAGCAGAGCTCAGGAACACATACAGAAATAGAAGAATATCCAGTACACAAAAAGTCTGGCATCAAATAAAATTAAGCAAGAATGCAGAAAATAAAATTTTCTGCATTTTGGCATCAAATAAATGTCTGGCATCAAATGATGTCTGGCGTCAAATAAAATTAAGCAAGAATGCAGAAAAGTAGAAAATTGTGGTTCATAAGTAGAATAATCAACCAATCAAACCAACCCATAACTGACATTATGTTAAAATAGTTATTGGAACAATTTAAATGTATCAAAGACATTTAAAAA... | TTTTATCCACATCATTTAACGGAATCCCAGAGCAGAGCTCAGGAACACATACAGAAATAGAAGAATATCCAGTACACAAAAAGTCTGGCATCAAATAAAATTAAGCAAGAATGCAGAAAATAAAATTTTCTGCATTTTGGCATCAAATAAATGTCTGGCATCAAATGATGTCTGGCGTCAAATAAAATTAAGCAAGAATGCAGAAAAGTAGAAAATTGTGGTTCATAAGTAGAATAATCAACCAATCAAACCAACCCATAACTGACATTATGTTAAAATAGTTATTGGAACAATTTAAATGTATCAAAGACATTTAAAAA... |
Task1_train_41969 | Here is a mutation located on Chromosome 12. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AGAGAAGACCTTTTACTATTTTCCTTAGTATGAGATGGAGGTGTTCAGTGACAAATTCTCCCCGTTTGGCTGTTTAATATATATTTATTCACCTTTTATTTTTGAAGGCTGTTTTTGCTGGGGGTAGAATTCTAACGTTGGCAGTGATTTTCTTTCAGTATTTGAAAGATATAATGCTTTGTATTCTGCATTCCACTGTTGCTATTGAGAAGTCAGCTGTGAACCTTATGGTTGTCCCTTTGAGAGTATTTTGATGATAGTCTCTCTTTTCTCTGACTTCTTTTAACATTTTATCTTTTGTTAAGTTTTAGATGTACTAT... | AGAGAAGACCTTTTACTATTTTCCTTAGTATGAGATGGAGGTGTTCAGTGACAAATTCTCCCCGTTTGGCTGTTTAATATATATTTATTCACCTTTTATTTTTGAAGGCTGTTTTTGCTGGGGGTAGAATTCTAACGTTGGCAGTGATTTTCTTTCAGTATTTGAAAGATATAATGCTTTGTATTCTGCATTCCACTGTTGCTATTGAGAAGTCAGCTGTGAACCTTATGGTTGTCCCTTTGAGAGTATTTTGATGATAGTCTCTCTTTTCTCTGACTTCTTTTAACATTTTATCTTTTGTTAAGTTTTAGATGTACTAT... |
Task1_train_41970 | A mutation located on Chromosome 12 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TGTTCAATTAAAAAATATATGACAGTGTGCAAAGAAGGGTCCAACTTAGTGGAAAGAAATGTCAGGTGTCATTGCATTATGAAGGTAAGGAACTGGTATTCTGTGCTACTTGCACATAAGCTTTTGAGGTTAGCTATGGGCCATGTAGTAATTTTGTACTGTTTATCGGTTCCTCCAATCTAAGATGTTTTATTATATTAATGCTTACATATATGGGTAATATTTCTGCTGTATTCTGTTTTTGTGCCTACTGCTATTATAGAGTCAAGAGGGAGTTTGAATCTTCTAAATCAGACTAGCTTTCATGCATTATTTAGTCT... | TGTTCAATTAAAAAATATATGACAGTGTGCAAAGAAGGGTCCAACTTAGTGGAAAGAAATGTCAGGTGTCATTGCATTATGAAGGTAAGGAACTGGTATTCTGTGCTACTTGCACATAAGCTTTTGAGGTTAGCTATGGGCCATGTAGTAATTTTGTACTGTTTATCGGTTCCTCCAATCTAAGATGTTTTATTATATTAATGCTTACATATATGGGTAATATTTCTGCTGTATTCTGTTTTTGTGCCTACTGCTATTATAGAGTCAAGAGGGAGTTTGAATCTTCTAAATCAGACTAGCTTTCATGCATTATTTAGTCT... |
Task1_train_41971 | Chromosome 12 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | AATGTCAGGTGTCATTGCATTATGAAGGTAAGGAACTGGTATTCTGTGCTACTTGCACATAAGCTTTTGAGGTTAGCTATGGGCCATGTAGTAATTTTGTACTGTTTATCGGTTCCTCCAATCTAAGATGTTTTATTATATTAATGCTTACATATATGGGTAATATTTCTGCTGTATTCTGTTTTTGTGCCTACTGCTATTATAGAGTCAAGAGGGAGTTTGAATCTTCTAAATCAGACTAGCTTTCATGCATTATTTAGTCTAGAGGTCAAGAAATTTTCTGTAAAGGGCCAGATAGTAAATATGTCCACATATGGGTT... | AATGTCAGGTGTCATTGCATTATGAAGGTAAGGAACTGGTATTCTGTGCTACTTGCACATAAGCTTTTGAGGTTAGCTATGGGCCATGTAGTAATTTTGTACTGTTTATCGGTTCCTCCAATCTAAGATGTTTTATTATATTAATGCTTACATATATGGGTAATATTTCTGCTGTATTCTGTTTTTGTGCCTACTGCTATTATAGAGTCAAGAGGGAGTTTGAATCTTCTAAATCAGACTAGCTTTCATGCATTATTTAGTCTAGAGGTCAAGAAATTTTCTGTAAAGGGCCAGATAGTAAATATGTCCACATATGGGTT... |
