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_40800 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | ATATAACATTGATGTTTTATATGTGTGTGTGTGATTATATACATACACATTTACACATAAAATATTTTGAGGGAAAGGGCAGGTGACAGATATAGATACAGGTATTAAATTAAATCCTCACTGTGTGTAACAGAGTAGTTGGTAATCTATTAAAGTTTAAACATAGCTTGGAGTAAAAGACATAACCACCAAAAAGAAGAACAACAAAAACATACACATACACAAACAATATATATATATTTTTATATTTTTTTTATTATACTTTAAGTTCTGAGGTACATGTGCACAACGTGCAGGTTTGTTACATATGTATACATGTG... | ATATAACATTGATGTTTTATATGTGTGTGTGTGATTATATACATACACATTTACACATAAAATATTTTGAGGGAAAGGGCAGGTGACAGATATAGATACAGGTATTAAATTAAATCCTCACTGTGTGTAACAGAGTAGTTGGTAATCTATTAAAGTTTAAACATAGCTTGGAGTAAAAGACATAACCACCAAAAAGAAGAACAACAAAAACATACACATACACAAACAATATATATATATTTTTATATTTTTTTTATTATACTTTAAGTTCTGAGGTACATGTGCACAACGTGCAGGTTTGTTACATATGTATACATGTG... |
Task1_train_40801 | A mutation located on Chromosome 11 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TTTTATATTTTTTTTATTATACTTTAAGTTCTGAGGTACATGTGCACAACGTGCAGGTTTGTTACATATGTATACATGTGCCATGTTGGTGTGCTGCACCCATTAACTCGTCATTTAACATTAGGTATATCTCCTAATGCTATCCCTCCCCCCTCCCCCCACCCCACAACAGGCCCCGGTGTGTGATGTTCCCCTTCCTGTGTCCAAGTGTTCTCATTGTTCAATTCCCACCTATGAGTGAGAACATGCAGTGTTTGGTTTTTTGTCCTTGCGATAGTTTGCTGAGAATGATGGTTTCCAGCTTCATCCATGTCCCTACA... | TTTTATATTTTTTTTATTATACTTTAAGTTCTGAGGTACATGTGCACAACGTGCAGGTTTGTTACATATGTATACATGTGCCATGTTGGTGTGCTGCACCCATTAACTCGTCATTTAACATTAGGTATATCTCCTAATGCTATCCCTCCCCCCTCCCCCCACCCCACAACAGGCCCCGGTGTGTGATGTTCCCCTTCCTGTGTCCAAGTGTTCTCATTGTTCAATTCCCACCTATGAGTGAGAACATGCAGTGTTTGGTTTTTTGTCCTTGCGATAGTTTGCTGAGAATGATGGTTTCCAGCTTCATCCATGTCCCTACA... |
Task1_train_40802 | A mutation on Chromosome 11 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TATATCTCCTAATGCTATCCCTCCCCCCTCCCCCCACCCCACAACAGGCCCCGGTGTGTGATGTTCCCCTTCCTGTGTCCAAGTGTTCTCATTGTTCAATTCCCACCTATGAGTGAGAACATGCAGTGTTTGGTTTTTTGTCCTTGCGATAGTTTGCTGAGAATGATGGTTTCCAGCTTCATCCATGTCCCTACAAAGGACATGAGCTCATCCTTTTTTATGGCTGCATAGTATTCCATGGTGTATATGTGCCACATTTTCTTTATCCAGTCTATCATTGTTGAACATTTGGGTTGGTTCCAAGTCTTTGCTACACAAAC... | TATATCTCCTAATGCTATCCCTCCCCCCTCCCCCCACCCCACAACAGGCCCCGGTGTGTGATGTTCCCCTTCCTGTGTCCAAGTGTTCTCATTGTTCAATTCCCACCTATGAGTGAGAACATGCAGTGTTTGGTTTTTTGTCCTTGCGATAGTTTGCTGAGAATGATGGTTTCCAGCTTCATCCATGTCCCTACAAAGGACATGAGCTCATCCTTTTTTATGGCTGCATAGTATTCCATGGTGTATATGTGCCACATTTTCTTTATCCAGTCTATCATTGTTGAACATTTGGGTTGGTTCCAAGTCTTTGCTACACAAAC... |
Task1_train_40803 | 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 | TGTGTCCAAGTGTTCTCATTGTTCAATTCCCACCTATGAGTGAGAACATGCAGTGTTTGGTTTTTTGTCCTTGCGATAGTTTGCTGAGAATGATGGTTTCCAGCTTCATCCATGTCCCTACAAAGGACATGAGCTCATCCTTTTTTATGGCTGCATAGTATTCCATGGTGTATATGTGCCACATTTTCTTTATCCAGTCTATCATTGTTGAACATTTGGGTTGGTTCCAAGTCTTTGCTACACAAACAATATTTTTAAGAGGCCATCACTAAAAAGGGACTAGATGGAGGACATTTTCAAAAGGAAAGTTTAATTTTTTT... | TGTGTCCAAGTGTTCTCATTGTTCAATTCCCACCTATGAGTGAGAACATGCAGTGTTTGGTTTTTTGTCCTTGCGATAGTTTGCTGAGAATGATGGTTTCCAGCTTCATCCATGTCCCTACAAAGGACATGAGCTCATCCTTTTTTATGGCTGCATAGTATTCCATGGTGTATATGTGCCACATTTTCTTTATCCAGTCTATCATTGTTGAACATTTGGGTTGGTTCCAAGTCTTTGCTACACAAACAATATTTTTAAGAGGCCATCACTAAAAAGGGACTAGATGGAGGACATTTTCAAAAGGAAAGTTTAATTTTTTT... |
Task1_train_40804 | 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 | TGTCCTTGCGATAGTTTGCTGAGAATGATGGTTTCCAGCTTCATCCATGTCCCTACAAAGGACATGAGCTCATCCTTTTTTATGGCTGCATAGTATTCCATGGTGTATATGTGCCACATTTTCTTTATCCAGTCTATCATTGTTGAACATTTGGGTTGGTTCCAAGTCTTTGCTACACAAACAATATTTTTAAGAGGCCATCACTAAAAAGGGACTAGATGGAGGACATTTTCAAAAGGAAAGTTTAATTTTTTTATGATGATGTTGTCTTTGTTGTTTTATTATGATTTGTATAAATATGCACATATTATTTATGCTAA... | TGTCCTTGCGATAGTTTGCTGAGAATGATGGTTTCCAGCTTCATCCATGTCCCTACAAAGGACATGAGCTCATCCTTTTTTATGGCTGCATAGTATTCCATGGTGTATATGTGCCACATTTTCTTTATCCAGTCTATCATTGTTGAACATTTGGGTTGGTTCCAAGTCTTTGCTACACAAACAATATTTTTAAGAGGCCATCACTAAAAAGGGACTAGATGGAGGACATTTTCAAAAGGAAAGTTTAATTTTTTTATGATGATGTTGTCTTTGTTGTTTTATTATGATTTGTATAAATATGCACATATTATTTATGCTAA... |
Task1_train_40805 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | TTGTTGGAAATTCCCCAGGGAAACAAAAAATTTTATGTAAGAAGATGTCATCCTAGATTTCAAACAACTCCTAAAGATTCTCAGCCATGCACAGAGATTTGATTGTGCCTAGCACTGAGGTGAGATTGGTCAATTTTCATAAATCCCTATTTTAGGAAAGGGTAAAGACATTTTTGGCAAAGAATGCAACAGCCTGATACACTGAAACAGTTTTAAAAAGTAATAGCAGTAAGGGGCAATGTTTTTTACTTTCTCTTTCACTTCTTAAGAGGTAATGGCTCTTTTTCTTTCTGGGTGGCTTCCACTGGACTTAATCTTAT... | TTGTTGGAAATTCCCCAGGGAAACAAAAAATTTTATGTAAGAAGATGTCATCCTAGATTTCAAACAACTCCTAAAGATTCTCAGCCATGCACAGAGATTTGATTGTGCCTAGCACTGAGGTGAGATTGGTCAATTTTCATAAATCCCTATTTTAGGAAAGGGTAAAGACATTTTTGGCAAAGAATGCAACAGCCTGATACACTGAAACAGTTTTAAAAAGTAATAGCAGTAAGGGGCAATGTTTTTTACTTTCTCTTTCACTTCTTAAGAGGTAATGGCTCTTTTTCTTTCTGGGTGGCTTCCACTGGACTTAATCTTAT... |
Task1_train_40806 | A variant has been detected on Chromosome 11. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GCAGTAAGGGGCAATGTTTTTTACTTTCTCTTTCACTTCTTAAGAGGTAATGGCTCTTTTTCTTTCTGGGTGGCTTCCACTGGACTTAATCTTATTTTCTTTTCATTCCATTCATTTCAATGTGGTGTACACATAAAAGATGGTAGACACTAGAAATTTTAATCTTTAAGTTTGTCTTGTCTAAGAACATAAAATGATGGTTTCTTGAAACAGTGACATTCTGGAGAGGTACTGTGAGAACTTCCTTATAAGAAGGGATTATTTATATGAGATCCAGTCAGGTAGTATTCAGAGATCACGAGCTTCTGAAACATGTGGTT... | GCAGTAAGGGGCAATGTTTTTTACTTTCTCTTTCACTTCTTAAGAGGTAATGGCTCTTTTTCTTTCTGGGTGGCTTCCACTGGACTTAATCTTATTTTCTTTTCATTCCATTCATTTCAATGTGGTGTACACATAAAAGATGGTAGACACTAGAAATTTTAATCTTTAAGTTTGTCTTGTCTAAGAACATAAAATGATGGTTTCTTGAAACAGTGACATTCTGGAGAGGTACTGTGAGAACTTCCTTATAAGAAGGGATTATTTATATGAGATCCAGTCAGGTAGTATTCAGAGATCACGAGCTTCTGAAACATGTGGTT... |
Task1_train_40807 | A mutation found on Chromosome 11 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AGTGATTTCTAGAATGTTTCGGTCACAGAACTCTAAGCCTTGTGGATTCACAACCATGTAATCCATGCCATCACACTGCAAATGTATATCTATTTCTGCTAGATAGTGAGGAATGTTTGGCATTGGCTTTGCTCCATGGGGTCTACTACAGAACTTAAGGATTAGGGTTTTATTCCGAATAAAAAAAAAATTGAATAATTAGGACACTTCAACTTTCTTCAAACACCCCTGAAGCTATAAATTCCTTCAAATACTATTCAATTCTTTCTACTGCTCCATCAAGAAATAGCAATCCAAAGATGTGGTGCTATTTTTTAATT... | AGTGATTTCTAGAATGTTTCGGTCACAGAACTCTAAGCCTTGTGGATTCACAACCATGTAATCCATGCCATCACACTGCAAATGTATATCTATTTCTGCTAGATAGTGAGGAATGTTTGGCATTGGCTTTGCTCCATGGGGTCTACTACAGAACTTAAGGATTAGGGTTTTATTCCGAATAAAAAAAAAATTGAATAATTAGGACACTTCAACTTTCTTCAAACACCCCTGAAGCTATAAATTCCTTCAAATACTATTCAATTCTTTCTACTGCTCCATCAAGAAATAGCAATCCAAAGATGTGGTGCTATTTTTTAATT... |
Task1_train_40808 | A variant was discovered on Chromosome 11. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | AGAAAAGAAAAAGAAAGAAAGAAAGGAACGAACAAACAACGTGGATGGAACTGGATGACATTATGTTAAGTGAAATAAATCACGCAAATATCACACGTCCTCACTCTTATGTGGAGCTTAAAAAAAATTGATCTCATGGAGACAGAGTAGAATGATGGTTACCACAGGCTGTAAAGGGTAGTGAGGAGGGCAGGATAGAGGGATTGGTTAATAGGTACAAAAATACAGTTACAAGGAATAAGATCTAGCATTCAGTAGCATAATTGAGTGACTATAGTTAACAATACTGTATTATATATTTCAAAATAACTAGCAGAGTA... | AGAAAAGAAAAAGAAAGAAAGAAAGGAACGAACAAACAACGTGGATGGAACTGGATGACATTATGTTAAGTGAAATAAATCACGCAAATATCACACGTCCTCACTCTTATGTGGAGCTTAAAAAAAATTGATCTCATGGAGACAGAGTAGAATGATGGTTACCACAGGCTGTAAAGGGTAGTGAGGAGGGCAGGATAGAGGGATTGGTTAATAGGTACAAAAATACAGTTACAAGGAATAAGATCTAGCATTCAGTAGCATAATTGAGTGACTATAGTTAACAATACTGTATTATATATTTCAAAATAACTAGCAGAGTA... |
Task1_train_40809 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | AAAAAATTGATCTCATGGAGACAGAGTAGAATGATGGTTACCACAGGCTGTAAAGGGTAGTGAGGAGGGCAGGATAGAGGGATTGGTTAATAGGTACAAAAATACAGTTACAAGGAATAAGATCTAGCATTCAGTAGCATAATTGAGTGACTATAGTTAACAATACTGTATTATATATTTCAAAATAACTAGCAGAGTAGAAGTAGAATTTTCCTAACACAAAAAAATTATAAATTCTTGAGGTGACAGATACACCAATTTTTCTAATATAATCATTACACATTGTATCCTTGTGTCAAAATTTCACAATACCCCATATA... | AAAAAATTGATCTCATGGAGACAGAGTAGAATGATGGTTACCACAGGCTGTAAAGGGTAGTGAGGAGGGCAGGATAGAGGGATTGGTTAATAGGTACAAAAATACAGTTACAAGGAATAAGATCTAGCATTCAGTAGCATAATTGAGTGACTATAGTTAACAATACTGTATTATATATTTCAAAATAACTAGCAGAGTAGAAGTAGAATTTTCCTAACACAAAAAAATTATAAATTCTTGAGGTGACAGATACACCAATTTTTCTAATATAATCATTACACATTGTATCCTTGTGTCAAAATTTCACAATACCCCATATA... |
Task1_train_40810 | An alteration has been detected on Chromosome 11. Is it pathogenic, and if so, what disease is involved? | Benign | GTATCCTTGTGTCAAAATTTCACAATACCCCATATATATGTACAACTAGTATGTGTCCACAAACTATTAAATAAATATGCTGAACAAATTTTATGCATAAAAAGTTGACACACATTAGACATGTTATGAAATGATAGAATTCAAAGTACCAATTATAACAGAGAAAAAATACATAAGAGTCAAGAATATTTCTCCATCTCAAAATATAACTTCAAAATAATTGCAACAATGGTCACTGAAATTAAAAATATAATTGGTATATCAAAATTTGTAGAGACTTTAATGCAACTCTTATAAAAACAAGCTGTTTGAGAACGCAA... | GTATCCTTGTGTCAAAATTTCACAATACCCCATATATATGTACAACTAGTATGTGTCCACAAACTATTAAATAAATATGCTGAACAAATTTTATGCATAAAAAGTTGACACACATTAGACATGTTATGAAATGATAGAATTCAAAGTACCAATTATAACAGAGAAAAAATACATAAGAGTCAAGAATATTTCTCCATCTCAAAATATAACTTCAAAATAATTGCAACAATGGTCACTGAAATTAAAAATATAATTGGTATATCAAAATTTGTAGAGACTTTAATGCAACTCTTATAAAAACAAGCTGTTTGAGAACGCAA... |
Task1_train_40811 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | AGTATGTGTCCACAAACTATTAAATAAATATGCTGAACAAATTTTATGCATAAAAAGTTGACACACATTAGACATGTTATGAAATGATAGAATTCAAAGTACCAATTATAACAGAGAAAAAATACATAAGAGTCAAGAATATTTCTCCATCTCAAAATATAACTTCAAAATAATTGCAACAATGGTCACTGAAATTAAAAATATAATTGGTATATCAAAATTTGTAGAGACTTTAATGCAACTCTTATAAAAACAAGCTGTTTGAGAACGCAAAAGTAAGTAAAAGTAAAGAGAATGTGCATTTAAAAAATAATTGGAGA... | AGTATGTGTCCACAAACTATTAAATAAATATGCTGAACAAATTTTATGCATAAAAAGTTGACACACATTAGACATGTTATGAAATGATAGAATTCAAAGTACCAATTATAACAGAGAAAAAATACATAAGAGTCAAGAATATTTCTCCATCTCAAAATATAACTTCAAAATAATTGCAACAATGGTCACTGAAATTAAAAATATAATTGGTATATCAAAATTTGTAGAGACTTTAATGCAACTCTTATAAAAACAAGCTGTTTGAGAACGCAAAAGTAAGTAAAAGTAAAGAGAATGTGCATTTAAAAAATAATTGGAGA... |
