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_41500 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GTCCCAGGTTTAATTTTCTATGATGTGTGGAGGCCTCAGTTTAATGCTCCAACTTGATAGATGAAACACAGTTCCCACCTCTACACATTTCCCCTGTCTCAGGAGTTGTATATATTCTCAGTTGTCTGTCCAACTTATGCCCACTCTTTGAGATATTAATCAAGGCACTCCCTTGATAACACTTGCATATTATTATCAAAATTATGCAATTCTTTCTAATATCAGCCCACAAATACATCTCTTCCATTAAAAGTTTGACTTAATTATCTATACTACTCATTTGAAAACTAACATAGTTAAGTTGTATTTTTAGCCATGAA... | GTCCCAGGTTTAATTTTCTATGATGTGTGGAGGCCTCAGTTTAATGCTCCAACTTGATAGATGAAACACAGTTCCCACCTCTACACATTTCCCCTGTCTCAGGAGTTGTATATATTCTCAGTTGTCTGTCCAACTTATGCCCACTCTTTGAGATATTAATCAAGGCACTCCCTTGATAACACTTGCATATTATTATCAAAATTATGCAATTCTTTCTAATATCAGCCCACAAATACATCTCTTCCATTAAAAGTTTGACTTAATTATCTATACTACTCATTTGAAAACTAACATAGTTAAGTTGTATTTTTAGCCATGAA... |
Task1_train_41501 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | TTTCTCATTTTTGCCTATCAGAATACTAACCATCACTAAAGGCACTGCTCACATATGCAAGGCTTTGGCATTTCTAAAACAGCATATGTTATGTCTCATCAATTTTAAAGTTTTTCCAGTATAGTCATAATACTTAGGAGGGGGAAGAAGAGAAGAGAGGAGCTGTGAGAAAGATAATAGCTTTTATGTACCACTTAACTGTGTATTTTGTGTTATTTTAATTAATCCTTACATTACCTTCATGACATAAATATAATTCCCATTTTGTAGAATAAAGAAGATCAAACAGATACAATTTTACAAATCTTCCCTGTCTCAAC... | TTTCTCATTTTTGCCTATCAGAATACTAACCATCACTAAAGGCACTGCTCACATATGCAAGGCTTTGGCATTTCTAAAACAGCATATGTTATGTCTCATCAATTTTAAAGTTTTTCCAGTATAGTCATAATACTTAGGAGGGGGAAGAAGAGAAGAGAGGAGCTGTGAGAAAGATAATAGCTTTTATGTACCACTTAACTGTGTATTTTGTGTTATTTTAATTAATCCTTACATTACCTTCATGACATAAATATAATTCCCATTTTGTAGAATAAAGAAGATCAAACAGATACAATTTTACAAATCTTCCCTGTCTCAAC... |
Task1_train_41502 | A mutation is present on Chromosome 11. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TAAATAAATACAGTGCTTTTTCCTCCTCCTTTCCCCCAACTTTCTCATCTTGTAATACCAGCTGTGAACACTGGCTAATATAAAAAAGTTCCCTGCAGAAAAACTGAGATAAAAATTATGTGAAAAAGTATTTGGTCTATCTCCAAAACTGGGGAAAAAATAAACTCGCAGTTTGGAAGTTTAAGAAAATCCATTAATATATACAACTTACAGCATAAATGACTTCATGTACATAAAAATGTTCTGTATATACTATATGTATATAAGCAGACATATATACATACAAGCTATAGAAATGTAAGGCATCGTTAATGGGGTAA... | TAAATAAATACAGTGCTTTTTCCTCCTCCTTTCCCCCAACTTTCTCATCTTGTAATACCAGCTGTGAACACTGGCTAATATAAAAAAGTTCCCTGCAGAAAAACTGAGATAAAAATTATGTGAAAAAGTATTTGGTCTATCTCCAAAACTGGGGAAAAAATAAACTCGCAGTTTGGAAGTTTAAGAAAATCCATTAATATATACAACTTACAGCATAAATGACTTCATGTACATAAAAATGTTCTGTATATACTATATGTATATAAGCAGACATATATACATACAAGCTATAGAAATGTAAGGCATCGTTAATGGGGTAA... |
Task1_train_41503 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AGACCTCATGTGTTTATTAGAAGAAACCTTTTCTTGTTTATTGAATTATAATTATTTATTTGTTGGTTTTTCCATTATATTGTAAGCAACTTGAGGGGCGAGGTGAGGTCTTACTCTCTGGGTGCCCATCTGAAATGTATAGGTTTCAAGACAGTTCCTGGATTGGATGGATGAAAGAAATAAATGAAATGGGTTTAGCTTTACAGACTATTTTTTTCAACCCATTGGCTTAAAACCTAGAAGTTAAACTTTATAAAGTGTGTGATCAACAGATTATGATATTACTTTGTTGTATAAAAAATTAATTAATTAATTCAACT... | AGACCTCATGTGTTTATTAGAAGAAACCTTTTCTTGTTTATTGAATTATAATTATTTATTTGTTGGTTTTTCCATTATATTGTAAGCAACTTGAGGGGCGAGGTGAGGTCTTACTCTCTGGGTGCCCATCTGAAATGTATAGGTTTCAAGACAGTTCCTGGATTGGATGGATGAAAGAAATAAATGAAATGGGTTTAGCTTTACAGACTATTTTTTTCAACCCATTGGCTTAAAACCTAGAAGTTAAACTTTATAAAGTGTGTGATCAACAGATTATGATATTACTTTGTTGTATAAAAAATTAATTAATTAATTCAACT... |
Task1_train_41504 | A mutation on Chromosome 11 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TCATGTGTTTATTAGAAGAAACCTTTTCTTGTTTATTGAATTATAATTATTTATTTGTTGGTTTTTCCATTATATTGTAAGCAACTTGAGGGGCGAGGTGAGGTCTTACTCTCTGGGTGCCCATCTGAAATGTATAGGTTTCAAGACAGTTCCTGGATTGGATGGATGAAAGAAATAAATGAAATGGGTTTAGCTTTACAGACTATTTTTTTCAACCCATTGGCTTAAAACCTAGAAGTTAAACTTTATAAAGTGTGTGATCAACAGATTATGATATTACTTTGTTGTATAAAAAATTAATTAATTAATTCAACTGCAAC... | TCATGTGTTTATTAGAAGAAACCTTTTCTTGTTTATTGAATTATAATTATTTATTTGTTGGTTTTTCCATTATATTGTAAGCAACTTGAGGGGCGAGGTGAGGTCTTACTCTCTGGGTGCCCATCTGAAATGTATAGGTTTCAAGACAGTTCCTGGATTGGATGGATGAAAGAAATAAATGAAATGGGTTTAGCTTTACAGACTATTTTTTTCAACCCATTGGCTTAAAACCTAGAAGTTAAACTTTATAAAGTGTGTGATCAACAGATTATGATATTACTTTGTTGTATAAAAAATTAATTAATTAATTCAACTGCAAC... |
Task1_train_41505 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AATGTGACAATACTAGAAACACATTTAAAGCATCCCTACAGTGATATATAAACAGAATTTGGCTATTTGGGAAAATTTGTAAATTCATATTTTTATTCTTATTTATTTTTTACAAAATTTGATATTCTGGTAGGTTCAACAACTTGTAACACACATCTCAAATGATTAAAATCATTGAGAAGTGCTATTTAATACGCAATCTAACTGAGCCTCAAGTCTTTGTGAAGTAGTGAGACAGTGATGTTCTCCCCATATACAGATGAGAAACTCAAGACACAGCTAGGGTTACATACTGAGTTAATGACAACACCTGTATTATA... | AATGTGACAATACTAGAAACACATTTAAAGCATCCCTACAGTGATATATAAACAGAATTTGGCTATTTGGGAAAATTTGTAAATTCATATTTTTATTCTTATTTATTTTTTACAAAATTTGATATTCTGGTAGGTTCAACAACTTGTAACACACATCTCAAATGATTAAAATCATTGAGAAGTGCTATTTAATACGCAATCTAACTGAGCCTCAAGTCTTTGTGAAGTAGTGAGACAGTGATGTTCTCCCCATATACAGATGAGAAACTCAAGACACAGCTAGGGTTACATACTGAGTTAATGACAACACCTGTATTATA... |
Task1_train_41506 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | ATTCCATAACAAATCTTTCGTTCCTATCCAAGTTTTCTCAGAACTTACTGTAAAAACAAGAAATGTAAATTGAACTGTTGTTGCTGATCCCTGTCTCATTCTAGCAATAATTTGTTCACCCACTGAACAAATGTGTTAAGATAACACTTCACTGTCCCACTCATTGCATTAAAAGATATATTTCTAATCAAATTTTATGGTTATACATTATTTATAAGAATTGCAATGATGTTGTTAGACTTAATTTGATACTGCTAGTAATTATAATTATAACTTAATCTATCTTTTTTTTTTTTTTTGAGACCAAGTCTTACTCTGTC... | ATTCCATAACAAATCTTTCGTTCCTATCCAAGTTTTCTCAGAACTTACTGTAAAAACAAGAAATGTAAATTGAACTGTTGTTGCTGATCCCTGTCTCATTCTAGCAATAATTTGTTCACCCACTGAACAAATGTGTTAAGATAACACTTCACTGTCCCACTCATTGCATTAAAAGATATATTTCTAATCAAATTTTATGGTTATACATTATTTATAAGAATTGCAATGATGTTGTTAGACTTAATTTGATACTGCTAGTAATTATAATTATAACTTAATCTATCTTTTTTTTTTTTTTTGAGACCAAGTCTTACTCTGTC... |
Task1_train_41507 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CTGTCTCATTCTAGCAATAATTTGTTCACCCACTGAACAAATGTGTTAAGATAACACTTCACTGTCCCACTCATTGCATTAAAAGATATATTTCTAATCAAATTTTATGGTTATACATTATTTATAAGAATTGCAATGATGTTGTTAGACTTAATTTGATACTGCTAGTAATTATAATTATAACTTAATCTATCTTTTTTTTTTTTTTTGAGACCAAGTCTTACTCTGTCGCCCAGGCTGGAGTGCAGTGGTATGATCTTGGCTCACTGCAACCTCCACCTCCCGTGTTCAAGCAATTCTCGTGCCTCAGCCCCCGAGTA... | CTGTCTCATTCTAGCAATAATTTGTTCACCCACTGAACAAATGTGTTAAGATAACACTTCACTGTCCCACTCATTGCATTAAAAGATATATTTCTAATCAAATTTTATGGTTATACATTATTTATAAGAATTGCAATGATGTTGTTAGACTTAATTTGATACTGCTAGTAATTATAATTATAACTTAATCTATCTTTTTTTTTTTTTTTGAGACCAAGTCTTACTCTGTCGCCCAGGCTGGAGTGCAGTGGTATGATCTTGGCTCACTGCAACCTCCACCTCCCGTGTTCAAGCAATTCTCGTGCCTCAGCCCCCGAGTA... |
Task1_train_41508 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | AAAGGGGGCTGTCTACAGCTGAGGCAATCCTTGAAGGGGCTGACAGATGAAGATTGTCTGCAGAGAGCCTCCCCTGCAGCTGGAGCAAAAAGTCCTTCGTTGACCATGAATCTGGACAGCTCATCTGGTGCCCAGCACAAATACATTTTACTTTAGAGTAAAATTCTGTGGGGGAAGATGGACAATATACAAGTTCAAGAAAAAAAAAGAGATGACAAAATTTTGACTGTAAAGAAGAGCATGTTCATGTAATTTTTAAAATTGATGATGTTGAATAGTAAATAAATACAGTATTTAAATTGCTTTGGATCAATATAAAA... | AAAGGGGGCTGTCTACAGCTGAGGCAATCCTTGAAGGGGCTGACAGATGAAGATTGTCTGCAGAGAGCCTCCCCTGCAGCTGGAGCAAAAAGTCCTTCGTTGACCATGAATCTGGACAGCTCATCTGGTGCCCAGCACAAATACATTTTACTTTAGAGTAAAATTCTGTGGGGGAAGATGGACAATATACAAGTTCAAGAAAAAAAAAGAGATGACAAAATTTTGACTGTAAAGAAGAGCATGTTCATGTAATTTTTAAAATTGATGATGTTGAATAGTAAATAAATACAGTATTTAAATTGCTTTGGATCAATATAAAA... |
Task1_train_41509 | A genomic variant on Chromosome 11 is under review. What is the biological outcome — benign or pathogenic? | Benign | TCATTGTGTCTCTATAATTTTCAAAATCGAGAACAAAGGACAGGAGGTACTATATGATTGGGACACCATTCATCTCACTTGTTTTATATTTTTACATTGTATTAATTTTTCTTTCTCAAATAATACAAATAATCATAGATTCTGAAATTTCTAATGTTAAAATGTAAAATTTACAAATAAAGCAAAACTCCTCAATGCAAACTACTCTCAAACTTAGTCCTCTCTCCAAAGGTATTACTGTCCTCAGTTTTGGGTGTTCCCATCATGTTGGCATTAATATATAGAATTTAGCTTCACAAAGCACCAAAAGCATAGTGGGT... | TCATTGTGTCTCTATAATTTTCAAAATCGAGAACAAAGGACAGGAGGTACTATATGATTGGGACACCATTCATCTCACTTGTTTTATATTTTTACATTGTATTAATTTTTCTTTCTCAAATAATACAAATAATCATAGATTCTGAAATTTCTAATGTTAAAATGTAAAATTTACAAATAAAGCAAAACTCCTCAATGCAAACTACTCTCAAACTTAGTCCTCTCTCCAAAGGTATTACTGTCCTCAGTTTTGGGTGTTCCCATCATGTTGGCATTAATATATAGAATTTAGCTTCACAAAGCACCAAAAGCATAGTGGGT... |
Task1_train_41510 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | TCTCAAAGATCTCAAGCACTTCTGAAGGGGACATATAAACAGGGACCAGTAGAGAATAATAATAATTGATATGTGATACTGTGAGAATGCCAAAGGGGAACAAAAAAATCATGTTGATCATTTCAGATGGATTTTCTGAGGAGTCCTGCATTCTCGTGAGGGCCTATCATGTGTTGCTTACTGCTGTAGCCCAACAAAATGATACAGAAGTGAACAAAAGAAGAAATAGATCGCTTACCCTAGGAGTCTATAATCTAGTGGGGGAATTCAATCTACAAATTAAAATGTAAACTTTATAATAAATAATGTTCGTGAAGTGC... | TCTCAAAGATCTCAAGCACTTCTGAAGGGGACATATAAACAGGGACCAGTAGAGAATAATAATAATTGATATGTGATACTGTGAGAATGCCAAAGGGGAACAAAAAAATCATGTTGATCATTTCAGATGGATTTTCTGAGGAGTCCTGCATTCTCGTGAGGGCCTATCATGTGTTGCTTACTGCTGTAGCCCAACAAAATGATACAGAAGTGAACAAAAGAAGAAATAGATCGCTTACCCTAGGAGTCTATAATCTAGTGGGGGAATTCAATCTACAAATTAAAATGTAAACTTTATAATAAATAATGTTCGTGAAGTGC... |
Task1_train_41511 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GCTTTCCTGCTGCATGGGACATGGCAATAAATGGGAGTTTCCTGCACACAGAGATAAAATTCACTTGCTGAAGATGTCAGTCTTCTTCTTGACCAACTCCTATGTTGGTACAAACATGTGAGAGAAATGCACCTTCTGAATCATTTCAAATTCGTGGTCTTTGTTAGAGCACATAAGCCGGTGCGCTAGGAGATGTAGCTATTACATTCTATTATAGAATTTTCCATTCTCTATCATCTGGATTCTTATTTGAAATGTAACCAAAGTTTGTTCTTTCTACTGCATAAGAAGGTTTATACCACTTTATGCTTAGCAAGTAA... | GCTTTCCTGCTGCATGGGACATGGCAATAAATGGGAGTTTCCTGCACACAGAGATAAAATTCACTTGCTGAAGATGTCAGTCTTCTTCTTGACCAACTCCTATGTTGGTACAAACATGTGAGAGAAATGCACCTTCTGAATCATTTCAAATTCGTGGTCTTTGTTAGAGCACATAAGCCGGTGCGCTAGGAGATGTAGCTATTACATTCTATTATAGAATTTTCCATTCTCTATCATCTGGATTCTTATTTGAAATGTAACCAAAGTTTGTTCTTTCTACTGCATAAGAAGGTTTATACCACTTTATGCTTAGCAAGTAA... |
Task1_train_41512 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | AGTATTTTAGCAGCGAAAAAGTGTTGATGTTTTGTTTTTTATACATATATACATATCAGTTAACAGTTCTGAAAAATAGATTGAAAAAAACTGTGGAGTGTTAGAACTGTATAAGTCTCTAGGGAAGTTCTTTGCTAAAAGGGGAGAGAACAAGTTTCCATTCTTTATCTTGAGAAGGAAGCAGTGGATGCATCAGTCTCCCCAAAACCCCGCTATTTCAGACAAAGATGTCAGGGGAGTCTGCCAAGAAGTGGAACTCAGAATTTCGTTTCTAAATATTCTCAAGGCCATAAAGCTAAGGAACCTTACACATTTGGAGC... | AGTATTTTAGCAGCGAAAAAGTGTTGATGTTTTGTTTTTTATACATATATACATATCAGTTAACAGTTCTGAAAAATAGATTGAAAAAAACTGTGGAGTGTTAGAACTGTATAAGTCTCTAGGGAAGTTCTTTGCTAAAAGGGGAGAGAACAAGTTTCCATTCTTTATCTTGAGAAGGAAGCAGTGGATGCATCAGTCTCCCCAAAACCCCGCTATTTCAGACAAAGATGTCAGGGGAGTCTGCCAAGAAGTGGAACTCAGAATTTCGTTTCTAAATATTCTCAAGGCCATAAAGCTAAGGAACCTTACACATTTGGAGC... |
