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_41700 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | ATCTCAGCTCACTGCAACCTCCACCTCCCGGGTTCAAGCAATTCTCCTGCCTTAGTCTCCAGAGTAGCTGAAATTATAGGGGCCCTCACCTCTTTTTTCACTCCTCTTTTATGCTTTGTGTATCCAATGGAGAGGAAAATTTGGAGTCCTCAGTTTACAAAGTATTCTCAGAATTCAGAATGAACAGAGAGCATGGATCTACTGGCCAGAAGAATAGATCTTATTTGCTTGGTTTATCTTTGAGCCCATTGTGCTGGCCCATCAGCTCACAAACCCCATTCTTGTTATTTCACTTTACAATCAGGAATTTGGACTTGATT... | ATCTCAGCTCACTGCAACCTCCACCTCCCGGGTTCAAGCAATTCTCCTGCCTTAGTCTCCAGAGTAGCTGAAATTATAGGGGCCCTCACCTCTTTTTTCACTCCTCTTTTATGCTTTGTGTATCCAATGGAGAGGAAAATTTGGAGTCCTCAGTTTACAAAGTATTCTCAGAATTCAGAATGAACAGAGAGCATGGATCTACTGGCCAGAAGAATAGATCTTATTTGCTTGGTTTATCTTTGAGCCCATTGTGCTGGCCCATCAGCTCACAAACCCCATTCTTGTTATTTCACTTTACAATCAGGAATTTGGACTTGATT... |
Task1_train_41701 | A mutation found on Chromosome 11 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AGCATGGATCTACTGGCCAGAAGAATAGATCTTATTTGCTTGGTTTATCTTTGAGCCCATTGTGCTGGCCCATCAGCTCACAAACCCCATTCTTGTTATTTCACTTTACAATCAGGAATTTGGACTTGATTTTATATTATTAAAGTAACAGAAACTCTAAATGAGCCCATATGTGGATATCTTCATTTGATTCTTTCTTTGATGTATGACAGCCAGGACATTTTTGGAAGCAGTATAGATTATATGTAGCACTTGTCTTGGGTCTGATTGCTTTTTGGAATGTAGTGTAGAGCTTCTTCTGGAGTGCAGGTGACATGATT... | AGCATGGATCTACTGGCCAGAAGAATAGATCTTATTTGCTTGGTTTATCTTTGAGCCCATTGTGCTGGCCCATCAGCTCACAAACCCCATTCTTGTTATTTCACTTTACAATCAGGAATTTGGACTTGATTTTATATTATTAAAGTAACAGAAACTCTAAATGAGCCCATATGTGGATATCTTCATTTGATTCTTTCTTTGATGTATGACAGCCAGGACATTTTTGGAAGCAGTATAGATTATATGTAGCACTTGTCTTGGGTCTGATTGCTTTTTGGAATGTAGTGTAGAGCTTCTTCTGGAGTGCAGGTGACATGATT... |
Task1_train_41702 | A genetic alteration is present on Chromosome 11. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GCCAGAAGAATAGATCTTATTTGCTTGGTTTATCTTTGAGCCCATTGTGCTGGCCCATCAGCTCACAAACCCCATTCTTGTTATTTCACTTTACAATCAGGAATTTGGACTTGATTTTATATTATTAAAGTAACAGAAACTCTAAATGAGCCCATATGTGGATATCTTCATTTGATTCTTTCTTTGATGTATGACAGCCAGGACATTTTTGGAAGCAGTATAGATTATATGTAGCACTTGTCTTGGGTCTGATTGCTTTTTGGAATGTAGTGTAGAGCTTCTTCTGGAGTGCAGGTGACATGATTGTAAACAGAGAAATT... | GCCAGAAGAATAGATCTTATTTGCTTGGTTTATCTTTGAGCCCATTGTGCTGGCCCATCAGCTCACAAACCCCATTCTTGTTATTTCACTTTACAATCAGGAATTTGGACTTGATTTTATATTATTAAAGTAACAGAAACTCTAAATGAGCCCATATGTGGATATCTTCATTTGATTCTTTCTTTGATGTATGACAGCCAGGACATTTTTGGAAGCAGTATAGATTATATGTAGCACTTGTCTTGGGTCTGATTGCTTTTTGGAATGTAGTGTAGAGCTTCTTCTGGAGTGCAGGTGACATGATTGTAAACAGAGAAATT... |
Task1_train_41703 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TTTTGGAAGCAGTATAGATTATATGTAGCACTTGTCTTGGGTCTGATTGCTTTTTGGAATGTAGTGTAGAGCTTCTTCTGGAGTGCAGGTGACATGATTGTAAACAGAGAAATTCCAAATATACAGGAAATGGGCAAAAGAGAAACAGGTAGATGATCAAGTTGCTTTAGAAGACTGTGAGGAGAAATTACTATCTGATAGTACCACACAGATCCTTGCACAAGAGGAATGATATCCAATTCTTGCCAGGCATTGAGTGAGTTATCTTATTTCCTTCATCAAACGTTTATTGAAAAAGGCACTGTTCTTTGCACTGAGAG... | TTTTGGAAGCAGTATAGATTATATGTAGCACTTGTCTTGGGTCTGATTGCTTTTTGGAATGTAGTGTAGAGCTTCTTCTGGAGTGCAGGTGACATGATTGTAAACAGAGAAATTCCAAATATACAGGAAATGGGCAAAAGAGAAACAGGTAGATGATCAAGTTGCTTTAGAAGACTGTGAGGAGAAATTACTATCTGATAGTACCACACAGATCCTTGCACAAGAGGAATGATATCCAATTCTTGCCAGGCATTGAGTGAGTTATCTTATTTCCTTCATCAAACGTTTATTGAAAAAGGCACTGTTCTTTGCACTGAGAG... |
Task1_train_41704 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GCTAAATGGTTATACAAGCTGACTCTGACATTTCTGGCTATAAGTAAATTAAGGTGTGTTTGACTTTTGGAATGTTCTTTTTTGTTGTGAAACCAAATATTTCTCTCCATCATTTGAAGCACTTAGTTTTTATTTTTTCTCTCTTAGAGACATATACAAGGAGCCCTATACCTCTTAGATATTTTGAACATTTGGATATAAATGCCATGTGCCACATATATTTATATTGTGCTAGCTAAAACCTCAGTTATGTCAGTCATTATTCAAATGACAATATTTTTAGATCATGTTTCTGATATTGTCCAGTTTTTCTATATTCC... | GCTAAATGGTTATACAAGCTGACTCTGACATTTCTGGCTATAAGTAAATTAAGGTGTGTTTGACTTTTGGAATGTTCTTTTTTGTTGTGAAACCAAATATTTCTCTCCATCATTTGAAGCACTTAGTTTTTATTTTTTCTCTCTTAGAGACATATACAAGGAGCCCTATACCTCTTAGATATTTTGAACATTTGGATATAAATGCCATGTGCCACATATATTTATATTGTGCTAGCTAAAACCTCAGTTATGTCAGTCATTATTCAAATGACAATATTTTTAGATCATGTTTCTGATATTGTCCAGTTTTTCTATATTCC... |
Task1_train_41705 | A variant was discovered on Chromosome 11. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TTCTAAGATATTGCCAAGCAGTTTTCCGAAGTAGTTGTACGGTTTTACACCTCTCCTCACCAGCTATGTGTGAGAGCTTGAGTTATCCCATATCCTTGGCAAACTTTGGAACTGTAAGTTTTTGTTTATTTTGTTTTTTCTTTCTTTTATAATTTTTAGCCATTTCCATGTGGCTGTGTAGTGGTATGTAATTTTCCTGATGAATAATGAATTTGGTATCTTTTTACGTGCTTATCAACTATTTACATATCTTCTGTCATATATCATCTATACAAATACTTTTCTTATATTTTAATTTGGTCTATTGTCTTTGTATCATT... | TTCTAAGATATTGCCAAGCAGTTTTCCGAAGTAGTTGTACGGTTTTACACCTCTCCTCACCAGCTATGTGTGAGAGCTTGAGTTATCCCATATCCTTGGCAAACTTTGGAACTGTAAGTTTTTGTTTATTTTGTTTTTTCTTTCTTTTATAATTTTTAGCCATTTCCATGTGGCTGTGTAGTGGTATGTAATTTTCCTGATGAATAATGAATTTGGTATCTTTTTACGTGCTTATCAACTATTTACATATCTTCTGTCATATATCATCTATACAAATACTTTTCTTATATTTTAATTTGGTCTATTGTCTTTGTATCATT... |
Task1_train_41706 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | CTGTAAGTTTTTGTTTATTTTGTTTTTTCTTTCTTTTATAATTTTTAGCCATTTCCATGTGGCTGTGTAGTGGTATGTAATTTTCCTGATGAATAATGAATTTGGTATCTTTTTACGTGCTTATCAACTATTTACATATCTTCTGTCATATATCATCTATACAAATACTTTTCTTATATTTTAATTTGGTCTATTGTCTTTGTATCATTGACATGTTGATATTATTTGTATATATTTACATAAAAGGCCATAGTCAGATATACGTATTTTTTGTGGCTTACTCTTAATTTTCTTTTTTTAACTTTTATTTTAAGTTTAGA... | CTGTAAGTTTTTGTTTATTTTGTTTTTTCTTTCTTTTATAATTTTTAGCCATTTCCATGTGGCTGTGTAGTGGTATGTAATTTTCCTGATGAATAATGAATTTGGTATCTTTTTACGTGCTTATCAACTATTTACATATCTTCTGTCATATATCATCTATACAAATACTTTTCTTATATTTTAATTTGGTCTATTGTCTTTGTATCATTGACATGTTGATATTATTTGTATATATTTACATAAAAGGCCATAGTCAGATATACGTATTTTTTGTGGCTTACTCTTAATTTTCTTTTTTTAACTTTTATTTTAAGTTTAGA... |
Task1_train_41707 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GGGGAGTTTGTTGTACAGATTATTTTATCACCCAGGTATTAAACCCAGTACCCGTGAGTTACTTTTCCTGATCTTTTCCCTCCTCCCACCTTCCACTGGCTCTGATAGGCCCCAGTGTGTGTTGTCCCCCTCTATGTGTCCAAGTGGTCATGTGTTCAAATCATTTAGCTCCCACTTAGAAGTGAGAACATATGGTATTTGGTTTTCTGTTCCTGTGTCGGTTTGCTAAGGATAATACATTCATGTCCCTGCAATGGACATAATCTTGTGCTTTTTTAATGGTACCTTTGGAGATGTGCTTTTAATTAGGATAAAAAAGG... | GGGGAGTTTGTTGTACAGATTATTTTATCACCCAGGTATTAAACCCAGTACCCGTGAGTTACTTTTCCTGATCTTTTCCCTCCTCCCACCTTCCACTGGCTCTGATAGGCCCCAGTGTGTGTTGTCCCCCTCTATGTGTCCAAGTGGTCATGTGTTCAAATCATTTAGCTCCCACTTAGAAGTGAGAACATATGGTATTTGGTTTTCTGTTCCTGTGTCGGTTTGCTAAGGATAATACATTCATGTCCCTGCAATGGACATAATCTTGTGCTTTTTTAATGGTACCTTTGGAGATGTGCTTTTAATTAGGATAAAAAAGG... |
Task1_train_41708 | Chromosome 11 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | ATTCATGTCCCTGCAATGGACATAATCTTGTGCTTTTTTAATGGTACCTTTGGAGATGTGCTTTTAATTAGGATAAAAAAGGATTTATCAATGTTATATGGCTAATTCATGTGTGCATATATGTCCTAAGGAATCTAATTGGATTACTCCACTATATTGAAATTTTCCTCTAGTGTTTTTTCCTAAAGTTTAATAGTTTATTGTTTATGCTTAAATTTAAGATTTATTTCAATATTCTTGTTTGCATGGGTGTGAGATAGAAGATTTTAGATTTTCTGTTTCTACTTTATTTAAAATTCAAGTATGACTTATTTGGAATT... | ATTCATGTCCCTGCAATGGACATAATCTTGTGCTTTTTTAATGGTACCTTTGGAGATGTGCTTTTAATTAGGATAAAAAAGGATTTATCAATGTTATATGGCTAATTCATGTGTGCATATATGTCCTAAGGAATCTAATTGGATTACTCCACTATATTGAAATTTTCCTCTAGTGTTTTTTCCTAAAGTTTAATAGTTTATTGTTTATGCTTAAATTTAAGATTTATTTCAATATTCTTGTTTGCATGGGTGTGAGATAGAAGATTTTAGATTTTCTGTTTCTACTTTATTTAAAATTCAAGTATGACTTATTTGGAATT... |
Task1_train_41709 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | CTAAGGAATCTAATTGGATTACTCCACTATATTGAAATTTTCCTCTAGTGTTTTTTCCTAAAGTTTAATAGTTTATTGTTTATGCTTAAATTTAAGATTTATTTCAATATTCTTGTTTGCATGGGTGTGAGATAGAAGATTTTAGATTTTCTGTTTCTACTTTATTTAAAATTCAAGTATGACTTATTTGGAATTTTACATTAATGTATCAAATGACAAAATCTTTTGTTTAGTGCATAACAGAGGCTACATTTATATATTTCCTAATTTTATAACTCCATCTTTGGCACACTCCTAATTAAAGAAAGAGGAAAGAGATT... | CTAAGGAATCTAATTGGATTACTCCACTATATTGAAATTTTCCTCTAGTGTTTTTTCCTAAAGTTTAATAGTTTATTGTTTATGCTTAAATTTAAGATTTATTTCAATATTCTTGTTTGCATGGGTGTGAGATAGAAGATTTTAGATTTTCTGTTTCTACTTTATTTAAAATTCAAGTATGACTTATTTGGAATTTTACATTAATGTATCAAATGACAAAATCTTTTGTTTAGTGCATAACAGAGGCTACATTTATATATTTCCTAATTTTATAACTCCATCTTTGGCACACTCCTAATTAAAGAAAGAGGAAAGAGATT... |
Task1_train_41710 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | ATATTGAAATTTTCCTCTAGTGTTTTTTCCTAAAGTTTAATAGTTTATTGTTTATGCTTAAATTTAAGATTTATTTCAATATTCTTGTTTGCATGGGTGTGAGATAGAAGATTTTAGATTTTCTGTTTCTACTTTATTTAAAATTCAAGTATGACTTATTTGGAATTTTACATTAATGTATCAAATGACAAAATCTTTTGTTTAGTGCATAACAGAGGCTACATTTATATATTTCCTAATTTTATAACTCCATCTTTGGCACACTCCTAATTAAAGAAAGAGGAAAGAGATTAATGAAAATGTGTGAACATCATGTTTAC... | ATATTGAAATTTTCCTCTAGTGTTTTTTCCTAAAGTTTAATAGTTTATTGTTTATGCTTAAATTTAAGATTTATTTCAATATTCTTGTTTGCATGGGTGTGAGATAGAAGATTTTAGATTTTCTGTTTCTACTTTATTTAAAATTCAAGTATGACTTATTTGGAATTTTACATTAATGTATCAAATGACAAAATCTTTTGTTTAGTGCATAACAGAGGCTACATTTATATATTTCCTAATTTTATAACTCCATCTTTGGCACACTCCTAATTAAAGAAAGAGGAAAGAGATTAATGAAAATGTGTGAACATCATGTTTAC... |
Task1_train_41711 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | ATTGAAATTTTCCTCTAGTGTTTTTTCCTAAAGTTTAATAGTTTATTGTTTATGCTTAAATTTAAGATTTATTTCAATATTCTTGTTTGCATGGGTGTGAGATAGAAGATTTTAGATTTTCTGTTTCTACTTTATTTAAAATTCAAGTATGACTTATTTGGAATTTTACATTAATGTATCAAATGACAAAATCTTTTGTTTAGTGCATAACAGAGGCTACATTTATATATTTCCTAATTTTATAACTCCATCTTTGGCACACTCCTAATTAAAGAAAGAGGAAAGAGATTAATGAAAATGTGTGAACATCATGTTTACTA... | ATTGAAATTTTCCTCTAGTGTTTTTTCCTAAAGTTTAATAGTTTATTGTTTATGCTTAAATTTAAGATTTATTTCAATATTCTTGTTTGCATGGGTGTGAGATAGAAGATTTTAGATTTTCTGTTTCTACTTTATTTAAAATTCAAGTATGACTTATTTGGAATTTTACATTAATGTATCAAATGACAAAATCTTTTGTTTAGTGCATAACAGAGGCTACATTTATATATTTCCTAATTTTATAACTCCATCTTTGGCACACTCCTAATTAAAGAAAGAGGAAAGAGATTAATGAAAATGTGTGAACATCATGTTTACTA... |
Task1_train_41712 | A mutation on Chromosome 11 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GATTACTAAAAACATTGGATATATTTTCATAAACTTACTGACCAGTCATATATCTTTTCTGTGAGATAGCTCTTCTGATATTTCACTAGTAGTTAATATTTGGTTGTCTGTGTACTATTATTTGCATATGTTATTTACGTATTTTAGATAAAAGTCCTCTGTCAGGCATATGTGTTACCTTGAGCTTGCCATTTCATTTTCTTAATGTCATTAATTTTGTTTTCATTTTGATGAAATATAATCGAAACATTGTTAGTTTTTGGTTCTTTTGCTTTTTAAAAAATATTTTATTTTTTATTATACTTTAAGCTTTAGGGTAC... | GATTACTAAAAACATTGGATATATTTTCATAAACTTACTGACCAGTCATATATCTTTTCTGTGAGATAGCTCTTCTGATATTTCACTAGTAGTTAATATTTGGTTGTCTGTGTACTATTATTTGCATATGTTATTTACGTATTTTAGATAAAAGTCCTCTGTCAGGCATATGTGTTACCTTGAGCTTGCCATTTCATTTTCTTAATGTCATTAATTTTGTTTTCATTTTGATGAAATATAATCGAAACATTGTTAGTTTTTGGTTCTTTTGCTTTTTAAAAAATATTTTATTTTTTATTATACTTTAAGCTTTAGGGTAC... |
