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_45300 | Chromosome 17 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TTAGTTATTCTTTCTGTATGCTTGCATGCCATGCTGCTCACCTCCCAGTCACAGCAGAATCCCTCAGCATTGCAATTATTATTATGATAACTTGTCTTTCTTCTTCACTAGATTTGGGAGAGACTTGAGGGCACTTGAGACTTGAGGTAATAGCATTTCTTTTATCTTTTTACTCCTGGCATCAATATGATGCCTGACATAGGGCAAACACTCAGGAAATATGGACAAATGAATGAGTGAATGGACTAGATCTCTTGTTGACAATATCCTCTGTAGTGTCCCATAGACTCCATGGCTGCTAAGTTCTGTTCATTTAAGGT... | TTAGTTATTCTTTCTGTATGCTTGCATGCCATGCTGCTCACCTCCCAGTCACAGCAGAATCCCTCAGCATTGCAATTATTATTATGATAACTTGTCTTTCTTCTTCACTAGATTTGGGAGAGACTTGAGGGCACTTGAGACTTGAGGTAATAGCATTTCTTTTATCTTTTTACTCCTGGCATCAATATGATGCCTGACATAGGGCAAACACTCAGGAAATATGGACAAATGAATGAGTGAATGGACTAGATCTCTTGTTGACAATATCCTCTGTAGTGTCCCATAGACTCCATGGCTGCTAAGTTCTGTTCATTTAAGGT... |
Task1_train_45301 | This mutation on Chromosome 17 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | AGTTCTGAGACCACAACTTAACCAGCAGCACAGAGTAACTTATTCTGAAGCCCACAGTCTCTGAAATAGCCGTCTTTAAATCTTACAAACTTTCCCACACGTTTCTTTATATCTATTTTCTTAATTTCATTCTCTCCATAAATTTTGGAGTCAGACAGAGTTGCATTCAGATTTCAGTTTTGTTTCTAAACTTATGAGCTATGTGACTGTAAGCAAGCTATTTAACTTCTTTTAGACTTACTTATCTACAAGCCAGGATCACAATATCTATTTCACAGGATCAGTATAGATGTTATGTGAAGCAAAGTTCGCATGATGTG... | AGTTCTGAGACCACAACTTAACCAGCAGCACAGAGTAACTTATTCTGAAGCCCACAGTCTCTGAAATAGCCGTCTTTAAATCTTACAAACTTTCCCACACGTTTCTTTATATCTATTTTCTTAATTTCATTCTCTCCATAAATTTTGGAGTCAGACAGAGTTGCATTCAGATTTCAGTTTTGTTTCTAAACTTATGAGCTATGTGACTGTAAGCAAGCTATTTAACTTCTTTTAGACTTACTTATCTACAAGCCAGGATCACAATATCTATTTCACAGGATCAGTATAGATGTTATGTGAAGCAAAGTTCGCATGATGTG... |
Task1_train_45302 | A variant on Chromosome 17 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CCCACAGTCTCTGAAATAGCCGTCTTTAAATCTTACAAACTTTCCCACACGTTTCTTTATATCTATTTTCTTAATTTCATTCTCTCCATAAATTTTGGAGTCAGACAGAGTTGCATTCAGATTTCAGTTTTGTTTCTAAACTTATGAGCTATGTGACTGTAAGCAAGCTATTTAACTTCTTTTAGACTTACTTATCTACAAGCCAGGATCACAATATCTATTTCACAGGATCAGTATAGATGTTATGTGAAGCAAAGTTCGCATGATGTGTACCTGGCACATGCACAGCATATGGTACTAACAAGGCCACGCTGGTTCAC... | CCCACAGTCTCTGAAATAGCCGTCTTTAAATCTTACAAACTTTCCCACACGTTTCTTTATATCTATTTTCTTAATTTCATTCTCTCCATAAATTTTGGAGTCAGACAGAGTTGCATTCAGATTTCAGTTTTGTTTCTAAACTTATGAGCTATGTGACTGTAAGCAAGCTATTTAACTTCTTTTAGACTTACTTATCTACAAGCCAGGATCACAATATCTATTTCACAGGATCAGTATAGATGTTATGTGAAGCAAAGTTCGCATGATGTGTACCTGGCACATGCACAGCATATGGTACTAACAAGGCCACGCTGGTTCAC... |
Task1_train_45303 | This variant lies on Chromosome 17. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ATCTGATTCAATAAATGTTTATTGAATAGGTGGAGTAAAAGGCTTGATTCATGGATATCAATACCACTCAAACATGATTAAAGAGAACTTTCAAGCTGTAGTACTTCTCATGAAAGAGTCTTGTTATTTGCTGTAAAGAGACTAGGAAATGTGTTTTTTGGTTTATTTTATTTTATTTTTTGGATTTAGTAGTGGAACCGGGCTCGGGAAAAAATATCTAGGAGTTATGACACTTTGAAAAATGTACTGCCATCTACTTTATTCCTCTTGGAAATTGCATAATTTTGTGTGTAATCCATCATTGCTACCAATTAAATATA... | ATCTGATTCAATAAATGTTTATTGAATAGGTGGAGTAAAAGGCTTGATTCATGGATATCAATACCACTCAAACATGATTAAAGAGAACTTTCAAGCTGTAGTACTTCTCATGAAAGAGTCTTGTTATTTGCTGTAAAGAGACTAGGAAATGTGTTTTTTGGTTTATTTTATTTTATTTTTTGGATTTAGTAGTGGAACCGGGCTCGGGAAAAAATATCTAGGAGTTATGACACTTTGAAAAATGTACTGCCATCTACTTTATTCCTCTTGGAAATTGCATAATTTTGTGTGTAATCCATCATTGCTACCAATTAAATATA... |
Task1_train_45304 | A mutation on Chromosome 17 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | AGGTGGAGTAAAAGGCTTGATTCATGGATATCAATACCACTCAAACATGATTAAAGAGAACTTTCAAGCTGTAGTACTTCTCATGAAAGAGTCTTGTTATTTGCTGTAAAGAGACTAGGAAATGTGTTTTTTGGTTTATTTTATTTTATTTTTTGGATTTAGTAGTGGAACCGGGCTCGGGAAAAAATATCTAGGAGTTATGACACTTTGAAAAATGTACTGCCATCTACTTTATTCCTCTTGGAAATTGCATAATTTTGTGTGTAATCCATCATTGCTACCAATTAAATATAGAGGTAAGTTCTGGGAGCTTGTAAATA... | AGGTGGAGTAAAAGGCTTGATTCATGGATATCAATACCACTCAAACATGATTAAAGAGAACTTTCAAGCTGTAGTACTTCTCATGAAAGAGTCTTGTTATTTGCTGTAAAGAGACTAGGAAATGTGTTTTTTGGTTTATTTTATTTTATTTTTTGGATTTAGTAGTGGAACCGGGCTCGGGAAAAAATATCTAGGAGTTATGACACTTTGAAAAATGTACTGCCATCTACTTTATTCCTCTTGGAAATTGCATAATTTTGTGTGTAATCCATCATTGCTACCAATTAAATATAGAGGTAAGTTCTGGGAGCTTGTAAATA... |
Task1_train_45305 | Given a variant located on Chromosome 17, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CATATGTTAATTAGTTTGATTTAGCCATTGTACGAAGTATACATATTCCAAAAAAATGTGTTGTACACAATAAATACATATAATTTTTGTCAATTCAAATAAATAAATAAATGAACTCATTTAACCATATGTGTATTTGAGGGTTTATTTCTAGGCTCTCTGTTCTTTTCCATTGCTTTATATATCTGTCTTTATATCAGTATCACACTGTTATGATTACTGTAGCTTTACAGTAAATTTTGAAACAGGAAAATGTGAGACCAACTTTGTTCTTTTTTAAGATTGTTTTGGCTATATAGGACCCCTTCTAATTTCATATG... | CATATGTTAATTAGTTTGATTTAGCCATTGTACGAAGTATACATATTCCAAAAAAATGTGTTGTACACAATAAATACATATAATTTTTGTCAATTCAAATAAATAAATAAATGAACTCATTTAACCATATGTGTATTTGAGGGTTTATTTCTAGGCTCTCTGTTCTTTTCCATTGCTTTATATATCTGTCTTTATATCAGTATCACACTGTTATGATTACTGTAGCTTTACAGTAAATTTTGAAACAGGAAAATGTGAGACCAACTTTGTTCTTTTTTAAGATTGTTTTGGCTATATAGGACCCCTTCTAATTTCATATG... |
Task1_train_45306 | A mutation on Chromosome 17 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CATTCTAACTGGTGTGAGATGGTATCTCATTGTGGTTTTGATTTGCATTTCTCTGATGGCCAGTGATGATGAGCATTTTTTCATGTGTCTGTTGGCTGCATAAATGTCTTCTTTTGAGAAGTGTCTGTTCATATCCTTCACCCACTTATTGATGGGGTTGTTTGTTTTTTTCTTGTAAATTTGTTTGAGTTCTTTGTAGATTCTGGATATTAGCCCTTTGTCAGATGAGTAGATTGCAAAAATTTGGGAGAAAATATTTTCAAACTATGCATCTGACCAGGGGTTAATATCTAGAATATATAAGGAACTTGAACAACTCA... | CATTCTAACTGGTGTGAGATGGTATCTCATTGTGGTTTTGATTTGCATTTCTCTGATGGCCAGTGATGATGAGCATTTTTTCATGTGTCTGTTGGCTGCATAAATGTCTTCTTTTGAGAAGTGTCTGTTCATATCCTTCACCCACTTATTGATGGGGTTGTTTGTTTTTTTCTTGTAAATTTGTTTGAGTTCTTTGTAGATTCTGGATATTAGCCCTTTGTCAGATGAGTAGATTGCAAAAATTTGGGAGAAAATATTTTCAAACTATGCATCTGACCAGGGGTTAATATCTAGAATATATAAGGAACTTGAACAACTCA... |
Task1_train_45307 | This alteration on Chromosome 17 may affect genome function. Does it lead to a disease or is it benign? | Benign | TTGTTGCAATTGCTTTTGAGGACTTAGTCATAAATTCTTTCCCAAGGTTGATGTTAAGAATTATGTTTTCTAGATTTTCTCCTAGGGTTTTTAAAGTTTGAGGTCTTACATTTAAATCTTTAATCCATCTTGAGTTAATTTTTCTATATGGTGAAAGTCAGGGTCTAGTTTCAATCATCTGCATAAAGCTAGCCAGCTATCCCAGCACCACTTATTGAATAGGGAGTCCTATCCTCATTGCTTATTTTTGTTAATGATATCAAAGATTAGATTGTTGTATGAGCATGGCTTTATTTCTGGGTTCTCTATTCTGTTCCTTT... | TTGTTGCAATTGCTTTTGAGGACTTAGTCATAAATTCTTTCCCAAGGTTGATGTTAAGAATTATGTTTTCTAGATTTTCTCCTAGGGTTTTTAAAGTTTGAGGTCTTACATTTAAATCTTTAATCCATCTTGAGTTAATTTTTCTATATGGTGAAAGTCAGGGTCTAGTTTCAATCATCTGCATAAAGCTAGCCAGCTATCCCAGCACCACTTATTGAATAGGGAGTCCTATCCTCATTGCTTATTTTTGTTAATGATATCAAAGATTAGATTGTTGTATGAGCATGGCTTTATTTCTGGGTTCTCTATTCTGTTCCTTT... |
Task1_train_45308 | A genomic variant on Chromosome 17 is under review. What is the biological outcome — benign or pathogenic? | Benign | ATGGAATACTATACAGCCATAAAAAAGGAAATTATGTCCTTTGTAGCAATGTGGATGAAGCTGGAGGCCATTATCCTAAGCAAACTAACACAGATACAGAAAACCAAATACGGCATGTTCTCACTTATAAGTGGTAGCTAAACATTGAGTACATATGGACACAAATAAGGGAACAACAGATACTGAAGCTTACTTGAGGGCAGATGGTGGGAAGAGGGTGAGGATAAAAAAACCATCTATCTGTTACTATGCTTTTGTTTAATTAAATTAATTAATTAATTAAGTTTTGAGACAGAGTCTCACTCTGTCACCCAGGCAGG... | ATGGAATACTATACAGCCATAAAAAAGGAAATTATGTCCTTTGTAGCAATGTGGATGAAGCTGGAGGCCATTATCCTAAGCAAACTAACACAGATACAGAAAACCAAATACGGCATGTTCTCACTTATAAGTGGTAGCTAAACATTGAGTACATATGGACACAAATAAGGGAACAACAGATACTGAAGCTTACTTGAGGGCAGATGGTGGGAAGAGGGTGAGGATAAAAAAACCATCTATCTGTTACTATGCTTTTGTTTAATTAAATTAATTAATTAATTAAGTTTTGAGACAGAGTCTCACTCTGTCACCCAGGCAGG... |
Task1_train_45309 | This variant is found on Chromosome 17. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GCCATTATCCTAAGCAAACTAACACAGATACAGAAAACCAAATACGGCATGTTCTCACTTATAAGTGGTAGCTAAACATTGAGTACATATGGACACAAATAAGGGAACAACAGATACTGAAGCTTACTTGAGGGCAGATGGTGGGAAGAGGGTGAGGATAAAAAAACCATCTATCTGTTACTATGCTTTTGTTTAATTAAATTAATTAATTAATTAAGTTTTGAGACAGAGTCTCACTCTGTCACCCAGGCAGGAGTGCAGTGGCGCAACCTTGTCTCACCAAAGCCTCTGCCTCCCAGGTTCAAGCGATTCTCCTGATT... | GCCATTATCCTAAGCAAACTAACACAGATACAGAAAACCAAATACGGCATGTTCTCACTTATAAGTGGTAGCTAAACATTGAGTACATATGGACACAAATAAGGGAACAACAGATACTGAAGCTTACTTGAGGGCAGATGGTGGGAAGAGGGTGAGGATAAAAAAACCATCTATCTGTTACTATGCTTTTGTTTAATTAAATTAATTAATTAATTAAGTTTTGAGACAGAGTCTCACTCTGTCACCCAGGCAGGAGTGCAGTGGCGCAACCTTGTCTCACCAAAGCCTCTGCCTCCCAGGTTCAAGCGATTCTCCTGATT... |
Task1_train_45310 | Here is a variant on Chromosome 17. Please identify whether it is a benign mutation or associated with a disorder. | Benign | ACGGCATGTTCTCACTTATAAGTGGTAGCTAAACATTGAGTACATATGGACACAAATAAGGGAACAACAGATACTGAAGCTTACTTGAGGGCAGATGGTGGGAAGAGGGTGAGGATAAAAAAACCATCTATCTGTTACTATGCTTTTGTTTAATTAAATTAATTAATTAATTAAGTTTTGAGACAGAGTCTCACTCTGTCACCCAGGCAGGAGTGCAGTGGCGCAACCTTGTCTCACCAAAGCCTCTGCCTCCCAGGTTCAAGCGATTCTCCTGATTCAGCCTCCTGAGTAGCTTGGATTACAGGCGCATGCCACCATGC... | ACGGCATGTTCTCACTTATAAGTGGTAGCTAAACATTGAGTACATATGGACACAAATAAGGGAACAACAGATACTGAAGCTTACTTGAGGGCAGATGGTGGGAAGAGGGTGAGGATAAAAAAACCATCTATCTGTTACTATGCTTTTGTTTAATTAAATTAATTAATTAATTAAGTTTTGAGACAGAGTCTCACTCTGTCACCCAGGCAGGAGTGCAGTGGCGCAACCTTGTCTCACCAAAGCCTCTGCCTCCCAGGTTCAAGCGATTCTCCTGATTCAGCCTCCTGAGTAGCTTGGATTACAGGCGCATGCCACCATGC... |
Task1_train_45311 | A mutation found on Chromosome 17 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GTGTGTGTGTGTGTGTGTATGCATTTGCACATGTGTTTGTGTGATACAGGGGTTGGGACAGGACTACTGGAGAAGACTGAATTGAATCTTGGAAATGAATCAGAGTTAAGTAGGTGATGAAGGTGAAGAGAAAGAGTGTGTAAAAGAACAGATAAGTGAAAGAACATGAGGAAAAGCGAAACATTTGGAACTGCAAATGTTTAATAACTATAAGGTCAGTGTTGCTTGAAGTGAATCTTAGTGGGGAGCAGTGAGACATGGATCTATAGAGATGGGCAAAGGACAGGCAGCAGACCACCTGATGTGCACACACTTCCTAG... | GTGTGTGTGTGTGTGTGTATGCATTTGCACATGTGTTTGTGTGATACAGGGGTTGGGACAGGACTACTGGAGAAGACTGAATTGAATCTTGGAAATGAATCAGAGTTAAGTAGGTGATGAAGGTGAAGAGAAAGAGTGTGTAAAAGAACAGATAAGTGAAAGAACATGAGGAAAAGCGAAACATTTGGAACTGCAAATGTTTAATAACTATAAGGTCAGTGTTGCTTGAAGTGAATCTTAGTGGGGAGCAGTGAGACATGGATCTATAGAGATGGGCAAAGGACAGGCAGCAGACCACCTGATGTGCACACACTTCCTAG... |