Task1_train_41513 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | TCAGGAGTTCGAGAACAGCCTGGCCAACATGGTGAAACCCCGTGTCTATTAAAAATACAAAAATTAGCCAGGCGTCGTGGTGAGAGGTGACAGCATGCTGGCAGCCCTCGCTCGCTCTCGGCGCCTCCTCGGCCTTGGCGCCCACTCTGGCCACGCTTGAGGAGCCCTTCAGCCCGCCGCTGCACTGTGGGAGCCCCTTTCTGGGCTGGCCAAGGCTGGAGCCGGCTCCCTCAGCTTGCTGGGAGCTGTGGAGGGAAGGAGCGGGCGGGAACCGGGGCTGCGCGGGCGCTTGCGGCCCAGCGAGAGTTCCGGGTGGGCGT... | TCAGGAGTTCGAGAACAGCCTGGCCAACATGGTGAAACCCCGTGTCTATTAAAAATACAAAAATTAGCCAGGCGTCGTGGTGAGAGGTGACAGCATGCTGGCAGCCCTCGCTCGCTCTCGGCGCCTCCTCGGCCTTGGCGCCCACTCTGGCCACGCTTGAGGAGCCCTTCAGCCCGCCGCTGCACTGTGGGAGCCCCTTTCTGGGCTGGCCAAGGCTGGAGCCGGCTCCCTCAGCTTGCTGGGAGCTGTGGAGGGAAGGAGCGGGCGGGAACCGGGGCTGCGCGGGCGCTTGCGGCCCAGCGAGAGTTCCGGGTGGGCGT... |
Task1_train_41514 | 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 | CCTAACTTTGACTGCTTTGCTATAGTAATTATTTTTAATGCTAAAAAAGACAAAGCAAATTTCTAGAGAAATAAATCAATAAGCACTTTTTATTAACTTTTTTGACAAACCGATAGTAAAACATATGCTACCTAACGATAACTGTGTCCCTTTATGTATGAGTCTAAGAGAAATATTCGGATTTTTATCTGGACAAGAAATTCAAAGGCTCCTTAAGAAGAAAGTAAATACCATGGTCACTAATGTAACCAGACTAAATATAAAAGCTACATATGTATGTGTGTGTGTGTGTGTATAAATCAATGTTTTGATCAATGTAA... | CCTAACTTTGACTGCTTTGCTATAGTAATTATTTTTAATGCTAAAAAAGACAAAGCAAATTTCTAGAGAAATAAATCAATAAGCACTTTTTATTAACTTTTTTGACAAACCGATAGTAAAACATATGCTACCTAACGATAACTGTGTCCCTTTATGTATGAGTCTAAGAGAAATATTCGGATTTTTATCTGGACAAGAAATTCAAAGGCTCCTTAAGAAGAAAGTAAATACCATGGTCACTAATGTAACCAGACTAAATATAAAAGCTACATATGTATGTGTGTGTGTGTGTGTATAAATCAATGTTTTGATCAATGTAA... |
Task1_train_41515 | A genomic variant on Chromosome 11 is under review. What is the biological outcome — benign or pathogenic? | Benign | GAAGTAACAAGCAAATGGACATTCTTCATTCTTTCTTTAATATCCATCCTTTCTTTATCAGTTTTAAGAGTTTTGGCAAAATTAATATTTTATGGGTGAGAAGCTACAAGACAGTAGCAGTGGTTAAGTGTCCAGGGCTTCTAACATTGGGTCTGACCCTGGCTAAATTTCTCACTGAGCTACTCGCTAGTAGTTCCTTCAGTTTTCCTCGTATACGTCGATTAAAAAAAATACCGTTTGTGAAGCTGTGTTTATTCTAGAATAAGTGTTTAACATATGTAAGTTACCAACTGTGTCTCCCTTAAACACCCTTTAACTTC... | GAAGTAACAAGCAAATGGACATTCTTCATTCTTTCTTTAATATCCATCCTTTCTTTATCAGTTTTAAGAGTTTTGGCAAAATTAATATTTTATGGGTGAGAAGCTACAAGACAGTAGCAGTGGTTAAGTGTCCAGGGCTTCTAACATTGGGTCTGACCCTGGCTAAATTTCTCACTGAGCTACTCGCTAGTAGTTCCTTCAGTTTTCCTCGTATACGTCGATTAAAAAAAATACCGTTTGTGAAGCTGTGTTTATTCTAGAATAAGTGTTTAACATATGTAAGTTACCAACTGTGTCTCCCTTAAACACCCTTTAACTTC... |
Task1_train_41516 | The following genetic variant occurs on Chromosome 11. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GCACAATAAAAGATGGTAATACCTTGAAGCATTTTAAAAAGATTATAATTATAAAAGTAATTATGTAACTATTGATGAACAATGTTCATTGAAGAAAAGTTAGAAAATGCAAATATGCCACCAAATCCCAAAACACAGTTAATCCTTTTTAAATATAAAAATTCATTTGCACATATAGGTGTTTATATAATAATAGAACTCATGCTATATATACTGTTTGATGACCTTTTTTCCTTAGCATTACATCTTACTGCATCTGAAAATGCACATCTTTTATGTCTCTATTTTTAATGACTGCATAATATTTTATTTTATGAATA... | GCACAATAAAAGATGGTAATACCTTGAAGCATTTTAAAAAGATTATAATTATAAAAGTAATTATGTAACTATTGATGAACAATGTTCATTGAAGAAAAGTTAGAAAATGCAAATATGCCACCAAATCCCAAAACACAGTTAATCCTTTTTAAATATAAAAATTCATTTGCACATATAGGTGTTTATATAATAATAGAACTCATGCTATATATACTGTTTGATGACCTTTTTTCCTTAGCATTACATCTTACTGCATCTGAAAATGCACATCTTTTATGTCTCTATTTTTAATGACTGCATAATATTTTATTTTATGAATA... |
Task1_train_41517 | This is a variant located on Chromosome 11. Is this mutation a likely cause of disease or not? | Benign | TGAAGTGATTTCCCCTTATAAAGTTCTGTGGATCACCTGTTGGATTCACACTCAATTCTATGACACTATTCATTGCAAGCTTGAACGTTTACTCATAAGATCATTGAACTTTTTATTATTGTCATCACAAAATGGCCATGTTTAGGTGGCAAAGTAATAAATCATGCCGACATCAAAGACAACATTGTTTAATATTCACATTTGGGGGGGCTGGAATCAAAATGACCTCTTTATTAGATATACTTTGTCTTTTAAAATAAGCAAGTATCTTCTTGAAATAGATGTTACATGAACATGACCATTTTGTGTTCAGACATGGA... | TGAAGTGATTTCCCCTTATAAAGTTCTGTGGATCACCTGTTGGATTCACACTCAATTCTATGACACTATTCATTGCAAGCTTGAACGTTTACTCATAAGATCATTGAACTTTTTATTATTGTCATCACAAAATGGCCATGTTTAGGTGGCAAAGTAATAAATCATGCCGACATCAAAGACAACATTGTTTAATATTCACATTTGGGGGGGCTGGAATCAAAATGACCTCTTTATTAGATATACTTTGTCTTTTAAAATAAGCAAGTATCTTCTTGAAATAGATGTTACATGAACATGACCATTTTGTGTTCAGACATGGA... |
Task1_train_41518 | A variant was discovered on Chromosome 11. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TTAACATTGAAGACATAAATGACAATTCTCCAGTCTTTGTGGGCCTCCCATACTATGCTGCTGTTCAAGTGGATGCGGAACCCGGGACTCTGATTTATCAGGTGACAGCCATTGACAAAGATAAAGGTCCAAATGGAGAAGTGACCTATGTCCTGCAGGATGACTATGGCCACTTTGAAATTAACCCTAATTCAGGGAATGTTATTTTAAAGGAAGCATTCAACTCTGACTTGTCCAACATTGAGTATGGAGTCACCATCCTAGCCAAGGATGGCGGAAAACCTTCTTTGTCTACATCTGTGGAGCTTCCCATCACTATT... | TTAACATTGAAGACATAAATGACAATTCTCCAGTCTTTGTGGGCCTCCCATACTATGCTGCTGTTCAAGTGGATGCGGAACCCGGGACTCTGATTTATCAGGTGACAGCCATTGACAAAGATAAAGGTCCAAATGGAGAAGTGACCTATGTCCTGCAGGATGACTATGGCCACTTTGAAATTAACCCTAATTCAGGGAATGTTATTTTAAAGGAAGCATTCAACTCTGACTTGTCCAACATTGAGTATGGAGTCACCATCCTAGCCAAGGATGGCGGAAAACCTTCTTTGTCTACATCTGTGGAGCTTCCCATCACTATT... |
Task1_train_41519 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | AGGCCTGAGGTTAAGCTACTAGCTGTGGTTAGCTCGTTCCTTTGTTACTTAAAGGATCTCACCCTTCATGCCTGAGTTAAAATATTCCCTTCCTTTGGGAAGACTTCTGACATTCTCCCAGGAGACAGAATTTTTCCTCCTCTGGTCCCTCCATTGTGCTCACCTACCTGCCAAAGCAGTTATCTTATTATATTATCATCATGTGTTTTCATGTTGTTTCTTGAGGTGAGAGAAAGGAGGCATCATATCCTTTCATCTTTACATTCCCAGGCCTTATACCTCTTTGGCCCCAAACAATTATTTGTTGAATAAATGCACCA... | AGGCCTGAGGTTAAGCTACTAGCTGTGGTTAGCTCGTTCCTTTGTTACTTAAAGGATCTCACCCTTCATGCCTGAGTTAAAATATTCCCTTCCTTTGGGAAGACTTCTGACATTCTCCCAGGAGACAGAATTTTTCCTCCTCTGGTCCCTCCATTGTGCTCACCTACCTGCCAAAGCAGTTATCTTATTATATTATCATCATGTGTTTTCATGTTGTTTCTTGAGGTGAGAGAAAGGAGGCATCATATCCTTTCATCTTTACATTCCCAGGCCTTATACCTCTTTGGCCCCAAACAATTATTTGTTGAATAAATGCACCA... |
Task1_train_41520 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CATGCTCCTGACACGCCTGTTATACTTTACTAGTTAATGTTTCCACTTTCTGAAGTGCTCCTTCATATCTTTTTTTTGTCTTCAAATCTCCTACACTGTTCCCCTGAATCCTGGCTAATGGGTAGCCTCTATCTCCCTGAGAATACAGAAGCCAGACAAGAGTTCTCTTCTTTCCTCACACCAGTTTAGAAGTGCATCTGAATTTGCATCTGGCTTCTGATTCCTTTCTACTACAAGAAAGAAAGCCTCCCTCTCCTAACAAATAATATTTCTTCCTTGGGTTTTGGATGAGCTCACTTTAAGGAGTTCTGGATTAGCTC... | CATGCTCCTGACACGCCTGTTATACTTTACTAGTTAATGTTTCCACTTTCTGAAGTGCTCCTTCATATCTTTTTTTTGTCTTCAAATCTCCTACACTGTTCCCCTGAATCCTGGCTAATGGGTAGCCTCTATCTCCCTGAGAATACAGAAGCCAGACAAGAGTTCTCTTCTTTCCTCACACCAGTTTAGAAGTGCATCTGAATTTGCATCTGGCTTCTGATTCCTTTCTACTACAAGAAAGAAAGCCTCCCTCTCCTAACAAATAATATTTCTTCCTTGGGTTTTGGATGAGCTCACTTTAAGGAGTTCTGGATTAGCTC... |
Task1_train_41521 | Here is a genetic alteration on Chromosome 11. Based on the data, is it a benign variant or a cause of disease? | Benign | CCCTTGTGGGTGAATAAGTCCAGGTGTGCCATCTACTTCACTTGAAGGGCTGACTCAGGTGAAATCCCAGCTGGGCGGCTCTCAGCCTCCCTTTTTCTGTACCCCGTGGAATCCACACAGAGCCTGGCCTCTCCAATTGCTGTGCTTTGGGGGCTCTTTCCACCTGCCTGACCCTCTAGACCCCCAAAGCCACCACAGCCTCTGTGGCAATGGGACAGACACATGGTGGCTGTGGAGTTTCCATGTCTGTGTCTTTGCTGACTTGGGAGTTCCTCCTGCACACCATCCCAGCCGCCCTCTGCATTCCGCCACCCTAAGGC... | CCCTTGTGGGTGAATAAGTCCAGGTGTGCCATCTACTTCACTTGAAGGGCTGACTCAGGTGAAATCCCAGCTGGGCGGCTCTCAGCCTCCCTTTTTCTGTACCCCGTGGAATCCACACAGAGCCTGGCCTCTCCAATTGCTGTGCTTTGGGGGCTCTTTCCACCTGCCTGACCCTCTAGACCCCCAAAGCCACCACAGCCTCTGTGGCAATGGGACAGACACATGGTGGCTGTGGAGTTTCCATGTCTGTGTCTTTGCTGACTTGGGAGTTCCTCCTGCACACCATCCCAGCCGCCCTCTGCATTCCGCCACCCTAAGGC... |
Task1_train_41522 | A mutation is present on Chromosome 11. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TGAATCATCCAACAGTGGAGAATAGATATTTTCATCAATATGTGATTAGAACAATTACAATAATTACTAACTTTAAGTCTTTTCTCATTTTGTACAAAATTAATACCAAATAACTAAATAATTAAATGTAAAATAATGAAATTATAAAACAAATAGAAGAAAATACAAGTGAATATTAGCTTTTAGGATGAAAAGAAAAAATATAAAAGCAAGGAAGAAGTCACAAGGGAAAAAGACTGACAGATTTCATTAAATAAAAATTGTAAAAAACTTTGTGTATAAAATATATCACACACTAAAATTAAAACTTAAAATCACAT... | TGAATCATCCAACAGTGGAGAATAGATATTTTCATCAATATGTGATTAGAACAATTACAATAATTACTAACTTTAAGTCTTTTCTCATTTTGTACAAAATTAATACCAAATAACTAAATAATTAAATGTAAAATAATGAAATTATAAAACAAATAGAAGAAAATACAAGTGAATATTAGCTTTTAGGATGAAAAGAAAAAATATAAAAGCAAGGAAGAAGTCACAAGGGAAAAAGACTGACAGATTTCATTAAATAAAAATTGTAAAAAACTTTGTGTATAAAATATATCACACACTAAAATTAAAACTTAAAATCACAT... |
Task1_train_41523 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | TCTTCATGTGTAAGATTGAGTAATAATCATACCTACCTCATGAGGCTGTGTGAGAAATAAATATATGTAAAATATCAAGCTACTATTGTTTACACAGTAACTATGAGTAACTAAGCCCCAGGCGCTAGATTTGGCTTTACAAATACACTATTTCAACTTAACCCTCCCCACAATCCTATGAGGCAAGATAACCTCTAAGTGGACTCAGAGGGGTTCCAGCAGCAAAATCTGCACCAAAACCCAAGTTTGTTCTAAAAGCCTTATTTTCTACTAGGGCTCACCTTCCTGAAAGTGACTTTACCAGTTCTTTACAGACAGGG... | TCTTCATGTGTAAGATTGAGTAATAATCATACCTACCTCATGAGGCTGTGTGAGAAATAAATATATGTAAAATATCAAGCTACTATTGTTTACACAGTAACTATGAGTAACTAAGCCCCAGGCGCTAGATTTGGCTTTACAAATACACTATTTCAACTTAACCCTCCCCACAATCCTATGAGGCAAGATAACCTCTAAGTGGACTCAGAGGGGTTCCAGCAGCAAAATCTGCACCAAAACCCAAGTTTGTTCTAAAAGCCTTATTTTCTACTAGGGCTCACCTTCCTGAAAGTGACTTTACCAGTTCTTTACAGACAGGG... |
Task1_train_41524 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | ATTGTTTACACAGTAACTATGAGTAACTAAGCCCCAGGCGCTAGATTTGGCTTTACAAATACACTATTTCAACTTAACCCTCCCCACAATCCTATGAGGCAAGATAACCTCTAAGTGGACTCAGAGGGGTTCCAGCAGCAAAATCTGCACCAAAACCCAAGTTTGTTCTAAAAGCCTTATTTTCTACTAGGGCTCACCTTCCTGAAAGTGACTTTACCAGTTCTTTACAGACAGGGAAACTGAGGTTCAGTGGGGTTAAGTAATCCACAATTCTGAGTGGTAGACTGGGAACTAAATGCTGATCAGGTAATTGCAAGACA... | ATTGTTTACACAGTAACTATGAGTAACTAAGCCCCAGGCGCTAGATTTGGCTTTACAAATACACTATTTCAACTTAACCCTCCCCACAATCCTATGAGGCAAGATAACCTCTAAGTGGACTCAGAGGGGTTCCAGCAGCAAAATCTGCACCAAAACCCAAGTTTGTTCTAAAAGCCTTATTTTCTACTAGGGCTCACCTTCCTGAAAGTGACTTTACCAGTTCTTTACAGACAGGGAAACTGAGGTTCAGTGGGGTTAAGTAATCCACAATTCTGAGTGGTAGACTGGGAACTAAATGCTGATCAGGTAATTGCAAGACA... |
