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_47600 | A variant was discovered on Chromosome 19. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TGGTTACCGTTTCGTTAGGGCTGGACACGTGGCCCACCCCCTGCACCGTCCGTTTTCCGCCCACTTGGGCCCAGCCGTCCAATCGACACTCATCATGCTCTGCCTCGCCGCTCTCTCCGGCCAATCCGCATGTGCCACTGCCTCTGCCCGCAATCGGCGCTCACCAACTCACCCCGCCCCCTGCCTCTCAACCAATCCGCATATGCAGCTGCTTTGCTCCCGCCCCAGGGGGGGCGGTGCCGGCAAGGCTGTCAGTCTCAAGAAAATGATTAGCTCGCAAAGGCGCCGTGGGGGCGGGGCAGCAGGTCGTTCTGCCAATG... | TGGTTACCGTTTCGTTAGGGCTGGACACGTGGCCCACCCCCTGCACCGTCCGTTTTCCGCCCACTTGGGCCCAGCCGTCCAATCGACACTCATCATGCTCTGCCTCGCCGCTCTCTCCGGCCAATCCGCATGTGCCACTGCCTCTGCCCGCAATCGGCGCTCACCAACTCACCCCGCCCCCTGCCTCTCAACCAATCCGCATATGCAGCTGCTTTGCTCCCGCCCCAGGGGGGGCGGTGCCGGCAAGGCTGTCAGTCTCAAGAAAATGATTAGCTCGCAAAGGCGCCGTGGGGGCGGGGCAGCAGGTCGTTCTGCCAATG... |
Task1_train_47601 | Chromosome 19 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | AGGACAGGGTTGCCTGCCAAGAACAGGAGGGGAGAGGAGGGGCTGGAGGTTTCAGGAGAAAGAAGCATGTCAGGTAGTCACCTGGGGAGTGCATGGGCCAGAGACATGTAGTGTGAGCCAGGGAGGGTGATGGTGAGGGGGCCGCAGATTTTGTGGGCTTGAAGGGAAAGTGAGACTGAGGCCAGGCAAGGGGGTGCCTGTCATGGCCACCTGCAGCGTTTGTGCAGGGTCGGGCAGGAGTGAGGATGTGGGTTGGCTGGAGGTGAAAGGGCGCGCTGGATGGTAGATGGGCTGGAGTCTAAGGATTTGGGGAGTTGGAG... | AGGACAGGGTTGCCTGCCAAGAACAGGAGGGGAGAGGAGGGGCTGGAGGTTTCAGGAGAAAGAAGCATGTCAGGTAGTCACCTGGGGAGTGCATGGGCCAGAGACATGTAGTGTGAGCCAGGGAGGGTGATGGTGAGGGGGCCGCAGATTTTGTGGGCTTGAAGGGAAAGTGAGACTGAGGCCAGGCAAGGGGGTGCCTGTCATGGCCACCTGCAGCGTTTGTGCAGGGTCGGGCAGGAGTGAGGATGTGGGTTGGCTGGAGGTGAAAGGGCGCGCTGGATGGTAGATGGGCTGGAGTCTAAGGATTTGGGGAGTTGGAG... |
Task1_train_47602 | This mutation is located on Chromosome 19. Is it associated with a disease or is it a benign polymorphism? | Benign | CTTTCAAAGGCTCCTCGGCCCTGCTCTACCACCAGCGAGGCCACACGGGCGAGCGGCCCTACCAGTGCCCCGACTGTCCCAAGGCCTTCAAGCGCTCCTCTCTGCTGCAGATCCACCGTAGCGTGCACACCGGCCTGCGGGCCTTCATCTGCGGCCAGTGCGGCCTGGCCTTCAAGTGGTCGTCCCACTACCAGTACCACTTAAGGCAGCACACAGGCGAGCGCCCCTACCCGTGCCCGGACTGCCCCAAGGCCTTCAAGAACTCGTCCAGCCTGCGGCGCCACCGCCACGTGCACACCGGCGAGCGGCCCTACACCTGT... | CTTTCAAAGGCTCCTCGGCCCTGCTCTACCACCAGCGAGGCCACACGGGCGAGCGGCCCTACCAGTGCCCCGACTGTCCCAAGGCCTTCAAGCGCTCCTCTCTGCTGCAGATCCACCGTAGCGTGCACACCGGCCTGCGGGCCTTCATCTGCGGCCAGTGCGGCCTGGCCTTCAAGTGGTCGTCCCACTACCAGTACCACTTAAGGCAGCACACAGGCGAGCGCCCCTACCCGTGCCCGGACTGCCCCAAGGCCTTCAAGAACTCGTCCAGCCTGCGGCGCCACCGCCACGTGCACACCGGCGAGCGGCCCTACACCTGT... |