Task1_train_40812 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TATTACAAACCCCAACTCTGATTCAATTAAATGCTGAACAACTGGGAACCAACATTCATGTGGCAGTTTTGAGAGTATTACAATGATTACCCCTGGTTCTCAACTCTTAGTTGCAGCTATTCTCTTTGTAGAAATAAGGCCAGTACATGCATAAATATTATACAATCCAGGTTACATTAGTTGCTACAGAGTTGTACAGTGTCTTTAGGGATGCAAAGTTAAAATAAGGTAATTTTCCTTGTTATTGTCAAGGAATCAATGAAGAGTCCTTAAAACATTTTAATTTCAATATTAAAATTTGCTAAATATTTGATCTGTTT... | TATTACAAACCCCAACTCTGATTCAATTAAATGCTGAACAACTGGGAACCAACATTCATGTGGCAGTTTTGAGAGTATTACAATGATTACCCCTGGTTCTCAACTCTTAGTTGCAGCTATTCTCTTTGTAGAAATAAGGCCAGTACATGCATAAATATTATACAATCCAGGTTACATTAGTTGCTACAGAGTTGTACAGTGTCTTTAGGGATGCAAAGTTAAAATAAGGTAATTTTCCTTGTTATTGTCAAGGAATCAATGAAGAGTCCTTAAAACATTTTAATTTCAATATTAAAATTTGCTAAATATTTGATCTGTTT... |
Task1_train_40813 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TTATACAATCCAGGTTACATTAGTTGCTACAGAGTTGTACAGTGTCTTTAGGGATGCAAAGTTAAAATAAGGTAATTTTCCTTGTTATTGTCAAGGAATCAATGAAGAGTCCTTAAAACATTTTAATTTCAATATTAAAATTTGCTAAATATTTGATCTGTTTACACCTGAAGGTAGGCACAATTTTGGGACATGGGAATTTTTTTTATGTTACTAACTGATGTTATAGATTGTAAGGAAGATAAACATAATTTGGCAGATACACACAAGGCATTTTATTGGAAGGATATCAGGGAATCAGAATGACAGGATCTTGGAGA... | TTATACAATCCAGGTTACATTAGTTGCTACAGAGTTGTACAGTGTCTTTAGGGATGCAAAGTTAAAATAAGGTAATTTTCCTTGTTATTGTCAAGGAATCAATGAAGAGTCCTTAAAACATTTTAATTTCAATATTAAAATTTGCTAAATATTTGATCTGTTTACACCTGAAGGTAGGCACAATTTTGGGACATGGGAATTTTTTTTATGTTACTAACTGATGTTATAGATTGTAAGGAAGATAAACATAATTTGGCAGATACACACAAGGCATTTTATTGGAAGGATATCAGGGAATCAGAATGACAGGATCTTGGAGA... |
Task1_train_40814 | An alteration has been detected on Chromosome 11. Is it pathogenic, and if so, what disease is involved? | Benign | ATTGTCAAGGAATCAATGAAGAGTCCTTAAAACATTTTAATTTCAATATTAAAATTTGCTAAATATTTGATCTGTTTACACCTGAAGGTAGGCACAATTTTGGGACATGGGAATTTTTTTTATGTTACTAACTGATGTTATAGATTGTAAGGAAGATAAACATAATTTGGCAGATACACACAAGGCATTTTATTGGAAGGATATCAGGGAATCAGAATGACAGGATCTTGGAGAAACTGGATTGTTCATGAAGATTTAGAAGCATCAAAATTAGTAATTAATCCATAATAGAAATGCACTTATCAGTTTAGCTGAGTTAG... | ATTGTCAAGGAATCAATGAAGAGTCCTTAAAACATTTTAATTTCAATATTAAAATTTGCTAAATATTTGATCTGTTTACACCTGAAGGTAGGCACAATTTTGGGACATGGGAATTTTTTTTATGTTACTAACTGATGTTATAGATTGTAAGGAAGATAAACATAATTTGGCAGATACACACAAGGCATTTTATTGGAAGGATATCAGGGAATCAGAATGACAGGATCTTGGAGAAACTGGATTGTTCATGAAGATTTAGAAGCATCAAAATTAGTAATTAATCCATAATAGAAATGCACTTATCAGTTTAGCTGAGTTAG... |
Task1_train_40815 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CTCAGCTTGAAGAATACTGGTATATAGAAATGCTACTCATCTTTGTATGTTGATTTTGTGATACTAACTTTCCTATAATCAGATCCCATAAGGAGAAAAAGATGATTAATACAACTCAGGAAATGATCATATCATAAAGTATCTTCCCTCCCTTTAGCAGAATCGTGACATATCTTGGGAAGCAATTCCACACCATGAAATTGGACAGAATCTGAGAAGATACAAACCCAAATACACATACCACTATACTTCCAAAGCAGTTCTTTGGGCCTGCATTATAGCCAAGTCATAGGGATAGTTTTTCTTTAGGATTAGTAGCA... | CTCAGCTTGAAGAATACTGGTATATAGAAATGCTACTCATCTTTGTATGTTGATTTTGTGATACTAACTTTCCTATAATCAGATCCCATAAGGAGAAAAAGATGATTAATACAACTCAGGAAATGATCATATCATAAAGTATCTTCCCTCCCTTTAGCAGAATCGTGACATATCTTGGGAAGCAATTCCACACCATGAAATTGGACAGAATCTGAGAAGATACAAACCCAAATACACATACCACTATACTTCCAAAGCAGTTCTTTGGGCCTGCATTATAGCCAAGTCATAGGGATAGTTTTTCTTTAGGATTAGTAGCA... |
Task1_train_40816 | A genomic change on Chromosome 11 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CATTTATGAGATTTTGCGATGTCTTTCAGATGGCTGGATAATTGTGCTTGGAGTCGAATTTTCAAATTAAATTGCCTCATGTCCAGGTGGAATAAGGTAGTAGGAAGAGGTGCAAAGATTTAGAATTAAGAGTCTCTCCTCTATCCTCTGGTTCCACTTGTATTTTCTAATTATGACTTACCAGAGAACCCTGCATTAAAGACATTTTTAAACAAACAAAAACTGCAAACCTTTACAAGAGGGAATTCTAAAAGATATACTTCAGGCAAAAGAATACATATCCCACTTGGAAGATCTGAGATGAAAAACGTATACTTTTT... | CATTTATGAGATTTTGCGATGTCTTTCAGATGGCTGGATAATTGTGCTTGGAGTCGAATTTTCAAATTAAATTGCCTCATGTCCAGGTGGAATAAGGTAGTAGGAAGAGGTGCAAAGATTTAGAATTAAGAGTCTCTCCTCTATCCTCTGGTTCCACTTGTATTTTCTAATTATGACTTACCAGAGAACCCTGCATTAAAGACATTTTTAAACAAACAAAAACTGCAAACCTTTACAAGAGGGAATTCTAAAAGATATACTTCAGGCAAAAGAATACATATCCCACTTGGAAGATCTGAGATGAAAAACGTATACTTTTT... |
Task1_train_40817 | A mutation located on Chromosome 11 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CAACAAAGATTACCAAAAAAATGGTGGTTTAACCCAGATACAGGTTTATTTCTGTTTCAGGTTCAAGTCATGGTTGGTGGCCCAGACAGTGTCAGGAACACAGCTCTTCTGTATTGTTACTCTTCCATCTTCAGTTCACATTTCTGTCTTGTGATCCAAGAAAGCTGCCTGAGATGAAGCTTAGACTCTCTAGGGTTAAGAGAGTTTGTTACAATAGATGTAATACATCATACCCTGATTTTCTCTAGGACAATTTACCAGAGTTTAAGCCCTAGACTGGGAATGAAGCTGATTAGAATGTGCAATTCCTCCTGCAATAA... | CAACAAAGATTACCAAAAAAATGGTGGTTTAACCCAGATACAGGTTTATTTCTGTTTCAGGTTCAAGTCATGGTTGGTGGCCCAGACAGTGTCAGGAACACAGCTCTTCTGTATTGTTACTCTTCCATCTTCAGTTCACATTTCTGTCTTGTGATCCAAGAAAGCTGCCTGAGATGAAGCTTAGACTCTCTAGGGTTAAGAGAGTTTGTTACAATAGATGTAATACATCATACCCTGATTTTCTCTAGGACAATTTACCAGAGTTTAAGCCCTAGACTGGGAATGAAGCTGATTAGAATGTGCAATTCCTCCTGCAATAA... |
Task1_train_40818 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | TCAGTTCACATTTCTGTCTTGTGATCCAAGAAAGCTGCCTGAGATGAAGCTTAGACTCTCTAGGGTTAAGAGAGTTTGTTACAATAGATGTAATACATCATACCCTGATTTTCTCTAGGACAATTTACCAGAGTTTAAGCCCTAGACTGGGAATGAAGCTGATTAGAATGTGCAATTCCTCCTGCAATAAAAACAGCTCATACCAGTCCTCCCTAATTCATCTACTTGCAACGGCCAAGTTAAAGGCCTGATACTAAGCCTCTCAGACAGAGTACTAGTTATTATGAGTAAAATTTACTAAGAAAAGAAAAACTAGAAAA... | TCAGTTCACATTTCTGTCTTGTGATCCAAGAAAGCTGCCTGAGATGAAGCTTAGACTCTCTAGGGTTAAGAGAGTTTGTTACAATAGATGTAATACATCATACCCTGATTTTCTCTAGGACAATTTACCAGAGTTTAAGCCCTAGACTGGGAATGAAGCTGATTAGAATGTGCAATTCCTCCTGCAATAAAAACAGCTCATACCAGTCCTCCCTAATTCATCTACTTGCAACGGCCAAGTTAAAGGCCTGATACTAAGCCTCTCAGACAGAGTACTAGTTATTATGAGTAAAATTTACTAAGAAAAGAAAAACTAGAAAA... |
Task1_train_40819 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GAAAGCTGCCTGAGATGAAGCTTAGACTCTCTAGGGTTAAGAGAGTTTGTTACAATAGATGTAATACATCATACCCTGATTTTCTCTAGGACAATTTACCAGAGTTTAAGCCCTAGACTGGGAATGAAGCTGATTAGAATGTGCAATTCCTCCTGCAATAAAAACAGCTCATACCAGTCCTCCCTAATTCATCTACTTGCAACGGCCAAGTTAAAGGCCTGATACTAAGCCTCTCAGACAGAGTACTAGTTATTATGAGTAAAATTTACTAAGAAAAGAAAAACTAGAAAAAACAACTATTAACTCTACCCCTCCTACCA... | GAAAGCTGCCTGAGATGAAGCTTAGACTCTCTAGGGTTAAGAGAGTTTGTTACAATAGATGTAATACATCATACCCTGATTTTCTCTAGGACAATTTACCAGAGTTTAAGCCCTAGACTGGGAATGAAGCTGATTAGAATGTGCAATTCCTCCTGCAATAAAAACAGCTCATACCAGTCCTCCCTAATTCATCTACTTGCAACGGCCAAGTTAAAGGCCTGATACTAAGCCTCTCAGACAGAGTACTAGTTATTATGAGTAAAATTTACTAAGAAAAGAAAAACTAGAAAAAACAACTATTAACTCTACCCCTCCTACCA... |
Task1_train_40820 | A mutation on Chromosome 11 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | AGCTGATTAGAATGTGCAATTCCTCCTGCAATAAAAACAGCTCATACCAGTCCTCCCTAATTCATCTACTTGCAACGGCCAAGTTAAAGGCCTGATACTAAGCCTCTCAGACAGAGTACTAGTTATTATGAGTAAAATTTACTAAGAAAAGAAAAACTAGAAAAAACAACTATTAACTCTACCCCTCCTACCAATATGAAATCCCAAAATAAATCTTATCTCCCGAGCATCTTACATCAAAGTAGCAATGACTTGACTTCTTCCATGACTAAACAAAATGTGTTACCTTCTAGGAACAAAAATAATTAGGCCAGATCTCA... | AGCTGATTAGAATGTGCAATTCCTCCTGCAATAAAAACAGCTCATACCAGTCCTCCCTAATTCATCTACTTGCAACGGCCAAGTTAAAGGCCTGATACTAAGCCTCTCAGACAGAGTACTAGTTATTATGAGTAAAATTTACTAAGAAAAGAAAAACTAGAAAAAACAACTATTAACTCTACCCCTCCTACCAATATGAAATCCCAAAATAAATCTTATCTCCCGAGCATCTTACATCAAAGTAGCAATGACTTGACTTCTTCCATGACTAAACAAAATGTGTTACCTTCTAGGAACAAAAATAATTAGGCCAGATCTCA... |
Task1_train_40821 | A variant was discovered on Chromosome 11. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GACAAAAAACCAAACACCGCATTTTCTCACTCATAGGTGGGAGTTGAACAATGAGAACACATGGACACAGGAAGGGGAACATCACACACCGGGGACTGTTGTGGGTTAGGGGGAGTGGGGAGGGATAGCATTAGGAGATATACCTAATGTTAAATGACGAGTTAATGGGTGCAGCACGCCAACATGGCACATGTATACATATGTAACAAACCTGCACATTGTGCACATGTACTCTAAAACTTAAAACATAATAAAAAAATAAAAAATAAAAAAACCTGGTAGGAAAGATGGGGTTTGGCAAATGGTGATAATGGTAAAAG... | GACAAAAAACCAAACACCGCATTTTCTCACTCATAGGTGGGAGTTGAACAATGAGAACACATGGACACAGGAAGGGGAACATCACACACCGGGGACTGTTGTGGGTTAGGGGGAGTGGGGAGGGATAGCATTAGGAGATATACCTAATGTTAAATGACGAGTTAATGGGTGCAGCACGCCAACATGGCACATGTATACATATGTAACAAACCTGCACATTGTGCACATGTACTCTAAAACTTAAAACATAATAAAAAAATAAAAAATAAAAAAACCTGGTAGGAAAGATGGGGTTTGGCAAATGGTGATAATGGTAAAAG... |
Task1_train_40822 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | TTCCTGGCTTGCCCCCATCTCTGCCTCCTTACTCTACTTCCTGAGTCACCAGCCCATCAGCACTGAGCAAAGAGATACAAAACAGAGTTAATGTGGCACAGGTGGGAGGGAGAAAGGCCCTGAGGGAAGCAGGTAGAACAGCCACATAAAGAGCCCCACAGGCACTGATTAAAGCGAAGAGAAGCTGCCAACACACAGTGCTCGAGATCTTTCCCAGTCAAGCCTTCTGCTGGTGATTTCTTCCTCATTCATTTATCCATTCAACATGTATTAAGCTTCTTAGGTGGGCTGGATCCCACCTAAGTCAATCTACTTGTCCT... | TTCCTGGCTTGCCCCCATCTCTGCCTCCTTACTCTACTTCCTGAGTCACCAGCCCATCAGCACTGAGCAAAGAGATACAAAACAGAGTTAATGTGGCACAGGTGGGAGGGAGAAAGGCCCTGAGGGAAGCAGGTAGAACAGCCACATAAAGAGCCCCACAGGCACTGATTAAAGCGAAGAGAAGCTGCCAACACACAGTGCTCGAGATCTTTCCCAGTCAAGCCTTCTGCTGGTGATTTCTTCCTCATTCATTTATCCATTCAACATGTATTAAGCTTCTTAGGTGGGCTGGATCCCACCTAAGTCAATCTACTTGTCCT... |
Task1_train_40823 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | ACTTCCTGAGTCACCAGCCCATCAGCACTGAGCAAAGAGATACAAAACAGAGTTAATGTGGCACAGGTGGGAGGGAGAAAGGCCCTGAGGGAAGCAGGTAGAACAGCCACATAAAGAGCCCCACAGGCACTGATTAAAGCGAAGAGAAGCTGCCAACACACAGTGCTCGAGATCTTTCCCAGTCAAGCCTTCTGCTGGTGATTTCTTCCTCATTCATTTATCCATTCAACATGTATTAAGCTTCTTAGGTGGGCTGGATCCCACCTAAGTCAATCTACTTGTCCTGCCTCCTCCAATGTCAGAGATGCTTCTTCCTCAGA... | ACTTCCTGAGTCACCAGCCCATCAGCACTGAGCAAAGAGATACAAAACAGAGTTAATGTGGCACAGGTGGGAGGGAGAAAGGCCCTGAGGGAAGCAGGTAGAACAGCCACATAAAGAGCCCCACAGGCACTGATTAAAGCGAAGAGAAGCTGCCAACACACAGTGCTCGAGATCTTTCCCAGTCAAGCCTTCTGCTGGTGATTTCTTCCTCATTCATTTATCCATTCAACATGTATTAAGCTTCTTAGGTGGGCTGGATCCCACCTAAGTCAATCTACTTGTCCTGCCTCCTCCAATGTCAGAGATGCTTCTTCCTCAGA... |
Task1_train_40824 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TCTCTTTTTCTTGAGACTCTGTGGAGTGCAGTGGTGCCATCTCGGCTCACTGCAACCTCCGCTTCCCAGGTTCAAGCAATTCTCCTGCCTCAGTATCATGAGTAGCTGGGATTACAGGCGTGTGCCACCACACCCAGCTAATTTTTCTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGTCAGGATGGTCTCCAACTCCTGACCTCAGGTGATCCACCTGTCTCGGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCAGGGTGCACAGCCGAGGATTCTTTTTTCCCTACCTCCTGAGTGACTAAGTTCTACTAAT... | TCTCTTTTTCTTGAGACTCTGTGGAGTGCAGTGGTGCCATCTCGGCTCACTGCAACCTCCGCTTCCCAGGTTCAAGCAATTCTCCTGCCTCAGTATCATGAGTAGCTGGGATTACAGGCGTGTGCCACCACACCCAGCTAATTTTTCTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGTCAGGATGGTCTCCAACTCCTGACCTCAGGTGATCCACCTGTCTCGGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCAGGGTGCACAGCCGAGGATTCTTTTTTCCCTACCTCCTGAGTGACTAAGTTCTACTAAT... |