Task1_train_41525 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | ACAGTAACTATGAGTAACTAAGCCCCAGGCGCTAGATTTGGCTTTACAAATACACTATTTCAACTTAACCCTCCCCACAATCCTATGAGGCAAGATAACCTCTAAGTGGACTCAGAGGGGTTCCAGCAGCAAAATCTGCACCAAAACCCAAGTTTGTTCTAAAAGCCTTATTTTCTACTAGGGCTCACCTTCCTGAAAGTGACTTTACCAGTTCTTTACAGACAGGGAAACTGAGGTTCAGTGGGGTTAAGTAATCCACAATTCTGAGTGGTAGACTGGGAACTAAATGCTGATCAGGTAATTGCAAGACATGCAGACTG... | ACAGTAACTATGAGTAACTAAGCCCCAGGCGCTAGATTTGGCTTTACAAATACACTATTTCAACTTAACCCTCCCCACAATCCTATGAGGCAAGATAACCTCTAAGTGGACTCAGAGGGGTTCCAGCAGCAAAATCTGCACCAAAACCCAAGTTTGTTCTAAAAGCCTTATTTTCTACTAGGGCTCACCTTCCTGAAAGTGACTTTACCAGTTCTTTACAGACAGGGAAACTGAGGTTCAGTGGGGTTAAGTAATCCACAATTCTGAGTGGTAGACTGGGAACTAAATGCTGATCAGGTAATTGCAAGACATGCAGACTG... |
Task1_train_41526 | A genetic alteration is present on Chromosome 11. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TAGTGAAAAGAGGGCTTGTAAGACCATCTGAGGGATTCCAACATCTAGAAGATGGCTAGAGAAAGGGCAGATAGCAAAGTCAGTAAAAGGAGTGGCCAGAGAAGTAAGGGAGAATATGGTGTTGAAGTCCAAAAAAGGGAACTCTCATAGTCAATCCGTGACCAAGTTCTTTTGATAAAGGGCCTGGCTGGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCCAGGCGGGCAGATGACGAGGTCAGGAGGTCGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCCACTAAAAATACAAAAGATTA... | TAGTGAAAAGAGGGCTTGTAAGACCATCTGAGGGATTCCAACATCTAGAAGATGGCTAGAGAAAGGGCAGATAGCAAAGTCAGTAAAAGGAGTGGCCAGAGAAGTAAGGGAGAATATGGTGTTGAAGTCCAAAAAAGGGAACTCTCATAGTCAATCCGTGACCAAGTTCTTTTGATAAAGGGCCTGGCTGGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCCAGGCGGGCAGATGACGAGGTCAGGAGGTCGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCCACTAAAAATACAAAAGATTA... |
Task1_train_41527 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | GAACCAACTTTGAAAACAGCTGCATTGGGCCGGGTGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGTCTGAGGCAGGTGGATTGCTTGAGGCCAGGAGTTTGAGATCAGCCTGGCCAACATGGTGAAATCCCATCTCTACTAAAAAACACAAAAATTAGTTGGGTGTGATGGCATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGAACCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGTGCCACTGCACTCCAGCCTGGACAACATAGTGAGACCCCATCTCAAAAAAAAAAAAAGGAAAA... | GAACCAACTTTGAAAACAGCTGCATTGGGCCGGGTGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGTCTGAGGCAGGTGGATTGCTTGAGGCCAGGAGTTTGAGATCAGCCTGGCCAACATGGTGAAATCCCATCTCTACTAAAAAACACAAAAATTAGTTGGGTGTGATGGCATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGAACCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGTGCCACTGCACTCCAGCCTGGACAACATAGTGAGACCCCATCTCAAAAAAAAAAAAAGGAAAA... |
Task1_train_41528 | 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 | TAAACAATAGTTATTCTTATGGAAAAGGCCATTATTACAAAACCGTATGGCTTTTGACATACTCACCGAAGCCCAGGGAGGAACTTGCATTATCATAAAAACTGTGTGTTATGTCTGTATCCCAGATGAATCAGATAATATCACTACGTTAATGGATAATATGAAAACCTTAACAACTAACCTTTCAGATCCAACACATCTTTAAACAACTGGCTAAGCAGCTAGTTTTGATCTTGAAGACTTGGTGGCAAAAGCTTTGCTTATTCTAGGAATCATAATCATTTGTTGTTGTCTTGTTTTTGTCTGCACTATTAGACTGC... | TAAACAATAGTTATTCTTATGGAAAAGGCCATTATTACAAAACCGTATGGCTTTTGACATACTCACCGAAGCCCAGGGAGGAACTTGCATTATCATAAAAACTGTGTGTTATGTCTGTATCCCAGATGAATCAGATAATATCACTACGTTAATGGATAATATGAAAACCTTAACAACTAACCTTTCAGATCCAACACATCTTTAAACAACTGGCTAAGCAGCTAGTTTTGATCTTGAAGACTTGGTGGCAAAAGCTTTGCTTATTCTAGGAATCATAATCATTTGTTGTTGTCTTGTTTTTGTCTGCACTATTAGACTGC... |
Task1_train_41529 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CACATATTTCCTATATGTGGTTAGGAGACAGGATGGTGAGTTGAATTGGGTATTGGCAGTGCAGGTGGAGGGGTGTCAGATTTGCTATATTTAGGAGAGAGAAGCAAGAGAATTTGAAAATTGGTTATGGCAGCTGTGAGAAATGGAGTGTTGAAGATGGTGCTCCAGGATTCCGACTTGGGTGCACAGGTGGCTGGTGGTACATTTAGTAAGATGGGGAAGATGGAGTTCAGGTTTAAGGGGAAGATGAAGACTGAAGTCCTGGCCGTTATGAGTTTGAAGCCCTATGAGCCATCTACGCGGAGAGAGCTGTATACGCT... | CACATATTTCCTATATGTGGTTAGGAGACAGGATGGTGAGTTGAATTGGGTATTGGCAGTGCAGGTGGAGGGGTGTCAGATTTGCTATATTTAGGAGAGAGAAGCAAGAGAATTTGAAAATTGGTTATGGCAGCTGTGAGAAATGGAGTGTTGAAGATGGTGCTCCAGGATTCCGACTTGGGTGCACAGGTGGCTGGTGGTACATTTAGTAAGATGGGGAAGATGGAGTTCAGGTTTAAGGGGAAGATGAAGACTGAAGTCCTGGCCGTTATGAGTTTGAAGCCCTATGAGCCATCTACGCGGAGAGAGCTGTATACGCT... |
Task1_train_41530 | Assess the clinical impact of this variant found on Chromosome 11. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TCTGTGAATTCAACTGCTTATTTCAGCTGTCTTATTGGGATGATTACTGAATCACTGAAGTCGAAGCTTTTCTAATTTGTTTTGGGGGAAGTTACATGTTTCTTTGGCATTTTCCCAGATTCCAGAGTAGGGCAAAAATGGAGCCGTATGCCTTAGTTGCTTCTTAAAACCATAAAAGTTAACAAAAACCCAGCAGAAGCCTTCGTGATAGCTGCAGGTTTCTTAACTGGGATTTTGTTCAGGGAACGGGAGTAATTTTATTTTTTTATTTTCCTTCTGTGATTAGAACGTACACACCATGTGTCACCATGCAGTTGCTG... | TCTGTGAATTCAACTGCTTATTTCAGCTGTCTTATTGGGATGATTACTGAATCACTGAAGTCGAAGCTTTTCTAATTTGTTTTGGGGGAAGTTACATGTTTCTTTGGCATTTTCCCAGATTCCAGAGTAGGGCAAAAATGGAGCCGTATGCCTTAGTTGCTTCTTAAAACCATAAAAGTTAACAAAAACCCAGCAGAAGCCTTCGTGATAGCTGCAGGTTTCTTAACTGGGATTTTGTTCAGGGAACGGGAGTAATTTTATTTTTTTATTTTCCTTCTGTGATTAGAACGTACACACCATGTGTCACCATGCAGTTGCTG... |
Task1_train_41531 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TAGATAGGGAGTCGAGAATACCTGAAATTATATCCCAGCTCTGCTACTCACCGCTGAGCCTCAGTTCCCCACAGCTAAAACAAGGAGGGTGTTCATATTGGAGGTCTTTTTGAGACCTCAGATCCTGTAGACAGTACCAGGCCAGTGCCTGGCTCCTTGTTTGTGCTCAGCATTCAGTGGCTGTGATTACCCAGGTGTGGAGAATGTCATTTTCCAACATTAGTATATGCTTTACACATCAGTTGTAGCTGAACACCACAGAATGTATTTTATTCCATTAAAAAAACGCTTTTAGTGTTTTGTTTTCATTTCCTTTGTAT... | TAGATAGGGAGTCGAGAATACCTGAAATTATATCCCAGCTCTGCTACTCACCGCTGAGCCTCAGTTCCCCACAGCTAAAACAAGGAGGGTGTTCATATTGGAGGTCTTTTTGAGACCTCAGATCCTGTAGACAGTACCAGGCCAGTGCCTGGCTCCTTGTTTGTGCTCAGCATTCAGTGGCTGTGATTACCCAGGTGTGGAGAATGTCATTTTCCAACATTAGTATATGCTTTACACATCAGTTGTAGCTGAACACCACAGAATGTATTTTATTCCATTAAAAAAACGCTTTTAGTGTTTTGTTTTCATTTCCTTTGTAT... |
Task1_train_41532 | 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 | GGGAAGCAGATGATGTGAGCAAGTTCAGTTTCAGTTAACAGCCAAGAGGTCTAAGTGACAAACTCTTTCTCCCTCAAACCTTAGTTTCCTACTGAGCTCATATCCATGCTTTGATTTCAGAGTTTATCTGGTGCTAGAAGAAAACCTAAAAGCAGTGTGTCAGTAACAATTGTTTAGAGCAGGTGAATTAAGCTCGATTCTGCCTGACAGGTCTCTTTTCTGGGTGACACAGTGAGTCACTCAGGACCAGACAGAAGGTGATAAAAACAATCAGTCCCTGGAATGAGATTTCTCTGGCAAGTTAGACCCTTAAGAATTGA... | GGGAAGCAGATGATGTGAGCAAGTTCAGTTTCAGTTAACAGCCAAGAGGTCTAAGTGACAAACTCTTTCTCCCTCAAACCTTAGTTTCCTACTGAGCTCATATCCATGCTTTGATTTCAGAGTTTATCTGGTGCTAGAAGAAAACCTAAAAGCAGTGTGTCAGTAACAATTGTTTAGAGCAGGTGAATTAAGCTCGATTCTGCCTGACAGGTCTCTTTTCTGGGTGACACAGTGAGTCACTCAGGACCAGACAGAAGGTGATAAAAACAATCAGTCCCTGGAATGAGATTTCTCTGGCAAGTTAGACCCTTAAGAATTGA... |
Task1_train_41533 | An alteration has been detected on Chromosome 11. Is it pathogenic, and if so, what disease is involved? | Benign | ATGAGTCAATCAAATGAAATCTAGGTGTTTTTGCTTTCAAATTATATAAACCCATATTAGGTAAGGATATAGTGAATATAAGTCATTTAGAATAACTTTTTGGAAATTATTTCTGCCATTTGGACTTCTGATAGGTGAGTTGCCATAATTCACCTATCAGAACTCATGGTGAGTTGCCATAACTCACCCATCAAATTATTTCAGCCATATGGACTTCTGATAGCCGAAGGGCTTAGCAAAAGCCAAGGCATGTTGGCAGTAACATAGCTGGGTGAGAATGGCGATGAATTCACTCCAAACATGTTAGGTAAAAGTTATAC... | ATGAGTCAATCAAATGAAATCTAGGTGTTTTTGCTTTCAAATTATATAAACCCATATTAGGTAAGGATATAGTGAATATAAGTCATTTAGAATAACTTTTTGGAAATTATTTCTGCCATTTGGACTTCTGATAGGTGAGTTGCCATAATTCACCTATCAGAACTCATGGTGAGTTGCCATAACTCACCCATCAAATTATTTCAGCCATATGGACTTCTGATAGCCGAAGGGCTTAGCAAAAGCCAAGGCATGTTGGCAGTAACATAGCTGGGTGAGAATGGCGATGAATTCACTCCAAACATGTTAGGTAAAAGTTATAC... |
Task1_train_41534 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TTCTTTTTCAGTTGAGAGGAGTCGACACTTGAAGTCTTTCTGGCTCCGTGCCCGCTTTGTCTGCCTTCCTCCTTCTGGAATGCACATGCCCTGAGCTGAGGGAGTAAAGTTTCTCTTAAAAGAAGCAGCTGCCTCAGAGAGCACCCATGCTGTTTTCTAGACCCCCTTTTATCCAGTCAAATATATCACCTTCTGTAACTTCTTCACCCAAACATCACTTCACATGTATGGAGGGCTATTTTTTTTCCTGCAACCATTATCCCTGAATATAGTAAATATTTATGCATAACCATATTTTGCTTTGAGAGTTTCAGATGCAT... | TTCTTTTTCAGTTGAGAGGAGTCGACACTTGAAGTCTTTCTGGCTCCGTGCCCGCTTTGTCTGCCTTCCTCCTTCTGGAATGCACATGCCCTGAGCTGAGGGAGTAAAGTTTCTCTTAAAAGAAGCAGCTGCCTCAGAGAGCACCCATGCTGTTTTCTAGACCCCCTTTTATCCAGTCAAATATATCACCTTCTGTAACTTCTTCACCCAAACATCACTTCACATGTATGGAGGGCTATTTTTTTTCCTGCAACCATTATCCCTGAATATAGTAAATATTTATGCATAACCATATTTTGCTTTGAGAGTTTCAGATGCAT... |
Task1_train_41535 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | CGATCTCCTGACCTCGGGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGAGTATAGGCGTGAGCCACCGCGCCTGGCCTATACTTGATTTTTAATGAAAACATTCTTAAATTCATATGGCTAACGCAAATTTATTTTCTGTAGGCATAACATCAAAAACACCTGGCAGGATTGCCCCATTCCCAGCACTGTCTATTTCTCCCCTAGTATCAGTGGGACTCCACTGATGCACAGCTGTGATCTACTAAAACTTCTCTCAAAACTTTCTCCTCTCCTTAGGTCAGCAGCCCCGCCCCTGATCTATTTGGAAATCCCCTGAA... | CGATCTCCTGACCTCGGGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGAGTATAGGCGTGAGCCACCGCGCCTGGCCTATACTTGATTTTTAATGAAAACATTCTTAAATTCATATGGCTAACGCAAATTTATTTTCTGTAGGCATAACATCAAAAACACCTGGCAGGATTGCCCCATTCCCAGCACTGTCTATTTCTCCCCTAGTATCAGTGGGACTCCACTGATGCACAGCTGTGATCTACTAAAACTTCTCTCAAAACTTTCTCCTCTCCTTAGGTCAGCAGCCCCGCCCCTGATCTATTTGGAAATCCCCTGAA... |
Task1_train_41536 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | AACAGTTTGTTAAACATTTGGGTTTCTTTCTTGCATGATTAAATTTGTTCATATTTAAACAGAAGTATTTTAGGACCTGTGACATTCTGAAACGGGAATCATGGTAAAAATCCCAGTCACTGTTTTTTTGAAATGAGTTGTGCTTCACTGCATATATATTGTAATTAGGGAGGAAAAGAAAGAAAACTGTGACAGCTTCTAGTATGCCCTCCTCCCTGTCCCAGGAAAGAAAGACTGATTATTATGTAGTCAGTTTTCAAAGTGGAAGACATCCTGATATTGACCTTTATATTTCTCTATTTTATCTTATCATACAAAGT... | AACAGTTTGTTAAACATTTGGGTTTCTTTCTTGCATGATTAAATTTGTTCATATTTAAACAGAAGTATTTTAGGACCTGTGACATTCTGAAACGGGAATCATGGTAAAAATCCCAGTCACTGTTTTTTTGAAATGAGTTGTGCTTCACTGCATATATATTGTAATTAGGGAGGAAAAGAAAGAAAACTGTGACAGCTTCTAGTATGCCCTCCTCCCTGTCCCAGGAAAGAAAGACTGATTATTATGTAGTCAGTTTTCAAAGTGGAAGACATCCTGATATTGACCTTTATATTTCTCTATTTTATCTTATCATACAAAGT... |