Task1_train_47603 | A change on Chromosome 19 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GCTGAGCGTGGCCGGCTCCTCCCGCGAAGGCCCCGGCACGGATGAGAATCCACGCGCTGGCGTCGCCGCCCGGCGCTCAGGTTGCTCAGCAACGAGGGAACGTGGGGCGGGAGCTCGCGCTGGTCCCCAGCCCGCCGCCCGTCTCCTGCCGGCTTCCGCTCCCGTTCTTCCCCAGGTCCCCTTTCCCCGTTGCTCCTTCTCTAGGGATAGGAGAGGTCGCTTCCCGGCCCTCCGCAGGGTCACAGCTCGGTTCCTCCCAGCCCGCCCTCCGGGGAGCTTAGCAACGGTTGCTACGGCCCGGAGCGGGCGCCGCCCCGCCC... | GCTGAGCGTGGCCGGCTCCTCCCGCGAAGGCCCCGGCACGGATGAGAATCCACGCGCTGGCGTCGCCGCCCGGCGCTCAGGTTGCTCAGCAACGAGGGAACGTGGGGCGGGAGCTCGCGCTGGTCCCCAGCCCGCCGCCCGTCTCCTGCCGGCTTCCGCTCCCGTTCTTCCCCAGGTCCCCTTTCCCCGTTGCTCCTTCTCTAGGGATAGGAGAGGTCGCTTCCCGGCCCTCCGCAGGGTCACAGCTCGGTTCCTCCCAGCCCGCCCTCCGGGGAGCTTAGCAACGGTTGCTACGGCCCGGAGCGGGCGCCGCCCCGCCC... |
Task1_train_47604 | Consider a variant on Chromosome 19. Determine its clinical classification and disease relevance. | Benign | TAACTTTGGTTAACTGTGGATCTTTTGGATTAATTTTGATTGTTTAAAAATATTGCATAAAAACGCTTGAGCCCAGGAGTTCGAGGTTACAGTGAGCTATGATCTTGCCACCGCACTCCAGCTTGGGCGACACAGCCAGACTTTATCTTAAAAAATAAAAAAATCCATAAAAGTATTTATTTTGATTACTAACATTACCCTTCGGAGCCCTCTTTGGTCTCCCTGCCTCCCCTGGCTCCGCACATCTCCCAGTCCCCCGCTGGCTCAGAATCCTCCCGTATGCTGCACGCTTCTGAGCACTCCCGCCCCCTCCCGCACCC... | TAACTTTGGTTAACTGTGGATCTTTTGGATTAATTTTGATTGTTTAAAAATATTGCATAAAAACGCTTGAGCCCAGGAGTTCGAGGTTACAGTGAGCTATGATCTTGCCACCGCACTCCAGCTTGGGCGACACAGCCAGACTTTATCTTAAAAAATAAAAAAATCCATAAAAGTATTTATTTTGATTACTAACATTACCCTTCGGAGCCCTCTTTGGTCTCCCTGCCTCCCCTGGCTCCGCACATCTCCCAGTCCCCCGCTGGCTCAGAATCCTCCCGTATGCTGCACGCTTCTGAGCACTCCCGCCCCCTCCCGCACCC... |