Task1_train_40825 | This is a variant located on Chromosome 11. Is this mutation a likely cause of disease or not? | Benign | TTGTTATTTTGGGTTTTGTTTGAGACAGAGTCTCACTCTGTTGTGCAGGCTGGAGTGCAGTGGCACTATCATAGCTCATTGCAGCCTTGAACTCCTGGGTTCAAGCAATCTTTCTGCCTCAAACTCCTGAGTAGCTATGACTATAGGCACGTATCACCACACCCAGCTAATTTTTTATGTTTTGTAGAGACGGGACTTTGCTATGTTGCTCAGGCTGATCTCAAGCTCCTGGCCTCAGGTGATCCTCCCGCCTTGGCCTCTCAAAGTGCTGGGATTACAAAGATAAGCCACTGCACTCAGCTGTTCATTACAATCTTATG... | TTGTTATTTTGGGTTTTGTTTGAGACAGAGTCTCACTCTGTTGTGCAGGCTGGAGTGCAGTGGCACTATCATAGCTCATTGCAGCCTTGAACTCCTGGGTTCAAGCAATCTTTCTGCCTCAAACTCCTGAGTAGCTATGACTATAGGCACGTATCACCACACCCAGCTAATTTTTTATGTTTTGTAGAGACGGGACTTTGCTATGTTGCTCAGGCTGATCTCAAGCTCCTGGCCTCAGGTGATCCTCCCGCCTTGGCCTCTCAAAGTGCTGGGATTACAAAGATAAGCCACTGCACTCAGCTGTTCATTACAATCTTATG... |
Task1_train_40826 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TTCCCCATTTGCTCTCAAAATAACTTACATGTAACCATCATTCATTACAATTGGTGATGGTATCTCCCTCTAAATCCCGAGCTCCCCAAGGTGTTCATGAGACCTAGCATAGGGCCTGGAACAAAGTAGGTATTAAAAACGTTGTTATATGATAGTGACTGAATGAAGGAGTAGGTGACTGTGCTCCTCATCCTTAACCACCACTCCCACTTCCAGTTTTTTGTTTTTCCTTTTTTTTTTTTTTTGAAACATGGTCTCATTCTGTCACCCAGGCTGGAGGGCGGTGGCATGATCTTGGCTTACTGCAACCCCTGCCTCCT... | TTCCCCATTTGCTCTCAAAATAACTTACATGTAACCATCATTCATTACAATTGGTGATGGTATCTCCCTCTAAATCCCGAGCTCCCCAAGGTGTTCATGAGACCTAGCATAGGGCCTGGAACAAAGTAGGTATTAAAAACGTTGTTATATGATAGTGACTGAATGAAGGAGTAGGTGACTGTGCTCCTCATCCTTAACCACCACTCCCACTTCCAGTTTTTTGTTTTTCCTTTTTTTTTTTTTTTGAAACATGGTCTCATTCTGTCACCCAGGCTGGAGGGCGGTGGCATGATCTTGGCTTACTGCAACCCCTGCCTCCT... |
Task1_train_40827 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GATCTTGGCTTACTGCAACCCCTGCCTCCTGAGCTCAAGTGATCCTCCCACCTCAGCCCCCCAAGTAGCTGGGACTACAGGCACAAGCCACCACATCCAGCTAATTTTTGTAATTTTTGTAGAAATGGGGTTTCATCATTTTGCCAAGGCTGGATTTGAGCTCCCAAGGTCAAGTCCTCCACCCACCTTGGCCTCCCAAAGTGCTAAGATTACAGGCATGAGCCACCGTGCCCAGCCCCTTCTGTAATATTCTTGCTTTACTGCAGCAGGGAACTCTCCTCAGCCCCTCAAGAAGGTCTACCGTGTGCCAGACACAGTAT... | GATCTTGGCTTACTGCAACCCCTGCCTCCTGAGCTCAAGTGATCCTCCCACCTCAGCCCCCCAAGTAGCTGGGACTACAGGCACAAGCCACCACATCCAGCTAATTTTTGTAATTTTTGTAGAAATGGGGTTTCATCATTTTGCCAAGGCTGGATTTGAGCTCCCAAGGTCAAGTCCTCCACCCACCTTGGCCTCCCAAAGTGCTAAGATTACAGGCATGAGCCACCGTGCCCAGCCCCTTCTGTAATATTCTTGCTTTACTGCAGCAGGGAACTCTCCTCAGCCCCTCAAGAAGGTCTACCGTGTGCCAGACACAGTAT... |
Task1_train_40828 | 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 | TGTTCAATAAATAGCTGTTGAACGAAATGGAATTTAAAAGGTAGAAGATACTTGCTACTTTTGAAGCACTTTTCAACTGTGGCTCAAGACAGTGGTATGGGGTGTACGCAGCTGGTAGGGGAGGCCTAGGCATGAATGTCAACCGAAAAGTACCCTGAGTAAAAAGAGGGCCAAGAAAGGAATCCTGGAAAACTCAACTTTTAGGAGGTGCCAAGGAAAGAAAAGACTAAGAGGAAAACCATTAGTTGACACTGAGTAAGCACCTACAGCAAGGACTATACTGGATGCTAAAAAAAAAAACACACACACACACTCACACA... | TGTTCAATAAATAGCTGTTGAACGAAATGGAATTTAAAAGGTAGAAGATACTTGCTACTTTTGAAGCACTTTTCAACTGTGGCTCAAGACAGTGGTATGGGGTGTACGCAGCTGGTAGGGGAGGCCTAGGCATGAATGTCAACCGAAAAGTACCCTGAGTAAAAAGAGGGCCAAGAAAGGAATCCTGGAAAACTCAACTTTTAGGAGGTGCCAAGGAAAGAAAAGACTAAGAGGAAAACCATTAGTTGACACTGAGTAAGCACCTACAGCAAGGACTATACTGGATGCTAAAAAAAAAAACACACACACACACTCACACA... |
Task1_train_40829 | 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 | GTTAGGAGCCTGCTTTTGGACATTTTAAGTTTGAGATACCTATAAGCTCTCCAGGTGGAGACATTAAGTAGGCAGTTGGATATACTAATCTGATTTCAGAGGAGAGGTGGGCTGAATTTCTTTTTTTATTTTAATCATCAACTTTTTTTTTTTTTTTTTTTTTTTTGAGATAGAGTCTCCCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTCTGCTCACTGCAAGCTCCGCCTCCTGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCCAGTAGCTGGGACTACAGGCGCCCACCGCCACGCTCGGCTAATTTTT... | GTTAGGAGCCTGCTTTTGGACATTTTAAGTTTGAGATACCTATAAGCTCTCCAGGTGGAGACATTAAGTAGGCAGTTGGATATACTAATCTGATTTCAGAGGAGAGGTGGGCTGAATTTCTTTTTTTATTTTAATCATCAACTTTTTTTTTTTTTTTTTTTTTTTTGAGATAGAGTCTCCCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTCTGCTCACTGCAAGCTCCGCCTCCTGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCCAGTAGCTGGGACTACAGGCGCCCACCGCCACGCTCGGCTAATTTTT... |
Task1_train_40830 | Assess the clinical impact of this variant found on Chromosome 11. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | ATAGATGTTGAGCTCCTTGAGATCAAGGATTTTGTTTTATTCGGGCTTCTTTTGGGGAGGTGGGATAGGGTAGATGGATACGTTGGGGGTGGGGATGGGGGAGTACCAAAGACATACCAAAGACCTGGCACTAGTTTAGATACTCAGCGAATGGATATAAACACCTGCTTACGACACCCTCTGGATTGCTAGTCTCCCGAGTCAACCGTACTGCACGTGCAGTTCAGACCCCGCCTGGTCCTCTACAGGTCCCTGTCCCAGGCAAGCCTTAGCCCACAGGTTGAACCTAGTTCTGCCCCTCCAGGCTTGGGCTCTGCCCT... | ATAGATGTTGAGCTCCTTGAGATCAAGGATTTTGTTTTATTCGGGCTTCTTTTGGGGAGGTGGGATAGGGTAGATGGATACGTTGGGGGTGGGGATGGGGGAGTACCAAAGACATACCAAAGACCTGGCACTAGTTTAGATACTCAGCGAATGGATATAAACACCTGCTTACGACACCCTCTGGATTGCTAGTCTCCCGAGTCAACCGTACTGCACGTGCAGTTCAGACCCCGCCTGGTCCTCTACAGGTCCCTGTCCCAGGCAAGCCTTAGCCCACAGGTTGAACCTAGTTCTGCCCCTCCAGGCTTGGGCTCTGCCCT... |
Task1_train_40831 | This is a variant located on Chromosome 11. Is this mutation a likely cause of disease or not? | Benign | CAGAAGTGAATGAGACAGACTCAATCCCTTCACTTGAGGTATTACAGTTTAGTTAGGGAGATATAGTTAAGTTGATAACAAGTAAAATATAATTACAAATTGTAATAAGTGCTATAAAACAAAAGAATACTGTCTTTTGCCTGGCTGCTTCTCTGCAGGTGGGAGAGAGAGAGAGAGGGAGTGTAGTTAGGGGGAAAGCATGTGGGGGGAGTGTTCAAGTCTAGATTAGATTAACAAAAACATCAAACAGAGTTTCAAGGAGGAGGGAGCAGTCAGTAGTATTACATGTTAAATGAGACAAGTAAGAAGAATGAAAATGT... | CAGAAGTGAATGAGACAGACTCAATCCCTTCACTTGAGGTATTACAGTTTAGTTAGGGAGATATAGTTAAGTTGATAACAAGTAAAATATAATTACAAATTGTAATAAGTGCTATAAAACAAAAGAATACTGTCTTTTGCCTGGCTGCTTCTCTGCAGGTGGGAGAGAGAGAGAGAGGGAGTGTAGTTAGGGGGAAAGCATGTGGGGGGAGTGTTCAAGTCTAGATTAGATTAACAAAAACATCAAACAGAGTTTCAAGGAGGAGGGAGCAGTCAGTAGTATTACATGTTAAATGAGACAAGTAAGAAGAATGAAAATGT... |
Task1_train_40832 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | TTGTTTTAAGGGAGAATCTGTGGATGGAAAATTTTCTGAGTCTTTGTATATCTAAAAATGTTTTTATTTATCCTCAAACTTTAATGATATTCTGGCTAGGTATAGAATTCCAAGTTTTTTATTGTTATCATTACTTTTGAGACAGAATCTCACTCTGTTGCCCATGCAGTGGCATGATCAGGGATCACTGCAGCCTCAACTTCCCGGGCTCAGGTGATCCTCCCACCTCAGCCTCCCGAGTAGCTGGGACTACAGCAGTTGATACCGCCACGCCTGGCTAATTTTTTGTATTTTTTGCAGAGATCGGGTTTCACCATGTT... | TTGTTTTAAGGGAGAATCTGTGGATGGAAAATTTTCTGAGTCTTTGTATATCTAAAAATGTTTTTATTTATCCTCAAACTTTAATGATATTCTGGCTAGGTATAGAATTCCAAGTTTTTTATTGTTATCATTACTTTTGAGACAGAATCTCACTCTGTTGCCCATGCAGTGGCATGATCAGGGATCACTGCAGCCTCAACTTCCCGGGCTCAGGTGATCCTCCCACCTCAGCCTCCCGAGTAGCTGGGACTACAGCAGTTGATACCGCCACGCCTGGCTAATTTTTTGTATTTTTTGCAGAGATCGGGTTTCACCATGTT... |
Task1_train_40833 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GCTCATAGAAAACTGGAAATTTTAGCTTTTCTTAACTTTCAAAAGAAGACTTGGTTCAAAATAGTTCTCTAACCTCTAAGTTTCACTTTCTATTGTTTTTCTGTATTAAAAAAAGATGGCTTACTTTCTGAGGTTTTCTGGTTTCCCTCCCCTACCTTCATCTAGACTTTTCCTTTTTCTCTATTGCTGCTCAATCCTTATTCTACTCCCAGCATTTTCTCCATGACGAGCTCTGTCCCAAAAGGGAGCCCTGACTGTTTGGTTTCAAGAGTACACAGGGCATAGATTACTTAAGCTTCTATAGACCTTACCTCACCTGT... | GCTCATAGAAAACTGGAAATTTTAGCTTTTCTTAACTTTCAAAAGAAGACTTGGTTCAAAATAGTTCTCTAACCTCTAAGTTTCACTTTCTATTGTTTTTCTGTATTAAAAAAAGATGGCTTACTTTCTGAGGTTTTCTGGTTTCCCTCCCCTACCTTCATCTAGACTTTTCCTTTTTCTCTATTGCTGCTCAATCCTTATTCTACTCCCAGCATTTTCTCCATGACGAGCTCTGTCCCAAAAGGGAGCCCTGACTGTTTGGTTTCAAGAGTACACAGGGCATAGATTACTTAAGCTTCTATAGACCTTACCTCACCTGT... |
Task1_train_40834 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | TTCTCCATGACGAGCTCTGTCCCAAAAGGGAGCCCTGACTGTTTGGTTTCAAGAGTACACAGGGCATAGATTACTTAAGCTTCTATAGACCTTACCTCACCTGTTCTTGGAGGGGGTAAGACCCCCTTCCAGTTTTACCTGCTGTTCTGAAATGGGCCCTCTGCCTCCCAGTAAATGCTTGATGACTGTTTGGGGGTTTTCTTATTCTTAGGTCCATCTGTTGCTTCATTGTTTCCCTCTGCATCATTCATCACAAATGGTGATGCCATGTGTGTTTTGAGGTTGCAGATGGTTTGACCCCACCTACTTGTATTTTAGGA... | TTCTCCATGACGAGCTCTGTCCCAAAAGGGAGCCCTGACTGTTTGGTTTCAAGAGTACACAGGGCATAGATTACTTAAGCTTCTATAGACCTTACCTCACCTGTTCTTGGAGGGGGTAAGACCCCCTTCCAGTTTTACCTGCTGTTCTGAAATGGGCCCTCTGCCTCCCAGTAAATGCTTGATGACTGTTTGGGGGTTTTCTTATTCTTAGGTCCATCTGTTGCTTCATTGTTTCCCTCTGCATCATTCATCACAAATGGTGATGCCATGTGTGTTTTGAGGTTGCAGATGGTTTGACCCCACCTACTTGTATTTTAGGA... |
Task1_train_40835 | A mutation has occurred on Chromosome 11. What is the medical relevance of this mutation? | Benign | GGCTTCCTCTCAGCAGGTTTTCTTATTATCAGGTCTTAGTACCCAGTCATCTTGGTTACTTCCTCCAAGTCTCTGAAAGTGACATACCCAGTATGTCTCAATTATCTGTCCCCCAAACTCACTATTTTACTTACTAGTTGCAGAGATGCTAATAGAGGATCGGTCAGTTTACTTTGCACATAACATAAAAAATATTTTTAAATACTTTTTATAAACATATATTTTTATGTTTACATTTATATTTATAACATAAACATGTTTATATTTAAAATATAATGAAGTGGAGCCATGCTGCCTGAGTCTGAATCCTTGCTCTGCCA... | GGCTTCCTCTCAGCAGGTTTTCTTATTATCAGGTCTTAGTACCCAGTCATCTTGGTTACTTCCTCCAAGTCTCTGAAAGTGACATACCCAGTATGTCTCAATTATCTGTCCCCCAAACTCACTATTTTACTTACTAGTTGCAGAGATGCTAATAGAGGATCGGTCAGTTTACTTTGCACATAACATAAAAAATATTTTTAAATACTTTTTATAAACATATATTTTTATGTTTACATTTATATTTATAACATAAACATGTTTATATTTAAAATATAATGAAGTGGAGCCATGCTGCCTGAGTCTGAATCCTTGCTCTGCCA... |
Task1_train_40836 | 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 | TTAAAGTACTTGAAATAGTGTCTGGTATGTAGAAAGCACTCTATACTCTATTTGGTGTACCATATTTCTATATTGTATTTTTCCTATTCTGTGCATATTTTAACATCTCTGAACTTTAAAGGTGTCTCATGATTGAAGATGTGTTAGAGTTTAGATGGCATCAGTTTTTTTTCTTTGTTAGTGGTATATAAAATAATGGTGCTTCTTACAACGGGATCTTAGATTTTATGAGGTATCATATGGGTGTTATCCCTGCCCTCTGAGATAATAAAGTTGTTCATACTGCCAAGGGCAGCTTCCAGGATTACTTTCTAGCCCCT... | TTAAAGTACTTGAAATAGTGTCTGGTATGTAGAAAGCACTCTATACTCTATTTGGTGTACCATATTTCTATATTGTATTTTTCCTATTCTGTGCATATTTTAACATCTCTGAACTTTAAAGGTGTCTCATGATTGAAGATGTGTTAGAGTTTAGATGGCATCAGTTTTTTTTCTTTGTTAGTGGTATATAAAATAATGGTGCTTCTTACAACGGGATCTTAGATTTTATGAGGTATCATATGGGTGTTATCCCTGCCCTCTGAGATAATAAAGTTGTTCATACTGCCAAGGGCAGCTTCCAGGATTACTTTCTAGCCCCT... |
