ID stringlengths 13 17 | question stringlengths 88 1.13k | answer stringlengths 6 156 | reference_sequence stringlengths 4.1k 4.1k | variant_sequence stringlengths 4.1k 4.1k |
|---|---|---|---|---|
Task1_train_40900 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TCTCTAAGGACCTCTACATAGAAGTATATCCAGGGACCTATTCTGTCACTGTGGGCTCAAATGACTTAACCAAGAAGACTCATGTGGTAGCAGTTGATTCTGGACAAAGCGTGGACCTGGTCTTCCCTGTGTGATGTTGACCATCACTGCCATCACATCACCTTTTTTTAAGTAGTAAGAATAAAGCCACTGTATGATTCTCTTAATAGCTATACATTAATCCTGTTTTTAGTGCTGACTGGGTCAGCCTTCCGGGAACTGGAGTCTGTCTCTTTCAGTGCTTTTTTGTTTGTTTGGTTGGTTTTTTTTTGAGACAGTCT... | TCTCTAAGGACCTCTACATAGAAGTATATCCAGGGACCTATTCTGTCACTGTGGGCTCAAATGACTTAACCAAGAAGACTCATGTGGTAGCAGTTGATTCTGGACAAAGCGTGGACCTGGTCTTCCCTGTGTGATGTTGACCATCACTGCCATCACATCACCTTTTTTTAAGTAGTAAGAATAAAGCCACTGTATGATTCTCTTAATAGCTATACATTAATCCTGTTTTTAGTGCTGACTGGGTCAGCCTTCCGGGAACTGGAGTCTGTCTCTTTCAGTGCTTTTTTGTTTGTTTGGTTGGTTTTTTTTTGAGACAGTCT... |
Task1_train_40901 | A genomic variant on Chromosome 11 is under review. What is the biological outcome — benign or pathogenic? | Benign | CAAATGACTTAACCAAGAAGACTCATGTGGTAGCAGTTGATTCTGGACAAAGCGTGGACCTGGTCTTCCCTGTGTGATGTTGACCATCACTGCCATCACATCACCTTTTTTTAAGTAGTAAGAATAAAGCCACTGTATGATTCTCTTAATAGCTATACATTAATCCTGTTTTTAGTGCTGACTGGGTCAGCCTTCCGGGAACTGGAGTCTGTCTCTTTCAGTGCTTTTTTGTTTGTTTGGTTGGTTTTTTTTTGAGACAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAAGTTCCG... | CAAATGACTTAACCAAGAAGACTCATGTGGTAGCAGTTGATTCTGGACAAAGCGTGGACCTGGTCTTCCCTGTGTGATGTTGACCATCACTGCCATCACATCACCTTTTTTTAAGTAGTAAGAATAAAGCCACTGTATGATTCTCTTAATAGCTATACATTAATCCTGTTTTTAGTGCTGACTGGGTCAGCCTTCCGGGAACTGGAGTCTGTCTCTTTCAGTGCTTTTTTGTTTGTTTGGTTGGTTTTTTTTTGAGACAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAAGTTCCG... |
Task1_train_40902 | A mutation on Chromosome 11 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GCTGTGCTGGAGCAAGAGGCATTGGGAGCTATGGAGAATTTAGCATGAAAACTCTAGAGTTCGGTGCCATCTTCTTTATGCCCTCTCTACAAGTGATAATATAAAGAAAATGGTGCCAAACTCTAGAGTTTTCATGCTAAATTCTCCATAACTTCATTTCTTTCGAATGGAGAAAGAAACCGGCATTTCTTTCTTTTCTTTTTTTTTATTTTTGCAGACAGAGTCTCGCTGTGTCGCCCAGGCTGGAGTGTAGTGGCTTACCCTGCCTCCCAGCTTCAACTGATTCTCATACCTCAGCCTCCCAACTAGCTGGGATTACA... | GCTGTGCTGGAGCAAGAGGCATTGGGAGCTATGGAGAATTTAGCATGAAAACTCTAGAGTTCGGTGCCATCTTCTTTATGCCCTCTCTACAAGTGATAATATAAAGAAAATGGTGCCAAACTCTAGAGTTTTCATGCTAAATTCTCCATAACTTCATTTCTTTCGAATGGAGAAAGAAACCGGCATTTCTTTCTTTTCTTTTTTTTTATTTTTGCAGACAGAGTCTCGCTGTGTCGCCCAGGCTGGAGTGTAGTGGCTTACCCTGCCTCCCAGCTTCAACTGATTCTCATACCTCAGCCTCCCAACTAGCTGGGATTACA... |
Task1_train_40903 | A mutation found on Chromosome 11 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CTGCCTCCCAGCTTCAACTGATTCTCATACCTCAGCCTCCCAACTAGCTGGGATTACAGACGTGCATCACAATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACTTTGTTGGTCAGGCTGGTCTCAAACCCCTGACCTCAAGTGATCCACCCCCCACCCCCACCCCCCGGCCTCCCAAAGTGCTGGGTGAGCCACTGTGCCCAGCGAAATCGCCACTTCTGAGTGGCTGCTGCCAAGGCTTGCCATTGCAAGATTGGAGTAACCCATTTCACAGAAGCCCAGGACCCACCTCCCCATTTTATGTTTTCA... | CTGCCTCCCAGCTTCAACTGATTCTCATACCTCAGCCTCCCAACTAGCTGGGATTACAGACGTGCATCACAATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACTTTGTTGGTCAGGCTGGTCTCAAACCCCTGACCTCAAGTGATCCACCCCCCACCCCCACCCCCCGGCCTCCCAAAGTGCTGGGTGAGCCACTGTGCCCAGCGAAATCGCCACTTCTGAGTGGCTGCTGCCAAGGCTTGCCATTGCAAGATTGGAGTAACCCATTTCACAGAAGCCCAGGACCCACCTCCCCATTTTATGTTTTCA... |
Task1_train_40904 | A mutation on Chromosome 11 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CCCATTTTATGTTTTCAATACAAAGTTTCCTCCTGGAGAGTGGAGGAAGAGCACAGCTGGGCCTATGAGAGATAGGGGAAAAATCCTCATATAAAATCCAAGTGCAGCAGACACACTCCTCCCCACCCCTCCCAAAGCCCAGGGGTTCAGAGGAGTCACCAGGAAAGCTTCTCATTACAAACAATTTCTCAACTTCCTGGAACTGAACACTAATAAAATCCTTACCCTTGGGGCAAGATTTAAATCTTCATTGGTGCCAGCTTGGTGGTTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCAGATCACTTA... | CCCATTTTATGTTTTCAATACAAAGTTTCCTCCTGGAGAGTGGAGGAAGAGCACAGCTGGGCCTATGAGAGATAGGGGAAAAATCCTCATATAAAATCCAAGTGCAGCAGACACACTCCTCCCCACCCCTCCCAAAGCCCAGGGGTTCAGAGGAGTCACCAGGAAAGCTTCTCATTACAAACAATTTCTCAACTTCCTGGAACTGAACACTAATAAAATCCTTACCCTTGGGGCAAGATTTAAATCTTCATTGGTGCCAGCTTGGTGGTTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCAGATCACTTA... |
Task1_train_40905 | This is a variant located on Chromosome 11. Is this mutation a likely cause of disease or not? | Benign | CAGAAGAACCCATGAGACAGAACTTCTAGGTCTCTCAAAATAGGGGGAACAGAGCTCATTGCTCTGCAGAGACTATCTGACCCTTTTTCAGAGAACTTTGATGAAGACAGACATATATTTTTCACTTTTCTCTCTGGTTAAGACCACATTTTATTTTTTATTCATCTTTTAAAAAAATTATTATTATTTTGAGATGAGGTCTCTCTCTGTTGCCCAGGCTGGAGTGCAGTGGTGCGATCATGGCTCACTGCGCCCTTCACCTCCTGGGCTCAAGCCTCCCAAGAAGCTGGGACCATATGCAAGTGCCATCAGGCCTGGCT... | CAGAAGAACCCATGAGACAGAACTTCTAGGTCTCTCAAAATAGGGGGAACAGAGCTCATTGCTCTGCAGAGACTATCTGACCCTTTTTCAGAGAACTTTGATGAAGACAGACATATATTTTTCACTTTTCTCTCTGGTTAAGACCACATTTTATTTTTTATTCATCTTTTAAAAAAATTATTATTATTTTGAGATGAGGTCTCTCTCTGTTGCCCAGGCTGGAGTGCAGTGGTGCGATCATGGCTCACTGCGCCCTTCACCTCCTGGGCTCAAGCCTCCCAAGAAGCTGGGACCATATGCAAGTGCCATCAGGCCTGGCT... |
Task1_train_40906 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CTAATAAAGAAAACCAAGTTAAAATGACTATTTTTTTTTTTTTTTGCTTACCAGATTTGCAAAAATGAAAAGGATCAATGATAAATAATCCATGTTAGCAAAGATGTAGGATGCTTCCAACGTTGGAAGCGACATGCATAGGCATGATCTTTTGGGAAAGTAATTTGGCAGTATCTATTAAAGTTTTAAATATGCAAGTTCTTTGAGTCGGCCATTGTACTTTTGCAAGTCTATCCTTCAGAAATATTGGCCATGTGTACAAAGAATGATATTCATTGAGCACTATTTGCCATATAAAAATTAGCAATAACTTCTATGTT... | CTAATAAAGAAAACCAAGTTAAAATGACTATTTTTTTTTTTTTTTGCTTACCAGATTTGCAAAAATGAAAAGGATCAATGATAAATAATCCATGTTAGCAAAGATGTAGGATGCTTCCAACGTTGGAAGCGACATGCATAGGCATGATCTTTTGGGAAAGTAATTTGGCAGTATCTATTAAAGTTTTAAATATGCAAGTTCTTTGAGTCGGCCATTGTACTTTTGCAAGTCTATCCTTCAGAAATATTGGCCATGTGTACAAAGAATGATATTCATTGAGCACTATTTGCCATATAAAAATTAGCAATAACTTCTATGTT... |
Task1_train_40907 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | TTTTTTTTTTTTTGCTTACCAGATTTGCAAAAATGAAAAGGATCAATGATAAATAATCCATGTTAGCAAAGATGTAGGATGCTTCCAACGTTGGAAGCGACATGCATAGGCATGATCTTTTGGGAAAGTAATTTGGCAGTATCTATTAAAGTTTTAAATATGCAAGTTCTTTGAGTCGGCCATTGTACTTTTGCAAGTCTATCCTTCAGAAATATTGGCCATGTGTACAAAGAATGATATTCATTGAGCACTATTTGCCATATAAAAATTAGCAATAACTTCTATGTTCACCAGTAGGGGTAGGGCTAATCAATACTGGT... | TTTTTTTTTTTTTGCTTACCAGATTTGCAAAAATGAAAAGGATCAATGATAAATAATCCATGTTAGCAAAGATGTAGGATGCTTCCAACGTTGGAAGCGACATGCATAGGCATGATCTTTTGGGAAAGTAATTTGGCAGTATCTATTAAAGTTTTAAATATGCAAGTTCTTTGAGTCGGCCATTGTACTTTTGCAAGTCTATCCTTCAGAAATATTGGCCATGTGTACAAAGAATGATATTCATTGAGCACTATTTGCCATATAAAAATTAGCAATAACTTCTATGTTCACCAGTAGGGGTAGGGCTAATCAATACTGGT... |
Task1_train_40908 | This is a variant located on Chromosome 11. Is this mutation a likely cause of disease or not? | Benign | TTTGAGCTCTTTTCTGCAAATACCGAAAATCATTTCTAAAAGGAACTATCCTAAGCTTGTCTCCACTGTACCATCCAGAGCTCAGAAAACATCAGCAAGCCTGGTCTTTATGAAGTCCTAACACCATCAAATAGACCAGGACTAGAAGACAGACAGACAGACACACACACACACACACACACACACACACACACACACACACACAGCCTTGTCTATGCCACATGCTGCCTTCTGGATAAAAAGCCTTTCTAATTAACACACCTGACACTTCTTTACACCCACTTCCTCCCTCAGCAGCAAGAGGGAATGTCACTGGTAAC... | TTTGAGCTCTTTTCTGCAAATACCGAAAATCATTTCTAAAAGGAACTATCCTAAGCTTGTCTCCACTGTACCATCCAGAGCTCAGAAAACATCAGCAAGCCTGGTCTTTATGAAGTCCTAACACCATCAAATAGACCAGGACTAGAAGACAGACAGACAGACACACACACACACACACACACACACACACACACACACACACACAGCCTTGTCTATGCCACATGCTGCCTTCTGGATAAAAAGCCTTTCTAATTAACACACCTGACACTTCTTTACACCCACTTCCTCCCTCAGCAGCAAGAGGGAATGTCACTGGTAAC... |
Task1_train_40909 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CCAAGGGAAAAATTATAACTTTCCAGTTAAGAAACCACAGACACCATCTTAACCAAGTAAGCAGATTAGTATCACCAAAAATGAGACAAAATGACATCATATGCCTGCCTCCTGTAATCATGAAAACTGACAGTATGTGCCTCCTAATATAATGCACTGAGAGAAGCACATCACTTCTATGGTATTTTAGGCAAAAATTTATAATCTGAATCTAATCATGAAAACATCAGACAAAACCAAATTAAGGGACAGTCTATAAAATAACTTGCTTGTACTCTTCAAAAATGTCTATGTCATGAAAGACAAAAGCTGAGAAACTC... | CCAAGGGAAAAATTATAACTTTCCAGTTAAGAAACCACAGACACCATCTTAACCAAGTAAGCAGATTAGTATCACCAAAAATGAGACAAAATGACATCATATGCCTGCCTCCTGTAATCATGAAAACTGACAGTATGTGCCTCCTAATATAATGCACTGAGAGAAGCACATCACTTCTATGGTATTTTAGGCAAAAATTTATAATCTGAATCTAATCATGAAAACATCAGACAAAACCAAATTAAGGGACAGTCTATAAAATAACTTGCTTGTACTCTTCAAAAATGTCTATGTCATGAAAGACAAAAGCTGAGAAACTC... |
Task1_train_40910 | With a mutation on Chromosome 11, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CAGCTAAAGTACTTTTCAACTTTGACAACTAATAACAGTCATGGGTGAAGGTAAAACTGACAGAGTACTTTAGATCAGCTATGTCCTACAGTCAAGGAATCAAGGGCATTACCCATTTACCAAGCAGCAAAAAGCACTTTCATTTTTCCAGAACTATTTAAATACAGTAGTTGCCATGTGATCAGTTAATTTTACTTTGTGAGTTAGATAAAGTAAAGACTAAATTGGGAAACTGCAATAAGTAATCAAAAGTAGCTCCAAACAACAAAGCCATCAATAGAAACAAAAGGCATTTTTCTAGGTGTATCATGCATAAAAAG... | CAGCTAAAGTACTTTTCAACTTTGACAACTAATAACAGTCATGGGTGAAGGTAAAACTGACAGAGTACTTTAGATCAGCTATGTCCTACAGTCAAGGAATCAAGGGCATTACCCATTTACCAAGCAGCAAAAAGCACTTTCATTTTTCCAGAACTATTTAAATACAGTAGTTGCCATGTGATCAGTTAATTTTACTTTGTGAGTTAGATAAAGTAAAGACTAAATTGGGAAACTGCAATAAGTAATCAAAAGTAGCTCCAAACAACAAAGCCATCAATAGAAACAAAAGGCATTTTTCTAGGTGTATCATGCATAAAAAG... |
Task1_train_40911 | Here is a genetic alteration on Chromosome 11. Based on the data, is it a benign variant or a cause of disease? | Benign | GCCCAAGCCAGGCCATGGGAAGAGTCCAGTGAGGATGCCGCTGGCGCCCATGTTGGTACCAGGCATCAGCAGTGCCATCGCTCCTGCTGTCACTCAACACTGCATATTACTGCCACCGGCAAGATGAATTCTCTACTGGCTCTGCTTCTTTGTGCCAGGTGCTTCAGAGTCAAAGTTCCAGAAGGAGCATCTACATAGCCAAGCCCAGCTTGTGCCTCCACCATACCCTAGCTGCCAAGGGGTGGGAGGGCAGGTGTCTGGCCTGTGGATTCTATAGCGGGAAATGAGCCCTACCTTCCATCAAGTCTTCTACTATGGCA... | GCCCAAGCCAGGCCATGGGAAGAGTCCAGTGAGGATGCCGCTGGCGCCCATGTTGGTACCAGGCATCAGCAGTGCCATCGCTCCTGCTGTCACTCAACACTGCATATTACTGCCACCGGCAAGATGAATTCTCTACTGGCTCTGCTTCTTTGTGCCAGGTGCTTCAGAGTCAAAGTTCCAGAAGGAGCATCTACATAGCCAAGCCCAGCTTGTGCCTCCACCATACCCTAGCTGCCAAGGGGTGGGAGGGCAGGTGTCTGGCCTGTGGATTCTATAGCGGGAAATGAGCCCTACCTTCCATCAAGTCTTCTACTATGGCA... |