Task1_train_41972 | This variant is present on Chromosome 12. Is the change likely to result in a pathogenic outcome? | Benign | GAGGAATTAAGGAACTTGCCAAAGACCATAAAACTCCTAAGTGACAGAGCCAGGATTCTGCCAGCTGTCTGGTTGCCCAGTGGAGTCTCTGTCCATCTTGTCACCAGCCCCCGCACTGTGTACAGGAATGGAATCAGCATTCATTGCTATAAACTGCAGTAAGGTAAGTGAACATTCATAAAAGTTGGCCTGTAGTTTAGTATTTAAACTGGAAAAATAAAAAAAGGCAAGACAACCAGATTCAGCCTTCAAGGATCTTACCATCCAGTTCTTTTATCACATTAAAAAATAACAGCCTGATTCTTTATACACATTTCTAG... | GAGGAATTAAGGAACTTGCCAAAGACCATAAAACTCCTAAGTGACAGAGCCAGGATTCTGCCAGCTGTCTGGTTGCCCAGTGGAGTCTCTGTCCATCTTGTCACCAGCCCCCGCACTGTGTACAGGAATGGAATCAGCATTCATTGCTATAAACTGCAGTAAGGTAAGTGAACATTCATAAAAGTTGGCCTGTAGTTTAGTATTTAAACTGGAAAAATAAAAAAAGGCAAGACAACCAGATTCAGCCTTCAAGGATCTTACCATCCAGTTCTTTTATCACATTAAAAAATAACAGCCTGATTCTTTATACACATTTCTAG... |
Task1_train_41973 | Here is a variant on Chromosome 12. Please identify whether it is a benign mutation or associated with a disorder. | Benign | AGATCTTTGTGTATCATGTTAATGCCCAGCAGAGATATAACTTTACAACGAGCTGGACAGGATGACTTGGCCACCAGATATCCACCTGACTCTTTTTTCTGGCCATCTCTCCTTATGTAACTGACCCACGATAACAGTGGCCATGGTGGCAGAGATGGAAGCAATGCATGGGTCTACAATATGGACTTTTCCTCAATGTGGCTGATTGAGGACATCACTTCTAAGTATCCAACCAGTCAGTTTCTGAAGTAAAACCTCCACCCCGGGCGTGGCACCATTTCTTAGGTTGCTGGGAGAGTAGATAACAAGCTGCAGGTTAA... | AGATCTTTGTGTATCATGTTAATGCCCAGCAGAGATATAACTTTACAACGAGCTGGACAGGATGACTTGGCCACCAGATATCCACCTGACTCTTTTTTCTGGCCATCTCTCCTTATGTAACTGACCCACGATAACAGTGGCCATGGTGGCAGAGATGGAAGCAATGCATGGGTCTACAATATGGACTTTTCCTCAATGTGGCTGATTGAGGACATCACTTCTAAGTATCCAACCAGTCAGTTTCTGAAGTAAAACCTCCACCCCGGGCGTGGCACCATTTCTTAGGTTGCTGGGAGAGTAGATAACAAGCTGCAGGTTAA... |
Task1_train_41974 | A mutation has occurred on Chromosome 12. What is the medical relevance of this mutation? | Benign | ATGAGTGTCCAGGATAACACCCTGGGAAAATGTCAGTTATCAAAAATCAAGTCCTTTTGAGGAGCCAGAAGGCCAAGATGATGAAAAGGGAGAGAATGAAACTGAGTAGCATAAGGTGAACCTAGAGAGTGTGTAGTGTCACGGGTCGTTAAGGAACTTCCAAGTCAACTGAGGAATTATAAATGTTATCCTGAGATAATGGGGAACCACTGAAAAACTATAACCAGTGGAGATATTTGGTTAGTGTCTTAAATAAAACATACATAATTGGATTACTGTATAAGGCACAAAAATGAATTGCAGAAAATGGAAAAGGAGTC... | ATGAGTGTCCAGGATAACACCCTGGGAAAATGTCAGTTATCAAAAATCAAGTCCTTTTGAGGAGCCAGAAGGCCAAGATGATGAAAAGGGAGAGAATGAAACTGAGTAGCATAAGGTGAACCTAGAGAGTGTGTAGTGTCACGGGTCGTTAAGGAACTTCCAAGTCAACTGAGGAATTATAAATGTTATCCTGAGATAATGGGGAACCACTGAAAAACTATAACCAGTGGAGATATTTGGTTAGTGTCTTAAATAAAACATACATAATTGGATTACTGTATAAGGCACAAAAATGAATTGCAGAAAATGGAAAAGGAGTC... |
Task1_train_41975 | A variant found on Chromosome 12 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GGATGAAATATTTTTGTGGATGCACTAGTGACATCGAAATACTTGATGTGATGATTTTCCAGTGACTTATAGTGCATTTTCCAAGCTCTTTAATATAATTTTTCTAAATAGTTTATTTCATAATAGTCATGAAAACTAAAACATACACCAAACAATAACTTTAGAGTAGTGAAAAGAAGCCATAAGTTATATTCACACACTCTTTCCTTGTTTTCAATAATTTGTTTGTTGGCAAATATTTATAAAATGATTAAATGTATACATGCATAATTATTTTGTACACAACAGGATATTTACTCAAAAATAAGTATGTTTGAGGA... | GGATGAAATATTTTTGTGGATGCACTAGTGACATCGAAATACTTGATGTGATGATTTTCCAGTGACTTATAGTGCATTTTCCAAGCTCTTTAATATAATTTTTCTAAATAGTTTATTTCATAATAGTCATGAAAACTAAAACATACACCAAACAATAACTTTAGAGTAGTGAAAAGAAGCCATAAGTTATATTCACACACTCTTTCCTTGTTTTCAATAATTTGTTTGTTGGCAAATATTTATAAAATGATTAAATGTATACATGCATAATTATTTTGTACACAACAGGATATTTACTCAAAAATAAGTATGTTTGAGGA... |