Task1_train_45312 | A mutation located on Chromosome 17 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | AACTTGATCCTCAATGCAGCAGTGTTGGGAGGTGGGGCCTAACAGGAGATGTTTGGGTCATGGTGACACCACCCTCATGAGTGGATTAATGTTGTTATCACAAGAGTGGGTTCCTTATAAAAGGATGAGTTTGACTCCTTCTTTCTCTGTCTCACCCTCTCTCCCTTCCACAATGGGATAACATGGTATTCCTGGTTATCTATAACCAAGTCTCATTCTATAAACGGAATCCTAATTCCACAAGGTTCCACATATGCTATTTATCAGGGGACATGTTGCTTACCACATAAATAATTGTAGTTTTCCTGAAATGAAACTCT... | AACTTGATCCTCAATGCAGCAGTGTTGGGAGGTGGGGCCTAACAGGAGATGTTTGGGTCATGGTGACACCACCCTCATGAGTGGATTAATGTTGTTATCACAAGAGTGGGTTCCTTATAAAAGGATGAGTTTGACTCCTTCTTTCTCTGTCTCACCCTCTCTCCCTTCCACAATGGGATAACATGGTATTCCTGGTTATCTATAACCAAGTCTCATTCTATAAACGGAATCCTAATTCCACAAGGTTCCACATATGCTATTTATCAGGGGACATGTTGCTTACCACATAAATAATTGTAGTTTTCCTGAAATGAAACTCT... |
Task1_train_45313 | A variant on Chromosome 17 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | CCCCACTTAGAGTTGTCCCGGCCTTTTCCGGACGGAACCACTGTTCATCTTACATATGTTGATTGATGTCTCATGTCTCCCTAAAATGTATAAAACCAAGCTGTGCTCTGACCACTTTGGGCACCTGTCTTCAGAACCTCCTGAGGCTGTGTCACAGGTGTACATCCCCAACCTTGGCAAAATAAACTTTCTAAATAAACTGAGACCTGTCTCCGATTTTGCGGGTTCAGAAGGCTATACTGAATTGTCCCCTGTGTGAAGCCCAGCAGGAGCCTTTCACAGCAGGTTCTTTTCACTTGAACCTTTGTGCATCAGCACCT... | CCCCACTTAGAGTTGTCCCGGCCTTTTCCGGACGGAACCACTGTTCATCTTACATATGTTGATTGATGTCTCATGTCTCCCTAAAATGTATAAAACCAAGCTGTGCTCTGACCACTTTGGGCACCTGTCTTCAGAACCTCCTGAGGCTGTGTCACAGGTGTACATCCCCAACCTTGGCAAAATAAACTTTCTAAATAAACTGAGACCTGTCTCCGATTTTGCGGGTTCAGAAGGCTATACTGAATTGTCCCCTGTGTGAAGCCCAGCAGGAGCCTTTCACAGCAGGTTCTTTTCACTTGAACCTTTGTGCATCAGCACCT... |
Task1_train_45314 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | GAGAGGAAAACATTCCAAACAAAGAGATCATAATTTCATTTCAGGAAGACTAAACTAATTTACGTGGTAGGTAACATGTCATCTGATAAATAACATATGTGGAAAGTTGTGGAAGTTAAGATTCAATTTATAGAATGAGACTTGTTTATAGATAACCAGGAATACAGTGTTGAACGTGCATGCCTATATTCACACAGTAAAAAGACAGGAAGGAAGTAAACGCCAGATGGTAGCACTGGTTCTCCTTCACCTCCTGACTCCCTCGTTTTACTCTTGTCGATTGAAATAACTATTATTTCCAGTTTCGTATCAGTCAGCCA... | GAGAGGAAAACATTCCAAACAAAGAGATCATAATTTCATTTCAGGAAGACTAAACTAATTTACGTGGTAGGTAACATGTCATCTGATAAATAACATATGTGGAAAGTTGTGGAAGTTAAGATTCAATTTATAGAATGAGACTTGTTTATAGATAACCAGGAATACAGTGTTGAACGTGCATGCCTATATTCACACAGTAAAAAGACAGGAAGGAAGTAAACGCCAGATGGTAGCACTGGTTCTCCTTCACCTCCTGACTCCCTCGTTTTACTCTTGTCGATTGAAATAACTATTATTTCCAGTTTCGTATCAGTCAGCCA... |
Task1_train_45315 | A mutation has occurred on Chromosome 17. What is the medical relevance of this mutation? | Benign | CAGAGGGTTACAAGTTCCTGATACCTAGTACAACCTGGGAAAGAGAGCAAAAGCCCTTTATTCCTGATGCAGCTTCCCCAATCTCTAGCCAATTTGCACCAAAAGCCCAAGAAACTCCTAACTACAAATTCCTTCCTGGGGTGGGGTGTTTGGGAGGGTGGGCAGGGACTTCTCTGGGGTCCTGCATGCACAGCTAGGATCAAGGTTCAGCTTATAGTAACCATTTCCTCATTTTAATAGTAAAAACAACCACAACAAGAAAAACACCCCAAGGCGGAGATTTCATATGCTAATGATACATGCGATGGGTGTTAGACCAC... | CAGAGGGTTACAAGTTCCTGATACCTAGTACAACCTGGGAAAGAGAGCAAAAGCCCTTTATTCCTGATGCAGCTTCCCCAATCTCTAGCCAATTTGCACCAAAAGCCCAAGAAACTCCTAACTACAAATTCCTTCCTGGGGTGGGGTGTTTGGGAGGGTGGGCAGGGACTTCTCTGGGGTCCTGCATGCACAGCTAGGATCAAGGTTCAGCTTATAGTAACCATTTCCTCATTTTAATAGTAAAAACAACCACAACAAGAAAAACACCCCAAGGCGGAGATTTCATATGCTAATGATACATGCGATGGGTGTTAGACCAC... |
Task1_train_45316 | Consider a variant on Chromosome 17. Determine its clinical classification and disease relevance. | Benign | GTACAACCTGGGAAAGAGAGCAAAAGCCCTTTATTCCTGATGCAGCTTCCCCAATCTCTAGCCAATTTGCACCAAAAGCCCAAGAAACTCCTAACTACAAATTCCTTCCTGGGGTGGGGTGTTTGGGAGGGTGGGCAGGGACTTCTCTGGGGTCCTGCATGCACAGCTAGGATCAAGGTTCAGCTTATAGTAACCATTTCCTCATTTTAATAGTAAAAACAACCACAACAAGAAAAACACCCCAAGGCGGAGATTTCATATGCTAATGATACATGCGATGGGTGTTAGACCACGTGGATCCTGAGCACATGTGCCAACCG... | GTACAACCTGGGAAAGAGAGCAAAAGCCCTTTATTCCTGATGCAGCTTCCCCAATCTCTAGCCAATTTGCACCAAAAGCCCAAGAAACTCCTAACTACAAATTCCTTCCTGGGGTGGGGTGTTTGGGAGGGTGGGCAGGGACTTCTCTGGGGTCCTGCATGCACAGCTAGGATCAAGGTTCAGCTTATAGTAACCATTTCCTCATTTTAATAGTAAAAACAACCACAACAAGAAAAACACCCCAAGGCGGAGATTTCATATGCTAATGATACATGCGATGGGTGTTAGACCACGTGGATCCTGAGCACATGTGCCAACCG... |
Task1_train_45317 | Consider this mutation on Chromosome 17. Is this a benign change or a disease-causing variant? | Benign | GTCAGTCATTTGAGCTCTCAAATTAGCTATCATGAATTTCAAATTGTTTTGGGGGACAGGCTGGGTTCCCCAGGAAGCAGTCACTGAGATGGAGAGCAATATGCAGGAGGTTTATTGAAGCATGCTCTTGGGATTAACACTGGGGAGGGCAGGGGAGGGGAAAGGGAGGGGAGGGGAAAGGGAAAGGGAAGGGGAAGGGGAGGGAAAGGGAAGGGAAGGGAAGGGAAGGGAAGGGAAGGGAAGGGAAGGGAAGGGAAGGGAAGGGAAAGGAAGGGAAAGTGAGAGAAAGATCAAGTTTGACACTGGGATAAATCAAACTG... | GTCAGTCATTTGAGCTCTCAAATTAGCTATCATGAATTTCAAATTGTTTTGGGGGACAGGCTGGGTTCCCCAGGAAGCAGTCACTGAGATGGAGAGCAATATGCAGGAGGTTTATTGAAGCATGCTCTTGGGATTAACACTGGGGAGGGCAGGGGAGGGGAAAGGGAGGGGAGGGGAAAGGGAAAGGGAAGGGGAAGGGGAGGGAAAGGGAAGGGAAGGGAAGGGAAGGGAAGGGAAGGGAAGGGAAGGGAAGGGAAGGGAAGGGAAAGGAAGGGAAAGTGAGAGAAAGATCAAGTTTGACACTGGGATAAATCAAACTG... |
Task1_train_45318 | This variant is present on Chromosome 17. Is the change likely to result in a pathogenic outcome? | Benign | GAAATTTTGGATTTAAAGCAGTTTTAATATACTTTGGATTATTAGCTGAAATATAAACCCTTATATTTATATAAATAAGATATTTTGCACATATTGTGACACATTTTTTCATCTACATAGAATAACACTTGTTTGAGTTTTGATGATGAGAAAACTGAGTCTCAAGGAAAAGTCCCACCCATGTTCTCTTAAGACAAAGCAAGGTGATTAAAGCCCAAAACAAAGGAGTAAAACTATCAAGAAAATGAAAAAACCTCAGTAACATTAGGGGCTAAAATTATAAAGGAGTTTCAGTCTGGAAATACTAAGACTTTGAGCAT... | GAAATTTTGGATTTAAAGCAGTTTTAATATACTTTGGATTATTAGCTGAAATATAAACCCTTATATTTATATAAATAAGATATTTTGCACATATTGTGACACATTTTTTCATCTACATAGAATAACACTTGTTTGAGTTTTGATGATGAGAAAACTGAGTCTCAAGGAAAAGTCCCACCCATGTTCTCTTAAGACAAAGCAAGGTGATTAAAGCCCAAAACAAAGGAGTAAAACTATCAAGAAAATGAAAAAACCTCAGTAACATTAGGGGCTAAAATTATAAAGGAGTTTCAGTCTGGAAATACTAAGACTTTGAGCAT... |
Task1_train_45319 | This mutation is located on Chromosome 17. Is it associated with a disease or is it a benign polymorphism? | Benign | GAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAGGAGGAGGAGGAGGAGGAGGAGGAGGAAGAGGAGGAGGAGGAAGAAGGATAAGAAAAATATTTATTTAGAACATTTACCTATTTACTAGACAGTATACTCAAGAGTTGACCGTGACACCAGGGTAACCACTGATATTGTATAAAAATGATTTAATTATGTTACGTGAAATAGGCCAAGCACAGAAAGACAAATTGCTAATGGAATGGAACTCATGAAGATAAAGAATAGATTGCTGGTTATCAGAGTCAGAGGAGGGTGCCTGTGGGAAATGAAGAGGTGGA... | GAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAGGAGGAGGAGGAGGAGGAGGAGGAGGAAGAGGAGGAGGAGGAAGAAGGATAAGAAAAATATTTATTTAGAACATTTACCTATTTACTAGACAGTATACTCAAGAGTTGACCGTGACACCAGGGTAACCACTGATATTGTATAAAAATGATTTAATTATGTTACGTGAAATAGGCCAAGCACAGAAAGACAAATTGCTAATGGAATGGAACTCATGAAGATAAAGAATAGATTGCTGGTTATCAGAGTCAGAGGAGGGTGCCTGTGGGAAATGAAGAGGTGGA... |
Task1_train_45320 | A variant on Chromosome 17 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | AGAAGAAGAGGAGGAGGAGGAGGAGGAGGAGGAGGAAGAGGAGGAGGAGGAAGAAGGATAAGAAAAATATTTATTTAGAACATTTACCTATTTACTAGACAGTATACTCAAGAGTTGACCGTGACACCAGGGTAACCACTGATATTGTATAAAAATGATTTAATTATGTTACGTGAAATAGGCCAAGCACAGAAAGACAAATTGCTAATGGAATGGAACTCATGAAGATAAAGAATAGATTGCTGGTTATCAGAGTCAGAGGAGGGTGCCTGTGGGAAATGAAGAGGTGGATTGACGTGTACAAATATAAGTTAGAGATA... | AGAAGAAGAGGAGGAGGAGGAGGAGGAGGAGGAGGAAGAGGAGGAGGAGGAAGAAGGATAAGAAAAATATTTATTTAGAACATTTACCTATTTACTAGACAGTATACTCAAGAGTTGACCGTGACACCAGGGTAACCACTGATATTGTATAAAAATGATTTAATTATGTTACGTGAAATAGGCCAAGCACAGAAAGACAAATTGCTAATGGAATGGAACTCATGAAGATAAAGAATAGATTGCTGGTTATCAGAGTCAGAGGAGGGTGCCTGTGGGAAATGAAGAGGTGGATTGACGTGTACAAATATAAGTTAGAGATA... |
Task1_train_45321 | This alteration occurs on Chromosome 17. Is it associated with a disease or is it a benign variant? | Benign | GCTTACAAGATAATATGGAATAGTGGCTAACCCATGAATATAGTGAGAAAACTTTTTAAAAGTTATATTGGAGTAATCCCTTAGCTAATAATTATTATTGTAGTTTAGCTATTTGGCTATGACAAACTAATACTAGTTGCACCTCACTTGAAAATATATGATAGCAACTTAGTACATGGTATTGTACATATCTTCACTTGGTTAAACAACTTTTAGAGGATATGCTTAGTGATTTATATTTCAACTCTAAATTGTTAGTTTTCTTTTTTTTTATTATACTTTAAGTTTTAGGGTACATGTGCACATTGTGCAGGTTAGTT... | GCTTACAAGATAATATGGAATAGTGGCTAACCCATGAATATAGTGAGAAAACTTTTTAAAAGTTATATTGGAGTAATCCCTTAGCTAATAATTATTATTGTAGTTTAGCTATTTGGCTATGACAAACTAATACTAGTTGCACCTCACTTGAAAATATATGATAGCAACTTAGTACATGGTATTGTACATATCTTCACTTGGTTAAACAACTTTTAGAGGATATGCTTAGTGATTTATATTTCAACTCTAAATTGTTAGTTTTCTTTTTTTTTATTATACTTTAAGTTTTAGGGTACATGTGCACATTGTGCAGGTTAGTT... |
Task1_train_45322 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | GGTGCTTCTACTTCCAGCCTTGACTGCATATGAGCAAGTTCAAGGGCTCAAGCCTGATAAGGACACAGTAACCAAGGCTTAGAGCTCTCAGGATGAGGACTCGGGTTACCCTACCAAGCAAGTGACCTAGACCAGAAGCAGGGGTGCCCATGACCCCTCCTCTCATACGTTTCTCTAGAAACTGTGACCAACCAGTTGGAGTGAGCCTAATGAGAGAAACAGCTGCAGCTGAGCAGTGCCAGAGGTGGACTACAGGGCTCCCTATCCTGATCCCATTTACCAGAAAGATACCCCCATCCCCAAGCTAGTGTAAGTAGGAC... | GGTGCTTCTACTTCCAGCCTTGACTGCATATGAGCAAGTTCAAGGGCTCAAGCCTGATAAGGACACAGTAACCAAGGCTTAGAGCTCTCAGGATGAGGACTCGGGTTACCCTACCAAGCAAGTGACCTAGACCAGAAGCAGGGGTGCCCATGACCCCTCCTCTCATACGTTTCTCTAGAAACTGTGACCAACCAGTTGGAGTGAGCCTAATGAGAGAAACAGCTGCAGCTGAGCAGTGCCAGAGGTGGACTACAGGGCTCCCTATCCTGATCCCATTTACCAGAAAGATACCCCCATCCCCAAGCTAGTGTAAGTAGGAC... |
Task1_train_45323 | Here is a variant on Chromosome 17. Please identify whether it is a benign mutation or associated with a disorder. | Benign | AAAAAAAAAAGAATGTGACTTTCTTTATGACACTAATGTTATATTGCTCTACTGATATGATAATGTACTTTAATTTTTGCCATTTTCTTCTTCGTCCTTGTCTAAATTTTGCTTCTAACTAAAGTCCTTAACTCTTGGGCCTATTGATATTATTTGGTTATGGAATGGAAATTATCTCAAAGACATGAGAAACTGTGATAAGTTTGAACTTCCAAAAGGGAAAGTAGTTGCTAAAGAGCAGAGGAAACAACCAGATGGCTGCCTTGGAGCTAGGCTGCCTTGGGTAAAACATTCACTTGTCATGGGGAGATGAGAGGCTG... | AAAAAAAAAAGAATGTGACTTTCTTTATGACACTAATGTTATATTGCTCTACTGATATGATAATGTACTTTAATTTTTGCCATTTTCTTCTTCGTCCTTGTCTAAATTTTGCTTCTAACTAAAGTCCTTAACTCTTGGGCCTATTGATATTATTTGGTTATGGAATGGAAATTATCTCAAAGACATGAGAAACTGTGATAAGTTTGAACTTCCAAAAGGGAAAGTAGTTGCTAAAGAGCAGAGGAAACAACCAGATGGCTGCCTTGGAGCTAGGCTGCCTTGGGTAAAACATTCACTTGTCATGGGGAGATGAGAGGCTG... |
Task1_train_45324 | Here is a variant on Chromosome 17. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TTGAACTTCCAAAAGGGAAAGTAGTTGCTAAAGAGCAGAGGAAACAACCAGATGGCTGCCTTGGAGCTAGGCTGCCTTGGGTAAAACATTCACTTGTCATGGGGAGATGAGAGGCTGCTGTAAACATGGTGACACACGCTATAAAGACAAAACAGATAACATTTCTTGACAATTTGCTTTGCCTATCCCAGACAAGTGTGGACAGTAATTGGTATTTAGGTATAAATTATACCAATGAAAATGAGAAATCTACCAGTATTTCTCGCTTTACCTTCCTGCTGTCTACCCATCAGCTGAGTGGCACCCCCATCATTTGCAAT... | TTGAACTTCCAAAAGGGAAAGTAGTTGCTAAAGAGCAGAGGAAACAACCAGATGGCTGCCTTGGAGCTAGGCTGCCTTGGGTAAAACATTCACTTGTCATGGGGAGATGAGAGGCTGCTGTAAACATGGTGACACACGCTATAAAGACAAAACAGATAACATTTCTTGACAATTTGCTTTGCCTATCCCAGACAAGTGTGGACAGTAATTGGTATTTAGGTATAAATTATACCAATGAAAATGAGAAATCTACCAGTATTTCTCGCTTTACCTTCCTGCTGTCTACCCATCAGCTGAGTGGCACCCCCATCATTTGCAAT... |