Task1_train_41713 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CCCCCTCCCCCCACCCCACAACAGGCCCTGGTGTGTGATGTTCCCCTTCCTGTGTCCATGTGTTCTCATTGTTCAGTTCCCACCTATGAGTGAGAACATGCAGTGTTTGGTTTTTTGTCCTTGCGATAGTTTGCTGAGAATGATGGTTTCCAGCTTAATCCATGTTCTTTCTAAGAAATCATAAACTTTTCCAAGATATCAAGGATTTTATCAGTTGTTTTTCCAGAAGTTTTATAGTTAGTTTTATGCTCAGGTCTGATTTATTTCAGATTTATTTTGGTGTAGAAATGTGTTAAGAAATGTATAGATTTTCTAAATTT... | CCCCCTCCCCCCACCCCACAACAGGCCCTGGTGTGTGATGTTCCCCTTCCTGTGTCCATGTGTTCTCATTGTTCAGTTCCCACCTATGAGTGAGAACATGCAGTGTTTGGTTTTTTGTCCTTGCGATAGTTTGCTGAGAATGATGGTTTCCAGCTTAATCCATGTTCTTTCTAAGAAATCATAAACTTTTCCAAGATATCAAGGATTTTATCAGTTGTTTTTCCAGAAGTTTTATAGTTAGTTTTATGCTCAGGTCTGATTTATTTCAGATTTATTTTGGTGTAGAAATGTGTTAAGAAATGTATAGATTTTCTAAATTT... |
Task1_train_41714 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | AGAAGTTTTATAGTTAGTTTTATGCTCAGGTCTGATTTATTTCAGATTTATTTTGGTGTAGAAATGTGTTAAGAAATGTATAGATTTTCTAAATTTTGTATTTTTTTAAATAATTTGACTCATTCATTTGAAATGTAACTTTAGTGAATGGAATAGCTACATCATCTATTCACTGTTTAACAGAAAGGGGATCACACTTGTAATTCTGTTTTTTAATTGTGTGTCTCTACTTTTTACTCCCTTCTAATTCACAAAAGTTGAAGAAAATCAAAGGAAATACTGAGGTAGTAAGATTGCTGTTTCTGTACATTGAAATCAGT... | AGAAGTTTTATAGTTAGTTTTATGCTCAGGTCTGATTTATTTCAGATTTATTTTGGTGTAGAAATGTGTTAAGAAATGTATAGATTTTCTAAATTTTGTATTTTTTTAAATAATTTGACTCATTCATTTGAAATGTAACTTTAGTGAATGGAATAGCTACATCATCTATTCACTGTTTAACAGAAAGGGGATCACACTTGTAATTCTGTTTTTTAATTGTGTGTCTCTACTTTTTACTCCCTTCTAATTCACAAAAGTTGAAGAAAATCAAAGGAAATACTGAGGTAGTAAGATTGCTGTTTCTGTACATTGAAATCAGT... |
Task1_train_41715 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | AGTTTTATGCTCAGGTCTGATTTATTTCAGATTTATTTTGGTGTAGAAATGTGTTAAGAAATGTATAGATTTTCTAAATTTTGTATTTTTTTAAATAATTTGACTCATTCATTTGAAATGTAACTTTAGTGAATGGAATAGCTACATCATCTATTCACTGTTTAACAGAAAGGGGATCACACTTGTAATTCTGTTTTTTAATTGTGTGTCTCTACTTTTTACTCCCTTCTAATTCACAAAAGTTGAAGAAAATCAAAGGAAATACTGAGGTAGTAAGATTGCTGTTTCTGTACATTGAAATCAGTAATTTCTTACTATCT... | AGTTTTATGCTCAGGTCTGATTTATTTCAGATTTATTTTGGTGTAGAAATGTGTTAAGAAATGTATAGATTTTCTAAATTTTGTATTTTTTTAAATAATTTGACTCATTCATTTGAAATGTAACTTTAGTGAATGGAATAGCTACATCATCTATTCACTGTTTAACAGAAAGGGGATCACACTTGTAATTCTGTTTTTTAATTGTGTGTCTCTACTTTTTACTCCCTTCTAATTCACAAAAGTTGAAGAAAATCAAAGGAAATACTGAGGTAGTAAGATTGCTGTTTCTGTACATTGAAATCAGTAATTTCTTACTATCT... |
Task1_train_41716 | A mutation located on Chromosome 11 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GGGGGAAGAGGGTCTTAGCATAAAAATAATATTGCATCTAAATATACTGAGAAAGAGAAACAGTTCAATTGAATTATTGCAAAGCTAACAACTAAGAATACAGTTTTAAAATCTGGGTTTGGAACACCCTGTTTCTAAGAATCAAATCTGCTTAGAAAATAAAGTGATTTAGAAAGAATGCTTCAGTTTTATAACCCTAACAAGAGCAGAAGAAAAATGAGACTAAAAGTAAAATAAGTTAATTAAACTGGAATAAGAGAGAGAAGAGGACAGGTTAGAAAACTATGTGGCACCAAATGATAATTTGAAGGTCAGGATCC... | GGGGGAAGAGGGTCTTAGCATAAAAATAATATTGCATCTAAATATACTGAGAAAGAGAAACAGTTCAATTGAATTATTGCAAAGCTAACAACTAAGAATACAGTTTTAAAATCTGGGTTTGGAACACCCTGTTTCTAAGAATCAAATCTGCTTAGAAAATAAAGTGATTTAGAAAGAATGCTTCAGTTTTATAACCCTAACAAGAGCAGAAGAAAAATGAGACTAAAAGTAAAATAAGTTAATTAAACTGGAATAAGAGAGAGAAGAGGACAGGTTAGAAAACTATGTGGCACCAAATGATAATTTGAAGGTCAGGATCC... |
Task1_train_41717 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CTTCAGTTTTATAACCCTAACAAGAGCAGAAGAAAAATGAGACTAAAAGTAAAATAAGTTAATTAAACTGGAATAAGAGAGAGAAGAGGACAGGTTAGAAAACTATGTGGCACCAAATGATAATTTGAAGGTCAGGATCCTGGATTCAGAAAAGTGTTAATTGCACTATTAAAGCTGCTGAAAAAGAGTAAGTACTATGTGTCCCCCTCAAAAAGATCTTAAGGAATGGGAGGACTTGAGAAGATATAGGCACTGTATCTGAGAAACTCTAAGATAACATTAAAAAATATTAGAGCAAGGCATACAGAAGAGAAGATGTA... | CTTCAGTTTTATAACCCTAACAAGAGCAGAAGAAAAATGAGACTAAAAGTAAAATAAGTTAATTAAACTGGAATAAGAGAGAGAAGAGGACAGGTTAGAAAACTATGTGGCACCAAATGATAATTTGAAGGTCAGGATCCTGGATTCAGAAAAGTGTTAATTGCACTATTAAAGCTGCTGAAAAAGAGTAAGTACTATGTGTCCCCCTCAAAAAGATCTTAAGGAATGGGAGGACTTGAGAAGATATAGGCACTGTATCTGAGAAACTCTAAGATAACATTAAAAAATATTAGAGCAAGGCATACAGAAGAGAAGATGTA... |
Task1_train_41718 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | GTCCCCCTCAAAAAGATCTTAAGGAATGGGAGGACTTGAGAAGATATAGGCACTGTATCTGAGAAACTCTAAGATAACATTAAAAAATATTAGAGCAAGGCATACAGAAGAGAAGATGTATTAAGGGGAAGGTGAGCAAGGCCACGGTAAATGTTTAGGACCTGGTTCAACAAACTGATAGGAAGATGTATTCTGGGTGAGATTATCAAAATGTAGGAGCTAAAGGTAGACAAGCTTTGTTAGAACAGTAGGATTTTGGTAGATACAAAATTTACTGATTTCTTATTTCTTGCTTGGAATGATTCTTTAAGCTAAAATCT... | GTCCCCCTCAAAAAGATCTTAAGGAATGGGAGGACTTGAGAAGATATAGGCACTGTATCTGAGAAACTCTAAGATAACATTAAAAAATATTAGAGCAAGGCATACAGAAGAGAAGATGTATTAAGGGGAAGGTGAGCAAGGCCACGGTAAATGTTTAGGACCTGGTTCAACAAACTGATAGGAAGATGTATTCTGGGTGAGATTATCAAAATGTAGGAGCTAAAGGTAGACAAGCTTTGTTAGAACAGTAGGATTTTGGTAGATACAAAATTTACTGATTTCTTATTTCTTGCTTGGAATGATTCTTTAAGCTAAAATCT... |
Task1_train_41719 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | ATTTCTAGGTATTTTATTTGAGTTGTAGGTATTGTAAATAGGATTACTTCTTAAATTTCTTTTTCAGATTGCTCACTGTTGGCATGTAGAAATGCTACTGATTTTGTATGTCAACTTTATATCTTGCAACTTTACTGAGTTTGTTCAGTAGTACAAAATGAATTTAAACTTTTCTGAACAATTTGAACTTCTCTGAAAAGTTCAAAAAGTCCAGAAAAAAAGTTCAAATTGAATTTGAACTTTTCCAAATCAGTTCTAATAGTTTTTTTTGGTGGCATCTTTAGGCTTTTCTAAACATAAGATCATGTCATCTGCAAGCA... | ATTTCTAGGTATTTTATTTGAGTTGTAGGTATTGTAAATAGGATTACTTCTTAAATTTCTTTTTCAGATTGCTCACTGTTGGCATGTAGAAATGCTACTGATTTTGTATGTCAACTTTATATCTTGCAACTTTACTGAGTTTGTTCAGTAGTACAAAATGAATTTAAACTTTTCTGAACAATTTGAACTTCTCTGAAAAGTTCAAAAAGTCCAGAAAAAAAGTTCAAATTGAATTTGAACTTTTCCAAATCAGTTCTAATAGTTTTTTTTGGTGGCATCTTTAGGCTTTTCTAAACATAAGATCATGTCATCTGCAAGCA... |
Task1_train_41720 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | TTGTAAAGTGGAAGAAAAAGAGAAAGGGAATAAAAGAGATTATAGGAAAGGGGGAGTAGGCATGTTCAGATAGTGGAAAGGATAAAAAGAGATGGAATAGAAAGTATCAGAAGGTGATGAAATGAATGGATCATAAAACCTCAGTGTTAGCAATGAACAAAGGGATCAGTTTGGTCATATTCTTAGCCAGCATTTGATTCTTCTCAGAAATATTCCAGACAGAATGGTTGAATATTCTGTCTGGAATATGTACTTAAATCCCTACTGCTGGATAGTTCATAAATTCCCAAGATAGCTAATTATTTTTTGATAGTTCTGAT... | TTGTAAAGTGGAAGAAAAAGAGAAAGGGAATAAAAGAGATTATAGGAAAGGGGGAGTAGGCATGTTCAGATAGTGGAAAGGATAAAAAGAGATGGAATAGAAAGTATCAGAAGGTGATGAAATGAATGGATCATAAAACCTCAGTGTTAGCAATGAACAAAGGGATCAGTTTGGTCATATTCTTAGCCAGCATTTGATTCTTCTCAGAAATATTCCAGACAGAATGGTTGAATATTCTGTCTGGAATATGTACTTAAATCCCTACTGCTGGATAGTTCATAAATTCCCAAGATAGCTAATTATTTTTTGATAGTTCTGAT... |
Task1_train_41721 | A variant was discovered on Chromosome 11. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | AGGGTCCCTTAAGTAGGAGATGTCAAGAAATGATAAGACTTGCAACACATATTTTGTTATAAATGCCTATTAAGGATAAAACTGGAGGGAGCAAGAGTCAGCGATGAAGGCCTCAGACCAGGATGAAAGTCACCTACGAAAGGAGAAAAAAATGGAAAGATCGGTTAGGAAAATCTCAGACCATAGAGCAGTTCTAAAAAGTCTTGGTCAGGAGGATAGGAAGTCTCTAAACAAAGATTTCCTATCAGAAAAGACATATGTTAGATGGAAATTGCCAGCTCTCTTTAAGTCCCACCCACCCTGCTGAGTCATTGGTGGAG... | AGGGTCCCTTAAGTAGGAGATGTCAAGAAATGATAAGACTTGCAACACATATTTTGTTATAAATGCCTATTAAGGATAAAACTGGAGGGAGCAAGAGTCAGCGATGAAGGCCTCAGACCAGGATGAAAGTCACCTACGAAAGGAGAAAAAAATGGAAAGATCGGTTAGGAAAATCTCAGACCATAGAGCAGTTCTAAAAAGTCTTGGTCAGGAGGATAGGAAGTCTCTAAACAAAGATTTCCTATCAGAAAAGACATATGTTAGATGGAAATTGCCAGCTCTCTTTAAGTCCCACCCACCCTGCTGAGTCATTGGTGGAG... |
Task1_train_41722 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | AGAGTAAGAATGGACTCTGCCTAAACACCATGGTGGATCCAAAGAAGTGCAGCTATAGACTTTCAGTCAGCTATGCACCCCACTGCTGGGTCTCTTCATGGGGAGCTGAGCTGTTCTTCTCTGAGACTACCACACTCCACCTCCAAAAATATAAATTAAACCCCAAAGCTGTTCAGATTTATAATTGTCATTATTTTTGTATGTTATTAATTATTAATTAAAATAATACATTTATTATTGGTGTAAGAAGCAAGGTACTCCAATTCAGCCAGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGATGAAGCA... | AGAGTAAGAATGGACTCTGCCTAAACACCATGGTGGATCCAAAGAAGTGCAGCTATAGACTTTCAGTCAGCTATGCACCCCACTGCTGGGTCTCTTCATGGGGAGCTGAGCTGTTCTTCTCTGAGACTACCACACTCCACCTCCAAAAATATAAATTAAACCCCAAAGCTGTTCAGATTTATAATTGTCATTATTTTTGTATGTTATTAATTATTAATTAAAATAATACATTTATTATTGGTGTAAGAAGCAAGGTACTCCAATTCAGCCAGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGATGAAGCA... |
Task1_train_41723 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CTCTACCTCATGCTGTACACAAAAGTTAATCTAAAAATGGACCAAAACCATACACACACAAAAAACTTAAACTATAGGCTGAAGTGGAAGAATTACTTGAGCCCGGGAGTTGGAGGCTGCAGTAAGCTATGATCGAATCACTGCACTCCTATCTGGGTGACAACCTTTATATAAAATGTGTTTCATGTCTTATTGGTGAGATAAAGTTTAAGTAGGCTCACAAAATATTTGTAGAAATATAGTTTATTAATATTAATATACATTCCTTATGATAAACCACACTGGATAAGGAAAATGTTGTATAAAATATTTCTACTAAC... | CTCTACCTCATGCTGTACACAAAAGTTAATCTAAAAATGGACCAAAACCATACACACACAAAAAACTTAAACTATAGGCTGAAGTGGAAGAATTACTTGAGCCCGGGAGTTGGAGGCTGCAGTAAGCTATGATCGAATCACTGCACTCCTATCTGGGTGACAACCTTTATATAAAATGTGTTTCATGTCTTATTGGTGAGATAAAGTTTAAGTAGGCTCACAAAATATTTGTAGAAATATAGTTTATTAATATTAATATACATTCCTTATGATAAACCACACTGGATAAGGAAAATGTTGTATAAAATATTTCTACTAAC... |
Task1_train_41724 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | TGCCCTGACTTAGTTCTTGTTCCCGCTCATTTATACCAATGGTAATTGTTTTTTTTTCTTTATCCGTATCAAAGTAGATTTACTTTTGTCCTTCCTTATTCTTGATTCTTTTCTAATATCCCAAGACCCCCATGGACCTAGACACAGACAGTCCACTGGAGGGTGGGATTCAGCAAGGCCCAGAGGACTGACCAGCAGTGGTTGAGTAAGGTATTAAATCAATTCCAATGAATGAATTAATATATTTAAGGTACCTCAAATGGTGCACAAACACATGGTGCAAGTTCAGTAACTGTTAAGTGTCATTATTATCATAATCA... | TGCCCTGACTTAGTTCTTGTTCCCGCTCATTTATACCAATGGTAATTGTTTTTTTTTCTTTATCCGTATCAAAGTAGATTTACTTTTGTCCTTCCTTATTCTTGATTCTTTTCTAATATCCCAAGACCCCCATGGACCTAGACACAGACAGTCCACTGGAGGGTGGGATTCAGCAAGGCCCAGAGGACTGACCAGCAGTGGTTGAGTAAGGTATTAAATCAATTCCAATGAATGAATTAATATATTTAAGGTACCTCAAATGGTGCACAAACACATGGTGCAAGTTCAGTAACTGTTAAGTGTCATTATTATCATAATCA... |