Task1_train_41976 | A variant found on Chromosome 12 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CTCAAGGACAGAGATCCTATCTTCCTTTCTTCCAGCTTTTCTATCTTATTATACCATCTCCATAAAATCCTCCTCTAAGACTCTGATTAATTCTTCCATCCATGGGCATTCCAATCTACTTTATAACTATCACTCTAATCTAATATCTTATCATTTGCCTCTTTCTATCTAGAAAACCCTTGCTTCTGTCTATTTGCTAATCTATGGCCCTCAAAATCTTCAAGATCTAGTAAAACTCTGAAAATTTTTTTCTTAAAATGTGGCTTCATTCAATGATGATAAACTATCCTGTGAATTATTTTCAACTTAATATGTGTGTG... | CTCAAGGACAGAGATCCTATCTTCCTTTCTTCCAGCTTTTCTATCTTATTATACCATCTCCATAAAATCCTCCTCTAAGACTCTGATTAATTCTTCCATCCATGGGCATTCCAATCTACTTTATAACTATCACTCTAATCTAATATCTTATCATTTGCCTCTTTCTATCTAGAAAACCCTTGCTTCTGTCTATTTGCTAATCTATGGCCCTCAAAATCTTCAAGATCTAGTAAAACTCTGAAAATTTTTTTCTTAAAATGTGGCTTCATTCAATGATGATAAACTATCCTGTGAATTATTTTCAACTTAATATGTGTGTG... |
Task1_train_41977 | This mutation on Chromosome 12 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GATTCTGCTTTGCTCATTACTGCTGCCTGGAGGTTCTTACATTGATTTTCAAACTGTGTAAGCAACCTGTGGAGGCAAGGAACATTTTGTCCTATGTTCCCTGAACACTGTTTGCATGCTGACACTCACAAAGGGGCCCAGGCTTACAGTGATGCACATAAATGAAAGATGAAGATTCCCTATGACTTCTAAAATTACTGAGAGAAGCCCTACGAGAGTTATGTAAATGTCATCTGGAAGGCATGATCAGAAAGTCAGAGTCATGAAGAATGAAATTCTAATCAGTTCATACCATCTAACAGTGGACTTCAAATCAGCTA... | GATTCTGCTTTGCTCATTACTGCTGCCTGGAGGTTCTTACATTGATTTTCAAACTGTGTAAGCAACCTGTGGAGGCAAGGAACATTTTGTCCTATGTTCCCTGAACACTGTTTGCATGCTGACACTCACAAAGGGGCCCAGGCTTACAGTGATGCACATAAATGAAAGATGAAGATTCCCTATGACTTCTAAAATTACTGAGAGAAGCCCTACGAGAGTTATGTAAATGTCATCTGGAAGGCATGATCAGAAAGTCAGAGTCATGAAGAATGAAATTCTAATCAGTTCATACCATCTAACAGTGGACTTCAAATCAGCTA... |
Task1_train_41978 | Located on Chromosome 12, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TTATTTTTGGAGTCAGCAGGATTTCCAGCTGGATGTAATTTCAGGAAGTGATGTGACTATTTATTCAATAATGCTTTGCAAATTTCCTGGGAAATGATGGAATAATTCTGATGAAATTAAAGTGGCTATTGAAATATATGTCATACTATTTGCCAAGTGTTATTTCTTGTCTATTTAACCATATTAATTCATTTCATAATGAAAATAAACTCTTAGTAAATACTTTCCATAGACATATTTTCTAGGACTGAGAATATATTATCAAAATCCAGATCACCAAAGCCAACCAAATTAAATAAATGGACAGTGAATATCTCCTA... | TTATTTTTGGAGTCAGCAGGATTTCCAGCTGGATGTAATTTCAGGAAGTGATGTGACTATTTATTCAATAATGCTTTGCAAATTTCCTGGGAAATGATGGAATAATTCTGATGAAATTAAAGTGGCTATTGAAATATATGTCATACTATTTGCCAAGTGTTATTTCTTGTCTATTTAACCATATTAATTCATTTCATAATGAAAATAAACTCTTAGTAAATACTTTCCATAGACATATTTTCTAGGACTGAGAATATATTATCAAAATCCAGATCACCAAAGCCAACCAAATTAAATAAATGGACAGTGAATATCTCCTA... |
Task1_train_41979 | This variant lies on Chromosome 12. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CTGGAATGTCAAGATAATTAAGACAAAATTGGATTATTAAGATTATTATTAGTGAGGGCAAATGACATCTAAGATAGCCATGTTAAAAGTGGAGTATCATATTAAAAAGACAACTAGATCCCAGGGAACATCAATAGAGTTTAAGTCCATTGAACAGATACTGAATTCTTTTTCATAATCTGCCAAAAAAAGGTTAGCTTGAAAATTTTCTTTTAGTTTCTCAAATATCACACTGCTGCAGTACACGAACCTTTACTCATTAATAACTAAGGTCCTGATTTTTTTCATATGCTTTGCTCGAAGATGTAGTATTTTGCAGC... | CTGGAATGTCAAGATAATTAAGACAAAATTGGATTATTAAGATTATTATTAGTGAGGGCAAATGACATCTAAGATAGCCATGTTAAAAGTGGAGTATCATATTAAAAAGACAACTAGATCCCAGGGAACATCAATAGAGTTTAAGTCCATTGAACAGATACTGAATTCTTTTTCATAATCTGCCAAAAAAAGGTTAGCTTGAAAATTTTCTTTTAGTTTCTCAAATATCACACTGCTGCAGTACACGAACCTTTACTCATTAATAACTAAGGTCCTGATTTTTTTCATATGCTTTGCTCGAAGATGTAGTATTTTGCAGC... |