Task1_train_45325 | A mutation on Chromosome 17 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CCTGAGATTCACAGTCTCCGTTTATTACCACCAGTTCTATTCTCCCTTCACCGCTGGCCAGCACTCTTCTTGGTCTGGATAACTGCCTGATAACTGCCTTGATAACTTCCTTCCTAAATTGTCTGAGCCTCTAGTTACTATACCACTGTCCACTGTGATTGCTGTTCTTACCGATTTGTAGTTATCACTGGACATGGACACACTATGAGATTCTCCAGTGTTATGGGTTAATTTGTGTCCCCCAAAACTCATATTCAAATAGAATCATTTAAAGTGTTATGTGATAAGGCAAGGTCATATTGGAAACAATTAGGCCTCTG... | CCTGAGATTCACAGTCTCCGTTTATTACCACCAGTTCTATTCTCCCTTCACCGCTGGCCAGCACTCTTCTTGGTCTGGATAACTGCCTGATAACTGCCTTGATAACTTCCTTCCTAAATTGTCTGAGCCTCTAGTTACTATACCACTGTCCACTGTGATTGCTGTTCTTACCGATTTGTAGTTATCACTGGACATGGACACACTATGAGATTCTCCAGTGTTATGGGTTAATTTGTGTCCCCCAAAACTCATATTCAAATAGAATCATTTAAAGTGTTATGTGATAAGGCAAGGTCATATTGGAAACAATTAGGCCTCTG... |
Task1_train_45326 | This sequence change occurs on Chromosome 17. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TGGAAACAATTAGGCCTCTGATTAAATATGACTGTGTCTATTCACAAGGGAGAAATTCAGAGACAGTATGGATATAATAGAAAAATTATGTCAAACACACTTGGAGATGATAGACTTTGACACGTCAGGGAGAGAGACGTGGAACAGATACTTCCCTCGCAGTCTTCAGATGAAAACAACATTGCCAACACCTTAATTTCAGAAAAGAGGCCTTCAGAACTTTGATAAATAAATTTAAGCCACTTTTTTTCAGTAATTCATCAGGGCAGTGCTAGTAAATTAATATACTCAGTAAATCTCCTGAGCTATAGATATATTCT... | TGGAAACAATTAGGCCTCTGATTAAATATGACTGTGTCTATTCACAAGGGAGAAATTCAGAGACAGTATGGATATAATAGAAAAATTATGTCAAACACACTTGGAGATGATAGACTTTGACACGTCAGGGAGAGAGACGTGGAACAGATACTTCCCTCGCAGTCTTCAGATGAAAACAACATTGCCAACACCTTAATTTCAGAAAAGAGGCCTTCAGAACTTTGATAAATAAATTTAAGCCACTTTTTTTCAGTAATTCATCAGGGCAGTGCTAGTAAATTAATATACTCAGTAAATCTCCTGAGCTATAGATATATTCT... |
Task1_train_45327 | A variant affecting Chromosome 17 has been observed. Determine if it's benign or associated with disease. | Benign | CCAAAGGGCAGGGGGGAACAAGAGGGTGATATCAGCTGGGCCAGTTAGATGGGGAAGGCTAAAATGCTAAAATCAGTCTTTTAGTGCACTTTACTCAGGTTTGGCTAGGCATGTTTTATAGGCAATTGTAAATCATGGAGCAAATAAATCAACCTTAAGTGCAGCCATACAACTAAGTTGAAATGTGGTGTGTGTCTGTGTGTGAGTGTGTGTGTGCATGTATGTGTGTGCATCTGTATCTGAGTGTGTGTGTGTGTACCTGTATGCATCTATATGTGTGTGCATGTGTGTGGGTAGAAAAGGTACTGAAGGCAATACCC... | CCAAAGGGCAGGGGGGAACAAGAGGGTGATATCAGCTGGGCCAGTTAGATGGGGAAGGCTAAAATGCTAAAATCAGTCTTTTAGTGCACTTTACTCAGGTTTGGCTAGGCATGTTTTATAGGCAATTGTAAATCATGGAGCAAATAAATCAACCTTAAGTGCAGCCATACAACTAAGTTGAAATGTGGTGTGTGTCTGTGTGTGAGTGTGTGTGTGCATGTATGTGTGTGCATCTGTATCTGAGTGTGTGTGTGTGTACCTGTATGCATCTATATGTGTGTGCATGTGTGTGGGTAGAAAAGGTACTGAAGGCAATACCC... |
Task1_train_45328 | This alteration on Chromosome 17 may affect genome function. Does it lead to a disease or is it benign? | Benign | ATTCAAGAAGCATTCAATGCTTCTTGAATTCAATTCAAGAAGAGATTCAGTGCTGACATTAGTCAATTCAACTGCAGGTAGAAATTCTCCACCTGGACCCTTCCATGTTCAGGTGCTAGATTTTGTTCTTATGGCCATCCCCCTCTTTTTTGACCCAGAACCTTCTTTCAAGACTACGACCCTTGTGATTCTAAAACTGGGGATAAAACAATTAATAGTCTCTCTACAGATCCAAAGTATACCTCAGTGACAGAAAAATGTGAACTATGAAGATTTGTTTGCTAGTTACCAAATTATTGCTGCTCACCTACAGGTACACC... | ATTCAAGAAGCATTCAATGCTTCTTGAATTCAATTCAAGAAGAGATTCAGTGCTGACATTAGTCAATTCAACTGCAGGTAGAAATTCTCCACCTGGACCCTTCCATGTTCAGGTGCTAGATTTTGTTCTTATGGCCATCCCCCTCTTTTTTGACCCAGAACCTTCTTTCAAGACTACGACCCTTGTGATTCTAAAACTGGGGATAAAACAATTAATAGTCTCTCTACAGATCCAAAGTATACCTCAGTGACAGAAAAATGTGAACTATGAAGATTTGTTTGCTAGTTACCAAATTATTGCTGCTCACCTACAGGTACACC... |
Task1_train_45329 | This variant is found on Chromosome 17. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | AGATACAGAATTTATCCTATGAGTGTCTTGGAGGAAGTAGGAGAACATAAACAAAATTCTCACACAAGAAATCCAAGTTACCCAACCTTCTTTGTTGTAAGTATGATCCCTGATCCCCACTTGTTTTTCTTCCTGTGGACCCAAAAACAATTGGCTTCCTTTCCTCCCCAGTCTCTCTATATCCAGAACCATGTTCTTCCATTGAGTTCTCCACACCAACCAAGGCCAGAGGGATGTTCCAAAACCAGTGCTCTTCCTGTCACCTCCTTGCATGCAGCCCCTTGATGCTTTCATGTCAGCCCTGCATCAAACCGAAATAC... | AGATACAGAATTTATCCTATGAGTGTCTTGGAGGAAGTAGGAGAACATAAACAAAATTCTCACACAAGAAATCCAAGTTACCCAACCTTCTTTGTTGTAAGTATGATCCCTGATCCCCACTTGTTTTTCTTCCTGTGGACCCAAAAACAATTGGCTTCCTTTCCTCCCCAGTCTCTCTATATCCAGAACCATGTTCTTCCATTGAGTTCTCCACACCAACCAAGGCCAGAGGGATGTTCCAAAACCAGTGCTCTTCCTGTCACCTCCTTGCATGCAGCCCCTTGATGCTTTCATGTCAGCCCTGCATCAAACCGAAATAC... |
Task1_train_45330 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | AACATAAACAAAATTCTCACACAAGAAATCCAAGTTACCCAACCTTCTTTGTTGTAAGTATGATCCCTGATCCCCACTTGTTTTTCTTCCTGTGGACCCAAAAACAATTGGCTTCCTTTCCTCCCCAGTCTCTCTATATCCAGAACCATGTTCTTCCATTGAGTTCTCCACACCAACCAAGGCCAGAGGGATGTTCCAAAACCAGTGCTCTTCCTGTCACCTCCTTGCATGCAGCCCCTTGATGCTTTCATGTCAGCCCTGCATCAAACCGAAATACCTCTGTCTAGCATGCAAGACCCCACATAGACAGATCACTGTCT... | AACATAAACAAAATTCTCACACAAGAAATCCAAGTTACCCAACCTTCTTTGTTGTAAGTATGATCCCTGATCCCCACTTGTTTTTCTTCCTGTGGACCCAAAAACAATTGGCTTCCTTTCCTCCCCAGTCTCTCTATATCCAGAACCATGTTCTTCCATTGAGTTCTCCACACCAACCAAGGCCAGAGGGATGTTCCAAAACCAGTGCTCTTCCTGTCACCTCCTTGCATGCAGCCCCTTGATGCTTTCATGTCAGCCCTGCATCAAACCGAAATACCTCTGTCTAGCATGCAAGACCCCACATAGACAGATCACTGTCT... |
Task1_train_45331 | Chromosome 17 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TGTCTACGACCTGACCTCATGGCTCATTCCTCAAAGAACAACTCTCCCATGCCTCACCTAATGAACAATTTGCCCTCAAGCCCCATTCACTTGTACAAGTCTCCTTTGCCTAGAAAGTTTTTCCTTTCCTGTTTGTAACTGGTTAATTCCTACTCATACTGAAAGACTCGATGCCAGTATCACATTCTCCAATAATTCTTTCCTTGTTCCCCAACTATGCTCTGCTGAGTTCATGGTGCTCTATGCTTATCTCCAAGTACTTGGCACAAAGGAATGTCATAATTGTCTTGCTGCCCACCAGAGAGTGAGTTTCTTGAGAA... | TGTCTACGACCTGACCTCATGGCTCATTCCTCAAAGAACAACTCTCCCATGCCTCACCTAATGAACAATTTGCCCTCAAGCCCCATTCACTTGTACAAGTCTCCTTTGCCTAGAAAGTTTTTCCTTTCCTGTTTGTAACTGGTTAATTCCTACTCATACTGAAAGACTCGATGCCAGTATCACATTCTCCAATAATTCTTTCCTTGTTCCCCAACTATGCTCTGCTGAGTTCATGGTGCTCTATGCTTATCTCCAAGTACTTGGCACAAAGGAATGTCATAATTGTCTTGCTGCCCACCAGAGAGTGAGTTTCTTGAGAA... |
Task1_train_45332 | Consider a variant on Chromosome 17. Determine its clinical classification and disease relevance. | Benign | GCAAAATGAAAAATAGTGCATACTGCATGATTTCTTTTATATGAAATTCTAGACATGGTGAAATCTGTAGTAACATAAAGAACAGGTTGATGGTTGCCAGGGTCTGGGGGTGGGGGAAGAACTGACTGCAAAGACAAACTGGGAATTTTGGGGGTGATGGAAAGTTCCATAAAGATCTTGAGTGCAGTGGTGGTTACATAAGTATACACGAATGTCAGATCACATCATACTGTTCACTAAAAATGGGAACTTTTTATTATATGTAAATTATATTTCAATAAAGTTGACCATAAAAAATGAAACAAAAAAATTTTTTAAAG... | GCAAAATGAAAAATAGTGCATACTGCATGATTTCTTTTATATGAAATTCTAGACATGGTGAAATCTGTAGTAACATAAAGAACAGGTTGATGGTTGCCAGGGTCTGGGGGTGGGGGAAGAACTGACTGCAAAGACAAACTGGGAATTTTGGGGGTGATGGAAAGTTCCATAAAGATCTTGAGTGCAGTGGTGGTTACATAAGTATACACGAATGTCAGATCACATCATACTGTTCACTAAAAATGGGAACTTTTTATTATATGTAAATTATATTTCAATAAAGTTGACCATAAAAAATGAAACAAAAAAATTTTTTAAAG... |
Task1_train_45333 | Given this variant on Chromosome 17, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | AGATGTTTTGAGCACTAACAGCATTGTGTCTCCCCAGGAGGATGTATAAGCTCTGGGTGCTTGTTTGAAATCAATTTTGTCCTCTCATAATCACACCTCATGTGTAACTGACAAGCAGAGAGTGAACTCTGGGTTCAGTCCTGCCATTGATTCTTCCTCACTGTGAGGAAGAGAAAAAATTAGTAGCACAATTCCTGGCATTTGGTAGGTGTTCAATAAATATTAACTTCTGTCATCCCTGCTAGGGACTTAAAAGAATGAGTGGAACTGTCTAGAGATGCTCACCGTTGCATTTTACTGAGTAAGGTCCCATGAGAAAT... | AGATGTTTTGAGCACTAACAGCATTGTGTCTCCCCAGGAGGATGTATAAGCTCTGGGTGCTTGTTTGAAATCAATTTTGTCCTCTCATAATCACACCTCATGTGTAACTGACAAGCAGAGAGTGAACTCTGGGTTCAGTCCTGCCATTGATTCTTCCTCACTGTGAGGAAGAGAAAAAATTAGTAGCACAATTCCTGGCATTTGGTAGGTGTTCAATAAATATTAACTTCTGTCATCCCTGCTAGGGACTTAAAAGAATGAGTGGAACTGTCTAGAGATGCTCACCGTTGCATTTTACTGAGTAAGGTCCCATGAGAAAT... |
Task1_train_45334 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | GAATATAGGTGTTTCCTTCATTTGGGACAAAAAGGGGAAGACAGCTAACAAGACAACAGAGAACAGGTAATTAGAGATATTACAAGAAGACCCAGAGTGTGCAGGGTTATGGAAATCAATGAAGGTGTATTTTAAGGGAGGAGTAGGTATCTATATCAGCAAGGCAGCAGCAGCAGAGAGGTTGAGAGGAGAGAATCACTGCTCTTTGAACAGTTTCTGTAGAAGCAGTTTCTGTAGTTTCTTCAGGCAGTTTAGGAGAAAGGGAAGCAGAACATTCTATTCTGATGAGGGTGAGAGCTGGAGATAGCAGTGAAGTCTGG... | GAATATAGGTGTTTCCTTCATTTGGGACAAAAAGGGGAAGACAGCTAACAAGACAACAGAGAACAGGTAATTAGAGATATTACAAGAAGACCCAGAGTGTGCAGGGTTATGGAAATCAATGAAGGTGTATTTTAAGGGAGGAGTAGGTATCTATATCAGCAAGGCAGCAGCAGCAGAGAGGTTGAGAGGAGAGAATCACTGCTCTTTGAACAGTTTCTGTAGAAGCAGTTTCTGTAGTTTCTTCAGGCAGTTTAGGAGAAAGGGAAGCAGAACATTCTATTCTGATGAGGGTGAGAGCTGGAGATAGCAGTGAAGTCTGG... |
Task1_train_45335 | Given a variant located on Chromosome 17, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AGGCTTGGCTCAGTCATTTACTTCATTTTATTCTCCTAATGAAGGGGTATTTTTATGAAACAGCCATGATGAGTAATTTACAATGCATGAATATGAATGAGAAACATTTATTATGCCAGAGAAATGAAGTTTATTGGGAAGTAAATGAAGTCTCCTCCTTGCATTCCAGAGAATGCCAAAGAAAAAAGGAAAACAGGAAATGCAGTAGTACGTTCAGGAAACACCTTAAGTAGTAACTGGAGCTCAGATTACAGGGAGCTGAACATCTTTAGAAACAAACAGGCTCGACCCTCAACAGGAAGGAGTTGTCCAGACATTGG... | AGGCTTGGCTCAGTCATTTACTTCATTTTATTCTCCTAATGAAGGGGTATTTTTATGAAACAGCCATGATGAGTAATTTACAATGCATGAATATGAATGAGAAACATTTATTATGCCAGAGAAATGAAGTTTATTGGGAAGTAAATGAAGTCTCCTCCTTGCATTCCAGAGAATGCCAAAGAAAAAAGGAAAACAGGAAATGCAGTAGTACGTTCAGGAAACACCTTAAGTAGTAACTGGAGCTCAGATTACAGGGAGCTGAACATCTTTAGAAACAAACAGGCTCGACCCTCAACAGGAAGGAGTTGTCCAGACATTGG... |
Task1_train_45336 | A mutation located on Chromosome 17 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GGTTGTGCTGGGCCTGCAGCTCGATCTCCAGGGCGTTGACTGTGCGTCTCAGCTCGATGATCTCCGCCTGGTAGGACTGCAGCTGCTCTGAGCTGGATACCACCTGCTTGTTCAGCTCCTCGGTCTGAAACACCCAAGGGGAGAAAGGATCAGACCCTGCCTCCGGGGCCCTGGGGGGCCTTGGGTCCTGAGGGGCCACGTGCTTAGATGCCCACCTGCGTGGTGAACCATTGCTCCACTTCCCTGCGGTTGGTTTCCACCAGGGCCTCATACTGACTCCTGGTCTCGTTCAGCACCCGATTCAGGTCCACAGTGGGAGC... | GGTTGTGCTGGGCCTGCAGCTCGATCTCCAGGGCGTTGACTGTGCGTCTCAGCTCGATGATCTCCGCCTGGTAGGACTGCAGCTGCTCTGAGCTGGATACCACCTGCTTGTTCAGCTCCTCGGTCTGAAACACCCAAGGGGAGAAAGGATCAGACCCTGCCTCCGGGGCCCTGGGGGGCCTTGGGTCCTGAGGGGCCACGTGCTTAGATGCCCACCTGCGTGGTGAACCATTGCTCCACTTCCCTGCGGTTGGTTTCCACCAGGGCCTCATACTGACTCCTGGTCTCGTTCAGCACCCGATTCAGGTCCACAGTGGGAGC... |