Task1_train_41537 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | GAATCTGTGTTTGAAGTCCCTCCACTGGTGGCTTCAGCAGCCCCTGCCCCCAAAGGAAATGCACTTCAAAGAAGACGTGTGTGGACAGCAGCTGAGATCATCAAAGACTGTCCCAAGGACATTTAGCTCCCACCCCAGCTAGAGAGCTGGGAGGCAGTGCTGAGCCAGGCCTGGTCAAGGAGTTTGAAAATTTGCTCAGCTCTGGTAGCAACCTCCCTGGGAGTCCCCTGTTTGTGACGTGCAGCCAGGCAGGCATCTCTGGTGTCTGTGCCCGTATGCCCCAGGACCTGGCATGTCTAAACCAGGCCTGGGAGCCGGAG... | GAATCTGTGTTTGAAGTCCCTCCACTGGTGGCTTCAGCAGCCCCTGCCCCCAAAGGAAATGCACTTCAAAGAAGACGTGTGTGGACAGCAGCTGAGATCATCAAAGACTGTCCCAAGGACATTTAGCTCCCACCCCAGCTAGAGAGCTGGGAGGCAGTGCTGAGCCAGGCCTGGTCAAGGAGTTTGAAAATTTGCTCAGCTCTGGTAGCAACCTCCCTGGGAGTCCCCTGTTTGTGACGTGCAGCCAGGCAGGCATCTCTGGTGTCTGTGCCCGTATGCCCCAGGACCTGGCATGTCTAAACCAGGCCTGGGAGCCGGAG... |
Task1_train_41538 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | AAAGTGCCATTTTCTGGCCATTTAGAACCATTGTCGAGTTTGTACTGGGGCCAGGTGGTGTTGCAGAAGAAAATAAGATGCTTAGATTTTGGGTCAGGTGAGAGTTGAAGAGGTTTTAAGTTCTTGAGAACACAGGCTAAGGGAGAAGAAGGAGGAATGGAGGGTGGAAGGTTGCCCATAGTGAAGGAGGCAAGTTTAAAAAATAAGGGTAGAGACACAGAGAAGGGGGGTGGGGAGCAGCCCTGAGCTGCAACGTAGGGGAGCAGCCAAAGCAGCTGTCCCCACAGTTGATTTGCCCATCAAGGGAATGTGGGTGAATG... | AAAGTGCCATTTTCTGGCCATTTAGAACCATTGTCGAGTTTGTACTGGGGCCAGGTGGTGTTGCAGAAGAAAATAAGATGCTTAGATTTTGGGTCAGGTGAGAGTTGAAGAGGTTTTAAGTTCTTGAGAACACAGGCTAAGGGAGAAGAAGGAGGAATGGAGGGTGGAAGGTTGCCCATAGTGAAGGAGGCAAGTTTAAAAAATAAGGGTAGAGACACAGAGAAGGGGGGTGGGGAGCAGCCCTGAGCTGCAACGTAGGGGAGCAGCCAAAGCAGCTGTCCCCACAGTTGATTTGCCCATCAAGGGAATGTGGGTGAATG... |
Task1_train_41539 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | TGTATTGTTGACTTTCAATTTCATTTCATTTTGGCCAGTATATTCATTTAATATAATTTTTATTTGATATTTACTTTGTAGTCCTATATTGGTAAATTTATCTATTATAAACGTTACCTATGTACCGAAAAGCATTTCACATTTGCTTTTTAATTGTTACAATCTCTATCCTCAAAGTTCTTAAGCTTGTACATATTACTAAACATTAATTTTCTGCTCTACCTTATTGGTTTCTGAAAGGATAATGTTAAACACACACACACACACACAACTCCCAGCACGATTGCAGATTTTACTGTTTGACCTTACAACAACTCTCA... | TGTATTGTTGACTTTCAATTTCATTTCATTTTGGCCAGTATATTCATTTAATATAATTTTTATTTGATATTTACTTTGTAGTCCTATATTGGTAAATTTATCTATTATAAACGTTACCTATGTACCGAAAAGCATTTCACATTTGCTTTTTAATTGTTACAATCTCTATCCTCAAAGTTCTTAAGCTTGTACATATTACTAAACATTAATTTTCTGCTCTACCTTATTGGTTTCTGAAAGGATAATGTTAAACACACACACACACACACAACTCCCAGCACGATTGCAGATTTTACTGTTTGACCTTACAACAACTCTCA... |
Task1_train_41540 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | CCACTTGCTGCTATTATAAATACTGCCGCCCCAGGGCATAAAGATCAACAAGAATGCCTTGAGATTCTAGTATGTGTCAGGCCTTGGGCTGGGTTCTGGGGGAATATACATGGTTTCTGGTGTCAAGAATTTACAAGTTAGTTTGGGGGATAATGACATAATCCTAAATTAATCCTAAGCACTTTCCTTTTGTCCTTTCAGATAAGATGAAAATAATCATAAATAATATTGAATTTTTTTATAAAGAAAGCAGAACCAAGAAAGGATGTATATATTGATGGCAATTGATATATAGCACATGTCTAGATTGACCAAGACAC... | CCACTTGCTGCTATTATAAATACTGCCGCCCCAGGGCATAAAGATCAACAAGAATGCCTTGAGATTCTAGTATGTGTCAGGCCTTGGGCTGGGTTCTGGGGGAATATACATGGTTTCTGGTGTCAAGAATTTACAAGTTAGTTTGGGGGATAATGACATAATCCTAAATTAATCCTAAGCACTTTCCTTTTGTCCTTTCAGATAAGATGAAAATAATCATAAATAATATTGAATTTTTTTATAAAGAAAGCAGAACCAAGAAAGGATGTATATATTGATGGCAATTGATATATAGCACATGTCTAGATTGACCAAGACAC... |
Task1_train_41541 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | ATATAGCACATGTCTAGATTGACCAAGACACAAAATGAATTGTTAGTCATAGCAAATATTGGGGAGATTAAGTTCAAACAGCAACTGGTCTAATTTGAATTTTAGTTTTGCCTGATAAATACCTAATAACTGACACCAGACTGTACATTTTCCCCCATGTAATTTAAATGCGCTGATTAGAGTTGGTTATTTTTCATAAATCCGAAAATGTGTAAACATTCATTAGGAACATGTGCATTAAATTGCAACCAACATTGGTGGCTGATTAACTGAGTTGCAGTTCTGGCTTTATGGGCCTGTTGAGATCTACTCTCCCCTTG... | ATATAGCACATGTCTAGATTGACCAAGACACAAAATGAATTGTTAGTCATAGCAAATATTGGGGAGATTAAGTTCAAACAGCAACTGGTCTAATTTGAATTTTAGTTTTGCCTGATAAATACCTAATAACTGACACCAGACTGTACATTTTCCCCCATGTAATTTAAATGCGCTGATTAGAGTTGGTTATTTTTCATAAATCCGAAAATGTGTAAACATTCATTAGGAACATGTGCATTAAATTGCAACCAACATTGGTGGCTGATTAACTGAGTTGCAGTTCTGGCTTTATGGGCCTGTTGAGATCTACTCTCCCCTTG... |
Task1_train_41542 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | AAAAAAAAAAATTTATTGCTCTGTTCAAAAAATGGAGTCATTTTTTAAACACATGGAGCAGTAACCCATAATGAGGTATAATAGACCTAACCATGAAACACAGAAAACTTAACCATGTTCTACTTCTGCTTTGTATATAGTGATCACCAGCAGCTTGCAAAACTTATCCAGGAGTCGCCAACCGTTGAACTGAAAGACAAGTTGGAGTGTGAATTGGAGGCATTAGTGGGAAGGATGGAAGCAAAAGCCAACCAAATAACTAAAGTTCGAAAATACCAAGCCCAGGTAACTCAGTTTTCCTTCACTCAAGTTTCTAATGA... | AAAAAAAAAAATTTATTGCTCTGTTCAAAAAATGGAGTCATTTTTTAAACACATGGAGCAGTAACCCATAATGAGGTATAATAGACCTAACCATGAAACACAGAAAACTTAACCATGTTCTACTTCTGCTTTGTATATAGTGATCACCAGCAGCTTGCAAAACTTATCCAGGAGTCGCCAACCGTTGAACTGAAAGACAAGTTGGAGTGTGAATTGGAGGCATTAGTGGGAAGGATGGAAGCAAAAGCCAACCAAATAACTAAAGTTCGAAAATACCAAGCCCAGGTAACTCAGTTTTCCTTCACTCAAGTTTCTAATGA... |
Task1_train_41543 | This is a variant located on Chromosome 11. Is this mutation a likely cause of disease or not? | Benign | GCTCAGCCCTGAGGGACAAAACCTGGATATGAAGAGTCCATCTAGCATGTGGCAATGATTCATCACATCAGGGACAAAAGAACAAACAGAATGCTCCTAACAGACCACATTCCATTTTGTTGCTCACCCAAATCCAAATAATACGTCCAATGAAGGACAAATTGTTTTCCCTCTTGATTATGCGTTCCTTCAAACTCCGTGAAATACATTTGTACACACTGGTACTTGCCATCCCTGGTTCTTATCTCCAACCAAAACATGATATTTTCTAATCTCGGTTTTCTTCTCCAAACTTCCTTTTCTTATAAACCAGCCTCAGT... | GCTCAGCCCTGAGGGACAAAACCTGGATATGAAGAGTCCATCTAGCATGTGGCAATGATTCATCACATCAGGGACAAAAGAACAAACAGAATGCTCCTAACAGACCACATTCCATTTTGTTGCTCACCCAAATCCAAATAATACGTCCAATGAAGGACAAATTGTTTTCCCTCTTGATTATGCGTTCCTTCAAACTCCGTGAAATACATTTGTACACACTGGTACTTGCCATCCCTGGTTCTTATCTCCAACCAAAACATGATATTTTCTAATCTCGGTTTTCTTCTCCAAACTTCCTTTTCTTATAAACCAGCCTCAGT... |
Task1_train_41544 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | ACCCAAAATAGGATATCTCCTAATTGAGTATCCCTGTAATTTAAATGTCCAGGTGGCAAGTGAACCAGTGCCTACTGATATAAGGAAAACAGTCATTAACTTGCAGTGTAGAGATAACTGTAACTGGCATCTCTATAACTGCCAAATTTCTTGAAATTTGATTCATATCTCCAAATCCACTATTTTATTATAAATCATGAGATATAAATCAAGTCATGTCACACTTTATTTTAGTCAATATGGCCTTTTCTGAAATATTTGGAAAGAATGCACTCAAAGAAAAAAAATAAAAGTATATCCATCCAACACCTTGTTCCTAC... | ACCCAAAATAGGATATCTCCTAATTGAGTATCCCTGTAATTTAAATGTCCAGGTGGCAAGTGAACCAGTGCCTACTGATATAAGGAAAACAGTCATTAACTTGCAGTGTAGAGATAACTGTAACTGGCATCTCTATAACTGCCAAATTTCTTGAAATTTGATTCATATCTCCAAATCCACTATTTTATTATAAATCATGAGATATAAATCAAGTCATGTCACACTTTATTTTAGTCAATATGGCCTTTTCTGAAATATTTGGAAAGAATGCACTCAAAGAAAAAAAATAAAAGTATATCCATCCAACACCTTGTTCCTAC... |
Task1_train_41545 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GGGAGAAAGTGGGGCAAGAGTTGAAAAACTAACTATTGGGTACTGTGCTCTACCCTGGGTGACAGGATCAATCAATCCGAAACCTCATCATCATGCAATATACCCACCCAGGTAACAAACCTGCCCATGTATCCCCTGGATCTAAAATAAAAGTTAAAATTATAAAATAAATAAGTTGAATTAAAAAAAAAAAAAAAAACCTTGTGGTACTCAAAATTCTGCATGCCCAAGTGGATCAGGGGCCGAAAGTACAGGGCATTCATAAACTGTCTTTAATAGTTTATGTTAAATGTTGCCTCCTGTCAGTAAGAAAGCACTCC... | GGGAGAAAGTGGGGCAAGAGTTGAAAAACTAACTATTGGGTACTGTGCTCTACCCTGGGTGACAGGATCAATCAATCCGAAACCTCATCATCATGCAATATACCCACCCAGGTAACAAACCTGCCCATGTATCCCCTGGATCTAAAATAAAAGTTAAAATTATAAAATAAATAAGTTGAATTAAAAAAAAAAAAAAAAACCTTGTGGTACTCAAAATTCTGCATGCCCAAGTGGATCAGGGGCCGAAAGTACAGGGCATTCATAAACTGTCTTTAATAGTTTATGTTAAATGTTGCCTCCTGTCAGTAAGAAAGCACTCC... |
Task1_train_41546 | A variant was discovered on Chromosome 11. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TAAGCCCCAGTTCCACCTGCAAGAGGAGAATAAATAATTGTATTTACCATATAGGAATGTTATGAGGATCAAATAAGATAACATATATAAAAAGCTTCGTACAGTATGTGACATACAATAATCATTTATTAAATAATCAATTATGATCATGATGCTTCAGAAGACTTCTGGCTTGAAGAACCACTCCTGATGTTAGTATCTAAAAGTCACTTAGTTTGTGGTTATGTAGGGCTATTAAAACTACTTCAGACCAATCAACCTTGGATCAGTCAGTTTAATCCAACAGCGATTCTAATATATTAGCTGCATACAATGTTTTT... | TAAGCCCCAGTTCCACCTGCAAGAGGAGAATAAATAATTGTATTTACCATATAGGAATGTTATGAGGATCAAATAAGATAACATATATAAAAAGCTTCGTACAGTATGTGACATACAATAATCATTTATTAAATAATCAATTATGATCATGATGCTTCAGAAGACTTCTGGCTTGAAGAACCACTCCTGATGTTAGTATCTAAAAGTCACTTAGTTTGTGGTTATGTAGGGCTATTAAAACTACTTCAGACCAATCAACCTTGGATCAGTCAGTTTAATCCAACAGCGATTCTAATATATTAGCTGCATACAATGTTTTT... |
Task1_train_41547 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | GAAGTATATCCTCAAGTAACTATTTCAGAATGACTGCATGGGAGAGAATTATTTTTAAATGAATTCATTTCAATATTGTCATCATGGTACAGAGAAATGCTTTGGTTTTAGTGTCTTTTTACCTGTTACCTAGTTATGATATGAGGCTTTCCACATTGTTCCATATTAATTGTAATTGTTTTTAGTGACTAGACTGTACCACATCAGGGTCAAGTTCTCATATTGTGGAATTCATAGATGGCTTTGAAGAATGTAACTTTTTCATCCTTTTTGATCATTTCAAGGGAAATAGTTTGAAACTAGTCTCCTTCAGACTGTCC... | GAAGTATATCCTCAAGTAACTATTTCAGAATGACTGCATGGGAGAGAATTATTTTTAAATGAATTCATTTCAATATTGTCATCATGGTACAGAGAAATGCTTTGGTTTTAGTGTCTTTTTACCTGTTACCTAGTTATGATATGAGGCTTTCCACATTGTTCCATATTAATTGTAATTGTTTTTAGTGACTAGACTGTACCACATCAGGGTCAAGTTCTCATATTGTGGAATTCATAGATGGCTTTGAAGAATGTAACTTTTTCATCCTTTTTGATCATTTCAAGGGAAATAGTTTGAAACTAGTCTCCTTCAGACTGTCC... |
Task1_train_41548 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | AAAAGAAAACCCCGTGAAAGAATACTCCAGATAAATGGAAAAGTTACAATTGCTCTAGGATACTTATATTTTGCAGCTGATTAAGTAGCATATGGTTCAAAGCTTATTTTATAATGAAAGTGGCAATATCACCCTTTTATTGACCTTGGTCCATTTTTCTTATACGTAGATTTTTCATACTGCTCCAGACCCAAGCATTCCTCTTCCTCAGCCTCAGTCTCGATCTGGATCCCGAAGGACACGAGCAATCTGCCTCTCTACAGGGTCTAGGAAGCCCAGAGGGAGGTATACTCCATGCCTGGCCGAACCTGATAGTAAGT... | AAAAGAAAACCCCGTGAAAGAATACTCCAGATAAATGGAAAAGTTACAATTGCTCTAGGATACTTATATTTTGCAGCTGATTAAGTAGCATATGGTTCAAAGCTTATTTTATAATGAAAGTGGCAATATCACCCTTTTATTGACCTTGGTCCATTTTTCTTATACGTAGATTTTTCATACTGCTCCAGACCCAAGCATTCCTCTTCCTCAGCCTCAGTCTCGATCTGGATCCCGAAGGACACGAGCAATCTGCCTCTCTACAGGGTCTAGGAAGCCCAGAGGGAGGTATACTCCATGCCTGGCCGAACCTGATAGTAAGT... |
Task1_train_41549 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | AATTCATTCAATAGTGCTATTCCCAAAATGCAGACCATGAAAATATGGCTTTAAAAGTCCACAGGCCACAAGAGACTTTGATAATCTCAATGTTTCCCTGTTTGCAATTAATGGAAACAGTATGGGTAATACTAGTGTTGCCATTATTCTGATTTACTACACAAAAATTACATTTTGCAGCATTAAAAAAGTTGCCACCAAATTCAATGTAAGAGTTTTCTCTCATTCCTTTTTGTGGTTGTGTGGGGGTCAAAAAGTCCTGATAGATAACGGTTTCCGGTTAAAAAGGTCACTTAGCTTTTATCCAAAGTGAATAAGTC... | AATTCATTCAATAGTGCTATTCCCAAAATGCAGACCATGAAAATATGGCTTTAAAAGTCCACAGGCCACAAGAGACTTTGATAATCTCAATGTTTCCCTGTTTGCAATTAATGGAAACAGTATGGGTAATACTAGTGTTGCCATTATTCTGATTTACTACACAAAAATTACATTTTGCAGCATTAAAAAAGTTGCCACCAAATTCAATGTAAGAGTTTTCTCTCATTCCTTTTTGTGGTTGTGTGGGGGTCAAAAAGTCCTGATAGATAACGGTTTCCGGTTAAAAAGGTCACTTAGCTTTTATCCAAAGTGAATAAGTC... |