Task1_train_41980 | This sequence change occurs on Chromosome 12. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | AGATATACCTAATAGATAGACTCAGTATGATTCCGGGACAGATTAAATATAGTGATAGCCAGAGAGAGGAGAAAGAAGGATCAATGATAACTCACAAGTCTGCTTTAATGACTGGGCTTCCACTGATAAAGGGACAGGTCTATAGGGGAAGAAGTTGAGCTCATGTTGAGTTTGAAGTGCCTGAGTGACATGCTTCTGGAGATAAATAAATGGCAGTTACTGCATGATTCTGGAGCTTATGAGAAAAGACTGGATTAGAGAGATAGGTTTGGGAGATTTCAGCATGTAATTGATGGCCTTTCATCTCCAAAACAGTAATT... | AGATATACCTAATAGATAGACTCAGTATGATTCCGGGACAGATTAAATATAGTGATAGCCAGAGAGAGGAGAAAGAAGGATCAATGATAACTCACAAGTCTGCTTTAATGACTGGGCTTCCACTGATAAAGGGACAGGTCTATAGGGGAAGAAGTTGAGCTCATGTTGAGTTTGAAGTGCCTGAGTGACATGCTTCTGGAGATAAATAAATGGCAGTTACTGCATGATTCTGGAGCTTATGAGAAAAGACTGGATTAGAGAGATAGGTTTGGGAGATTTCAGCATGTAATTGATGGCCTTTCATCTCCAAAACAGTAATT... |
Task1_train_41981 | Located on Chromosome 12, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | AGCAAGGTGATAACCCACTTTGTTCATGGTGTATTGAAGTATCTTTCTTAGTGGACACTCCCATTTCACCCCCTCTCATCACCTGTTCTGAAATACATGCTGGGAAGTTGACAAACAAGATTCTGGTAATTTGGAGAAGACAGCGGTTCAAATAAAGGAGAAAATTTCTCTGTATTTCTGGGAAAACTGAAAATATTCAGTAGATAAGCAAAATGTTCAATTTCATGTTGCTCTTACAGTTATAGGTATTCTAAAGAAACCCATATTAATCCATCAGAAAATTCAACATCAAGTTTATCAACCTGTTTAATTAATCAAAC... | AGCAAGGTGATAACCCACTTTGTTCATGGTGTATTGAAGTATCTTTCTTAGTGGACACTCCCATTTCACCCCCTCTCATCACCTGTTCTGAAATACATGCTGGGAAGTTGACAAACAAGATTCTGGTAATTTGGAGAAGACAGCGGTTCAAATAAAGGAGAAAATTTCTCTGTATTTCTGGGAAAACTGAAAATATTCAGTAGATAAGCAAAATGTTCAATTTCATGTTGCTCTTACAGTTATAGGTATTCTAAAGAAACCCATATTAATCCATCAGAAAATTCAACATCAAGTTTATCAACCTGTTTAATTAATCAAAC... |
Task1_train_41982 | A variant on Chromosome 12 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | AAAACAGGTGAAACAGGATATTTTACATCTTGACCAGAATATAAGCACTCCTAGGATTATAGAAAAGTGATAACCCACTTTATCCATGGTGTGTTGAATTATCTGTCTTAGTAGATGCTCCCATTCCCGCCCCACCCCCACCCCCTCTTATCACCTCCTCTTCTGACATACATCCTGGGAAATTGACAAAGAGAAGTCCGGTAATTCAAAGACAGTGTCAATAAAGGGGAAAATTTTTCTGCATTTTTGGGAAAGGTGAAAATATTCAGCAGATAAGCAAAATGTTCAATCCAGTGTTACTCTTATAGTTACAGGTATTC... | AAAACAGGTGAAACAGGATATTTTACATCTTGACCAGAATATAAGCACTCCTAGGATTATAGAAAAGTGATAACCCACTTTATCCATGGTGTGTTGAATTATCTGTCTTAGTAGATGCTCCCATTCCCGCCCCACCCCCACCCCCTCTTATCACCTCCTCTTCTGACATACATCCTGGGAAATTGACAAAGAGAAGTCCGGTAATTCAAAGACAGTGTCAATAAAGGGGAAAATTTTTCTGCATTTTTGGGAAAGGTGAAAATATTCAGCAGATAAGCAAAATGTTCAATCCAGTGTTACTCTTATAGTTACAGGTATTC... |
Task1_train_41983 | Consider a variant on Chromosome 12. Determine its clinical classification and disease relevance. | Benign | ATTAATAAGTGCCTGTTAAGAATGGATAACATACCTAAATACCTATAGTCAGGAGAAAAGACATATTGGATTTATTCTCTATGTTCTTGTTGAAAACTAAGACTAATTGGTTAGAAAGAAAGGAAAATTTCAGTTCATTACAAAGACAATTTTTAAACAATGAGAACTGTTCAAAAGTTGAGCAAATTGCTCTCAGGTAGTCAGCTTCATGTCACTTGAGTTGTTTATTGATCTGTTTATTAAAAATAAGTAATACGTCACAATTGTATAGAAGTTCAGACCAGATGACATCCAAATTGCTGTCTGCCACAAAAATTTAA... | ATTAATAAGTGCCTGTTAAGAATGGATAACATACCTAAATACCTATAGTCAGGAGAAAAGACATATTGGATTTATTCTCTATGTTCTTGTTGAAAACTAAGACTAATTGGTTAGAAAGAAAGGAAAATTTCAGTTCATTACAAAGACAATTTTTAAACAATGAGAACTGTTCAAAAGTTGAGCAAATTGCTCTCAGGTAGTCAGCTTCATGTCACTTGAGTTGTTTATTGATCTGTTTATTAAAAATAAGTAATACGTCACAATTGTATAGAAGTTCAGACCAGATGACATCCAAATTGCTGTCTGCCACAAAAATTTAA... |