Task1_train_45337 | Given a variant located on Chromosome 17, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CTCTCAGGCTAGGATAACGAATGTGAGTAAAACCCCAGGGTCCAGGTGTCCTGACTGCACTGGTTACCCACCTGCCAGCCTCTAGCCTTCATTTTCTATGTACCTGAGTGGCACCTCCTGTCACACCTAGCCATGGGACCTCATAGGTAGAGCTTGTTAAGGGTGTGACCTGGCCAAGAAAGGTGGGGACAGGTCGGATCTCCACAACCCCATCACACTGAGGGTCAGGGAGGGTCATGGCCACTTCTTAAAACATGACTCTTGTGGGTTCCTCATTAGAAGAGCCCACCAAACAGTCTTGTCCTCTGACAGCCCAATGA... | CTCTCAGGCTAGGATAACGAATGTGAGTAAAACCCCAGGGTCCAGGTGTCCTGACTGCACTGGTTACCCACCTGCCAGCCTCTAGCCTTCATTTTCTATGTACCTGAGTGGCACCTCCTGTCACACCTAGCCATGGGACCTCATAGGTAGAGCTTGTTAAGGGTGTGACCTGGCCAAGAAAGGTGGGGACAGGTCGGATCTCCACAACCCCATCACACTGAGGGTCAGGGAGGGTCATGGCCACTTCTTAAAACATGACTCTTGTGGGTTCCTCATTAGAAGAGCCCACCAAACAGTCTTGTCCTCTGACAGCCCAATGA... |
Task1_train_45338 | A mutation on Chromosome 17 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GAGAATTCCATGGCTCCATGAAAGGGGCCAACTGGAGTGAGAGGAAAAACTTGGCAACTTGGCTCAGACAATTCTCAACACGACCTTCCTTTGACGATATTAGAATGCTAAGTGATGTGATTTTGCTCTTGGACAAAATAACAAGAGGCTGAAGATGCCAAAAGCATGGTAGGGACATGTTAGCTCTGAGCTGTTCTGAAAGAATTCAAACTTGGCAACTGGCATCACTTCCTTCCACCAGTCTATAGGGATCCCTGGGAAAGGTGAATACACATCCAACATCAGGAAGGGACCTTCATCCAGAGGCCCCAGAGCACCCC... | GAGAATTCCATGGCTCCATGAAAGGGGCCAACTGGAGTGAGAGGAAAAACTTGGCAACTTGGCTCAGACAATTCTCAACACGACCTTCCTTTGACGATATTAGAATGCTAAGTGATGTGATTTTGCTCTTGGACAAAATAACAAGAGGCTGAAGATGCCAAAAGCATGGTAGGGACATGTTAGCTCTGAGCTGTTCTGAAAGAATTCAAACTTGGCAACTGGCATCACTTCCTTCCACCAGTCTATAGGGATCCCTGGGAAAGGTGAATACACATCCAACATCAGGAAGGGACCTTCATCCAGAGGCCCCAGAGCACCCC... |
Task1_train_45339 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GGCAAGGTGAGGGCACTCCTGACCCCAGTGCAACCAGCCTCAATCTCCTAACTCGGGCCTTCAGAATCATCTCCCCATGCTGGCTCCATGGCCAGAGGGAGACCCACCGGTGACAGGGCCACAGCTTGGACAAGAAGTACAGGAGGCAGGCGTGGAACAGGGATTGCAGGGGAGTCTGCAGGGAGAGAAAGAAGAGTTACATTAAAAAGATGTCTCAGTGATTGATGGACAAGGGTAAGATCAGGGTGAAGGCTGGGCCTGCCACCAACAAGGCACACAGACCAGAGAATCTATACCAACAGTTCTCTCATCTGTGTCTT... | GGCAAGGTGAGGGCACTCCTGACCCCAGTGCAACCAGCCTCAATCTCCTAACTCGGGCCTTCAGAATCATCTCCCCATGCTGGCTCCATGGCCAGAGGGAGACCCACCGGTGACAGGGCCACAGCTTGGACAAGAAGTACAGGAGGCAGGCGTGGAACAGGGATTGCAGGGGAGTCTGCAGGGAGAGAAAGAAGAGTTACATTAAAAAGATGTCTCAGTGATTGATGGACAAGGGTAAGATCAGGGTGAAGGCTGGGCCTGCCACCAACAAGGCACACAGACCAGAGAATCTATACCAACAGTTCTCTCATCTGTGTCTT... |
Task1_train_45340 | A genomic variant on Chromosome 17 is under review. What is the biological outcome — benign or pathogenic? | Benign | TAACCCCCACTCACCTGGGCTTGGAACCACTGTTCCACATCCTGGTGGTTGGTCTCCACCATGGCCTCGTACTGAGCCCGCATCTCCCCCAACACCCTGTTCAGGTCAATGGTGGGCTCAATGTCCAGCTCGATCCGGAACTTCTCCCCCAGCTGACTCCTCAGAATCTTTACTTCCTGCAGAAATGGAAGCGATAGACAGCCTGCGTAAGGAAACGGCCTTTGATGGAGCAGACAGCACCAGGACTCCGTCCCTGGCAAGCAGTAGGAGGGGAGTCCCACACATAAGCAAATGGGAAAGTCTTGTCCAGAGTGCATTTG... | TAACCCCCACTCACCTGGGCTTGGAACCACTGTTCCACATCCTGGTGGTTGGTCTCCACCATGGCCTCGTACTGAGCCCGCATCTCCCCCAACACCCTGTTCAGGTCAATGGTGGGCTCAATGTCCAGCTCGATCCGGAACTTCTCCCCCAGCTGACTCCTCAGAATCTTTACTTCCTGCAGAAATGGAAGCGATAGACAGCCTGCGTAAGGAAACGGCCTTTGATGGAGCAGACAGCACCAGGACTCCGTCCCTGGCAAGCAGTAGGAGGGGAGTCCCACACATAAGCAAATGGGAAAGTCTTGTCCAGAGTGCATTTG... |
Task1_train_45341 | A variant found on Chromosome 17 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CCCCCACTCACCTGGGCTTGGAACCACTGTTCCACATCCTGGTGGTTGGTCTCCACCATGGCCTCGTACTGAGCCCGCATCTCCCCCAACACCCTGTTCAGGTCAATGGTGGGCTCAATGTCCAGCTCGATCCGGAACTTCTCCCCCAGCTGACTCCTCAGAATCTTTACTTCCTGCAGAAATGGAAGCGATAGACAGCCTGCGTAAGGAAACGGCCTTTGATGGAGCAGACAGCACCAGGACTCCGTCCCTGGCAAGCAGTAGGAGGGGAGTCCCACACATAAGCAAATGGGAAAGTCTTGTCCAGAGTGCATTTGGGA... | CCCCCACTCACCTGGGCTTGGAACCACTGTTCCACATCCTGGTGGTTGGTCTCCACCATGGCCTCGTACTGAGCCCGCATCTCCCCCAACACCCTGTTCAGGTCAATGGTGGGCTCAATGTCCAGCTCGATCCGGAACTTCTCCCCCAGCTGACTCCTCAGAATCTTTACTTCCTGCAGAAATGGAAGCGATAGACAGCCTGCGTAAGGAAACGGCCTTTGATGGAGCAGACAGCACCAGGACTCCGTCCCTGGCAAGCAGTAGGAGGGGAGTCCCACACATAAGCAAATGGGAAAGTCTTGTCCAGAGTGCATTTGGGA... |
Task1_train_45342 | A mutation is present on Chromosome 17. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CAGGTCAATGGTGGGCTCAATGTCCAGCTCGATCCGGAACTTCTCCCCCAGCTGACTCCTCAGAATCTTTACTTCCTGCAGAAATGGAAGCGATAGACAGCCTGCGTAAGGAAACGGCCTTTGATGGAGCAGACAGCACCAGGACTCCGTCCCTGGCAAGCAGTAGGAGGGGAGTCCCACACATAAGCAAATGGGAAAGTCTTGTCCAGAGTGCATTTGGGAGAGCCCACCTGGACACCTTCCTCATGCCCAAGGCAAGTCTGCACTTTCCACAGAGGCCCTCTGGACCCTCAGACCCACCTCAGCCCTGCATCCTTAGG... | CAGGTCAATGGTGGGCTCAATGTCCAGCTCGATCCGGAACTTCTCCCCCAGCTGACTCCTCAGAATCTTTACTTCCTGCAGAAATGGAAGCGATAGACAGCCTGCGTAAGGAAACGGCCTTTGATGGAGCAGACAGCACCAGGACTCCGTCCCTGGCAAGCAGTAGGAGGGGAGTCCCACACATAAGCAAATGGGAAAGTCTTGTCCAGAGTGCATTTGGGAGAGCCCACCTGGACACCTTCCTCATGCCCAAGGCAAGTCTGCACTTTCCACAGAGGCCCTCTGGACCCTCAGACCCACCTCAGCCCTGCATCCTTAGG... |
Task1_train_45343 | A mutation is present on Chromosome 17. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | AGAAATGGAAGCGATAGACAGCCTGCGTAAGGAAACGGCCTTTGATGGAGCAGACAGCACCAGGACTCCGTCCCTGGCAAGCAGTAGGAGGGGAGTCCCACACATAAGCAAATGGGAAAGTCTTGTCCAGAGTGCATTTGGGAGAGCCCACCTGGACACCTTCCTCATGCCCAAGGCAAGTCTGCACTTTCCACAGAGGCCCTCTGGACCCTCAGACCCACCTCAGCCCTGCATCCTTAGGCCAGCTGAGCCCAGGCAATGCTCTGAGAGCCCCAGGGCCGGGGAGCTCCCCTGTCTGCCCAGCGCCCTCCCCAGGAGTC... | AGAAATGGAAGCGATAGACAGCCTGCGTAAGGAAACGGCCTTTGATGGAGCAGACAGCACCAGGACTCCGTCCCTGGCAAGCAGTAGGAGGGGAGTCCCACACATAAGCAAATGGGAAAGTCTTGTCCAGAGTGCATTTGGGAGAGCCCACCTGGACACCTTCCTCATGCCCAAGGCAAGTCTGCACTTTCCACAGAGGCCCTCTGGACCCTCAGACCCACCTCAGCCCTGCATCCTTAGGCCAGCTGAGCCCAGGCAATGCTCTGAGAGCCCCAGGGCCGGGGAGCTCCCCTGTCTGCCCAGCGCCCTCCCCAGGAGTC... |
Task1_train_45344 | A variant found on Chromosome 17 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | AAAAATAGCTGGTAATCGCATTCAGAAATCAGGACCACAAATGGGCCTAATCTGCATTCCCCCCAAGTCTCCAAATTGAAGTTCTGCAGGGATCATAATGGCCCTTGGAATTACTGAGTGCCTCACAAGACCGAGGTGTGTTCTCCCATCACTTTAACCCTGGTGAACCCAAAGGGGAAAATGGAAACAAGACCACCCATGAAAGTGGGTCCTCTCTCCTTGGATGGACTCAATAGAAAGGAGTTCTGCCCCTCAAAGCAAAGTTTTCTCATTGTTTGGCCTAATGCAAATACTCAAATACAGTTTGCTCTAGGAAGCAA... | AAAAATAGCTGGTAATCGCATTCAGAAATCAGGACCACAAATGGGCCTAATCTGCATTCCCCCCAAGTCTCCAAATTGAAGTTCTGCAGGGATCATAATGGCCCTTGGAATTACTGAGTGCCTCACAAGACCGAGGTGTGTTCTCCCATCACTTTAACCCTGGTGAACCCAAAGGGGAAAATGGAAACAAGACCACCCATGAAAGTGGGTCCTCTCTCCTTGGATGGACTCAATAGAAAGGAGTTCTGCCCCTCAAAGCAAAGTTTTCTCATTGTTTGGCCTAATGCAAATACTCAAATACAGTTTGCTCTAGGAAGCAA... |
Task1_train_45345 | This sequence change occurs on Chromosome 17. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | AGAAACATCATCTCAGCTCATTAAGGAAGAACTGTGTGTTTGGAGGGTGAGGTTCAGAAAGGTGTTCAAGATTCCTGTCCCCAGCTCTCTCCTCTTTACCTGCCATGGCCAATCCATTGCCAAGTCAGGTCCATCACAGTGTCTCTTAGATTGATTCCTTATTTTTCCATGGTCCCTGACATTGTCTTGCCTGAGACCCTGTTAGCTTCTTCCACAGCCTAACCCCTCCTCTTAGCTATCCTGTCTGTGTTACTTGGTGATACTTTCTAAGATGCCACTCAAGTCATGTCATCTTTGGGCTCAAATCCTGCAGCAGCCCT... | AGAAACATCATCTCAGCTCATTAAGGAAGAACTGTGTGTTTGGAGGGTGAGGTTCAGAAAGGTGTTCAAGATTCCTGTCCCCAGCTCTCTCCTCTTTACCTGCCATGGCCAATCCATTGCCAAGTCAGGTCCATCACAGTGTCTCTTAGATTGATTCCTTATTTTTCCATGGTCCCTGACATTGTCTTGCCTGAGACCCTGTTAGCTTCTTCCACAGCCTAACCCCTCCTCTTAGCTATCCTGTCTGTGTTACTTGGTGATACTTTCTAAGATGCCACTCAAGTCATGTCATCTTTGGGCTCAAATCCTGCAGCAGCCCT... |
Task1_train_45346 | A change on Chromosome 17 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CCACCATGGCACATGTACACCTATGTAACAAACCTGCACGTTCTGCACATGTATCCCAGAAGTTAAAGTAAAATAAAATAAAATAAAGAAAAGCAGCTTCCTTAATAGGACCTGCATGATCCTGCTCCCACCTCTTGCCCCAGCCTCACCTGATAGCTCCATTGCTCTGGGAGCTGCAGGTACTCTGACCTTCTTCCAGCTCCTGCAGGGACTGTACTGCTCAGGCCACAGGGCTTGTGCCCTGTGCCGTACATCTCTGGAACCCTCTTCCCTCTCCACTCACCTACATTTCTTCTCTTGTTTAAGAGCTCAACTCAACT... | CCACCATGGCACATGTACACCTATGTAACAAACCTGCACGTTCTGCACATGTATCCCAGAAGTTAAAGTAAAATAAAATAAAATAAAGAAAAGCAGCTTCCTTAATAGGACCTGCATGATCCTGCTCCCACCTCTTGCCCCAGCCTCACCTGATAGCTCCATTGCTCTGGGAGCTGCAGGTACTCTGACCTTCTTCCAGCTCCTGCAGGGACTGTACTGCTCAGGCCACAGGGCTTGTGCCCTGTGCCGTACATCTCTGGAACCCTCTTCCCTCTCCACTCACCTACATTTCTTCTCTTGTTTAAGAGCTCAACTCAACT... |
Task1_train_45347 | A mutation is present on Chromosome 17. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TATGTAACAAACCTGCACGTTCTGCACATGTATCCCAGAAGTTAAAGTAAAATAAAATAAAATAAAGAAAAGCAGCTTCCTTAATAGGACCTGCATGATCCTGCTCCCACCTCTTGCCCCAGCCTCACCTGATAGCTCCATTGCTCTGGGAGCTGCAGGTACTCTGACCTTCTTCCAGCTCCTGCAGGGACTGTACTGCTCAGGCCACAGGGCTTGTGCCCTGTGCCGTACATCTCTGGAACCCTCTTCCCTCTCCACTCACCTACATTTCTTCTCTTGTTTAAGAGCTCAACTCAACTCTCACGTCCTCCTTGAAGCCT... | TATGTAACAAACCTGCACGTTCTGCACATGTATCCCAGAAGTTAAAGTAAAATAAAATAAAATAAAGAAAAGCAGCTTCCTTAATAGGACCTGCATGATCCTGCTCCCACCTCTTGCCCCAGCCTCACCTGATAGCTCCATTGCTCTGGGAGCTGCAGGTACTCTGACCTTCTTCCAGCTCCTGCAGGGACTGTACTGCTCAGGCCACAGGGCTTGTGCCCTGTGCCGTACATCTCTGGAACCCTCTTCCCTCTCCACTCACCTACATTTCTTCTCTTGTTTAAGAGCTCAACTCAACTCTCACGTCCTCCTTGAAGCCT... |
Task1_train_45348 | This alteration occurs on Chromosome 17. Is it associated with a disease or is it a benign variant? | Benign | GCAGCTTCCTTAATAGGACCTGCATGATCCTGCTCCCACCTCTTGCCCCAGCCTCACCTGATAGCTCCATTGCTCTGGGAGCTGCAGGTACTCTGACCTTCTTCCAGCTCCTGCAGGGACTGTACTGCTCAGGCCACAGGGCTTGTGCCCTGTGCCGTACATCTCTGGAACCCTCTTCCCTCTCCACTCACCTACATTTCTTCTCTTGTTTAAGAGCTCAACTCAACTCTCACGTCCTCCTTGAAGCCTCCCCCACCTCTCTGAGACAAAGCCCCCATGGTACATGTATCTCCTTTCATCGTGAGTAGTAATCATTCTAT... | GCAGCTTCCTTAATAGGACCTGCATGATCCTGCTCCCACCTCTTGCCCCAGCCTCACCTGATAGCTCCATTGCTCTGGGAGCTGCAGGTACTCTGACCTTCTTCCAGCTCCTGCAGGGACTGTACTGCTCAGGCCACAGGGCTTGTGCCCTGTGCCGTACATCTCTGGAACCCTCTTCCCTCTCCACTCACCTACATTTCTTCTCTTGTTTAAGAGCTCAACTCAACTCTCACGTCCTCCTTGAAGCCTCCCCCACCTCTCTGAGACAAAGCCCCCATGGTACATGTATCTCCTTTCATCGTGAGTAGTAATCATTCTAT... |
Task1_train_45349 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | CCTTAATAGGACCTGCATGATCCTGCTCCCACCTCTTGCCCCAGCCTCACCTGATAGCTCCATTGCTCTGGGAGCTGCAGGTACTCTGACCTTCTTCCAGCTCCTGCAGGGACTGTACTGCTCAGGCCACAGGGCTTGTGCCCTGTGCCGTACATCTCTGGAACCCTCTTCCCTCTCCACTCACCTACATTTCTTCTCTTGTTTAAGAGCTCAACTCAACTCTCACGTCCTCCTTGAAGCCTCCCCCACCTCTCTGAGACAAAGCCCCCATGGTACATGTATCTCCTTTCATCGTGAGTAGTAATCATTCTATTATGGTC... | CCTTAATAGGACCTGCATGATCCTGCTCCCACCTCTTGCCCCAGCCTCACCTGATAGCTCCATTGCTCTGGGAGCTGCAGGTACTCTGACCTTCTTCCAGCTCCTGCAGGGACTGTACTGCTCAGGCCACAGGGCTTGTGCCCTGTGCCGTACATCTCTGGAACCCTCTTCCCTCTCCACTCACCTACATTTCTTCTCTTGTTTAAGAGCTCAACTCAACTCTCACGTCCTCCTTGAAGCCTCCCCCACCTCTCTGAGACAAAGCCCCCATGGTACATGTATCTCCTTTCATCGTGAGTAGTAATCATTCTATTATGGTC... |