Task1_train_41550 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | GGGAAAGGAGCCTACCTTCCATTGCCCTCTTAAAGAAGACCTTACAGCTCCCACAGGTAAGGACACCATAATGACAGCCTGATGCTTCATCCCCACAGATTAAACAAATCTTCTGAGGTAATGACTCGAAGCTGTATTGTGGGCTCTGGCTGGCTTCTGAATCCGGCCTTGAAATGCAAAACAAAGTACTCCATTTATTTTTAAGTGCACCACTATCTAATACTAAAGGTTTCTTAAACCAGTATTAACAGGGTGAAAGGAGATTTTAAAAACAGAACTGTATATATACACTTGAAAGACATGCAAACTAAACTTGGTAA... | GGGAAAGGAGCCTACCTTCCATTGCCCTCTTAAAGAAGACCTTACAGCTCCCACAGGTAAGGACACCATAATGACAGCCTGATGCTTCATCCCCACAGATTAAACAAATCTTCTGAGGTAATGACTCGAAGCTGTATTGTGGGCTCTGGCTGGCTTCTGAATCCGGCCTTGAAATGCAAAACAAAGTACTCCATTTATTTTTAAGTGCACCACTATCTAATACTAAAGGTTTCTTAAACCAGTATTAACAGGGTGAAAGGAGATTTTAAAAACAGAACTGTATATATACACTTGAAAGACATGCAAACTAAACTTGGTAA... |
Task1_train_41551 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | ATTTGATTATTTGCCTCAATGTTCATAAACAAGGATGGAAAACAGATGCCAGAAAGACATATGGCCAGGGAAGAAGAAATAGTAAAGGAAATCAGTTTAATTAGAATTCAATCAAAATTTAAGAAATGTGTAACTCTAAGGATTGCCAAAAATAGTCTGTGTCAAAGCACCAGACACTCTGGAATACATTATGCTTTCGAACACACTGGTTATGGAAAAGGAAAATTATTCAGTTTAGGAAAGAGATTATAATTTAACTGGTCACAGAATGAGAATAGGGAGAATTCAAAAACTCCCCCCATTTTAATTCAGTTAAAATC... | ATTTGATTATTTGCCTCAATGTTCATAAACAAGGATGGAAAACAGATGCCAGAAAGACATATGGCCAGGGAAGAAGAAATAGTAAAGGAAATCAGTTTAATTAGAATTCAATCAAAATTTAAGAAATGTGTAACTCTAAGGATTGCCAAAAATAGTCTGTGTCAAAGCACCAGACACTCTGGAATACATTATGCTTTCGAACACACTGGTTATGGAAAAGGAAAATTATTCAGTTTAGGAAAGAGATTATAATTTAACTGGTCACAGAATGAGAATAGGGAGAATTCAAAAACTCCCCCCATTTTAATTCAGTTAAAATC... |
Task1_train_41552 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CTCACTACTGATATATAACCACAAGGTTTTTAATCAAATCATTTTTTGACAGACACAGCGACAAGTGATTATATGGATTACAGAATGAAAAAAGGTTTTGTTCATGGAACAGTCTAATTTTTAAAAAGCCGTATAAATTTTTAGTCACCTAGTTTAGCCAGGAGGTAATGTTGCCAAACCTATAACCCTCAGACATCGGAGATCTCAAGTTTAACCAATAAAAATTCCATCTATGTCTTAAACTTACACCTTCAAAGTACATTTTAAAATAGCAGCATTTCAGAATATCCAAGATTTATTTATTTTTCTTTCTATTCTTG... | CTCACTACTGATATATAACCACAAGGTTTTTAATCAAATCATTTTTTGACAGACACAGCGACAAGTGATTATATGGATTACAGAATGAAAAAAGGTTTTGTTCATGGAACAGTCTAATTTTTAAAAAGCCGTATAAATTTTTAGTCACCTAGTTTAGCCAGGAGGTAATGTTGCCAAACCTATAACCCTCAGACATCGGAGATCTCAAGTTTAACCAATAAAAATTCCATCTATGTCTTAAACTTACACCTTCAAAGTACATTTTAAAATAGCAGCATTTCAGAATATCCAAGATTTATTTATTTTTCTTTCTATTCTTG... |
Task1_train_41553 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | ACTTGAAAACATAGCAATAGAAATTATCCAAGCTGAAGCTTTGGGAGAAAAAGGCTGGAAAAAAATGAACAGTTTGTTAGTGACCTGTGAGACCATATAAAGCCATCAACACATTTAATTAAAAATAAAATTTAAATAAAATTTCACAAAGTAGGAATGGAAATGTTTAAAGAAACCATCGCTGGAAATGTTTCAAATTTGATGAAAATTATAAATCCACAGACTCAAGAAGCCCAACAAACTCCAAGAAGGATAAGTGTATGCACACACACATACCACAGAAAGGCACCTAAAAATCAGATTAAAGCCAGAGGGAAAAA... | ACTTGAAAACATAGCAATAGAAATTATCCAAGCTGAAGCTTTGGGAGAAAAAGGCTGGAAAAAAATGAACAGTTTGTTAGTGACCTGTGAGACCATATAAAGCCATCAACACATTTAATTAAAAATAAAATTTAAATAAAATTTCACAAAGTAGGAATGGAAATGTTTAAAGAAACCATCGCTGGAAATGTTTCAAATTTGATGAAAATTATAAATCCACAGACTCAAGAAGCCCAACAAACTCCAAGAAGGATAAGTGTATGCACACACACATACCACAGAAAGGCACCTAAAAATCAGATTAAAGCCAGAGGGAAAAA... |
Task1_train_41554 | With a mutation on Chromosome 11, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | AGAAATTATCCAAGCTGAAGCTTTGGGAGAAAAAGGCTGGAAAAAAATGAACAGTTTGTTAGTGACCTGTGAGACCATATAAAGCCATCAACACATTTAATTAAAAATAAAATTTAAATAAAATTTCACAAAGTAGGAATGGAAATGTTTAAAGAAACCATCGCTGGAAATGTTTCAAATTTGATGAAAATTATAAATCCACAGACTCAAGAAGCCCAACAAACTCCAAGAAGGATAAGTGTATGCACACACACATACCACAGAAAGGCACCTAAAAATCAGATTAAAGCCAGAGGGAAAAAAGATATGTTACATGCAGG... | AGAAATTATCCAAGCTGAAGCTTTGGGAGAAAAAGGCTGGAAAAAAATGAACAGTTTGTTAGTGACCTGTGAGACCATATAAAGCCATCAACACATTTAATTAAAAATAAAATTTAAATAAAATTTCACAAAGTAGGAATGGAAATGTTTAAAGAAACCATCGCTGGAAATGTTTCAAATTTGATGAAAATTATAAATCCACAGACTCAAGAAGCCCAACAAACTCCAAGAAGGATAAGTGTATGCACACACACATACCACAGAAAGGCACCTAAAAATCAGATTAAAGCCAGAGGGAAAAAAGATATGTTACATGCAGG... |
Task1_train_41555 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TGACCTGTGAGACCATATAAAGCCATCAACACATTTAATTAAAAATAAAATTTAAATAAAATTTCACAAAGTAGGAATGGAAATGTTTAAAGAAACCATCGCTGGAAATGTTTCAAATTTGATGAAAATTATAAATCCACAGACTCAAGAAGCCCAACAAACTCCAAGAAGGATAAGTGTATGCACACACACATACCACAGAAAGGCACCTAAAAATCAGATTAAAGCCAGAGGGAAAAAAGATATGTTACATGCAGGGCAATAAAGATAAGACGGACCGCTAAATGTAACTTATAAGCAAAACTTGAAATTGATCATAA... | TGACCTGTGAGACCATATAAAGCCATCAACACATTTAATTAAAAATAAAATTTAAATAAAATTTCACAAAGTAGGAATGGAAATGTTTAAAGAAACCATCGCTGGAAATGTTTCAAATTTGATGAAAATTATAAATCCACAGACTCAAGAAGCCCAACAAACTCCAAGAAGGATAAGTGTATGCACACACACATACCACAGAAAGGCACCTAAAAATCAGATTAAAGCCAGAGGGAAAAAAGATATGTTACATGCAGGGCAATAAAGATAAGACGGACCGCTAAATGTAACTTATAAGCAAAACTTGAAATTGATCATAA... |
Task1_train_41556 | 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 | TCCATGTTCTTAAAATCTATCAAGAAGTTTGATTTACTTTTATGTGTACTGAATCATATGTAGTGTCAAAACTGGAAGATTCCAATGGCCTATTCCAACATTTCCCAAAATGTGTTCCACACAATACTAGTTCCAAGAGATAGACAGTGTTAGCTCCCATTGAAGAGGGGCAGGGGGAGGGATTTATTCATTCAACAAGTATTTTGGTTAAAAATTTGGGAAACAGTTCATACTGTATTCCATCCTGGAAAATCATAATGTATATCAATATTTTAAAGGCTTAGAGAAGTCTTATAGTAAACTGTCTTAGTTTACTTTAG... | TCCATGTTCTTAAAATCTATCAAGAAGTTTGATTTACTTTTATGTGTACTGAATCATATGTAGTGTCAAAACTGGAAGATTCCAATGGCCTATTCCAACATTTCCCAAAATGTGTTCCACACAATACTAGTTCCAAGAGATAGACAGTGTTAGCTCCCATTGAAGAGGGGCAGGGGGAGGGATTTATTCATTCAACAAGTATTTTGGTTAAAAATTTGGGAAACAGTTCATACTGTATTCCATCCTGGAAAATCATAATGTATATCAATATTTTAAAGGCTTAGAGAAGTCTTATAGTAAACTGTCTTAGTTTACTTTAG... |
Task1_train_41557 | A mutation found on Chromosome 11 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GCTGTGAAAGCCTGGGTTCCTGGGCTCAGCTCTAATTTGCCTTTGAAAAGTGAATGTCTGTCCATTGTCAAAGATTTAGTTCAAACTGTTTCTAATTTTTAAAAATTAGAAATAATCCAGTATGGGATTGATTAAGTAATGATATATCTATTCATTGGAATAACATATAATATATAAAGGATGAGAATTAAAATCCGTTGACAGGAAAAAATAAAATTTTGTGAGTGAAAAAGTTTATAAATCAACACCACTAGTAAAATCCTATTTTTTTAGAAATCATTGCGCCCTACTCCCATATGTACAATATCTAGCTCTCTATC... | GCTGTGAAAGCCTGGGTTCCTGGGCTCAGCTCTAATTTGCCTTTGAAAAGTGAATGTCTGTCCATTGTCAAAGATTTAGTTCAAACTGTTTCTAATTTTTAAAAATTAGAAATAATCCAGTATGGGATTGATTAAGTAATGATATATCTATTCATTGGAATAACATATAATATATAAAGGATGAGAATTAAAATCCGTTGACAGGAAAAAATAAAATTTTGTGAGTGAAAAAGTTTATAAATCAACACCACTAGTAAAATCCTATTTTTTTAGAAATCATTGCGCCCTACTCCCATATGTACAATATCTAGCTCTCTATC... |
Task1_train_41558 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | TGCCTTGGCTTCCCAAAGTGCTAGGATTACAGGCATGAGCCACTGCGCCCAGCCCAGCAGTTTTTTCTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTTGAGATGGAGTCTCACTCTGTCATGAGGCTGGAATGCAGTTACGCGATCTTGGCTCACTGCAACCTCCACCTCCCTGGTTCAAGCGATTCTCCTGCCTCAGCCCCCCGAGTACTGGGACTGCAGGCGCGCACCACCAAGCCCAGTTAATTTTCGTATTTTTAGTAGACACAGGGTTTCACCATGTTAGCCAGGATGGTCGCAAT... | TGCCTTGGCTTCCCAAAGTGCTAGGATTACAGGCATGAGCCACTGCGCCCAGCCCAGCAGTTTTTTCTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTTGAGATGGAGTCTCACTCTGTCATGAGGCTGGAATGCAGTTACGCGATCTTGGCTCACTGCAACCTCCACCTCCCTGGTTCAAGCGATTCTCCTGCCTCAGCCCCCCGAGTACTGGGACTGCAGGCGCGCACCACCAAGCCCAGTTAATTTTCGTATTTTTAGTAGACACAGGGTTTCACCATGTTAGCCAGGATGGTCGCAAT... |
Task1_train_41559 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AGTATGTTTGGACATGTTCTCCTAAGTTTCAGCCCCCAAGTGCTCTCAAAGGCTAGTAATCTGATAAGATCATGATCATTAAACAGAAAATGTCAGTTAAATTTGATTTCAAGTAAACAATGACTAACTTTTGGTATAAATAAATACAAAATATTTTAAGGGATATATATATATACCAAAAAATTATTTGTTGTTTATCTGAAATTTATAGTGTCCTATATTTTTATTTGCCAAATCTGGCAACCTTAGTAAAAAGTGAACATTAAAGACAGATTAATTACCTTTATTTGGCAGAAAAAGAGACTTTTTTAGTTTTTATC... | AGTATGTTTGGACATGTTCTCCTAAGTTTCAGCCCCCAAGTGCTCTCAAAGGCTAGTAATCTGATAAGATCATGATCATTAAACAGAAAATGTCAGTTAAATTTGATTTCAAGTAAACAATGACTAACTTTTGGTATAAATAAATACAAAATATTTTAAGGGATATATATATATACCAAAAAATTATTTGTTGTTTATCTGAAATTTATAGTGTCCTATATTTTTATTTGCCAAATCTGGCAACCTTAGTAAAAAGTGAACATTAAAGACAGATTAATTACCTTTATTTGGCAGAAAAAGAGACTTTTTTAGTTTTTATC... |
Task1_train_41560 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GTGGCGCGACCTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGTGATTCTCATGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCGTGCCACCAGGCCCAGCTAATTTTTGTGTTTTTTAGTAGAGATGGGGTTTTGCCACGTTTGCCAGGCTGGTCTCAAACTCCTGAACTCAGGTGATCCGTCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACACCCAGTCCATATATTAAGAATCTTACATGAGAACCACAAGAATTGCTCAGGAAAAGATTTTTCTCGTTTATGTTGCCTATCT... | GTGGCGCGACCTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGTGATTCTCATGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCGTGCCACCAGGCCCAGCTAATTTTTGTGTTTTTTAGTAGAGATGGGGTTTTGCCACGTTTGCCAGGCTGGTCTCAAACTCCTGAACTCAGGTGATCCGTCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACACCCAGTCCATATATTAAGAATCTTACATGAGAACCACAAGAATTGCTCAGGAAAAGATTTTTCTCGTTTATGTTGCCTATCT... |
Task1_train_41561 | Here is a genetic alteration on Chromosome 11. Based on the data, is it a benign variant or a cause of disease? | Benign | CACTGCAACCTCTGCCTCCCAGGTTCAAGTGATTCTCATGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCGTGCCACCAGGCCCAGCTAATTTTTGTGTTTTTTAGTAGAGATGGGGTTTTGCCACGTTTGCCAGGCTGGTCTCAAACTCCTGAACTCAGGTGATCCGTCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACACCCAGTCCATATATTAAGAATCTTACATGAGAACCACAAGAATTGCTCAGGAAAAGATTTTTCTCGTTTATGTTGCCTATCTTGCTAAATTCATTTTTA... | CACTGCAACCTCTGCCTCCCAGGTTCAAGTGATTCTCATGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCGTGCCACCAGGCCCAGCTAATTTTTGTGTTTTTTAGTAGAGATGGGGTTTTGCCACGTTTGCCAGGCTGGTCTCAAACTCCTGAACTCAGGTGATCCGTCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACACCCAGTCCATATATTAAGAATCTTACATGAGAACCACAAGAATTGCTCAGGAAAAGATTTTTCTCGTTTATGTTGCCTATCTTGCTAAATTCATTTTTA... |
Task1_train_41562 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | ACCTCTGCCTCCCAGGTTCAAGTGATTCTCATGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCGTGCCACCAGGCCCAGCTAATTTTTGTGTTTTTTAGTAGAGATGGGGTTTTGCCACGTTTGCCAGGCTGGTCTCAAACTCCTGAACTCAGGTGATCCGTCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACACCCAGTCCATATATTAAGAATCTTACATGAGAACCACAAGAATTGCTCAGGAAAAGATTTTTCTCGTTTATGTTGCCTATCTTGCTAAATTCATTTTTATCTCAAG... | ACCTCTGCCTCCCAGGTTCAAGTGATTCTCATGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCGTGCCACCAGGCCCAGCTAATTTTTGTGTTTTTTAGTAGAGATGGGGTTTTGCCACGTTTGCCAGGCTGGTCTCAAACTCCTGAACTCAGGTGATCCGTCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACACCCAGTCCATATATTAAGAATCTTACATGAGAACCACAAGAATTGCTCAGGAAAAGATTTTTCTCGTTTATGTTGCCTATCTTGCTAAATTCATTTTTATCTCAAG... |