Task1_train_40837 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | AGCAGGATCGGTGGAGCTGGAGGGCATCATCATGAGTCTGGAGAGCGTGCTCTATGGGGTGTGTGCTCACTTCCCCCGCCTCTTCTTCCTTAGTGACAGTGAGCTGGTAGCCCTGCTGGCTGCTCGACTGGAATCATGCGAAGCCCAGCTATGGGTACGACGCTGCTTTCCTCATGTGCATGCTGTGAGCTTCAGGTCTTGCCCAACTGGTGAGAAAAACACAGATGACTGGGAGTCAAGCCCAAACACACAGACTCAGGTGGAGGCACTTGCAGTGCTAGGGGCAGGTGGGGAGGAGGTGAAGCTGCAGGGTCCCCTTC... | AGCAGGATCGGTGGAGCTGGAGGGCATCATCATGAGTCTGGAGAGCGTGCTCTATGGGGTGTGTGCTCACTTCCCCCGCCTCTTCTTCCTTAGTGACAGTGAGCTGGTAGCCCTGCTGGCTGCTCGACTGGAATCATGCGAAGCCCAGCTATGGGTACGACGCTGCTTTCCTCATGTGCATGCTGTGAGCTTCAGGTCTTGCCCAACTGGTGAGAAAAACACAGATGACTGGGAGTCAAGCCCAAACACACAGACTCAGGTGGAGGCACTTGCAGTGCTAGGGGCAGGTGGGGAGGAGGTGAAGCTGCAGGGTCCCCTTC... |
Task1_train_40838 | A mutation on Chromosome 11 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GCCTCTTCTTCCTTAGTGACAGTGAGCTGGTAGCCCTGCTGGCTGCTCGACTGGAATCATGCGAAGCCCAGCTATGGGTACGACGCTGCTTTCCTCATGTGCATGCTGTGAGCTTCAGGTCTTGCCCAACTGGTGAGAAAAACACAGATGACTGGGAGTCAAGCCCAAACACACAGACTCAGGTGGAGGCACTTGCAGTGCTAGGGGCAGGTGGGGAGGAGGTGAAGCTGCAGGGTCCCCTTCCTCTGCATCCAGATCTCCCTAAGTGGCTGGCCTCTCTGGAGAAGTGTCTGCGCTTGGCACTGGTGCACATGCTGCAG... | GCCTCTTCTTCCTTAGTGACAGTGAGCTGGTAGCCCTGCTGGCTGCTCGACTGGAATCATGCGAAGCCCAGCTATGGGTACGACGCTGCTTTCCTCATGTGCATGCTGTGAGCTTCAGGTCTTGCCCAACTGGTGAGAAAAACACAGATGACTGGGAGTCAAGCCCAAACACACAGACTCAGGTGGAGGCACTTGCAGTGCTAGGGGCAGGTGGGGAGGAGGTGAAGCTGCAGGGTCCCCTTCCTCTGCATCCAGATCTCCCTAAGTGGCTGGCCTCTCTGGAGAAGTGTCTGCGCTTGGCACTGGTGCACATGCTGCAG... |
Task1_train_40839 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | GGAACCGAAGTGCCAGAAGCCTCGCAGCCTAGCTGCCATTGAGGAGGCTGCCCTACTGCGCTCACCACTGTTTAGCATTCTCAATGGGCTCCACCTGCACAACCTCCGAGGGCTGTTGTGTGCGCTTTTCCCTAGCGCCAGCCAAGTGCTGGCAGAACCTATGACTTACAAGCTGATGAAGCCATTGGTGGTGGAGGAACTGCAACAGGTAGGTCTGGATCCCAGCCCTGACATTTTGGGGTCCTTGGAACAGTTGAGCCAGGCCCTGAGCCGGGCCTCAGGCATTCTGCTCCTGGGCCCTGCGGGCAGCGGCAAGACCA... | GGAACCGAAGTGCCAGAAGCCTCGCAGCCTAGCTGCCATTGAGGAGGCTGCCCTACTGCGCTCACCACTGTTTAGCATTCTCAATGGGCTCCACCTGCACAACCTCCGAGGGCTGTTGTGTGCGCTTTTCCCTAGCGCCAGCCAAGTGCTGGCAGAACCTATGACTTACAAGCTGATGAAGCCATTGGTGGTGGAGGAACTGCAACAGGTAGGTCTGGATCCCAGCCCTGACATTTTGGGGTCCTTGGAACAGTTGAGCCAGGCCCTGAGCCGGGCCTCAGGCATTCTGCTCCTGGGCCCTGCGGGCAGCGGCAAGACCA... |
Task1_train_40840 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | TCAGCTCCCCTTTATTTCCTGTTAGGGCAGGGTTGTTGGCTGCTCTGGTACTAGAACACCAGTTTAACTGGGGGCTCTCAGAAAAATACTACTCAGGAATAAAATGGAACAAACTAAGGAAACACGCAAAAACATGGATGAGTCTCAAAAACCTGCTGAGTAAAAGAAGATAGACATGATCAAGTACATACCGTATGATTCTATTTATATGAGGTTCTAGAACAGACAAAGCTAACCTATAGTGATGGAAATCCGATCAAATAACAATGCCTGTGATGGTGGTGGCAGAGGGATTGATTGGCTTTAAAGGAGCATGAGGA... | TCAGCTCCCCTTTATTTCCTGTTAGGGCAGGGTTGTTGGCTGCTCTGGTACTAGAACACCAGTTTAACTGGGGGCTCTCAGAAAAATACTACTCAGGAATAAAATGGAACAAACTAAGGAAACACGCAAAAACATGGATGAGTCTCAAAAACCTGCTGAGTAAAAGAAGATAGACATGATCAAGTACATACCGTATGATTCTATTTATATGAGGTTCTAGAACAGACAAAGCTAACCTATAGTGATGGAAATCCGATCAAATAACAATGCCTGTGATGGTGGTGGCAGAGGGATTGATTGGCTTTAAAGGAGCATGAGGA... |
Task1_train_40841 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | GCCTGAAAGTTAGGTCAGATCTGATCAGTGTTTGAAAGGGGCCAAGTGACAGAATGTCCCAGGTTGATATAACAGCATGTGAAAGGCCTAGAGGCAAAAGAGTGTGTGCCACATTGGAGGAACTGAAAGTCAGGAATGGCTGGAAAGTAGCGTGCTAGGAGAGAGAAAAGAGATGAGATTGAAATGATGAGTAGGGGCCTGGTCATGGGGGTATTGTCAATCAAATGTAGAAGTGACAAGTGTTAATGACAATGATTCAGTTTTTAGAAAACCAGCCAGGCTGCAGTGGGGGAATAAAAGGAGGGAAGTAAGAGTGGAAA... | GCCTGAAAGTTAGGTCAGATCTGATCAGTGTTTGAAAGGGGCCAAGTGACAGAATGTCCCAGGTTGATATAACAGCATGTGAAAGGCCTAGAGGCAAAAGAGTGTGTGCCACATTGGAGGAACTGAAAGTCAGGAATGGCTGGAAAGTAGCGTGCTAGGAGAGAGAAAAGAGATGAGATTGAAATGATGAGTAGGGGCCTGGTCATGGGGGTATTGTCAATCAAATGTAGAAGTGACAAGTGTTAATGACAATGATTCAGTTTTTAGAAAACCAGCCAGGCTGCAGTGGGGGAATAAAAGGAGGGAAGTAAGAGTGGAAA... |
Task1_train_40842 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | AATTTGGTCACATTTATTTTTTCTCTTTATTACAATGATTCTGAATCTACATGACTGATTGGTCCATGATCTTCCACTTCCCTGGTCTACTCAGCACTACCCAAATTTATCCAATGTTCAGAAATCCTGGGGAATATTTCTGTTGGCTCTGTTTGGATCGGGGACCCATCTGGGTGGAGTATTGGAAGGAACATTTTCTAGGAAAAGGAATAGAGTGTTTATTCCCCAGAAGAAGAGGCTGGGGATTGAGTTTGTGAGAAAAATGTGACCTTATTTGGAAAGGGGTCCTTTCAGATGTAATTAAGTTAAGGACTTTGAAT... | AATTTGGTCACATTTATTTTTTCTCTTTATTACAATGATTCTGAATCTACATGACTGATTGGTCCATGATCTTCCACTTCCCTGGTCTACTCAGCACTACCCAAATTTATCCAATGTTCAGAAATCCTGGGGAATATTTCTGTTGGCTCTGTTTGGATCGGGGACCCATCTGGGTGGAGTATTGGAAGGAACATTTTCTAGGAAAAGGAATAGAGTGTTTATTCCCCAGAAGAAGAGGCTGGGGATTGAGTTTGTGAGAAAAATGTGACCTTATTTGGAAAGGGGTCCTTTCAGATGTAATTAAGTTAAGGACTTTGAAT... |
Task1_train_40843 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | TCCAACAGGAACAACCCAGGCCCAGGTGTAGGTGGATCCATGGGTGTCAATACCTGGTAGAGGCTCTGTGAGAAGGCAGGTGCATTGTCATTGACATCCTCCACAAGCACTGTGAGGTTGGCACGGCCCTCATGAGGCCCATCATGTGCCAGCAGCTGCAGCTGGTAGCGGTCACACTGCTCAAAGTCCAGGGGCCCCGTGAGGGAGACACGGCCTCCATAGCGGCCAACACTGAAGGGATCCTGGGGCCCAGATGGGCTTAGCACATACCACAGCACGGGTCCTGAGTCCACATCATTCCCTGTTACCTGTGCAATCTC... | TCCAACAGGAACAACCCAGGCCCAGGTGTAGGTGGATCCATGGGTGTCAATACCTGGTAGAGGCTCTGTGAGAAGGCAGGTGCATTGTCATTGACATCCTCCACAAGCACTGTGAGGTTGGCACGGCCCTCATGAGGCCCATCATGTGCCAGCAGCTGCAGCTGGTAGCGGTCACACTGCTCAAAGTCCAGGGGCCCCGTGAGGGAGACACGGCCTCCATAGCGGCCAACACTGAAGGGATCCTGGGGCCCAGATGGGCTTAGCACATACCACAGCACGGGTCCTGAGTCCACATCATTCCCTGTTACCTGTGCAATCTC... |
Task1_train_40844 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TTGTTTTAATGTTTAAAAACACATTCACATATCTGCAAGTCCACATTTTAAAAAACTTAGACAATATTCCCAACAAATTTCTCTCATTGTTATTGTACTCACTTTAAAACTGGTACTTTCAATTCTATTTTATTCATTCTTTATTTTAGTTTTAATTTTAGGCAATGTAAAAATGCCCATTTTCAAAAAGACTGTCAAAATTTCCAAGTAGAAATATCTTTCTTTATCCTTTTCCATTCTTTCTTTCTATTTATTTATTTATTTATTGAAACGGAGTCTCTCTCTGTTGCTCAGGCTGGAGTGCAGTGGCGCGATCTCAG... | TTGTTTTAATGTTTAAAAACACATTCACATATCTGCAAGTCCACATTTTAAAAAACTTAGACAATATTCCCAACAAATTTCTCTCATTGTTATTGTACTCACTTTAAAACTGGTACTTTCAATTCTATTTTATTCATTCTTTATTTTAGTTTTAATTTTAGGCAATGTAAAAATGCCCATTTTCAAAAAGACTGTCAAAATTTCCAAGTAGAAATATCTTTCTTTATCCTTTTCCATTCTTTCTTTCTATTTATTTATTTATTTATTGAAACGGAGTCTCTCTCTGTTGCTCAGGCTGGAGTGCAGTGGCGCGATCTCAG... |
Task1_train_40845 | A mutation has occurred on Chromosome 11. What is the medical relevance of this mutation? | Benign | TTATCTAGCCAGCATTTTAGTCATATTCCTTCTAGTCTTGTTTAAACAAGCAAATATGGCTGATATTTTTGATACTGTTATATAACATAATATTTTTATTAAGTTAGAAATATTTTTTCTTTCATTAACTCTATTTAGATCACTTTATTTCAATTTCTGCATAGTTTTCCATGTAACATATGAGCTACAATTTATTTGACCAGTGCCCTGTTTGCGAAAGTTGAGCATATTTTGCTTATTTCCTTTCCTTGTTTCTGTATTTATAAGTAAAAGTGTCTATCTGCACAAATCTTTCCGAATCAGAATGGTTGCAATATTTT... | TTATCTAGCCAGCATTTTAGTCATATTCCTTCTAGTCTTGTTTAAACAAGCAAATATGGCTGATATTTTTGATACTGTTATATAACATAATATTTTTATTAAGTTAGAAATATTTTTTCTTTCATTAACTCTATTTAGATCACTTTATTTCAATTTCTGCATAGTTTTCCATGTAACATATGAGCTACAATTTATTTGACCAGTGCCCTGTTTGCGAAAGTTGAGCATATTTTGCTTATTTCCTTTCCTTGTTTCTGTATTTATAAGTAAAAGTGTCTATCTGCACAAATCTTTCCGAATCAGAATGGTTGCAATATTTT... |
Task1_train_40846 | The following genetic variant occurs on Chromosome 11. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CAACCTCCCGAGCTCTGGTGATCCTCCCACCTCAGCCTCCTGAGTAGCTAGGACAACAGGCATATGCCACCACAACTGGATATTTTCTCCATTTTTTGTAGAGATGGGGTTTCGCCACCTTGCTGAGGCTGGTCTCAAACTCCTAGGCTCAAGTGATCCACCTGCCTCAGGCTCCCAAAGTCCTGGGATTACAGGCATCAGCCACCACGCCTGGCCTACAGTGAAAGAGTTTCTAGTTGAGATGATCTGTCTTTTCATCATTGGTTCTTTTATTATTTTTTAAACTTACATTTGTTTTTCTGAAACCGAGCTAAAAACTG... | CAACCTCCCGAGCTCTGGTGATCCTCCCACCTCAGCCTCCTGAGTAGCTAGGACAACAGGCATATGCCACCACAACTGGATATTTTCTCCATTTTTTGTAGAGATGGGGTTTCGCCACCTTGCTGAGGCTGGTCTCAAACTCCTAGGCTCAAGTGATCCACCTGCCTCAGGCTCCCAAAGTCCTGGGATTACAGGCATCAGCCACCACGCCTGGCCTACAGTGAAAGAGTTTCTAGTTGAGATGATCTGTCTTTTCATCATTGGTTCTTTTATTATTTTTTAAACTTACATTTGTTTTTCTGAAACCGAGCTAAAAACTG... |
Task1_train_40847 | 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 | TTATTTTTTAAACTTACATTTGTTTTTCTGAAACCGAGCTAAAAACTGTAGACATTGCTTCATTTAATGTTTAGCATTTCTGAGAAATCTTAGATCAGTTTGATTATAATTCTTTTATAAGAATGGTGTTTTTTCCTTCATAGATTCTCTGGAATTTTAAACATAACCTTGAAGTTCAAATTATTCACCAAGACCTGACTAATATTTAGCCTCTTTTAAATAAGTTGTCTGCTGCTTGAAAATGGATTGTGCGTAAAGACGGAGGGTAATTATAGATATACCACCTAGTCTTCTTGATCCGAGGCCTACAGCTTTTGATC... | TTATTTTTTAAACTTACATTTGTTTTTCTGAAACCGAGCTAAAAACTGTAGACATTGCTTCATTTAATGTTTAGCATTTCTGAGAAATCTTAGATCAGTTTGATTATAATTCTTTTATAAGAATGGTGTTTTTTCCTTCATAGATTCTCTGGAATTTTAAACATAACCTTGAAGTTCAAATTATTCACCAAGACCTGACTAATATTTAGCCTCTTTTAAATAAGTTGTCTGCTGCTTGAAAATGGATTGTGCGTAAAGACGGAGGGTAATTATAGATATACCACCTAGTCTTCTTGATCCGAGGCCTACAGCTTTTGATC... |
Task1_train_40848 | 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 | TAAGTTGTCTGCTGCTTGAAAATGGATTGTGCGTAAAGACGGAGGGTAATTATAGATATACCACCTAGTCTTCTTGATCCGAGGCCTACAGCTTTTGATCCCTTCTCTATCCCATTCTATCAACAATGTCAGAGTGATCCTTCTAAGTAGCATTATGACAATGTCACTCTGCAGCTTCAAATATTCAGGTGAATCTCCTCATCTATAAAATAAAGTCCAAAATTCTCAGCATGTAATATAAGTCTATTAATGTAATATATCCAAAACACTGACCATATCTTTGTTTATCTTTTACTTTGTGTCAGTTCTGGTTTTTACTG... | TAAGTTGTCTGCTGCTTGAAAATGGATTGTGCGTAAAGACGGAGGGTAATTATAGATATACCACCTAGTCTTCTTGATCCGAGGCCTACAGCTTTTGATCCCTTCTCTATCCCATTCTATCAACAATGTCAGAGTGATCCTTCTAAGTAGCATTATGACAATGTCACTCTGCAGCTTCAAATATTCAGGTGAATCTCCTCATCTATAAAATAAAGTCCAAAATTCTCAGCATGTAATATAAGTCTATTAATGTAATATATCCAAAACACTGACCATATCTTTGTTTATCTTTTACTTTGTGTCAGTTCTGGTTTTTACTG... |
Task1_train_40849 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | CCCTTCTCTATCCCATTCTATCAACAATGTCAGAGTGATCCTTCTAAGTAGCATTATGACAATGTCACTCTGCAGCTTCAAATATTCAGGTGAATCTCCTCATCTATAAAATAAAGTCCAAAATTCTCAGCATGTAATATAAGTCTATTAATGTAATATATCCAAAACACTGACCATATCTTTGTTTATCTTTTACTTTGTGTCAGTTCTGGTTTTTACTGTTCCTAATAAAGTTTTTAATTTTTATTATTAATTTTTTTTAACCAGAGTTTGCTAACCACATTCATTTCTTTTTTTATTTATCCCAGCCTCTCAATTTC... | CCCTTCTCTATCCCATTCTATCAACAATGTCAGAGTGATCCTTCTAAGTAGCATTATGACAATGTCACTCTGCAGCTTCAAATATTCAGGTGAATCTCCTCATCTATAAAATAAAGTCCAAAATTCTCAGCATGTAATATAAGTCTATTAATGTAATATATCCAAAACACTGACCATATCTTTGTTTATCTTTTACTTTGTGTCAGTTCTGGTTTTTACTGTTCCTAATAAAGTTTTTAATTTTTATTATTAATTTTTTTTAACCAGAGTTTGCTAACCACATTCATTTCTTTTTTTATTTATCCCAGCCTCTCAATTTC... |