Task1_train_41725 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | ATTTATACCAATGGTAATTGTTTTTTTTTCTTTATCCGTATCAAAGTAGATTTACTTTTGTCCTTCCTTATTCTTGATTCTTTTCTAATATCCCAAGACCCCCATGGACCTAGACACAGACAGTCCACTGGAGGGTGGGATTCAGCAAGGCCCAGAGGACTGACCAGCAGTGGTTGAGTAAGGTATTAAATCAATTCCAATGAATGAATTAATATATTTAAGGTACCTCAAATGGTGCACAAACACATGGTGCAAGTTCAGTAACTGTTAAGTGTCATTATTATCATAATCAAAGCATAATCCAAGTATCAGAGTTTTTC... | ATTTATACCAATGGTAATTGTTTTTTTTTCTTTATCCGTATCAAAGTAGATTTACTTTTGTCCTTCCTTATTCTTGATTCTTTTCTAATATCCCAAGACCCCCATGGACCTAGACACAGACAGTCCACTGGAGGGTGGGATTCAGCAAGGCCCAGAGGACTGACCAGCAGTGGTTGAGTAAGGTATTAAATCAATTCCAATGAATGAATTAATATATTTAAGGTACCTCAAATGGTGCACAAACACATGGTGCAAGTTCAGTAACTGTTAAGTGTCATTATTATCATAATCAAAGCATAATCCAAGTATCAGAGTTTTTC... |
Task1_train_41726 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AAAGATCTTCCTCTAGCAGATTTGGAGAAGATAGATAGAGTTTGTCTCACGTCTCCTGTTGGTCAGACCTGTGCTGCAGTTGCTTCTCTGCCCTGCTCTCAGCTCTCCCTCAGAATGTCTCCTGGCCACGAGCTGGAGCACTGAACTCTTCAATGTAGAACAGCAGAACCTTTAGCAGAGTAATACAGAGTGGTCTTTGGCACTCAAAATCCAGATCCCTTCCAGACTCCCTGAGAGTGGGACGTGTAATATGACTCCTCTTTCTTTCCGATTCTATATTGATTAACTGTAATACACATACAGACACACACACACACACA... | AAAGATCTTCCTCTAGCAGATTTGGAGAAGATAGATAGAGTTTGTCTCACGTCTCCTGTTGGTCAGACCTGTGCTGCAGTTGCTTCTCTGCCCTGCTCTCAGCTCTCCCTCAGAATGTCTCCTGGCCACGAGCTGGAGCACTGAACTCTTCAATGTAGAACAGCAGAACCTTTAGCAGAGTAATACAGAGTGGTCTTTGGCACTCAAAATCCAGATCCCTTCCAGACTCCCTGAGAGTGGGACGTGTAATATGACTCCTCTTTCTTTCCGATTCTATATTGATTAACTGTAATACACATACAGACACACACACACACACA... |
Task1_train_41727 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | TTTAGGAATGGAATGATAAGATAGGAGGAAGACATATTTTCACTGTATAACCCCCATTTATATTGTTTAGTGCTGTACCATACGCAAATATTACTTAGTCAAAATATATGACTTTTTAAATGATACTTAGAGTTCATTTTTCTCATGACTAAGCAGAGTTCCAGGAAGATGAAGTGACTTGTCTCAGCTCATGGAAAAACTCAAGGAAGTGCTGATAATTACATAAAAGAATTATTGCAGGGTGATAACTAAAATGTAGTAAGTGCCCTGCATTTAATTCTTCAAAGACCCCACGAAGTCAGAATCATTACATCACTTTC... | TTTAGGAATGGAATGATAAGATAGGAGGAAGACATATTTTCACTGTATAACCCCCATTTATATTGTTTAGTGCTGTACCATACGCAAATATTACTTAGTCAAAATATATGACTTTTTAAATGATACTTAGAGTTCATTTTTCTCATGACTAAGCAGAGTTCCAGGAAGATGAAGTGACTTGTCTCAGCTCATGGAAAAACTCAAGGAAGTGCTGATAATTACATAAAAGAATTATTGCAGGGTGATAACTAAAATGTAGTAAGTGCCCTGCATTTAATTCTTCAAAGACCCCACGAAGTCAGAATCATTACATCACTTTC... |
Task1_train_41728 | Given this context: Chromosome 11 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GCATGTCTCAATCAGCTGAAGCTTCCCTTTCGGTCTTTTAGTTTACCCAACAACATTCTTACCTTAAAAAGTCTTAAAACCCAAGAATTAGAAGCACTTACCTTACATCAATGCCTGGCATATAGTATTTTTAAATGTTTGCTGAATGGAAATGAATTTTGAAGAGACTGCATCAGGGTCTGGATCACTCGGGATTGGATCATCAGTTTTGTATACTGATAAAACCAACCAGACAATCCTTGCTTTCGGGGGCCAGTACAATTCCCACAAGCATCCCTGTCACATATATATGCTAGCCATTGCTCAAACCACCAATTTGT... | GCATGTCTCAATCAGCTGAAGCTTCCCTTTCGGTCTTTTAGTTTACCCAACAACATTCTTACCTTAAAAAGTCTTAAAACCCAAGAATTAGAAGCACTTACCTTACATCAATGCCTGGCATATAGTATTTTTAAATGTTTGCTGAATGGAAATGAATTTTGAAGAGACTGCATCAGGGTCTGGATCACTCGGGATTGGATCATCAGTTTTGTATACTGATAAAACCAACCAGACAATCCTTGCTTTCGGGGGCCAGTACAATTCCCACAAGCATCCCTGTCACATATATATGCTAGCCATTGCTCAAACCACCAATTTGT... |
Task1_train_41729 | A variant has been detected on Chromosome 11. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | AGTAGCTTTGTCCTATTAGCTACTACTTTAATGTCTTTGTTAAAAAAAGAGAAAGCTTAAGAAGTCCCAAAGATAAATGTTATCAAATACACTAATTTAAATTTGTAATGGAGTAATTAATGGGTGGCAAATTCCTTGAACAATAGTAGGTTTTAAATATCTTAGTTTGTGGACCCAGTTTTCTAAGCAACAACATCCCCAAAGAAATACTACTGGAGCCAAGACCTGGAGAACTTTGGTGCAATTTCCCTCCTTTAGCTTACTCTAACTCATGATTGCGCCTATTAGACTTTATTATTGCTCTTTAGTGTGATCATTCT... | AGTAGCTTTGTCCTATTAGCTACTACTTTAATGTCTTTGTTAAAAAAAGAGAAAGCTTAAGAAGTCCCAAAGATAAATGTTATCAAATACACTAATTTAAATTTGTAATGGAGTAATTAATGGGTGGCAAATTCCTTGAACAATAGTAGGTTTTAAATATCTTAGTTTGTGGACCCAGTTTTCTAAGCAACAACATCCCCAAAGAAATACTACTGGAGCCAAGACCTGGAGAACTTTGGTGCAATTTCCCTCCTTTAGCTTACTCTAACTCATGATTGCGCCTATTAGACTTTATTATTGCTCTTTAGTGTGATCATTCT... |
Task1_train_41730 | This genomic variant is located on Chromosome 11. Can you determine its pathogenicity and name any linked disease? | Benign | GAGCCTGTGGCCCCAGTCCTATCCAGTCCCCACCTCCATTGATGGGTCCATGGGTAACCAGCTTCTGTCCCTGCTGGGTCCTGCCTGTCTTTAAGTACCTTGACCCTGGTGTCTGTCCTGGGGGAGAGAGAAAGGGTCTGTAGCTGTGGCCAACCCAGCCTGGGGTGGGGAGTGGAGCAGGTATGAGATCCGGAGTGACCACAGCCTTTGGATTGGGCATGTGAGTGCCGAAGATGAGGGAACGTACACCTGTGTGGCGGAGAACAGTGTGGGCCGCGCTGAAGCATCTGGCTCCCTCAGTGTTCACGGTGAGGGCTGTA... | GAGCCTGTGGCCCCAGTCCTATCCAGTCCCCACCTCCATTGATGGGTCCATGGGTAACCAGCTTCTGTCCCTGCTGGGTCCTGCCTGTCTTTAAGTACCTTGACCCTGGTGTCTGTCCTGGGGGAGAGAGAAAGGGTCTGTAGCTGTGGCCAACCCAGCCTGGGGTGGGGAGTGGAGCAGGTATGAGATCCGGAGTGACCACAGCCTTTGGATTGGGCATGTGAGTGCCGAAGATGAGGGAACGTACACCTGTGTGGCGGAGAACAGTGTGGGCCGCGCTGAAGCATCTGGCTCCCTCAGTGTTCACGGTGAGGGCTGTA... |
Task1_train_41731 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GGTAAGGTCAGAGTCCCTGGGCTCATGAGCATGAAATGTAACATCATAAAGCAACCCTCTCCCCCAAAACCATGACACCACGGCAGTTCATACAGTTCTTTCCTGCTATGCCAGGTCTATACTGGTGGCCCGGCCTGGAATAGGAGATCATGTTTGCCTCTCACAGAAGAGACAAGGGAGGAGGAAGGCAGGGAGAGGGGAGGAGGGAAGAAGGAAAGGGAGAGAGGTAGTCATTCATTTTGGCAGCTTCTGACTTCTGAGCCTTTTACCCATAGATAATAATATAGATTATTAAGACTAGAAGGGACCATGGAGGGGCC... | GGTAAGGTCAGAGTCCCTGGGCTCATGAGCATGAAATGTAACATCATAAAGCAACCCTCTCCCCCAAAACCATGACACCACGGCAGTTCATACAGTTCTTTCCTGCTATGCCAGGTCTATACTGGTGGCCCGGCCTGGAATAGGAGATCATGTTTGCCTCTCACAGAAGAGACAAGGGAGGAGGAAGGCAGGGAGAGGGGAGGAGGGAAGAAGGAAAGGGAGAGAGGTAGTCATTCATTTTGGCAGCTTCTGACTTCTGAGCCTTTTACCCATAGATAATAATATAGATTATTAAGACTAGAAGGGACCATGGAGGGGCC... |
Task1_train_41732 | A variant on Chromosome 11 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TGGGACCCAGCTCACAAAGACAGTGCCATTGCCAGGCTTTAGAGTCACTTCCTGAGGTGGGGCACTGGGCACTGGAGGGGTGGAAGAGAGACTATGAGGGGCTCTGAGGGAGAGGACTCTAGGGAAAGGAGCTGGGCTGGGGGACACAGCGTCAGAACCCTACTGAAGAGACAAGAAGCCTCTTGAAGCTCTGCTGGCCTGGCCAGGGCAGAAGGGAGTCCCAGGGTAGGACCCATAATCTCCCCTCAAGACTGAAGCAGAACAGTCCAGGGGCCCCCAAATAAGAAGGAGCCAGAGGGGATATTGTTGGCTTCTGAAGG... | TGGGACCCAGCTCACAAAGACAGTGCCATTGCCAGGCTTTAGAGTCACTTCCTGAGGTGGGGCACTGGGCACTGGAGGGGTGGAAGAGAGACTATGAGGGGCTCTGAGGGAGAGGACTCTAGGGAAAGGAGCTGGGCTGGGGGACACAGCGTCAGAACCCTACTGAAGAGACAAGAAGCCTCTTGAAGCTCTGCTGGCCTGGCCAGGGCAGAAGGGAGTCCCAGGGTAGGACCCATAATCTCCCCTCAAGACTGAAGCAGAACAGTCCAGGGGCCCCCAAATAAGAAGGAGCCAGAGGGGATATTGTTGGCTTCTGAAGG... |
Task1_train_41733 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GACAATCAGTGAAGGCTTCTATTCAGCCATCTTGCTTCACCTCCCTTGGTAATCTCATATTTAATGAGTGCTAAGTACTTTGAGCTCACTGTGCTTTTAAATTTTGTTTTACTTCTGACTGCTTAAAAATTTCCCCCATCTCTGGCAGGGAAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGCGGATCATGAGGTCAGGAGTTTGAGATCAGCCTGGCCAACATAGTGAAACCCTGTCTCTACCAAAAATACAAAAATTAGCTGGACATGGTGGCACGTGCTTGTAGTCCCAGCTACTCGGGAGG... | GACAATCAGTGAAGGCTTCTATTCAGCCATCTTGCTTCACCTCCCTTGGTAATCTCATATTTAATGAGTGCTAAGTACTTTGAGCTCACTGTGCTTTTAAATTTTGTTTTACTTCTGACTGCTTAAAAATTTCCCCCATCTCTGGCAGGGAAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGCGGATCATGAGGTCAGGAGTTTGAGATCAGCCTGGCCAACATAGTGAAACCCTGTCTCTACCAAAAATACAAAAATTAGCTGGACATGGTGGCACGTGCTTGTAGTCCCAGCTACTCGGGAGG... |
Task1_train_41734 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | AGTACTTTGAGCTCACTGTGCTTTTAAATTTTGTTTTACTTCTGACTGCTTAAAAATTTCCCCCATCTCTGGCAGGGAAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGCGGATCATGAGGTCAGGAGTTTGAGATCAGCCTGGCCAACATAGTGAAACCCTGTCTCTACCAAAAATACAAAAATTAGCTGGACATGGTGGCACGTGCTTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTTGTAGTGAGCCTAGACTGCGCCATTGCACTCCAG... | AGTACTTTGAGCTCACTGTGCTTTTAAATTTTGTTTTACTTCTGACTGCTTAAAAATTTCCCCCATCTCTGGCAGGGAAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGCGGATCATGAGGTCAGGAGTTTGAGATCAGCCTGGCCAACATAGTGAAACCCTGTCTCTACCAAAAATACAAAAATTAGCTGGACATGGTGGCACGTGCTTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTTGTAGTGAGCCTAGACTGCGCCATTGCACTCCAG... |
Task1_train_41735 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | ACCCCCAATTTAAGGCAGATTTGGCTTAAGCCTGGCAAGCTGGCCCCTCAGGGATTCAGCACCAGGGTATGGCATGTTCTCATCTCACCCTAACCTTCACCTGTGCATCTCAAGGCTGACCAGCAGGTACTCCTTATCCAAGTCCTGCTGCCTCTTCCACCTTCTTGAGAAACTTTTCCCCTACATGCATTATCTCATTATGGATGAGGCACCTGGGAAGTTTAGGGGAGCTGCGAAGGCACACCTGCTCAAATGAGCCTGGGGAAGTGCCGAGGGACAGGGAGCTGAGACAGGCATGCTGTGGGGTTCAGGGCAGAGGG... | ACCCCCAATTTAAGGCAGATTTGGCTTAAGCCTGGCAAGCTGGCCCCTCAGGGATTCAGCACCAGGGTATGGCATGTTCTCATCTCACCCTAACCTTCACCTGTGCATCTCAAGGCTGACCAGCAGGTACTCCTTATCCAAGTCCTGCTGCCTCTTCCACCTTCTTGAGAAACTTTTCCCCTACATGCATTATCTCATTATGGATGAGGCACCTGGGAAGTTTAGGGGAGCTGCGAAGGCACACCTGCTCAAATGAGCCTGGGGAAGTGCCGAGGGACAGGGAGCTGAGACAGGCATGCTGTGGGGTTCAGGGCAGAGGG... |
Task1_train_41736 | A variant found on Chromosome 11 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CTGGGGAAATCACCAGAACTGGTGTCCAAAGACCTAGGTTTGAAACCTAGATCTGCCACTCATTGACTTGTTTAATCCTGAGCAAGTCATTTAATCTCACAGCCTTGTTTTTTCTAATCTCTAAAATGTGCATGACACAAATATTTCACAGGGTTATTCTGAGTACTATAAAGCAGGGGTCCCCACCCCCAGGCCGAGGACTGGTACTGGTCCATAGCCTGTTAGGAAGGGAGCGGCAGAGCAGGAGGTGAGCGGTAGGCCAGAGAGCAAAGCTTCATATGTATTTACAGACATGCCCCATGGCTTGCATTATCGCCTGA... | CTGGGGAAATCACCAGAACTGGTGTCCAAAGACCTAGGTTTGAAACCTAGATCTGCCACTCATTGACTTGTTTAATCCTGAGCAAGTCATTTAATCTCACAGCCTTGTTTTTTCTAATCTCTAAAATGTGCATGACACAAATATTTCACAGGGTTATTCTGAGTACTATAAAGCAGGGGTCCCCACCCCCAGGCCGAGGACTGGTACTGGTCCATAGCCTGTTAGGAAGGGAGCGGCAGAGCAGGAGGTGAGCGGTAGGCCAGAGAGCAAAGCTTCATATGTATTTACAGACATGCCCCATGGCTTGCATTATCGCCTGA... |
Task1_train_41737 | A mutation located on Chromosome 11 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TACAAGTTCCTTATCAGATAGTTGATTTGCAAGTATTTTCTCCCATTCTGTAGACTGTTATCTTACTTGATTAATAGTATTGTTTATGGCATAAGATTTTTAAATTAGTCACTTCTTTTTTTCTTATGTTGCTTGTGCTTTTGATGAATTATCTAATAATAATTGTTTATCTTGAGATCATGAAGATTTATTCCTATGTGTTCTTTTAAGATTTTATAGTTTTTAGCTCTTAATTTTAGGTCTGTGATCCATTTCGAGTTAATTTTTATGTATGCTGTAAATAAGTGGTTCATCTTCATTCTTTTGAATATAGGTGTCTA... | TACAAGTTCCTTATCAGATAGTTGATTTGCAAGTATTTTCTCCCATTCTGTAGACTGTTATCTTACTTGATTAATAGTATTGTTTATGGCATAAGATTTTTAAATTAGTCACTTCTTTTTTTCTTATGTTGCTTGTGCTTTTGATGAATTATCTAATAATAATTGTTTATCTTGAGATCATGAAGATTTATTCCTATGTGTTCTTTTAAGATTTTATAGTTTTTAGCTCTTAATTTTAGGTCTGTGATCCATTTCGAGTTAATTTTTATGTATGCTGTAAATAAGTGGTTCATCTTCATTCTTTTGAATATAGGTGTCTA... |