Task1_train_41563 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | AAGTTTTAGGAAACATGATAGTCTGAAATTGATGCTACTATTAAAAATGGAATATTCAATTCTTATAGATCCTTTTGCATTTGTTACGTTGATATGATGAATCGCTTATACATCTCTCTCACTTTTCTTAGCACAGTCCCTGAAACATAATTAATAGTAGGTAGGTAGTTAATTCTTGCTGAATAAATCAATGAATGGAATGATAATATATACTTGTTTCAGTTTTCTTATTTTGTAAAATAATTTGAGAATAATGTATTAACATACTTGAGGAAATTTTTGAGGACCTCAAATATTTATAAAATATTTCACACACTCTG... | AAGTTTTAGGAAACATGATAGTCTGAAATTGATGCTACTATTAAAAATGGAATATTCAATTCTTATAGATCCTTTTGCATTTGTTACGTTGATATGATGAATCGCTTATACATCTCTCTCACTTTTCTTAGCACAGTCCCTGAAACATAATTAATAGTAGGTAGGTAGTTAATTCTTGCTGAATAAATCAATGAATGGAATGATAATATATACTTGTTTCAGTTTTCTTATTTTGTAAAATAATTTGAGAATAATGTATTAACATACTTGAGGAAATTTTTGAGGACCTCAAATATTTATAAAATATTTCACACACTCTG... |
Task1_train_41564 | 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 | GACCTCCAGTTCTCTGGTCATTTTGCAACCCTTTCTAAGTTACTACAGAGGTCTGATAACTTGACAGCCACAGGAACAATAACACAAATTAATTTGTAGGTTGGCTTTGAGAGAACAACTCTTTTTAGAAAGAACAGTTCCTCCACTCAGTGCTCCAGTTAATGGTTATGCATAAAAAAGGGTGTCTCATAAGGGATGAGGATCACATCACACAGGCAAAGTGCTACTCTACAGTCAGGAGACTGTCTTCTTGTTTTTACAAAAAAATTAGGACTAACATTAATTGACTTCTCTTGAGGTATTTGTTGCATCAGTGCAGT... | GACCTCCAGTTCTCTGGTCATTTTGCAACCCTTTCTAAGTTACTACAGAGGTCTGATAACTTGACAGCCACAGGAACAATAACACAAATTAATTTGTAGGTTGGCTTTGAGAGAACAACTCTTTTTAGAAAGAACAGTTCCTCCACTCAGTGCTCCAGTTAATGGTTATGCATAAAAAAGGGTGTCTCATAAGGGATGAGGATCACATCACACAGGCAAAGTGCTACTCTACAGTCAGGAGACTGTCTTCTTGTTTTTACAAAAAAATTAGGACTAACATTAATTGACTTCTCTTGAGGTATTTGTTGCATCAGTGCAGT... |
Task1_train_41565 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CCAATAACAGTTTTCTGCAGCACAAACACAGCTAGATTCAGCTTTTTAAAAATATTATAAAAAGGGTTTTATTGAATTTAGTAGTAGATATTATTTAACCAAGGCTCCAAGAATTGTGCAGAAAAGAACAGTTGTTCAAATAAAAGGCAATCATTTCATGCAACACAAACTTCAGTCTCGTGAGACAGAGTCTCACTCTGTTGCCCAGGCTGGAGTACAGTGGTACAATCTCGGCTCACTGCAGCCTCCATCTCCTGGGTTCAGTGATTCTCGTGCCTCAGCCTCCTGAGTCTTGTACTCAGGAAAGATGTTCTTTGCAT... | CCAATAACAGTTTTCTGCAGCACAAACACAGCTAGATTCAGCTTTTTAAAAATATTATAAAAAGGGTTTTATTGAATTTAGTAGTAGATATTATTTAACCAAGGCTCCAAGAATTGTGCAGAAAAGAACAGTTGTTCAAATAAAAGGCAATCATTTCATGCAACACAAACTTCAGTCTCGTGAGACAGAGTCTCACTCTGTTGCCCAGGCTGGAGTACAGTGGTACAATCTCGGCTCACTGCAGCCTCCATCTCCTGGGTTCAGTGATTCTCGTGCCTCAGCCTCCTGAGTCTTGTACTCAGGAAAGATGTTCTTTGCAT... |
Task1_train_41566 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | TCGATTTATTGCTCGTTCTAGATAATCCAATTATTTTTGGGTAGGATTGGACATTATTCCTGAAATGTTCCCGAGAGGTTTACGACCCACCTGATGCATCTTCTGTCCATTTTTCATCATCATCAAAGTGAATATCTCCATAAAGCCCAGGTCCAGGTGGGTAGGCATGAGCCAAACTGTGTCCTGGGCCATCAAAAGAGTAAAAGTCTCCATGTTCTGATAGGGAACAAATTAATGGAAATATAAGTGTTCAGAATTTCTTTTTACCCTGTTCCAATTAAACAACAGTAGATTCTATAGTCTGAATGTTGGTGTCTGCT... | TCGATTTATTGCTCGTTCTAGATAATCCAATTATTTTTGGGTAGGATTGGACATTATTCCTGAAATGTTCCCGAGAGGTTTACGACCCACCTGATGCATCTTCTGTCCATTTTTCATCATCATCAAAGTGAATATCTCCATAAAGCCCAGGTCCAGGTGGGTAGGCATGAGCCAAACTGTGTCCTGGGCCATCAAAAGAGTAAAAGTCTCCATGTTCTGATAGGGAACAAATTAATGGAAATATAAGTGTTCAGAATTTCTTTTTACCCTGTTCCAATTAAACAACAGTAGATTCTATAGTCTGAATGTTGGTGTCTGCT... |
Task1_train_41567 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GTTCACAGGCCACACCTACATTTACCTACCTACTCAGCTGAAATTAACCTTACTCATCTGTGCTTTCATAGTATCTTGTATTTCCACTCTAGCACATGTCACGTTCTCCTTGGTTTATGGTTACAGCAAGGTGCCCAATGTCTGGGCTGAGCATAATTACCAGCCTGTGGCCTGTTAGAAACCAGGCTGTATAGCAGGAGGCAAGCGGCAGGCGAGTGAGCCAGCATATCCACCTCCTGTCAGAACAGCAGCGGCATTCGATTCTCACAGGAATGCGAACCCTATTGTGAACTGTGCGTGCGAGGGATCTAGGTTGCATG... | GTTCACAGGCCACACCTACATTTACCTACCTACTCAGCTGAAATTAACCTTACTCATCTGTGCTTTCATAGTATCTTGTATTTCCACTCTAGCACATGTCACGTTCTCCTTGGTTTATGGTTACAGCAAGGTGCCCAATGTCTGGGCTGAGCATAATTACCAGCCTGTGGCCTGTTAGAAACCAGGCTGTATAGCAGGAGGCAAGCGGCAGGCGAGTGAGCCAGCATATCCACCTCCTGTCAGAACAGCAGCGGCATTCGATTCTCACAGGAATGCGAACCCTATTGTGAACTGTGCGTGCGAGGGATCTAGGTTGCATG... |
Task1_train_41568 | A mutation is present on Chromosome 11. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GTATAATGAATGTCCACGTATCCACCATTCAATTTTAATAGTCATTGACATTTTTCAATTCTTTTCTCATCTTTGTCTTCCCTGCCTTTCTCTTAACCTTTTTTTTTAAATGGAATATTTATAAAGCAGAGATATTGTATACTTCCACCCTTAAAACATAACCACAATGCCATTATCACAGCCAACAAAATGACGATAATTCCTTAATATCATTTTATGTCTAGCCAGCATGTATTTATCCTGATTTTCTCAGAAATTTGTAAATAGTTGGTTTACTTGAATGAGGTTGCAGACAAGGTGCACCCATTGTATTTGGTTGA... | GTATAATGAATGTCCACGTATCCACCATTCAATTTTAATAGTCATTGACATTTTTCAATTCTTTTCTCATCTTTGTCTTCCCTGCCTTTCTCTTAACCTTTTTTTTTAAATGGAATATTTATAAAGCAGAGATATTGTATACTTCCACCCTTAAAACATAACCACAATGCCATTATCACAGCCAACAAAATGACGATAATTCCTTAATATCATTTTATGTCTAGCCAGCATGTATTTATCCTGATTTTCTCAGAAATTTGTAAATAGTTGGTTTACTTGAATGAGGTTGCAGACAAGGTGCACCCATTGTATTTGGTTGA... |
Task1_train_41569 | A variant on Chromosome 11 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TTGCCATCATTTTAGACTGGAAGAGCCTAATTTCTCCCTGGCAAGTAGTATCTCTAAAGATATCGAGAGCTGTGCCCAAATTTGGGCCTTTTATGAAGAGTTTCAACAAGGATTTCAGGAAATGGCCAATGAAGACTGGATCACTTTTCGGTTTGATTCAAAAACAATATTTAGACTAATAATTTGGTTGTTTTATTTTTGGATGTAATCTTTGCAATGTGTTTTTGGTATTTTATAGGACTAAGACATACCTGTTTGAGGAATTTTTGATGAACTGGCATGACAGATTAAGGAAGGTTGAAGAACATTCAGTGATGACA... | TTGCCATCATTTTAGACTGGAAGAGCCTAATTTCTCCCTGGCAAGTAGTATCTCTAAAGATATCGAGAGCTGTGCCCAAATTTGGGCCTTTTATGAAGAGTTTCAACAAGGATTTCAGGAAATGGCCAATGAAGACTGGATCACTTTTCGGTTTGATTCAAAAACAATATTTAGACTAATAATTTGGTTGTTTTATTTTTGGATGTAATCTTTGCAATGTGTTTTTGGTATTTTATAGGACTAAGACATACCTGTTTGAGGAATTTTTGATGAACTGGCATGACAGATTAAGGAAGGTTGAAGAACATTCAGTGATGACA... |
Task1_train_41570 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | ACACGCTTCAACAGAGTTGATGAAGATTTTAGGTCAGTACAATGATGTAAGACATAGACACATATGGTATTTTTTTTAAATTAATTCATATTGTGAAGTGCTTAATACAGGCAAATTACTTTTACATGATTGGTATCCTCTGTGTATTCAAATTCTTTCCTAGTGGATCCTTTTGAGAAGCTATTCTCTCATTCAAGCATTTACTTCTTGAACCATTATGGTGTGGTCTCTGTTATTACCACTCTACCTAATAATACATACTTCATAAAATCACTAATTACTTTCTCTTTTAAATTCAAAAGGCATTTTCAATTTTTATT... | ACACGCTTCAACAGAGTTGATGAAGATTTTAGGTCAGTACAATGATGTAAGACATAGACACATATGGTATTTTTTTTAAATTAATTCATATTGTGAAGTGCTTAATACAGGCAAATTACTTTTACATGATTGGTATCCTCTGTGTATTCAAATTCTTTCCTAGTGGATCCTTTTGAGAAGCTATTCTCTCATTCAAGCATTTACTTCTTGAACCATTATGGTGTGGTCTCTGTTATTACCACTCTACCTAATAATACATACTTCATAAAATCACTAATTACTTTCTCTTTTAAATTCAAAAGGCATTTTCAATTTTTATT... |
Task1_train_41571 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | AGGTTTTTAACTTATGATATGGGACTTATACTCTTTCATAGTGATATTCTTTTTATGTTTTAGATACCTGAAATGTTATTCAGTGAAACAGGTGGTGGAGAAAAATACAATGATAAAAAACGAAAAGAAGAAAAGAAAAAAAATTCAGGTAGTATTTTGATAAAATCAGTTTGATCTGGTTTTTATTTATGAAATAATTGCCGTTTTTAATGCTACAGATCCATTAAAGATTCATGATTATAAATTTGAATAATGCTAAGTGTAACAAAATTAGATTTCTTCTGATGCAAACAAAATTTTGAAGCCCTTTTTATTTTTAA... | AGGTTTTTAACTTATGATATGGGACTTATACTCTTTCATAGTGATATTCTTTTTATGTTTTAGATACCTGAAATGTTATTCAGTGAAACAGGTGGTGGAGAAAAATACAATGATAAAAAACGAAAAGAAGAAAAGAAAAAAAATTCAGGTAGTATTTTGATAAAATCAGTTTGATCTGGTTTTTATTTATGAAATAATTGCCGTTTTTAATGCTACAGATCCATTAAAGATTCATGATTATAAATTTGAATAATGCTAAGTGTAACAAAATTAGATTTCTTCTGATGCAAACAAAATTTTGAAGCCCTTTTTATTTTTAA... |
Task1_train_41572 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | CAACTTCTGCCTCCCGAGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGTGATCACAGGCGCCCACCACCAGCCTGACTAATTTTTTTTGTATTTTTAGTAGAGATAGGGTTTCACCATGTTGGCCAGGCTGGTGTCAAACTCCTGACCTCAGGTGATCTGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTATAGGTGTGAGCCACTGTGCCCGGCTGAGAGGAGGAATTTGATTAGATATTCAAGGTAGGGATTCTTGCTAAAGTTACTTAGCAAAATTCTTATTAAAATAGGATACAAGGCAGGACACAAA... | CAACTTCTGCCTCCCGAGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGTGATCACAGGCGCCCACCACCAGCCTGACTAATTTTTTTTGTATTTTTAGTAGAGATAGGGTTTCACCATGTTGGCCAGGCTGGTGTCAAACTCCTGACCTCAGGTGATCTGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTATAGGTGTGAGCCACTGTGCCCGGCTGAGAGGAGGAATTTGATTAGATATTCAAGGTAGGGATTCTTGCTAAAGTTACTTAGCAAAATTCTTATTAAAATAGGATACAAGGCAGGACACAAA... |
Task1_train_41573 | A mutation on Chromosome 11 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CAAAGGTTCATCTCACTCATTCATTCATTCCCCTTCAAGGCAATGGCCCATCTACCCTATATCCCATTTTAGAGACCCTCTGTGTTATCCACACATTCCACTTTTTTACACTCCCCACCTCCAAGGGGTATGCACACTCTGTCCATTTTACTCAAGAAACATGTTTATTCTCTACTGCTTTGGCTTTGGGCCTCCTGACTTTCCACACTCTAGCAACAGCTCCCTCTTTGAACCACTGGAAAAGCCTCCTGACTGGCCCTCCTGCCACATTATGTCCTCCATGTGTTGCAAGAAGCCTCTTCCTTAAGTCAATTTAAAAA... | CAAAGGTTCATCTCACTCATTCATTCATTCCCCTTCAAGGCAATGGCCCATCTACCCTATATCCCATTTTAGAGACCCTCTGTGTTATCCACACATTCCACTTTTTTACACTCCCCACCTCCAAGGGGTATGCACACTCTGTCCATTTTACTCAAGAAACATGTTTATTCTCTACTGCTTTGGCTTTGGGCCTCCTGACTTTCCACACTCTAGCAACAGCTCCCTCTTTGAACCACTGGAAAAGCCTCCTGACTGGCCCTCCTGCCACATTATGTCCTCCATGTGTTGCAAGAAGCCTCTTCCTTAAGTCAATTTAAAAA... |
Task1_train_41574 | Given this context: Chromosome 11 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AAATTTCAATTTGAGTCTTATCTATTATCTAATGAAACAGGAATCTCTCAGGAATCTGCTCAGGAATCTCTTAACATTGACACAACAAGAAAGGGAGTAGTGGAGTGGTACAGGATCAGTAAAGCAATTTCCCACAGCACATAGGGACTTAGGTGGTTATCTCCTGACTAAATCAGATCATCGGTATATAGTGTGTATATATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAAACAGTTAAATAACAAATGAATAGCTAGGATTCTTCTTATCCTGCACTCCAGAATCCAATGCTTTGTTGGAAA... | AAATTTCAATTTGAGTCTTATCTATTATCTAATGAAACAGGAATCTCTCAGGAATCTGCTCAGGAATCTCTTAACATTGACACAACAAGAAAGGGAGTAGTGGAGTGGTACAGGATCAGTAAAGCAATTTCCCACAGCACATAGGGACTTAGGTGGTTATCTCCTGACTAAATCAGATCATCGGTATATAGTGTGTATATATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAAACAGTTAAATAACAAATGAATAGCTAGGATTCTTCTTATCCTGCACTCCAGAATCCAATGCTTTGTTGGAAA... |