Task1_train_40912 | Here is a genetic alteration on Chromosome 11. Based on the data, is it a benign variant or a cause of disease? | Benign | ATCGGCCCAGACAGTTTAAAGAGGACAGGGGATGGACTCACTACAAGGACAACAGATATTCATAAATTTTCTTACAACTTGAATAGAAAATAAATAATTAGCATTATTGTATTTTATCAACTTTAATATGTCATCAATTCTAAGACGCACTGTTATTTTATTGCCTAACAATAAAAACTGCTTATCAATTAAAAAACTGCCATTTAAACTATGACACTATTCTTTCTGATCACATCAATTGTAAGATGCATTGCAATTTCAAAGATACTAGTTGTCAGCCAGGCGCAGTGGTTCACGTCTGTAATCCCAGCACTTAGGAA... | ATCGGCCCAGACAGTTTAAAGAGGACAGGGGATGGACTCACTACAAGGACAACAGATATTCATAAATTTTCTTACAACTTGAATAGAAAATAAATAATTAGCATTATTGTATTTTATCAACTTTAATATGTCATCAATTCTAAGACGCACTGTTATTTTATTGCCTAACAATAAAAACTGCTTATCAATTAAAAAACTGCCATTTAAACTATGACACTATTCTTTCTGATCACATCAATTGTAAGATGCATTGCAATTTCAAAGATACTAGTTGTCAGCCAGGCGCAGTGGTTCACGTCTGTAATCCCAGCACTTAGGAA... |
Task1_train_40913 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | CATAAAAAAGAAGAAAGTGTGGGAAGTGGTTAAGAATAGTAGGATGAAGTGAATCTTTTAGAAAGAAAAGCTGAGCAAGTCCAAAGGTGAGGAAAAATGGTTAACTTTTGAAATATGTACAGCAGTATTTGCTCAAAATGTTTAATATTATCTGTCAAGCCAAGACTGGCCCCAAGAAGAGTAGGAGGAGGGTCTGTGTGTTCACATTTTGGTACCTGTTTGTGACAATGCTGTTGCTTCCGCTCTCCCAGTCACCTGGCGCTGATGTTCTTAGGAGCTTGTTTTTACTTGTGTCGAGTGGAACTAGCAGGTTCACCATG... | CATAAAAAAGAAGAAAGTGTGGGAAGTGGTTAAGAATAGTAGGATGAAGTGAATCTTTTAGAAAGAAAAGCTGAGCAAGTCCAAAGGTGAGGAAAAATGGTTAACTTTTGAAATATGTACAGCAGTATTTGCTCAAAATGTTTAATATTATCTGTCAAGCCAAGACTGGCCCCAAGAAGAGTAGGAGGAGGGTCTGTGTGTTCACATTTTGGTACCTGTTTGTGACAATGCTGTTGCTTCCGCTCTCCCAGTCACCTGGCGCTGATGTTCTTAGGAGCTTGTTTTTACTTGTGTCGAGTGGAACTAGCAGGTTCACCATG... |
Task1_train_40914 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GAAAATGGAACCTGCAATCCAAAACCAGCCAAGAATTTCCCAAGGGATAGGAGCTGAGGAAAACTGAATAGAAGGCAGCTTTGGCCCTAACTCAGTTGCCCCAGATCTAGCCTTGGTGCTGCTTAGCAAGGCCCTTAACTCTTAGGGACCCAGGTTTGTGAACCCTCTGAAATTATGTATGTGTATGTCTGTGTGTGGAGGGGTGTTTTTCTAGGAAAAACATCCACAGCTTTCAACAATTTCTCAGAGTTCCATGATCCAAAGAGGTTAGGGATCATTGGATGGGGTGATTCTTGCAAAGGTGATGTCTTCCTGCTCAG... | GAAAATGGAACCTGCAATCCAAAACCAGCCAAGAATTTCCCAAGGGATAGGAGCTGAGGAAAACTGAATAGAAGGCAGCTTTGGCCCTAACTCAGTTGCCCCAGATCTAGCCTTGGTGCTGCTTAGCAAGGCCCTTAACTCTTAGGGACCCAGGTTTGTGAACCCTCTGAAATTATGTATGTGTATGTCTGTGTGTGGAGGGGTGTTTTTCTAGGAAAAACATCCACAGCTTTCAACAATTTCTCAGAGTTCCATGATCCAAAGAGGTTAGGGATCATTGGATGGGGTGATTCTTGCAAAGGTGATGTCTTCCTGCTCAG... |
Task1_train_40915 | A mutation has occurred on Chromosome 11. What is the medical relevance of this mutation? | Benign | GCCCTTTGGATCTCCATATCCCAAACCCATGGGATCAAGATGTTGTAGAACTTGGCAGTCTTGTGGGTGGGGAGATGCCCTTCCCTTGAATGTCTAAGTGACAGGTGTCTATGTTGTCTTGTTTTATGTTTCCTGAGGATATACTCTGAAAGAACTTTTAATTATAAAGCATTGTAAGCAGGAAGAATTTAATATAAAAGCCTGTCTTCACTGACAGCAGGGGTGCATCTTTGCTGATCTTTTATTATCTTATATTTTAGGAATGCTTTTAGTCTTGGGGCAGCTGTTTGGGGGAGTTGCCCAGGATTTAAGAGCTACAT... | GCCCTTTGGATCTCCATATCCCAAACCCATGGGATCAAGATGTTGTAGAACTTGGCAGTCTTGTGGGTGGGGAGATGCCCTTCCCTTGAATGTCTAAGTGACAGGTGTCTATGTTGTCTTGTTTTATGTTTCCTGAGGATATACTCTGAAAGAACTTTTAATTATAAAGCATTGTAAGCAGGAAGAATTTAATATAAAAGCCTGTCTTCACTGACAGCAGGGGTGCATCTTTGCTGATCTTTTATTATCTTATATTTTAGGAATGCTTTTAGTCTTGGGGCAGCTGTTTGGGGGAGTTGCCCAGGATTTAAGAGCTACAT... |
Task1_train_40916 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | GGTCAGTGGTGGAGCCACACGGTCACTCCAGGGTCCACACTTTCCATAGGGACACTGTGCTGCCTCCATTACAAGATGTCATCTCCCCACTGTGATAATAAGGGAAGAGCTGGCCAACACTGAGCCCACCTCCTGACTCAGAGCCCGGGGTTATTTTCACCACACCTGTATGAGCAAAGTCAAGAATGTCTTCAGGCTTTCTTCTCCTCCTGATGAGCCAGGAAGCTTGGGCTCTCTGGAAACACCCTCTTGATTTGCTTATCAGCCACAGAACTCTCTGTGGCCTCTCTGTGTCCCTTCCCTGGTGGCCACTCTGGGAA... | GGTCAGTGGTGGAGCCACACGGTCACTCCAGGGTCCACACTTTCCATAGGGACACTGTGCTGCCTCCATTACAAGATGTCATCTCCCCACTGTGATAATAAGGGAAGAGCTGGCCAACACTGAGCCCACCTCCTGACTCAGAGCCCGGGGTTATTTTCACCACACCTGTATGAGCAAAGTCAAGAATGTCTTCAGGCTTTCTTCTCCTCCTGATGAGCCAGGAAGCTTGGGCTCTCTGGAAACACCCTCTTGATTTGCTTATCAGCCACAGAACTCTCTGTGGCCTCTCTGTGTCCCTTCCCTGGTGGCCACTCTGGGAA... |
Task1_train_40917 | 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 | CCAGGGATTCAGTTTCAAGTAGGTTTCACATGGCCCTAACTTCCTCACCCAAGATACTATTTAAATTCCCTGCTTTGTCACTTGGTGGCTGGGTGAGCTTGGACGAGTCATTTAACATCCCCTAGCCCCACTGTCCTCACCTGGAGCAGTAAGGTAAAGATACATCCCCCATGGCATTCTGTGAGGGGGCATGTGAAATCCCTCGTGGAAAGCCTCAGATGCACCATGTTGCAAGGGGGCCGGTGATTCCCCCGCTGCACTCTGACATGGGGTCCCAAGCAGACGGGAGCTGACCATGGAGGTCAAGAGCAGAGCCTCCA... | CCAGGGATTCAGTTTCAAGTAGGTTTCACATGGCCCTAACTTCCTCACCCAAGATACTATTTAAATTCCCTGCTTTGTCACTTGGTGGCTGGGTGAGCTTGGACGAGTCATTTAACATCCCCTAGCCCCACTGTCCTCACCTGGAGCAGTAAGGTAAAGATACATCCCCCATGGCATTCTGTGAGGGGGCATGTGAAATCCCTCGTGGAAAGCCTCAGATGCACCATGTTGCAAGGGGGCCGGTGATTCCCCCGCTGCACTCTGACATGGGGTCCCAAGCAGACGGGAGCTGACCATGGAGGTCAAGAGCAGAGCCTCCA... |
Task1_train_40918 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | ATTGAGACTAGAAGTTATCTTTAATGGTTCTGACCAAGAAGGGCTTATTCGTGGTTACCTCAAATCTCATATCAGCCAACAGGCCTGATTACTATTGTTCAAACTCAGGCCAGATGGGACTCAAGACAAGTTGGAAAAAGGAAGACGTCAGGCTCTGACATACAGGGGTTGGGAAACTGAGCCAGGAGTAGAGTGGTCTCCAAAGGTGTGGCAGAGACCCCTATTGCTCACTGACACCTGGGTGCTCCTCCATATTTCCCTGCACCCCTTGCAGTCAGGAGGGTGCAAATCGATGAGATGAGAGAGGACATGGCCTCTGC... | ATTGAGACTAGAAGTTATCTTTAATGGTTCTGACCAAGAAGGGCTTATTCGTGGTTACCTCAAATCTCATATCAGCCAACAGGCCTGATTACTATTGTTCAAACTCAGGCCAGATGGGACTCAAGACAAGTTGGAAAAAGGAAGACGTCAGGCTCTGACATACAGGGGTTGGGAAACTGAGCCAGGAGTAGAGTGGTCTCCAAAGGTGTGGCAGAGACCCCTATTGCTCACTGACACCTGGGTGCTCCTCCATATTTCCCTGCACCCCTTGCAGTCAGGAGGGTGCAAATCGATGAGATGAGAGAGGACATGGCCTCTGC... |
Task1_train_40919 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | ATGGCCTCTGCCACTTCCCGGGGAAGGCAGGTGACTATCCAGTGTGTCTCCTTAGGTGCACTTCTACTCCCCACCCCACCATCTGCTGGATGTTTAAGCCAGGGTGAACTTGAAGTTCAAAGATGCTGAACCCACAAGAGAAGCAATCAGAGTCCCCAAGTCACTACTTGGAGAAAAGCTGCACAGGAGAGCCTCCCAGCCAGCCTTCAGGGGACTGTGTGAGCAAAATAGGACATTTCCTGGGTAACCTCTATTTCCAGCAGTTCTGAGAGCTGCTGTTTCAGTCTGTGATGCTGCCAGTATGTAAAGAGGCAAGGTGA... | ATGGCCTCTGCCACTTCCCGGGGAAGGCAGGTGACTATCCAGTGTGTCTCCTTAGGTGCACTTCTACTCCCCACCCCACCATCTGCTGGATGTTTAAGCCAGGGTGAACTTGAAGTTCAAAGATGCTGAACCCACAAGAGAAGCAATCAGAGTCCCCAAGTCACTACTTGGAGAAAAGCTGCACAGGAGAGCCTCCCAGCCAGCCTTCAGGGGACTGTGTGAGCAAAATAGGACATTTCCTGGGTAACCTCTATTTCCAGCAGTTCTGAGAGCTGCTGTTTCAGTCTGTGATGCTGCCAGTATGTAAAGAGGCAAGGTGA... |
Task1_train_40920 | 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 | GCAAACTAAGGTTCAGGGTCACAGGATAATTTAGAAGCACAGTAAGATATGGATCCAAGAGCCTGCCTTTTGGAAGACAGGAAGTCATTATGGTTCAGAGCATAGCCTCTGGGGCCAAACAGTCTTGGTGTCAAGTCCTACATTTCCCATTTGCTGAACTGGTGACTTTAGGCAATTCACTTCACCTTCCAACACTCAGTTTCCTTGTCTATGAAATGGAGATAAAAGTGATAAATTCCAAAGATAGTTGCTGTGAGAATTAAATGAAGTAATACACAGAGACAGTTTATTTCATCACCTGGAAGAAGTTTAGAGGCCCC... | GCAAACTAAGGTTCAGGGTCACAGGATAATTTAGAAGCACAGTAAGATATGGATCCAAGAGCCTGCCTTTTGGAAGACAGGAAGTCATTATGGTTCAGAGCATAGCCTCTGGGGCCAAACAGTCTTGGTGTCAAGTCCTACATTTCCCATTTGCTGAACTGGTGACTTTAGGCAATTCACTTCACCTTCCAACACTCAGTTTCCTTGTCTATGAAATGGAGATAAAAGTGATAAATTCCAAAGATAGTTGCTGTGAGAATTAAATGAAGTAATACACAGAGACAGTTTATTTCATCACCTGGAAGAAGTTTAGAGGCCCC... |
Task1_train_40921 | This is a variant located on Chromosome 11. Is this mutation a likely cause of disease or not? | Benign | GTGAGCCATAGGCAGGAAATTGAAACTGGACTCCTTCCTTACACCATAAACAAAAATTAACTTAAGACAGATTAAAGACTTCAATGTAAAACCCGAAACTATACAAAACCTTAGAAAAAAATCTAGGCAATATTATTTAGGACATAGGTACAGGCACAGATTTCATGATGAAATTCCAAAAGCAATTGCAACAAAAGCAAAAATTGACAAATGGATCTAATTAAACTAAAGGGCTTCCACACAGCAAAAGAAACTATCATCAGAATGACCAGACAGCCTACAGAATGGGAGAAAATTTTTACAATCTATCCACCTGACAA... | GTGAGCCATAGGCAGGAAATTGAAACTGGACTCCTTCCTTACACCATAAACAAAAATTAACTTAAGACAGATTAAAGACTTCAATGTAAAACCCGAAACTATACAAAACCTTAGAAAAAAATCTAGGCAATATTATTTAGGACATAGGTACAGGCACAGATTTCATGATGAAATTCCAAAAGCAATTGCAACAAAAGCAAAAATTGACAAATGGATCTAATTAAACTAAAGGGCTTCCACACAGCAAAAGAAACTATCATCAGAATGACCAGACAGCCTACAGAATGGGAGAAAATTTTTACAATCTATCCACCTGACAA... |
Task1_train_40922 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | ACCTGATTCTGAGGAGGCTCTCAGTAGATATCTGTTGAGTAACCAGAATGTAGGGTGGTCCTGATGGTTTCTGACATTGAATAGAAAACAGCTCCCTATTTGATCTTAAAATAATCACTATAACCTGGACATACTGTACTAGATGCTGTTTTTGTCTGACTTCTACTCTGTCAATCTCTTTGCACCTCCATTTGTTCATCTGTGAAATGAAGAAAATGCTCATGGAGTTCAGTGAAGATTAAATGAATGAATATAGGTAGACTGCCTAATCTGGCACTTGCCACGCAGCTGACTTCAATATAGTAGCTCTAATATTATGG... | ACCTGATTCTGAGGAGGCTCTCAGTAGATATCTGTTGAGTAACCAGAATGTAGGGTGGTCCTGATGGTTTCTGACATTGAATAGAAAACAGCTCCCTATTTGATCTTAAAATAATCACTATAACCTGGACATACTGTACTAGATGCTGTTTTTGTCTGACTTCTACTCTGTCAATCTCTTTGCACCTCCATTTGTTCATCTGTGAAATGAAGAAAATGCTCATGGAGTTCAGTGAAGATTAAATGAATGAATATAGGTAGACTGCCTAATCTGGCACTTGCCACGCAGCTGACTTCAATATAGTAGCTCTAATATTATGG... |
Task1_train_40923 | A mutation is present on Chromosome 11. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GGGGACCTCTCTGGGCAGCAGGATCTCCCCATCTTGGTCACGGCTCCCCACGAAGGTCGGCTTGCACACATACACCAGGCTGTGGCTGGGGAGAGATGGGACAAAGCCAGGCTCTAAACGTGGGAGCCTGCCCAGGCCGAAAGCTAAGGCGCCCTGACTCTGTGGGGCTCCCAGCCTCACCTTCATGCCCCCTCCTCTCCTGTCTCTTCAACAGAGACACTTCACTTCCCGTCAACATCTATCTTAAAATGATGGCTGAGGGAGGCTCACTTTGGGAGAATGTGCTGGTGGGGGGCAGCTTCCCCTCCTCCAGCGCAGGC... | GGGGACCTCTCTGGGCAGCAGGATCTCCCCATCTTGGTCACGGCTCCCCACGAAGGTCGGCTTGCACACATACACCAGGCTGTGGCTGGGGAGAGATGGGACAAAGCCAGGCTCTAAACGTGGGAGCCTGCCCAGGCCGAAAGCTAAGGCGCCCTGACTCTGTGGGGCTCCCAGCCTCACCTTCATGCCCCCTCCTCTCCTGTCTCTTCAACAGAGACACTTCACTTCCCGTCAACATCTATCTTAAAATGATGGCTGAGGGAGGCTCACTTTGGGAGAATGTGCTGGTGGGGGGCAGCTTCCCCTCCTCCAGCGCAGGC... |
Task1_train_40924 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TCACCCTGCTACTGAGTGGCAGAGGAGGACCTGAGCCCAGGACAACTGCGAAGCACCGTTGGGTGGAGGGGGTATTGCCTCTCACATCCTCATCCGCCACTCATACAGTGCTGAGATTTAGGATTTCCATCTTCCCTCTCTGCCCCCACATTGCGTGAGAAGCAAGACAGCCCAGACAGACTGCCAGCAAAGCTCAGGGCTCTTTGCCTCTTTGTCCCTGCATGGCATCCTAACAAGCTCAAAGCATAACGGACAAGCTAGAACTTGGCGATGCCTGGAGCTTGTCCCGGGTTTCTGTGAAACCACAGTGCTGGAATACC... | TCACCCTGCTACTGAGTGGCAGAGGAGGACCTGAGCCCAGGACAACTGCGAAGCACCGTTGGGTGGAGGGGGTATTGCCTCTCACATCCTCATCCGCCACTCATACAGTGCTGAGATTTAGGATTTCCATCTTCCCTCTCTGCCCCCACATTGCGTGAGAAGCAAGACAGCCCAGACAGACTGCCAGCAAAGCTCAGGGCTCTTTGCCTCTTTGTCCCTGCATGGCATCCTAACAAGCTCAAAGCATAACGGACAAGCTAGAACTTGGCGATGCCTGGAGCTTGTCCCGGGTTTCTGTGAAACCACAGTGCTGGAATACC... |