Task1_train_41738 | A mutation on Chromosome 11 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GCTTGAATCCCTGTTCTGCCTCTTGCTATGTGACCTTGGGCAAGTTACCTTAACCTCTGACAGACTCAGTGTTCTTACCTATAAAATGGGGATAATAATGGTACCTATGTCATACTACTTAGGGCTGTCCTGAGGTTTAAATGAGACAGTGCAAACAAAGTGTTTGGCACAGGACCTGGCACACGGAAATCCCTTAAAGAATGTTAGCTATTTTCATGACTATCACTTAAAACATCAAAATGAAGGTTGAGAGGAAAGCTGTGAGAAGGAGTAATGGGACAGAAAAGGTCAATGTCATTGTCAAGATCCCATGGGTCTGA... | GCTTGAATCCCTGTTCTGCCTCTTGCTATGTGACCTTGGGCAAGTTACCTTAACCTCTGACAGACTCAGTGTTCTTACCTATAAAATGGGGATAATAATGGTACCTATGTCATACTACTTAGGGCTGTCCTGAGGTTTAAATGAGACAGTGCAAACAAAGTGTTTGGCACAGGACCTGGCACACGGAAATCCCTTAAAGAATGTTAGCTATTTTCATGACTATCACTTAAAACATCAAAATGAAGGTTGAGAGGAAAGCTGTGAGAAGGAGTAATGGGACAGAAAAGGTCAATGTCATTGTCAAGATCCCATGGGTCTGA... |
Task1_train_41739 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | GGTAAAGCCATGGTAAAGAACTCCAGAGAAGGATTCTGAGAGAGATGATAAAAATCCATTTAAAGACATGGGTGCTGGCAGGTATGGTCCCAGGTATGAGGACCAAAGAACTCCCAGAAGACTGTTGGGAAAATTCTAGCACATGCAGTTGGAGAAGCATGTCCTCAGCACCCTCAGGGCACCACATCAATTTCAGCCCAGGATCTGCAGTTAGGAGCCCAGGCTGCCAGGAATGGGAACACTTCATCTCGGGTGCAGGCCTGTGACTATCCCTATTTCATTTTCTTTTTTTTCTGTCCCCATGGTACGAGGTGGCTTTC... | GGTAAAGCCATGGTAAAGAACTCCAGAGAAGGATTCTGAGAGAGATGATAAAAATCCATTTAAAGACATGGGTGCTGGCAGGTATGGTCCCAGGTATGAGGACCAAAGAACTCCCAGAAGACTGTTGGGAAAATTCTAGCACATGCAGTTGGAGAAGCATGTCCTCAGCACCCTCAGGGCACCACATCAATTTCAGCCCAGGATCTGCAGTTAGGAGCCCAGGCTGCCAGGAATGGGAACACTTCATCTCGGGTGCAGGCCTGTGACTATCCCTATTTCATTTTCTTTTTTTTCTGTCCCCATGGTACGAGGTGGCTTTC... |
Task1_train_41740 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | GCTCTGAATGTTTATGTCCCACCCCCCAAATTTATATGCTAAAATCCTAATGCCCAAAGTGATGGTATTAGACAGTGAGACCTTGTGGAGGTGATGATATCATGGAGGTGGGATGCCCACAAGTATCTTTCTAAAAGAGGCCCAAGGGAGCACTTTAGACCCTTCTACCATGTGGGGACACAGTGAGAAGGTGCCGTCTGTGAACCAGAAAGCAGGTCCTCACCAGATATTGAATCTGCCAGTGCCTTGATCTTGGACTTCCCTGCCACCAGAGCTGTGAAAATCAACTTCTGTTGTTAATAAATTACTTAGTCTAACGT... | GCTCTGAATGTTTATGTCCCACCCCCCAAATTTATATGCTAAAATCCTAATGCCCAAAGTGATGGTATTAGACAGTGAGACCTTGTGGAGGTGATGATATCATGGAGGTGGGATGCCCACAAGTATCTTTCTAAAAGAGGCCCAAGGGAGCACTTTAGACCCTTCTACCATGTGGGGACACAGTGAGAAGGTGCCGTCTGTGAACCAGAAAGCAGGTCCTCACCAGATATTGAATCTGCCAGTGCCTTGATCTTGGACTTCCCTGCCACCAGAGCTGTGAAAATCAACTTCTGTTGTTAATAAATTACTTAGTCTAACGT... |
Task1_train_41741 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CTCAACTTTGAGGCTGGGGGATGTGGTAGTATGGCATTATCTTTTTGGTGCTTAACATGGTATATCTCTGACTGGGTTGTAAGATGGCATAAATGAGCATGAGTTGCTCTAAATTAGAGAAGTCAAATTGATGTCAGCATCTGGATCCTTTTGGGGGTGTTTTAGAAAGACCTTCAGATATTTACCAGGGTGTGCGTGGTTGAAAGAGGTTAACTGATACTTACAGGATGGCATCCTTTTGATTTGCTATCTTGCTTAGTTCCAGACTAATCCTGACAAAGGATGCTGGTGCTGAAATTCTTAATTCACTTAGCCTGTCA... | CTCAACTTTGAGGCTGGGGGATGTGGTAGTATGGCATTATCTTTTTGGTGCTTAACATGGTATATCTCTGACTGGGTTGTAAGATGGCATAAATGAGCATGAGTTGCTCTAAATTAGAGAAGTCAAATTGATGTCAGCATCTGGATCCTTTTGGGGGTGTTTTAGAAAGACCTTCAGATATTTACCAGGGTGTGCGTGGTTGAAAGAGGTTAACTGATACTTACAGGATGGCATCCTTTTGATTTGCTATCTTGCTTAGTTCCAGACTAATCCTGACAAAGGATGCTGGTGCTGAAATTCTTAATTCACTTAGCCTGTCA... |
Task1_train_41742 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | CATAGTCCTTAAGGAAGTTTTGGTCTTCTTACAGGGAAAGAAATACAGGCAGCTGTCTATATCCGATAGGCTACAGTTCTGGAAGTGTGGTTCTTGAATCATCATCACTAGCAGCAGCAGCTAGAAACTTGTTAGAAATAAATGCAAATTCTAGAGCCCCAACACAGACCTACTGAATCAGAAACTCTGGAGGTGGGGCTCAGCGATCTGTGCTTCGACACTCCTACCTCCTTGGTGACTACGATGCCCACTAGCATTTGAGAACCACCGATCTAAGGCAAAGAATGATTAAGTGCTAGAAGAGAACTAATGTGATATGG... | CATAGTCCTTAAGGAAGTTTTGGTCTTCTTACAGGGAAAGAAATACAGGCAGCTGTCTATATCCGATAGGCTACAGTTCTGGAAGTGTGGTTCTTGAATCATCATCACTAGCAGCAGCAGCTAGAAACTTGTTAGAAATAAATGCAAATTCTAGAGCCCCAACACAGACCTACTGAATCAGAAACTCTGGAGGTGGGGCTCAGCGATCTGTGCTTCGACACTCCTACCTCCTTGGTGACTACGATGCCCACTAGCATTTGAGAACCACCGATCTAAGGCAAAGAATGATTAAGTGCTAGAAGAGAACTAATGTGATATGG... |
Task1_train_41743 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | GAATAGAGGCTATTTCTATGTATTCTGTCTTTAACTGGTATTCTGCTGGAGTCTGTATATCTTTTTTTTTTTTTTTTTCAGGCTAAAAAGACTCCATCAGACACACAGGAAATTTGCAGGTCTTCCTCTTCGTATTCTTTGTTTTCAGCACACAGTGAGGAAACAAGAGAAAATGGGATAAATGATATAAAAACTTGCTTTTATTTTTATACCAGGCCCTGTGGCTCGCTTCTGTAATCCCAGTGACTTGGGATGCTGAGGTAGGAGGATCACTTGAGCTCAGGAGTTCCAGGCTGCAGTGAGCTAAGACTGCCCAATTG... | GAATAGAGGCTATTTCTATGTATTCTGTCTTTAACTGGTATTCTGCTGGAGTCTGTATATCTTTTTTTTTTTTTTTTTCAGGCTAAAAAGACTCCATCAGACACACAGGAAATTTGCAGGTCTTCCTCTTCGTATTCTTTGTTTTCAGCACACAGTGAGGAAACAAGAGAAAATGGGATAAATGATATAAAAACTTGCTTTTATTTTTATACCAGGCCCTGTGGCTCGCTTCTGTAATCCCAGTGACTTGGGATGCTGAGGTAGGAGGATCACTTGAGCTCAGGAGTTCCAGGCTGCAGTGAGCTAAGACTGCCCAATTG... |
Task1_train_41744 | Here is a genetic alteration on Chromosome 11. Based on the data, is it a benign variant or a cause of disease? | Benign | AGGCTATTTCTATGTATTCTGTCTTTAACTGGTATTCTGCTGGAGTCTGTATATCTTTTTTTTTTTTTTTTTCAGGCTAAAAAGACTCCATCAGACACACAGGAAATTTGCAGGTCTTCCTCTTCGTATTCTTTGTTTTCAGCACACAGTGAGGAAACAAGAGAAAATGGGATAAATGATATAAAAACTTGCTTTTATTTTTATACCAGGCCCTGTGGCTCGCTTCTGTAATCCCAGTGACTTGGGATGCTGAGGTAGGAGGATCACTTGAGCTCAGGAGTTCCAGGCTGCAGTGAGCTAAGACTGCCCAATTGCACTCC... | AGGCTATTTCTATGTATTCTGTCTTTAACTGGTATTCTGCTGGAGTCTGTATATCTTTTTTTTTTTTTTTTTCAGGCTAAAAAGACTCCATCAGACACACAGGAAATTTGCAGGTCTTCCTCTTCGTATTCTTTGTTTTCAGCACACAGTGAGGAAACAAGAGAAAATGGGATAAATGATATAAAAACTTGCTTTTATTTTTATACCAGGCCCTGTGGCTCGCTTCTGTAATCCCAGTGACTTGGGATGCTGAGGTAGGAGGATCACTTGAGCTCAGGAGTTCCAGGCTGCAGTGAGCTAAGACTGCCCAATTGCACTCC... |
Task1_train_41745 | A genomic variant on Chromosome 11 is under review. What is the biological outcome — benign or pathogenic? | Benign | AGATGGAGTTTCACTCTTGTCTCCCAGGCTGGAGTACAATGGCATGATCTCAGCTTACTGCAACCTCCGTCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTTCCAAGTAGCTGGGATTACAGGTGCCCACCACCACACCTGGCTAGGTTTTGTATTTTTAGTAGAGATGGGGTTTTTTCATGTTGGCCAGGCTGATCTGGAACTCCTGACCTCAAGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGGATTTTAGGTGTGAGCCACCTCGCCTGGCAAGGGATTCTGTTCTTAGTCCTTGAAAAAATAAAGTTCT... | AGATGGAGTTTCACTCTTGTCTCCCAGGCTGGAGTACAATGGCATGATCTCAGCTTACTGCAACCTCCGTCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTTCCAAGTAGCTGGGATTACAGGTGCCCACCACCACACCTGGCTAGGTTTTGTATTTTTAGTAGAGATGGGGTTTTTTCATGTTGGCCAGGCTGATCTGGAACTCCTGACCTCAAGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGGATTTTAGGTGTGAGCCACCTCGCCTGGCAAGGGATTCTGTTCTTAGTCCTTGAAAAAATAAAGTTCT... |
Task1_train_41746 | A genomic variant on Chromosome 11 is under review. What is the biological outcome — benign or pathogenic? | Benign | TCTCCCAACTAAAGTCTAAGTTGCAGCCACCAGGAAGCCTCAAGAAAGGAAAACAGTTCCCTCCTCAGCTTACATCTTCTACCCTAGGGTCTGCTTCTTTCCAGGATGATTGACAGTGAGAAACTTTACTCTCCTCATGGGAACCCTCTGTCTGCCTCTGAGCCTAACCTTTCTGTGCCCTCTCTTCTCCATTCCTAGAGGTATGTATTTTTTAAGTCTGCGTTCAGCCTTCCTTTTGCCTTTCTGCATTCCAATGATTTATACTTATGTATTCTCTCAGCTTTAATGAATGTCTTGTTGTAGATGACTCTCAATTCTAC... | TCTCCCAACTAAAGTCTAAGTTGCAGCCACCAGGAAGCCTCAAGAAAGGAAAACAGTTCCCTCCTCAGCTTACATCTTCTACCCTAGGGTCTGCTTCTTTCCAGGATGATTGACAGTGAGAAACTTTACTCTCCTCATGGGAACCCTCTGTCTGCCTCTGAGCCTAACCTTTCTGTGCCCTCTCTTCTCCATTCCTAGAGGTATGTATTTTTTAAGTCTGCGTTCAGCCTTCCTTTTGCCTTTCTGCATTCCAATGATTTATACTTATGTATTCTCTCAGCTTTAATGAATGTCTTGTTGTAGATGACTCTCAATTCTAC... |
Task1_train_41747 | A mutation is present on Chromosome 11. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | ACTTTTTAGTACTACAGGGTCACCTCACCTTTTGTATGCTATTTTACTTCCTAAATCTGGAACTGTTTCAGTGAAGTCTATTTCTGTGGTCCACCCCCCTTCTGTAGCAATTATGCAGCATTAGTTTATGATTTATATATTAGTATTGTTTTTAATTGTCCCATGTGTTATTTGCACTAGCAGCTTGAGGATAGAAAACATATTTGTATACCTGAAGTCTTGAACATGGGTAGGAAAAAACTAATTATTGGTTGGTAAGTAAAACTTTGGATCTCATAAACATGGTAGAATTGTAAATTAGAGGATCAGGGTCTTAGATC... | ACTTTTTAGTACTACAGGGTCACCTCACCTTTTGTATGCTATTTTACTTCCTAAATCTGGAACTGTTTCAGTGAAGTCTATTTCTGTGGTCCACCCCCCTTCTGTAGCAATTATGCAGCATTAGTTTATGATTTATATATTAGTATTGTTTTTAATTGTCCCATGTGTTATTTGCACTAGCAGCTTGAGGATAGAAAACATATTTGTATACCTGAAGTCTTGAACATGGGTAGGAAAAAACTAATTATTGGTTGGTAAGTAAAACTTTGGATCTCATAAACATGGTAGAATTGTAAATTAGAGGATCAGGGTCTTAGATC... |
Task1_train_41748 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CACTTGACATTTTCAAACTTACAGTCATATAAGACTAGAGGAAATTCTACAGCCATACTAGAGAAAAAGAGAAAAGAAAGTTTGAGAATACATAACATCCATCTAACAGTTCTTTAAAAACTAAGGGTTAGTTGCGTTAAGGGAGCCGGGTAGGGCGCCACCATTGATGTTAATATTGCCTAATAGCTGAGAAAATATCTCACCATCCCTAACCTTGAACACCTTTATTACAATAATGAAAAATGCAACAAATCATAGATCAACCTGATCTATGTAAGGTAAATGTCAGTGCTAACAAGACATGGCTCCATCATACTGCT... | CACTTGACATTTTCAAACTTACAGTCATATAAGACTAGAGGAAATTCTACAGCCATACTAGAGAAAAAGAGAAAAGAAAGTTTGAGAATACATAACATCCATCTAACAGTTCTTTAAAAACTAAGGGTTAGTTGCGTTAAGGGAGCCGGGTAGGGCGCCACCATTGATGTTAATATTGCCTAATAGCTGAGAAAATATCTCACCATCCCTAACCTTGAACACCTTTATTACAATAATGAAAAATGCAACAAATCATAGATCAACCTGATCTATGTAAGGTAAATGTCAGTGCTAACAAGACATGGCTCCATCATACTGCT... |
Task1_train_41749 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | CAAAAAATAAAAGGCAAATGACAAACTGAGAAGAAAAAAATAAGTGATGGTAAAGTGCGACCTTCCTCAATATATATTTCATGAATATATACATCAGTTTTAATGAAAAAGTAAAAAAAAAAAAAATCCAGCAACCTGAGAGTCAAATGGGCAAAGACCAAGCATTTCAAACAAAAAGAAAAAAGCTTATAAAAATTTTTTAAAAAAAATTTTAAATGCTCAATTTTACTCAGCTGAGATAAATGCAAAAGGATATGAACTATTTTTCAAGGAAGTGACTGCAAAGACAAAGTTTGATAGTATACCACTTTGGAGAGGGA... | CAAAAAATAAAAGGCAAATGACAAACTGAGAAGAAAAAAATAAGTGATGGTAAAGTGCGACCTTCCTCAATATATATTTCATGAATATATACATCAGTTTTAATGAAAAAGTAAAAAAAAAAAAAATCCAGCAACCTGAGAGTCAAATGGGCAAAGACCAAGCATTTCAAACAAAAAGAAAAAAGCTTATAAAAATTTTTTAAAAAAAATTTTAAATGCTCAATTTTACTCAGCTGAGATAAATGCAAAAGGATATGAACTATTTTTCAAGGAAGTGACTGCAAAGACAAAGTTTGATAGTATACCACTTTGGAGAGGGA... |