Task1_train_41575 | An alteration has been detected on Chromosome 11. Is it pathogenic, and if so, what disease is involved? | Benign | ACTATTTCTGTGCACAGTCTAAACACAAGGACACAGCTTTTTGGCTAATTGGAAATTTGATCCCGTCCCATAAAAGACAAGGTGGTCTCTAACAGGATGATGACATGTTTACTGAAAATGAGAGTTTAGAAATGAAACTGTAGGTAGATCACAGATAACACTGCATGGGCCTTGGAGTTGAATATATTCTGGAAAATTTAACATATTTATCGTGTTAGATGCAACCTTACGTTTTACACTGGTGATCTTTTGGTCCATATTGAGAAGTGTTTGGGTAAACATTTGATGAGCCACGCGATTCTTTCGCAAAGAGTCTACCA... | ACTATTTCTGTGCACAGTCTAAACACAAGGACACAGCTTTTTGGCTAATTGGAAATTTGATCCCGTCCCATAAAAGACAAGGTGGTCTCTAACAGGATGATGACATGTTTACTGAAAATGAGAGTTTAGAAATGAAACTGTAGGTAGATCACAGATAACACTGCATGGGCCTTGGAGTTGAATATATTCTGGAAAATTTAACATATTTATCGTGTTAGATGCAACCTTACGTTTTACACTGGTGATCTTTTGGTCCATATTGAGAAGTGTTTGGGTAAACATTTGATGAGCCACGCGATTCTTTCGCAAAGAGTCTACCA... |
Task1_train_41576 | A mutation is present on Chromosome 11. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GCCACCATGCCCAACCTCTCATGGTGTTTTATCTTTACTTTGCCAATGACTTAATCCGATGGCAGCACAAACTTGTGCTCCTTGCCACTGGGAGGATTTGTAGCATGGAAGAAAGCAGAAATTGCCTGTGTATTACTTATCTTCCCATCATGTACTTTTAAATGATTCAATTTTTTTTCTATTAACTAAAGTATTTCACATGAGGGTTTCGCCCACAGCCAGAGCCATGAACCACTGAGTTGAAGCATGTCAGAGTGACATCCCAGAAACAGAAGCCATGACTAGACCATATATCTGGGAATGTAGAACCATAAGCCTTG... | GCCACCATGCCCAACCTCTCATGGTGTTTTATCTTTACTTTGCCAATGACTTAATCCGATGGCAGCACAAACTTGTGCTCCTTGCCACTGGGAGGATTTGTAGCATGGAAGAAAGCAGAAATTGCCTGTGTATTACTTATCTTCCCATCATGTACTTTTAAATGATTCAATTTTTTTTCTATTAACTAAAGTATTTCACATGAGGGTTTCGCCCACAGCCAGAGCCATGAACCACTGAGTTGAAGCATGTCAGAGTGACATCCCAGAAACAGAAGCCATGACTAGACCATATATCTGGGAATGTAGAACCATAAGCCTTG... |
Task1_train_41577 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | CCAACACTGTTAACCTGGCAAATAGGATTAGGGTTGGAAGTGACATGAAAGGGAGATTTACTTTTTCATTTTATACTCACCTATGCTTCATATTCTTGTTTTATACTCTTCTGTCTATATTGTTTAAATTTTATACATATACATTTATTAAGATTACAAATGGCATGTTCTAAAAAATAATACTGGTGTAAATAACAAGAAAGGTAAAGATATATGAACAATACATACAAAGAAGTAAAAACTAATTCAACTAATTTTTCCAATCATGACCATTCACTTATAAGACAAAGATTATTTGTAACAACTAGGCATTCTTCAAG... | CCAACACTGTTAACCTGGCAAATAGGATTAGGGTTGGAAGTGACATGAAAGGGAGATTTACTTTTTCATTTTATACTCACCTATGCTTCATATTCTTGTTTTATACTCTTCTGTCTATATTGTTTAAATTTTATACATATACATTTATTAAGATTACAAATGGCATGTTCTAAAAAATAATACTGGTGTAAATAACAAGAAAGGTAAAGATATATGAACAATACATACAAAGAAGTAAAAACTAATTCAACTAATTTTTCCAATCATGACCATTCACTTATAAGACAAAGATTATTTGTAACAACTAGGCATTCTTCAAG... |
Task1_train_41578 | A variant was discovered on Chromosome 11. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TATTATTGGCTTTATGTTTACATTAATGTTTTATATTAAACTGTTTTTAACTAGCCCTTATAATGCAAGTGATTTTTTTTTGTTGACTTGTAAAGTAGTAACAAGTTGATTAATATTTATTAAACTTATATATGCCAGTTGCCAAGGATGTAAAAATATGACAGGGTGTCTGGCCTCAAAGGAGCATAGTCTAGTGGGAAGACTTGACATGTAAACATATAATAATATTAAAAGCATTGCATAGTAATTGGGGAACACAAAGGAGGAGAAACTGTTTCAAGAAAGGATAGAAATAAATGGTCAAGGCAGACATGAAGTAG... | TATTATTGGCTTTATGTTTACATTAATGTTTTATATTAAACTGTTTTTAACTAGCCCTTATAATGCAAGTGATTTTTTTTTGTTGACTTGTAAAGTAGTAACAAGTTGATTAATATTTATTAAACTTATATATGCCAGTTGCCAAGGATGTAAAAATATGACAGGGTGTCTGGCCTCAAAGGAGCATAGTCTAGTGGGAAGACTTGACATGTAAACATATAATAATATTAAAAGCATTGCATAGTAATTGGGGAACACAAAGGAGGAGAAACTGTTTCAAGAAAGGATAGAAATAAATGGTCAAGGCAGACATGAAGTAG... |
Task1_train_41579 | The following genetic variant occurs on Chromosome 11. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CCCATGATGTTTACTATAGATAGCCTTTAAGAGCTTTTATCATAAATGGATGCTTAACCTCACCAATGTTTTTTTCTGGTATCAACTTTGTAAGGGATAAAAACAAGTGTCAGACTGTGAAGACATCTGTGATATGTTACTAATAAAAGTATAACACCTCAACAGACAGGAAATTTAATAGAGAAGTAGGAAAAGGATATGAATAAGCAATTCACAGAAGGGAAAATATTATTTATAGTTATAAGAGAAGATTCCAAACTTTATTAGTAATCAGAATAAAGTAAAAGAATGATATGAGATACTACCACTTTAAATCCATC... | CCCATGATGTTTACTATAGATAGCCTTTAAGAGCTTTTATCATAAATGGATGCTTAACCTCACCAATGTTTTTTTCTGGTATCAACTTTGTAAGGGATAAAAACAAGTGTCAGACTGTGAAGACATCTGTGATATGTTACTAATAAAAGTATAACACCTCAACAGACAGGAAATTTAATAGAGAAGTAGGAAAAGGATATGAATAAGCAATTCACAGAAGGGAAAATATTATTTATAGTTATAAGAGAAGATTCCAAACTTTATTAGTAATCAGAATAAAGTAAAAGAATGATATGAGATACTACCACTTTAAATCCATC... |
Task1_train_41580 | A mutation located on Chromosome 11 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CTCTGCCTCCCAGCTTTAGATTCTTCTGTCTCAGCCTCCCAAGCAGCTGGGATTACAGGTGCCCACCACCATGCCAATTTTTGTATTTTTAGTAGATACGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCGGGTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGTCATGAGCCACTGAGCCCAGCCATAAACAAAGGATTTTAAAGACAGAGATCAATTAGAAAGGATTTTATAAAGGAAGAAATTCAAGTTTTTTTTTTTTTTTGAGACAGAGTCTCGCTCTTGTTGCCCAGGCT... | CTCTGCCTCCCAGCTTTAGATTCTTCTGTCTCAGCCTCCCAAGCAGCTGGGATTACAGGTGCCCACCACCATGCCAATTTTTGTATTTTTAGTAGATACGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCGGGTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGTCATGAGCCACTGAGCCCAGCCATAAACAAAGGATTTTAAAGACAGAGATCAATTAGAAAGGATTTTATAAAGGAAGAAATTCAAGTTTTTTTTTTTTTTTGAGACAGAGTCTCGCTCTTGTTGCCCAGGCT... |
Task1_train_41581 | Chromosome 11 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCGGGTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGTCATGAGCCACTGAGCCCAGCCATAAACAAAGGATTTTAAAGACAGAGATCAATTAGAAAGGATTTTATAAAGGAAGAAATTCAAGTTTTTTTTTTTTTTTGAGACAGAGTCTCGCTCTTGTTGCCCAGGCTGAAGTGCAATGGCATGATCTTGGCTCACTGAAACCTCTGTCTCCTGGGTTCACGAGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGTAATTACAGGCACCTGC... | TTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCGGGTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGTCATGAGCCACTGAGCCCAGCCATAAACAAAGGATTTTAAAGACAGAGATCAATTAGAAAGGATTTTATAAAGGAAGAAATTCAAGTTTTTTTTTTTTTTTGAGACAGAGTCTCGCTCTTGTTGCCCAGGCTGAAGTGCAATGGCATGATCTTGGCTCACTGAAACCTCTGTCTCCTGGGTTCACGAGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGTAATTACAGGCACCTGC... |
Task1_train_41582 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GAGACCCCATCTTTAAAAAAACTAAAAAAATTAGCTGAGTGTAGTGGTGCTTGCCTGTAGTCCTAGCTACCTGGGAGGCTGACATGGGTAGATCCCTTAAGTCCAGGAGGTCAAGGCTGCAGTGAGTCATAATGGGGCCACTGCACTCCAGCTTGGGTGACAGAGCGAGATATTCTGTCTCAAAAACAAGCAAAACTATGAAAAAAAAGTCAACATTTCTTGAAATACTTCTCATATTTGGTAGAGGAGGGAGATATATTGGGATAAAGGACATAGGAAGATAGGATTTTATTATAATATTAATTTCTGTAGTTATTCAA... | GAGACCCCATCTTTAAAAAAACTAAAAAAATTAGCTGAGTGTAGTGGTGCTTGCCTGTAGTCCTAGCTACCTGGGAGGCTGACATGGGTAGATCCCTTAAGTCCAGGAGGTCAAGGCTGCAGTGAGTCATAATGGGGCCACTGCACTCCAGCTTGGGTGACAGAGCGAGATATTCTGTCTCAAAAACAAGCAAAACTATGAAAAAAAAGTCAACATTTCTTGAAATACTTCTCATATTTGGTAGAGGAGGGAGATATATTGGGATAAAGGACATAGGAAGATAGGATTTTATTATAATATTAATTTCTGTAGTTATTCAA... |
Task1_train_41583 | Consider this mutation on Chromosome 11. Is this a benign change or a disease-causing variant? | Benign | TGTATAAACATAAATGTTTTCATCTTAAAAGGTAAACATTGCCTCCAGATTTAGTTTTAACTGTATTTAGCTTTATTCAGAAAGATTTGTTATACTCATTTTGTGTAGGAAAGGTACAATGATTTCCACTTCTCTTATTTACATTTTCTAATCCCTTTCTTTCTAGTTTTTAGAAGTACCCAGATTTGACAAAGAAAACCCTTTTGAAGGCCTGGATGATATAAATCTGTGGATTCCTCTAAGTGAAAATCATGACATTTGGATAAAGACACTGACTTGTGCTTTTTTGGACAGTGGAGGCACAAAATGTGAAATTCTTC... | TGTATAAACATAAATGTTTTCATCTTAAAAGGTAAACATTGCCTCCAGATTTAGTTTTAACTGTATTTAGCTTTATTCAGAAAGATTTGTTATACTCATTTTGTGTAGGAAAGGTACAATGATTTCCACTTCTCTTATTTACATTTTCTAATCCCTTTCTTTCTAGTTTTTAGAAGTACCCAGATTTGACAAAGAAAACCCTTTTGAAGGCCTGGATGATATAAATCTGTGGATTCCTCTAAGTGAAAATCATGACATTTGGATAAAGACACTGACTTGTGCTTTTTTGGACAGTGGAGGCACAAAATGTGAAATTCTTC... |
Task1_train_41584 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | ACTCCAGCCTGGGTGACAGAGCAAAACTCCGTCTCCAAAAAACAAAAACAAAACAAAACCAAACAAAAAACAAAAACAAAAAAAAGAAAATGTGAAAATGGATAGTTCTGAGGAAATGGGAAAAGCCAGTTGCTGAGAGAACTGCAGTAAAGGTAAGTCGGTCCCATGAAGGGATACCTACTTCCTACCTCTGCTCCTCAGCTATGTTCTCTTCATAAGCAGAAATTCTGTGACCAGGCAACTTTCTGTATGGTCAGGTTGCCTGGCCTAAGTCCTTGGCTTGACTAAAAGCCCTTAATAATCCAGCCAGTCCCCCACGG... | ACTCCAGCCTGGGTGACAGAGCAAAACTCCGTCTCCAAAAAACAAAAACAAAACAAAACCAAACAAAAAACAAAAACAAAAAAAAGAAAATGTGAAAATGGATAGTTCTGAGGAAATGGGAAAAGCCAGTTGCTGAGAGAACTGCAGTAAAGGTAAGTCGGTCCCATGAAGGGATACCTACTTCCTACCTCTGCTCCTCAGCTATGTTCTCTTCATAAGCAGAAATTCTGTGACCAGGCAACTTTCTGTATGGTCAGGTTGCCTGGCCTAAGTCCTTGGCTTGACTAAAAGCCCTTAATAATCCAGCCAGTCCCCCACGG... |
Task1_train_41585 | A variant has been detected on Chromosome 11. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CAGACTGCAGACTCTCTAAGTTTGGTTCATCTGACTGAGTCTCCTCACCAAGCTGTAGTTTATGCAATGCTGGAGTAAGGGCAAAGACTTGACTCTCTGAGTGAGAAAGTGTTTTATTAGTCATTTTTTGGCAGTTGGTTCCAATGTCCCCTCTGCCTTCCCTAGGCTGTGATCCACTGGAGCCATCACCTACAGCTGTGGATGTGTGATCTTTCTGGGGACACTTGCCACTTCCAGTAAATGGAATGGCTCTACCACTCCCTGTACACTCCCAAGAACTTCTTCTAGTTTGGGAATTTCCAATATTAACTTCTGAAAGA... | CAGACTGCAGACTCTCTAAGTTTGGTTCATCTGACTGAGTCTCCTCACCAAGCTGTAGTTTATGCAATGCTGGAGTAAGGGCAAAGACTTGACTCTCTGAGTGAGAAAGTGTTTTATTAGTCATTTTTTGGCAGTTGGTTCCAATGTCCCCTCTGCCTTCCCTAGGCTGTGATCCACTGGAGCCATCACCTACAGCTGTGGATGTGTGATCTTTCTGGGGACACTTGCCACTTCCAGTAAATGGAATGGCTCTACCACTCCCTGTACACTCCCAAGAACTTCTTCTAGTTTGGGAATTTCCAATATTAACTTCTGAAAGA... |
Task1_train_41586 | A variant has been detected on Chromosome 11. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CTTCAGGAAGAGAAACAGCTGCCTCAACAGAAGCCATTTCCTGTAATGTAGGAGCTAGGGGCCCCCTATTTGATAATCGGAAGGCAGTCATATTTTCAGTGGTGAGCGTCTGATCAGAGTTGACGGACATCTTTAGATTTTCACATGAAGGTGTTCCTGACTGCTCTCGTGTAGAATAATTCTGTTTGTCTTTTTCTAAAGCGTTAGGAAATGTTTCAGTCTCCACTTGAGGTGATTCTATAAGTAAATTAGTATTTTGTGTATACTGTTGAAGGAGGTTACAGAATTTTTTGCTGGGTTTCCTCGGTAGAGTGTAATAT... | CTTCAGGAAGAGAAACAGCTGCCTCAACAGAAGCCATTTCCTGTAATGTAGGAGCTAGGGGCCCCCTATTTGATAATCGGAAGGCAGTCATATTTTCAGTGGTGAGCGTCTGATCAGAGTTGACGGACATCTTTAGATTTTCACATGAAGGTGTTCCTGACTGCTCTCGTGTAGAATAATTCTGTTTGTCTTTTTCTAAAGCGTTAGGAAATGTTTCAGTCTCCACTTGAGGTGATTCTATAAGTAAATTAGTATTTTGTGTATACTGTTGAAGGAGGTTACAGAATTTTTTGCTGGGTTTCCTCGGTAGAGTGTAATAT... |