Task1_train_40925 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | CTTAAGACAGGAGACTTTCAGCATATTTAAATATAGACAGGAAAGATTCAGTAGACAAATGAGGACACAAGAATGACACTGTGGAGAGGGAGGAGGGAAGTGAGAGGGAGCCAAGTTCAGGTGAAGGCTCCATCTTGAAGAGGAAAAATGACACCTGTTCTCTGGACACTGTCCCTGGAGATGAGGTCACCTAGCTAGTTAGTGGCCAAGACAGAGCTGGGCGCATTCACTCATGAACTCATTCAGCAGACACTCACTGAACGCCTACCGTTCACCAGGTACCACCCTAGCAACAAATGAAACAGACAAAAATCACTGCT... | CTTAAGACAGGAGACTTTCAGCATATTTAAATATAGACAGGAAAGATTCAGTAGACAAATGAGGACACAAGAATGACACTGTGGAGAGGGAGGAGGGAAGTGAGAGGGAGCCAAGTTCAGGTGAAGGCTCCATCTTGAAGAGGAAAAATGACACCTGTTCTCTGGACACTGTCCCTGGAGATGAGGTCACCTAGCTAGTTAGTGGCCAAGACAGAGCTGGGCGCATTCACTCATGAACTCATTCAGCAGACACTCACTGAACGCCTACCGTTCACCAGGTACCACCCTAGCAACAAATGAAACAGACAAAAATCACTGCT... |
Task1_train_40926 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CTCACTGTAACCTCCCTCTCTTGTGTGCTCTTAAAATCTCAAACGACTCTTCCTGTCTGAGAGCCTCTTGGCACACATATGAGAAGAAAGAGCCCATCTCATTAGTCGTGGATGTCTATCCTGTCTGTGCCCATGGCTAAAGGTCTAGCATCTTGTGGGAAGAAAGCTCAGGTGGTTTATTGACTGAGTGATTTAACACAGCCCAGCTCCCAACCACAATGGTTTTAGGATGCTCTTTGGAGGCAGATGAGCATTTCTAAGAAATGTTCTGGAAATGCCCTGATACACCTCTCAAGAGCATCATCGCATGAGTCTGAAAC... | CTCACTGTAACCTCCCTCTCTTGTGTGCTCTTAAAATCTCAAACGACTCTTCCTGTCTGAGAGCCTCTTGGCACACATATGAGAAGAAAGAGCCCATCTCATTAGTCGTGGATGTCTATCCTGTCTGTGCCCATGGCTAAAGGTCTAGCATCTTGTGGGAAGAAAGCTCAGGTGGTTTATTGACTGAGTGATTTAACACAGCCCAGCTCCCAACCACAATGGTTTTAGGATGCTCTTTGGAGGCAGATGAGCATTTCTAAGAAATGTTCTGGAAATGCCCTGATACACCTCTCAAGAGCATCATCGCATGAGTCTGAAAC... |
Task1_train_40927 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | AGGTGAGTGTCCCTGAGGGTCCTGCCCAGGTGTCAGGAAGCTAACCTACCTGTACTCTTCCCACCTTCCACACTTATCTCTGGATTCCACGTGCTCATAGGTCAACCTAAGTGCAAAGCCAGCGCCAGAAGATACTCTGTCAAGGGTCTACCCCAGCTGCCTTCATGTATACCTTTCACAAAAGCTCCTGCTGTTCCTTCACAGCCATCCCTGAGGACACAGTCATTCCCTCAGCAAACTTTACAGGGTTTAGACTCCATGCCAGGTCTCCATGAGATACAGAGCTGCTAGGACACCTTTCCCTTGAGAACTTGCAAAGG... | AGGTGAGTGTCCCTGAGGGTCCTGCCCAGGTGTCAGGAAGCTAACCTACCTGTACTCTTCCCACCTTCCACACTTATCTCTGGATTCCACGTGCTCATAGGTCAACCTAAGTGCAAAGCCAGCGCCAGAAGATACTCTGTCAAGGGTCTACCCCAGCTGCCTTCATGTATACCTTTCACAAAAGCTCCTGCTGTTCCTTCACAGCCATCCCTGAGGACACAGTCATTCCCTCAGCAAACTTTACAGGGTTTAGACTCCATGCCAGGTCTCCATGAGATACAGAGCTGCTAGGACACCTTTCCCTTGAGAACTTGCAAAGG... |
Task1_train_40928 | This sequence change occurs on Chromosome 11. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CCCAGGTGTCAGGAAGCTAACCTACCTGTACTCTTCCCACCTTCCACACTTATCTCTGGATTCCACGTGCTCATAGGTCAACCTAAGTGCAAAGCCAGCGCCAGAAGATACTCTGTCAAGGGTCTACCCCAGCTGCCTTCATGTATACCTTTCACAAAAGCTCCTGCTGTTCCTTCACAGCCATCCCTGAGGACACAGTCATTCCCTCAGCAAACTTTACAGGGTTTAGACTCCATGCCAGGTCTCCATGAGATACAGAGCTGCTAGGACACCTTTCCCTTGAGAACTTGCAAAGGGCATTGAGGAATTTGCAGCTGTAG... | CCCAGGTGTCAGGAAGCTAACCTACCTGTACTCTTCCCACCTTCCACACTTATCTCTGGATTCCACGTGCTCATAGGTCAACCTAAGTGCAAAGCCAGCGCCAGAAGATACTCTGTCAAGGGTCTACCCCAGCTGCCTTCATGTATACCTTTCACAAAAGCTCCTGCTGTTCCTTCACAGCCATCCCTGAGGACACAGTCATTCCCTCAGCAAACTTTACAGGGTTTAGACTCCATGCCAGGTCTCCATGAGATACAGAGCTGCTAGGACACCTTTCCCTTGAGAACTTGCAAAGGGCATTGAGGAATTTGCAGCTGTAG... |
Task1_train_40929 | 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 | TCCTTCACAGCCATCCCTGAGGACACAGTCATTCCCTCAGCAAACTTTACAGGGTTTAGACTCCATGCCAGGTCTCCATGAGATACAGAGCTGCTAGGACACCTTTCCCTTGAGAACTTGCAAAGGGCATTGAGGAATTTGCAGCTGTAGGATGGCAGGCACAGAAGTGAGGGTCCCTTTGGTAGGGTCCAAGAACCTTGGAAGCAACATCTCCCTTGAATATAAAATGTCATCATTGGTATGCAGGCTGGACTCTTTCCTTCTGTATGTATTTATCAAGCCTCTGTTACCTGCCAGGCCTGTTCTAGACTCTGGAAAGT... | TCCTTCACAGCCATCCCTGAGGACACAGTCATTCCCTCAGCAAACTTTACAGGGTTTAGACTCCATGCCAGGTCTCCATGAGATACAGAGCTGCTAGGACACCTTTCCCTTGAGAACTTGCAAAGGGCATTGAGGAATTTGCAGCTGTAGGATGGCAGGCACAGAAGTGAGGGTCCCTTTGGTAGGGTCCAAGAACCTTGGAAGCAACATCTCCCTTGAATATAAAATGTCATCATTGGTATGCAGGCTGGACTCTTTCCTTCTGTATGTATTTATCAAGCCTCTGTTACCTGCCAGGCCTGTTCTAGACTCTGGAAAGT... |
Task1_train_40930 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | ACCAGGAAATGCGTCTGGGGGCGCCAGGAAAGATGAGAAGATAAAGTCACGATGCGTCCAGCTAGCTATAGACACAAGCAGAGGAGCCAGTAGGCCAAAGGAGACGCACAGCTGATCCGTGCCGAGGCGCGGGCTCCACTCCCTGAAGTGGAGGGACCCTTGAATCTTTCCTTGCGTAGGCGCGCGGCAGAGCAGCGATTTGGCGAAAAGGGCCGAGACTCAGGATGCCTGCAATGCGAGCGAGGGGCGGACAGGGCGCACGGGGCGCGGCAAGGCTGCGAGGGGCGGGCCTGGGCCCTGAGCCTCCTGCACTTCCAGCC... | ACCAGGAAATGCGTCTGGGGGCGCCAGGAAAGATGAGAAGATAAAGTCACGATGCGTCCAGCTAGCTATAGACACAAGCAGAGGAGCCAGTAGGCCAAAGGAGACGCACAGCTGATCCGTGCCGAGGCGCGGGCTCCACTCCCTGAAGTGGAGGGACCCTTGAATCTTTCCTTGCGTAGGCGCGCGGCAGAGCAGCGATTTGGCGAAAAGGGCCGAGACTCAGGATGCCTGCAATGCGAGCGAGGGGCGGACAGGGCGCACGGGGCGCGGCAAGGCTGCGAGGGGCGGGCCTGGGCCCTGAGCCTCCTGCACTTCCAGCC... |
Task1_train_40931 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TCTACTTGCTCCCTGCCATCTAATCACATCTTAGTTTTACCCTGAGAAGTTGGTGTTTTCCTTTTTTGTACTTTAGTCAAACATATCAAAAGGGAGCAAACGCCTCATTTTATTGTTCCTAGTTTTTCTTTTGCGCCATCCCTTTCAGCCTACTGGCTCACCAGATTCCAAAAATATACCTTCTCAATAATGACAGTAATGATGGAAATAACGATGGTGATAACATGCTTGTTGAGCCTCTCGCTGTGCTAAGTGTGTGACCTGCTGTATCTCATTTTCTGCATCTCCCTTAGCATAGCTGACCAGAGAGCTGAGCACAT... | TCTACTTGCTCCCTGCCATCTAATCACATCTTAGTTTTACCCTGAGAAGTTGGTGTTTTCCTTTTTTGTACTTTAGTCAAACATATCAAAAGGGAGCAAACGCCTCATTTTATTGTTCCTAGTTTTTCTTTTGCGCCATCCCTTTCAGCCTACTGGCTCACCAGATTCCAAAAATATACCTTCTCAATAATGACAGTAATGATGGAAATAACGATGGTGATAACATGCTTGTTGAGCCTCTCGCTGTGCTAAGTGTGTGACCTGCTGTATCTCATTTTCTGCATCTCCCTTAGCATAGCTGACCAGAGAGCTGAGCACAT... |
Task1_train_40932 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | AGTATATGTCAGGGATGTTTTATTCAATGGGGTTTCAGAGCAGCAGTCTGGACTAGGGAGCAGGCCTGGCAGCCAGGCCTTGGGTGGCAGCAGACCCTGGGGACCATCAAATCCTTGGCCTCTCTGGTGTGTTCAGATTGGCCTATCTCCAAGCATGTGTTGGGGATTAGGGCAAGTTACTGGTTTGGGTCCGACTGGTATTCACATCTGAGCTGGGGACCAGGATAGCATCTGCAACCACGTTGAGATTAAGGAGACGGGATTGATTGAGATATTTCCCCACTAATGATCCTATAGCTTCTTAGCAACGAGCTTGATCT... | AGTATATGTCAGGGATGTTTTATTCAATGGGGTTTCAGAGCAGCAGTCTGGACTAGGGAGCAGGCCTGGCAGCCAGGCCTTGGGTGGCAGCAGACCCTGGGGACCATCAAATCCTTGGCCTCTCTGGTGTGTTCAGATTGGCCTATCTCCAAGCATGTGTTGGGGATTAGGGCAAGTTACTGGTTTGGGTCCGACTGGTATTCACATCTGAGCTGGGGACCAGGATAGCATCTGCAACCACGTTGAGATTAAGGAGACGGGATTGATTGAGATATTTCCCCACTAATGATCCTATAGCTTCTTAGCAACGAGCTTGATCT... |
Task1_train_40933 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | ATTATTGCCTAAACAATACAGTATAACAACTATTTACATAGCATTTACATTGTATTAGGTATTATATGTAATCTTGCAATCTAGAAATGATTTAAAGTATGTGCGTAGGTTATATGCAAATACACCATTTTATATAAGGGACTGAGTATTTTGGTATCTGTGGGGCTTCCTGGCACCAGTCCTCCATGGATACCAAGGAATGACTACATACATATACTGTAAACATATATATATATTAAAAGAATGAAAAATAAAGACCAGGAAACAGTGACTGTTGGGGACTAGACTGTGCACTAGACTGTGTTGGGGAGAAAGATGTG... | ATTATTGCCTAAACAATACAGTATAACAACTATTTACATAGCATTTACATTGTATTAGGTATTATATGTAATCTTGCAATCTAGAAATGATTTAAAGTATGTGCGTAGGTTATATGCAAATACACCATTTTATATAAGGGACTGAGTATTTTGGTATCTGTGGGGCTTCCTGGCACCAGTCCTCCATGGATACCAAGGAATGACTACATACATATACTGTAAACATATATATATATTAAAAGAATGAAAAATAAAGACCAGGAAACAGTGACTGTTGGGGACTAGACTGTGCACTAGACTGTGTTGGGGAGAAAGATGTG... |
Task1_train_40934 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | ACTCATTTTCTCCCTGGAAGGCTGGAGTGAGGTAGGGACTGGAGCAGCCCAGCCCATGGAGAGCAGAGCAGAGAGGCAGGCGAACTCAGCAAACCAAGTCACTGAGAAAGGGGATAGAAAATTGGGAGGAGGGGGAGGGAGCACAGCAGCCTGTCTGGAAGCACCTCTCTGATACACAGCCCACACCCAGTGCTAAAATCTGCCTTCCTGCGCTCCTTGCCTGCAGTAAGCCCACCCTATTCCCCACACTTCTTGCCTTTGCCCCTCCCCGCCTTACATAAACTCAGCCGCCTCTTGCACTCCCCAGAATGTCAACTTCC... | ACTCATTTTCTCCCTGGAAGGCTGGAGTGAGGTAGGGACTGGAGCAGCCCAGCCCATGGAGAGCAGAGCAGAGAGGCAGGCGAACTCAGCAAACCAAGTCACTGAGAAAGGGGATAGAAAATTGGGAGGAGGGGGAGGGAGCACAGCAGCCTGTCTGGAAGCACCTCTCTGATACACAGCCCACACCCAGTGCTAAAATCTGCCTTCCTGCGCTCCTTGCCTGCAGTAAGCCCACCCTATTCCCCACACTTCTTGCCTTTGCCCCTCCCCGCCTTACATAAACTCAGCCGCCTCTTGCACTCCCCAGAATGTCAACTTCC... |
Task1_train_40935 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GCAGTGGCCACCTACAATCCAATCTCCTCACAGTGATCGTTCTAAAAACACACACCAAATCATGCCATTTCCCTGCTTAAAACCCTCCAATGACGTTTCACTGGGCTTAGAATAAAGTATGAAAATTCCTCACCCCGGCTCACAAAGCTTTGCGGCATTTACCTTTCTCCTACCTGTGACCTCTCCTCATGCCACTTTCTCCCTTGTGCACCACATTCCAGCCTTCCTGCTCCTTAAACTCCAAGCTCTTTTCTGCCTTAAGCCCTTGCCCTGGCTGTTCGCTCTTCCCGAAATGCTTTGCCAACTCATCATCACATGAT... | GCAGTGGCCACCTACAATCCAATCTCCTCACAGTGATCGTTCTAAAAACACACACCAAATCATGCCATTTCCCTGCTTAAAACCCTCCAATGACGTTTCACTGGGCTTAGAATAAAGTATGAAAATTCCTCACCCCGGCTCACAAAGCTTTGCGGCATTTACCTTTCTCCTACCTGTGACCTCTCCTCATGCCACTTTCTCCCTTGTGCACCACATTCCAGCCTTCCTGCTCCTTAAACTCCAAGCTCTTTTCTGCCTTAAGCCCTTGCCCTGGCTGTTCGCTCTTCCCGAAATGCTTTGCCAACTCATCATCACATGAT... |
Task1_train_40936 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TATAAAGATTAGCCAACTGTGGTGGCACATGCCTGTAGCCCCAGCTACTTGGGAAGCTAAGGTGGGAGGATCAACTCAGCCCAGGTGTCAAGGCTACAGTGAGCCAAGTGAGCCAAATGAGCCAACACTGCATCACTGCACTCCAGCCAGGGTAATAGAGCGAGACCGTTTCTCAAAAAGTAGAAATAAAAATAGTCCAGGCAGCCGGGCGCAGTGGTTCACGCCTGTAATCCCAGCACTTTGGAAGGCTGAGGCAGGTGGATCACAAGGTCAGGATATTGAGACCATCCTGGCTAACATGGTGAAATCCTGTCTCTACT... | TATAAAGATTAGCCAACTGTGGTGGCACATGCCTGTAGCCCCAGCTACTTGGGAAGCTAAGGTGGGAGGATCAACTCAGCCCAGGTGTCAAGGCTACAGTGAGCCAAGTGAGCCAAATGAGCCAACACTGCATCACTGCACTCCAGCCAGGGTAATAGAGCGAGACCGTTTCTCAAAAAGTAGAAATAAAAATAGTCCAGGCAGCCGGGCGCAGTGGTTCACGCCTGTAATCCCAGCACTTTGGAAGGCTGAGGCAGGTGGATCACAAGGTCAGGATATTGAGACCATCCTGGCTAACATGGTGAAATCCTGTCTCTACT... |