Task1_train_41984 | Consider this mutation on Chromosome 12. Is this a benign change or a disease-causing variant? | Benign | TGGGACGCTTAGTGTATTGCCTAGTACCCAATTGAAAACCAAACATTTGTGGAATGAATAAATAATTAATCTGTATGTAATAGTATGGTAGAGTGCCAAGGATAATAAAATGTTAAGTGAACAAAGTAAGTCACAAAACAGCATTTATGCATGATCCTATTTGGAAGTAAAATGAACTAAACCAATAATAATATGCATATGAAAAATATTGAAGGAATGTAGTTAAACTGTTAATAGTAGGATTGAAGGGTGCTCTTTCTGTGTTATGTAGTTTTGTAATTTTAAATCTTATAAAACTTATATTTTCAAAATTCAGATAT... | TGGGACGCTTAGTGTATTGCCTAGTACCCAATTGAAAACCAAACATTTGTGGAATGAATAAATAATTAATCTGTATGTAATAGTATGGTAGAGTGCCAAGGATAATAAAATGTTAAGTGAACAAAGTAAGTCACAAAACAGCATTTATGCATGATCCTATTTGGAAGTAAAATGAACTAAACCAATAATAATATGCATATGAAAAATATTGAAGGAATGTAGTTAAACTGTTAATAGTAGGATTGAAGGGTGCTCTTTCTGTGTTATGTAGTTTTGTAATTTTAAATCTTATAAAACTTATATTTTCAAAATTCAGATAT... |
Task1_train_41985 | This variant is found on Chromosome 12. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GTGAAGTATAAACAAAGCTTCATATAAAGTCCTGCTTAGGACACAACCAAGTTTTTCTGTTATTTGAATTTTAATTTGAGATTACCCCACTTTTTTCTTGAGAGTGTAGAAATATGACCTATTAGAATTTAATCCACTTAGGATTTCTGAGAAGCATCTGATTTGACTGAAGCACAAGATTTCAATTAATTTGGAATTAATTTATCCATCAGAAGTTAGGAGAAAGTCCTGATTAACCTGTTGTCAGAACTACCTACTTTACTAGGACAACAATCTATGTGCATTTTCATATATATACCTCCTGATGAGTTTAGCTAGGG... | GTGAAGTATAAACAAAGCTTCATATAAAGTCCTGCTTAGGACACAACCAAGTTTTTCTGTTATTTGAATTTTAATTTGAGATTACCCCACTTTTTTCTTGAGAGTGTAGAAATATGACCTATTAGAATTTAATCCACTTAGGATTTCTGAGAAGCATCTGATTTGACTGAAGCACAAGATTTCAATTAATTTGGAATTAATTTATCCATCAGAAGTTAGGAGAAAGTCCTGATTAACCTGTTGTCAGAACTACCTACTTTACTAGGACAACAATCTATGTGCATTTTCATATATATACCTCCTGATGAGTTTAGCTAGGG... |
Task1_train_41986 | A mutation located on Chromosome 12 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TGTACAGAAATGAAATAGTGTCTATTTGTCTACATAATCATTTTATTTATCGTAGCTTTCATATACTTTGAAATAACAAAAAGACTAAACTGTAGAGTTTCAAATGAAATAAATAGGCTTTTTATGAATTTTTAGTATAACGTATATACTGTACGTCTTTGCCTATAAGATTTTGATTATTTTTTATAAGACCTCAACACTTACACCTATACCCACTGAAGTATAGTTGTTCCCATCATTTCACTGAAGCTGTTATTCCTAAGGTCACTGTGTAGTTATAATTACAGTCAGATGCTCCTGAGAGAAAAGTTAAAATGGCA... | TGTACAGAAATGAAATAGTGTCTATTTGTCTACATAATCATTTTATTTATCGTAGCTTTCATATACTTTGAAATAACAAAAAGACTAAACTGTAGAGTTTCAAATGAAATAAATAGGCTTTTTATGAATTTTTAGTATAACGTATATACTGTACGTCTTTGCCTATAAGATTTTGATTATTTTTTATAAGACCTCAACACTTACACCTATACCCACTGAAGTATAGTTGTTCCCATCATTTCACTGAAGCTGTTATTCCTAAGGTCACTGTGTAGTTATAATTACAGTCAGATGCTCCTGAGAGAAAAGTTAAAATGGCA... |
Task1_train_41987 | This alteration occurs on Chromosome 12. Is it associated with a disease or is it a benign variant? | Benign | GTATTGAATTATCTTTCTTGCTGGACACTTCCATTTCACTTTTACCCATCACATCTCTTAAAACACATGCTGGGAAATTGACAGAAAGTACTCTGGTAATTTGGGGAAGATAATGGTGCAAATAAAGGGGAATATTTCTCTGTATTTCTAGGAAAAGTGAAAATATTCAGTAGATAAGCAAAATGTTTAATTCAGTGATGTTCTTACAGTTACAGGTATTCTAAAGAAACTAATATCAATTCATCAGAAAATTCAACATCGACCTTATCCACTTGTTTAATTAATCAAATTTTATCACTCAATAGAGCATCACCTGAGAT... | GTATTGAATTATCTTTCTTGCTGGACACTTCCATTTCACTTTTACCCATCACATCTCTTAAAACACATGCTGGGAAATTGACAGAAAGTACTCTGGTAATTTGGGGAAGATAATGGTGCAAATAAAGGGGAATATTTCTCTGTATTTCTAGGAAAAGTGAAAATATTCAGTAGATAAGCAAAATGTTTAATTCAGTGATGTTCTTACAGTTACAGGTATTCTAAAGAAACTAATATCAATTCATCAGAAAATTCAACATCGACCTTATCCACTTGTTTAATTAATCAAATTTTATCACTCAATAGAGCATCACCTGAGAT... |