Task1_train_41750 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | TCCCTGTGGTCGGGAGTCCTGTGTTGGGCAGGTAATTGGACCAGAAGAGTTTGGGGGCCTTTCTCAACTCTGTCCAGTGATTCTAATTTTACAATATCCTTTGAGCGAAAATGCAGGGAGCTCGTGGTCCTCTCCCCTGGGTCTGCCCCAGCCACGTCCTACCCTCCCCAATTCTGCATTATGGATGGGGTGAATCATCTGGTAAATAATTAACGAGTCATCGAGGCACTGAGGGTAACAGGAGAGCAGGGGTGGAGGCATGGGCAGGGCTAAAGTTGGCAACCTGAGCCAGACCACCATCCTCCCAGGGCTGGGCTCTG... | TCCCTGTGGTCGGGAGTCCTGTGTTGGGCAGGTAATTGGACCAGAAGAGTTTGGGGGCCTTTCTCAACTCTGTCCAGTGATTCTAATTTTACAATATCCTTTGAGCGAAAATGCAGGGAGCTCGTGGTCCTCTCCCCTGGGTCTGCCCCAGCCACGTCCTACCCTCCCCAATTCTGCATTATGGATGGGGTGAATCATCTGGTAAATAATTAACGAGTCATCGAGGCACTGAGGGTAACAGGAGAGCAGGGGTGGAGGCATGGGCAGGGCTAAAGTTGGCAACCTGAGCCAGACCACCATCCTCCCAGGGCTGGGCTCTG... |
Task1_train_41751 | This sequence change occurs on Chromosome 11. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CCTGTGTTGGGCAGGTAATTGGACCAGAAGAGTTTGGGGGCCTTTCTCAACTCTGTCCAGTGATTCTAATTTTACAATATCCTTTGAGCGAAAATGCAGGGAGCTCGTGGTCCTCTCCCCTGGGTCTGCCCCAGCCACGTCCTACCCTCCCCAATTCTGCATTATGGATGGGGTGAATCATCTGGTAAATAATTAACGAGTCATCGAGGCACTGAGGGTAACAGGAGAGCAGGGGTGGAGGCATGGGCAGGGCTAAAGTTGGCAACCTGAGCCAGACCACCATCCTCCCAGGGCTGGGCTCTGCTCTGGGTAGAAGGGGC... | CCTGTGTTGGGCAGGTAATTGGACCAGAAGAGTTTGGGGGCCTTTCTCAACTCTGTCCAGTGATTCTAATTTTACAATATCCTTTGAGCGAAAATGCAGGGAGCTCGTGGTCCTCTCCCCTGGGTCTGCCCCAGCCACGTCCTACCCTCCCCAATTCTGCATTATGGATGGGGTGAATCATCTGGTAAATAATTAACGAGTCATCGAGGCACTGAGGGTAACAGGAGAGCAGGGGTGGAGGCATGGGCAGGGCTAAAGTTGGCAACCTGAGCCAGACCACCATCCTCCCAGGGCTGGGCTCTGCTCTGGGTAGAAGGGGC... |
Task1_train_41752 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | GATGGTCAGGGTGGGTGGGCTGGTGAGTCCCCAGCCAGCAGGGGTGGGGGCGCTGGACACAGCTGGGCGTGTCCTGGGTCTGTAATAACACAGCGGGCCTCTCCCTCCTCTGGCCAGTGCCGGTGTCCAAGCCTCAAGTGCGACTGAGTAACCCGTCCCCTGTGGAGGGAGCCTCCGTGGTGGCCACGTGTGCAGTGCGGGAGGGCACAGAGCCCGTGACCTTTGCCTGGCAGCATCGGGCACCCCGAGGCCTTGGAGAGGCCCTGGTGGGGGTCACTGAGCCACTATTCCAGCTGGACCCTGTCAACCGGACACACCTA... | GATGGTCAGGGTGGGTGGGCTGGTGAGTCCCCAGCCAGCAGGGGTGGGGGCGCTGGACACAGCTGGGCGTGTCCTGGGTCTGTAATAACACAGCGGGCCTCTCCCTCCTCTGGCCAGTGCCGGTGTCCAAGCCTCAAGTGCGACTGAGTAACCCGTCCCCTGTGGAGGGAGCCTCCGTGGTGGCCACGTGTGCAGTGCGGGAGGGCACAGAGCCCGTGACCTTTGCCTGGCAGCATCGGGCACCCCGAGGCCTTGGAGAGGCCCTGGTGGGGGTCACTGAGCCACTATTCCAGCTGGACCCTGTCAACCGGACACACCTA... |
Task1_train_41753 | This genomic variant is located on Chromosome 11. Can you determine its pathogenicity and name any linked disease? | Benign | CCAACAGGACCCCAGGAGACAGGAATGGGGCCACAGTGGGAGGAGAGGGCAGCAAGCCTGAAGTTAGAAGTCAGGAGCCCCGGGTGAAAGATGAAGGCCAGGGTGGCCTGGAGCTCGCTGTCCCACATGGCAGCCACGCATGTGTATCTTCGGTCACTTGAGATGGAGCCAATCCAAACTGAGCTGTGCTGTAGGCATGGAAGGCACACTTGATTTTGAAGCTTTAGTCCAAAAGAAAGAATGTAAAATATCCGTAACTTCTATATTGATTATATATTGAAATAACATTCTGGATATATTTGGTTAAATAAATATATTCT... | CCAACAGGACCCCAGGAGACAGGAATGGGGCCACAGTGGGAGGAGAGGGCAGCAAGCCTGAAGTTAGAAGTCAGGAGCCCCGGGTGAAAGATGAAGGCCAGGGTGGCCTGGAGCTCGCTGTCCCACATGGCAGCCACGCATGTGTATCTTCGGTCACTTGAGATGGAGCCAATCCAAACTGAGCTGTGCTGTAGGCATGGAAGGCACACTTGATTTTGAAGCTTTAGTCCAAAAGAAAGAATGTAAAATATCCGTAACTTCTATATTGATTATATATTGAAATAACATTCTGGATATATTTGGTTAAATAAATATATTCT... |
Task1_train_41754 | A genetic alteration is present on Chromosome 11. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TTGCTATTCCTCCCTTCTCCTTCTCTAACATCCTTTGGGGTTCACTATAGCTTTCAAGGAAAGATTCAACTTTGAAGCATATCACACAAGGCATTCCCCACAGTAACCAGTCACACTAAATAAAATCTCTAACCTCTCAATCTCTAAACATAATAGAACATATCAGCCACTTGTCGAGATGTCTTTGCTAGAAACTCTTTTGCTGTTTCATCTGTCTGTATCGTCGTTCTCCTTTGAAGTTTAGCTTATGATGCAGAGAAGCCTCTCTTATCTACTCACCCTTGTCTACACTGAGTGACTGACTTAGATATTTCTCGTGA... | TTGCTATTCCTCCCTTCTCCTTCTCTAACATCCTTTGGGGTTCACTATAGCTTTCAAGGAAAGATTCAACTTTGAAGCATATCACACAAGGCATTCCCCACAGTAACCAGTCACACTAAATAAAATCTCTAACCTCTCAATCTCTAAACATAATAGAACATATCAGCCACTTGTCGAGATGTCTTTGCTAGAAACTCTTTTGCTGTTTCATCTGTCTGTATCGTCGTTCTCCTTTGAAGTTTAGCTTATGATGCAGAGAAGCCTCTCTTATCTACTCACCCTTGTCTACACTGAGTGACTGACTTAGATATTTCTCGTGA... |
Task1_train_41755 | A mutation on Chromosome 11 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CCCAACAAGTTCAGAAGCCACGCCTCTGCTATGCTCTATTGGTGCTACCTCAACTCAACCGCCATAACCTAAAAATCAACAGTGATTTTCATTACATCTGAAAGAAAGAGGACAGACATATCTCTTTTTTTTTTTTTTCAAAATTCACAGACATCAATTTAATGACCACTACTATAAAGCTGTATCTCCTCTATTTCTTCTTGTTTGAACAAAGGGCAAAATTCTCCACATGTATTCACTCTGTCACCTTGGCCAAAATTCCCTTCTGTAAGTTACATTTTTAAAGCATGTACAGAACTCTTCTATAATGCATTCATGTA... | CCCAACAAGTTCAGAAGCCACGCCTCTGCTATGCTCTATTGGTGCTACCTCAACTCAACCGCCATAACCTAAAAATCAACAGTGATTTTCATTACATCTGAAAGAAAGAGGACAGACATATCTCTTTTTTTTTTTTTTCAAAATTCACAGACATCAATTTAATGACCACTACTATAAAGCTGTATCTCCTCTATTTCTTCTTGTTTGAACAAAGGGCAAAATTCTCCACATGTATTCACTCTGTCACCTTGGCCAAAATTCCCTTCTGTAAGTTACATTTTTAAAGCATGTACAGAACTCTTCTATAATGCATTCATGTA... |
Task1_train_41756 | A mutation on Chromosome 11 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | AAGCAAAACGAAATAAAGGGGCCAGAGAGCACCAGGCATATTATTTTAGATAGGACCATGAGGGCTATCTTTTCCAAGGAAGTGAAATCTGATGGGGGTCTGAAGGAACTGAGGGAGTGAGGCCTCAGGGTATGGGGCCGTAATTATTTGTATATTGTAACCATTTGTTTTAGTCCTCTCCACTCATGCCTTCTTGTATCCACAGTTCGTCCCTAGCACACAGAGCTTAGAAGTAGCTTATTTAATGAGCATTTGTTCTGTGTGTGCCACCGGCTTTTCACAAAAGGTCTCACCTGTGGAATGTTCCAGCCATTTTCCCC... | AAGCAAAACGAAATAAAGGGGCCAGAGAGCACCAGGCATATTATTTTAGATAGGACCATGAGGGCTATCTTTTCCAAGGAAGTGAAATCTGATGGGGGTCTGAAGGAACTGAGGGAGTGAGGCCTCAGGGTATGGGGCCGTAATTATTTGTATATTGTAACCATTTGTTTTAGTCCTCTCCACTCATGCCTTCTTGTATCCACAGTTCGTCCCTAGCACACAGAGCTTAGAAGTAGCTTATTTAATGAGCATTTGTTCTGTGTGTGCCACCGGCTTTTCACAAAAGGTCTCACCTGTGGAATGTTCCAGCCATTTTCCCC... |
Task1_train_41757 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | AAATAGGTGAAAGAAATGCCTCCACTTATACCACCTCTACTGCCATCAGCAGGCCTCATACCAGTACTTCTTCACCACCTGACGGGTTCTAAACAACTCTTGGACTTGATGTGCCATGTCCTTGTCCCAAGCCAACACCATTACACCTGTGGTTTCCTTGTCCAGCCGGTGGCACAGATGCAAGGGCTCTGCCTTGTGGCCATGAAGCATCTTTGCCAGGATAGGTAGTACATCAGTGATGCAGAGCTGGACCCCAGGGCCACCTAAGAAGGAAAAAGCCAAAGGTTTGAGCGGCCAGGAAAAGATCTCGCCAAAGAACT... | AAATAGGTGAAAGAAATGCCTCCACTTATACCACCTCTACTGCCATCAGCAGGCCTCATACCAGTACTTCTTCACCACCTGACGGGTTCTAAACAACTCTTGGACTTGATGTGCCATGTCCTTGTCCCAAGCCAACACCATTACACCTGTGGTTTCCTTGTCCAGCCGGTGGCACAGATGCAAGGGCTCTGCCTTGTGGCCATGAAGCATCTTTGCCAGGATAGGTAGTACATCAGTGATGCAGAGCTGGACCCCAGGGCCACCTAAGAAGGAAAAAGCCAAAGGTTTGAGCGGCCAGGAAAAGATCTCGCCAAAGAACT... |
Task1_train_41758 | Given this context: Chromosome 11 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CCATGCCCAGCTAATTTTTGTATTTTCAGTAGAGACAGGGGTTTTACCATGTTGGCCAGGCTAGGCTTGAACTCCTGACTTCAGGTGATCCGCCGCCTTGGCCTCCCAAAATGCTAGGATTACAGGCGTGAGCCATTGTGCCTGGCCACATTCTTTAAATTTTGAAACCTTTTATTTTAGTGTGTCTAATAATACTTGCTTCCATGAGTTCTCAGGTTTGTTTTGATCTCACAGATCCACCAAAGAGAAAGCAGCCCTGTGCCAGTTGCTCTGCCAGCCTTTCACAGGAGAAGTGTCACTAGAATACTACAGCCCCCACA... | CCATGCCCAGCTAATTTTTGTATTTTCAGTAGAGACAGGGGTTTTACCATGTTGGCCAGGCTAGGCTTGAACTCCTGACTTCAGGTGATCCGCCGCCTTGGCCTCCCAAAATGCTAGGATTACAGGCGTGAGCCATTGTGCCTGGCCACATTCTTTAAATTTTGAAACCTTTTATTTTAGTGTGTCTAATAATACTTGCTTCCATGAGTTCTCAGGTTTGTTTTGATCTCACAGATCCACCAAAGAGAAAGCAGCCCTGTGCCAGTTGCTCTGCCAGCCTTTCACAGGAGAAGTGTCACTAGAATACTACAGCCCCCACA... |
Task1_train_41759 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TCCTCCTGGCCAGGTGGAGCAGAGAACAGTTCCTCAGCTGGTCATGCTGAGCTCATACCCTGTAAGTCTGACCACACTACACAGCTTTGGCTTTATCTAGAATCCAGCTCCAATCACAGTCGTGTCTGGCCCTAATCTCATGAGGAATGAAAGACCCATTTAGAGAAGAAGCCTCTGTCAGGCATTAGGAGAGAAACAGAACTTCGCAGAGCTCATCCATGGGGAATGAGAGCAGGGTAAGTGCAGCCTTTGTGATTCTCTCTCTCTACCCTCTGTAGGATGGCTGCTCCATGAGGTCAAGACTGGGTCTCCTCCCTCCT... | TCCTCCTGGCCAGGTGGAGCAGAGAACAGTTCCTCAGCTGGTCATGCTGAGCTCATACCCTGTAAGTCTGACCACACTACACAGCTTTGGCTTTATCTAGAATCCAGCTCCAATCACAGTCGTGTCTGGCCCTAATCTCATGAGGAATGAAAGACCCATTTAGAGAAGAAGCCTCTGTCAGGCATTAGGAGAGAAACAGAACTTCGCAGAGCTCATCCATGGGGAATGAGAGCAGGGTAAGTGCAGCCTTTGTGATTCTCTCTCTCTACCCTCTGTAGGATGGCTGCTCCATGAGGTCAAGACTGGGTCTCCTCCCTCCT... |
Task1_train_41760 | This is a variant located on Chromosome 11. Is this mutation a likely cause of disease or not? | Benign | ATCATCGACCTCCCTCCCAGCTCCTGGCTCTCGGCCTAAGAAGCCTCTAGGCAAGATGGCTGGTGAGTGGAACCGGACTCGCGACTCTGCTGTGTTCCTGAGTGTAGTGCTCAGCCTCCATAGGGCGCGGTGGGAGGCCTGCCTGGTCCAAACTCAGAGAGACGCAGGAAGGCTGACGTGGGGAACTCCTGACCTGAATTCAGGGCCTGGATGCTTTGTGGAGAGTGAGGAGGGGAGGCCTGCGTCAGCTCAGCCAGATCTTTATCCTTTTGGCTCAAAGGTTTTCCAGGCCTGCTCAGCTAGCTTTCCTAGCCTGGAAA... | ATCATCGACCTCCCTCCCAGCTCCTGGCTCTCGGCCTAAGAAGCCTCTAGGCAAGATGGCTGGTGAGTGGAACCGGACTCGCGACTCTGCTGTGTTCCTGAGTGTAGTGCTCAGCCTCCATAGGGCGCGGTGGGAGGCCTGCCTGGTCCAAACTCAGAGAGACGCAGGAAGGCTGACGTGGGGAACTCCTGACCTGAATTCAGGGCCTGGATGCTTTGTGGAGAGTGAGGAGGGGAGGCCTGCGTCAGCTCAGCCAGATCTTTATCCTTTTGGCTCAAAGGTTTTCCAGGCCTGCTCAGCTAGCTTTCCTAGCCTGGAAA... |
Task1_train_41761 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | TCCTCGGGGACCTGGCTGGCAGGGACCTCCCGGCCAGCCCAGAACTGCCAACATGTCTGCCAGCACTGCCCCTCCATTCCCAGTCCTGGGGGGAGGCTCTGTCTGGGCAGCTTGAGGCCTGACCTACTGTGGCTGCTTCCTCTGCTCCCCAGCCTGGGTCCTGAGGGCCTGGCTTAAGGGAACTGCTGCCAGAAGGCTGGGAGTGTAGGCAGTGTTCGGGTGCCCAGCTGTGCCCTGTCTGACCTCATGGCCACCCACAAGCTGGCACCCCCCACAGGCCTCTTGGGGAAGCCTGTACTTTCCACCGCCGGAGGCGGGTA... | TCCTCGGGGACCTGGCTGGCAGGGACCTCCCGGCCAGCCCAGAACTGCCAACATGTCTGCCAGCACTGCCCCTCCATTCCCAGTCCTGGGGGGAGGCTCTGTCTGGGCAGCTTGAGGCCTGACCTACTGTGGCTGCTTCCTCTGCTCCCCAGCCTGGGTCCTGAGGGCCTGGCTTAAGGGAACTGCTGCCAGAAGGCTGGGAGTGTAGGCAGTGTTCGGGTGCCCAGCTGTGCCCTGTCTGACCTCATGGCCACCCACAAGCTGGCACCCCCCACAGGCCTCTTGGGGAAGCCTGTACTTTCCACCGCCGGAGGCGGGTA... |
Task1_train_41762 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GAATCCTGCTGCCTGCTGAGAAACATGGTCAGCAAGTCCCGTGAGTGTCATCCGAGGGCTCCCCCACCCTGGAGGACAGGCCTCAGAAGCCGTCTTCAGCAGGATCCTGGGACCTCTGGGGGCTGTGGAGGGACAGACAGGGAGCCAGGGGCCCTTCTCTTCATCTTGAAGGACAGTGGGTACAATCAGGGTCAAGCCCTCAGCCAGGGCCAGGAGAGGGCCAGAGACTGCTTCTGTTGAGTTAGGGGTCGGAGGGACTCAGAAGGGGGCAGGTGGGAAGGTGGACGGGGGTTGTACCTGCCTGTTGCTGCCTCTAGCTC... | GAATCCTGCTGCCTGCTGAGAAACATGGTCAGCAAGTCCCGTGAGTGTCATCCGAGGGCTCCCCCACCCTGGAGGACAGGCCTCAGAAGCCGTCTTCAGCAGGATCCTGGGACCTCTGGGGGCTGTGGAGGGACAGACAGGGAGCCAGGGGCCCTTCTCTTCATCTTGAAGGACAGTGGGTACAATCAGGGTCAAGCCCTCAGCCAGGGCCAGGAGAGGGCCAGAGACTGCTTCTGTTGAGTTAGGGGTCGGAGGGACTCAGAAGGGGGCAGGTGGGAAGGTGGACGGGGGTTGTACCTGCCTGTTGCTGCCTCTAGCTC... |