Task1_train_45350 | A genomic change on Chromosome 17 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GAAAAGAACCTGGGCATCAGGATGGGTGATATTGAGATCCATAGGTTTGGAAGGGCAGGCTAAGCACAGAACAAGCCTTCTTGTGGAGTTGAGTTTGACAGTGTCCACCTAACCCATGTCTGATTTGAAACATCCCTTTTTTATCTCTGAGCTGGATCTCGGGAGAAACCTCCCTCCGGGAAAAGTCAACAGGATGAGCATCCATGGTGGCTGAAATCTGAGCCTCCTCTTCCTCTTTCCTGGGGACCTGCACCTATGCTCAGTACCGCCTAGGATCCGGAGGGATGGGTGCCCACCCAGCAGCTCTCACCAGGCTGTGC... | GAAAAGAACCTGGGCATCAGGATGGGTGATATTGAGATCCATAGGTTTGGAAGGGCAGGCTAAGCACAGAACAAGCCTTCTTGTGGAGTTGAGTTTGACAGTGTCCACCTAACCCATGTCTGATTTGAAACATCCCTTTTTTATCTCTGAGCTGGATCTCGGGAGAAACCTCCCTCCGGGAAAAGTCAACAGGATGAGCATCCATGGTGGCTGAAATCTGAGCCTCCTCTTCCTCTTTCCTGGGGACCTGCACCTATGCTCAGTACCGCCTAGGATCCGGAGGGATGGGTGCCCACCCAGCAGCTCTCACCAGGCTGTGC... |
Task1_train_45351 | Mutation context: Chromosome 17. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | AGAGGTTGAGAGTCAACCAGGGAGGGGGGAAAAACACCATGGCTCAGGTGGGCTTGGCAGCACACAGGTGCCCAAAGCAGAGGGCTTCCCCTCCAAGAAACTTCAGGAGATAAGGAAAAATCAGAAAGTAAAGGGCTTCAGCTTGAGCATTTTATATGCAAACAGAAGGGAGGACAAAATAAGGATAGGGGCAAAAAGAGGAGACCACTGCAGCTGTACTCCCTCTCAGAAGAGATGGGACTGCTTCTGAGAGTTGAGCCAGGCAGAGATGGACAGGCCATTCAACGTGAGATCTGGAACATAACTCACCCCGGCACCAC... | AGAGGTTGAGAGTCAACCAGGGAGGGGGGAAAAACACCATGGCTCAGGTGGGCTTGGCAGCACACAGGTGCCCAAAGCAGAGGGCTTCCCCTCCAAGAAACTTCAGGAGATAAGGAAAAATCAGAAAGTAAAGGGCTTCAGCTTGAGCATTTTATATGCAAACAGAAGGGAGGACAAAATAAGGATAGGGGCAAAAAGAGGAGACCACTGCAGCTGTACTCCCTCTCAGAAGAGATGGGACTGCTTCTGAGAGTTGAGCCAGGCAGAGATGGACAGGCCATTCAACGTGAGATCTGGAACATAACTCACCCCGGCACCAC... |
Task1_train_45352 | A mutation has occurred on Chromosome 17. What is the medical relevance of this mutation? | Benign | TTCACTTTAGCTGGCCTGGTTTACCGGGAAGGAAACGTCAGAAGTGAAACTCTGGCCAGGGAAATGTGGATGCCCAGCCTCATAGCAATCCAGTCGTCCAGCTGGAAGGGAGAGTTGGTGGTGATGAGCCATCTTCAAATGCCCTGCATATGCTGGGCAAAGCATTCTCGGCCTCACTTCACAGCATAAGTGTCATGTTCTCTATTTAACTGAAGCTCAGAAATGGACAATGACCTGCTAAACCTCCCACATGTAGTTAGTGGTGGGTGGGGATTTGAACCCAGGTCCATCTGACTCCACATTCGGAGCCCACGTTTATT... | TTCACTTTAGCTGGCCTGGTTTACCGGGAAGGAAACGTCAGAAGTGAAACTCTGGCCAGGGAAATGTGGATGCCCAGCCTCATAGCAATCCAGTCGTCCAGCTGGAAGGGAGAGTTGGTGGTGATGAGCCATCTTCAAATGCCCTGCATATGCTGGGCAAAGCATTCTCGGCCTCACTTCACAGCATAAGTGTCATGTTCTCTATTTAACTGAAGCTCAGAAATGGACAATGACCTGCTAAACCTCCCACATGTAGTTAGTGGTGGGTGGGGATTTGAACCCAGGTCCATCTGACTCCACATTCGGAGCCCACGTTTATT... |
Task1_train_45353 | Given this context: Chromosome 17 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CCACCTCAACATTGAGGCGGTCACCAAGTTGGCAGCGCAGTGAGTTCACTTCCTATAGCACAGACCAGGATGAGTACTAATTCCCAGAGGGCTGCCTCCAAGGTTCACCTCCTCCTCATGTTCACCTCCTCCCCATGCTCACCCCTCCTAATGCTCACCTCCTCCCCATGCTCATCTGCTCCCCATGCCCACCTCCTCCCCATGCTCACCTCCTCTGCATGCTCACCTGCTCTCTATGCTCACCTGCTCCCCATGCTCACCTCCTCTTCCCTATGCACACCTGCTCCCTCATGTTCACCTCCCCCTATGCTCACCTCATC... | CCACCTCAACATTGAGGCGGTCACCAAGTTGGCAGCGCAGTGAGTTCACTTCCTATAGCACAGACCAGGATGAGTACTAATTCCCAGAGGGCTGCCTCCAAGGTTCACCTCCTCCTCATGTTCACCTCCTCCCCATGCTCACCCCTCCTAATGCTCACCTCCTCCCCATGCTCATCTGCTCCCCATGCCCACCTCCTCCCCATGCTCACCTCCTCTGCATGCTCACCTGCTCTCTATGCTCACCTGCTCCCCATGCTCACCTCCTCTTCCCTATGCACACCTGCTCCCTCATGTTCACCTCCCCCTATGCTCACCTCATC... |
Task1_train_45354 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | TGCTCAGCAAGTGATTGAAGAGTCCCATTTAGCAGCAAGTAGCTGATGACATGAGGCAGAGCCAGGTCATGGATGTCTTGGCCATGACCCAGAGGAGAGCCCAGAGGAGAGTGAGCACAAGAGAGGGGGAGGAGGGAAGAGAGACAGAGACAGAGAGCGAGACAGAGAGAGAGAGAGAGAGAAATTGTACTGAGAAGAGCTCCAGAGCCAGGGTCAGAATAGCCAGGTGATGGCCAGGTCTCTGCCACTCACTGCTCTGTGGCCTGGAACAAGTCACTGCCCTCTCTGGGCCTGTTTTCTCAAGTGAAGACTGGAGCAGG... | TGCTCAGCAAGTGATTGAAGAGTCCCATTTAGCAGCAAGTAGCTGATGACATGAGGCAGAGCCAGGTCATGGATGTCTTGGCCATGACCCAGAGGAGAGCCCAGAGGAGAGTGAGCACAAGAGAGGGGGAGGAGGGAAGAGAGACAGAGACAGAGAGCGAGACAGAGAGAGAGAGAGAGAGAAATTGTACTGAGAAGAGCTCCAGAGCCAGGGTCAGAATAGCCAGGTGATGGCCAGGTCTCTGCCACTCACTGCTCTGTGGCCTGGAACAAGTCACTGCCCTCTCTGGGCCTGTTTTCTCAAGTGAAGACTGGAGCAGG... |
Task1_train_45355 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | AAGACTGGAGCAGGGGCAAAGGAACCAACCGTGAGGCCCTCAGACCTCTCCCAGGCCATGCTTCTCTGATCAGAGGGGTGTCCAGAGCTGGCAGAGTTAGGCCCCACCTGCAGACCTGCCTAACTCAGCCAGTGGAATCCAGGGCTCTGAACTCTGCTCCACAGTGAAGCCTGGCTGTCCTCTCCCCAGACTCCATGTCTGAGCACCCACCCCCACCCCACTGTCCCTGGCACCCTTCAGTTTGGCCCTATGTGCCTTGTTGGGACATGGATTCACCTGCCCTCCACCTTCACCTCCCTGCTCTCCCTGACTGCCCTCCC... | AAGACTGGAGCAGGGGCAAAGGAACCAACCGTGAGGCCCTCAGACCTCTCCCAGGCCATGCTTCTCTGATCAGAGGGGTGTCCAGAGCTGGCAGAGTTAGGCCCCACCTGCAGACCTGCCTAACTCAGCCAGTGGAATCCAGGGCTCTGAACTCTGCTCCACAGTGAAGCCTGGCTGTCCTCTCCCCAGACTCCATGTCTGAGCACCCACCCCCACCCCACTGTCCCTGGCACCCTTCAGTTTGGCCCTATGTGCCTTGTTGGGACATGGATTCACCTGCCCTCCACCTTCACCTCCCTGCTCTCCCTGACTGCCCTCCC... |
Task1_train_45356 | Located on Chromosome 17, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | GAGCCCAGCACTGGCTCCCTCCCTCCCCGCCAGCTCCCACCCCCATTGGGGCAGTGAATGGGAGGCTAACTCTGCCTCCCCCTACACCACGGGGCTGTTCCCTTACCTGCTGAGGAAGGGAAACCAATCATCCTGGGAGAGAGGACAGAGGTGGCCATGAGCAGAGGGTAACTGAGGGCAGGTGCTTACCTGTTCCTCTGGGGAAGTGCCTCGGCTTATCATTTCAAGCCCCTGGGCTGGACTCTAGTGCCTCCTAGCTGTGCCCCCAGCTCAAGGGACAGCAGCATCAGGTGCCCACTGGGACTGTCTGTCTTTCCTGT... | GAGCCCAGCACTGGCTCCCTCCCTCCCCGCCAGCTCCCACCCCCATTGGGGCAGTGAATGGGAGGCTAACTCTGCCTCCCCCTACACCACGGGGCTGTTCCCTTACCTGCTGAGGAAGGGAAACCAATCATCCTGGGAGAGAGGACAGAGGTGGCCATGAGCAGAGGGTAACTGAGGGCAGGTGCTTACCTGTTCCTCTGGGGAAGTGCCTCGGCTTATCATTTCAAGCCCCTGGGCTGGACTCTAGTGCCTCCTAGCTGTGCCCCCAGCTCAAGGGACAGCAGCATCAGGTGCCCACTGGGACTGTCTGTCTTTCCTGT... |
Task1_train_45357 | A variant affecting Chromosome 17 has been observed. Determine if it's benign or associated with disease. | Benign | GCCGACCACCTGGTTGCTAAATTCCTTCATCTCCTGTGGGGATGGGAAAGGAAGATGTGTGAGGCTACTCATCCTCCCTCTCCTTGGCTCTGAGTGCTGGCAGAGTGTTCTGGAGAGTGTTTCCAGGTCCCACAGTGGAGGACTGTGTCCAGTTGCAGGGGAGGGCTCCTCCTTCTCACTGGAGGTTGTTGAGCCCAGGGCAGCCTGCAATTCCCGCTCACCTCTTCATGGTTCTTCTTCATGTAGGCTAGCTCTTCATTCAGGCTCTCGATCTGCATCTCCAGGTCAGTCTTAGACAGAGTGAGCTCATCCAGCACCCG... | GCCGACCACCTGGTTGCTAAATTCCTTCATCTCCTGTGGGGATGGGAAAGGAAGATGTGTGAGGCTACTCATCCTCCCTCTCCTTGGCTCTGAGTGCTGGCAGAGTGTTCTGGAGAGTGTTTCCAGGTCCCACAGTGGAGGACTGTGTCCAGTTGCAGGGGAGGGCTCCTCCTTCTCACTGGAGGTTGTTGAGCCCAGGGCAGCCTGCAATTCCCGCTCACCTCTTCATGGTTCTTCTTCATGTAGGCTAGCTCTTCATTCAGGCTCTCGATCTGCATCTCCAGGTCAGTCTTAGACAGAGTGAGCTCATCCAGCACCCG... |
Task1_train_45358 | This genomic variant is located on Chromosome 17. Can you determine its pathogenicity and name any linked disease? | Benign | ACAATCAACGCGATCAGTCACTTGGTAAATATTCATAATTATTAGATGTGTTGAGTTCTGTGCTGGGTACACCAAACTCTTTTTAGGGAACCTCCCCACCCTCACTTCCCTGGTCACCCCATGGTGACCCAGAAGAGCAAATTACCTGAGTAGCACTATGTTTGTCCCAGCCACTGGTGCCCTGGGTACCCAAAAGAATTGTGGCCACGCAGGGAAGAGGCCAAAGTGGGGGGAGATATCACCATGTGGACCCTGGGTCTCCTCAGAGATCAGAGGCCAACCAGGACCCCATCAAGAAAAACTGGACATACTGCCAAGAG... | ACAATCAACGCGATCAGTCACTTGGTAAATATTCATAATTATTAGATGTGTTGAGTTCTGTGCTGGGTACACCAAACTCTTTTTAGGGAACCTCCCCACCCTCACTTCCCTGGTCACCCCATGGTGACCCAGAAGAGCAAATTACCTGAGTAGCACTATGTTTGTCCCAGCCACTGGTGCCCTGGGTACCCAAAAGAATTGTGGCCACGCAGGGAAGAGGCCAAAGTGGGGGGAGATATCACCATGTGGACCCTGGGTCTCCTCAGAGATCAGAGGCCAACCAGGACCCCATCAAGAAAAACTGGACATACTGCCAAGAG... |
Task1_train_45359 | This mutation is located on Chromosome 17. Is it associated with a disease or is it a benign polymorphism? | Benign | TCCTGGCTCTGCCCGTAACACACCCCAACCGCTGTTCCCCATTGCACATGAAGAGGTTTGGTCACATGGACCCCTCAGCTCTAAGGAGTTCTCTGCTGCTCTAGGTCCTACCAAGGGAGGACCCCGAGACTGTAGGGCCCTGATGTGAGCTCACAAAGCCAATCAGGAAGTCAACCATTCATACGGGCCACCTGGGCTGGCTGTGGGCCTGGGCTACCAGACACTGCCCCTTCCTCTCCATGAGGACACCTGGTTTTGTGGGGTAGGTGTGTTTCTGAACCACTAAGCCCCAGGCCAACTATGAGGAAGTACCAACAGCC... | TCCTGGCTCTGCCCGTAACACACCCCAACCGCTGTTCCCCATTGCACATGAAGAGGTTTGGTCACATGGACCCCTCAGCTCTAAGGAGTTCTCTGCTGCTCTAGGTCCTACCAAGGGAGGACCCCGAGACTGTAGGGCCCTGATGTGAGCTCACAAAGCCAATCAGGAAGTCAACCATTCATACGGGCCACCTGGGCTGGCTGTGGGCCTGGGCTACCAGACACTGCCCCTTCCTCTCCATGAGGACACCTGGTTTTGTGGGGTAGGTGTGTTTCTGAACCACTAAGCCCCAGGCCAACTATGAGGAAGTACCAACAGCC... |
Task1_train_45360 | Chromosome 17 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GCCTTGTGGGTGGTTTAAGGAGCCAATCTTGAAAATGGCGTGGTTGAACACAGTGCCCATTGATTGCTCAGATATGAACATTCCTGCGGGCTGGGGATAAGGCAGTTCATCTTGCTGCAGAAATCAGGAGGGGGTTGCACTTCTAGCTTCAGCCAACAAATAATGCAGAAGTCCTCCAACTATGATTCCTTCCTATACTTCAAGGGCAGCTGGGGAAGTGGAAAGTGCCTCTCCCTAAAGCAGCGGTTCTGAAACCTGGCTGTGGACCAGAATCACCCAGGTAACCTGCTATAAATAGCTGAATCAAAACTCCAAGGGTG... | GCCTTGTGGGTGGTTTAAGGAGCCAATCTTGAAAATGGCGTGGTTGAACACAGTGCCCATTGATTGCTCAGATATGAACATTCCTGCGGGCTGGGGATAAGGCAGTTCATCTTGCTGCAGAAATCAGGAGGGGGTTGCACTTCTAGCTTCAGCCAACAAATAATGCAGAAGTCCTCCAACTATGATTCCTTCCTATACTTCAAGGGCAGCTGGGGAAGTGGAAAGTGCCTCTCCCTAAAGCAGCGGTTCTGAAACCTGGCTGTGGACCAGAATCACCCAGGTAACCTGCTATAAATAGCTGAATCAAAACTCCAAGGGTG... |
Task1_train_45361 | A mutation on Chromosome 17 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CTGCGCAGGCCATTGATGTCGGCCTCCACACTCAGGCGCAGGGCCTGCTCTGTCTCAAACCTGCCGTGGGAATCAGAGACTTCAGCCCAGGCTGCTTGGACCTGCAGATCCAGGTCCTGGCTGCTCACCTGCCTTCATTTTGCCAGGACTCTAAGGAGTTGGAAGGGCTGATGAGAGGGTCGAGTGGAAACGAATTCCAGCCCCGGGACCCCGGGACCATCACAGGGCCAGATCCCACGCCCACCAGCTTCCTTACTTCTCTCTGCCTCCCGCCTCCCGCCTCCCCTCCTTCTCTTCTATTCCCTGCCTAAGCTCAGCAA... | CTGCGCAGGCCATTGATGTCGGCCTCCACACTCAGGCGCAGGGCCTGCTCTGTCTCAAACCTGCCGTGGGAATCAGAGACTTCAGCCCAGGCTGCTTGGACCTGCAGATCCAGGTCCTGGCTGCTCACCTGCCTTCATTTTGCCAGGACTCTAAGGAGTTGGAAGGGCTGATGAGAGGGTCGAGTGGAAACGAATTCCAGCCCCGGGACCCCGGGACCATCACAGGGCCAGATCCCACGCCCACCAGCTTCCTTACTTCTCTCTGCCTCCCGCCTCCCGCCTCCCCTCCTTCTCTTCTATTCCCTGCCTAAGCTCAGCAA... |
Task1_train_45362 | Consider this mutation on Chromosome 17. Is this a benign change or a disease-causing variant? | Benign | TCTTTTATGTCCCTGACCCTGCACGGAATACACCAACAGGGTTAACACCCACTTCTGCCTCCCTCCTGCATGATTTAACCTTCATAGCCCACCCCACAGCTACTTGCCATAGGAACAAATCCATTCTAGACAGGCTCAGACAGGTCAAATGACTTGCCCAAGGACACACAGTCAGGAAAGGGACCACGCTGGGCCTTAGTCCCAGGTGTTCCCAGCTCCTAAGCCAGTGCCTGTCACCTCTCAGCCCATAGTCAGTTGAAAAGAAAGCTTCAGTCCCCACTCAGAGCTGCCTGGAATCAGACGGCCACCCAGGGGGCAAG... | TCTTTTATGTCCCTGACCCTGCACGGAATACACCAACAGGGTTAACACCCACTTCTGCCTCCCTCCTGCATGATTTAACCTTCATAGCCCACCCCACAGCTACTTGCCATAGGAACAAATCCATTCTAGACAGGCTCAGACAGGTCAAATGACTTGCCCAAGGACACACAGTCAGGAAAGGGACCACGCTGGGCCTTAGTCCCAGGTGTTCCCAGCTCCTAAGCCAGTGCCTGTCACCTCTCAGCCCATAGTCAGTTGAAAAGAAAGCTTCAGTCCCCACTCAGAGCTGCCTGGAATCAGACGGCCACCCAGGGGGCAAG... |