Task1_train_41988 | A variant on Chromosome 12 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TTGGTGGATTTAGATCATTGACATTAAAAGTGACTACTGATGTTGTGAGACCAATGTTGATTATAATTTTACTATTGTCTATTTGTTATACTTGTTCTTTGATCCTATTTTTGTCTTCTATTCTTTTTTCTTCTGTTGTGTTCTTAACTAAATAGTCTATATGACTCTGATTTTATATGACTATATAATCATAACTTTTTATGTTACCTTTCTTTATGTATATCAAGTTTCTGACCTATATGAGTCTCTCTAAAAAGCTTCTCTTAACATTTCTTACAAGGAAGATGTACTGGAAAAACATTTCTTCAATTGTTGTTTGT... | TTGGTGGATTTAGATCATTGACATTAAAAGTGACTACTGATGTTGTGAGACCAATGTTGATTATAATTTTACTATTGTCTATTTGTTATACTTGTTCTTTGATCCTATTTTTGTCTTCTATTCTTTTTTCTTCTGTTGTGTTCTTAACTAAATAGTCTATATGACTCTGATTTTATATGACTATATAATCATAACTTTTTATGTTACCTTTCTTTATGTATATCAAGTTTCTGACCTATATGAGTCTCTCTAAAAAGCTTCTCTTAACATTTCTTACAAGGAAGATGTACTGGAAAAACATTTCTTCAATTGTTGTTTGT... |
Task1_train_41989 | Mutation context: Chromosome 12. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TTTTTAGACTAACTTTGGAAGGCTCTTGACCAAGAGGAGGTCCATTCAGTGCTGGGAGCAGGGGGTGGGAGGGTTGAATTTTATTTGTGGCTTAGAGGCTGTATATACTGATTCATAAACTACCATCTTTCTCACTGTGTCTTCACATGGCAGAAAATGCAGTGAATCTCTCTTAGTCCTCTATTATAAAGCCACTGAACCCATTCATAAAGGCTTTACCTTTGTGACCTAATCACCTCTCGAAGGCCCCACTTCCTACTGCCATCACCTTAGAAATTAGGATTTCAACATGGGAATTTGGATGGGACACATTCACACCA... | TTTTTAGACTAACTTTGGAAGGCTCTTGACCAAGAGGAGGTCCATTCAGTGCTGGGAGCAGGGGGTGGGAGGGTTGAATTTTATTTGTGGCTTAGAGGCTGTATATACTGATTCATAAACTACCATCTTTCTCACTGTGTCTTCACATGGCAGAAAATGCAGTGAATCTCTCTTAGTCCTCTATTATAAAGCCACTGAACCCATTCATAAAGGCTTTACCTTTGTGACCTAATCACCTCTCGAAGGCCCCACTTCCTACTGCCATCACCTTAGAAATTAGGATTTCAACATGGGAATTTGGATGGGACACATTCACACCA... |
Task1_train_41990 | This genomic variant is located on Chromosome 12. Can you determine its pathogenicity and name any linked disease? | Benign | TTCAGAGAAGTGTCCAAAGTCACATAAACGTATACATGACAAATACAGTAGCAATGACACTCAGCAAACATCCACAAGATACAAAGTGATGTAACAAAAAACAGCAAACATTCAACAGGTCTAGCACCAATTGCTATGTGACTAAATTACTATGTTAGGCAAAGTTGCATATGCTGTTCCTCCAAGCCTCTTTCCCTACCTGTAAAACTGGGAGGATGGCAATCTTATAAATAAGTTGGATAGATTCAAATGTACCAGATTAAGCAAAATACATCAACATAAATAATAAAATTAATCATCTAACATTTTATTGAGCCCTT... | TTCAGAGAAGTGTCCAAAGTCACATAAACGTATACATGACAAATACAGTAGCAATGACACTCAGCAAACATCCACAAGATACAAAGTGATGTAACAAAAAACAGCAAACATTCAACAGGTCTAGCACCAATTGCTATGTGACTAAATTACTATGTTAGGCAAAGTTGCATATGCTGTTCCTCCAAGCCTCTTTCCCTACCTGTAAAACTGGGAGGATGGCAATCTTATAAATAAGTTGGATAGATTCAAATGTACCAGATTAAGCAAAATACATCAACATAAATAATAAAATTAATCATCTAACATTTTATTGAGCCCTT... |
Task1_train_41991 | This mutation occurs on Chromosome 12. Does this change lead to a known medical condition, or is it benign? | Benign | CTTTTGAGATGGCACTAATGATGATGACTAAGTCTTGTGTGTGTGTCAAAGGAAGATATGGGTTGAAGAATCTCCTTTGCATGCTATGAATACATGAAGCTTTTGTTTTCCGCCTGCAGCTACTATATGAGAGACCTGGACTTCTTGATTGCTTCCGGGACTTATTTGGAATATAAAGGTGTCCTGAAGTCTTGACTTAAGATGAACTTTACTGATTTCTTTTAGCAAGGCTGTCCTCCAGTATCTGATTCTTCCCTATTATAACAAGCATTCTGATGCAAGCCTGACACATTTGTTTTATCTCCTTTGTAATAATTCCA... | CTTTTGAGATGGCACTAATGATGATGACTAAGTCTTGTGTGTGTGTCAAAGGAAGATATGGGTTGAAGAATCTCCTTTGCATGCTATGAATACATGAAGCTTTTGTTTTCCGCCTGCAGCTACTATATGAGAGACCTGGACTTCTTGATTGCTTCCGGGACTTATTTGGAATATAAAGGTGTCCTGAAGTCTTGACTTAAGATGAACTTTACTGATTTCTTTTAGCAAGGCTGTCCTCCAGTATCTGATTCTTCCCTATTATAACAAGCATTCTGATGCAAGCCTGACACATTTGTTTTATCTCCTTTGTAATAATTCCA... |