Task1_train_40850 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TTAGTAGAGACAGGGTTTCTCTATGTTGGTCAGGCTGGTCTTGAACTCCCGATCTCAGGTGATCAGCCAGCCTCCACCTCCCAAAGAGCTGTGATTACAGGCGTGAGCCTCCGTGCCTGGCTTAACAGAATTTGTTTATAACCTGTCTTCCCTATGATGAGTTTTATGAGGGCAGAGATTTTTGCTTGTTTTATTTACTAATGTATTATCTTCAGTATCTAAAACAGAGCATAGCATACAGAATTATCTTCTGATAATCAATATTTACTGAATTAATTATTTTATTTTAGAGATTGAATAGTAGGGGCTATAGTGAGTTT... | TTAGTAGAGACAGGGTTTCTCTATGTTGGTCAGGCTGGTCTTGAACTCCCGATCTCAGGTGATCAGCCAGCCTCCACCTCCCAAAGAGCTGTGATTACAGGCGTGAGCCTCCGTGCCTGGCTTAACAGAATTTGTTTATAACCTGTCTTCCCTATGATGAGTTTTATGAGGGCAGAGATTTTTGCTTGTTTTATTTACTAATGTATTATCTTCAGTATCTAAAACAGAGCATAGCATACAGAATTATCTTCTGATAATCAATATTTACTGAATTAATTATTTTATTTTAGAGATTGAATAGTAGGGGCTATAGTGAGTTT... |
Task1_train_40851 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | CTTGTTCCCTGGCTTCTAATTGGAATACAATAGTGGGGGATCAGAAGGTGGGTGGAAAATGGGCTTGAGAAATATTTCTTCTCATGGCTTCCTTGCCTTCACATAGCCTAAGTCCACAGTTACTGCCTTGTGCCCTTAGCATATTTCTACCCTCTCCAGGTTCTAGTTCCCTCCTCTTGGTCATTCAGGCTTAGCGTTAGTTACAGCTTCTCACTCTTGCTATGTGTCACTATTCTTGGAATATGTCACTATTTCTTGCTGGTTTCCACAACTCCTATATTCATCTTTATGAAGATGTATCCTGATAAATATGATCCTTA... | CTTGTTCCCTGGCTTCTAATTGGAATACAATAGTGGGGGATCAGAAGGTGGGTGGAAAATGGGCTTGAGAAATATTTCTTCTCATGGCTTCCTTGCCTTCACATAGCCTAAGTCCACAGTTACTGCCTTGTGCCCTTAGCATATTTCTACCCTCTCCAGGTTCTAGTTCCCTCCTCTTGGTCATTCAGGCTTAGCGTTAGTTACAGCTTCTCACTCTTGCTATGTGTCACTATTCTTGGAATATGTCACTATTTCTTGCTGGTTTCCACAACTCCTATATTCATCTTTATGAAGATGTATCCTGATAAATATGATCCTTA... |
Task1_train_40852 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CAGTTACTGCCTTGTGCCCTTAGCATATTTCTACCCTCTCCAGGTTCTAGTTCCCTCCTCTTGGTCATTCAGGCTTAGCGTTAGTTACAGCTTCTCACTCTTGCTATGTGTCACTATTCTTGGAATATGTCACTATTTCTTGCTGGTTTCCACAACTCCTATATTCATCTTTATGAAGATGTATCCTGATAAATATGATCCTTATGTTTCTAAAAGAGTGTGAGAAGGAGAGCAGAGCTCATATATTCTGCTTCATTGTACCCATGCTCTTCATTACCCATGTTAAGCACACATACAGGTGCACATGCCAACATACATGT... | CAGTTACTGCCTTGTGCCCTTAGCATATTTCTACCCTCTCCAGGTTCTAGTTCCCTCCTCTTGGTCATTCAGGCTTAGCGTTAGTTACAGCTTCTCACTCTTGCTATGTGTCACTATTCTTGGAATATGTCACTATTTCTTGCTGGTTTCCACAACTCCTATATTCATCTTTATGAAGATGTATCCTGATAAATATGATCCTTATGTTTCTAAAAGAGTGTGAGAAGGAGAGCAGAGCTCATATATTCTGCTTCATTGTACCCATGCTCTTCATTACCCATGTTAAGCACACATACAGGTGCACATGCCAACATACATGT... |
Task1_train_40853 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | TGTTTTAATTATTGAGTTATAATAATATTGAATATTTTTCTTATATTTAGTAGCTATTTGTATTTCTTCTTTTAAATAGTCTGTTCATATCTTTGGCCCATTATTTCTTGGACTTCACAATTTTCATATAGCTTTCTACAAACTCTTAATGTAATCAGGTCATTTAATTTGACTTCTTTTCCTATTTGGATGCCTTTCATTTTTTTCTCTTCTAGTACTATATTGAATATGAGTGGTAAGAGTGGGTATCCTTGTCTTGTTCCAGTTCTCAGTCAGAATGGTTCCAGCTTTTGCCCATTCAGTAAGATGTTGGCTGTGGG... | TGTTTTAATTATTGAGTTATAATAATATTGAATATTTTTCTTATATTTAGTAGCTATTTGTATTTCTTCTTTTAAATAGTCTGTTCATATCTTTGGCCCATTATTTCTTGGACTTCACAATTTTCATATAGCTTTCTACAAACTCTTAATGTAATCAGGTCATTTAATTTGACTTCTTTTCCTATTTGGATGCCTTTCATTTTTTTCTCTTCTAGTACTATATTGAATATGAGTGGTAAGAGTGGGTATCCTTGTCTTGTTCCAGTTCTCAGTCAGAATGGTTCCAGCTTTTGCCCATTCAGTAAGATGTTGGCTGTGGG... |
Task1_train_40854 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CTTGTCTTGTTCCAGTTCTCAGTCAGAATGGTTCCAGCTTTTGCCCATTCAGTAAGATGTTGGCTGTGGGTCTGTTACTGATATACCATCTTTCACCAATCAGAATGGCTTTCATCAAAAAGTCAAGAAATAACATATGATGGTGAGGCTGCAGAAAAAAGGGAACACTAATACGCTGTTAGTAGAAGGTAAATTAGTGCAGCCACTGTGGAGAGCAGTTTAGGGACTTCTCAAGGAACTAAGAATTAAAGTAATATTTGATCCAACAATCCCACTGCTGTATATACACCCAAAGGAAAATAAATCATTCCACCAAAAAG... | CTTGTCTTGTTCCAGTTCTCAGTCAGAATGGTTCCAGCTTTTGCCCATTCAGTAAGATGTTGGCTGTGGGTCTGTTACTGATATACCATCTTTCACCAATCAGAATGGCTTTCATCAAAAAGTCAAGAAATAACATATGATGGTGAGGCTGCAGAAAAAAGGGAACACTAATACGCTGTTAGTAGAAGGTAAATTAGTGCAGCCACTGTGGAGAGCAGTTTAGGGACTTCTCAAGGAACTAAGAATTAAAGTAATATTTGATCCAACAATCCCACTGCTGTATATACACCCAAAGGAAAATAAATCATTCCACCAAAAAG... |
Task1_train_40855 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | ACTTATTTGAATGTTGAATGATCTGTGCAGGCAGGCATTGCCATGGACAAGGTCACACAAACTTTTGGCCAATATGTAAGATCTAACATTGTAACATACATGTGTGCATATGATCTACTGAGAGCTTACTGTGTGTCAAGAAATGAGATGATAGCTCTTTTAATCCCTATAATTTGATCAGATATTTTTATATCCATTTTACAGTTGAGAATGCAAACTTGGGTTAATATAATTTGCTCAGCTTTATACATATAGTAACTAGTACATCTGGGATAGAAACTCATGTATCTATGACTCCAAAGTATGTAGTCTCATTTATA... | ACTTATTTGAATGTTGAATGATCTGTGCAGGCAGGCATTGCCATGGACAAGGTCACACAAACTTTTGGCCAATATGTAAGATCTAACATTGTAACATACATGTGTGCATATGATCTACTGAGAGCTTACTGTGTGTCAAGAAATGAGATGATAGCTCTTTTAATCCCTATAATTTGATCAGATATTTTTATATCCATTTTACAGTTGAGAATGCAAACTTGGGTTAATATAATTTGCTCAGCTTTATACATATAGTAACTAGTACATCTGGGATAGAAACTCATGTATCTATGACTCCAAAGTATGTAGTCTCATTTATA... |
Task1_train_40856 | Consider this mutation on Chromosome 11. Is this a benign change or a disease-causing variant? | Benign | TGTACAGATGGGTTTTTGGTGTGGATGTCCTTTCTGTTTGTTAGTTTTCCTTCTAACAGACAGGACCCTCAGCTGCAGGTCTGTTGGAGTTTGCTAGAGGTCCACTCCAGACCCTGTTTGCCTGGGTACCAGCAATGGTGGCTGCAGAACAGCGGATTTTTGTGAACCAGAATGCTGCTGTCTGATCGTTTCTCTGGAAGTTTTGTCTCAGAGGAATACCCGGCCGTGTGAGATGTCAGTCTGCCCCTACTGGGGAGTGCCTGCCAGTTAGGCTGCTCGGGGGTCAGGGTTCAGGGACCCACTTGAGGAGGCAGTCTGCC... | TGTACAGATGGGTTTTTGGTGTGGATGTCCTTTCTGTTTGTTAGTTTTCCTTCTAACAGACAGGACCCTCAGCTGCAGGTCTGTTGGAGTTTGCTAGAGGTCCACTCCAGACCCTGTTTGCCTGGGTACCAGCAATGGTGGCTGCAGAACAGCGGATTTTTGTGAACCAGAATGCTGCTGTCTGATCGTTTCTCTGGAAGTTTTGTCTCAGAGGAATACCCGGCCGTGTGAGATGTCAGTCTGCCCCTACTGGGGAGTGCCTGCCAGTTAGGCTGCTCGGGGGTCAGGGTTCAGGGACCCACTTGAGGAGGCAGTCTGCC... |
Task1_train_40857 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | ATAATTAAGACTGTGTATTCCGACTAACTCTATTCTGAGATAATGGCCAAACTCTCTTTTTACATAATTAGCTTCAGGGTTCATCGTTGCACAGAGTTCTGAGTTCAATGCTGTCCTTGCAGATATTTCTCTATTACCACTCTGTTCTACTGAGATTAAATAAAATTCTACTGCTTGGATCTCTAATTCCGAACCAATGGAGTATCTTCCATTTCTAGCACTTTTGTCCATACCCTTCACACCTTAGAGAAAATTCTGTACTTCTTGTTGTTTGGTATCTGAACCTATTATTAAGCGTGGAAAACCGGAAAGGGAAGGGA... | ATAATTAAGACTGTGTATTCCGACTAACTCTATTCTGAGATAATGGCCAAACTCTCTTTTTACATAATTAGCTTCAGGGTTCATCGTTGCACAGAGTTCTGAGTTCAATGCTGTCCTTGCAGATATTTCTCTATTACCACTCTGTTCTACTGAGATTAAATAAAATTCTACTGCTTGGATCTCTAATTCCGAACCAATGGAGTATCTTCCATTTCTAGCACTTTTGTCCATACCCTTCACACCTTAGAGAAAATTCTGTACTTCTTGTTGTTTGGTATCTGAACCTATTATTAAGCGTGGAAAACCGGAAAGGGAAGGGA... |
Task1_train_40858 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | AGTATCTTCCATTTCTAGCACTTTTGTCCATACCCTTCACACCTTAGAGAAAATTCTGTACTTCTTGTTGTTTGGTATCTGAACCTATTATTAAGCGTGGAAAACCGGAAAGGGAAGGGATGAGTGCACTGTAGTCACCTCAAAGTGAAGCACCCCTGCAACAGAAGGATGGTCCCTGGGTTTTCTGGTTGACAGAGATAACAACTCAGATACACTGTCTCAGACACAATGTCATACAATGCTTTCCTATCTTTTATTAGGTGGCTTTTGTCCATAAACAATTGAATTCTACCGGCCAAAACTGAGTTTTAAGTTCTATG... | AGTATCTTCCATTTCTAGCACTTTTGTCCATACCCTTCACACCTTAGAGAAAATTCTGTACTTCTTGTTGTTTGGTATCTGAACCTATTATTAAGCGTGGAAAACCGGAAAGGGAAGGGATGAGTGCACTGTAGTCACCTCAAAGTGAAGCACCCCTGCAACAGAAGGATGGTCCCTGGGTTTTCTGGTTGACAGAGATAACAACTCAGATACACTGTCTCAGACACAATGTCATACAATGCTTTCCTATCTTTTATTAGGTGGCTTTTGTCCATAAACAATTGAATTCTACCGGCCAAAACTGAGTTTTAAGTTCTATG... |
Task1_train_40859 | A mutation on Chromosome 11 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | AGGGGAGTTAAGAGATGTCGTTTAACAGTTGGCCAACCAGTTTCAATTCAAACCAAAATTTAAGTAAATATTTTGAAGACAGTGAAAATACAAAATTGAACACACAATTTCATGCACATTAAAATGCACAGAAAAAAAGACTAGAATGAAATAGAATGAAGAGTTTTCTCCTTAAATGTTTAATATATTTATGACTGTATTATATTTATAGTAGGTAAAGAAAAATACACTATAATTTTAAATATATAGGGTTTTTTCTAAAGATCTCCTTTTGAAGCAAATAATTCTTAGTGGGAGATAGGGGAAACTATAAATGTTGC... | AGGGGAGTTAAGAGATGTCGTTTAACAGTTGGCCAACCAGTTTCAATTCAAACCAAAATTTAAGTAAATATTTTGAAGACAGTGAAAATACAAAATTGAACACACAATTTCATGCACATTAAAATGCACAGAAAAAAAGACTAGAATGAAATAGAATGAAGAGTTTTCTCCTTAAATGTTTAATATATTTATGACTGTATTATATTTATAGTAGGTAAAGAAAAATACACTATAATTTTAAATATATAGGGTTTTTTCTAAAGATCTCCTTTTGAAGCAAATAATTCTTAGTGGGAGATAGGGGAAACTATAAATGTTGC... |
Task1_train_40860 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CAGTGGAATTGTGGTGGCAAAAGTTCTATTGCAGTGGATTGAGGAGGTATAATATAATAGGTGATAGAGTATAGAAGATTGAAGAAGTTTGACTATGAAGATGAAGGGGATTTGGAGTAAAGGGAATATTTGTAAAAGACTAAGTGAGATTTGGGCACATTTAAGTGCTAATGAGTAGGACTTAGGGGACAGGGAGAAGTTGAAGATCAAGAAGATAGATTTCTAATGGATTAAATCCCTTCAGGAACAATTGCTTATGAGATTTAGATCACAGGTAGAGAAATAAGCTATAGAAAAGGGAAGAGAGCGCCCCTCATTTG... | CAGTGGAATTGTGGTGGCAAAAGTTCTATTGCAGTGGATTGAGGAGGTATAATATAATAGGTGATAGAGTATAGAAGATTGAAGAAGTTTGACTATGAAGATGAAGGGGATTTGGAGTAAAGGGAATATTTGTAAAAGACTAAGTGAGATTTGGGCACATTTAAGTGCTAATGAGTAGGACTTAGGGGACAGGGAGAAGTTGAAGATCAAGAAGATAGATTTCTAATGGATTAAATCCCTTCAGGAACAATTGCTTATGAGATTTAGATCACAGGTAGAGAAATAAGCTATAGAAAAGGGAAGAGAGCGCCCCTCATTTG... |
Task1_train_40861 | This is a variant located on Chromosome 11. Is this mutation a likely cause of disease or not? | Benign | TCTTATGGACCTATACCAAATAACAGCTGGTCAGTGCTACAGATAGCAAGCAGTAAGGACAACAAAAACATTTATAACTTGCTGACTTTTAAGGAGCTTTGGGCTTTGGAAATTTTTGCCAAGGATGTTGTTTTGGTAGCACTATTAAGAGGAAGTCGTGCAGGCTCTTAAGAAGGAACTAAATATAAGTGATAAGCTAATCTGTCTCCTGTTTTGCTGGCTTACATTTAGGGGTCAGTTTGGAGCCATAATCCTCAGCTTTTGGCTTCCCTTTTGATTGAATCACTGGTGATTGATGTTATATATTAATACAGGTGAGA... | TCTTATGGACCTATACCAAATAACAGCTGGTCAGTGCTACAGATAGCAAGCAGTAAGGACAACAAAAACATTTATAACTTGCTGACTTTTAAGGAGCTTTGGGCTTTGGAAATTTTTGCCAAGGATGTTGTTTTGGTAGCACTATTAAGAGGAAGTCGTGCAGGCTCTTAAGAAGGAACTAAATATAAGTGATAAGCTAATCTGTCTCCTGTTTTGCTGGCTTACATTTAGGGGTCAGTTTGGAGCCATAATCCTCAGCTTTTGGCTTCCCTTTTGATTGAATCACTGGTGATTGATGTTATATATTAATACAGGTGAGA... |
Task1_train_40862 | 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 | TTGAGTTGTATGCTTAGACATACATATTCCCTTTCTTCTTCTCCAACAAAGATATTTAAGGTTACAACTTCCCTTCAAATGACTGCGTTAACTTAATCATAAAATTTTGATGTTGTATGCAGTGTTTTTGTTATTTTTGAGTCCACAATATTTGTAAACTTCCCTAGAACTTTTTTCTTCAACTAATAGGTTATTTGTAAACATACTCCTTAATTTTCAAGCATGAGGCTTTTCTTTTTATATTCAGTCTGTAGAATTGTTGTCTGAGAACATACTGTGCATGAGTACAGTTCTTTGAAGTTTGTTGTCATTTGCTACAT... | TTGAGTTGTATGCTTAGACATACATATTCCCTTTCTTCTTCTCCAACAAAGATATTTAAGGTTACAACTTCCCTTCAAATGACTGCGTTAACTTAATCATAAAATTTTGATGTTGTATGCAGTGTTTTTGTTATTTTTGAGTCCACAATATTTGTAAACTTCCCTAGAACTTTTTTCTTCAACTAATAGGTTATTTGTAAACATACTCCTTAATTTTCAAGCATGAGGCTTTTCTTTTTATATTCAGTCTGTAGAATTGTTGTCTGAGAACATACTGTGCATGAGTACAGTTCTTTGAAGTTTGTTGTCATTTGCTACAT... |