Task1_train_45363 | Chromosome 17 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AGAGAGAGGCTAGGCCCCTAAGAGAACCTTCCCCATCCCCTAGTTCTCTAGGGTACCAGACCAGAGTCTGCCATTAACCCACTGTGGAACCTGGCTCAGTTTCCCCTCATGGAAAAAGAAGATCAGACCAGATTGGCTCTGAGAGCTCTTCCAGCCTGAACATCCCACATCGACCTGTCTTCCATAAGAAGGACCCTAACCTGGGGCCCCAGAGAGACTGCCAATCAGGAAATAAACAAGACCCCCACCCCTACAGGACAAAACTAGAATAAGGGCTTGCCTGGATCAGGAAGGCAGTACACACCTCCTCCAGCAAATAT... | AGAGAGAGGCTAGGCCCCTAAGAGAACCTTCCCCATCCCCTAGTTCTCTAGGGTACCAGACCAGAGTCTGCCATTAACCCACTGTGGAACCTGGCTCAGTTTCCCCTCATGGAAAAAGAAGATCAGACCAGATTGGCTCTGAGAGCTCTTCCAGCCTGAACATCCCACATCGACCTGTCTTCCATAAGAAGGACCCTAACCTGGGGCCCCAGAGAGACTGCCAATCAGGAAATAAACAAGACCCCCACCCCTACAGGACAAAACTAGAATAAGGGCTTGCCTGGATCAGGAAGGCAGTACACACCTCCTCCAGCAAATAT... |
Task1_train_45364 | A variant has been detected on Chromosome 17. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GTCAGGAAACGCTACCACTGCAGATGTGCTTCCCCGGAAGACCCACCTATGGGAGGAAGGAGTGAGGTCACTGAGCCCCCAGCCTTGACCCAGCCCTTTTTCCAGACTCAGACTCTGCCCTTTCAGCTCTCATCCCGATCAAAGGCCTAGGGGAGGGGCTTGGAGTGGGACAGGGAGTCCTCCTAGGAACAGAGGTGGACAGGGCCCAGGCCAGATCACCTGGCACATCTGGAGAGAAAGTAGGGGTGGGGCAGTGAGAACTTGGCTTCCCAGCCTTGACTCTACCTTCAAGTGGGAAGACAACTCTGCCGCCCTGCCCC... | GTCAGGAAACGCTACCACTGCAGATGTGCTTCCCCGGAAGACCCACCTATGGGAGGAAGGAGTGAGGTCACTGAGCCCCCAGCCTTGACCCAGCCCTTTTTCCAGACTCAGACTCTGCCCTTTCAGCTCTCATCCCGATCAAAGGCCTAGGGGAGGGGCTTGGAGTGGGACAGGGAGTCCTCCTAGGAACAGAGGTGGACAGGGCCCAGGCCAGATCACCTGGCACATCTGGAGAGAAAGTAGGGGTGGGGCAGTGAGAACTTGGCTTCCCAGCCTTGACTCTACCTTCAAGTGGGAAGACAACTCTGCCGCCCTGCCCC... |
Task1_train_45365 | Chromosome 17 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TGCCTCAGCCTCCTGAGTAACTGGGACTACAGGCGCCCGCCACCACACCTGGCTAATGTTTTGTATTTTTAGTAAAGACGGGGTTTCACTGTGTTAGCCAGGATTGTAGAATAGGCCTTTTCAAAATGTGAAACCAGCTCCCACCCCACCTCTGCTCTCCCGTCTTTTCTTGGAGAGCCAATAGTATAATGGCAAATTTTAGAACTCAGCTGACTACATATTAGCTGTGTGACCTTGGGCAAGGCACTGAGTCTCTCAAGTCTCCATTGCTCTCATTAAGAAAAATGAGAACAAGAATGCCCACCTCACAGGGGAGACAA... | TGCCTCAGCCTCCTGAGTAACTGGGACTACAGGCGCCCGCCACCACACCTGGCTAATGTTTTGTATTTTTAGTAAAGACGGGGTTTCACTGTGTTAGCCAGGATTGTAGAATAGGCCTTTTCAAAATGTGAAACCAGCTCCCACCCCACCTCTGCTCTCCCGTCTTTTCTTGGAGAGCCAATAGTATAATGGCAAATTTTAGAACTCAGCTGACTACATATTAGCTGTGTGACCTTGGGCAAGGCACTGAGTCTCTCAAGTCTCCATTGCTCTCATTAAGAAAAATGAGAACAAGAATGCCCACCTCACAGGGGAGACAA... |
Task1_train_45366 | Given this context: Chromosome 17 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CCTTCAGGGGCCTTGCATCTCCAGCTGGACCCCCTGGCACAGGATGTGCTGCAGTAGCCCGTTGACCACATCCAGAGTCTCGTCCTTCTCCAGCACGATGTCATAGGAGTCCATGTAGCGCTCCCGCCGCTCCTCCACCTGCCCGGAATGAGAGGCAGAAGCCAGAGGGTCCCCAAATGCCCTGCCCTCCGTAGCTCACTCTCAAAGCCCCTGGGGCTGGGGAGGAGAGCATTCAAGCAGCAACTCCCAGCTCCCTTTTGAGAGCCAAAGGAGTTCAAGGTTACCGGGCCTACCCTTTGGAGACAGACGAGGGATGGGCA... | CCTTCAGGGGCCTTGCATCTCCAGCTGGACCCCCTGGCACAGGATGTGCTGCAGTAGCCCGTTGACCACATCCAGAGTCTCGTCCTTCTCCAGCACGATGTCATAGGAGTCCATGTAGCGCTCCCGCCGCTCCTCCACCTGCCCGGAATGAGAGGCAGAAGCCAGAGGGTCCCCAAATGCCCTGCCCTCCGTAGCTCACTCTCAAAGCCCCTGGGGCTGGGGAGGAGAGCATTCAAGCAGCAACTCCCAGCTCCCTTTTGAGAGCCAAAGGAGTTCAAGGTTACCGGGCCTACCCTTTGGAGACAGACGAGGGATGGGCA... |
Task1_train_45367 | Here’s a variant located on Chromosome 17. What is the predicted biological effect — harmless or disease-causing? | Benign | GGGAACTCGATGTCACCCCACTTCACTTTGCAGATGTAGTCGGCAGTGGCGTCCACCTTGGCCGCCAAGTCAAGGACATAGACTCCATCTTTGGTCACTACTTCAAGGGGAGCAGAGGCAATCATCAGACACCGGCTCTGGGTAGAGACAACCACCAACCTCCAACCCCTCCACAAACACCGATCCCATGGTGGCCCATTCAGGCCTCAGAACTCTCTAAGCTCAGTAAGAAACCAGAGAGGCCCTTATGGAGACAGAGCTTTTCCCCATTAAAGGCAAAACAAATTCTACAAGGCCATTCCCCTCTCCCTGACCTATAG... | GGGAACTCGATGTCACCCCACTTCACTTTGCAGATGTAGTCGGCAGTGGCGTCCACCTTGGCCGCCAAGTCAAGGACATAGACTCCATCTTTGGTCACTACTTCAAGGGGAGCAGAGGCAATCATCAGACACCGGCTCTGGGTAGAGACAACCACCAACCTCCAACCCCTCCACAAACACCGATCCCATGGTGGCCCATTCAGGCCTCAGAACTCTCTAAGCTCAGTAAGAAACCAGAGAGGCCCTTATGGAGACAGAGCTTTTCCCCATTAAAGGCAAAACAAATTCTACAAGGCCATTCCCCTCTCCCTGACCTATAG... |
Task1_train_45368 | A mutation on Chromosome 17 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GCAGCAATGAGGTGGTCAGTCCAGGGAGAGGTCCGACAAGTTCTCGGCACAATGCTGCAGGAAGTCAAAGTCAGGCACGGAGAAGGGCACGCGGGACCACTTTTTGGCCTGGATCCGCCCCTGAGGGGTCTCCAGCAGCATGCTGCGGACTTTGAGCACTGGCAGCTTCACTGACTTGTAGATCATCTGCAGACCCCAGACCTGGAGGTGAGACAGAGAGGGTAGGGTCTGGGTCTCTGGCCTCAGACTGGGCTTCTCTCCTCAAGTTGGAATTCCCTGAATACAGGGCCTTTTCCTCCCACCTGAGATGTCACAGACTG... | GCAGCAATGAGGTGGTCAGTCCAGGGAGAGGTCCGACAAGTTCTCGGCACAATGCTGCAGGAAGTCAAAGTCAGGCACGGAGAAGGGCACGCGGGACCACTTTTTGGCCTGGATCCGCCCCTGAGGGGTCTCCAGCAGCATGCTGCGGACTTTGAGCACTGGCAGCTTCACTGACTTGTAGATCATCTGCAGACCCCAGACCTGGAGGTGAGACAGAGAGGGTAGGGTCTGGGTCTCTGGCCTCAGACTGGGCTTCTCTCCTCAAGTTGGAATTCCCTGAATACAGGGCCTTTTCCTCCCACCTGAGATGTCACAGACTG... |
Task1_train_45369 | Here is a genetic alteration on Chromosome 17. Based on the data, is it a benign variant or a cause of disease? | Benign | TACCTTCTCATTCGCTCACATTCAAACCAGACCCATTGAGACCTAGCTGAAATGCAACCTCCTCAATTGAGAAAATCTGTGTGAAGATCCTTGGCACAGTGGCCCGGAACACAGAGGGTAACATAATGAATGGATGGAGGATGGGGGAAGGTTACTCTCTAGGAGATAGTGGATGGAGGATGGCCCAGGGATGGCCAAGCTCTCTTGATATCTTCGGAATAGGTAGGACCAGAGGGTCAATGTGTGGTCTTTTGACACTTAGTATCCTGAATTCCAGTTCTTGCTCAACCAGATAGTGGCTGTGGGAACTTGGGCAAGTC... | TACCTTCTCATTCGCTCACATTCAAACCAGACCCATTGAGACCTAGCTGAAATGCAACCTCCTCAATTGAGAAAATCTGTGTGAAGATCCTTGGCACAGTGGCCCGGAACACAGAGGGTAACATAATGAATGGATGGAGGATGGGGGAAGGTTACTCTCTAGGAGATAGTGGATGGAGGATGGCCCAGGGATGGCCAAGCTCTCTTGATATCTTCGGAATAGGTAGGACCAGAGGGTCAATGTGTGGTCTTTTGACACTTAGTATCCTGAATTCCAGTTCTTGCTCAACCAGATAGTGGCTGTGGGAACTTGGGCAAGTC... |
Task1_train_45370 | Located on Chromosome 17, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | ATAAACACAAAATTACATATAAAAGTGAGTTTTGTTTTTTTTTTTAAGTTTCGGATACCACGGCACATTACTGGAATCTTGGAGACTGGCTTCTCTCCCTTTTGATCTCCATGCACAACTTACCTGAGATGTATTCTAATAGCAACCTGGCTTCCCCTCCACACTCAGCCTTTCAAGCGCCCATTAGCTTCGCAGTAAATCTCCCACACTAGGTATCCAGCCTTTGCCTTTTTCTTTTTTCTTTTTTTTTTTCCAGAGGGAGTTTCGCTTTTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCACTCTGTCACCCAGG... | ATAAACACAAAATTACATATAAAAGTGAGTTTTGTTTTTTTTTTTAAGTTTCGGATACCACGGCACATTACTGGAATCTTGGAGACTGGCTTCTCTCCCTTTTGATCTCCATGCACAACTTACCTGAGATGTATTCTAATAGCAACCTGGCTTCCCCTCCACACTCAGCCTTTCAAGCGCCCATTAGCTTCGCAGTAAATCTCCCACACTAGGTATCCAGCCTTTGCCTTTTTCTTTTTTCTTTTTTTTTTTCCAGAGGGAGTTTCGCTTTTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCACTCTGTCACCCAGG... |
Task1_train_45371 | Here is a genetic alteration on Chromosome 17. Based on the data, is it a benign variant or a cause of disease? | Benign | GCAGTGTAGACACTAGGGAGCAGAGCACTGCAGCGTGGTCTGGCAGGAAGTGGGGGGCCCAGTATGGTTGGCTTTGGGTTGAAGGGAAGAGGTCAGCATTTAAGAAAGCCATTGTGTGGCCGGGCGCGGTGGCTCACCCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATCACGAGGTCAGGAGACCGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCCACTAAAAAATACAAAAAAATTAGCCGGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTG... | GCAGTGTAGACACTAGGGAGCAGAGCACTGCAGCGTGGTCTGGCAGGAAGTGGGGGGCCCAGTATGGTTGGCTTTGGGTTGAAGGGAAGAGGTCAGCATTTAAGAAAGCCATTGTGTGGCCGGGCGCGGTGGCTCACCCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATCACGAGGTCAGGAGACCGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCCACTAAAAAATACAAAAAAATTAGCCGGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTG... |
Task1_train_45372 | This genomic variant is located on Chromosome 17. Can you determine its pathogenicity and name any linked disease? | Benign | AATTTTCTGTTTTATATTTAGTGTGCCTCCCTCCACGAGACTATAGGCCTAATGAAGGGAAAGACGGTGCCTGTTCCTCTCTGTGGTCTTCCCAGAGCCAGGCACAGTGTATGGCACATGTGGGTACTCACGTGTTTGTTTACTGCCCTGCGTAGTCCGAGAGTATCTCATGGTGCCCCAGAAACAGTACTTTTCTTTCTTTTTATTTTTTATTTATATTTATATATATATATATATATTATATATATTTATACTTTTTTATTTATATTTTTTACAGAGATGGCATCTTGCTGTGTTGCTCAGGCTGGTGTCCAACTCCT... | AATTTTCTGTTTTATATTTAGTGTGCCTCCCTCCACGAGACTATAGGCCTAATGAAGGGAAAGACGGTGCCTGTTCCTCTCTGTGGTCTTCCCAGAGCCAGGCACAGTGTATGGCACATGTGGGTACTCACGTGTTTGTTTACTGCCCTGCGTAGTCCGAGAGTATCTCATGGTGCCCCAGAAACAGTACTTTTCTTTCTTTTTATTTTTTATTTATATTTATATATATATATATATATTATATATATTTATACTTTTTTATTTATATTTTTTACAGAGATGGCATCTTGCTGTGTTGCTCAGGCTGGTGTCCAACTCCT... |
Task1_train_45373 | With a mutation on Chromosome 17, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | AGTCGTCCAGGCTGGAGTGCGGTGGTGTGATCTTGGCTCCACCGTTTCCCAGGTTCAAGTGATTCTCCCGTCTTAGCCTCCCAAGTAGCTGGGATTACAGGTGCCCGCCATCATGCCCAGCTAATTTTTGTATTTTAGTAGAGATAGGGTATCACCATGTTGGCCAGGCTGGTCTTAAACTCCTGACTTCAGGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCGCGCCCAGCCTGATGTTTTAAGATCAGAAGCAGGGGGAGAGGGATGAGTGAGATAACAAGCTCTCCCTCCCCAT... | AGTCGTCCAGGCTGGAGTGCGGTGGTGTGATCTTGGCTCCACCGTTTCCCAGGTTCAAGTGATTCTCCCGTCTTAGCCTCCCAAGTAGCTGGGATTACAGGTGCCCGCCATCATGCCCAGCTAATTTTTGTATTTTAGTAGAGATAGGGTATCACCATGTTGGCCAGGCTGGTCTTAAACTCCTGACTTCAGGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCGCGCCCAGCCTGATGTTTTAAGATCAGAAGCAGGGGGAGAGGGATGAGTGAGATAACAAGCTCTCCCTCCCCAT... |
Task1_train_45374 | Chromosome 17 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CTTACCCTGAGACCTGGTTTTACACCCTCTCTAACTTGCAAATATAAATTTCTTTGTTGTTATTGTTGTTTTGAGACAGGGTCTTGCTCTGTCACCCAGGCTGGAGTGCCTGGTGGGATCTTGGCTCACTGCAGCCTTGACCTCCTGGGCTCAAGTGATCCTCCCACCTCAGCTTCCTGAGTAGCTGGGACTACAAGCATGTGCCTCCACACTTCGCACTTGGCTATTTTTTTTTTTTTAGAGATGGGCTTTTGCCATGTTGCCCAGGGTGGTCTTGAACTCCTGGGCTCAAGTCATCTGCCTGCCTTGGCCTCCCAAAG... | CTTACCCTGAGACCTGGTTTTACACCCTCTCTAACTTGCAAATATAAATTTCTTTGTTGTTATTGTTGTTTTGAGACAGGGTCTTGCTCTGTCACCCAGGCTGGAGTGCCTGGTGGGATCTTGGCTCACTGCAGCCTTGACCTCCTGGGCTCAAGTGATCCTCCCACCTCAGCTTCCTGAGTAGCTGGGACTACAAGCATGTGCCTCCACACTTCGCACTTGGCTATTTTTTTTTTTTTAGAGATGGGCTTTTGCCATGTTGCCCAGGGTGGTCTTGAACTCCTGGGCTCAAGTCATCTGCCTGCCTTGGCCTCCCAAAG... |