Task1_train_40937 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GTATTCCACGGGACTTGGGCCCAAAGTCCAGTAATTCTGTGATTTTTGCAGACTCTTAAAAGTACCACCTTGGTGGTCTTGGATAAGATCCAGAAGAATTCTCTAGATTACCAGGCAGAGACTCTTGTTCTTTTCCCTTACTTTCTTCCAAACAAATGGTCTCTCTCTCTGTGCTGAGCCACCTGGAACTGGAGGTGTGGTGATGCAAGTACCTTTATGGCCATCACCACGGAACTGTGCTGGGTCAAGCCTGAAGCCAACATGGCACTGGGCCTTGCCCAAGGCCCTTTCCTTCATGGTGGCGAGTTCCCCCAGATCCT... | GTATTCCACGGGACTTGGGCCCAAAGTCCAGTAATTCTGTGATTTTTGCAGACTCTTAAAAGTACCACCTTGGTGGTCTTGGATAAGATCCAGAAGAATTCTCTAGATTACCAGGCAGAGACTCTTGTTCTTTTCCCTTACTTTCTTCCAAACAAATGGTCTCTCTCTCTGTGCTGAGCCACCTGGAACTGGAGGTGTGGTGATGCAAGTACCTTTATGGCCATCACCACGGAACTGTGCTGGGTCAAGCCTGAAGCCAACATGGCACTGGGCCTTGCCCAAGGCCCTTTCCTTCATGGTGGCGAGTTCCCCCAGATCCT... |
Task1_train_40938 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CAGCATTTTTAAAGAGTAGGCATCCTGTGTTTTTTGTCTTATCTGGCTACAGGAGCAGTGATGCATAGCTGTGAGGGTATGGTAGAAGCCAGTTAGCATAAGGTGTGGTGGGGATAAAAGGGTGCTGGGCCCAACTCTGTATGATTTTTTTTCCCTGACAGCTTCCCCAGCCAGCAGATTGTTGCTGGATCAAGTGGGCATGAAAGAGAATGAAGACAAATATATGTGTGAGTCAAGTGGGTTCTACCCAGAGGCTATTAATATAACATGGGAGAAGCAGACCCAGAAGTTTCCCCATCCCATAGAGATTTCTGAGGATG... | CAGCATTTTTAAAGAGTAGGCATCCTGTGTTTTTTGTCTTATCTGGCTACAGGAGCAGTGATGCATAGCTGTGAGGGTATGGTAGAAGCCAGTTAGCATAAGGTGTGGTGGGGATAAAAGGGTGCTGGGCCCAACTCTGTATGATTTTTTTTCCCTGACAGCTTCCCCAGCCAGCAGATTGTTGCTGGATCAAGTGGGCATGAAAGAGAATGAAGACAAATATATGTGTGAGTCAAGTGGGTTCTACCCAGAGGCTATTAATATAACATGGGAGAAGCAGACCCAGAAGTTTCCCCATCCCATAGAGATTTCTGAGGATG... |
Task1_train_40939 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | TCCATCCCCTGACACATGCACAGTAAGGGGAACAAAGCCACATGGAGTAACTCAAGCTAAGGGCTTGCATGCACACTACGAGGATGGGGTGGAGCTACCAGAAATGTGTGCCTTATGCCTTTGTATTCAGCTGTGAAATGGCAACCCTCTTTTGGGCCCCCTCTCTGCAGTGGAGTGCTTTCTTCTTTTGCTTATTAAACTTTCACTTCAACTTCATCTTTGGGGTCCGCGCTCCTTAATTTTCTTGGTCATGAGACAAAGAACTTCAGGTGATACCTTGGGCAATGAGAGACTGCTACATTGTGGTGCATTGACGAGAC... | TCCATCCCCTGACACATGCACAGTAAGGGGAACAAAGCCACATGGAGTAACTCAAGCTAAGGGCTTGCATGCACACTACGAGGATGGGGTGGAGCTACCAGAAATGTGTGCCTTATGCCTTTGTATTCAGCTGTGAAATGGCAACCCTCTTTTGGGCCCCCTCTCTGCAGTGGAGTGCTTTCTTCTTTTGCTTATTAAACTTTCACTTCAACTTCATCTTTGGGGTCCGCGCTCCTTAATTTTCTTGGTCATGAGACAAAGAACTTCAGGTGATACCTTGGGCAATGAGAGACTGCTACATTGTGGTGCATTGACGAGAC... |
Task1_train_40940 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | ATGATGAGGGTGGGGGGTGACCCACCCTTCTAAGACCACCCTGGAGGCTGTGTGGCAGATGGACTACAGTGGGTGAGATGGAGACAAGGGGACCAGGTCACAGGCATTGCCACAGCCCCTAAAATCGTGGTCTCAGCTAGGAGGGGACACCGTGTGGAAAGAAAGACCTGGCAAAGAAACATGACCAAGGGCAAAATAAAAGCACCGTCTCTCTTTAACACTTGTTTGGCCGTTTCCTCAGCATGTAGCTGATTCAGCAGCAATCACAATAGTTAACATTTATTGAGCACTTACTGTAGACCAGGCACTTCAGCATTTTA... | ATGATGAGGGTGGGGGGTGACCCACCCTTCTAAGACCACCCTGGAGGCTGTGTGGCAGATGGACTACAGTGGGTGAGATGGAGACAAGGGGACCAGGTCACAGGCATTGCCACAGCCCCTAAAATCGTGGTCTCAGCTAGGAGGGGACACCGTGTGGAAAGAAAGACCTGGCAAAGAAACATGACCAAGGGCAAAATAAAAGCACCGTCTCTCTTTAACACTTGTTTGGCCGTTTCCTCAGCATGTAGCTGATTCAGCAGCAATCACAATAGTTAACATTTATTGAGCACTTACTGTAGACCAGGCACTTCAGCATTTTA... |
Task1_train_40941 | A genetic alteration is present on Chromosome 11. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | CTGCTGGGCCCCTGGGGAAATCTCAGAGCTGGAAAGGCTGGGTTCTGCCTCCTGGTGCAGCCTTGAGGCCTTACCTCCCTCCCTGCTGCTCACCCTTCTGAGAGGCTGAGTCTCCCACCTGAAAGGCTCAGCCTCCCCTTTTGCTCCATCCTGCACTTGCTTATAGTCATCTCCACCAAATACTGAACTTGTCAAGTCGCTTTCTTGCTCAAAACCCTTCTCCCTTTTTGTCCATGGGCATAGCCCACACTCCTTGCTCTGGCATTCAGGGCTCTCTGATATGATGCCCTCCCCACTGCTGTAATCTCTCTCCCACCTCC... | CTGCTGGGCCCCTGGGGAAATCTCAGAGCTGGAAAGGCTGGGTTCTGCCTCCTGGTGCAGCCTTGAGGCCTTACCTCCCTCCCTGCTGCTCACCCTTCTGAGAGGCTGAGTCTCCCACCTGAAAGGCTCAGCCTCCCCTTTTGCTCCATCCTGCACTTGCTTATAGTCATCTCCACCAAATACTGAACTTGTCAAGTCGCTTTCTTGCTCAAAACCCTTCTCCCTTTTTGTCCATGGGCATAGCCCACACTCCTTGCTCTGGCATTCAGGGCTCTCTGATATGATGCCCTCCCCACTGCTGTAATCTCTCTCCCACCTCC... |
Task1_train_40942 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | GAAGATGCCCCCTTGGCATGGGGGACTCGCAATCTCTGTCTCACAAGGATCCCTGACTGTACCCGCTGTACCCTGCAGGAGGAGCCAGACCCTGAACTGACCAGTTGTGTGACCTGGGGCAAGACACCTGACCTCTCTGGGCCCCCGTATAGTGAGAAGTAGGACTAAATGGTCCTGCCAGGCTTCAGACTCCAAACTTGGGGCAAACCTGAGACACGGGCTTCTGTCTGCCATCCTTACAGGGTCCTTGAGTGCCCAACCAACCCAGCTGCATAGCCAGGAGTAGTTACCGAGGCCTCCTGGCAGTGCCTTCACCACCA... | GAAGATGCCCCCTTGGCATGGGGGACTCGCAATCTCTGTCTCACAAGGATCCCTGACTGTACCCGCTGTACCCTGCAGGAGGAGCCAGACCCTGAACTGACCAGTTGTGTGACCTGGGGCAAGACACCTGACCTCTCTGGGCCCCCGTATAGTGAGAAGTAGGACTAAATGGTCCTGCCAGGCTTCAGACTCCAAACTTGGGGCAAACCTGAGACACGGGCTTCTGTCTGCCATCCTTACAGGGTCCTTGAGTGCCCAACCAACCCAGCTGCATAGCCAGGAGTAGTTACCGAGGCCTCCTGGCAGTGCCTTCACCACCA... |
Task1_train_40943 | A genomic change on Chromosome 11 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GGTGCTGGGGGCCGGGCTGGGCTCAGCCACCAGGCATGGGCCACAGCTAGTATCCGAAAGTGCCACCCCATCCCCAGGCTCCCTTGTGGCCCCCAACCCAGACACACTCCTCCTTGGACTCTTCCCCACCCCTCTCCCTGAGCCTCTCACCCAGGAGCCCCTCGTAGCTCTCTGCCTCGGTTTTCAGGAGCCCATGGATGCGCTTCACAGCCCCCAGCTGGAGCTCCATGTCTGCCAGGTTCCTCACCATCCAGTTGAGGTAGTTGGAGACCTGTGGGGAGCAAGCCAGTGGCGCACACTCCATGGTCGCTTAGTTCTGT... | GGTGCTGGGGGCCGGGCTGGGCTCAGCCACCAGGCATGGGCCACAGCTAGTATCCGAAAGTGCCACCCCATCCCCAGGCTCCCTTGTGGCCCCCAACCCAGACACACTCCTCCTTGGACTCTTCCCCACCCCTCTCCCTGAGCCTCTCACCCAGGAGCCCCTCGTAGCTCTCTGCCTCGGTTTTCAGGAGCCCATGGATGCGCTTCACAGCCCCCAGCTGGAGCTCCATGTCTGCCAGGTTCCTCACCATCCAGTTGAGGTAGTTGGAGACCTGTGGGGAGCAAGCCAGTGGCGCACACTCCATGGTCGCTTAGTTCTGT... |
Task1_train_40944 | With a mutation on Chromosome 11, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CTCTCCAGCATTTGTTGTTTCCTGACTTTTTAACGATCACCATTCTAACGGGTGTGAGATGGTATCTCATTGTGGTTTTGATTTTTACATGAATCTTTCATCAACTAGTTTCAAGTGCTTCTTGGAAGTAGGTGGGTATAAATAACAGATTCGTGATTGACTGAGCCTGGGGTTCTGGCTCTTTAATTAAGACAGTGATCTTTGCCCAGAAACCAACATTTATTGGTTACATCTGGATCTTCAGAACACCCACTTATGGTGTGTAGGTCAGTGCAGCTCAGGACCAAGCTGGAAACCAATGTTGGTGTTGCAATTTCCCA... | CTCTCCAGCATTTGTTGTTTCCTGACTTTTTAACGATCACCATTCTAACGGGTGTGAGATGGTATCTCATTGTGGTTTTGATTTTTACATGAATCTTTCATCAACTAGTTTCAAGTGCTTCTTGGAAGTAGGTGGGTATAAATAACAGATTCGTGATTGACTGAGCCTGGGGTTCTGGCTCTTTAATTAAGACAGTGATCTTTGCCCAGAAACCAACATTTATTGGTTACATCTGGATCTTCAGAACACCCACTTATGGTGTGTAGGTCAGTGCAGCTCAGGACCAAGCTGGAAACCAATGTTGGTGTTGCAATTTCCCA... |
Task1_train_40945 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | TCACAACCCTGAGGGGCTGGGGGTGGTTTGGAGGTGAGGACCCACTGGGCTGGGAGCTGTGTAGGGAAGGGAGCCCCTCTTCCTGGGAAAAAAGGCAGAAGTCCGACACAGCAGGCCCAAGTTTTGGGCCTTAGAGGACCATGCTGGGAGTAGCAAGGGGAGGCCGGGCACTCACCACCGCCTGGTACTTGCTGGCTGGGCCCTGAGGTGTGGGCTCATGGGGGGCACACTGCTCCTCACGGATCTCTGCACTGGACAGGAACTCGCTTAGCTTTTGCACGCTGCTCGGGAAGCACAGAGACACCCCTCACCCCTGCCAG... | TCACAACCCTGAGGGGCTGGGGGTGGTTTGGAGGTGAGGACCCACTGGGCTGGGAGCTGTGTAGGGAAGGGAGCCCCTCTTCCTGGGAAAAAAGGCAGAAGTCCGACACAGCAGGCCCAAGTTTTGGGCCTTAGAGGACCATGCTGGGAGTAGCAAGGGGAGGCCGGGCACTCACCACCGCCTGGTACTTGCTGGCTGGGCCCTGAGGTGTGGGCTCATGGGGGGCACACTGCTCCTCACGGATCTCTGCACTGGACAGGAACTCGCTTAGCTTTTGCACGCTGCTCGGGAAGCACAGAGACACCCCTCACCCCTGCCAG... |
Task1_train_40946 | A variant was discovered on Chromosome 11. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | AGGATCACCAGCAGCCCTGTGAGGCAGAAGCGTAGCTGCGAGAAGCCGATGGCGTGGTCCAAGAACTTGACAAACTTGATGGTCTTGGTGATGAAGGCCAGGGTCCAATACACCAGCAGGGCTGCCGAGGAGAGATGGAAGATCGCAGAGACGTGTGTGCATCATGTGTGTACACTCACATAATGTGTGCAAGTATGTGGCAGAGAAGGAGACAGAATAAGCGTGCCTGGGTGTGTACATTTCCGAGTAAGTGGATGTGCACGTGTGAATATATCAGAGTACATGACTCTAAGATGACGCACGTACGTCTTAACATTCAT... | AGGATCACCAGCAGCCCTGTGAGGCAGAAGCGTAGCTGCGAGAAGCCGATGGCGTGGTCCAAGAACTTGACAAACTTGATGGTCTTGGTGATGAAGGCCAGGGTCCAATACACCAGCAGGGCTGCCGAGGAGAGATGGAAGATCGCAGAGACGTGTGTGCATCATGTGTGTACACTCACATAATGTGTGCAAGTATGTGGCAGAGAAGGAGACAGAATAAGCGTGCCTGGGTGTGTACATTTCCGAGTAAGTGGATGTGCACGTGTGAATATATCAGAGTACATGACTCTAAGATGACGCACGTACGTCTTAACATTCAT... |
Task1_train_40947 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ATAGGTTTCTCCTGTGAATGAAGAGTTGGTAAATGGGTCTTGTGGCTAGTTAGACAGTACTTTTGTTTCCCTTTCCTGAAATTTTGCTGGGTTCAAGGTTGCCAAATTCCAGGTTGGCTAGGGGTCCCTGTACCAGGAAAACTGGGAAAGTGGTCAAGGCTGCTGGAGCCCGCCATCTTTTCTTGCACTCCCAGTTTTCCTCCTCTCTTGGCTTCTGTTTCCACTTGGTTCCTGCTCCCCACCAAAAAAATAAAGCAGATGTTTGTTTATATTCTATCCTGTCTGGGAGAAAGGAACTTGGAGTCACTCACTCTAAGATT... | ATAGGTTTCTCCTGTGAATGAAGAGTTGGTAAATGGGTCTTGTGGCTAGTTAGACAGTACTTTTGTTTCCCTTTCCTGAAATTTTGCTGGGTTCAAGGTTGCCAAATTCCAGGTTGGCTAGGGGTCCCTGTACCAGGAAAACTGGGAAAGTGGTCAAGGCTGCTGGAGCCCGCCATCTTTTCTTGCACTCCCAGTTTTCCTCCTCTCTTGGCTTCTGTTTCCACTTGGTTCCTGCTCCCCACCAAAAAAATAAAGCAGATGTTTGTTTATATTCTATCCTGTCTGGGAGAAAGGAACTTGGAGTCACTCACTCTAAGATT... |
Task1_train_40948 | A mutation located on Chromosome 11 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GCCGGGCGTGGGAGTCTGAGCGGGCCAGGCAGGTGGTGGTGGTGGGCGGGGTGTGTACTGGCTGCCCTCCCACTCTCTCCTTTTGGATTCTGTGCCCAGATGCCTTTGAGATCCGTAGGCTGTCCTCCGTGTTCCTGCGGGTGAGGACGAACGTGGGCGTGCGGGTGCTCTACGACCGTGAAGGGCTCCGACTGTACCTGCAAGTGGACCAGCGATGGGTGGAGGATACCGTGGGCCTCTGCGGCACCTTCAATGGCAACACGCAGGATGACTTCCTGTACGTAGCCCTGCCACGGAACCCGAAGAAGAGGGGAAATGGG... | GCCGGGCGTGGGAGTCTGAGCGGGCCAGGCAGGTGGTGGTGGTGGGCGGGGTGTGTACTGGCTGCCCTCCCACTCTCTCCTTTTGGATTCTGTGCCCAGATGCCTTTGAGATCCGTAGGCTGTCCTCCGTGTTCCTGCGGGTGAGGACGAACGTGGGCGTGCGGGTGCTCTACGACCGTGAAGGGCTCCGACTGTACCTGCAAGTGGACCAGCGATGGGTGGAGGATACCGTGGGCCTCTGCGGCACCTTCAATGGCAACACGCAGGATGACTTCCTGTACGTAGCCCTGCCACGGAACCCGAAGAAGAGGGGAAATGGG... |
Task1_train_40949 | A genomic change on Chromosome 11 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | ATTACTTTTCCCTGTGTCCTTATGCACCTGGTTGGCTGAGGGTGGGGTCCCTGTCCTTGGCAGTCTCTGCCCTAGCTCCTGAGCCTGCTCACCTTTCTTTGCTCCCATTTTTTTATAGGAACCAGTGCTCCTGCCACTTCCAGGGAGTGGACTATCCCCCCGGAGACAGTGACATCCCATCCCTGGGCCACTGGTGAGCTCCGTAGGTAGCAGCCTTCTTGTCCTCTCTTTAAAGGGAGGCTGCTGACTGAAGACAGTGCAGCTGATGGAACTTTCTGTGAAGGGACACCCAGCCCTGCTCTGTGCAGGGAGGGGGAAGT... | ATTACTTTTCCCTGTGTCCTTATGCACCTGGTTGGCTGAGGGTGGGGTCCCTGTCCTTGGCAGTCTCTGCCCTAGCTCCTGAGCCTGCTCACCTTTCTTTGCTCCCATTTTTTTATAGGAACCAGTGCTCCTGCCACTTCCAGGGAGTGGACTATCCCCCCGGAGACAGTGACATCCCATCCCTGGGCCACTGGTGAGCTCCGTAGGTAGCAGCCTTCTTGTCCTCTCTTTAAAGGGAGGCTGCTGACTGAAGACAGTGCAGCTGATGGAACTTTCTGTGAAGGGACACCCAGCCCTGCTCTGTGCAGGGAGGGGGAAGT... |