Task1_train_40863 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CCATGTATTGACTTATGATTTTGTCTGTAACTTCTGCTTTCCTGAAATTTACATTTTCCTTTAAAAACCTTTACCTGTAAGCCATCATGGAGGTCAGAATTTAAGAGTAGCTGCCTGGTCTTCCTTGCTTGGAGCCCTGCAAATAAATGCCCTCCTTTTTCCTGCTGCAAACCTCAGTGTGGCTATCTGGTCTTATTGTGCCAGGAGAGCATATCTCAGTTAGGTTTGATTAGTAAGTGGCACAAGTGAACCCTCTGGAGTGATGGAAATGTTATAGATTTTAATGTGGGTCATGGTTACATGGATATACACACGTAAAA... | CCATGTATTGACTTATGATTTTGTCTGTAACTTCTGCTTTCCTGAAATTTACATTTTCCTTTAAAAACCTTTACCTGTAAGCCATCATGGAGGTCAGAATTTAAGAGTAGCTGCCTGGTCTTCCTTGCTTGGAGCCCTGCAAATAAATGCCCTCCTTTTTCCTGCTGCAAACCTCAGTGTGGCTATCTGGTCTTATTGTGCCAGGAGAGCATATCTCAGTTAGGTTTGATTAGTAAGTGGCACAAGTGAACCCTCTGGAGTGATGGAAATGTTATAGATTTTAATGTGGGTCATGGTTACATGGATATACACACGTAAAA... |
Task1_train_40864 | A genetic alteration is present on Chromosome 11. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GGTGGGTGATTAGTGATTAGGAGGCTATTTTAGGATAAAGAGGAATGCTCAGCATAACAATATCTGTGGTGACAAGGGAGAATACTTTCAAATGTGTCTGGGGGTCCCTTAATTCCATTTTTACGTCTTTATTTCATTGTCTGAAGAAAGGAAGAGAAGGGCAAATTCAAATGTTTACTCTGCCTCTCCAACTGTTTACCAATCCCTAAGAGACATCCCAGCTGTTCTCTTTCACCTTCTAGTAAAGAGGCTATTTTAATTAAGGTTGTTGAGCGAATGCATACAATACAATATAATGACTCTAAACTCTGAGCTAAAAA... | GGTGGGTGATTAGTGATTAGGAGGCTATTTTAGGATAAAGAGGAATGCTCAGCATAACAATATCTGTGGTGACAAGGGAGAATACTTTCAAATGTGTCTGGGGGTCCCTTAATTCCATTTTTACGTCTTTATTTCATTGTCTGAAGAAAGGAAGAGAAGGGCAAATTCAAATGTTTACTCTGCCTCTCCAACTGTTTACCAATCCCTAAGAGACATCCCAGCTGTTCTCTTTCACCTTCTAGTAAAGAGGCTATTTTAATTAAGGTTGTTGAGCGAATGCATACAATACAATATAATGACTCTAAACTCTGAGCTAAAAA... |
Task1_train_40865 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | GGTAGGTGTGGAGCACCAGAGGAAGGCTGGAGACAGTGGAAGTGGGGGCTGGTTTGGAGAAGGGGAAGTACAGGGCAGGATATGATGACAGTAGGGACAAGAAAAGCAACTGGACTGGGGGTGTGGAAAGCACAGCCTGCCAGGTTTGATCTCAAGGGGCAAAGTCTGCTTCACCCACAGGAAGCAAGGTGACCAGGCTATCCTAGAAAATAAAGCCACAGCCATCCTCAGACCAGCTGTTCTCCTAGAGTTGTTTGAGAGAGGGCCTGAACTGTCTCTCCTCATGTACCCATTTATTCGTCCATTCCCCAGTGTTTGTG... | GGTAGGTGTGGAGCACCAGAGGAAGGCTGGAGACAGTGGAAGTGGGGGCTGGTTTGGAGAAGGGGAAGTACAGGGCAGGATATGATGACAGTAGGGACAAGAAAAGCAACTGGACTGGGGGTGTGGAAAGCACAGCCTGCCAGGTTTGATCTCAAGGGGCAAAGTCTGCTTCACCCACAGGAAGCAAGGTGACCAGGCTATCCTAGAAAATAAAGCCACAGCCATCCTCAGACCAGCTGTTCTCCTAGAGTTGTTTGAGAGAGGGCCTGAACTGTCTCTCCTCATGTACCCATTTATTCGTCCATTCCCCAGTGTTTGTG... |
Task1_train_40866 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GTAGGTGTGGAGCACCAGAGGAAGGCTGGAGACAGTGGAAGTGGGGGCTGGTTTGGAGAAGGGGAAGTACAGGGCAGGATATGATGACAGTAGGGACAAGAAAAGCAACTGGACTGGGGGTGTGGAAAGCACAGCCTGCCAGGTTTGATCTCAAGGGGCAAAGTCTGCTTCACCCACAGGAAGCAAGGTGACCAGGCTATCCTAGAAAATAAAGCCACAGCCATCCTCAGACCAGCTGTTCTCCTAGAGTTGTTTGAGAGAGGGCCTGAACTGTCTCTCCTCATGTACCCATTTATTCGTCCATTCCCCAGTGTTTGTGA... | GTAGGTGTGGAGCACCAGAGGAAGGCTGGAGACAGTGGAAGTGGGGGCTGGTTTGGAGAAGGGGAAGTACAGGGCAGGATATGATGACAGTAGGGACAAGAAAAGCAACTGGACTGGGGGTGTGGAAAGCACAGCCTGCCAGGTTTGATCTCAAGGGGCAAAGTCTGCTTCACCCACAGGAAGCAAGGTGACCAGGCTATCCTAGAAAATAAAGCCACAGCCATCCTCAGACCAGCTGTTCTCCTAGAGTTGTTTGAGAGAGGGCCTGAACTGTCTCTCCTCATGTACCCATTTATTCGTCCATTCCCCAGTGTTTGTGA... |
Task1_train_40867 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | TCCTGAAGATTTAATCCATAGCTAAAATACTGCCTGGCATAATGGTATGTATCTAAAATGTTATTATTCACCATAGTTCATTTTTTAAAATATGAAACTTAAAAATGTTGGTTACTTTTTCTTCATGTTTTAGTGTTTCAGGCTGATAATGGATTTCAGCTTTTCGTTTTGTCTTTTATGATAAACCATTAGGTCACTGTAAAAAGTCATGATATCAATGTACTGAGAAGTCTTAGTTTCTTTTGCTGAACTGGATTTAGACTTAGAAGTGAGCAGATTTCAGCCAAGTTAAACAGAAAGAATGCATTTGGGCTGCCACC... | TCCTGAAGATTTAATCCATAGCTAAAATACTGCCTGGCATAATGGTATGTATCTAAAATGTTATTATTCACCATAGTTCATTTTTTAAAATATGAAACTTAAAAATGTTGGTTACTTTTTCTTCATGTTTTAGTGTTTCAGGCTGATAATGGATTTCAGCTTTTCGTTTTGTCTTTTATGATAAACCATTAGGTCACTGTAAAAAGTCATGATATCAATGTACTGAGAAGTCTTAGTTTCTTTTGCTGAACTGGATTTAGACTTAGAAGTGAGCAGATTTCAGCCAAGTTAAACAGAAAGAATGCATTTGGGCTGCCACC... |
Task1_train_40868 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TTTTCTTCATGTTTTAGTGTTTCAGGCTGATAATGGATTTCAGCTTTTCGTTTTGTCTTTTATGATAAACCATTAGGTCACTGTAAAAAGTCATGATATCAATGTACTGAGAAGTCTTAGTTTCTTTTGCTGAACTGGATTTAGACTTAGAAGTGAGCAGATTTCAGCCAAGTTAAACAGAAAGAATGCATTTGGGCTGCCACCTCATTAAAATGTGCAAAACCCAACATTTTGGCAGCCTGGACAGGCTCCCAGGGACAAATGTAACCCTCCACCCTAGCCTTTGCCACACCCTGGCATTGATTATTCATACTTAATGG... | TTTTCTTCATGTTTTAGTGTTTCAGGCTGATAATGGATTTCAGCTTTTCGTTTTGTCTTTTATGATAAACCATTAGGTCACTGTAAAAAGTCATGATATCAATGTACTGAGAAGTCTTAGTTTCTTTTGCTGAACTGGATTTAGACTTAGAAGTGAGCAGATTTCAGCCAAGTTAAACAGAAAGAATGCATTTGGGCTGCCACCTCATTAAAATGTGCAAAACCCAACATTTTGGCAGCCTGGACAGGCTCCCAGGGACAAATGTAACCCTCCACCCTAGCCTTTGCCACACCCTGGCATTGATTATTCATACTTAATGG... |
Task1_train_40869 | Chromosome 11 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GTGAGCAAAGCCCACCCCCAGAGTCCTGCCCTTTTGAAAGTAGAGTTAGTTCAGGATGGCTGAGAGTGTTGGGCCACAGGGATTAATAAACACCCACCCACAAAGGTTTGCGTGTAAGGTGGACCAAGTTGATAGAAAGAGCCCGTTCTTGTTTTTTTTTTTTTTTTTAACATTTTTTTTGGTTAAAAGTGGAATGTTAACCATGTGTCAACTCCAGGAATATGTTTCAATAATTCATTAATCATTTGGGAAAATAAAAATGGAGATCTTAAAGTAGGCATATTAATTTAGATTAGTTCCTTTTTAAACAGGCGCTTTAT... | GTGAGCAAAGCCCACCCCCAGAGTCCTGCCCTTTTGAAAGTAGAGTTAGTTCAGGATGGCTGAGAGTGTTGGGCCACAGGGATTAATAAACACCCACCCACAAAGGTTTGCGTGTAAGGTGGACCAAGTTGATAGAAAGAGCCCGTTCTTGTTTTTTTTTTTTTTTTTAACATTTTTTTTGGTTAAAAGTGGAATGTTAACCATGTGTCAACTCCAGGAATATGTTTCAATAATTCATTAATCATTTGGGAAAATAAAAATGGAGATCTTAAAGTAGGCATATTAATTTAGATTAGTTCCTTTTTAAACAGGCGCTTTAT... |
Task1_train_40870 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TTTTTTGCACCATGGTGCCTGGGATTCTTTTGTTTGCTTGTGCTTCCTGTTGCCCCAAACATCCGTTACCTGCACTTTGTGTCTCACAGTAGCCATAGACCTCTAAGCTCCCACCCTCCACTGGGGAGACACATGCTATAAAGTCATCATAGTGATTAAAGGAGATGAGGAGATGGTGCAAAGGAGAGGGGGAGGGAAAGACAAAATGGAAAGATGGGTGTCACAGTAGAAGAGAAGAGAAGAGACAGAGGAGGGGGAAGAGGAGCCCGTAGAAGCTAGACATTTCAGAATAGGTATCCCTACTTGTAGATCCAAAATTA... | TTTTTTGCACCATGGTGCCTGGGATTCTTTTGTTTGCTTGTGCTTCCTGTTGCCCCAAACATCCGTTACCTGCACTTTGTGTCTCACAGTAGCCATAGACCTCTAAGCTCCCACCCTCCACTGGGGAGACACATGCTATAAAGTCATCATAGTGATTAAAGGAGATGAGGAGATGGTGCAAAGGAGAGGGGGAGGGAAAGACAAAATGGAAAGATGGGTGTCACAGTAGAAGAGAAGAGAAGAGACAGAGGAGGGGGAAGAGGAGCCCGTAGAAGCTAGACATTTCAGAATAGGTATCCCTACTTGTAGATCCAAAATTA... |
Task1_train_40871 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CACTTTGGGCTGCGTAATACTCTGTGATGGAAATACTCTGTGATGGAGGCTCTCCTGTGGGTTTTAAGATGTTTAGCAGCATCCTTGGTCTCTACCCTCTAAATGCTAATAGAGGGTAGATGCACCCCTTCTGTAGCTGACAACCAACATGTCTTTGGACTTTGTTATCTGTTCCCTGAGCAGCAAAATCACCCTCAGTTGAGAACCAGTAGGTGAGAGAATGGGGTCGGAGTTGGGGGCCCAGGGAAAGAAAAATCTGATAAAGTCGGCAGGAGCAAACCAAGAAGGGCCTTGGGAGCCAGGCCCTGGAGTGTGTCCTG... | CACTTTGGGCTGCGTAATACTCTGTGATGGAAATACTCTGTGATGGAGGCTCTCCTGTGGGTTTTAAGATGTTTAGCAGCATCCTTGGTCTCTACCCTCTAAATGCTAATAGAGGGTAGATGCACCCCTTCTGTAGCTGACAACCAACATGTCTTTGGACTTTGTTATCTGTTCCCTGAGCAGCAAAATCACCCTCAGTTGAGAACCAGTAGGTGAGAGAATGGGGTCGGAGTTGGGGGCCCAGGGAAAGAAAAATCTGATAAAGTCGGCAGGAGCAAACCAAGAAGGGCCTTGGGAGCCAGGCCCTGGAGTGTGTCCTG... |
Task1_train_40872 | The following genetic variant occurs on Chromosome 11. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | AGGCTCTCCTGTGGGTTTTAAGATGTTTAGCAGCATCCTTGGTCTCTACCCTCTAAATGCTAATAGAGGGTAGATGCACCCCTTCTGTAGCTGACAACCAACATGTCTTTGGACTTTGTTATCTGTTCCCTGAGCAGCAAAATCACCCTCAGTTGAGAACCAGTAGGTGAGAGAATGGGGTCGGAGTTGGGGGCCCAGGGAAAGAAAAATCTGATAAAGTCGGCAGGAGCAAACCAAGAAGGGCCTTGGGAGCCAGGCCCTGGAGTGTGTCCTGGAGAGATGGGGGTGGCCAGAGTGGGGTCTCCCTTGAAAGCAGTGAA... | AGGCTCTCCTGTGGGTTTTAAGATGTTTAGCAGCATCCTTGGTCTCTACCCTCTAAATGCTAATAGAGGGTAGATGCACCCCTTCTGTAGCTGACAACCAACATGTCTTTGGACTTTGTTATCTGTTCCCTGAGCAGCAAAATCACCCTCAGTTGAGAACCAGTAGGTGAGAGAATGGGGTCGGAGTTGGGGGCCCAGGGAAAGAAAAATCTGATAAAGTCGGCAGGAGCAAACCAAGAAGGGCCTTGGGAGCCAGGCCCTGGAGTGTGTCCTGGAGAGATGGGGGTGGCCAGAGTGGGGTCTCCCTTGAAAGCAGTGAA... |
Task1_train_40873 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | CTGCAGGGACCCTGAAGCCCTGCTGCTGTCTGTCAGCTGTCAGCATTGACGAGGAAGGAGAACACAACGAGGTATACCGAGGTGTGTGAATCAGTACAGCCAGCTGGAGTTGTCCGGCAGGGTGTGGCCTGGTGTTAGTGGAACTGCGCAGAATTGCTCAGTAGGGTAGCGCCCTCTGCCGACCAGGGACCTGTATGACAAGCAGGTACAGCCGGGAGCAGTGTGAGAGGCGCGCCTGTGGGGTGCTCTGTGCACAGTGGTTGCTGGGATGCTGTCTGGGCTGCAGCAGCTGTCTGGGGGCTCAGCATGTCCAGGTGAGG... | CTGCAGGGACCCTGAAGCCCTGCTGCTGTCTGTCAGCTGTCAGCATTGACGAGGAAGGAGAACACAACGAGGTATACCGAGGTGTGTGAATCAGTACAGCCAGCTGGAGTTGTCCGGCAGGGTGTGGCCTGGTGTTAGTGGAACTGCGCAGAATTGCTCAGTAGGGTAGCGCCCTCTGCCGACCAGGGACCTGTATGACAAGCAGGTACAGCCGGGAGCAGTGTGAGAGGCGCGCCTGTGGGGTGCTCTGTGCACAGTGGTTGCTGGGATGCTGTCTGGGCTGCAGCAGCTGTCTGGGGGCTCAGCATGTCCAGGTGAGG... |
Task1_train_40874 | A variant was discovered on Chromosome 11. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GTTGATCCCACTAAGCCCTCCCACAGATGCAGGCACCCAAGCAGCATGAGCTCAGTCAATGCAGGAGAAATGAAAACAAGAGCCCAGCTCAGCAAACATTCCATCCTACCACTGCAAGCTCAGCAGGAACTGACCTGGTTGGCAAAGATGAGGGACATCCTGGTCCTGTCACTGGGGTCCTTGGTGATGTGGCGAATGAGCTGCAACATGGGTGTGATGCCTGGAACACAGTGAGCGAGCAGCCAGCTTTCTCCCTGTCTCTGAAGCCCACAGTCCCTGACCTGCAGCAAGCTTCATACCTTCCCCCAGCCCAAGTTATC... | GTTGATCCCACTAAGCCCTCCCACAGATGCAGGCACCCAAGCAGCATGAGCTCAGTCAATGCAGGAGAAATGAAAACAAGAGCCCAGCTCAGCAAACATTCCATCCTACCACTGCAAGCTCAGCAGGAACTGACCTGGTTGGCAAAGATGAGGGACATCCTGGTCCTGTCACTGGGGTCCTTGGTGATGTGGCGAATGAGCTGCAACATGGGTGTGATGCCTGGAACACAGTGAGCGAGCAGCCAGCTTTCTCCCTGTCTCTGAAGCCCACAGTCCCTGACCTGCAGCAAGCTTCATACCTTCCCCCAGCCCAAGTTATC... |