Task1_train_41763 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | TAACTTCTACTGTTATCAAGAGCCTGGTCTTGCCCACTGCCGGCTCACTCTCCAAAGCCACAAGGGTCAGAGATTCAGCACATGTGTCTTGGAGCCGGCTAACCCAGAAGCAAGCCTTGGATCTACAGCTTGCTCAGTGACCTCATGTCCTTTACTTAACCTCCTTTGCAAAATACAGATAATGGTCTCCCTTCATGACAGACCCAGCCCCAAGGAATGCAATGAGCTGACAGCCTCCAGTGACAGGGGCCTGCACATCAAGGCCATGTGCTTCCCAGGCAGAGCCCAGCTGATGATGACTGCCATGGTGGGCTCCTCTA... | TAACTTCTACTGTTATCAAGAGCCTGGTCTTGCCCACTGCCGGCTCACTCTCCAAAGCCACAAGGGTCAGAGATTCAGCACATGTGTCTTGGAGCCGGCTAACCCAGAAGCAAGCCTTGGATCTACAGCTTGCTCAGTGACCTCATGTCCTTTACTTAACCTCCTTTGCAAAATACAGATAATGGTCTCCCTTCATGACAGACCCAGCCCCAAGGAATGCAATGAGCTGACAGCCTCCAGTGACAGGGGCCTGCACATCAAGGCCATGTGCTTCCCAGGCAGAGCCCAGCTGATGATGACTGCCATGGTGGGCTCCTCTA... |
Task1_train_41764 | This sequence change occurs on Chromosome 11. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CTGTTATCAAGAGCCTGGTCTTGCCCACTGCCGGCTCACTCTCCAAAGCCACAAGGGTCAGAGATTCAGCACATGTGTCTTGGAGCCGGCTAACCCAGAAGCAAGCCTTGGATCTACAGCTTGCTCAGTGACCTCATGTCCTTTACTTAACCTCCTTTGCAAAATACAGATAATGGTCTCCCTTCATGACAGACCCAGCCCCAAGGAATGCAATGAGCTGACAGCCTCCAGTGACAGGGGCCTGCACATCAAGGCCATGTGCTTCCCAGGCAGAGCCCAGCTGATGATGACTGCCATGGTGGGCTCCTCTACGGGCAGTC... | CTGTTATCAAGAGCCTGGTCTTGCCCACTGCCGGCTCACTCTCCAAAGCCACAAGGGTCAGAGATTCAGCACATGTGTCTTGGAGCCGGCTAACCCAGAAGCAAGCCTTGGATCTACAGCTTGCTCAGTGACCTCATGTCCTTTACTTAACCTCCTTTGCAAAATACAGATAATGGTCTCCCTTCATGACAGACCCAGCCCCAAGGAATGCAATGAGCTGACAGCCTCCAGTGACAGGGGCCTGCACATCAAGGCCATGTGCTTCCCAGGCAGAGCCCAGCTGATGATGACTGCCATGGTGGGCTCCTCTACGGGCAGTC... |
Task1_train_41765 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | AACTCGTGGGTGTTAAACATGTTTTACATGTCTCCAGAGTTATAAAGAGCTATACCTGAAATGCTGGTGTAGATGGTAATTACAAGAAGACTGTGACCACACAAGTATAGAGTAAGCAAACGACAGTAATGCCTTAGGACAGCAATAACTGCCCAGAACTCCACTGGTGAAACGGGGCTGTGAACTAAGCAGTTATTGCAGGAACTTGCAGTCTAATAATAGATAATGCGTAGCTACTTAAATTCCCAGGGACCTCGTACTCTGGTTTAGGAACAGAAACAAACATGGAAATTTATATTCATAATAAATTATGCGTGTCT... | AACTCGTGGGTGTTAAACATGTTTTACATGTCTCCAGAGTTATAAAGAGCTATACCTGAAATGCTGGTGTAGATGGTAATTACAAGAAGACTGTGACCACACAAGTATAGAGTAAGCAAACGACAGTAATGCCTTAGGACAGCAATAACTGCCCAGAACTCCACTGGTGAAACGGGGCTGTGAACTAAGCAGTTATTGCAGGAACTTGCAGTCTAATAATAGATAATGCGTAGCTACTTAAATTCCCAGGGACCTCGTACTCTGGTTTAGGAACAGAAACAAACATGGAAATTTATATTCATAATAAATTATGCGTGTCT... |
Task1_train_41766 | A variant has been detected on Chromosome 11. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TTCTTTACCACTTTCTAACAAGGATAACCTTTCTTCTAGTTTCCAATACCTTGTTCTTTATTTCTGTCTGAGACCTCATCAGAATTGCCTTCACCATCGGTATCTCTATCAACATTCTGTTCATGACCACTTAGGCAATCTCTAAGAACGAGGCTTTCCCCACAGCTCATATCCCACATCTACAGCTCTCCTCTTCTTCTGAGCCCTCACCAGAATCATCCTTAGTGCTCCGTTCATGGCAATCCAGGCTTTTTTCAGCACTCACTTCAAAGCTGTTCCAGCTTGTATTCATTATCCAGTTCCAAAGCCACCCCCACATT... | TTCTTTACCACTTTCTAACAAGGATAACCTTTCTTCTAGTTTCCAATACCTTGTTCTTTATTTCTGTCTGAGACCTCATCAGAATTGCCTTCACCATCGGTATCTCTATCAACATTCTGTTCATGACCACTTAGGCAATCTCTAAGAACGAGGCTTTCCCCACAGCTCATATCCCACATCTACAGCTCTCCTCTTCTTCTGAGCCCTCACCAGAATCATCCTTAGTGCTCCGTTCATGGCAATCCAGGCTTTTTTCAGCACTCACTTCAAAGCTGTTCCAGCTTGTATTCATTATCCAGTTCCAAAGCCACCCCCACATT... |
Task1_train_41767 | An alteration has been detected on Chromosome 11. Is it pathogenic, and if so, what disease is involved? | Benign | TTTAGGAGATGATGCATTTTTACTCTACTTGTTTGGGGATTTGAATTAACTATTTTGAGGAAATGAGTAAGTTTTCCCCCTTAATTTTATAACTAAGTCAAACACAAGGCCCAAAGAGTATCTCAGGTCCAGTTCATCAGAGGTGGGTGATAAACTGATGAAATGAACAGGCATTTACCCTCAGCTTGCTATAATTCCAGTGGCCACGAGAACCACCTTGGGCTGTGCCTTGGTGTCATACCTTAAATTGCTTCCCACAGGTGGAACACAGGAAGTCTTTGCGGTCCGAATGCCGGAGCATGTGGAGTCGCAGTTTATCG... | TTTAGGAGATGATGCATTTTTACTCTACTTGTTTGGGGATTTGAATTAACTATTTTGAGGAAATGAGTAAGTTTTCCCCCTTAATTTTATAACTAAGTCAAACACAAGGCCCAAAGAGTATCTCAGGTCCAGTTCATCAGAGGTGGGTGATAAACTGATGAAATGAACAGGCATTTACCCTCAGCTTGCTATAATTCCAGTGGCCACGAGAACCACCTTGGGCTGTGCCTTGGTGTCATACCTTAAATTGCTTCCCACAGGTGGAACACAGGAAGTCTTTGCGGTCCGAATGCCGGAGCATGTGGAGTCGCAGTTTATCG... |
Task1_train_41768 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TAATTTTCTCCCAAGACCTAAAGAACTAAAGCAGAAATGAAGTTTTGTAAAACACTTTCTGAGTGGTCAGCTTTGGAGGATTGAATTCTTGAAGGCCTGAGCTTGGCACATGGCCTGATGCCTGATATTGAAGGTCTGGAAGCAGATGGCCCAAGAACACATTTGGGAGAGAAATAATGTATGTGTTGCTATCGAAGTCACGCACTCTTAGGGTGGAATCCTTGCTCTTATACTGCCTTGGCTTTGGACCTAACTTTTTAATGTCAGTTTTCTCTAGTGAAGGATAGTAGATCCCCAAGATAATATAAACTAATTTAATC... | TAATTTTCTCCCAAGACCTAAAGAACTAAAGCAGAAATGAAGTTTTGTAAAACACTTTCTGAGTGGTCAGCTTTGGAGGATTGAATTCTTGAAGGCCTGAGCTTGGCACATGGCCTGATGCCTGATATTGAAGGTCTGGAAGCAGATGGCCCAAGAACACATTTGGGAGAGAAATAATGTATGTGTTGCTATCGAAGTCACGCACTCTTAGGGTGGAATCCTTGCTCTTATACTGCCTTGGCTTTGGACCTAACTTTTTAATGTCAGTTTTCTCTAGTGAAGGATAGTAGATCCCCAAGATAATATAAACTAATTTAATC... |
Task1_train_41769 | Here is a genetic alteration on Chromosome 11. Based on the data, is it a benign variant or a cause of disease? | Benign | TGCCGACATTCCTTTCAACAGCACAACTGAGATGTTTATAGAGAAAGATGAGTTTTCTAGAAGTTTAACTGGCTTTTGCTTTTGTACTGAACTGTTATGAGTTGGGACAATTTAAACATTAACTTTGGTGTCTTGAAGTCACTTGTTTATGTTAAGAAACGTGGGGGCTATACCACCAAAAATCTATTATAACAGTCTGGACTGGTGGTAGGTTTTTTTTTTTTTTTTTTTTTTTTGAGATGGGGTCTTGCTGTTGCCCAGGCTGGAGTGCAGTGGTGCGGTCTTGGCTCACTGCAGCCTCCTCCTCTGGGGCTCAAGCA... | TGCCGACATTCCTTTCAACAGCACAACTGAGATGTTTATAGAGAAAGATGAGTTTTCTAGAAGTTTAACTGGCTTTTGCTTTTGTACTGAACTGTTATGAGTTGGGACAATTTAAACATTAACTTTGGTGTCTTGAAGTCACTTGTTTATGTTAAGAAACGTGGGGGCTATACCACCAAAAATCTATTATAACAGTCTGGACTGGTGGTAGGTTTTTTTTTTTTTTTTTTTTTTTTGAGATGGGGTCTTGCTGTTGCCCAGGCTGGAGTGCAGTGGTGCGGTCTTGGCTCACTGCAGCCTCCTCCTCTGGGGCTCAAGCA... |
Task1_train_41770 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TTGTAAGCCTGGCCAGCAAGGTGAAGGACGCGGTGAGTGCAGCCTGCCCAGAGTCCTGCTGGGCTGTGTGCGCTGGTGTCCCACCTGCTGGGCAGGAGGGACATGCCTCGCCTGTGCTCCCAGGGCCCTGGGATGGGGGTGATCTGCAAAGGGGACCCGGGCCCTGGAGGGGAGGGAGCAGCCCGGGCTTGGGGCAGGGTCATCGCCGCATGGGGCTCACCTTGAGTCTCTGCCCTTCCTCAGCTGAAGCTGCTGTACAGCGGAGTCCCATTCCTGGGCCCCTACCACAAGGAGTCGGCTGTGACGGCCTTCAGGTGGGT... | TTGTAAGCCTGGCCAGCAAGGTGAAGGACGCGGTGAGTGCAGCCTGCCCAGAGTCCTGCTGGGCTGTGTGCGCTGGTGTCCCACCTGCTGGGCAGGAGGGACATGCCTCGCCTGTGCTCCCAGGGCCCTGGGATGGGGGTGATCTGCAAAGGGGACCCGGGCCCTGGAGGGGAGGGAGCAGCCCGGGCTTGGGGCAGGGTCATCGCCGCATGGGGCTCACCTTGAGTCTCTGCCCTTCCTCAGCTGAAGCTGCTGTACAGCGGAGTCCCATTCCTGGGCCCCTACCACAAGGAGTCGGCTGTGACGGCCTTCAGGTGGGT... |
Task1_train_41771 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TGGCCTTGCCTAGTGCCCCTACAGCATCCTCTCTGCCCATGGTGCCAGATATCTGAATGGGAGGACAAAGGGGGCACAGGTGGTGAAAAAAACCAAGATGCACATTTGGGTATTTTCCTTCTTTTGCTAGAATGTCATTTCTTGATGTCTGTTTCTTGTCACCCATTTGTGATCAGGGACTAAGTAAGTTCCCTCTGCACCAGACCAGGTGGAAGACTGAGCCAGAGTTCCTCTGAGCCACAGGAGAGATGAGGAGCTATGGAGCGGAGTAGGGGCTGAGGATCTGGTGCCCCCAGCTAAACTAAAAGGAGGCAGGCAGC... | TGGCCTTGCCTAGTGCCCCTACAGCATCCTCTCTGCCCATGGTGCCAGATATCTGAATGGGAGGACAAAGGGGGCACAGGTGGTGAAAAAAACCAAGATGCACATTTGGGTATTTTCCTTCTTTTGCTAGAATGTCATTTCTTGATGTCTGTTTCTTGTCACCCATTTGTGATCAGGGACTAAGTAAGTTCCCTCTGCACCAGACCAGGTGGAAGACTGAGCCAGAGTTCCTCTGAGCCACAGGAGAGATGAGGAGCTATGGAGCGGAGTAGGGGCTGAGGATCTGGTGCCCCCAGCTAAACTAAAAGGAGGCAGGCAGC... |
Task1_train_41772 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CCTGGTATCTCCCGAACATTTGAGCATCTCTATCTGCTATTTCCAAACTGTCACAAAGACCCACACTATATTCAGGACAATCTGTGATTTAAAACGATGGCATCCCACTCTCACCACCACAAGCCCAGGCCTGCTGGCTTCATGGGGACCTGTGCCTGCCTCCTCTCCATCCTGCCACGTGCTGCTGCCAGACCAACCCATCTGAAGTTAGATGTGGGTTGCTTTCCACCCCCAAATCCTAAAATTAAAGCTGTTCTTCCTGCCAAGGTTCCCTGCCCAAACTGTGCATCTGAATGCCTGGGGAGACTTTGCCAAGGCAG... | CCTGGTATCTCCCGAACATTTGAGCATCTCTATCTGCTATTTCCAAACTGTCACAAAGACCCACACTATATTCAGGACAATCTGTGATTTAAAACGATGGCATCCCACTCTCACCACCACAAGCCCAGGCCTGCTGGCTTCATGGGGACCTGTGCCTGCCTCCTCTCCATCCTGCCACGTGCTGCTGCCAGACCAACCCATCTGAAGTTAGATGTGGGTTGCTTTCCACCCCCAAATCCTAAAATTAAAGCTGTTCTTCCTGCCAAGGTTCCCTGCCCAAACTGTGCATCTGAATGCCTGGGGAGACTTTGCCAAGGCAG... |
Task1_train_41773 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | GACCACTGAGCGTCCCATAACATGTTTGCTGGCCTGTGCATCACCTGCATTTATTGAGCTTTTAAATTAAATTAAATTATTATTATTATTATTATTATTTTGAGATGCAGTCTTGCTCTGTCATCCAGGCTGGAGTGCAGTGGCACGATCTCAGCTCACTGCATCCTCTGCTTATGGGGTTGAGGCGATTCTCCCACCTCAGCCTCCCAAGTAGTTAGGACTACAGGCGTGCACCACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTATCCAGGCTGGTCTCAAACTCCTGACCTCGGA... | GACCACTGAGCGTCCCATAACATGTTTGCTGGCCTGTGCATCACCTGCATTTATTGAGCTTTTAAATTAAATTAAATTATTATTATTATTATTATTATTTTGAGATGCAGTCTTGCTCTGTCATCCAGGCTGGAGTGCAGTGGCACGATCTCAGCTCACTGCATCCTCTGCTTATGGGGTTGAGGCGATTCTCCCACCTCAGCCTCCCAAGTAGTTAGGACTACAGGCGTGCACCACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTATCCAGGCTGGTCTCAAACTCCTGACCTCGGA... |
Task1_train_41774 | Consider this mutation on Chromosome 11. Is this a benign change or a disease-causing variant? | Benign | CTTGCTTAAAGAAAGGAGTCAGAGGAGAGGGCTGGTGCTCCCACCGCTCCGTGCTCTCAGGACAGGCAGGGAAACAGGTGTTAAATCAGCGTGACCCAAAGCTGCTCTGCCCTGCTTTTGGGGAAGCAAATACCACAAGGGCTTGCAGGGGTGCGTCCCTGGGGTGTAGTCAGCACCTGCAGTAGCCAGAGGGGCAGCCACGTGGACTCTCACCCACAGCAGTTCCCATCCTAATCATCTGTTTCTCCCTGGGTCTTTCCTACCCTGCCTTTCCCAGTGATAGAGGGTGGGAAAGATGGGGTGAGAAACAGAAGGCTGAT... | CTTGCTTAAAGAAAGGAGTCAGAGGAGAGGGCTGGTGCTCCCACCGCTCCGTGCTCTCAGGACAGGCAGGGAAACAGGTGTTAAATCAGCGTGACCCAAAGCTGCTCTGCCCTGCTTTTGGGGAAGCAAATACCACAAGGGCTTGCAGGGGTGCGTCCCTGGGGTGTAGTCAGCACCTGCAGTAGCCAGAGGGGCAGCCACGTGGACTCTCACCCACAGCAGTTCCCATCCTAATCATCTGTTTCTCCCTGGGTCTTTCCTACCCTGCCTTTCCCAGTGATAGAGGGTGGGAAAGATGGGGTGAGAAACAGAAGGCTGAT... |