Task1_train_41992 | Here’s a variant located on Chromosome 12. What is the predicted biological effect — harmless or disease-causing? | Benign | TCTTCCATTGCTTCACTTCTAGAATGTTTTAATCTTTGTCCTTTCTTTTTTCGTCTTTTCATATCAAATTCAGTCGTTTGAGCGATGAACAGCTTGACTTAGCATATTTTTAACCAGCTGGTCTAGCACCTAGCTTGCATTGCATAGTCAGATACAACAAATGTTTATACAGAAGGTAGCTTTCATGAAAATGAAAAAAAGCCTGGGTATCATGCATCCTGGCTTTTTTTAGCTTTTTTTTTTTTAATTCACCATACAGAATACAAAGTTTGAATTCTTTTTAATGGCAAACAAAATTCTATTTATAGTTCAAAAAAATG... | TCTTCCATTGCTTCACTTCTAGAATGTTTTAATCTTTGTCCTTTCTTTTTTCGTCTTTTCATATCAAATTCAGTCGTTTGAGCGATGAACAGCTTGACTTAGCATATTTTTAACCAGCTGGTCTAGCACCTAGCTTGCATTGCATAGTCAGATACAACAAATGTTTATACAGAAGGTAGCTTTCATGAAAATGAAAAAAAGCCTGGGTATCATGCATCCTGGCTTTTTTTAGCTTTTTTTTTTTTAATTCACCATACAGAATACAAAGTTTGAATTCTTTTTAATGGCAAACAAAATTCTATTTATAGTTCAAAAAAATG... |
Task1_train_41993 | A variant on Chromosome 12 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | AATCCAAGAATAGAAGACAACATTGAATTAAATGACAAAATGTGTGTTACAATTATAAATCCTAGGAGAGATCAGAAAGAATGGAGTCCCATGATTAAAAACTGATTCTAGAATTTCAAGAGAGGAGTGTATTTTAGACTTCACGTTGAGAGATCATTCTTCTTCTTCTTCTTCTTTTCTTTTTTTTTTTGGACAGAGTCTTGCTCTGTCCCCCCGGCTAGAGTGCCGTAGCATGATCTCAGCTCACTGCAACCTCTGCCTCCAATGTTGAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGTCGCCT... | AATCCAAGAATAGAAGACAACATTGAATTAAATGACAAAATGTGTGTTACAATTATAAATCCTAGGAGAGATCAGAAAGAATGGAGTCCCATGATTAAAAACTGATTCTAGAATTTCAAGAGAGGAGTGTATTTTAGACTTCACGTTGAGAGATCATTCTTCTTCTTCTTCTTCTTTTCTTTTTTTTTTTGGACAGAGTCTTGCTCTGTCCCCCCGGCTAGAGTGCCGTAGCATGATCTCAGCTCACTGCAACCTCTGCCTCCAATGTTGAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGTCGCCT... |
Task1_train_41994 | Here is a variant on Chromosome 12. Please identify whether it is a benign mutation or associated with a disorder. | Benign | ATTCATGGAAATTTCTGTTAATGTCCTAAAAAATCATAGTTTTTGAAATCAGTAATTCCATAACTATTCAACTATTTGTTGTAACTATTGAAACTATTTTAACCTTTTGCCTAGAGTATTTAAAAAATATCTGTCTAATCTAATCTAATCTAATCTGTCCATCCATCCCTCTGTTGCCCAGGCTGGAGTACCTGTGGTGACACCTTCATGGCTCACTGAAGCCCTCCCATACTCAAGTGACCCTCCCACCCCCACCTCCTGAGTAGCTGGAACTACAGGCACGCACCACCACACCCAGCCTAGATTATTTTAAATCTTAC... | ATTCATGGAAATTTCTGTTAATGTCCTAAAAAATCATAGTTTTTGAAATCAGTAATTCCATAACTATTCAACTATTTGTTGTAACTATTGAAACTATTTTAACCTTTTGCCTAGAGTATTTAAAAAATATCTGTCTAATCTAATCTAATCTAATCTGTCCATCCATCCCTCTGTTGCCCAGGCTGGAGTACCTGTGGTGACACCTTCATGGCTCACTGAAGCCCTCCCATACTCAAGTGACCCTCCCACCCCCACCTCCTGAGTAGCTGGAACTACAGGCACGCACCACCACACCCAGCCTAGATTATTTTAAATCTTAC... |
Task1_train_41995 | A mutation on Chromosome 12 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CTGTATTGAACACTTGTAGCAAAATATTTGCATGTACCCTTATTTATTTCCTTAGGATGAGTGGGGCTTATTTGTTCCCAGAGAGCTTCTCTGCTTGGACAGGATTTAAGAAAGTAATTCTCTGAAGAAAATAAGAAAGCTTCACTGATGGGAAATGGGATGTGTATTAGCCAGGGCTCTCTGGTGGGAAGAGATATTTATATTTGTATCTGTCAATTTAATCTAGCTAGCTAAAGAGACTTATTATAAGGAATTGGGTCATGCGATCATGGAGGCGGGCAAGTCCCAAGATCTGCAGGATGTCAGCAAGCCAGGGATTC... | CTGTATTGAACACTTGTAGCAAAATATTTGCATGTACCCTTATTTATTTCCTTAGGATGAGTGGGGCTTATTTGTTCCCAGAGAGCTTCTCTGCTTGGACAGGATTTAAGAAAGTAATTCTCTGAAGAAAATAAGAAAGCTTCACTGATGGGAAATGGGATGTGTATTAGCCAGGGCTCTCTGGTGGGAAGAGATATTTATATTTGTATCTGTCAATTTAATCTAGCTAGCTAAAGAGACTTATTATAAGGAATTGGGTCATGCGATCATGGAGGCGGGCAAGTCCCAAGATCTGCAGGATGTCAGCAAGCCAGGGATTC... |