Task1_train_40875 | A mutation on Chromosome 11 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CCAAAAGAGAGAAGAAATTCTGCCTGTGAGGAACAACTTCAGCCCATGCTGTGGATTCCGGTGTTTCTATGATTTTCCCTTTCTGAGCACCTGGCCTGTAGATTTACCTGCTTAGTCAGCCCCCACAATTGTGTAAGCCAATTCTGGTGTATCCGTTTGCTAGGGTTGCCATGACAAAGTACCACAAACTAGGTGGCTTAGAACAACAGAAATTTATTGTCTCATAGTTCTGGAGGCTAGAAGTCCAAGATCAACGTGTCAGCAGGGATGGCTCTGTCTGAGGGCTGTGACGAGGAGTCTGCCCCAAGCCTCTCCTCTAG... | CCAAAAGAGAGAAGAAATTCTGCCTGTGAGGAACAACTTCAGCCCATGCTGTGGATTCCGGTGTTTCTATGATTTTCCCTTTCTGAGCACCTGGCCTGTAGATTTACCTGCTTAGTCAGCCCCCACAATTGTGTAAGCCAATTCTGGTGTATCCGTTTGCTAGGGTTGCCATGACAAAGTACCACAAACTAGGTGGCTTAGAACAACAGAAATTTATTGTCTCATAGTTCTGGAGGCTAGAAGTCCAAGATCAACGTGTCAGCAGGGATGGCTCTGTCTGAGGGCTGTGACGAGGAGTCTGCCCCAAGCCTCTCCTCTAG... |
Task1_train_40876 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TCAGCCCATGCTGTGGATTCCGGTGTTTCTATGATTTTCCCTTTCTGAGCACCTGGCCTGTAGATTTACCTGCTTAGTCAGCCCCCACAATTGTGTAAGCCAATTCTGGTGTATCCGTTTGCTAGGGTTGCCATGACAAAGTACCACAAACTAGGTGGCTTAGAACAACAGAAATTTATTGTCTCATAGTTCTGGAGGCTAGAAGTCCAAGATCAACGTGTCAGCAGGGATGGCTCTGTCTGAGGGCTGTGACGAGGAGTCTGCCCCAAGCCTCTCCTCTAGCTTCTGGTGGTTTACTGACAGTCACTGGTGCCCCTTGG... | TCAGCCCATGCTGTGGATTCCGGTGTTTCTATGATTTTCCCTTTCTGAGCACCTGGCCTGTAGATTTACCTGCTTAGTCAGCCCCCACAATTGTGTAAGCCAATTCTGGTGTATCCGTTTGCTAGGGTTGCCATGACAAAGTACCACAAACTAGGTGGCTTAGAACAACAGAAATTTATTGTCTCATAGTTCTGGAGGCTAGAAGTCCAAGATCAACGTGTCAGCAGGGATGGCTCTGTCTGAGGGCTGTGACGAGGAGTCTGCCCCAAGCCTCTCCTCTAGCTTCTGGTGGTTTACTGACAGTCACTGGTGCCCCTTGG... |
Task1_train_40877 | A variant on Chromosome 11 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | AACTAAAGATTTGAACTAAAGTGTCTTAGAGACCATCTGGCCCACACTATTTTCTTTATGGATGAGGGCCAGAGTTAGGAAAAGGCTCGCCCAAAGTCACAGAGTGAATTCATCGCAGGATCGCAATGGAACAAAGGGGATGAGACCCTATATAAGTAGGGACACTTTCAGGGCAAGGTGTGTAGCTTACTGACCACATCGGCACTGCCTTGCCCTCTTTCCTTGAGTCTCTGATTCCAAGCTAGTGTTTGGCAAAGGTTGGCTGAATTGGGACAGAGCTCTGGATTGCTAAGAAATGAAATGGGAGGGCAACTGGGGCT... | AACTAAAGATTTGAACTAAAGTGTCTTAGAGACCATCTGGCCCACACTATTTTCTTTATGGATGAGGGCCAGAGTTAGGAAAAGGCTCGCCCAAAGTCACAGAGTGAATTCATCGCAGGATCGCAATGGAACAAAGGGGATGAGACCCTATATAAGTAGGGACACTTTCAGGGCAAGGTGTGTAGCTTACTGACCACATCGGCACTGCCTTGCCCTCTTTCCTTGAGTCTCTGATTCCAAGCTAGTGTTTGGCAAAGGTTGGCTGAATTGGGACAGAGCTCTGGATTGCTAAGAAATGAAATGGGAGGGCAACTGGGGCT... |
Task1_train_40878 | 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 | ACTATTTGACCCCTATAGCTTCTTCAAGCCTATTCTTTACCCTACCTCTCCAATATACTTTCTAATTTTTGCTTATCCTATTTGTGATACTTGATTTGATTCTAAAATGACTTACTATGTACAAGTAAATACTTTTTCTTATGACATTCATCACATGCCATGATGACTATTCTGTCTTTCAACCCAACTAGGCTGTAGGCTCCTCAAAGATATAAACTTAACCTTAAAAATATCTATATCCATAATATCTAGCACAGTTCTTGATGCATAGAAGTCCTTGAGACTCACCTGCCAGGGATAGGAACCCTTCTCCACTTGGC... | ACTATTTGACCCCTATAGCTTCTTCAAGCCTATTCTTTACCCTACCTCTCCAATATACTTTCTAATTTTTGCTTATCCTATTTGTGATACTTGATTTGATTCTAAAATGACTTACTATGTACAAGTAAATACTTTTTCTTATGACATTCATCACATGCCATGATGACTATTCTGTCTTTCAACCCAACTAGGCTGTAGGCTCCTCAAAGATATAAACTTAACCTTAAAAATATCTATATCCATAATATCTAGCACAGTTCTTGATGCATAGAAGTCCTTGAGACTCACCTGCCAGGGATAGGAACCCTTCTCCACTTGGC... |
Task1_train_40879 | A mutation on Chromosome 11 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | ATAGCTTCTTCAAGCCTATTCTTTACCCTACCTCTCCAATATACTTTCTAATTTTTGCTTATCCTATTTGTGATACTTGATTTGATTCTAAAATGACTTACTATGTACAAGTAAATACTTTTTCTTATGACATTCATCACATGCCATGATGACTATTCTGTCTTTCAACCCAACTAGGCTGTAGGCTCCTCAAAGATATAAACTTAACCTTAAAAATATCTATATCCATAATATCTAGCACAGTTCTTGATGCATAGAAGTCCTTGAGACTCACCTGCCAGGGATAGGAACCCTTCTCCACTTGGCTTCCTCCAAGAATG... | ATAGCTTCTTCAAGCCTATTCTTTACCCTACCTCTCCAATATACTTTCTAATTTTTGCTTATCCTATTTGTGATACTTGATTTGATTCTAAAATGACTTACTATGTACAAGTAAATACTTTTTCTTATGACATTCATCACATGCCATGATGACTATTCTGTCTTTCAACCCAACTAGGCTGTAGGCTCCTCAAAGATATAAACTTAACCTTAAAAATATCTATATCCATAATATCTAGCACAGTTCTTGATGCATAGAAGTCCTTGAGACTCACCTGCCAGGGATAGGAACCCTTCTCCACTTGGCTTCCTCCAAGAATG... |
Task1_train_40880 | The following genetic variant occurs on Chromosome 11. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | AACTTGATATGAAAGAAAGTAATAGTGGCGTAAAACAATAGCCAAGGAAGTTAGAATTACGGGATGTTTGGTTCTCCTGTAGAAACTTAAGATAGCATCTTAACAACATATGTCCCTGGGTTGTTTTTCAGAAACCTGGACCCCCACCAGATGAAAAATTCCATCTGCTGGCACATAGACCTCAGATAAGGAGGAAATGAGGACTGAAGTCTGACCACAGCCATGCTTTGCTCTAAATTTCTTCCTGATGGGCATGGGAGGGGTCACACTCCAAGGCCAGAACTAATATTCTTTTCTGCTAATCCCAAAGTTTTAAACAA... | AACTTGATATGAAAGAAAGTAATAGTGGCGTAAAACAATAGCCAAGGAAGTTAGAATTACGGGATGTTTGGTTCTCCTGTAGAAACTTAAGATAGCATCTTAACAACATATGTCCCTGGGTTGTTTTTCAGAAACCTGGACCCCCACCAGATGAAAAATTCCATCTGCTGGCACATAGACCTCAGATAAGGAGGAAATGAGGACTGAAGTCTGACCACAGCCATGCTTTGCTCTAAATTTCTTCCTGATGGGCATGGGAGGGGTCACACTCCAAGGCCAGAACTAATATTCTTTTCTGCTAATCCCAAAGTTTTAAACAA... |
Task1_train_40881 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | AAACAAAGTTTTGCCTCCTGAACCAACTGCAAATCAGAAAATCTTCGAGTCCACCTATGATCTGTTCCCTATCTCCACTTCAAGATCTGCCACCCTTTTAGGTCAAACCAATGTATTGCCTCCATATTCCGATTTATGACTTTGCCTGTCAACTCTGCCTCCCCACCTTTAAAAATCCTTACTTGCAAGCCATTGGAAAGATCGGGACTTGAGCAAGGGCTGCTTGATTCTCCTTGCTTGGCACTCTGCAAATAAATGCTCTCCTTTCTCCTGCTATAAACCTGGTGTAGATGTTTGGCGTTATTGTGCAGGGCAAGTGG... | AAACAAAGTTTTGCCTCCTGAACCAACTGCAAATCAGAAAATCTTCGAGTCCACCTATGATCTGTTCCCTATCTCCACTTCAAGATCTGCCACCCTTTTAGGTCAAACCAATGTATTGCCTCCATATTCCGATTTATGACTTTGCCTGTCAACTCTGCCTCCCCACCTTTAAAAATCCTTACTTGCAAGCCATTGGAAAGATCGGGACTTGAGCAAGGGCTGCTTGATTCTCCTTGCTTGGCACTCTGCAAATAAATGCTCTCCTTTCTCCTGCTATAAACCTGGTGTAGATGTTTGGCGTTATTGTGCAGGGCAAGTGG... |
Task1_train_40882 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | GGACTTGAGCAAGGGCTGCTTGATTCTCCTTGCTTGGCACTCTGCAAATAAATGCTCTCCTTTCTCCTGCTATAAACCTGGTGTAGATGTTTGGCGTTATTGTGCAGGGCAAGTGGATCCCAGTTCAGTTGGAAAACAGGCTCCCTGATTGGCCCCACTGAAACATAATTTTTCCATTGGTTTTTGTCTAGAGTAAGGCAGGAAGTGCCTAAATGTTTTCTTTTCTCTCCAGGCCACCCTTTTCCCAGTTCTTTGACCAGGAGAGAACAGTCTTTTCTTACAGTTGTTTTTTGTTTTTTGCTTTTGTCTGTGTCTGTTGG... | GGACTTGAGCAAGGGCTGCTTGATTCTCCTTGCTTGGCACTCTGCAAATAAATGCTCTCCTTTCTCCTGCTATAAACCTGGTGTAGATGTTTGGCGTTATTGTGCAGGGCAAGTGGATCCCAGTTCAGTTGGAAAACAGGCTCCCTGATTGGCCCCACTGAAACATAATTTTTCCATTGGTTTTTGTCTAGAGTAAGGCAGGAAGTGCCTAAATGTTTTCTTTTCTCTCCAGGCCACCCTTTTCCCAGTTCTTTGACCAGGAGAGAACAGTCTTTTCTTACAGTTGTTTTTTGTTTTTTGCTTTTGTCTGTGTCTGTTGG... |
Task1_train_40883 | A genomic variant on Chromosome 11 is under review. What is the biological outcome — benign or pathogenic? | Benign | CCAATAGTTCCTAGGCAGTTAACCCTTTTTATTCCACCTTTGAAAGTCTTCCTACTTGTTTTTGTGCTACATATAGGGATTTTTTGGTAATAAGAGGAAGGGCCTGGAAGAAATGGGGCTACTTCAGCATCAAGGTAATCAAAAATCTATGCCTTCAAACATGTAGAAATATGCAGTTTCTTATGTATTTCATGCCACAAAGTTGGTGTAATACAAATTAGCCTGCCATATCCAGATATAGAAGTCTCTATACTTACTGTGAACAGAAAGGGTTTGCTAGAAAGAAATGTGTCAGAGACAAATGAAAGTTCATGGTGAAG... | CCAATAGTTCCTAGGCAGTTAACCCTTTTTATTCCACCTTTGAAAGTCTTCCTACTTGTTTTTGTGCTACATATAGGGATTTTTTGGTAATAAGAGGAAGGGCCTGGAAGAAATGGGGCTACTTCAGCATCAAGGTAATCAAAAATCTATGCCTTCAAACATGTAGAAATATGCAGTTTCTTATGTATTTCATGCCACAAAGTTGGTGTAATACAAATTAGCCTGCCATATCCAGATATAGAAGTCTCTATACTTACTGTGAACAGAAAGGGTTTGCTAGAAAGAAATGTGTCAGAGACAAATGAAAGTTCATGGTGAAG... |
Task1_train_40884 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | AGATGGGATCCAATCAAAGGCTTTTGCTGAGGGCTGTTTGGTGCCCAAATGAAAACAGTATTATACAACATTCAGATATCACTGATAGCGACAGGAGGCAGCCAAATGCCTAGGCAGATGGGGTGGGTTCCTGGTGAAACCCCACCTCTAAACAAAAGACAGTTTAAAGCCTGAAAGCCAAACTGCAAGTTAAACTCTGGGACCGGATTGAGAACTTATCTTCCCATTTCACATACTTTCCTCTGATTGTTCCCCGCTCTTCACCTATTTTACATATACCTACCCTTTCCTAATTGGTTTTTCTACACTGTCATGCCCAC... | AGATGGGATCCAATCAAAGGCTTTTGCTGAGGGCTGTTTGGTGCCCAAATGAAAACAGTATTATACAACATTCAGATATCACTGATAGCGACAGGAGGCAGCCAAATGCCTAGGCAGATGGGGTGGGTTCCTGGTGAAACCCCACCTCTAAACAAAAGACAGTTTAAAGCCTGAAAGCCAAACTGCAAGTTAAACTCTGGGACCGGATTGAGAACTTATCTTCCCATTTCACATACTTTCCTCTGATTGTTCCCCGCTCTTCACCTATTTTACATATACCTACCCTTTCCTAATTGGTTTTTCTACACTGTCATGCCCAC... |
Task1_train_40885 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GTAGGGGAACCACCCCCCATATCCCCTCTCTGCTGACAGTTGTTCTGTCCTTCAGTAAAATTCTTCTCCACCATCCTTACCCTTCAATGCCCAGCATATCCTCATTCTTCTTGGGTGTGGTACAAAAGCTTGGGAACTGCTGAATGCAGGTACAAGCTATAACAGAGGTGAGCTGGGGCATGCCAGGTGGGCTGTTGCCGGTCAGGGGTCCCCAGCTTCCAAAGTGACTGAGAAGAAAAGTCCTGCATCATTACCCACAAGGTTCCAGCCTTCTTCTCATGAAATTTCTCTCTTTTTTTGAAATTCAAATAGATTTGCAA... | GTAGGGGAACCACCCCCCATATCCCCTCTCTGCTGACAGTTGTTCTGTCCTTCAGTAAAATTCTTCTCCACCATCCTTACCCTTCAATGCCCAGCATATCCTCATTCTTCTTGGGTGTGGTACAAAAGCTTGGGAACTGCTGAATGCAGGTACAAGCTATAACAGAGGTGAGCTGGGGCATGCCAGGTGGGCTGTTGCCGGTCAGGGGTCCCCAGCTTCCAAAGTGACTGAGAAGAAAAGTCCTGCATCATTACCCACAAGGTTCCAGCCTTCTTCTCATGAAATTTCTCTCTTTTTTTGAAATTCAAATAGATTTGCAA... |
Task1_train_40886 | A mutation located on Chromosome 11 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | ACCATCCTTACCCTTCAATGCCCAGCATATCCTCATTCTTCTTGGGTGTGGTACAAAAGCTTGGGAACTGCTGAATGCAGGTACAAGCTATAACAGAGGTGAGCTGGGGCATGCCAGGTGGGCTGTTGCCGGTCAGGGGTCCCCAGCTTCCAAAGTGACTGAGAAGAAAAGTCCTGCATCATTACCCACAAGGTTCCAGCCTTCTTCTCATGAAATTTCTCTCTTTTTTTGAAATTCAAATAGATTTGCAACTTCACCTTTATTTTTGGCAGAAGGAGTAGTGAAGAAAAGAAGGGTTTTCCATCCAATGAATGATTGTT... | ACCATCCTTACCCTTCAATGCCCAGCATATCCTCATTCTTCTTGGGTGTGGTACAAAAGCTTGGGAACTGCTGAATGCAGGTACAAGCTATAACAGAGGTGAGCTGGGGCATGCCAGGTGGGCTGTTGCCGGTCAGGGGTCCCCAGCTTCCAAAGTGACTGAGAAGAAAAGTCCTGCATCATTACCCACAAGGTTCCAGCCTTCTTCTCATGAAATTTCTCTCTTTTTTTGAAATTCAAATAGATTTGCAACTTCACCTTTATTTTTGGCAGAAGGAGTAGTGAAGAAAAGAAGGGTTTTCCATCCAATGAATGATTGTT... |
Task1_train_40887 | Here is a genetic alteration on Chromosome 11. Based on the data, is it a benign variant or a cause of disease? | Benign | GGCTCTCTCTCGTCACACTGAGTTTTCTGAGGGTAGAGATTGAGCCTCTGTTCCTAGCACCTGGCACTGAGCAATTGACTGCTAAATGAATGAATGAGCTAGAAGAGAACAGCAGTATTTATCTCTAATAAGGGAATCCTATCCTAAGGCCAAAAGTAAACCTGAGCCAGGAACCCAGGGCTCTCCTCATGAATCAACCCCTCACAGTGAACGAAGGGAAATAACACAGAAAACAATTTATCTAAACAGTAAAGAGCACCTGTTATTTTTCACCTTTCGTGTACAATACATCTAGATTGCATTCAGTATATTTTAAACTG... | GGCTCTCTCTCGTCACACTGAGTTTTCTGAGGGTAGAGATTGAGCCTCTGTTCCTAGCACCTGGCACTGAGCAATTGACTGCTAAATGAATGAATGAGCTAGAAGAGAACAGCAGTATTTATCTCTAATAAGGGAATCCTATCCTAAGGCCAAAAGTAAACCTGAGCCAGGAACCCAGGGCTCTCCTCATGAATCAACCCCTCACAGTGAACGAAGGGAAATAACACAGAAAACAATTTATCTAAACAGTAAAGAGCACCTGTTATTTTTCACCTTTCGTGTACAATACATCTAGATTGCATTCAGTATATTTTAAACTG... |