Task1_train_40950 | A variant was discovered on Chromosome 11. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GGTGGGGATGGTGAGGATGATGGTGGTGGTGATGGTGATAATGCAATGGTGATGGTGGTGGTGATGGTGAGGATGATGGTGGTGGTGATGGTGAGGATGGTGGTGGTGGTGATGGTGATAATGCAATGATGGTGGTGGTGGGGACAGTGAGGGTGATGGTGATAATGCAGTGACGATGGTGATGGTGGTGATAATGCAATGACAATGGTGGTAGTGGGGAAGGTGAGGATGATGGTGGTGGTGAAGATGATAATGGCAATGATGATGATGATGTTGATGACAATCATGACGGTAGCTAATGTTTACTGAGAGCTTACTAA... | GGTGGGGATGGTGAGGATGATGGTGGTGGTGATGGTGATAATGCAATGGTGATGGTGGTGGTGATGGTGAGGATGATGGTGGTGGTGATGGTGAGGATGGTGGTGGTGGTGATGGTGATAATGCAATGATGGTGGTGGTGGGGACAGTGAGGGTGATGGTGATAATGCAGTGACGATGGTGATGGTGGTGATAATGCAATGACAATGGTGGTAGTGGGGAAGGTGAGGATGATGGTGGTGGTGAAGATGATAATGGCAATGATGATGATGATGTTGATGACAATCATGACGGTAGCTAATGTTTACTGAGAGCTTACTAA... |
Task1_train_40951 | A genomic change on Chromosome 11 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | ACATAAATTCTCCCGTAGTCAGACGCCCTGGTCTTGGAGGAGCCTCCTGGGTGGGATTCAGGCCTCCAGGGTCCCTGACAGTCCCCGTTAGTCCCGCCTCTCCTCCACGGGTTAGTGTCCACTGTCGCCCAGGTACTCCTCTCGGAAGCCCACTGCACTGGAGGCAGGCAGCCGCATTGCTATGTCCAGCAATGTCCCTTCTGCTAGATGGCCTGATCTCTGGGGGCAAGGGAGGGGGAGGGCCCCTGCTCCCCACGTCTGGCACAGGCTATTGGGCCTGCAGTGCATGCTGGGTAGTGAGCTGTATCCCCTGGGCTTGC... | ACATAAATTCTCCCGTAGTCAGACGCCCTGGTCTTGGAGGAGCCTCCTGGGTGGGATTCAGGCCTCCAGGGTCCCTGACAGTCCCCGTTAGTCCCGCCTCTCCTCCACGGGTTAGTGTCCACTGTCGCCCAGGTACTCCTCTCGGAAGCCCACTGCACTGGAGGCAGGCAGCCGCATTGCTATGTCCAGCAATGTCCCTTCTGCTAGATGGCCTGATCTCTGGGGGCAAGGGAGGGGGAGGGCCCCTGCTCCCCACGTCTGGCACAGGCTATTGGGCCTGCAGTGCATGCTGGGTAGTGAGCTGTATCCCCTGGGCTTGC... |
Task1_train_40952 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | GATTTTGGTTTCTTCCAGCAGGTGCTGAAAGAGGTAGGAGGGAGCTCTGAACTGGAACCTTGTGAGAGAGAGTGCGTTGGTTCTTTGTGAGTAGTAACTGTTCAGGCAGTACGGGCCTGAGTGCTATCCGGTGTGGGATTGCTTTCTGGCCTGTGTGTCTGATACAGGCCTTTAGGACAGTGGGTGGTGGGCCAGTGTCCTTGGGCTTGCTCCCATATGGATCACCTCTGGGCCATCTGACTGCTCCATCTCTGTGGTTTGTTTGGTCACCTTGGCAAGTCAAGCTCCGAGTGCATGGAGATATCCTTCTTCCCATTCCT... | GATTTTGGTTTCTTCCAGCAGGTGCTGAAAGAGGTAGGAGGGAGCTCTGAACTGGAACCTTGTGAGAGAGAGTGCGTTGGTTCTTTGTGAGTAGTAACTGTTCAGGCAGTACGGGCCTGAGTGCTATCCGGTGTGGGATTGCTTTCTGGCCTGTGTGTCTGATACAGGCCTTTAGGACAGTGGGTGGTGGGCCAGTGTCCTTGGGCTTGCTCCCATATGGATCACCTCTGGGCCATCTGACTGCTCCATCTCTGTGGTTTGTTTGGTCACCTTGGCAAGTCAAGCTCCGAGTGCATGGAGATATCCTTCTTCCCATTCCT... |
Task1_train_40953 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | TGTGAGTAGTAACTGTTCAGGCAGTACGGGCCTGAGTGCTATCCGGTGTGGGATTGCTTTCTGGCCTGTGTGTCTGATACAGGCCTTTAGGACAGTGGGTGGTGGGCCAGTGTCCTTGGGCTTGCTCCCATATGGATCACCTCTGGGCCATCTGACTGCTCCATCTCTGTGGTTTGTTTGGTCACCTTGGCAAGTCAAGCTCCGAGTGCATGGAGATATCCTTCTTCCCATTCCTCAAGTTCTTGGAGACTGTACTGGCCTCTATTGGTCCTGAGAGGTGGGGAACCAAGGGATTTGCTGGCCAGGGCAGCCATGTTTCT... | TGTGAGTAGTAACTGTTCAGGCAGTACGGGCCTGAGTGCTATCCGGTGTGGGATTGCTTTCTGGCCTGTGTGTCTGATACAGGCCTTTAGGACAGTGGGTGGTGGGCCAGTGTCCTTGGGCTTGCTCCCATATGGATCACCTCTGGGCCATCTGACTGCTCCATCTCTGTGGTTTGTTTGGTCACCTTGGCAAGTCAAGCTCCGAGTGCATGGAGATATCCTTCTTCCCATTCCTCAAGTTCTTGGAGACTGTACTGGCCTCTATTGGTCCTGAGAGGTGGGGAACCAAGGGATTTGCTGGCCAGGGCAGCCATGTTTCT... |
Task1_train_40954 | A mutation on Chromosome 11 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CACCAAGCCTGGCTAATTTTTGTATTTTTAGCAGAGACAGGGTTTCACCATGTTAGCCAGACTGACTTTGAACTCCTGACCTCAGGTAATCTGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTATAGGTGTGAGCCACAGCACCTGGCTGTAAAACATATATCTTATACCCAATAATGCTTAACAATGGAACTCTAGGATTATTCCTACTAAAATCAGGAAGAAGGTAAGGATGTTTTCTACCATCACTATTATTTTACACCAGAGACTCTAGGCAACCCAGAAAGACAAGAAGAATAAACCAGAGATAGACAAGTGATA... | CACCAAGCCTGGCTAATTTTTGTATTTTTAGCAGAGACAGGGTTTCACCATGTTAGCCAGACTGACTTTGAACTCCTGACCTCAGGTAATCTGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTATAGGTGTGAGCCACAGCACCTGGCTGTAAAACATATATCTTATACCCAATAATGCTTAACAATGGAACTCTAGGATTATTCCTACTAAAATCAGGAAGAAGGTAAGGATGTTTTCTACCATCACTATTATTTTACACCAGAGACTCTAGGCAACCCAGAAAGACAAGAAGAATAAACCAGAGATAGACAAGTGATA... |
Task1_train_40955 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GGGCCAATCAGAGCTGTGGCAGCTTGTCTCCCTAAGAGAGCTCATGATGGATGCACTCACTCCTGATGCTCCTCTATACTCCCAGAGGAGGATGCATCTTCTTTCCACCTGGAGAGCTCCTGCCCATGTGCATTCTTGGGATTCCAGAGCAAACGTGGCCTCTGATAGGCAAAAAAGAACTCCTGAATTTGTTCCTAAATGGCACGCACTCACCTCTATTTTTCCCTTATTTCATTTGCTTCTCATTCTCTATCTGGAGTTTGTTTAGGTTAATTTTTTTTTTCAGCCCACAATTTTGACTGTCAACTTGGATTTAACTT... | GGGCCAATCAGAGCTGTGGCAGCTTGTCTCCCTAAGAGAGCTCATGATGGATGCACTCACTCCTGATGCTCCTCTATACTCCCAGAGGAGGATGCATCTTCTTTCCACCTGGAGAGCTCCTGCCCATGTGCATTCTTGGGATTCCAGAGCAAACGTGGCCTCTGATAGGCAAAAAAGAACTCCTGAATTTGTTCCTAAATGGCACGCACTCACCTCTATTTTTCCCTTATTTCATTTGCTTCTCATTCTCTATCTGGAGTTTGTTTAGGTTAATTTTTTTTTTCAGCCCACAATTTTGACTGTCAACTTGGATTTAACTT... |
Task1_train_40956 | This sequence change occurs on Chromosome 11. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TGTTTAGGTTAATTTTTTTTTTCAGCCCACAATTTTGACTGTCAACTTGGATTTAACTTGAGAATCACTCCTCTACTTTACCCCCCTCTAACATGTATAATCGACACATAGTGGTGCTGGGTCCAAAGGGCTGGTGAAAAAATGGATCATGAGTCAGCCCTGCTGGGCTCACATTCATACTATATAATATATAACCCCCCGGACAAATAATATCCTCTCTTTATACTCTAATTTCATTATCTGCAATACAGGAATAATACTAATTTTTACCTCCTAGGCTCTTCAGATGATTAAAAGAGGCAATACCTAATAAACTGTCA... | TGTTTAGGTTAATTTTTTTTTTCAGCCCACAATTTTGACTGTCAACTTGGATTTAACTTGAGAATCACTCCTCTACTTTACCCCCCTCTAACATGTATAATCGACACATAGTGGTGCTGGGTCCAAAGGGCTGGTGAAAAAATGGATCATGAGTCAGCCCTGCTGGGCTCACATTCATACTATATAATATATAACCCCCCGGACAAATAATATCCTCTCTTTATACTCTAATTTCATTATCTGCAATACAGGAATAATACTAATTTTTACCTCCTAGGCTCTTCAGATGATTAAAAGAGGCAATACCTAATAAACTGTCA... |
Task1_train_40957 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GACAAATAATATCCTCTCTTTATACTCTAATTTCATTATCTGCAATACAGGAATAATACTAATTTTTACCTCCTAGGCTCTTCAGATGATTAAAAGAGGCAATACCTAATAAACTGTCAATCAGCTGCTGTTATTCTCCCAAATTAGACCTAATCCTCATTCTCCAGTTGAAATTTGCATGAATATCTCTCTTTACAACCCAAGCCCTACACTTCTCCTATTTCCACTCATGGACTCCTCTCATACAAATGTTTGCATCAACAAAGAAACGCTACCAAAGATCTCCCGAAAGAGAGAATGAAATAGGTTTACATTGTGTA... | GACAAATAATATCCTCTCTTTATACTCTAATTTCATTATCTGCAATACAGGAATAATACTAATTTTTACCTCCTAGGCTCTTCAGATGATTAAAAGAGGCAATACCTAATAAACTGTCAATCAGCTGCTGTTATTCTCCCAAATTAGACCTAATCCTCATTCTCCAGTTGAAATTTGCATGAATATCTCTCTTTACAACCCAAGCCCTACACTTCTCCTATTTCCACTCATGGACTCCTCTCATACAAATGTTTGCATCAACAAAGAAACGCTACCAAAGATCTCCCGAAAGAGAGAATGAAATAGGTTTACATTGTGTA... |
Task1_train_40958 | With a mutation on Chromosome 11, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TCTCCTATTTCCACTCATGGACTCCTCTCATACAAATGTTTGCATCAACAAAGAAACGCTACCAAAGATCTCCCGAAAGAGAGAATGAAATAGGTTTACATTGTGTATACTCAGCAGAACACTTAGTAGTCCCCCATACATATTCCCACACTTCAATTACCTGCTGCAGTGGCACTCAGGCTCACCCTCACTTACTCTTTCCTCTGTTCTGTTGCTGAGCAATTCAGCTCAGACCCACACCCTACCCAAACACTGTGTACAAAATGCTTCTAGGGGTTCGGCAAAGCCACACTGAGTCCTTATTTTAAAGGCACATCAGT... | TCTCCTATTTCCACTCATGGACTCCTCTCATACAAATGTTTGCATCAACAAAGAAACGCTACCAAAGATCTCCCGAAAGAGAGAATGAAATAGGTTTACATTGTGTATACTCAGCAGAACACTTAGTAGTCCCCCATACATATTCCCACACTTCAATTACCTGCTGCAGTGGCACTCAGGCTCACCCTCACTTACTCTTTCCTCTGTTCTGTTGCTGAGCAATTCAGCTCAGACCCACACCCTACCCAAACACTGTGTACAAAATGCTTCTAGGGGTTCGGCAAAGCCACACTGAGTCCTTATTTTAAAGGCACATCAGT... |
Task1_train_40959 | This is a variant located on Chromosome 11. Is this mutation a likely cause of disease or not? | Benign | TCTTATGTTATATGAGGATAATACCATAGATGGTCTTTAAGGAACACAGGCTAAATGTTGGTGATACTACAGGGAAAATGACAGGTATGACTTAGTCCTTATGGAGCTTTGGTTTTCATGAGGAAGACAAACATATCATACCATAAATATAGATAGAGAAACTCTTTAGTGCCCTGAGTGTGGATAACAGAGGCTCTCCTTTTCCTCCCATTTCCTTTCTGGGCCAATCAGGGCTGTGGCACCTTGCCCCTCTAAGAGAGCTCATGATGGATGCATTCACTCCTGATGCTTCTCTGTACTCCCAGCAAAGGGTGCATCTT... | TCTTATGTTATATGAGGATAATACCATAGATGGTCTTTAAGGAACACAGGCTAAATGTTGGTGATACTACAGGGAAAATGACAGGTATGACTTAGTCCTTATGGAGCTTTGGTTTTCATGAGGAAGACAAACATATCATACCATAAATATAGATAGAGAAACTCTTTAGTGCCCTGAGTGTGGATAACAGAGGCTCTCCTTTTCCTCCCATTTCCTTTCTGGGCCAATCAGGGCTGTGGCACCTTGCCCCTCTAAGAGAGCTCATGATGGATGCATTCACTCCTGATGCTTCTCTGTACTCCCAGCAAAGGGTGCATCTT... |
Task1_train_40960 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CTTGCAATTGCAATTAAAAATGGCAGCTATTCTAATTACTATTTGCTGACTTCCCATACCCCAGCAAAATTTGGATTGCCACCAGTGTGTGCTTCTGTTGAGGCTCTTACTAAACTGTGTTGTCTATCTACATATCTCACTTCCCCTTTAGGACAGGAAGTAGAATTTTATTTGAACTAAAAGCCAACGAAATGCCGGCCAGGTGCAGTGGTTCAGGCCTACATTTTCAGACCCTTGGCCAGTTGAGCCCATGAGTTAGCCCAGCCCGGCCAACATGGTGAACCCCCTTTTTTATTAAAAACCCAAAAATTAGCCAGGTG... | CTTGCAATTGCAATTAAAAATGGCAGCTATTCTAATTACTATTTGCTGACTTCCCATACCCCAGCAAAATTTGGATTGCCACCAGTGTGTGCTTCTGTTGAGGCTCTTACTAAACTGTGTTGTCTATCTACATATCTCACTTCCCCTTTAGGACAGGAAGTAGAATTTTATTTGAACTAAAAGCCAACGAAATGCCGGCCAGGTGCAGTGGTTCAGGCCTACATTTTCAGACCCTTGGCCAGTTGAGCCCATGAGTTAGCCCAGCCCGGCCAACATGGTGAACCCCCTTTTTTATTAAAAACCCAAAAATTAGCCAGGTG... |
Task1_train_40961 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GAGCCGTAAGGGACGGGGCATCCAGTAACAACGCACACGGGGTATTTTTGGGCTTCCTTAAGATTTGAGCCGCTGCCTTAGGTTGTGCTGCCCAATGTGCCTGGGGAGCTGCTAAACAGATTAGAGAGTCGAGGATTGTTGTCAGTTACTCAGAGAAAGAACAATCATCCTTTCCAGGAGCACCTGAGCTGTTTGTTTTGCGTAGAAGATGCAAAATAAGGCCTGCAATGGGTATAAAATGTCCCTCAGCATAAATCGCATAGGAGTATGACTAAGGCTGTTGACTCTTCTGTCTTCTTTCTCCTTCCTCCTTCGATTTC... | GAGCCGTAAGGGACGGGGCATCCAGTAACAACGCACACGGGGTATTTTTGGGCTTCCTTAAGATTTGAGCCGCTGCCTTAGGTTGTGCTGCCCAATGTGCCTGGGGAGCTGCTAAACAGATTAGAGAGTCGAGGATTGTTGTCAGTTACTCAGAGAAAGAACAATCATCCTTTCCAGGAGCACCTGAGCTGTTTGTTTTGCGTAGAAGATGCAAAATAAGGCCTGCAATGGGTATAAAATGTCCCTCAGCATAAATCGCATAGGAGTATGACTAAGGCTGTTGACTCTTCTGTCTTCTTTCTCCTTCCTCCTTCGATTTC... |