Task1_train_45375 | A mutation is present on Chromosome 17. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CAAATCCTACTACTCAGAAATAGGTGGTCACATTACATCAGACATCTCTTTATGCATGTGCATTCAAAAGGAAGAGTAGATAGAATTTTGTAAAACAGATGTTGTATGTAATTTATAATAAAAAGTATTAGAGGAATTTTACTTGAATTTATTGTTTGACCTGTTAAGTATCTAGAGTCCTCTGGAGAATACTAAGGAGTCTGGCCAGGGAAATTAGCGCTGGGGGCCAGAGGGCAAGGGGGATAGACCTGGCCAAGGAATGTCATTTGGAAAGCTAAAGGGGCAGGGGGTGGGGGTCTTTGGAAGGAAAACGATAGTTT... | CAAATCCTACTACTCAGAAATAGGTGGTCACATTACATCAGACATCTCTTTATGCATGTGCATTCAAAAGGAAGAGTAGATAGAATTTTGTAAAACAGATGTTGTATGTAATTTATAATAAAAAGTATTAGAGGAATTTTACTTGAATTTATTGTTTGACCTGTTAAGTATCTAGAGTCCTCTGGAGAATACTAAGGAGTCTGGCCAGGGAAATTAGCGCTGGGGGCCAGAGGGCAAGGGGGATAGACCTGGCCAAGGAATGTCATTTGGAAAGCTAAAGGGGCAGGGGGTGGGGGTCTTTGGAAGGAAAACGATAGTTT... |
Task1_train_45376 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GGCAACAAGAGAGAAACTCTGTCTCAAAAAAAAAAAAAAGAAAAGAAGAAAAAGAAAGAAAGAGAGAGAGGGGGAGGGAGGAAGGGAGGGAGAGAGAGAGAGAGAAAGAAAGAAAAGAAAGAAAGAAAGAAAGAAAAGAAAGAATAAGACTCATCAATTAATTTCTACAGTGGAAACTACTTCTGGGACTGGAATATAGAAAACAAGAATTGGCAGAGGCCGGGTGCAGTGGCTCACAGCTGTAATCCCAGCACTTTAGGAGGCCGATGCAGGTGGATCACCTGTGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGTT... | GGCAACAAGAGAGAAACTCTGTCTCAAAAAAAAAAAAAAGAAAAGAAGAAAAAGAAAGAAAGAGAGAGAGGGGGAGGGAGGAAGGGAGGGAGAGAGAGAGAGAGAAAGAAAGAAAAGAAAGAAAGAAAGAAAGAAAAGAAAGAATAAGACTCATCAATTAATTTCTACAGTGGAAACTACTTCTGGGACTGGAATATAGAAAACAAGAATTGGCAGAGGCCGGGTGCAGTGGCTCACAGCTGTAATCCCAGCACTTTAGGAGGCCGATGCAGGTGGATCACCTGTGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGTT... |
Task1_train_45377 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | AAGTCAAAGCTACAGTGAACCATGACTGCACTACTCCATTCCAGCCTGGGTAACAGAGTAAGAGACCCTGTGTCAAAGAAACCAAAAAGAAAAAAATAACTAGATTTTAAAAGGGAAAAAAAAAAAGAAGAAGAGAAAGAAGTATCCACAAAACAGTGAAAGGCTAGATGGTCTCTATTAGGAAGAGAACCCTATAGTCTCCAACTTGGTACCAAGAATAAACACCAAAATTGCGATTGCTGGCAATAATATTGGTGAGAGTTCTGTACCTGGCTGTGTGGCCTTAGGCAGTTTGCTTACCTTCTCTGACCTGCAGTAGG... | AAGTCAAAGCTACAGTGAACCATGACTGCACTACTCCATTCCAGCCTGGGTAACAGAGTAAGAGACCCTGTGTCAAAGAAACCAAAAAGAAAAAAATAACTAGATTTTAAAAGGGAAAAAAAAAAAGAAGAAGAGAAAGAAGTATCCACAAAACAGTGAAAGGCTAGATGGTCTCTATTAGGAAGAGAACCCTATAGTCTCCAACTTGGTACCAAGAATAAACACCAAAATTGCGATTGCTGGCAATAATATTGGTGAGAGTTCTGTACCTGGCTGTGTGGCCTTAGGCAGTTTGCTTACCTTCTCTGACCTGCAGTAGG... |
Task1_train_45378 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | GTGTTTTTGTTTGTTTGTTTTTGAGATGGAGTCTCACTTTGTCACCCAGGCTGGAGTGCAGTGGTACAATCCCAGCTCAGTGCAACCTCCGCCTCCCAGGTTCAGGCGATTCTCCTGTCTCAGCCTCCAGAATAGCTGGGATTACAAGGCATTGGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGATGTGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTTCTGACCTGAGGTGATCCACCCACCTTGGCCTCCCAAAGTGCTGGGATTAGCAAATGGGTTTCGAAGGTTTAGCTTATTCATTAAAATCA... | GTGTTTTTGTTTGTTTGTTTTTGAGATGGAGTCTCACTTTGTCACCCAGGCTGGAGTGCAGTGGTACAATCCCAGCTCAGTGCAACCTCCGCCTCCCAGGTTCAGGCGATTCTCCTGTCTCAGCCTCCAGAATAGCTGGGATTACAAGGCATTGGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGATGTGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTTCTGACCTGAGGTGATCCACCCACCTTGGCCTCCCAAAGTGCTGGGATTAGCAAATGGGTTTCGAAGGTTTAGCTTATTCATTAAAATCA... |
Task1_train_45379 | Consider this mutation on Chromosome 17. Is this a benign change or a disease-causing variant? | Benign | GGGCAAACACAAAAACCTGGTTCCAATACCTAAGTTTGAATCCATGCTTTGCTCTTCTTGATTATTTTCTTCCAAGCCCGTTCCTCTTTCTTCATCATCTGAAACCAATTCCTTGTCACTCAGACCAACTCCCTGGCTTTCAGACTGATGCCTCATTTGTTTGGAAGAACCAATCAAGAAAGGATCCTGGGTGTTTGTATTTGCAGTCAAGTCTTCCAATTCACTGCACTGTGAAGAAAACAAGCTAGCAGAACATTTTGTTTCCTCACTAAGGTGATGTTCCTGAGATGCCTTTGCCAATATTACCTGGTTACTGCAGT... | GGGCAAACACAAAAACCTGGTTCCAATACCTAAGTTTGAATCCATGCTTTGCTCTTCTTGATTATTTTCTTCCAAGCCCGTTCCTCTTTCTTCATCATCTGAAACCAATTCCTTGTCACTCAGACCAACTCCCTGGCTTTCAGACTGATGCCTCATTTGTTTGGAAGAACCAATCAAGAAAGGATCCTGGGTGTTTGTATTTGCAGTCAAGTCTTCCAATTCACTGCACTGTGAAGAAAACAAGCTAGCAGAACATTTTGTTTCCTCACTAAGGTGATGTTCCTGAGATGCCTTTGCCAATATTACCTGGTTACTGCAGT... |
Task1_train_45380 | This mutation on Chromosome 17 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | ATACATGCTTGAGAGTCACTTGCCTACAGATTATAGCAGAAGCCATCTGATGGAATGAGATGATCCAGGAATAATGGGGAAAGCAAGAAGCAACCTTTAAGGATCAGGGAAAGGAATACTCTGAAAGAAAGCTGGGAACTAGGAGGAAAATGAAGAGAGAGAGTTCTATGCTGGAACTTAAGGAAGGGTGTTTTAATAAGGGGGACATGGTCAACGGTGTTAGATGCTACAGAGAGATATGAACTGGTGGTGAGGAATTTGAGAGTAGAAGTATGCCACACTTTCAAATAGACAGGCTACAACAGGCAGAAGCTAGGATA... | ATACATGCTTGAGAGTCACTTGCCTACAGATTATAGCAGAAGCCATCTGATGGAATGAGATGATCCAGGAATAATGGGGAAAGCAAGAAGCAACCTTTAAGGATCAGGGAAAGGAATACTCTGAAAGAAAGCTGGGAACTAGGAGGAAAATGAAGAGAGAGAGTTCTATGCTGGAACTTAAGGAAGGGTGTTTTAATAAGGGGGACATGGTCAACGGTGTTAGATGCTACAGAGAGATATGAACTGGTGGTGAGGAATTTGAGAGTAGAAGTATGCCACACTTTCAAATAGACAGGCTACAACAGGCAGAAGCTAGGATA... |
Task1_train_45381 | Consider a variant on Chromosome 17. Determine its clinical classification and disease relevance. | Benign | GCTAGAGTTCCTATCTCCCATTGAAGAAGGGGCTTCTTCAAGCAGACAGACCAAACATCATTTCAAAATGAGGACTGCATTTGAAATCTACTGAAGGGGGTGATACCGGGGGCCTGAAGCCTGGGGTTTGAGCTCACTTCTAGGGTGACCAATTCTTCTGTTTGCCTGGGACTGTGGGGTTTCCTACGACAGGATTTTCAGTGCTAAAACTGGAAAAGTCCTGGGCAAATGGAGATGAGCTGCTCACTCTAGTTTGACCCCATTCTTTCTGTGTTCTCACCAACTTTCAGTCTTTCATTTTGCAGATTGAGAGAATCAAG... | GCTAGAGTTCCTATCTCCCATTGAAGAAGGGGCTTCTTCAAGCAGACAGACCAAACATCATTTCAAAATGAGGACTGCATTTGAAATCTACTGAAGGGGGTGATACCGGGGGCCTGAAGCCTGGGGTTTGAGCTCACTTCTAGGGTGACCAATTCTTCTGTTTGCCTGGGACTGTGGGGTTTCCTACGACAGGATTTTCAGTGCTAAAACTGGAAAAGTCCTGGGCAAATGGAGATGAGCTGCTCACTCTAGTTTGACCCCATTCTTTCTGTGTTCTCACCAACTTTCAGTCTTTCATTTTGCAGATTGAGAGAATCAAG... |
Task1_train_45382 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CCTCCCAAAGTGCTAGGATTACAGGCATTATCCTGCATAACAACTTTGCATGTGCTGGTCACACTTCAGGGGCAGCTGCCCTCCCTGGCCTGGCTCTCTGTAGATCAGCTCAAGACCAATTTCACTTGATAAGAATCCAATACTCTCTAAGTGTAAAGAAGTCCCCATCTTTTTACTAGAAAGTTCTGAAGAATGTGATCCTGTTACGTGGACCTACCAGTTCATGAGCTAGAGCGTTGCAAAGGTATCCTTGTGTAGAAGGTAAAATGGAAATTTCTAAATGGGTGGCAAACCTTCTCCCTGGTGCTTCACCTTCAACT... | CCTCCCAAAGTGCTAGGATTACAGGCATTATCCTGCATAACAACTTTGCATGTGCTGGTCACACTTCAGGGGCAGCTGCCCTCCCTGGCCTGGCTCTCTGTAGATCAGCTCAAGACCAATTTCACTTGATAAGAATCCAATACTCTCTAAGTGTAAAGAAGTCCCCATCTTTTTACTAGAAAGTTCTGAAGAATGTGATCCTGTTACGTGGACCTACCAGTTCATGAGCTAGAGCGTTGCAAAGGTATCCTTGTGTAGAAGGTAAAATGGAAATTTCTAAATGGGTGGCAAACCTTCTCCCTGGTGCTTCACCTTCAACT... |
Task1_train_45383 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | CTTCCAGGGAAGACATTACAGAGGAGTTGACCTTGAGCTTGTGCTGAAGGACAGAAAGAAGTGCTTTAGGCAGAGATGGAAAGGAAAGGCATCGCACACAGAGGAACAGCATGTCCAAGGCACGGAGGTGGGCAGGAGGCTGGTTTAGTCGGGAATAGAGGATGACTCTATGGCTGGAGCACCGAACAGAGAAAGAGGCGAAGCTGACAAGGTGGTTCAAAGCCTCAAAGCCTGAGTTTTGTTCTTTGCTTTTTTTTTTTTTTAGAGACGAAGTTTTGCTGTTGTTGCCCAGGCTGGAGTGCAGTGGCGCAATCTTGGCT... | CTTCCAGGGAAGACATTACAGAGGAGTTGACCTTGAGCTTGTGCTGAAGGACAGAAAGAAGTGCTTTAGGCAGAGATGGAAAGGAAAGGCATCGCACACAGAGGAACAGCATGTCCAAGGCACGGAGGTGGGCAGGAGGCTGGTTTAGTCGGGAATAGAGGATGACTCTATGGCTGGAGCACCGAACAGAGAAAGAGGCGAAGCTGACAAGGTGGTTCAAAGCCTCAAAGCCTGAGTTTTGTTCTTTGCTTTTTTTTTTTTTTAGAGACGAAGTTTTGCTGTTGTTGCCCAGGCTGGAGTGCAGTGGCGCAATCTTGGCT... |
Task1_train_45384 | With a mutation on Chromosome 17, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GCCCTGTGGCCCCCAAGGGACCTGTGTCCAAGCAGGGAACTTCTCTGCAGCTATGGCAGAGTCAGCTTTAGAGTCTTCTCTCCTTCCAGAACCATTGAACTGCAAATACTCCTTAAAAACCCTGATCCAGCCCAGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAAGCAGGCAGATCACGAGGTCAGGAGATTGAGACCATCCTGGCCAACACGGTGAAACCCCGTCTCTACCAAAAATACAACAATTAGCTAGGTGTGGTGGTGAGAACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAG... | GCCCTGTGGCCCCCAAGGGACCTGTGTCCAAGCAGGGAACTTCTCTGCAGCTATGGCAGAGTCAGCTTTAGAGTCTTCTCTCCTTCCAGAACCATTGAACTGCAAATACTCCTTAAAAACCCTGATCCAGCCCAGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAAGCAGGCAGATCACGAGGTCAGGAGATTGAGACCATCCTGGCCAACACGGTGAAACCCCGTCTCTACCAAAAATACAACAATTAGCTAGGTGTGGTGGTGAGAACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAG... |
Task1_train_45385 | With a mutation on Chromosome 17, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CCTCAACCTCCCAGGCATAAGTGATCCTCCCACCTCAGCCTCCTCAGTAGCTGGGCCTACAGGTGTGTGCCACCATGCCCAGCTAATTTTTCGTTTTTTTGTAGAGACAGGGTCTTACTAAGTTGCCCAGGCTGGTCTCAAATTCCTGGGCTCAAATGATCCTTCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCAGTGGGCCCGTCCTGATTTTTGCTTTTACAAATAATTCACAACTGCCAGTTTTGTCAAGGAGATGTGTCCTTGTCTTTGTCTTTCAGCTTTGGAGATATGTGATTACAGGCTGA... | CCTCAACCTCCCAGGCATAAGTGATCCTCCCACCTCAGCCTCCTCAGTAGCTGGGCCTACAGGTGTGTGCCACCATGCCCAGCTAATTTTTCGTTTTTTTGTAGAGACAGGGTCTTACTAAGTTGCCCAGGCTGGTCTCAAATTCCTGGGCTCAAATGATCCTTCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCAGTGGGCCCGTCCTGATTTTTGCTTTTACAAATAATTCACAACTGCCAGTTTTGTCAAGGAGATGTGTCCTTGTCTTTGTCTTTCAGCTTTGGAGATATGTGATTACAGGCTGA... |
Task1_train_45386 | A change on Chromosome 17 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CGGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACGAGGTCAGGAGATCGAAACCATCCTATTCTTGGCTAATACGGCGAAACCTTGTCTCTACTAAAAATACAAAAAATTAGCCAGGTGTGGTGGCAGGCGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCGAGGTCGCGCCACTGCACTCCAGCCTGGGTGACAGAGCGAGACTCCATCTCAAAAAAAAAATAATAATAAATAAAAATACAAAAATCAGCTGG... | CGGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACGAGGTCAGGAGATCGAAACCATCCTATTCTTGGCTAATACGGCGAAACCTTGTCTCTACTAAAAATACAAAAAATTAGCCAGGTGTGGTGGCAGGCGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCGAGGTCGCGCCACTGCACTCCAGCCTGGGTGACAGAGCGAGACTCCATCTCAAAAAAAAAATAATAATAAATAAAAATACAAAAATCAGCTGG... |