Task1_train_40888 | 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 | AGTACTATAAAGGATGGCAAATAGAGGCTAAGGTAGAGCAACGATTTCCTGGGGCAAAAACTACAGTGTGCTCACAAAGATGCAGGAGGGACATTTCAACACTTCCTTCTGCATGGGATTCTGCCACTCCCCCTAATATTCTTCCTCCATCCTTGCCAGAAGACCTAGCTGAAACTGAACCCTTCTTTGTCCTCCATCTTACATTCTGGTTTTTCCTTCTTGGCCTTTCTATATCCACGTTTTCTTGGTTGTTGTCCACTTCTATCAACCTCCTGAAGCCACCCTTTCAGATCCTCAGCCAGCCTGGTAGCAAGAGGAGT... | AGTACTATAAAGGATGGCAAATAGAGGCTAAGGTAGAGCAACGATTTCCTGGGGCAAAAACTACAGTGTGCTCACAAAGATGCAGGAGGGACATTTCAACACTTCCTTCTGCATGGGATTCTGCCACTCCCCCTAATATTCTTCCTCCATCCTTGCCAGAAGACCTAGCTGAAACTGAACCCTTCTTTGTCCTCCATCTTACATTCTGGTTTTTCCTTCTTGGCCTTTCTATATCCACGTTTTCTTGGTTGTTGTCCACTTCTATCAACCTCCTGAAGCCACCCTTTCAGATCCTCAGCCAGCCTGGTAGCAAGAGGAGT... |
Task1_train_40889 | A variant was discovered on Chromosome 11. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GGCATGACCTTGTCCTTAGGCCCTGTGCAGGGAGCATGCAGCCAGCAGAGGTACGCACTCAAACACCGACTGGGAAAATCTTGGGCCAGGCCCCCGCTACAGCCCCTACAAGGCTCACGTTCCTTTTGCTCAGCCAGGCTTGCAGCAGGCCTGGCTCCCTTCCCAGTGGTCCTGAGCCCCTCCCAGGGCTCTATATTTGGGCTATTACCAGAACATGGGTGAATGGCTGGAACCTCCGTACTCAGGGGAGACCCTAGCCCACTAAATTATAGCCCAAAATGAAGGGAGACAGTGAGAGGCCCCAGCACGTGAAGCAGCTG... | GGCATGACCTTGTCCTTAGGCCCTGTGCAGGGAGCATGCAGCCAGCAGAGGTACGCACTCAAACACCGACTGGGAAAATCTTGGGCCAGGCCCCCGCTACAGCCCCTACAAGGCTCACGTTCCTTTTGCTCAGCCAGGCTTGCAGCAGGCCTGGCTCCCTTCCCAGTGGTCCTGAGCCCCTCCCAGGGCTCTATATTTGGGCTATTACCAGAACATGGGTGAATGGCTGGAACCTCCGTACTCAGGGGAGACCCTAGCCCACTAAATTATAGCCCAAAATGAAGGGAGACAGTGAGAGGCCCCAGCACGTGAAGCAGCTG... |
Task1_train_40890 | A mutation located on Chromosome 11 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | ACATCCTCACTTACCCTGTCTGCTAGTTTTCCAAGAGCTCTGCCATTGTTTCAAAAGGTGTGATTACCCTGGCTTTTGAGAAATTCCCAAACCTAAGCATGGGAAAGTTCCTTAGAGGACATCAAGGGAAGACAAGCTCCTACCCACCTTGCAAGAATTACTGTTATGGCATTTATAACAAGTAGCCTTCCAGAGTCTGCTTGAATACTTCCAATGATGGGGAGGTGGAAGGTTTGTTACCCACGGCCCAGCCTTTTTCCATTGCTGGTGAACTCTGACTATGGAAAAATTTTTCCTGTCGATGAAACCTACATTCCTAA... | ACATCCTCACTTACCCTGTCTGCTAGTTTTCCAAGAGCTCTGCCATTGTTTCAAAAGGTGTGATTACCCTGGCTTTTGAGAAATTCCCAAACCTAAGCATGGGAAAGTTCCTTAGAGGACATCAAGGGAAGACAAGCTCCTACCCACCTTGCAAGAATTACTGTTATGGCATTTATAACAAGTAGCCTTCCAGAGTCTGCTTGAATACTTCCAATGATGGGGAGGTGGAAGGTTTGTTACCCACGGCCCAGCCTTTTTCCATTGCTGGTGAACTCTGACTATGGAAAAATTTTTCCTGTCGATGAAACCTACATTCCTAA... |
Task1_train_40891 | A mutation found on Chromosome 11 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CATCCTCACTTACCCTGTCTGCTAGTTTTCCAAGAGCTCTGCCATTGTTTCAAAAGGTGTGATTACCCTGGCTTTTGAGAAATTCCCAAACCTAAGCATGGGAAAGTTCCTTAGAGGACATCAAGGGAAGACAAGCTCCTACCCACCTTGCAAGAATTACTGTTATGGCATTTATAACAAGTAGCCTTCCAGAGTCTGCTTGAATACTTCCAATGATGGGGAGGTGGAAGGTTTGTTACCCACGGCCCAGCCTTTTTCCATTGCTGGTGAACTCTGACTATGGAAAAATTTTTCCTGTCGATGAAACCTACATTCCTAAA... | CATCCTCACTTACCCTGTCTGCTAGTTTTCCAAGAGCTCTGCCATTGTTTCAAAAGGTGTGATTACCCTGGCTTTTGAGAAATTCCCAAACCTAAGCATGGGAAAGTTCCTTAGAGGACATCAAGGGAAGACAAGCTCCTACCCACCTTGCAAGAATTACTGTTATGGCATTTATAACAAGTAGCCTTCCAGAGTCTGCTTGAATACTTCCAATGATGGGGAGGTGGAAGGTTTGTTACCCACGGCCCAGCCTTTTTCCATTGCTGGTGAACTCTGACTATGGAAAAATTTTTCCTGTCGATGAAACCTACATTCCTAAA... |
Task1_train_40892 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TCTTTTAAAAAGATGAACACAAGTAACACTCAAGAGGCTGCCTATGGGTAAGTGTTGGGTCAGGCACTGATGGGCCAGTTTCTCACCTTCAAGATGAGCTCAGAAATCACTTGTTCTCAGTACACCAGTGTTGCCTCCTCTGAGGAGTCTTTTTGTCCAGCCTCTGCCATGTCAGCCAAGTGCTGGGATTCCAGCAGTGCTTGAGAATCCAGCTCACACTCCATGGAAAAGAGGCTCCCAGGGAGTTCTCCCCTGAGTATGCAGTCTATGGAGATGGGCAGGAGGCAGTGATGGGGCAAAAGGATGAAACTAGCATCCAT... | TCTTTTAAAAAGATGAACACAAGTAACACTCAAGAGGCTGCCTATGGGTAAGTGTTGGGTCAGGCACTGATGGGCCAGTTTCTCACCTTCAAGATGAGCTCAGAAATCACTTGTTCTCAGTACACCAGTGTTGCCTCCTCTGAGGAGTCTTTTTGTCCAGCCTCTGCCATGTCAGCCAAGTGCTGGGATTCCAGCAGTGCTTGAGAATCCAGCTCACACTCCATGGAAAAGAGGCTCCCAGGGAGTTCTCCCCTGAGTATGCAGTCTATGGAGATGGGCAGGAGGCAGTGATGGGGCAAAAGGATGAAACTAGCATCCAT... |
Task1_train_40893 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | ATGAGCTCAGAAATCACTTGTTCTCAGTACACCAGTGTTGCCTCCTCTGAGGAGTCTTTTTGTCCAGCCTCTGCCATGTCAGCCAAGTGCTGGGATTCCAGCAGTGCTTGAGAATCCAGCTCACACTCCATGGAAAAGAGGCTCCCAGGGAGTTCTCCCCTGAGTATGCAGTCTATGGAGATGGGCAGGAGGCAGTGATGGGGCAAAAGGATGAAACTAGCATCCATTCAGCACCAGGCAAGGTCCTAGGCACTGTACATGCGCAAGCAGGGTCTAAAAAGTTTAACTGCATAAAATGCAGAGTTACATTATTGTGTGTA... | ATGAGCTCAGAAATCACTTGTTCTCAGTACACCAGTGTTGCCTCCTCTGAGGAGTCTTTTTGTCCAGCCTCTGCCATGTCAGCCAAGTGCTGGGATTCCAGCAGTGCTTGAGAATCCAGCTCACACTCCATGGAAAAGAGGCTCCCAGGGAGTTCTCCCCTGAGTATGCAGTCTATGGAGATGGGCAGGAGGCAGTGATGGGGCAAAAGGATGAAACTAGCATCCATTCAGCACCAGGCAAGGTCCTAGGCACTGTACATGCGCAAGCAGGGTCTAAAAAGTTTAACTGCATAAAATGCAGAGTTACATTATTGTGTGTA... |
Task1_train_40894 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | ATATTCACTTTAGCAATCATAACCTAGTTTTGACTTACATTTTAGCTTGTGGCCCTCTATGAACCCTAGACCCTTCTCTGCCATCACATGGATTATTCTATATCTCCTCAAAAGAACTGGGCCTCAGGGGAAGACATTGAAGCATGATCTGAAGTTGTCAGTACTGAAGCGTAAATGTGAGGCCTTATATTCTATAATAAAGTAAAAATCTGTAAAGCTGCTTTGAAGATATAACTGTGATTACAGATTTAAAGGGGATACCACTATAGAAAAAGTGAGAGAAGGGTAGAGAAAAGAGGATAGAACAGGAGGTTCTGGGG... | ATATTCACTTTAGCAATCATAACCTAGTTTTGACTTACATTTTAGCTTGTGGCCCTCTATGAACCCTAGACCCTTCTCTGCCATCACATGGATTATTCTATATCTCCTCAAAAGAACTGGGCCTCAGGGGAAGACATTGAAGCATGATCTGAAGTTGTCAGTACTGAAGCGTAAATGTGAGGCCTTATATTCTATAATAAAGTAAAAATCTGTAAAGCTGCTTTGAAGATATAACTGTGATTACAGATTTAAAGGGGATACCACTATAGAAAAAGTGAGAGAAGGGTAGAGAAAAGAGGATAGAACAGGAGGTTCTGGGG... |
Task1_train_40895 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | CTTCTACCCTCAAACTTAACTACAGCATTGTCCCCTTCCTGTCCTCCCATCTCAGACGAAGGGACTGTCCTTGTGTTTAAGGTCAACCAGTTCACTCTATATCCTTCCTCCTGCTTTCTCAGTGTACTTACCCCACCACACACCCCTCCTCTCTATCTTCAACCTCTTCTCCCATATACATGTGTGCAAATGTTTTCCAAGCTTAAAAAAAAGTTTCCCCCAACTCTGCCATCTTCTCAGGCTATGTTTTTATTTTTCTTCTTTTCACTTCTGTCTCTACTTCGTCACCACCCATCCTCAGTCTCCTCATTCTAGCTTTT... | CTTCTACCCTCAAACTTAACTACAGCATTGTCCCCTTCCTGTCCTCCCATCTCAGACGAAGGGACTGTCCTTGTGTTTAAGGTCAACCAGTTCACTCTATATCCTTCCTCCTGCTTTCTCAGTGTACTTACCCCACCACACACCCCTCCTCTCTATCTTCAACCTCTTCTCCCATATACATGTGTGCAAATGTTTTCCAAGCTTAAAAAAAAGTTTCCCCCAACTCTGCCATCTTCTCAGGCTATGTTTTTATTTTTCTTCTTTTCACTTCTGTCTCTACTTCGTCACCACCCATCCTCAGTCTCCTCATTCTAGCTTTT... |
Task1_train_40896 | A genomic change on Chromosome 11 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CCCAGGCTAGAGTGCAGTGGTGTGATCATACTCGCTGTACCCTCAACCTCCTGGGCTCAAGCTATCCTCCCTCCTCAGCCTCCCAAGTAGCTGAGACTGCAGGCACATGCCAACACTCCAGCTAATTTTTTAAATTTTTTGTAGAGATGAGGTCTCATTATGTTGCCCAGGCTGTCTCGAACTCCTGGTCTTAAATGATCCTCCCACTTTAGCCTCCCAAAGTGCTGGAATTACAGGTGTAAGCCACCTCACCTGGACTGCATTTTTTTTAAAATAAAAAAGTATATTAAATATAAGAATCACACTTGGTATAACAGACA... | CCCAGGCTAGAGTGCAGTGGTGTGATCATACTCGCTGTACCCTCAACCTCCTGGGCTCAAGCTATCCTCCCTCCTCAGCCTCCCAAGTAGCTGAGACTGCAGGCACATGCCAACACTCCAGCTAATTTTTTAAATTTTTTGTAGAGATGAGGTCTCATTATGTTGCCCAGGCTGTCTCGAACTCCTGGTCTTAAATGATCCTCCCACTTTAGCCTCCCAAAGTGCTGGAATTACAGGTGTAAGCCACCTCACCTGGACTGCATTTTTTTTAAAATAAAAAAGTATATTAAATATAAGAATCACACTTGGTATAACAGACA... |
Task1_train_40897 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CACCTGGACTGCATTTTTTTTAAAATAAAAAAGTATATTAAATATAAGAATCACACTTGGTATAACAGACACAAACTTACCATCTCTACTCCTCATGGAACATGTTCACTGTGTGAAATGGCATACAGAACAGACTGCACTTCTGGAACTGTTTCTCTTTTTCCAAGAGCACAGATTTAAGTTTGCTAAGTTAATTCTTACATGAAGGGACTCCTCCATATATGGTATACGTGTGTATATATTATATATAAATGCAGTGTGGGGTGGAATATGTGTAAAACCTTCAGGCTGATGAACTCTCCCCCCCACTCCCTTTGGTC... | CACCTGGACTGCATTTTTTTTAAAATAAAAAAGTATATTAAATATAAGAATCACACTTGGTATAACAGACACAAACTTACCATCTCTACTCCTCATGGAACATGTTCACTGTGTGAAATGGCATACAGAACAGACTGCACTTCTGGAACTGTTTCTCTTTTTCCAAGAGCACAGATTTAAGTTTGCTAAGTTAATTCTTACATGAAGGGACTCCTCCATATATGGTATACGTGTGTATATATTATATATAAATGCAGTGTGGGGTGGAATATGTGTAAAACCTTCAGGCTGATGAACTCTCCCCCCCACTCCCTTTGGTC... |
Task1_train_40898 | Consider this mutation on Chromosome 11. Is this a benign change or a disease-causing variant? | Benign | AAATGGAAAAAAAAAGATGGCAGAGCCAGAATTCAAACCAGCTCTCCCGAGTGGATATACAGGACCCCATGCACGTACAACCACTATGTTCTAAAGGAGGCACTTGATAAACCCTTATTGAAGGAAATGTTTTGGAATACCAATAAAATGAAAAAAAAATCATCTCAAGAATAATGTAGGGTTTCACTCACTGTTATTCTTTTTTATAAGGGGAAAGCAGGAAATTTGCAAAAGTTAAGTAGCATAGAAGGAGGTCGTATTGGTCGGCTACTACTCACCTGGTACCTGATAATTGCTCATCAAGCCATCTGTTGAGACTA... | AAATGGAAAAAAAAAGATGGCAGAGCCAGAATTCAAACCAGCTCTCCCGAGTGGATATACAGGACCCCATGCACGTACAACCACTATGTTCTAAAGGAGGCACTTGATAAACCCTTATTGAAGGAAATGTTTTGGAATACCAATAAAATGAAAAAAAAATCATCTCAAGAATAATGTAGGGTTTCACTCACTGTTATTCTTTTTTATAAGGGGAAAGCAGGAAATTTGCAAAAGTTAAGTAGCATAGAAGGAGGTCGTATTGGTCGGCTACTACTCACCTGGTACCTGATAATTGCTCATCAAGCCATCTGTTGAGACTA... |
Task1_train_40899 | A mutation on Chromosome 11 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GGGATAGGATTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTGAGACAGGGTCTTACTCTGTCACCCAGGCTAGAGTGCAGTGGAGCAATCATGGCTTACTGCAGCCTTGACTTCCTGGGCAGGTGATCCTCCCACCTGAACCTCCCAAGTAGCTGGGACTACAGGCACATGCCACCACACCCAGCTAATTTTTAATGTTTTTAATAGAGATGGGGTTTTGCTATGTTGCCCAGGCTGGGGGAAAAGATTTTTAATAATTACATTTTTTACTATAAGGTGATAACTGTCATGTCTTTGGTAATTTTTTTTTTTTTTTGA... | GGGATAGGATTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTGAGACAGGGTCTTACTCTGTCACCCAGGCTAGAGTGCAGTGGAGCAATCATGGCTTACTGCAGCCTTGACTTCCTGGGCAGGTGATCCTCCCACCTGAACCTCCCAAGTAGCTGGGACTACAGGCACATGCCACCACACCCAGCTAATTTTTAATGTTTTTAATAGAGATGGGGTTTTGCTATGTTGCCCAGGCTGGGGGAAAAGATTTTTAATAATTACATTTTTTACTATAAGGTGATAACTGTCATGTCTTTGGTAATTTTTTTTTTTTTTTGA... |
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