Task1_train_41996 | This sequence change occurs on Chromosome 12. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | AAGACAAAACTTGGTCAGGCAAAGAATCCTAGCTCACTGGTTTTGTTTTTTTTTTTTTTTTTTGGCTACAGGGAAGGAGTGAATCATAGATTAAGCAGCATCATCGATGATTCTGTTTGTGAACAGGATGGCATAAAATCAGATGGAACAAGTATGTATGTGTTTCTTCAGGATTGTTCTGTTTTCTTACGGTTTGTAGAAAATGATTTTTTTTCATAAAACTCTTGTATGTGTTTCAGTGAAGATGAGCACAGATATAACAGATTCTACATTGGGGAGCTTCGAGGCTTTGGGAGGAGAAACATCTAAAGGAGTCTTGT... | AAGACAAAACTTGGTCAGGCAAAGAATCCTAGCTCACTGGTTTTGTTTTTTTTTTTTTTTTTTGGCTACAGGGAAGGAGTGAATCATAGATTAAGCAGCATCATCGATGATTCTGTTTGTGAACAGGATGGCATAAAATCAGATGGAACAAGTATGTATGTGTTTCTTCAGGATTGTTCTGTTTTCTTACGGTTTGTAGAAAATGATTTTTTTTCATAAAACTCTTGTATGTGTTTCAGTGAAGATGAGCACAGATATAACAGATTCTACATTGGGGAGCTTCGAGGCTTTGGGAGGAGAAACATCTAAAGGAGTCTTGT... |
Task1_train_41997 | Here is a mutation located on Chromosome 12. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GGTGGCTCATGCCTGTAATCCCAGCACTTTCGGAGGCCGAGACAGGCGGATCTCGAGGTCAGGAAATCGAGACCATCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAATACAAAAAATTAGCCGGGCATGGTGGTGCGTGCCTGTAGTCCCAGCTACCCGGGAGGCTGAGGCAGGGGAATCGCTTCAACCCGGGAGCCAAAGGTTGCAGTGAGCTGAGATCGCGCCAGTGCACTCCAGCCTGGAGACAGAGCGAGACTCCGTCTCAAAAAAAACAAACAAACAAACAAACAAAAAAAAACAGTTACAGAGTTTTCT... | GGTGGCTCATGCCTGTAATCCCAGCACTTTCGGAGGCCGAGACAGGCGGATCTCGAGGTCAGGAAATCGAGACCATCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAATACAAAAAATTAGCCGGGCATGGTGGTGCGTGCCTGTAGTCCCAGCTACCCGGGAGGCTGAGGCAGGGGAATCGCTTCAACCCGGGAGCCAAAGGTTGCAGTGAGCTGAGATCGCGCCAGTGCACTCCAGCCTGGAGACAGAGCGAGACTCCGTCTCAAAAAAAACAAACAAACAAACAAACAAAAAAAAACAGTTACAGAGTTTTCT... |
Task1_train_41998 | Chromosome 12 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CATATGACAACATAGATAAACCTGGAGGACACTATCCCAAGTAAAATAAGTGAGTCACAGAACAACAAATACTGCACGATCCCACTTCTCTGAGGTATCTAAAATAGTTAAACTAATAGAAAGAGAGAGAATAGTGGTTGCCAGGAGCTAGGGGAGGGGAAATGAGGAGTTGCTACTCAATAGGTATAAAGTTTCAGTTATGCAAGATGAAGATGTTCTAGAGATCTGCTGTACAACATTATGCCTGTAGTTAATAATACTGTATTGTACACTTAAAAATTTGTTAAGTGGGTAAATCTCCTGTTAAATGTTCCTGCCAC... | CATATGACAACATAGATAAACCTGGAGGACACTATCCCAAGTAAAATAAGTGAGTCACAGAACAACAAATACTGCACGATCCCACTTCTCTGAGGTATCTAAAATAGTTAAACTAATAGAAAGAGAGAGAATAGTGGTTGCCAGGAGCTAGGGGAGGGGAAATGAGGAGTTGCTACTCAATAGGTATAAAGTTTCAGTTATGCAAGATGAAGATGTTCTAGAGATCTGCTGTACAACATTATGCCTGTAGTTAATAATACTGTATTGTACACTTAAAAATTTGTTAAGTGGGTAAATCTCCTGTTAAATGTTCCTGCCAC... |
Task1_train_41999 | A variant was discovered on Chromosome 12. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | AAAATGGGAGAAAATTTTTGCAACCTACTCATCTGACAAAGGGCTAACATCCAGAATCTACAATGAACTCAAACAAATTTACAAGAAAAAAACAAACAATGCCATCAAAAAGTGGGCGAAGGACATGAACAGATACTTCTCTAAAGAAGACATTTATGCAGCCAAAAAACACATGAAAAAATGCTCACCATCACTGGCCATCAGAGAAATGCAAATTAAAACCACAATGAGATACCATCTCACACCAGTTAGAATGGCAATCATTAAAAAGTCAGGAAACAACAGGTGCTGGAGAGGATGTGGAGAAATAGGAACACTTT... | AAAATGGGAGAAAATTTTTGCAACCTACTCATCTGACAAAGGGCTAACATCCAGAATCTACAATGAACTCAAACAAATTTACAAGAAAAAAACAAACAATGCCATCAAAAAGTGGGCGAAGGACATGAACAGATACTTCTCTAAAGAAGACATTTATGCAGCCAAAAAACACATGAAAAAATGCTCACCATCACTGGCCATCAGAGAAATGCAAATTAAAACCACAATGAGATACCATCTCACACCAGTTAGAATGGCAATCATTAAAAAGTCAGGAAACAACAGGTGCTGGAGAGGATGTGGAGAAATAGGAACACTTT... |
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