Task1_train_40962 | Chromosome 11 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GGGCATCCAGTAACAACGCACACGGGGTATTTTTGGGCTTCCTTAAGATTTGAGCCGCTGCCTTAGGTTGTGCTGCCCAATGTGCCTGGGGAGCTGCTAAACAGATTAGAGAGTCGAGGATTGTTGTCAGTTACTCAGAGAAAGAACAATCATCCTTTCCAGGAGCACCTGAGCTGTTTGTTTTGCGTAGAAGATGCAAAATAAGGCCTGCAATGGGTATAAAATGTCCCTCAGCATAAATCGCATAGGAGTATGACTAAGGCTGTTGACTCTTCTGTCTTCTTTCTCCTTCCTCCTTCGATTTCCTAGTTGGATAATGT... | GGGCATCCAGTAACAACGCACACGGGGTATTTTTGGGCTTCCTTAAGATTTGAGCCGCTGCCTTAGGTTGTGCTGCCCAATGTGCCTGGGGAGCTGCTAAACAGATTAGAGAGTCGAGGATTGTTGTCAGTTACTCAGAGAAAGAACAATCATCCTTTCCAGGAGCACCTGAGCTGTTTGTTTTGCGTAGAAGATGCAAAATAAGGCCTGCAATGGGTATAAAATGTCCCTCAGCATAAATCGCATAGGAGTATGACTAAGGCTGTTGACTCTTCTGTCTTCTTTCTCCTTCCTCCTTCGATTTCCTAGTTGGATAATGT... |
Task1_train_40963 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | AGTTAAGTAGCTGCACAAAGTCTTCTCTCTTAAACTCAAATGTCAACCCTGGTCCCATGGAGTAGCTAGAAAAGAATTCTGAAAAGACTCCAAGTCTGAGCCCAAACTGACCATTAGAAAGGATCAGCTAAAGACTAATGATACGTGGAAACTATTACCATCAGAGATTTTTAATTTTTGATCTCTTGAGGGTGGGGGCACCTACATCTGCAACAACTCAAATACCAGCTGCTAAAACAGAGGGAAGCTAGACTCTCCCCAAGGTAAATGAGAAGTTAATAGCTCCATATGACAAGTTATATGGAAAACAAGAGACTTCC... | AGTTAAGTAGCTGCACAAAGTCTTCTCTCTTAAACTCAAATGTCAACCCTGGTCCCATGGAGTAGCTAGAAAAGAATTCTGAAAAGACTCCAAGTCTGAGCCCAAACTGACCATTAGAAAGGATCAGCTAAAGACTAATGATACGTGGAAACTATTACCATCAGAGATTTTTAATTTTTGATCTCTTGAGGGTGGGGGCACCTACATCTGCAACAACTCAAATACCAGCTGCTAAAACAGAGGGAAGCTAGACTCTCCCCAAGGTAAATGAGAAGTTAATAGCTCCATATGACAAGTTATATGGAAAACAAGAGACTTCC... |
Task1_train_40964 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TTTATGGGCAAGAGGGAGAAAAAGATATAGTATTCTGGCTTGAGACTGAAGTGAATTATTTACCTATAATAACATTATGGCCGGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTAGGAAGCCGAGCCAGGCGGATCACCTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATATGGTGAAACCCCATCTCTACTAAAAATTACAAAAATTAGCTGGGCGTGGTAGCGCACACCTGTAGTCCCAGCTACTTGGGAAGCTGAGGCAGAAGAATCGCTTGAACCCGGGGAGGTGGGGGTTGCAGTGAGCCGTGACCA... | TTTATGGGCAAGAGGGAGAAAAAGATATAGTATTCTGGCTTGAGACTGAAGTGAATTATTTACCTATAATAACATTATGGCCGGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTAGGAAGCCGAGCCAGGCGGATCACCTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATATGGTGAAACCCCATCTCTACTAAAAATTACAAAAATTAGCTGGGCGTGGTAGCGCACACCTGTAGTCCCAGCTACTTGGGAAGCTGAGGCAGAAGAATCGCTTGAACCCGGGGAGGTGGGGGTTGCAGTGAGCCGTGACCA... |
Task1_train_40965 | Assess the clinical impact of this variant found on Chromosome 11. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TATCTATAACTGGATAAAAAAGGTCTGTAACCATGGAGACCACAGCAATGGAGTGTCATGGAAGGTTCAGGAGTAGCAGAAGGTGAGATGAGAGGTGGGGGAGGGGGAAACCTTCTTGGTTTGGGATTTTACCATGAGAGGAAAGCTGGGGGAAATTTAAGCAACAGAAAGCAAGGCAGGCCAGCTTTGCATTTAGAGTTCATGCTGCTAGCTGTGTGGCTATGAAGACAGTAGACTGGGAAGGAATAAAATGCTTCCCCCTATGTGTGCACACATGAGTAGAAACATGGCATGCATGTACAAAAGGGAGGGTTCCCTTC... | TATCTATAACTGGATAAAAAAGGTCTGTAACCATGGAGACCACAGCAATGGAGTGTCATGGAAGGTTCAGGAGTAGCAGAAGGTGAGATGAGAGGTGGGGGAGGGGGAAACCTTCTTGGTTTGGGATTTTACCATGAGAGGAAAGCTGGGGGAAATTTAAGCAACAGAAAGCAAGGCAGGCCAGCTTTGCATTTAGAGTTCATGCTGCTAGCTGTGTGGCTATGAAGACAGTAGACTGGGAAGGAATAAAATGCTTCCCCCTATGTGTGCACACATGAGTAGAAACATGGCATGCATGTACAAAAGGGAGGGTTCCCTTC... |
Task1_train_40966 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | GCATGTGATATGACTGGACAACGTTGACAATTCCTGCCCAAAATGATGTTCTGTTTTTACTCTGGAATCGGTCTGTCTCATGAGACAGCCAGAGAGATGTTCCTGTGGAATTCCCCACAGATCAGTGTTCCTTCCTGGCTTAAGGTCTCCATGCTGACCCCTGGGTTCCCCACTGAGCACCAGGCTATCTCACTGACCTATGGGATTTCCTGCAAACACTTCTTCTGTCTCCAGTGGGTCACTCACACCTTCTGAATTGACTGCCAGGATACGGAACTGGTAGGCTTTTCCCTCTTCCACCTTGTTGGTGGAGAAGTTGG... | GCATGTGATATGACTGGACAACGTTGACAATTCCTGCCCAAAATGATGTTCTGTTTTTACTCTGGAATCGGTCTGTCTCATGAGACAGCCAGAGAGATGTTCCTGTGGAATTCCCCACAGATCAGTGTTCCTTCCTGGCTTAAGGTCTCCATGCTGACCCCTGGGTTCCCCACTGAGCACCAGGCTATCTCACTGACCTATGGGATTTCCTGCAAACACTTCTTCTGTCTCCAGTGGGTCACTCACACCTTCTGAATTGACTGCCAGGATACGGAACTGGTAGGCTTTTCCCTCTTCCACCTTGTTGGTGGAGAAGTTGG... |
Task1_train_40967 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ACTCCACCCGGCCCTGTGGAGGCTTTGGACGGTCTGGGGACAGAGAACAGCTTCAGAATGGGGCTTTGGAACAAAGGATCAGAAGGGCCTCCTCCCACTCACCAAAGGTCTGCCCAGACTAGGGTATAGCTGGATTTTGAGCTTTTTGGATCCTTTGCCCCTCCCTGTGTCCACCATCCCTCCTTCTAAGACTTGCCCAAAGAGTTTGATCCTTGCCCCCGTGAGTTTCCCATCTGCCTAGCAATGGGTAGACTAGAGACCTTAGGGGCCCCTGCCCTTAGCTGATCTCCCTGTCCCCTTCCAAACAAGTTCTCCCCCTC... | ACTCCACCCGGCCCTGTGGAGGCTTTGGACGGTCTGGGGACAGAGAACAGCTTCAGAATGGGGCTTTGGAACAAAGGATCAGAAGGGCCTCCTCCCACTCACCAAAGGTCTGCCCAGACTAGGGTATAGCTGGATTTTGAGCTTTTTGGATCCTTTGCCCCTCCCTGTGTCCACCATCCCTCCTTCTAAGACTTGCCCAAAGAGTTTGATCCTTGCCCCCGTGAGTTTCCCATCTGCCTAGCAATGGGTAGACTAGAGACCTTAGGGGCCCCTGCCCTTAGCTGATCTCCCTGTCCCCTTCCAAACAAGTTCTCCCCCTC... |
Task1_train_40968 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | AAAGGGCTGGTAGCGATGGTCATGGGACTGGTCAGGGGTGCTGCGTCAATCAAAATAATTTATGATGAGCAGGCGGCTTGCCAATGTGGTCAATAGGTGATTAGGGGGTGGTCAGTGGGGGGAACTGGAGCAACACATGGGAGGGGGATGGGGAAAGGTCAGTGGCTTGGGAAATGGTGACCAGGAAAACTGGGAGATGGCTAGTGGGGAATTGATTAGTGGAGCGTGGTCAGCAGGGACTTAGGATGCTGGGTTGGAGAGGGAAATAGATGGTGAAGATGCAGGTGGTTACTGGAGTTGGGATGTTTAGTTGTGGTTAC... | AAAGGGCTGGTAGCGATGGTCATGGGACTGGTCAGGGGTGCTGCGTCAATCAAAATAATTTATGATGAGCAGGCGGCTTGCCAATGTGGTCAATAGGTGATTAGGGGGTGGTCAGTGGGGGGAACTGGAGCAACACATGGGAGGGGGATGGGGAAAGGTCAGTGGCTTGGGAAATGGTGACCAGGAAAACTGGGAGATGGCTAGTGGGGAATTGATTAGTGGAGCGTGGTCAGCAGGGACTTAGGATGCTGGGTTGGAGAGGGAAATAGATGGTGAAGATGCAGGTGGTTACTGGAGTTGGGATGTTTAGTTGTGGTTAC... |
Task1_train_40969 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | ATCAAAATAATTTATGATGAGCAGGCGGCTTGCCAATGTGGTCAATAGGTGATTAGGGGGTGGTCAGTGGGGGGAACTGGAGCAACACATGGGAGGGGGATGGGGAAAGGTCAGTGGCTTGGGAAATGGTGACCAGGAAAACTGGGAGATGGCTAGTGGGGAATTGATTAGTGGAGCGTGGTCAGCAGGGACTTAGGATGCTGGGTTGGAGAGGGAAATAGATGGTGAAGATGCAGGTGGTTACTGGAGTTGGGATGTTTAGTTGTGGTTACGCTAGACTGTGGGATACATAGACTGTGGGATACATACATACATGTCAT... | ATCAAAATAATTTATGATGAGCAGGCGGCTTGCCAATGTGGTCAATAGGTGATTAGGGGGTGGTCAGTGGGGGGAACTGGAGCAACACATGGGAGGGGGATGGGGAAAGGTCAGTGGCTTGGGAAATGGTGACCAGGAAAACTGGGAGATGGCTAGTGGGGAATTGATTAGTGGAGCGTGGTCAGCAGGGACTTAGGATGCTGGGTTGGAGAGGGAAATAGATGGTGAAGATGCAGGTGGTTACTGGAGTTGGGATGTTTAGTTGTGGTTACGCTAGACTGTGGGATACATAGACTGTGGGATACATACATACATGTCAT... |
Task1_train_40970 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | ATTCCCTGGGCCCCTTGGGAGGAGCTACTCTGAGCCCAGGCCTTACAAGGGAAATTACTGGGCTGCAGCTGCTGTTGGGATCTGTGGAGCTAACATGGGATAAGAGTTTGGCCAACAGGGAGGGGCCTGGGTGTGACCTGAATGTCTCCTTACCCTAGCCTTGGCTTCTCTGGCACATCTGTTGGAAATGGTGACCTGCCAGCCACTGTGCCTTCCCTGGAAGCCTTCCACACCTGTCCTTGAGGCTCCCCATGGCCCAGAGCATGTGTCAGGGCCAGGGCTGAGGCTGTGTGAGAATCCTGCAGAATGTTCCCAGTTTG... | ATTCCCTGGGCCCCTTGGGAGGAGCTACTCTGAGCCCAGGCCTTACAAGGGAAATTACTGGGCTGCAGCTGCTGTTGGGATCTGTGGAGCTAACATGGGATAAGAGTTTGGCCAACAGGGAGGGGCCTGGGTGTGACCTGAATGTCTCCTTACCCTAGCCTTGGCTTCTCTGGCACATCTGTTGGAAATGGTGACCTGCCAGCCACTGTGCCTTCCCTGGAAGCCTTCCACACCTGTCCTTGAGGCTCCCCATGGCCCAGAGCATGTGTCAGGGCCAGGGCTGAGGCTGTGTGAGAATCCTGCAGAATGTTCCCAGTTTG... |
Task1_train_40971 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AACTGAAGCTCAGAGGGAAAGCAGCTTGCCCAAGATGGTGGGAGAGCTGATAATAAAGTGATACTAATCTACTGCAGATGCTGAGTTCCAGGCACCACGCTCCACCACCTGGGCAGGTGGATGATTGACATGGGTCTGCACACAGTGGGGCGACCGGCTCAAGGGAACTCACAAAGAATTCCGCCTGCAGCAGGAAAGGGTCCAGGGCCTTTTCATGAAGCTCTTCTGCTTGGAGGACACGGGAGGCGCTGAGCAGGTACTCGCGGGCGGACTCCTCACGTGGGGACATGAGATAGCCAAAGCCCTCCTCGTTGCAGCCC... | AACTGAAGCTCAGAGGGAAAGCAGCTTGCCCAAGATGGTGGGAGAGCTGATAATAAAGTGATACTAATCTACTGCAGATGCTGAGTTCCAGGCACCACGCTCCACCACCTGGGCAGGTGGATGATTGACATGGGTCTGCACACAGTGGGGCGACCGGCTCAAGGGAACTCACAAAGAATTCCGCCTGCAGCAGGAAAGGGTCCAGGGCCTTTTCATGAAGCTCTTCTGCTTGGAGGACACGGGAGGCGCTGAGCAGGTACTCGCGGGCGGACTCCTCACGTGGGGACATGAGATAGCCAAAGCCCTCCTCGTTGCAGCCC... |
Task1_train_40972 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TACTGTCCCTTTTAAGAATTTTTCATTATTCCACACAGAAATTCTGTGCTCATTTAATAATGGCTACATATTCTCCCCATCATCTAGCACCAGGATCCTCCTAATTTAATTTCTGTGTTCACGAATTTCCTAGTTTGGATACCTGGTAGAATTTGAACTTACTGTTCTTTGGTATCTGGCTTATTTTCCTTAGCAGAATGTTTCCAGGTTCATCTATGTCAAGCATGTATCAGAATTCTATACCAACTGTAAGTTATTATCAAGATACCATAATTGACATTAGCATGGAAAAGTCAGATGTTATCAGTCTTGCCTCTCAT... | TACTGTCCCTTTTAAGAATTTTTCATTATTCCACACAGAAATTCTGTGCTCATTTAATAATGGCTACATATTCTCCCCATCATCTAGCACCAGGATCCTCCTAATTTAATTTCTGTGTTCACGAATTTCCTAGTTTGGATACCTGGTAGAATTTGAACTTACTGTTCTTTGGTATCTGGCTTATTTTCCTTAGCAGAATGTTTCCAGGTTCATCTATGTCAAGCATGTATCAGAATTCTATACCAACTGTAAGTTATTATCAAGATACCATAATTGACATTAGCATGGAAAAGTCAGATGTTATCAGTCTTGCCTCTCAT... |
Task1_train_40973 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AAATATTTTGTCTTGAATGAAGTTTGAGTCACATAGGTGTATTCATTTAACAAAACTCATTAAGCTGTACATTTATGATCTGTGCATATCATTCTCTTAATTATACCTTAATTAAAAATAATAAAAAATTATTAAAAGATGCAGCATTTACAATTAGTATTTTATTCTGTGGAACACGTAACTTTTAAAAATATGTGCAATTTAATTAACAAAATAAATGCTCCGAGTTCTTCGGAATAAAAGGTAAATCTGACATACAGCCTGTCCTCCAAGAACATGGAGTCTATAAGACCACTGGAAACTTCCAGGACGAATTAGAG... | AAATATTTTGTCTTGAATGAAGTTTGAGTCACATAGGTGTATTCATTTAACAAAACTCATTAAGCTGTACATTTATGATCTGTGCATATCATTCTCTTAATTATACCTTAATTAAAAATAATAAAAAATTATTAAAAGATGCAGCATTTACAATTAGTATTTTATTCTGTGGAACACGTAACTTTTAAAAATATGTGCAATTTAATTAACAAAATAAATGCTCCGAGTTCTTCGGAATAAAAGGTAAATCTGACATACAGCCTGTCCTCCAAGAACATGGAGTCTATAAGACCACTGGAAACTTCCAGGACGAATTAGAG... |
Task1_train_40974 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | CCTGTTGCCCATAAAACTCTTAAGATAAATGTCAGAAATTAGGCTCTTTTTAGAGGGAATCTCAGTAAAAACTCGCATTTTATGTCTTTCCTAAAATTTTCTTCAGGTCCTGGACCTTCTCAAGTGGTTGTCGGGGGACCTGTAGGTAGTATCTGGGAAGGGCATAGAGAGCTATGGAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTTCTAAACCAGCAAAACCTGAATGTATATTCTTATTATGTTTCTAAAATAAAGGGAGTATTTATTTTCCAGTAAAATGTTAAAGTTGACATTTAAAAGATGGAGAGT... | CCTGTTGCCCATAAAACTCTTAAGATAAATGTCAGAAATTAGGCTCTTTTTAGAGGGAATCTCAGTAAAAACTCGCATTTTATGTCTTTCCTAAAATTTTCTTCAGGTCCTGGACCTTCTCAAGTGGTTGTCGGGGGACCTGTAGGTAGTATCTGGGAAGGGCATAGAGAGCTATGGAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTTCTAAACCAGCAAAACCTGAATGTATATTCTTATTATGTTTCTAAAATAAAGGGAGTATTTATTTTCCAGTAAAATGTTAAAGTTGACATTTAAAAGATGGAGAGT... |