Task1_train_41775 | A mutation on Chromosome 11 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TCTTCCTGGCAGGCTCAGGGAAGTAAATACTGAAACCAGTAAAGCATTTGGTACTGAGCAGTTAAGAAAATTGGGACGAGGCCTCAGGGGGTTTTGGATAATATGAAAACTCTATTTCCGAATCCTTCCTAAAACCAGACCTCCATGTACCAACCAATAAAACTTTCACTGCAGAGACTATAGGATCCAAATGTCTCTGTCTCTTCTTTCCTTGTCCCCGTGTGAACAGCAAGCCTGGCTCATTCTCAGTCCCCAGGTAGTTATCCTGAGCCTGCCTTTCTCAGCAGCAAGGGCAAGGGCAGAGAGGTGGGGTGGGGAAG... | TCTTCCTGGCAGGCTCAGGGAAGTAAATACTGAAACCAGTAAAGCATTTGGTACTGAGCAGTTAAGAAAATTGGGACGAGGCCTCAGGGGGTTTTGGATAATATGAAAACTCTATTTCCGAATCCTTCCTAAAACCAGACCTCCATGTACCAACCAATAAAACTTTCACTGCAGAGACTATAGGATCCAAATGTCTCTGTCTCTTCTTTCCTTGTCCCCGTGTGAACAGCAAGCCTGGCTCATTCTCAGTCCCCAGGTAGTTATCCTGAGCCTGCCTTTCTCAGCAGCAAGGGCAAGGGCAGAGAGGTGGGGTGGGGAAG... |
Task1_train_41776 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AATACTGAAACCAGTAAAGCATTTGGTACTGAGCAGTTAAGAAAATTGGGACGAGGCCTCAGGGGGTTTTGGATAATATGAAAACTCTATTTCCGAATCCTTCCTAAAACCAGACCTCCATGTACCAACCAATAAAACTTTCACTGCAGAGACTATAGGATCCAAATGTCTCTGTCTCTTCTTTCCTTGTCCCCGTGTGAACAGCAAGCCTGGCTCATTCTCAGTCCCCAGGTAGTTATCCTGAGCCTGCCTTTCTCAGCAGCAAGGGCAAGGGCAGAGAGGTGGGGTGGGGAAGGGGGAAGGTAATTAAAATGGCCACC... | AATACTGAAACCAGTAAAGCATTTGGTACTGAGCAGTTAAGAAAATTGGGACGAGGCCTCAGGGGGTTTTGGATAATATGAAAACTCTATTTCCGAATCCTTCCTAAAACCAGACCTCCATGTACCAACCAATAAAACTTTCACTGCAGAGACTATAGGATCCAAATGTCTCTGTCTCTTCTTTCCTTGTCCCCGTGTGAACAGCAAGCCTGGCTCATTCTCAGTCCCCAGGTAGTTATCCTGAGCCTGCCTTTCTCAGCAGCAAGGGCAAGGGCAGAGAGGTGGGGTGGGGAAGGGGGAAGGTAATTAAAATGGCCACC... |
Task1_train_41777 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | GTCCGTGGAGGGGAAAGGGCAGGGAGAGGGAGCAAAACCCTTAGTGCTGAAGCACCAGGAAGAAAGGCAAGACACAAAAGAGGGAAGAAGGCAGTAATTTAGTGGTTGTCTTGACGACCAGAGTCCCTATTGTTCATGGGGGCTTTACCTCACAGGGAGATCTCCCTGTTCTGCTCTGCACATAGAACTCCCACCACAGGAAAGGAGGATGGGAAGGGAAGGGTTGCAGGAGGCAGAAGTGATAAGTAATTATGTGCTCGCAGAAGGGGCTGACCTCCAAATTTCTGCAAATATTACGGATAACAGATTTAGAGTGTGCT... | GTCCGTGGAGGGGAAAGGGCAGGGAGAGGGAGCAAAACCCTTAGTGCTGAAGCACCAGGAAGAAAGGCAAGACACAAAAGAGGGAAGAAGGCAGTAATTTAGTGGTTGTCTTGACGACCAGAGTCCCTATTGTTCATGGGGGCTTTACCTCACAGGGAGATCTCCCTGTTCTGCTCTGCACATAGAACTCCCACCACAGGAAAGGAGGATGGGAAGGGAAGGGTTGCAGGAGGCAGAAGTGATAAGTAATTATGTGCTCGCAGAAGGGGCTGACCTCCAAATTTCTGCAAATATTACGGATAACAGATTTAGAGTGTGCT... |
Task1_train_41778 | A variant on Chromosome 11 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | ATTGTTCATGGGGGCTTTACCTCACAGGGAGATCTCCCTGTTCTGCTCTGCACATAGAACTCCCACCACAGGAAAGGAGGATGGGAAGGGAAGGGTTGCAGGAGGCAGAAGTGATAAGTAATTATGTGCTCGCAGAAGGGGCTGACCTCCAAATTTCTGCAAATATTACGGATAACAGATTTAGAGTGTGCTCAGCCATGATTTGGAAGAAAATTATTAGGGATTTATTTAAATCAGCAGACATGGGAGGACTTCAAATTATGCTGTGAAAATGGCTACAGGAGGCTGGAAAAGACCAGCCTTGAGGAGAATAAAGAATA... | ATTGTTCATGGGGGCTTTACCTCACAGGGAGATCTCCCTGTTCTGCTCTGCACATAGAACTCCCACCACAGGAAAGGAGGATGGGAAGGGAAGGGTTGCAGGAGGCAGAAGTGATAAGTAATTATGTGCTCGCAGAAGGGGCTGACCTCCAAATTTCTGCAAATATTACGGATAACAGATTTAGAGTGTGCTCAGCCATGATTTGGAAGAAAATTATTAGGGATTTATTTAAATCAGCAGACATGGGAGGACTTCAAATTATGCTGTGAAAATGGCTACAGGAGGCTGGAAAAGACCAGCCTTGAGGAGAATAAAGAATA... |
Task1_train_41779 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AGGTTTAGCATTTGCTTGGAGCTGCCACCATGTGGTAACAATTAGTTACAGCAGTGAAAAATAAGAAAGCAAACAAGGTACCACCAAGTCAGTTGCCTTAAAGAAAATGGTAGATTTTTTTTTGTTTTTTATAATCATATGAGCATTTTGAGTCTCTCAGAGATAGAAGAAGGGTTTCAGGCCTAAACCATCCCTCTAGAGATATGATGTTCAACATGTACAGGCTGGACTTTGCCTAGAATGATATTCTTACCACACTGACCCTGCCCCCCACCATCTTTACAGTCTCTTAGAGTTCTCTGATGCTTTCACTGTCATAT... | AGGTTTAGCATTTGCTTGGAGCTGCCACCATGTGGTAACAATTAGTTACAGCAGTGAAAAATAAGAAAGCAAACAAGGTACCACCAAGTCAGTTGCCTTAAAGAAAATGGTAGATTTTTTTTTGTTTTTTATAATCATATGAGCATTTTGAGTCTCTCAGAGATAGAAGAAGGGTTTCAGGCCTAAACCATCCCTCTAGAGATATGATGTTCAACATGTACAGGCTGGACTTTGCCTAGAATGATATTCTTACCACACTGACCCTGCCCCCCACCATCTTTACAGTCTCTTAGAGTTCTCTGATGCTTTCACTGTCATAT... |
Task1_train_41780 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | ATACCACGGATGGCATGGAATCTGCAACTCAGCATGGGGGCACACTTCTTGACAGGGTAGTTAAGACACAATGAAACGCTGTGGGAGAAGTATATATGTGCGCCTTCTCATTAGGAATGGGCTATTATTTTTCGGTTGAGGTATACTGTGGGCAAGAGGTGGAAAAAACTACCTCCTCGTTGGTGGGAGTTGTGGCTGGTGCTTTACAATTTTCTGGAGACAGGGTATTCATTATGAGCTGATGTGAGCAAAGCAGTCCCTCAGAACAGCACTGAGAAGGAAAGACCAAGTAAGAGCAACAGGTGGCATTCAGGGTGGGG... | ATACCACGGATGGCATGGAATCTGCAACTCAGCATGGGGGCACACTTCTTGACAGGGTAGTTAAGACACAATGAAACGCTGTGGGAGAAGTATATATGTGCGCCTTCTCATTAGGAATGGGCTATTATTTTTCGGTTGAGGTATACTGTGGGCAAGAGGTGGAAAAAACTACCTCCTCGTTGGTGGGAGTTGTGGCTGGTGCTTTACAATTTTCTGGAGACAGGGTATTCATTATGAGCTGATGTGAGCAAAGCAGTCCCTCAGAACAGCACTGAGAAGGAAAGACCAAGTAAGAGCAACAGGTGGCATTCAGGGTGGGG... |
Task1_train_41781 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | GTTGGTGGGAGTTGTGGCTGGTGCTTTACAATTTTCTGGAGACAGGGTATTCATTATGAGCTGATGTGAGCAAAGCAGTCCCTCAGAACAGCACTGAGAAGGAAAGACCAAGTAAGAGCAACAGGTGGCATTCAGGGTGGGGCTCTCAAGCCTGGAGCATTTGGAACTATGAGGCTTTCTGTGGAATATGCTGCTCCTCGAGGGCCAATTTTCAACACCGTTATGGTTACTTCCATCACATAAACCGAAAACTATTTACTATCAGAAAGTATAATAATATTGATATACAATTTAAAATCAGTTATATGTCCATATAAAAA... | GTTGGTGGGAGTTGTGGCTGGTGCTTTACAATTTTCTGGAGACAGGGTATTCATTATGAGCTGATGTGAGCAAAGCAGTCCCTCAGAACAGCACTGAGAAGGAAAGACCAAGTAAGAGCAACAGGTGGCATTCAGGGTGGGGCTCTCAAGCCTGGAGCATTTGGAACTATGAGGCTTTCTGTGGAATATGCTGCTCCTCGAGGGCCAATTTTCAACACCGTTATGGTTACTTCCATCACATAAACCGAAAACTATTTACTATCAGAAAGTATAATAATATTGATATACAATTTAAAATCAGTTATATGTCCATATAAAAA... |
Task1_train_41782 | Located on Chromosome 11, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | CAGGGTATTCATTATGAGCTGATGTGAGCAAAGCAGTCCCTCAGAACAGCACTGAGAAGGAAAGACCAAGTAAGAGCAACAGGTGGCATTCAGGGTGGGGCTCTCAAGCCTGGAGCATTTGGAACTATGAGGCTTTCTGTGGAATATGCTGCTCCTCGAGGGCCAATTTTCAACACCGTTATGGTTACTTCCATCACATAAACCGAAAACTATTTACTATCAGAAAGTATAATAATATTGATATACAATTTAAAATCAGTTATATGTCCATATAAAAATCTAAACCCAATTTCAAACTACTCATAATTGGCTATATTATT... | CAGGGTATTCATTATGAGCTGATGTGAGCAAAGCAGTCCCTCAGAACAGCACTGAGAAGGAAAGACCAAGTAAGAGCAACAGGTGGCATTCAGGGTGGGGCTCTCAAGCCTGGAGCATTTGGAACTATGAGGCTTTCTGTGGAATATGCTGCTCCTCGAGGGCCAATTTTCAACACCGTTATGGTTACTTCCATCACATAAACCGAAAACTATTTACTATCAGAAAGTATAATAATATTGATATACAATTTAAAATCAGTTATATGTCCATATAAAAATCTAAACCCAATTTCAAACTACTCATAATTGGCTATATTATT... |
Task1_train_41783 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | AGCAGTCCCTCAGAACAGCACTGAGAAGGAAAGACCAAGTAAGAGCAACAGGTGGCATTCAGGGTGGGGCTCTCAAGCCTGGAGCATTTGGAACTATGAGGCTTTCTGTGGAATATGCTGCTCCTCGAGGGCCAATTTTCAACACCGTTATGGTTACTTCCATCACATAAACCGAAAACTATTTACTATCAGAAAGTATAATAATATTGATATACAATTTAAAATCAGTTATATGTCCATATAAAAATCTAAACCCAATTTCAAACTACTCATAATTGGCTATATTATTTCGTTCTCATTTTTTACTTTACTCTTTTCTA... | AGCAGTCCCTCAGAACAGCACTGAGAAGGAAAGACCAAGTAAGAGCAACAGGTGGCATTCAGGGTGGGGCTCTCAAGCCTGGAGCATTTGGAACTATGAGGCTTTCTGTGGAATATGCTGCTCCTCGAGGGCCAATTTTCAACACCGTTATGGTTACTTCCATCACATAAACCGAAAACTATTTACTATCAGAAAGTATAATAATATTGATATACAATTTAAAATCAGTTATATGTCCATATAAAAATCTAAACCCAATTTCAAACTACTCATAATTGGCTATATTATTTCGTTCTCATTTTTTACTTTACTCTTTTCTA... |
Task1_train_41784 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | ACAGGTGGCATTCAGGGTGGGGCTCTCAAGCCTGGAGCATTTGGAACTATGAGGCTTTCTGTGGAATATGCTGCTCCTCGAGGGCCAATTTTCAACACCGTTATGGTTACTTCCATCACATAAACCGAAAACTATTTACTATCAGAAAGTATAATAATATTGATATACAATTTAAAATCAGTTATATGTCCATATAAAAATCTAAACCCAATTTCAAACTACTCATAATTGGCTATATTATTTCGTTCTCATTTTTTACTTTACTCTTTTCTAATGCTTAATTGAAGCAGTAGCAGATGTCAAAATCTAGCCAACAACAA... | ACAGGTGGCATTCAGGGTGGGGCTCTCAAGCCTGGAGCATTTGGAACTATGAGGCTTTCTGTGGAATATGCTGCTCCTCGAGGGCCAATTTTCAACACCGTTATGGTTACTTCCATCACATAAACCGAAAACTATTTACTATCAGAAAGTATAATAATATTGATATACAATTTAAAATCAGTTATATGTCCATATAAAAATCTAAACCCAATTTCAAACTACTCATAATTGGCTATATTATTTCGTTCTCATTTTTTACTTTACTCTTTTCTAATGCTTAATTGAAGCAGTAGCAGATGTCAAAATCTAGCCAACAACAA... |
Task1_train_41785 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | GTGGAATATGCTGCTCCTCGAGGGCCAATTTTCAACACCGTTATGGTTACTTCCATCACATAAACCGAAAACTATTTACTATCAGAAAGTATAATAATATTGATATACAATTTAAAATCAGTTATATGTCCATATAAAAATCTAAACCCAATTTCAAACTACTCATAATTGGCTATATTATTTCGTTCTCATTTTTTACTTTACTCTTTTCTAATGCTTAATTGAAGCAGTAGCAGATGTCAAAATCTAGCCAACAACAAAAAAGAACAAATAATGGGAGAAAGACTGGGAACTTAAACATTCTATCCATCAACTTAATT... | GTGGAATATGCTGCTCCTCGAGGGCCAATTTTCAACACCGTTATGGTTACTTCCATCACATAAACCGAAAACTATTTACTATCAGAAAGTATAATAATATTGATATACAATTTAAAATCAGTTATATGTCCATATAAAAATCTAAACCCAATTTCAAACTACTCATAATTGGCTATATTATTTCGTTCTCATTTTTTACTTTACTCTTTTCTAATGCTTAATTGAAGCAGTAGCAGATGTCAAAATCTAGCCAACAACAAAAAAGAACAAATAATGGGAGAAAGACTGGGAACTTAAACATTCTATCCATCAACTTAATT... |
Task1_train_41786 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GTACATTGGCATATGGGATCTGAGTTTCTTTCTTAACAGGCATAGAGAGCTGCTAGAGATGGGATCCTGCAAACAATGACTCTTGCCCTGACACCATGAACTTTTGAGCTGGTCTCTCCCCCTTCTTGACTCATGAGCACAAAGCTTTTTTTTACTAACCAGGTACCCTTGAGCCCCCAGTAATGCTGAACAGGTAGCAGACTGTCCCGGGGAGAGCCAGGGACACAGAGCTGAGTGCCCTTACTAAAGGCAGCAAGCAGTGGTCTCGTGAGCCGTGGAATTCACCCTTCTGAATTCAGTCTTCTGAATTCCTCTCCTAT... | GTACATTGGCATATGGGATCTGAGTTTCTTTCTTAACAGGCATAGAGAGCTGCTAGAGATGGGATCCTGCAAACAATGACTCTTGCCCTGACACCATGAACTTTTGAGCTGGTCTCTCCCCCTTCTTGACTCATGAGCACAAAGCTTTTTTTTACTAACCAGGTACCCTTGAGCCCCCAGTAATGCTGAACAGGTAGCAGACTGTCCCGGGGAGAGCCAGGGACACAGAGCTGAGTGCCCTTACTAAAGGCAGCAAGCAGTGGTCTCGTGAGCCGTGGAATTCACCCTTCTGAATTCAGTCTTCTGAATTCCTCTCCTAT... |
Task1_train_41787 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | GTAATTTGAAAAGTAAGATACTTCTAGGATTAAGAGCCGCCATGGCCAGGGCATGAACAGGAGACTTGTGATCATGTAACCGTAATTGGTAATAAGGGCTCAAGACCCATTCAGATTTTTTAGACCAGATGCTCAAAGCAGTCATCTCTCTCTAGTTTGTACTGTTATGGGGGGACTTTGTGAGAGAAGGCAGGTAATGAAATGACCCCTAAGTGTACCTCTTTCTCACAGCTCCTCGGGTTTCTGTATTTTCCTACAGGATCCTTCCTGATCCTCTGTAACTGTAAGGCATTATGCATTTTAGCATCCCCTTCTCTTTG... | GTAATTTGAAAAGTAAGATACTTCTAGGATTAAGAGCCGCCATGGCCAGGGCATGAACAGGAGACTTGTGATCATGTAACCGTAATTGGTAATAAGGGCTCAAGACCCATTCAGATTTTTTAGACCAGATGCTCAAAGCAGTCATCTCTCTCTAGTTTGTACTGTTATGGGGGGACTTTGTGAGAGAAGGCAGGTAATGAAATGACCCCTAAGTGTACCTCTTTCTCACAGCTCCTCGGGTTTCTGTATTTTCCTACAGGATCCTTCCTGATCCTCTGTAACTGTAAGGCATTATGCATTTTAGCATCCCCTTCTCTTTG... |