Task1_train_45387 | A variant was discovered on Chromosome 17. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | AGGCTGAGGCAGGCAGATCACGAGGTCAGGAGATCAAGACCATCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGCATGGCAGCGCATGCCTGCAGTCCCAGCTACTCAGGAGGCTGAGGCAGAAGAATTGCTTCAACCCAGGAGGCAGAGACTGCAGTGAGCCAAGATGGAGCTACTGCACTCCAGCCTGGGCGACAGAGCAAGACTCTGCCTCAAAAAAAAAAAAAAAAGATTGGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGGATCACGAG... | AGGCTGAGGCAGGCAGATCACGAGGTCAGGAGATCAAGACCATCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGCATGGCAGCGCATGCCTGCAGTCCCAGCTACTCAGGAGGCTGAGGCAGAAGAATTGCTTCAACCCAGGAGGCAGAGACTGCAGTGAGCCAAGATGGAGCTACTGCACTCCAGCCTGGGCGACAGAGCAAGACTCTGCCTCAAAAAAAAAAAAAAAAGATTGGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGGATCACGAG... |
Task1_train_45388 | Chromosome 17 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CTGAGGCAGAAGAATTGCTTCAACCCAGGAGGCAGAGACTGCAGTGAGCCAAGATGGAGCTACTGCACTCCAGCCTGGGCGACAGAGCAAGACTCTGCCTCAAAAAAAAAAAAAAAAGATTGGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGGATCACGAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCATCTCTACTAAAAAAATACAAAAAAATTAGCCGGGCATGGTGATGGGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCAG... | CTGAGGCAGAAGAATTGCTTCAACCCAGGAGGCAGAGACTGCAGTGAGCCAAGATGGAGCTACTGCACTCCAGCCTGGGCGACAGAGCAAGACTCTGCCTCAAAAAAAAAAAAAAAAGATTGGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGGATCACGAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCATCTCTACTAAAAAAATACAAAAAAATTAGCCGGGCATGGTGATGGGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCAG... |
Task1_train_45389 | A genomic change on Chromosome 17 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GTAAATGTTTGTGGAATGAATGAATGAGTGAACTAATGAGTGTTTGGAGGGAGGAACCAAACACTTAGGAGGCCTGAGTCCCAGGCCCAATCCCTGGATCATCCTTGCCTGTACCTTGTCCTCACCAGGACGCCTCTCTCTGGGCCCAGAGAAGAGGGTCTCAAGGTAGGGGCTGGGAGCAGAGTGGGGAAGGGAGGAGTCACAGGGGAAGGGAAAGTGGACGCATGACTGACAGAGGACAGAGCTCGGACCTTGAAATCAGAAGGCCTGGTTCAAATCCCAGCTGCACGGCTCAGTTCAAATCCCAGCTATGTGACCTT... | GTAAATGTTTGTGGAATGAATGAATGAGTGAACTAATGAGTGTTTGGAGGGAGGAACCAAACACTTAGGAGGCCTGAGTCCCAGGCCCAATCCCTGGATCATCCTTGCCTGTACCTTGTCCTCACCAGGACGCCTCTCTCTGGGCCCAGAGAAGAGGGTCTCAAGGTAGGGGCTGGGAGCAGAGTGGGGAAGGGAGGAGTCACAGGGGAAGGGAAAGTGGACGCATGACTGACAGAGGACAGAGCTCGGACCTTGAAATCAGAAGGCCTGGTTCAAATCCCAGCTGCACGGCTCAGTTCAAATCCCAGCTATGTGACCTT... |
Task1_train_45390 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | GGGGCCTCGGGACATCCTGGGGACGTCCTGGTCCCACCGCCCTCAGCGGCCAGCGCAGACGCGCGGGGGGAGGGGCGGGACCGGCCGTGCCCACTGCTCCCTCTCCCAAGCTACGACTACCTGACGGACGAGGAGGAGCGGCACAGCGCCGAGAGCAGCACGAGCGAGGACAACTCGCCCGAGCACCCGTACCTCCCGCTCGTCACCGATGAGGACAGCTGGTACAGCAAGTGGCACAAGATGGAGCAGAAGTTCCGCATCGTCTACGCGCAGAAGGTGCGCGACGCCGGCGGGCCCGGGGGGCGGGCGGGCCGGGCGGG... | GGGGCCTCGGGACATCCTGGGGACGTCCTGGTCCCACCGCCCTCAGCGGCCAGCGCAGACGCGCGGGGGGAGGGGCGGGACCGGCCGTGCCCACTGCTCCCTCTCCCAAGCTACGACTACCTGACGGACGAGGAGGAGCGGCACAGCGCCGAGAGCAGCACGAGCGAGGACAACTCGCCCGAGCACCCGTACCTCCCGCTCGTCACCGATGAGGACAGCTGGTACAGCAAGTGGCACAAGATGGAGCAGAAGTTCCGCATCGTCTACGCGCAGAAGGTGCGCGACGCCGGCGGGCCCGGGGGGCGGGCGGGCCGGGCGGG... |
Task1_train_45391 | This is a variant located on Chromosome 17. Is this mutation a likely cause of disease or not? | Benign | GGGCAAGAGAGCTCAAATAAAAACCAGAGGACTGAGGGCAGCCTTGTATGTGGGGGGCTGGGGAAGGGCCCCGTCCTGAGGTCTGAAGGAAGTGGAGTCAGTGCCTGACCGAAGACCAAGGTCAGGCAGCACTAGCATGTGCCCTGTGGGGACAGGCAGGCCAGCACTCAGGGAGGGGGTAGCTTCTGTGTCCAAAATATTAGGTCTGCCTAGGGCAGGCCCAAGACATGCAACTGCCCCCCAACCCAACAGCCTTTAAGAACTTGCTCAAAACCAGGCTGAGGCGGCCGAGCACGCCAGGGGCAGGATGGAGGCACACC... | GGGCAAGAGAGCTCAAATAAAAACCAGAGGACTGAGGGCAGCCTTGTATGTGGGGGGCTGGGGAAGGGCCCCGTCCTGAGGTCTGAAGGAAGTGGAGTCAGTGCCTGACCGAAGACCAAGGTCAGGCAGCACTAGCATGTGCCCTGTGGGGACAGGCAGGCCAGCACTCAGGGAGGGGGTAGCTTCTGTGTCCAAAATATTAGGTCTGCCTAGGGCAGGCCCAAGACATGCAACTGCCCCCCAACCCAACAGCCTTTAAGAACTTGCTCAAAACCAGGCTGAGGCGGCCGAGCACGCCAGGGGCAGGATGGAGGCACACC... |
Task1_train_45392 | A mutation is present on Chromosome 17. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCCAGCCCCTACCACCCCCAATTCTAACCCTAACATGGGGGGGAGGTCCCCAAAGGGACCTCACCACCAGAATGTCTACTTGTGGTCCCTTACACTCTAGGTCCTCACCCCGACTCTCGCCAAACTGGAGAGGTCCTCTTCATAGGTGCCACTCTGGGCAGCCAAACCAGCACCAGGGTCCCTCCCAAGCCTCCCTCCCAGCCACCCCAGGCCCCAGAGGGACAGGCACCAGGCAGAAGTTCATCATCTTTAGACTTAAGGAATTAAC... | CCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCCAGCCCCTACCACCCCCAATTCTAACCCTAACATGGGGGGGAGGTCCCCAAAGGGACCTCACCACCAGAATGTCTACTTGTGGTCCCTTACACTCTAGGTCCTCACCCCGACTCTCGCCAAACTGGAGAGGTCCTCTTCATAGGTGCCACTCTGGGCAGCCAAACCAGCACCAGGGTCCCTCCCAAGCCTCCCTCCCAGCCACCCCAGGCCCCAGAGGGACAGGCACCAGGCAGAAGTTCATCATCTTTAGACTTAAGGAATTAAC... |
Task1_train_45393 | A variant found on Chromosome 17 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CACCGTGCCCAGCCCCTACCACCCCCAATTCTAACCCTAACATGGGGGGGAGGTCCCCAAAGGGACCTCACCACCAGAATGTCTACTTGTGGTCCCTTACACTCTAGGTCCTCACCCCGACTCTCGCCAAACTGGAGAGGTCCTCTTCATAGGTGCCACTCTGGGCAGCCAAACCAGCACCAGGGTCCCTCCCAAGCCTCCCTCCCAGCCACCCCAGGCCCCAGAGGGACAGGCACCAGGCAGAAGTTCATCATCTTTAGACTTAAGGAATTAACAAGGGTCAGGGAGACTACACCAGGCTGAGGGCTTCTTGGTTCCTG... | CACCGTGCCCAGCCCCTACCACCCCCAATTCTAACCCTAACATGGGGGGGAGGTCCCCAAAGGGACCTCACCACCAGAATGTCTACTTGTGGTCCCTTACACTCTAGGTCCTCACCCCGACTCTCGCCAAACTGGAGAGGTCCTCTTCATAGGTGCCACTCTGGGCAGCCAAACCAGCACCAGGGTCCCTCCCAAGCCTCCCTCCCAGCCACCCCAGGCCCCAGAGGGACAGGCACCAGGCAGAAGTTCATCATCTTTAGACTTAAGGAATTAACAAGGGTCAGGGAGACTACACCAGGCTGAGGGCTTCTTGGTTCCTG... |
Task1_train_45394 | A variant affecting Chromosome 17 has been observed. Determine if it's benign or associated with disease. | Benign | TTGCAGTGAGCCAAGATCATGCCATTGTACTCCAGCCTGGGCAACAGAGTGAGAATCCATCTCAAAAAAAAAAATTAATGAATTTTTAATTTAATTTACTTCAATTTAATATGTAGCTAGTGGCTACTGCATTAGACAGTTTAGGTCGTGTGTGTGTGTGTGTGTGTGTGTGTGTTGGGGTGGAGGGGACAGACATACAAACAATTCCAATACAATATGGTCACAGCTAACATTTATTAATCTTTAAGCTATGCTGGGCACTGTTCTAAGCAGGTTACCTATATTAACCCCTGCAATTAGGAAAATAGCCCCTGAGCTAG... | TTGCAGTGAGCCAAGATCATGCCATTGTACTCCAGCCTGGGCAACAGAGTGAGAATCCATCTCAAAAAAAAAAATTAATGAATTTTTAATTTAATTTACTTCAATTTAATATGTAGCTAGTGGCTACTGCATTAGACAGTTTAGGTCGTGTGTGTGTGTGTGTGTGTGTGTGTGTTGGGGTGGAGGGGACAGACATACAAACAATTCCAATACAATATGGTCACAGCTAACATTTATTAATCTTTAAGCTATGCTGGGCACTGTTCTAAGCAGGTTACCTATATTAACCCCTGCAATTAGGAAAATAGCCCCTGAGCTAG... |
Task1_train_45395 | A mutation found on Chromosome 17 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TGCCTCACTCAAGGGGAAGGGCAGGGCTAGGAAGAAGTGCATCTTGTCCTTGAGACCAGCCAGGAATTCCTGAAGGCAGGACTTACACCCTCTATACCCTCTATATCCTCTGAATCTTTTTGGTGGCAGGGGTGTCTAAAGGCCTCAGAATTTCAGGTGCTATCCTTTCCAGTGGTATGTGTCTGGAAGGGTTCCCAGGAGAATGACATTTTTGTGTTTGTTTTGCCTTTTTTGCTCTACTAGAGAAAGACATTCTATTTTTTTCTTTTTTTTTTGAGATGGAGGCTCGCTCTGTTGCCCAAGCTGGAGTGCAGTGGTGT... | TGCCTCACTCAAGGGGAAGGGCAGGGCTAGGAAGAAGTGCATCTTGTCCTTGAGACCAGCCAGGAATTCCTGAAGGCAGGACTTACACCCTCTATACCCTCTATATCCTCTGAATCTTTTTGGTGGCAGGGGTGTCTAAAGGCCTCAGAATTTCAGGTGCTATCCTTTCCAGTGGTATGTGTCTGGAAGGGTTCCCAGGAGAATGACATTTTTGTGTTTGTTTTGCCTTTTTTGCTCTACTAGAGAAAGACATTCTATTTTTTTCTTTTTTTTTTGAGATGGAGGCTCGCTCTGTTGCCCAAGCTGGAGTGCAGTGGTGT... |
Task1_train_45396 | Here is a mutation located on Chromosome 17. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TTAGGGATGGCTCCCAAATCTGTTACATTTAAGCGACAACTGCAAAATTGCTGTGGTGTCTAGGATGACCATATCGCATTTCACTTTTTTATCCAATATTAATATAGAGTCACAAAAATAGAATAGAGCATCAGGTTCATATGGTTTTCAAATTGCAAATGAGGAAGCTGAGCAGGTGTTGATGGAATAATGTATAATAAGACAAGACTTGCTTTCAGGAGCAGCTATGATACCAAGCATGTCTGTGACATCATAGATGACAGATTTATATCTTGGTCACCTAAAATGAAAACCATGTGTTGTGGAGAAATAAGAGGTAA... | TTAGGGATGGCTCCCAAATCTGTTACATTTAAGCGACAACTGCAAAATTGCTGTGGTGTCTAGGATGACCATATCGCATTTCACTTTTTTATCCAATATTAATATAGAGTCACAAAAATAGAATAGAGCATCAGGTTCATATGGTTTTCAAATTGCAAATGAGGAAGCTGAGCAGGTGTTGATGGAATAATGTATAATAAGACAAGACTTGCTTTCAGGAGCAGCTATGATACCAAGCATGTCTGTGACATCATAGATGACAGATTTATATCTTGGTCACCTAAAATGAAAACCATGTGTTGTGGAGAAATAAGAGGTAA... |
Task1_train_45397 | A mutation found on Chromosome 17 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TCCTGGTACCCTCCAAAGAGAATGAAGCAGAGGTCAGAAAACTCAAGTGGTCCTACTCACGGAACAAGGGAAACAACAGCAAAGGTGCCAAGGGGCAAACCCTTACAATGAAATCAGGACGTCTGGATGGGTGGAGGTGGCAGCCAACTGAGTACATGGGATATGAGGAACCTGGAGCACCAACACCAAAGTGGGAAGGGTCAGAAGAACACCTTGGGGTCCCCCAGGGCTTCCTTCCTTATGGCCCTGGTAGAGTAGGAAAACAGCTGTACCAGGAGGTGGGAGCCAGCAGTGTGGCTCAAGGGCCCAGGGCGGAGCAA... | TCCTGGTACCCTCCAAAGAGAATGAAGCAGAGGTCAGAAAACTCAAGTGGTCCTACTCACGGAACAAGGGAAACAACAGCAAAGGTGCCAAGGGGCAAACCCTTACAATGAAATCAGGACGTCTGGATGGGTGGAGGTGGCAGCCAACTGAGTACATGGGATATGAGGAACCTGGAGCACCAACACCAAAGTGGGAAGGGTCAGAAGAACACCTTGGGGTCCCCCAGGGCTTCCTTCCTTATGGCCCTGGTAGAGTAGGAAAACAGCTGTACCAGGAGGTGGGAGCCAGCAGTGTGGCTCAAGGGCCCAGGGCGGAGCAA... |
Task1_train_45398 | A mutation has occurred on Chromosome 17. What is the medical relevance of this mutation? | Benign | TGACTTACTCTTGAAGACCAGAGCTATGTCTCCATTCATGAGTAGGAAAATTCCAGTATAAATGAGAATCTCAAATCATGGCGTGGATTCCTTGGGGCCCTCCCTGTTTCATCCCCAGTTTCCTCATCTGAAAATGAGGCCGCCAAGGACCACAGCTTTCCCAGTGCTCAGACAGTAGTGAGATGAAGACAGTAAGATGAAGAGCTACAGGCTCCCCTCCCTGTCACTGTTGCAGAACAGCTGGAAGAGCTCCTGACTCCCTTTCCTTCCTTTGTGGTCCAGGAGAAAGCCCCCCTCCAGCCCGAGACGTCTGCTGACTT... | TGACTTACTCTTGAAGACCAGAGCTATGTCTCCATTCATGAGTAGGAAAATTCCAGTATAAATGAGAATCTCAAATCATGGCGTGGATTCCTTGGGGCCCTCCCTGTTTCATCCCCAGTTTCCTCATCTGAAAATGAGGCCGCCAAGGACCACAGCTTTCCCAGTGCTCAGACAGTAGTGAGATGAAGACAGTAAGATGAAGAGCTACAGGCTCCCCTCCCTGTCACTGTTGCAGAACAGCTGGAAGAGCTCCTGACTCCCTTTCCTTCCTTTGTGGTCCAGGAGAAAGCCCCCCTCCAGCCCGAGACGTCTGCTGACTT... |
Task1_train_45399 | A mutation on Chromosome 17 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CTTTCCCAGTGCTCAGACAGTAGTGAGATGAAGACAGTAAGATGAAGAGCTACAGGCTCCCCTCCCTGTCACTGTTGCAGAACAGCTGGAAGAGCTCCTGACTCCCTTTCCTTCCTTTGTGGTCCAGGAGAAAGCCCCCCTCCAGCCCGAGACGTCTGCTGACTTCTATCGTGATTGGCGACGACACTTGCCAAGTGGGCCAGAGCGCTACCAGGCTCTACTGCAGCTTGGGGGTCCAAGGCTCGGCTGCCTCTTCCAGACAGATGTGGGATTTGGACTTCTTGGGGAGCTGCTGGTGGCACTGGCTGATCACGTGGGGC... | CTTTCCCAGTGCTCAGACAGTAGTGAGATGAAGACAGTAAGATGAAGAGCTACAGGCTCCCCTCCCTGTCACTGTTGCAGAACAGCTGGAAGAGCTCCTGACTCCCTTTCCTTCCTTTGTGGTCCAGGAGAAAGCCCCCCTCCAGCCCGAGACGTCTGCTGACTTCTATCGTGATTGGCGACGACACTTGCCAAGTGGGCCAGAGCGCTACCAGGCTCTACTGCAGCTTGGGGGTCCAAGGCTCGGCTGCCTCTTCCAGACAGATGTGGGATTTGGACTTCTTGGGGAGCTGCTGGTGGCACTGGCTGATCACGTGGGGC... |
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