Task1_train_40975 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | CCACTGAGCAACAGAATAGGCCTAGGCTCAGGGGTGGAGGACGCATTGCCTTGGCCCTAGTGCATTCCTTCCTTTGATAGTGTCAAGAAGGAGCTAAGCCTCTACTATTTCTCCACAAGACCAAGGGATTATGGAGGCAGCGAGGGTCAGAGCTGCAAGGACCAGGAGGAAAACCAGATCTGTCCCTATGATCACTAAGTAACGTGCAACATCGACAACAGAACTGTTAGTGCGGGGTAGGCAGGAGGGAGATAGACATGTCATGATAAACTCCAGTGAGGCCAAACTGAGTTCACCCTCCTCCAGTCACCCCCTCTGCC... | CCACTGAGCAACAGAATAGGCCTAGGCTCAGGGGTGGAGGACGCATTGCCTTGGCCCTAGTGCATTCCTTCCTTTGATAGTGTCAAGAAGGAGCTAAGCCTCTACTATTTCTCCACAAGACCAAGGGATTATGGAGGCAGCGAGGGTCAGAGCTGCAAGGACCAGGAGGAAAACCAGATCTGTCCCTATGATCACTAAGTAACGTGCAACATCGACAACAGAACTGTTAGTGCGGGGTAGGCAGGAGGGAGATAGACATGTCATGATAAACTCCAGTGAGGCCAAACTGAGTTCACCCTCCTCCAGTCACCCCCTCTGCC... |
Task1_train_40976 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | ACAATAATAACCTCTGCCACATAGAATGAAGATTGAATGAGTTAACGTGTGTAAAATGTTTATGTCAGTGCCTGGCATGTAGTAGGCACTGTATGTTAGTTGGATTTATTAAGCTCCTTCTCTGCATAAGGCACTCTTTCAAAAGTGCTCTTGTAGGTACTTGGCATACGTCATTAAACAAAACATACCCAAATCCCTACTCTTGTGGAGCCTACAGAACCGGGACCTGAACCCATGTCTGCTTCTTTTCCTTTTAATGTTTATTTTCCTTCCTCTCTCCCTCTTAATAATTTTCTTTAATGATCTTTTAAATTTCAAGT... | ACAATAATAACCTCTGCCACATAGAATGAAGATTGAATGAGTTAACGTGTGTAAAATGTTTATGTCAGTGCCTGGCATGTAGTAGGCACTGTATGTTAGTTGGATTTATTAAGCTCCTTCTCTGCATAAGGCACTCTTTCAAAAGTGCTCTTGTAGGTACTTGGCATACGTCATTAAACAAAACATACCCAAATCCCTACTCTTGTGGAGCCTACAGAACCGGGACCTGAACCCATGTCTGCTTCTTTTCCTTTTAATGTTTATTTTCCTTCCTCTCTCCCTCTTAATAATTTTCTTTAATGATCTTTTAAATTTCAAGT... |
Task1_train_40977 | A genetic alteration is present on Chromosome 11. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GTGGTGCCTGGCAGACAGCAAGCATGGAGTAAATTCTGGTTGGATGAATGTACTGGAAGTGTTTAGAGGAAGGAAACTGACCTGAGGTAGTTGGGACAAAGAATGGGCAACTTTAGTTTCTGTAAGATTGAGATAAAGATAACAGTACTTGAGTACTTGTGTACTTACCCTTTCTGATTAAATAGAGGCTGAGATCGGATAAGATAATTTTGCTAATGTCTGTTGTGGCCTGAAAAGCGTGTGTTCCTTGGCTCCTTCCTAGGCTCATTCATTCGCTCATCAAGCTTTGAGTGAGCTCCTGCCCTGTGCCCACATGTAGG... | GTGGTGCCTGGCAGACAGCAAGCATGGAGTAAATTCTGGTTGGATGAATGTACTGGAAGTGTTTAGAGGAAGGAAACTGACCTGAGGTAGTTGGGACAAAGAATGGGCAACTTTAGTTTCTGTAAGATTGAGATAAAGATAACAGTACTTGAGTACTTGTGTACTTACCCTTTCTGATTAAATAGAGGCTGAGATCGGATAAGATAATTTTGCTAATGTCTGTTGTGGCCTGAAAAGCGTGTGTTCCTTGGCTCCTTCCTAGGCTCATTCATTCGCTCATCAAGCTTTGAGTGAGCTCCTGCCCTGTGCCCACATGTAGG... |
Task1_train_40978 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | AGGGTAGGGTACGAGGAGTGACTGCTAATGATATGGGATTTCTTTTCAGGGTGATGAAATATTTTAAAACTTAGATCGTGATGAAGGTTACAGAGTTCTGTGTATATACTAAAAACCACCTATTAAAAAAAAAAGAATGGCCAAGCGCGGTGGCTCTCGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGTGGATCACTTGAGGTCAGGAGTTCGAGACCAGCCTGGTCAACATGGTGACAACCCCGTCACTACTAAAAATACAAAAATTAGCCAGGCATAATGGCGGATGCCTGTAATCCCAGCTACTTGGGAGG... | AGGGTAGGGTACGAGGAGTGACTGCTAATGATATGGGATTTCTTTTCAGGGTGATGAAATATTTTAAAACTTAGATCGTGATGAAGGTTACAGAGTTCTGTGTATATACTAAAAACCACCTATTAAAAAAAAAAGAATGGCCAAGCGCGGTGGCTCTCGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGTGGATCACTTGAGGTCAGGAGTTCGAGACCAGCCTGGTCAACATGGTGACAACCCCGTCACTACTAAAAATACAAAAATTAGCCAGGCATAATGGCGGATGCCTGTAATCCCAGCTACTTGGGAGG... |
Task1_train_40979 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | ACATGTCATATGAGATAGTTTTATATCATTTTCTTAATATAGAGGAATAGGTCAGATATAAAAGCTAAAGCCAAATATACACATTAACATATATACGTACACAAAAATTGTTATATTTTGTTGAATGGATTGCACCTTGGGCCACATTATTTCTTCTATTATTTAACTCCTTAATTATGTGTTAAACTGTGAGTCTCACCTTTTTTGCAAAGATGTAGAGAAGGTATCAGTAATGGAATCTTTATATTCTGAAAATAAATATAACAGGTGGTTATGTTTTACTTGTGTTATTTCACTACCATCTTGAAAAGCATTCAGAT... | ACATGTCATATGAGATAGTTTTATATCATTTTCTTAATATAGAGGAATAGGTCAGATATAAAAGCTAAAGCCAAATATACACATTAACATATATACGTACACAAAAATTGTTATATTTTGTTGAATGGATTGCACCTTGGGCCACATTATTTCTTCTATTATTTAACTCCTTAATTATGTGTTAAACTGTGAGTCTCACCTTTTTTGCAAAGATGTAGAGAAGGTATCAGTAATGGAATCTTTATATTCTGAAAATAAATATAACAGGTGGTTATGTTTTACTTGTGTTATTTCACTACCATCTTGAAAAGCATTCAGAT... |
Task1_train_40980 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | TACTCTAGGCTGTTGTCCCTTTAAAACTTGAATCCAAGGGGGTAATGATTTATCAAACTTGTATTATCAAGAAAATGTCAAACCAAGGGCACCTTGCTTTGCACTGACGCAAACCCGGCCTTTCCCAAGGAGATATAGAAAGCGCCTCTCCTGCCTGAGCCAAACCCAGTCTTGTCAATAGCGGGTTTCACCCTCCACCAGTTCAGTCTGTTGCCTGTGTCAGACATGGTGAGTGTTTGCTTTTGTTCTTTCAAGAGGAAAGGGGGCTGAGGGGACAGGGAAAGCAGATTCGTTTTGGCTATTTCTTTTGGAGATGTCTG... | TACTCTAGGCTGTTGTCCCTTTAAAACTTGAATCCAAGGGGGTAATGATTTATCAAACTTGTATTATCAAGAAAATGTCAAACCAAGGGCACCTTGCTTTGCACTGACGCAAACCCGGCCTTTCCCAAGGAGATATAGAAAGCGCCTCTCCTGCCTGAGCCAAACCCAGTCTTGTCAATAGCGGGTTTCACCCTCCACCAGTTCAGTCTGTTGCCTGTGTCAGACATGGTGAGTGTTTGCTTTTGTTCTTTCAAGAGGAAAGGGGGCTGAGGGGACAGGGAAAGCAGATTCGTTTTGGCTATTTCTTTTGGAGATGTCTG... |
Task1_train_40981 | A mutation has occurred on Chromosome 11. What is the medical relevance of this mutation? | Benign | TAATGCACTTTTAATGTAGCCTACCTGTGAGTCGAGCGCTGTCAGTGTGATTAAGTTGAGGACTGGGGAGTCCTAGGCCAGACTGTGAAATGGTACTTCTGTTTCCAGTGCCCTGGGCCTGTTCCACTTTGTGTGGATTGTAAGTGACACTGTACTCTTCCAATAGCCCCATGAAGAATCTACTATTGTTGCCACTTTGCAGGTGTGGACACTGAGGGTCAGAGACTCAGAGAGGTTAAGTTGCTGCCTCAGTGAGTGCTGGAGTCAGGATTTGGTGACACAGTTCGTAAGTGCTGGAGTCAGAATTTGGACCCAGGCTC... | TAATGCACTTTTAATGTAGCCTACCTGTGAGTCGAGCGCTGTCAGTGTGATTAAGTTGAGGACTGGGGAGTCCTAGGCCAGACTGTGAAATGGTACTTCTGTTTCCAGTGCCCTGGGCCTGTTCCACTTTGTGTGGATTGTAAGTGACACTGTACTCTTCCAATAGCCCCATGAAGAATCTACTATTGTTGCCACTTTGCAGGTGTGGACACTGAGGGTCAGAGACTCAGAGAGGTTAAGTTGCTGCCTCAGTGAGTGCTGGAGTCAGGATTTGGTGACACAGTTCGTAAGTGCTGGAGTCAGAATTTGGACCCAGGCTC... |
Task1_train_40982 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | TAGCCTACCTGTGAGTCGAGCGCTGTCAGTGTGATTAAGTTGAGGACTGGGGAGTCCTAGGCCAGACTGTGAAATGGTACTTCTGTTTCCAGTGCCCTGGGCCTGTTCCACTTTGTGTGGATTGTAAGTGACACTGTACTCTTCCAATAGCCCCATGAAGAATCTACTATTGTTGCCACTTTGCAGGTGTGGACACTGAGGGTCAGAGACTCAGAGAGGTTAAGTTGCTGCCTCAGTGAGTGCTGGAGTCAGGATTTGGTGACACAGTTCGTAAGTGCTGGAGTCAGAATTTGGACCCAGGCTCGTGGGACTGCAGAGCC... | TAGCCTACCTGTGAGTCGAGCGCTGTCAGTGTGATTAAGTTGAGGACTGGGGAGTCCTAGGCCAGACTGTGAAATGGTACTTCTGTTTCCAGTGCCCTGGGCCTGTTCCACTTTGTGTGGATTGTAAGTGACACTGTACTCTTCCAATAGCCCCATGAAGAATCTACTATTGTTGCCACTTTGCAGGTGTGGACACTGAGGGTCAGAGACTCAGAGAGGTTAAGTTGCTGCCTCAGTGAGTGCTGGAGTCAGGATTTGGTGACACAGTTCGTAAGTGCTGGAGTCAGAATTTGGACCCAGGCTCGTGGGACTGCAGAGCC... |
Task1_train_40983 | This is a variant located on Chromosome 11. Is this mutation a likely cause of disease or not? | Benign | TTGGCATTACTTGTAGGTAAATTTATTAAGATGATCTTTGCTTAGAAGTAATGATAATAGGGTGCAGTGGCTCACACTTGTAATCCCAGCACTTTGGAAGGCCAAGGTGGGTGGATCCCCTGAGCTCAGGAGTTCAAGACCAGCCTGGGCAACATGGGGAAACCCTGTCTCTACCAAAAATACAAAAAAAAAAAAAAAAAAAAAGGCGGGCATGGTGGCACACACCTGTGGTCCCAACTACTTGGGAGGCTGAAGTGGGAGATCGCTTGAGCCCGGGAGGTGGAGGTTGCAGTGAGCCGAGATCATGCCACTGCACTTCA... | TTGGCATTACTTGTAGGTAAATTTATTAAGATGATCTTTGCTTAGAAGTAATGATAATAGGGTGCAGTGGCTCACACTTGTAATCCCAGCACTTTGGAAGGCCAAGGTGGGTGGATCCCCTGAGCTCAGGAGTTCAAGACCAGCCTGGGCAACATGGGGAAACCCTGTCTCTACCAAAAATACAAAAAAAAAAAAAAAAAAAAAGGCGGGCATGGTGGCACACACCTGTGGTCCCAACTACTTGGGAGGCTGAAGTGGGAGATCGCTTGAGCCCGGGAGGTGGAGGTTGCAGTGAGCCGAGATCATGCCACTGCACTTCA... |
Task1_train_40984 | Chromosome 11 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GAGAAAAGATAGTCTTTTCAACAAATGGTACTAGAACTTGACATCTACATGAAAATGATAATGATAATAATCTGGACACTGACACCTTTCAGTAACATTAACTCGCTATGGATCATAAACCTAAATGTAACATACACAACTGCAAAACTTCTAGGAGATAATACATAAGAGAACTAATGTGACCTTAAATTTGGCAATAAATTTTCAGATATATAGCCAAAAGATTTAAGTGATTAACCTTATGTAGTCATCTAACATATGGCAAAACAAGAAGTGGAGTCCAGAACAACCTGGTTTCAAAGATAATCCTCTTTTCATTA... | GAGAAAAGATAGTCTTTTCAACAAATGGTACTAGAACTTGACATCTACATGAAAATGATAATGATAATAATCTGGACACTGACACCTTTCAGTAACATTAACTCGCTATGGATCATAAACCTAAATGTAACATACACAACTGCAAAACTTCTAGGAGATAATACATAAGAGAACTAATGTGACCTTAAATTTGGCAATAAATTTTCAGATATATAGCCAAAAGATTTAAGTGATTAACCTTATGTAGTCATCTAACATATGGCAAAACAAGAAGTGGAGTCCAGAACAACCTGGTTTCAAAGATAATCCTCTTTTCATTA... |
Task1_train_40985 | A variant has been detected on Chromosome 11. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | ATAATTAAGAATTTAAAGTGTATCTTAGGCCAAGATCTTTCAGCAGCTGATGCACAAAATGATTAATGATATAAACTTCCTGGAGTTGCTAATCAACACAGACATGATTCTATGTGTCAACATGTATGAGTAACATAAACAGCATATCTTCGAGGTGCCGTATTTTATCTGGAAGAAGTATAATTGAAGACATCACCTATTAAGACCAAACAAGACCAAGATAAAATATGACACAAGGAGAACAGGCCCACAAAAGGCCTCTGTCCTTCCTTACTGACCCTATTCTACATTTAAACATTGTAAGACTTTTTAAAAGATTC... | ATAATTAAGAATTTAAAGTGTATCTTAGGCCAAGATCTTTCAGCAGCTGATGCACAAAATGATTAATGATATAAACTTCCTGGAGTTGCTAATCAACACAGACATGATTCTATGTGTCAACATGTATGAGTAACATAAACAGCATATCTTCGAGGTGCCGTATTTTATCTGGAAGAAGTATAATTGAAGACATCACCTATTAAGACCAAACAAGACCAAGATAAAATATGACACAAGGAGAACAGGCCCACAAAAGGCCTCTGTCCTTCCTTACTGACCCTATTCTACATTTAAACATTGTAAGACTTTTTAAAAGATTC... |
Task1_train_40986 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | ATTTCTGATTTTTAAATTAAATAGCTCCAGATAAAAGCATGTTATTTTCCACATACGCTATCTTTGTATTCTGCACAGAGTTCCAAGGCAAAGATTGCTCCTGGCTTTATGAATTACCAGAGATGATGACTTGTGTGGCTGACTTATCACAGGTCTTTTACTCTTCCTTCCTGATAGATCCTTAGCTTCTTTGGGAGGTGGCATATGAATTGGTTTCCACGGAATTGGATTATAAAAGGCTGGTTCTGGATAGGAATTTCCACTGTAAAAACCTAAAATTATTGAAAAATCAGATCAAAACAAGGAAAAACTTTCTTGAC... | ATTTCTGATTTTTAAATTAAATAGCTCCAGATAAAAGCATGTTATTTTCCACATACGCTATCTTTGTATTCTGCACAGAGTTCCAAGGCAAAGATTGCTCCTGGCTTTATGAATTACCAGAGATGATGACTTGTGTGGCTGACTTATCACAGGTCTTTTACTCTTCCTTCCTGATAGATCCTTAGCTTCTTTGGGAGGTGGCATATGAATTGGTTTCCACGGAATTGGATTATAAAAGGCTGGTTCTGGATAGGAATTTCCACTGTAAAAACCTAAAATTATTGAAAAATCAGATCAAAACAAGGAAAAACTTTCTTGAC... |
Task1_train_40987 | 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 | TAAGTTTCTGAAGCATTTGACAATAATCACTGCATGTATCTGTTCTTTAGGAAGTGGGAAATGGACATGCAGTCAGCAAACGTTTATTGAGCACCTAATAAGCATCTGACACTTGCCACACACAATGCTTGACAACTTCAGCATTCTCTTTTCAAACCCACGTCCCAGCTACTCCTTTGATTCATAGGGACTGAAATGTGATAAGGAAGGCAGCCTTAGCCCTGTGGTGCTACCAGCTCATTCTGGCTTTGGATAAGTGAGACGTACATACGTTCACCTCCTCCCCTGGCAGGCTCCACTTAGTCAGGGCTTTGGCTCTT... | TAAGTTTCTGAAGCATTTGACAATAATCACTGCATGTATCTGTTCTTTAGGAAGTGGGAAATGGACATGCAGTCAGCAAACGTTTATTGAGCACCTAATAAGCATCTGACACTTGCCACACACAATGCTTGACAACTTCAGCATTCTCTTTTCAAACCCACGTCCCAGCTACTCCTTTGATTCATAGGGACTGAAATGTGATAAGGAAGGCAGCCTTAGCCCTGTGGTGCTACCAGCTCATTCTGGCTTTGGATAAGTGAGACGTACATACGTTCACCTCCTCCCCTGGCAGGCTCCACTTAGTCAGGGCTTTGGCTCTT... |