Task1_train_41788 | A variant has been detected on Chromosome 11. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CAGCCCTTTTTTTCCCTGGAGACTTTGATCATGGGGTGTCAGAACCCACACTCGACCGATTTTAGGGTCATTCCCCACAAAAGTCACCAGGCTGAGACCGAGACAGTGCTTTCCCCCAATTTACTAAGTTGCAGAAGGTCAGACTCTGAATTCAAACCCGTGTCTAGCTCCCATCTCACCCAACTGAACCATGCTCTGTTTAGTTTCCGATTTCCTCATATAGTCGGCCCTCAGCATCCATGGAGGATTGATTCCAGGGCCCCTGTGGACACAAAATCGGTCGGTGTTCAAGTTCTTGACATAAAATTGTGTGGCACTTC... | CAGCCCTTTTTTTCCCTGGAGACTTTGATCATGGGGTGTCAGAACCCACACTCGACCGATTTTAGGGTCATTCCCCACAAAAGTCACCAGGCTGAGACCGAGACAGTGCTTTCCCCCAATTTACTAAGTTGCAGAAGGTCAGACTCTGAATTCAAACCCGTGTCTAGCTCCCATCTCACCCAACTGAACCATGCTCTGTTTAGTTTCCGATTTCCTCATATAGTCGGCCCTCAGCATCCATGGAGGATTGATTCCAGGGCCCCTGTGGACACAAAATCGGTCGGTGTTCAAGTTCTTGACATAAAATTGTGTGGCACTTC... |
Task1_train_41789 | This variant is found on Chromosome 12. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TGGACATGTGTGTGAAGAACGGAACAACACAATAACAAACATGCGAAGCGTACTCATAGCCCTTCCTCCTTCCCATCCCATTCCTATAAAAGAGGAAAGAACAACTCATTTCCTTCACGGGGCATGGTGGTATGCATCTGTAGTCCCACCTACTCAGGAAGCTGAGGCTAGAGGATTCCTTGATCCCAGGAGGTCAAGGATGGAGTAAGCTATGATCCTGCCACTGCACTCCAGCCTCGGTGACAGACAAGACTTTAAAAAAAAAAAAAAGTAAAGGAAAAGAAAAGGAAAGGGATATTTCCCTGCCAAATTAATTTAAA... | TGGACATGTGTGTGAAGAACGGAACAACACAATAACAAACATGCGAAGCGTACTCATAGCCCTTCCTCCTTCCCATCCCATTCCTATAAAAGAGGAAAGAACAACTCATTTCCTTCACGGGGCATGGTGGTATGCATCTGTAGTCCCACCTACTCAGGAAGCTGAGGCTAGAGGATTCCTTGATCCCAGGAGGTCAAGGATGGAGTAAGCTATGATCCTGCCACTGCACTCCAGCCTCGGTGACAGACAAGACTTTAAAAAAAAAAAAAAGTAAAGGAAAAGAAAAGGAAAGGGATATTTCCCTGCCAAATTAATTTAAA... |
Task1_train_41790 | A genomic change on Chromosome 12 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TAAGTGGCATGTCTGGTTGTGAATAGGAAACACTCGCACTTCCCAAACTTCTCTGAGGGCTGATCAGAGTCTAGGATGCCACCATTTAAGCCCATCACCTTCACACAGGCCTTGTCCCTTATTTAAAGGCAGAAGCCTCTGGGGGCATGGCTGTCATACCTCCCCAGTCCTTTCCTGAGAAGTTTCCATAGGGAGGAAAAGTGAGAGCGTAGCAACCTGAGAGGAGAAAACCCACGGACAGGAGGACAGAGCCGAGAGGAGGCACGCTGGCCCCCTGACAGAAGTTTTCCTGGGATCAGATCTGCCCAGGTGAGGTGCCA... | TAAGTGGCATGTCTGGTTGTGAATAGGAAACACTCGCACTTCCCAAACTTCTCTGAGGGCTGATCAGAGTCTAGGATGCCACCATTTAAGCCCATCACCTTCACACAGGCCTTGTCCCTTATTTAAAGGCAGAAGCCTCTGGGGGCATGGCTGTCATACCTCCCCAGTCCTTTCCTGAGAAGTTTCCATAGGGAGGAAAAGTGAGAGCGTAGCAACCTGAGAGGAGAAAACCCACGGACAGGAGGACAGAGCCGAGAGGAGGCACGCTGGCCCCCTGACAGAAGTTTTCCTGGGATCAGATCTGCCCAGGTGAGGTGCCA... |
Task1_train_41791 | Assess the clinical impact of this variant found on Chromosome 12. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GGCTGTCATACCTCCCCAGTCCTTTCCTGAGAAGTTTCCATAGGGAGGAAAAGTGAGAGCGTAGCAACCTGAGAGGAGAAAACCCACGGACAGGAGGACAGAGCCGAGAGGAGGCACGCTGGCCCCCTGACAGAAGTTTTCCTGGGATCAGATCTGCCCAGGTGAGGTGCCATGCCCCCGAGCCCACCCCACCCAGCCCTGCCCTGGTTGGACAGCTCCCACCGTAAGAGCAGAGGTGACTCAAATTGGGGAACTCTTGGTAATGGTGGCCTGGAGGGACCCCCATTCTTGAGACACCCACTCAACTTTTTAGCAAATCC... | GGCTGTCATACCTCCCCAGTCCTTTCCTGAGAAGTTTCCATAGGGAGGAAAAGTGAGAGCGTAGCAACCTGAGAGGAGAAAACCCACGGACAGGAGGACAGAGCCGAGAGGAGGCACGCTGGCCCCCTGACAGAAGTTTTCCTGGGATCAGATCTGCCCAGGTGAGGTGCCATGCCCCCGAGCCCACCCCACCCAGCCCTGCCCTGGTTGGACAGCTCCCACCGTAAGAGCAGAGGTGACTCAAATTGGGGAACTCTTGGTAATGGTGGCCTGGAGGGACCCCCATTCTTGAGACACCCACTCAACTTTTTAGCAAATCC... |
Task1_train_41792 | Mutation context: Chromosome 12. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CTTGGCTGCCAGGCAGGTTCTGCTACACTTATACTCCCCGTCGTTGCTTGGATTCACCAGCCACCGCAGCCCAGCCCCTAACAGGCAACATCCCAGGGGCTGAAATGATGGATACCTGTGTTCCAAAAGTTGTTGCAGGTCGTCCAGGGCAGCTCAGAAGTGAAGGAGCTGAACAGGTAGAAGAGAGCCCAGGCAAGGATGATGATGTAGTAGACATTCAAATATGACTCGATGACCACAGATGCCAGACCAATGCCTTCCAGAGTGGGGGAGAGATGGGGAGGGACAAGAGAGATCAATGTTAGCAAAAAAGTCACATA... | CTTGGCTGCCAGGCAGGTTCTGCTACACTTATACTCCCCGTCGTTGCTTGGATTCACCAGCCACCGCAGCCCAGCCCCTAACAGGCAACATCCCAGGGGCTGAAATGATGGATACCTGTGTTCCAAAAGTTGTTGCAGGTCGTCCAGGGCAGCTCAGAAGTGAAGGAGCTGAACAGGTAGAAGAGAGCCCAGGCAAGGATGATGATGTAGTAGACATTCAAATATGACTCGATGACCACAGATGCCAGACCAATGCCTTCCAGAGTGGGGGAGAGATGGGGAGGGACAAGAGAGATCAATGTTAGCAAAAAAGTCACATA... |
Task1_train_41793 | This sequence change occurs on Chromosome 12. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TGTTACTGCGGGTACTCATCTCTCTCTCTCCACCCCACCCCACGGCCAGGACAGAGGCCACAGCCACAGCAGCAGCCAGCATGACAGGACAGAGGCAGGGTGGGCGCCCGACACCGCGGCCCTGCCTCCCAGGCCCTAGTGCTGTCTCCCTCCCAGATGGCTGGGTGAGGAGTGTGCCGTGACGCAGAAATGGTTCCAAGGCCCTCTGCAGTCCTGGGCAAATCCTCCTCCACTAAAGGAGGGCTTAGTCTGAGCACCTCCATCTCCAGCCCTAACATCCTATATGCCATGAGATGGTGGCCCTGGATGAAGAAGGAAAC... | TGTTACTGCGGGTACTCATCTCTCTCTCTCCACCCCACCCCACGGCCAGGACAGAGGCCACAGCCACAGCAGCAGCCAGCATGACAGGACAGAGGCAGGGTGGGCGCCCGACACCGCGGCCCTGCCTCCCAGGCCCTAGTGCTGTCTCCCTCCCAGATGGCTGGGTGAGGAGTGTGCCGTGACGCAGAAATGGTTCCAAGGCCCTCTGCAGTCCTGGGCAAATCCTCCTCCACTAAAGGAGGGCTTAGTCTGAGCACCTCCATCTCCAGCCCTAACATCCTATATGCCATGAGATGGTGGCCCTGGATGAAGAAGGAAAC... |
Task1_train_41794 | Chromosome 12 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TTTTGGGGAGAAAAGAAAAAAAACTTCAGAATGACATAATAAACCTTTGCTATCAATAATTTTCCTTCTGTACTCTAAAAGTTTTCATATCACAATGAAGAACCTTCTGAAAACCCATAAACAGAAAAAACAGCAAAACGTACACTTCCATTTAGAAAATTTAAGATAAATTAGTAATACTTAAAGTAATTAAAAAATAATACTTAAAGTAATTAAAAAGTAATACTTAAAATCTTAATAAATCAGATTAACACTCCTGGCAAAGTTCCATTAAAACCAAAACCAAAACCAAACCAAAACAAAACAAACTCTGAAAACTA... | TTTTGGGGAGAAAAGAAAAAAAACTTCAGAATGACATAATAAACCTTTGCTATCAATAATTTTCCTTCTGTACTCTAAAAGTTTTCATATCACAATGAAGAACCTTCTGAAAACCCATAAACAGAAAAAACAGCAAAACGTACACTTCCATTTAGAAAATTTAAGATAAATTAGTAATACTTAAAGTAATTAAAAAATAATACTTAAAGTAATTAAAAAGTAATACTTAAAATCTTAATAAATCAGATTAACACTCCTGGCAAAGTTCCATTAAAACCAAAACCAAAACCAAACCAAAACAAAACAAACTCTGAAAACTA... |
Task1_train_41795 | Here is a variant on Chromosome 12. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CTCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGCAGGTCACAAGGTCAGGCGTTTGAGACCAGCCTGGCCAACATGGTGAAACTCCGTCTCTACTAAAAAAAAAAAAAAAAATTAACTGGGCATGGTGGTGTGCACCTGTAATCTCAGCTACTTGGGAGGCGGAGGCAGGAGAATTGCTTGAACCCAGTTGGTGGAGGTTGCAGTGAGCTCAGATCACGCCACTGCACTCCAGCCTGGGCAACAGAGCAAGACTCCATCTCAAAAAAAAAAAAAAAGAAATGTTAAGTAAACTAGTATTTCTCTCACAAGTTTTTA... | CTCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGCAGGTCACAAGGTCAGGCGTTTGAGACCAGCCTGGCCAACATGGTGAAACTCCGTCTCTACTAAAAAAAAAAAAAAAAATTAACTGGGCATGGTGGTGTGCACCTGTAATCTCAGCTACTTGGGAGGCGGAGGCAGGAGAATTGCTTGAACCCAGTTGGTGGAGGTTGCAGTGAGCTCAGATCACGCCACTGCACTCCAGCCTGGGCAACAGAGCAAGACTCCATCTCAAAAAAAAAAAAAAAGAAATGTTAAGTAAACTAGTATTTCTCTCACAAGTTTTTA... |
Task1_train_41796 | The following genetic variant occurs on Chromosome 12. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CCACCTCAGCCTCCCAAAGTGTTGGGATTACAGGCGGGAGCCATCGCGCCCGGTCTGCTATGTTTCTTTTAACATAGTATAATGTGTTTGCATTTGGCCAGTATTTCTCCACCTTCATTTTTATTTTTAGTATTTTTGCACTTAAGTATAGCATCTTGACATTTCAATGGGTTTTGTTTTTAAGGAACAGATATTTTAATATTGTCATAGTAATTTGTAATTTTATATCTGTTTTCCAGAATACCAGTAACCTTCCTTGTTTAGCGTTATCTGCATATCTGAGCACATGATCGGTTCCTTCCATTAGATGGATCTTCCTA... | CCACCTCAGCCTCCCAAAGTGTTGGGATTACAGGCGGGAGCCATCGCGCCCGGTCTGCTATGTTTCTTTTAACATAGTATAATGTGTTTGCATTTGGCCAGTATTTCTCCACCTTCATTTTTATTTTTAGTATTTTTGCACTTAAGTATAGCATCTTGACATTTCAATGGGTTTTGTTTTTAAGGAACAGATATTTTAATATTGTCATAGTAATTTGTAATTTTATATCTGTTTTCCAGAATACCAGTAACCTTCCTTGTTTAGCGTTATCTGCATATCTGAGCACATGATCGGTTCCTTCCATTAGATGGATCTTCCTA... |
Task1_train_41797 | This alteration on Chromosome 12 may affect genome function. Does it lead to a disease or is it benign? | Benign | GCACGCCTGAACCCACAACTGCTAGCCAGCAGATCCTCAGGGCTGGGAAGGGATGAGCTCTTGCTTTAGATCATGTGTTTGGGTTGGGATTAGCAGATGAACAAGCAGTTTTCCCCTGAGCTCATCCAGAAATGGAGGGTATAGTCTGGGAGCATTCTTTCTCTTTCTCCCTCACTCCTCATATTTTCACATCACTTCAGTGGCCCCAGCATCCTGCTTCCCCAGAACACACCCCTGCCCTGAACTCGCCAGACCTCTTCCTGCCAGCTGGGCCAGCCTGGAAACAGGAGAGACCTTGATGGCAGAGGGATAAAGCTGCA... | GCACGCCTGAACCCACAACTGCTAGCCAGCAGATCCTCAGGGCTGGGAAGGGATGAGCTCTTGCTTTAGATCATGTGTTTGGGTTGGGATTAGCAGATGAACAAGCAGTTTTCCCCTGAGCTCATCCAGAAATGGAGGGTATAGTCTGGGAGCATTCTTTCTCTTTCTCCCTCACTCCTCATATTTTCACATCACTTCAGTGGCCCCAGCATCCTGCTTCCCCAGAACACACCCCTGCCCTGAACTCGCCAGACCTCTTCCTGCCAGCTGGGCCAGCCTGGAAACAGGAGAGACCTTGATGGCAGAGGGATAAAGCTGCA... |
Task1_train_41798 | A mutation on Chromosome 12 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GGCAGGGGGTGTGAGAGGAGGGAGGGGGGTGTGGGAGGAGGGGAGTGGGGAGGTGGGGAGAGGAGTAAGGAGTGGGGAGGTGGGAGGAGTGGGGCAGAGAGTGCGGACAGGGAGGAGTGGGGAGCGAGTCTGAGGCTGGGGAAGGACCACAGCGATTCGGCTTGGGACACCCAGCGCAGCATCTCTGGGGCCCTCTGGCCTTGGCCGGGTGCTGACTCGCGCTGCAGGTCATCCGGCTGCTCCGGGCTCCTGGCAAGGCGGGCTGCCTCCTGCGTGGGCAACGCTCACTCCTTCACTCCCTTCTGTTTTCTCTCCTACCT... | GGCAGGGGGTGTGAGAGGAGGGAGGGGGGTGTGGGAGGAGGGGAGTGGGGAGGTGGGGAGAGGAGTAAGGAGTGGGGAGGTGGGAGGAGTGGGGCAGAGAGTGCGGACAGGGAGGAGTGGGGAGCGAGTCTGAGGCTGGGGAAGGACCACAGCGATTCGGCTTGGGACACCCAGCGCAGCATCTCTGGGGCCCTCTGGCCTTGGCCGGGTGCTGACTCGCGCTGCAGGTCATCCGGCTGCTCCGGGCTCCTGGCAAGGCGGGCTGCCTCCTGCGTGGGCAACGCTCACTCCTTCACTCCCTTCTGTTTTCTCTCCTACCT... |
Task1_train_41799 | This alteration on Chromosome 12 may affect genome function. Does it lead to a disease or is it benign? | Benign | TTGAACCACTGCACTCCAGCCTGGGTGACAGAGTGAGATCCTGTCAAAAAAAACAAACAAACAAAAAAAACAACAAAGTTTCTTTACTCCTCACCCCTCTCAAAAAAATGACAACTGACGCTAAGGGGATGTTCAGCCCATGGTAGGAAATCCAGTTATCGGTACTGTACGAGGGAGGGGACCTTCTGGCCTCTTAGAAGTTTCTAGACCTTATTGAGGCTATCCCTGCACAGTGACTCTAAGATCAAACGGTGCCTTGTACCTGGGGCTGTGTGCTGAGTCCTCTGCTGCCAGGGTGCTCCTCAAATGGCCCTGCTCCA... | TTGAACCACTGCACTCCAGCCTGGGTGACAGAGTGAGATCCTGTCAAAAAAAACAAACAAACAAAAAAAACAACAAAGTTTCTTTACTCCTCACCCCTCTCAAAAAAATGACAACTGACGCTAAGGGGATGTTCAGCCCATGGTAGGAAATCCAGTTATCGGTACTGTACGAGGGAGGGGACCTTCTGGCCTCTTAGAAGTTTCTAGACCTTATTGAGGCTATCCCTGCACAGTGACTCTAAGATCAAACGGTGCCTTGTACCTGGGGCTGTGTGCTGAGTCCTCTGCTGCCAGGGTGCTCCTCAAATGGCCCTGCTCCA... |
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