Task1_train_41587 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CCCAGGGTGCTCGTAGGTAAGGAGGAGGTCCTGAATCACAGTCCATTTTGCAGATTGATTTTCTATTTCAGATCAACACTGCCAAAGAAAGTTAGGTTCTACCTGAGATTATAGAGCCCTTCAGAATGTATGACCTGATTTATATCACCTGTCGTAATACAATGCCCCCTTTAATAAACACTTCTTTTCCCACATATAGGATTCATATCCAAATATTTAGGTCACATTCAAATTTAAAAATAAAAACGACATGCTTTTATATTTCATCTTCTGAAACCTCTTAGGAGCAAAACCCAGTGCCTTTAATTATATTCTGCACC... | CCCAGGGTGCTCGTAGGTAAGGAGGAGGTCCTGAATCACAGTCCATTTTGCAGATTGATTTTCTATTTCAGATCAACACTGCCAAAGAAAGTTAGGTTCTACCTGAGATTATAGAGCCCTTCAGAATGTATGACCTGATTTATATCACCTGTCGTAATACAATGCCCCCTTTAATAAACACTTCTTTTCCCACATATAGGATTCATATCCAAATATTTAGGTCACATTCAAATTTAAAAATAAAAACGACATGCTTTTATATTTCATCTTCTGAAACCTCTTAGGAGCAAAACCCAGTGCCTTTAATTATATTCTGCACC... |
Task1_train_41588 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GGAAGTGGGGAATTAATCAAAGGAAAAGACAGTACTAGAAATCATTGCCTTGGGTATTTGGTCCACACATCTACTTTCCTTAAATGATTTTTGTATTTTAATGGTGATATTTTTCAAATTGTTTGGGCAATTAAATACTTTTAATAATTAGTATAATACAGTATCGATTTTGTCTTAGCATTATGGCTTTTTCTGTTGATGCTTCCATTAGAATATGAGTGCCATGAAATTAGAAAATGTGTTTTGACCTTCCTTCTAATGCCCAGCCCAATGGCTTTGTGTAGATACACGTGCTTTGTGTAGATCTATGTGGAGATCCA... | GGAAGTGGGGAATTAATCAAAGGAAAAGACAGTACTAGAAATCATTGCCTTGGGTATTTGGTCCACACATCTACTTTCCTTAAATGATTTTTGTATTTTAATGGTGATATTTTTCAAATTGTTTGGGCAATTAAATACTTTTAATAATTAGTATAATACAGTATCGATTTTGTCTTAGCATTATGGCTTTTTCTGTTGATGCTTCCATTAGAATATGAGTGCCATGAAATTAGAAAATGTGTTTTGACCTTCCTTCTAATGCCCAGCCCAATGGCTTTGTGTAGATACACGTGCTTTGTGTAGATCTATGTGGAGATCCA... |
Task1_train_41589 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GGAGGAAAGGGTCTTAATGGGCAGTCATTCTGAGCAGAAACCCCAGTGTCGGGCCCAGGAAGAGCGGGATGAAAGGGGGAGGGAAGCCCGCTGGTAGCCAGGCGGAGCCAGAAAAATAGGAGGTGCAGAGCGAAGGCCTCTGCTAGGCCGCTGGCCTGCCACCTGGGCCCAGAGCGACTTCTTGCTGTGCCACACCCACTAGCTGCCATGTTCATTCCTCAAAACCTGAGATTTCCCCTCAAAACACAGATGGGGGATGCGGGAATCAGTCTGGCCAGCCAGTCTGGCTCCGGTGTTCATGGCCAGGGCAGCCTAAGTCA... | GGAGGAAAGGGTCTTAATGGGCAGTCATTCTGAGCAGAAACCCCAGTGTCGGGCCCAGGAAGAGCGGGATGAAAGGGGGAGGGAAGCCCGCTGGTAGCCAGGCGGAGCCAGAAAAATAGGAGGTGCAGAGCGAAGGCCTCTGCTAGGCCGCTGGCCTGCCACCTGGGCCCAGAGCGACTTCTTGCTGTGCCACACCCACTAGCTGCCATGTTCATTCCTCAAAACCTGAGATTTCCCCTCAAAACACAGATGGGGGATGCGGGAATCAGTCTGGCCAGCCAGTCTGGCTCCGGTGTTCATGGCCAGGGCAGCCTAAGTCA... |
Task1_train_41590 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GCAAATCATCTCAGACCAGAGGTTGGCAATGTTTTTCTATTATAAGCCAGAGAGAAAATATTTTAGGCTTTGTATGCTGCACAGTCTCTGTCACAACTACTCAACTCTGCAAAAGCAGCCCTAGACAATATTCAAATGATAGACAGAGCTGTGTTCCAATAAAACTTTATTTACAAATGGAGTGGCAGGCCTGATTTGGCACAGAGGCCATAGTTTGCAGACCACTATTTTAGACCCTTGGAAAATTTTGCAATATCCTATCACCCAAGAATATTTAGACTGTGGCTTTTTAACTATTCTAATCAAAGTGTGGAAAAGAA... | GCAAATCATCTCAGACCAGAGGTTGGCAATGTTTTTCTATTATAAGCCAGAGAGAAAATATTTTAGGCTTTGTATGCTGCACAGTCTCTGTCACAACTACTCAACTCTGCAAAAGCAGCCCTAGACAATATTCAAATGATAGACAGAGCTGTGTTCCAATAAAACTTTATTTACAAATGGAGTGGCAGGCCTGATTTGGCACAGAGGCCATAGTTTGCAGACCACTATTTTAGACCCTTGGAAAATTTTGCAATATCCTATCACCCAAGAATATTTAGACTGTGGCTTTTTAACTATTCTAATCAAAGTGTGGAAAAGAA... |
Task1_train_41591 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GGTAAGCTCCTGGTGAAGATATGGTTCAAAGCACCTTCTACATGAAAGGACTTATCTTGACTCCTGGCAAAATAGACACCAATATGAAGTCTGTCATTATTAAAATAAGCAAGTATTTTTAGAGACCGAATCAATTAATTGGCAGGGCCTATTGAGTCTGTCTATGAGATTTTGTTATCATTAGTGAGAGAGATGAAAACGCAGAAGGCTTAAACCTATGCTATTACCTACCTATATCCAGTGCACTTGTACCCTGCCACAGCCTTACAGCTGAATGGATACACGTCGCTTAAAATGAGCCCCCCCAGGGCTGCCATGGC... | GGTAAGCTCCTGGTGAAGATATGGTTCAAAGCACCTTCTACATGAAAGGACTTATCTTGACTCCTGGCAAAATAGACACCAATATGAAGTCTGTCATTATTAAAATAAGCAAGTATTTTTAGAGACCGAATCAATTAATTGGCAGGGCCTATTGAGTCTGTCTATGAGATTTTGTTATCATTAGTGAGAGAGATGAAAACGCAGAAGGCTTAAACCTATGCTATTACCTACCTATATCCAGTGCACTTGTACCCTGCCACAGCCTTACAGCTGAATGGATACACGTCGCTTAAAATGAGCCCCCCCAGGGCTGCCATGGC... |
Task1_train_41592 | This is a variant located on Chromosome 11. Is this mutation a likely cause of disease or not? | Benign | CATACAGCTCTGTATAGGAGATATAATGCAGACTTAAAGAACTCTAATGTATGGTAAAAAGTTATAAATACAGGGAAAGATAAAGTTTTATGTGAGTTGAAAGAGAAGCTAACTTCAGGGAAGGCATCATTTGAGCTAGAAGGAAGGAAATGATCATTTATTACTCATTTATTGTGTTATCTAGTTACTCAACTCTCACTTCTTTTTGTTCTCTTTGACTGTAGCAGTGCTTTTAGTCCCTCAATGCCTACATCTCAAAATTACCTTAAAAATTTAGCTAATTCTCCATATTGTATTGGGAATACTGAAGTTTTTCCTGT... | CATACAGCTCTGTATAGGAGATATAATGCAGACTTAAAGAACTCTAATGTATGGTAAAAAGTTATAAATACAGGGAAAGATAAAGTTTTATGTGAGTTGAAAGAGAAGCTAACTTCAGGGAAGGCATCATTTGAGCTAGAAGGAAGGAAATGATCATTTATTACTCATTTATTGTGTTATCTAGTTACTCAACTCTCACTTCTTTTTGTTCTCTTTGACTGTAGCAGTGCTTTTAGTCCCTCAATGCCTACATCTCAAAATTACCTTAAAAATTTAGCTAATTCTCCATATTGTATTGGGAATACTGAAGTTTTTCCTGT... |
Task1_train_41593 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CTTTGTTCTCTATTTTTTGTTATCTCAATAAACCTCCAGAGGCTTAAAGATATTATGGCAATTGAAGATATTTTTATTTTAAAATATTCTTTATTGTTATTGTTTCTGATTACAAAGGTAATAATCATTCATTGCAGAAAATTTAACTTCTGCAACGAGCAGAAAATAAAAAGCACCATAAATAAAGCACCCAGAGATGATGGGAACATTTTAGTGTATTTCCATATATTTTTTAAATGTGCACAGTTTTTATTCCAAAACATACCTTTTTACTAACTTAATAAAAAGTAAAATTTTCCATGATGTTCGGTGTTCTTCCA... | CTTTGTTCTCTATTTTTTGTTATCTCAATAAACCTCCAGAGGCTTAAAGATATTATGGCAATTGAAGATATTTTTATTTTAAAATATTCTTTATTGTTATTGTTTCTGATTACAAAGGTAATAATCATTCATTGCAGAAAATTTAACTTCTGCAACGAGCAGAAAATAAAAAGCACCATAAATAAAGCACCCAGAGATGATGGGAACATTTTAGTGTATTTCCATATATTTTTTAAATGTGCACAGTTTTTATTCCAAAACATACCTTTTTACTAACTTAATAAAAAGTAAAATTTTCCATGATGTTCGGTGTTCTTCCA... |
Task1_train_41594 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | ATTTATAAGTCCTGGGCGGGCATGGTGGCTCGCGCCTGTAATCTCAGCACTTTGGGAGGCCGAGGCAGGTGGATCACCTGAAGTCAGGAGTTTGAGACCAGCATGACTAACATGGTGAAACCCCGTATCTACTAAAAACACAAAATTAGCTGGGCATGGTGGCACGTGCCTGTAATCCCAGCACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCGGGATCATGCCACTGCACTCCAGCCTGGGCGACAGAGTGAGACTCCATCCCCAAATAATAGTAATAAGTCCTTTCAGT... | ATTTATAAGTCCTGGGCGGGCATGGTGGCTCGCGCCTGTAATCTCAGCACTTTGGGAGGCCGAGGCAGGTGGATCACCTGAAGTCAGGAGTTTGAGACCAGCATGACTAACATGGTGAAACCCCGTATCTACTAAAAACACAAAATTAGCTGGGCATGGTGGCACGTGCCTGTAATCCCAGCACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCGGGATCATGCCACTGCACTCCAGCCTGGGCGACAGAGTGAGACTCCATCCCCAAATAATAGTAATAAGTCCTTTCAGT... |
Task1_train_41595 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GAGATAGGGTTTCACCATGTTGCCCAGGCTGGTCTCGAACCCCTGAGCTCAGGCAATCCACCCCCCTTCGGCCTCCCAAAATCCTAGGATTACAGGCATGAGTCACCGTACCCAGCCAAAACCTCTGACTGTACTAAGGTGGACTTCAGTAAATCCTTACATTTGGCTAAAATGACAGCAATTAAGTCTAAAGAGACAGGTAAGTCTTGAAATATGGGCAATGTCTAAAAAGGAATTATGGGTATCACTGACTGGAATCAAAATGCTACCAGCCTGGACTAAAAGAAACTGCCTTCAAAATTTAAAACAATCCTTTGAGC... | GAGATAGGGTTTCACCATGTTGCCCAGGCTGGTCTCGAACCCCTGAGCTCAGGCAATCCACCCCCCTTCGGCCTCCCAAAATCCTAGGATTACAGGCATGAGTCACCGTACCCAGCCAAAACCTCTGACTGTACTAAGGTGGACTTCAGTAAATCCTTACATTTGGCTAAAATGACAGCAATTAAGTCTAAAGAGACAGGTAAGTCTTGAAATATGGGCAATGTCTAAAAAGGAATTATGGGTATCACTGACTGGAATCAAAATGCTACCAGCCTGGACTAAAAGAAACTGCCTTCAAAATTTAAAACAATCCTTTGAGC... |
Task1_train_41596 | A variant on Chromosome 11 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GAAATATTAGATCACAAGTACAGTAAGTAATATTTCTCTAACATGTCATCCCTCTTGAAGGAGCTGTCTATAATGTGCTCCACTTCCTCAACACTGAGTCTCTTTTAGCCTGTATTAATTGGGGTCTTATCCCAACTATATAACTTAGGTTATTCTTACCAAGGGCACTGAAGGCCTTCATCTTTCCAAATCCGGTTGTCTATTTTCTGCCCTCCACTTGCTTGAAGTCTCAGCCGCCTTCAACTCAATTAACAATTCTCCCCATAAGTCACTTTTCTTTGGCTTTCCAGATGCATAGAAGTCTCCTCTGCCAGATCCTT... | GAAATATTAGATCACAAGTACAGTAAGTAATATTTCTCTAACATGTCATCCCTCTTGAAGGAGCTGTCTATAATGTGCTCCACTTCCTCAACACTGAGTCTCTTTTAGCCTGTATTAATTGGGGTCTTATCCCAACTATATAACTTAGGTTATTCTTACCAAGGGCACTGAAGGCCTTCATCTTTCCAAATCCGGTTGTCTATTTTCTGCCCTCCACTTGCTTGAAGTCTCAGCCGCCTTCAACTCAATTAACAATTCTCCCCATAAGTCACTTTTCTTTGGCTTTCCAGATGCATAGAAGTCTCCTCTGCCAGATCCTT... |
Task1_train_41597 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | CAACTAGCAAGCACATTCCTTGCCAGTCACAGCCCATGGTCCTAAGATGTTTACAGTTGAGGAAACAGACTGAAGATACCAACAAGGACACACTCCTGTAACAGCGGAAAGTCCAGATGTCCCAATACCCTTGACAATATATGCTTTCAAGATAATTATAGTTACGCTTTGATGGACTTACACACTAAAATGTCAGGGATAGTTTTCTTTACATCAATAAAGTAATAAATTTTGTCATGCTGTCAGCCCACCCACACACAGGCACAGCTTAGTTTAGTCTTTACATAGACAAGGCCCCTATACAAGAAAAACTTAAAGAC... | CAACTAGCAAGCACATTCCTTGCCAGTCACAGCCCATGGTCCTAAGATGTTTACAGTTGAGGAAACAGACTGAAGATACCAACAAGGACACACTCCTGTAACAGCGGAAAGTCCAGATGTCCCAATACCCTTGACAATATATGCTTTCAAGATAATTATAGTTACGCTTTGATGGACTTACACACTAAAATGTCAGGGATAGTTTTCTTTACATCAATAAAGTAATAAATTTTGTCATGCTGTCAGCCCACCCACACACAGGCACAGCTTAGTTTAGTCTTTACATAGACAAGGCCCCTATACAAGAAAAACTTAAAGAC... |
Task1_train_41598 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | AACTGAAAAACCACCTGGCTATCAATAAGAGAATGGATTAACTATGGTATATATAATGGTTTAAATGAATCAACTGGAACCATGTGTATCAAGAACACATCTCTAAAGCATCTTAAGAGAAAAAAGTAGGTTGCAAATGAATGCACATTTTATACAACTATTTTAAAAAATTGTTTAAATATTACATACACAAATATTCTGGTAGATTGCAAGAATGGTTACAAATTCCTTTCTTCCCATCAAGAGTGGAGCCTATTTCTCTGCCACTTGAATCTGGGTTGGCCATGTGTGTTGCTTTGGCCAAAAGGATGTTTGCAAAC... | AACTGAAAAACCACCTGGCTATCAATAAGAGAATGGATTAACTATGGTATATATAATGGTTTAAATGAATCAACTGGAACCATGTGTATCAAGAACACATCTCTAAAGCATCTTAAGAGAAAAAAGTAGGTTGCAAATGAATGCACATTTTATACAACTATTTTAAAAAATTGTTTAAATATTACATACACAAATATTCTGGTAGATTGCAAGAATGGTTACAAATTCCTTTCTTCCCATCAAGAGTGGAGCCTATTTCTCTGCCACTTGAATCTGGGTTGGCCATGTGTGTTGCTTTGGCCAAAAGGATGTTTGCAAAC... |
Task1_train_41599 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | TATTTGGATGGAGACGTGTGTAAATGAGACAATCCCTAAGAAAGGTTGTAATGGACATTCTTTCACTTCCTAAAACTCTTTTTTGCCCCAGGACCTTTGCAGCTTCTGTTTCCCCACTCCCCTCTATTTACCTAGCGAAGGTCTACTCACTATTCAGCTTAACCATCACCTCCTCAGGGAGCTCTTCCCTGATCTACTCCAGTAGGTCCCCATTATATGCCTTCACTGTACCTCTGATTCTCCATATTACTAACCCCAACATAGGTATATAATCATTAGTGAAACACTTTCATTAATGACTGGACCCCCTATTTGAATAA... | TATTTGGATGGAGACGTGTGTAAATGAGACAATCCCTAAGAAAGGTTGTAATGGACATTCTTTCACTTCCTAAAACTCTTTTTTGCCCCAGGACCTTTGCAGCTTCTGTTTCCCCACTCCCCTCTATTTACCTAGCGAAGGTCTACTCACTATTCAGCTTAACCATCACCTCCTCAGGGAGCTCTTCCCTGATCTACTCCAGTAGGTCCCCATTATATGCCTTCACTGTACCTCTGATTCTCCATATTACTAACCCCAACATAGGTATATAATCATTAGTGAAACACTTTCATTAATGACTGGACCCCCTATTTGAATAA... |
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