Task1_train_40988 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | AAATTATCCAGAGGTGGGATGGTGGGCATAAGTCGGCTTGAGTGTGGTCCTCCAGTCGAGAACCTCTTGAGCACAGTTAGATAATGTAGGCACTTAAAGCACGAGGTCCAAGCAGCTTGACACATGTCATTCCAGAGCCACCTCTGAAGGGTCCTTCAGAGGCCTTCGTTTTGGAATGTCTCAAATACCATGCCCCACCTCCACCTAGACCTTGGGATGGCCACTCAGAAATTCCTCCCGCACTGCCGGTAAATGCAATGCCAACTCCACATAGCCTCCATTTGGCTGTTCAGTCTCATGTCACTGGCAATGTGGATTCC... | AAATTATCCAGAGGTGGGATGGTGGGCATAAGTCGGCTTGAGTGTGGTCCTCCAGTCGAGAACCTCTTGAGCACAGTTAGATAATGTAGGCACTTAAAGCACGAGGTCCAAGCAGCTTGACACATGTCATTCCAGAGCCACCTCTGAAGGGTCCTTCAGAGGCCTTCGTTTTGGAATGTCTCAAATACCATGCCCCACCTCCACCTAGACCTTGGGATGGCCACTCAGAAATTCCTCCCGCACTGCCGGTAAATGCAATGCCAACTCCACATAGCCTCCATTTGGCTGTTCAGTCTCATGTCACTGGCAATGTGGATTCC... |
Task1_train_40989 | A variant was discovered on Chromosome 11. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | AATCAAGAATTAAGTTGGTCTAAGGTCTGTTTCAGACTTTCAAGAACTGGCCTATTTCTAGGTTGCCCTACTCCTAGTGAAACACCCTTCAGGGATCTCAAATAAAATCCTAATGTGTTTAACAGGGTCTTTTCTTCATGGTGGTCCCTGAACTCCAATTTTTCTGTGAAAGCCTCATAAGAACATCAAAACTCTGCTTAATACTTTAGCCTCTTAGCAGCTACTTTCAGCTAGGCATCTTAGCCTCTCATTCCACAAAGCTGAGAACTTGGCGAATACCTTGAGGACAAAACCTGTACAGAATAATTTTGTTTCCCTAG... | AATCAAGAATTAAGTTGGTCTAAGGTCTGTTTCAGACTTTCAAGAACTGGCCTATTTCTAGGTTGCCCTACTCCTAGTGAAACACCCTTCAGGGATCTCAAATAAAATCCTAATGTGTTTAACAGGGTCTTTTCTTCATGGTGGTCCCTGAACTCCAATTTTTCTGTGAAAGCCTCATAAGAACATCAAAACTCTGCTTAATACTTTAGCCTCTTAGCAGCTACTTTCAGCTAGGCATCTTAGCCTCTCATTCCACAAAGCTGAGAACTTGGCGAATACCTTGAGGACAAAACCTGTACAGAATAATTTTGTTTCCCTAG... |
Task1_train_40990 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CTTTCATATTGCAAAACAGGAAATTGAAGCTAAGCATAAAGTGAAATGATTTGACTAGGGTCACAAAGCTAGTAGTTCAAAGAGCCAGAAATAGGTCCTAGTTCCCCCAATTCTCAGTAGCAATGTGCTTCCACCATAGCAGTCTTTCCCAAACAGTGTGAAATATGCACTGCTGGTGCTATTTTAAGTGATTTTACATGTACAAGACATATATTAAACATTGACTCACAAATGACTCAATAGGAGTCATTATTAAAAAATTATAGATTAGTTCATATGGCAAAAATCTTATGAATGGCTTAAGTTTACAAAATCCGTCT... | CTTTCATATTGCAAAACAGGAAATTGAAGCTAAGCATAAAGTGAAATGATTTGACTAGGGTCACAAAGCTAGTAGTTCAAAGAGCCAGAAATAGGTCCTAGTTCCCCCAATTCTCAGTAGCAATGTGCTTCCACCATAGCAGTCTTTCCCAAACAGTGTGAAATATGCACTGCTGGTGCTATTTTAAGTGATTTTACATGTACAAGACATATATTAAACATTGACTCACAAATGACTCAATAGGAGTCATTATTAAAAAATTATAGATTAGTTCATATGGCAAAAATCTTATGAATGGCTTAAGTTTACAAAATCCGTCT... |
Task1_train_40991 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GTTGTTCCAGAGTTCACTTTTTAGGCGTATACATTGTACGTTCATTACTGGGAACCCCGCAGCATACTGTTATTTTTAAGTGGAACAGAGCCAAGCCATTGGATGTCGGTTCCTTAATAAAATGAATCTATGAGATATTACAGATATATAGTCAATTTAATTGAAGTACTATTAAATTACATAAGTGGATTAAATAGTTCCAGTGGGCAATGTTTATAGCATGGAGATTGAGTTCAGGCTCTGGGGGTAGACTGTGTTACAATTTTAGCTTTACGGCTCTCTAGCTATGTGGCCTTTGGCAAATTACTTCTCTGTTTTCC... | GTTGTTCCAGAGTTCACTTTTTAGGCGTATACATTGTACGTTCATTACTGGGAACCCCGCAGCATACTGTTATTTTTAAGTGGAACAGAGCCAAGCCATTGGATGTCGGTTCCTTAATAAAATGAATCTATGAGATATTACAGATATATAGTCAATTTAATTGAAGTACTATTAAATTACATAAGTGGATTAAATAGTTCCAGTGGGCAATGTTTATAGCATGGAGATTGAGTTCAGGCTCTGGGGGTAGACTGTGTTACAATTTTAGCTTTACGGCTCTCTAGCTATGTGGCCTTTGGCAAATTACTTCTCTGTTTTCC... |
Task1_train_40992 | This is a variant located on Chromosome 11. Is this mutation a likely cause of disease or not? | Benign | AAAAAAGAATGCAATCCTGTCATTTGCAACAACACACATGGAACTGGAGGACATTTTGTTAAGTAAAATAAGCCAAGCACAAAAAGACAAATATTGTATGTTTTCACTCATACATAGGAGCAAAAAAATAAATAAAATTTAACTCATGGAGATAGAGACTAGAATGATGGTTGCCAGAGCCTGGGAAAGGTAGCGGGGAGGAGGGAATAAAGGGAGGTTGTTTAATAGGTACAAAACTACAGTTTAGATAGAATGAATAAGATCTAGTAGTCAGTAGCACGATAGAATGACTAAACAGCAATTTACTGTATATTTTTAAA... | AAAAAAGAATGCAATCCTGTCATTTGCAACAACACACATGGAACTGGAGGACATTTTGTTAAGTAAAATAAGCCAAGCACAAAAAGACAAATATTGTATGTTTTCACTCATACATAGGAGCAAAAAAATAAATAAAATTTAACTCATGGAGATAGAGACTAGAATGATGGTTGCCAGAGCCTGGGAAAGGTAGCGGGGAGGAGGGAATAAAGGGAGGTTGTTTAATAGGTACAAAACTACAGTTTAGATAGAATGAATAAGATCTAGTAGTCAGTAGCACGATAGAATGACTAAACAGCAATTTACTGTATATTTTTAAA... |
Task1_train_40993 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | AAAATACATAATGAGCAAACTTCTGCTTATTTTTCTTCATTTTTATATTTCCAAATAAAACTTAAGTATCATATTAAAACTGCTGAATGTAAAGCTATGAATTATTACAACTTAGTGGAAGAAAAAAGCTTTAGGAGAAATGGCAAAGAGCATAGGTTTCAAAATATTCTTAAATTTCATATAATGTTGAAATCTTTACAGACTGCCCAAACAGACAATCACAGAGACACTAAAATGTTAAATTTTGTTCATAATTTAATATTTAATAAAATATATTTTTCATCAATTTTGAGTCATAAAGAATTTTTTAATGAAAGCAG... | AAAATACATAATGAGCAAACTTCTGCTTATTTTTCTTCATTTTTATATTTCCAAATAAAACTTAAGTATCATATTAAAACTGCTGAATGTAAAGCTATGAATTATTACAACTTAGTGGAAGAAAAAAGCTTTAGGAGAAATGGCAAAGAGCATAGGTTTCAAAATATTCTTAAATTTCATATAATGTTGAAATCTTTACAGACTGCCCAAACAGACAATCACAGAGACACTAAAATGTTAAATTTTGTTCATAATTTAATATTTAATAAAATATATTTTTCATCAATTTTGAGTCATAAAGAATTTTTTAATGAAAGCAG... |
Task1_train_40994 | 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 | GAGCTGAGACTGGGAACTTTTAGCACAAAGCGAACTGGTAAACGGAACTGGTTACAGATGTACTAGTATTCCATTGGTGCCAACAAATTACCATAAACTTAGTTGCTTAAAACAACACATATTTATAATCTTACAGTTGATAGGTCAGAAGTCTAACATGGGTACCACTGGGCTAAAAAATCAAGACTGTTTCTTTCTAAAGGCTTTAGGGGAGAATCCATTTCCTTGCCTTTCCCAACTTCTAGAAGCACTAACATTCCTTTACTCATAGCCCCTTTGTTCCATCTCAAAGCCTTTAATCTCCCTGGCCATTATTCCAT... | GAGCTGAGACTGGGAACTTTTAGCACAAAGCGAACTGGTAAACGGAACTGGTTACAGATGTACTAGTATTCCATTGGTGCCAACAAATTACCATAAACTTAGTTGCTTAAAACAACACATATTTATAATCTTACAGTTGATAGGTCAGAAGTCTAACATGGGTACCACTGGGCTAAAAAATCAAGACTGTTTCTTTCTAAAGGCTTTAGGGGAGAATCCATTTCCTTGCCTTTCCCAACTTCTAGAAGCACTAACATTCCTTTACTCATAGCCCCTTTGTTCCATCTCAAAGCCTTTAATCTCCCTGGCCATTATTCCAT... |
Task1_train_40995 | Assess the clinical impact of this variant found on Chromosome 11. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GAAGCAGAGCTATGCGGATGCTTGGGCGGGGATTCTCCAGCCTGTAGGAAAGGGTCTGCCACTATTGCCGCTGAACACCAAGATGGACCAGAGAATCTGCGCAGGACAGCAACAATGCCTGCTGTGGTAACCCTGAGCCAAAGCAAAGCCCATGTTATGGGGTGGCAGGAACCAAGAGCCCTGCCGAGAAGGCTGACCTGCCAAAAGGAAAATGAGGTAGAGAAGCACGAGAAGCAAGACAGACAACGCAGTCACAGAGAGCAGAGCCTGGCCGTCACACCCACTGTCTCCAGCAGCCGCCCACAGGAGCCCACCCGGCA... | GAAGCAGAGCTATGCGGATGCTTGGGCGGGGATTCTCCAGCCTGTAGGAAAGGGTCTGCCACTATTGCCGCTGAACACCAAGATGGACCAGAGAATCTGCGCAGGACAGCAACAATGCCTGCTGTGGTAACCCTGAGCCAAAGCAAAGCCCATGTTATGGGGTGGCAGGAACCAAGAGCCCTGCCGAGAAGGCTGACCTGCCAAAAGGAAAATGAGGTAGAGAAGCACGAGAAGCAAGACAGACAACGCAGTCACAGAGAGCAGAGCCTGGCCGTCACACCCACTGTCTCCAGCAGCCGCCCACAGGAGCCCACCCGGCA... |
Task1_train_40996 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | TGGACCAGAGAATCTGCGCAGGACAGCAACAATGCCTGCTGTGGTAACCCTGAGCCAAAGCAAAGCCCATGTTATGGGGTGGCAGGAACCAAGAGCCCTGCCGAGAAGGCTGACCTGCCAAAAGGAAAATGAGGTAGAGAAGCACGAGAAGCAAGACAGACAACGCAGTCACAGAGAGCAGAGCCTGGCCGTCACACCCACTGTCTCCAGCAGCCGCCCACAGGAGCCCACCCGGCACAGTCACCAGATGTGACCCAGGACTTGTATTCCGGCAATGACTCTTCCATTTTCCTCCCATAATTATTTCCAGCTCTTGCTCA... | TGGACCAGAGAATCTGCGCAGGACAGCAACAATGCCTGCTGTGGTAACCCTGAGCCAAAGCAAAGCCCATGTTATGGGGTGGCAGGAACCAAGAGCCCTGCCGAGAAGGCTGACCTGCCAAAAGGAAAATGAGGTAGAGAAGCACGAGAAGCAAGACAGACAACGCAGTCACAGAGAGCAGAGCCTGGCCGTCACACCCACTGTCTCCAGCAGCCGCCCACAGGAGCCCACCCGGCACAGTCACCAGATGTGACCCAGGACTTGTATTCCGGCAATGACTCTTCCATTTTCCTCCCATAATTATTTCCAGCTCTTGCTCA... |
Task1_train_40997 | An alteration has been detected on Chromosome 11. Is it pathogenic, and if so, what disease is involved? | Benign | GGTGTTCTAGTGAAAATGTTTCCTATTCTTGTGTTCAACCACAATAAACCATGTCTGGCCTCTTCATAGTCTGATCCCAATTGCTTGAATAAGAGGGAAAGAAGAATCCATCATAGAAATAGTTTAGACCACGAGGTAGACAAATGGAAAGTGAAGAGGAAGGGATTGGAAGAAGGGAAAGGAAAAGCACTGCCTAGAAGGAATCAGTGAAAACAAAATTTCTGCAGAAAACTTAGGAATAATTCAGTTGATTATCAATAATAATAATAAAATAGACAATATCCTTTGGGAGGAGAAAAACAGAATTTGGTAAAAATTGA... | GGTGTTCTAGTGAAAATGTTTCCTATTCTTGTGTTCAACCACAATAAACCATGTCTGGCCTCTTCATAGTCTGATCCCAATTGCTTGAATAAGAGGGAAAGAAGAATCCATCATAGAAATAGTTTAGACCACGAGGTAGACAAATGGAAAGTGAAGAGGAAGGGATTGGAAGAAGGGAAAGGAAAAGCACTGCCTAGAAGGAATCAGTGAAAACAAAATTTCTGCAGAAAACTTAGGAATAATTCAGTTGATTATCAATAATAATAATAAAATAGACAATATCCTTTGGGAGGAGAAAAACAGAATTTGGTAAAAATTGA... |
Task1_train_40998 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | ACCACTTCGACCAAAGCATAAATAGTGTTTCAAAGAACTGTTAAGCACGTTCTTTGGATAAAGAAGGATGTGACCATCACCTGGCATAGGTACTCTGTCCACCTGCTGCCTTCATTACTTGATGCAGCAGTTTTTGAAGTCTTTAATCAAGACCTTTTTACGCTCTTTTACATTATCAAGGACCCCAAAGAGCTTTCACTTATGTGAATTTTATCTAATGATATTTATTATCTAACATTAAAACTGAGAAATTTTCAAAATATTATTTGAAATCAAGACAACAAAGCTTACTTTTTGTTATGTTTATGCATAGACTCAAG... | ACCACTTCGACCAAAGCATAAATAGTGTTTCAAAGAACTGTTAAGCACGTTCTTTGGATAAAGAAGGATGTGACCATCACCTGGCATAGGTACTCTGTCCACCTGCTGCCTTCATTACTTGATGCAGCAGTTTTTGAAGTCTTTAATCAAGACCTTTTTACGCTCTTTTACATTATCAAGGACCCCAAAGAGCTTTCACTTATGTGAATTTTATCTAATGATATTTATTATCTAACATTAAAACTGAGAAATTTTCAAAATATTATTTGAAATCAAGACAACAAAGCTTACTTTTTGTTATGTTTATGCATAGACTCAAG... |
Task1_train_40999 | A mutation on Chromosome 11 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TATTCAAATAAAATATCTGTCTCCTCCTTTATCTTGTAAGCAAACAAATAGAACTTTTCATCATGAGCTAATGAATGTGGCAAGTGACTGCCTACCATGAATACATTCCAGATTTCTGACAGAGGAGGAATTGTGTTGAGCTCTCTAAGTAAACTTGTGATCCTCTCAGTCACCTCTCAACTATTGAAGGGCCAATTATCCAGTTCCTAGATTTACACAGACCTTTTGCTTTTCTTCTTTCTCGCAATTTTTCTCTCTCCTTCCCTTCCAATTCAGATCTCATTATTACCTCAAAAGGAAAAATGGTGCTCTAAGAGACA... | TATTCAAATAAAATATCTGTCTCCTCCTTTATCTTGTAAGCAAACAAATAGAACTTTTCATCATGAGCTAATGAATGTGGCAAGTGACTGCCTACCATGAATACATTCCAGATTTCTGACAGAGGAGGAATTGTGTTGAGCTCTCTAAGTAAACTTGTGATCCTCTCAGTCACCTCTCAACTATTGAAGGGCCAATTATCCAGTTCCTAGATTTACACAGACCTTTTGCTTTTCTTCTTTCTCGCAATTTTTCTCTCTCCTTCCCTTCCAATTCAGATCTCATTATTACCTCAAAAGGAAAAATGGTGCTCTAAGAGACA... |
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