Task1_train_47605 | A mutation has occurred on Chromosome 19. What is the medical relevance of this mutation? | Benign | CTGGATCTCTGCATCCGTGGCTCTTCCTGAGGTGTGCTGTTGTGTGGCTGTGTTATTGCCCTCTGTGTTATTACTGAATTGTGTATCCCCAAAACTCGTATGTGGGAGTCCTAACCCCCCCAGTGCTGAATGTGGCTGTATTTGGAGATGGGGTCTTTAAAGAGGTAAAATGAGGTCACTAGAGTGGGCAGGCCCTCATCCAATGTGACTGGTGTCCTTATAAGAAGAGGAGATCAGGACACAGACACACACAGAGGGACGACCATGTGAGGACACAGGGAGAAGACGGCCAAATGCAAGCCAAGGAGAGAGGCCTCAGG... | CTGGATCTCTGCATCCGTGGCTCTTCCTGAGGTGTGCTGTTGTGTGGCTGTGTTATTGCCCTCTGTGTTATTACTGAATTGTGTATCCCCAAAACTCGTATGTGGGAGTCCTAACCCCCCCAGTGCTGAATGTGGCTGTATTTGGAGATGGGGTCTTTAAAGAGGTAAAATGAGGTCACTAGAGTGGGCAGGCCCTCATCCAATGTGACTGGTGTCCTTATAAGAAGAGGAGATCAGGACACAGACACACACAGAGGGACGACCATGTGAGGACACAGGGAGAAGACGGCCAAATGCAAGCCAAGGAGAGAGGCCTCAGG... |
Task1_train_47606 | Mutation context: Chromosome 19. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | ATCCATCCACCCATCCATCCACCCACCAATCCTTCCTTCTATCGATCCATCCATCCATCCATCCATCCGTCCATCCACCCACCAATCCTTCCTTCCATCCATCCATCCACCCACCAATCCTTTCATCCATCCATCCACCCCTCCATCTACCCACCCACCCATCCATCCACCCACCCATCCATCCATCCATCCACCCATCCATCCATCCACCCACGGATCCTTCCATCCACCCACCCACCCGTCCACTCAACCAATCCTTTCATCCACCCACCCACCCACCCATCCACTCATCCATCCATCCACTCACCCACCAAACCTTT... | ATCCATCCACCCATCCATCCACCCACCAATCCTTCCTTCTATCGATCCATCCATCCATCCATCCATCCGTCCATCCACCCACCAATCCTTCCTTCCATCCATCCATCCACCCACCAATCCTTTCATCCATCCATCCACCCCTCCATCTACCCACCCACCCATCCATCCACCCACCCATCCATCCATCCATCCACCCATCCATCCATCCACCCACGGATCCTTCCATCCACCCACCCACCCGTCCACTCAACCAATCCTTTCATCCACCCACCCACCCACCCATCCACTCATCCATCCATCCACTCACCCACCAAACCTTT... |
Task1_train_47607 | This sequence variant lies on Chromosome 19. Is it clinically significant, and what condition might it cause if any? | Benign | TTCGAGACCAGCCTGGCCAATGTGGTGAAACCCGTCTCTACTAAAAATACAAAAAATTAGTTGGTTGTGGTAGCAGGCTCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCCCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCAAGGTCGTGCCATTGTACTCCAGCCTGGGCGACAAGAGTGAAACTCTCTCTCTCTCTCAAAAAAAAAAAAAGAGTGAAGAGTGTGACTGAGGAACCGAACTTTTACATTTATTTCATCTTAATGTCTTTACATTTCCATATTCTAAATTTAAACGGAAATAGCCAC... | TTCGAGACCAGCCTGGCCAATGTGGTGAAACCCGTCTCTACTAAAAATACAAAAAATTAGTTGGTTGTGGTAGCAGGCTCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCCCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCAAGGTCGTGCCATTGTACTCCAGCCTGGGCGACAAGAGTGAAACTCTCTCTCTCTCTCAAAAAAAAAAAAAGAGTGAAGAGTGTGACTGAGGAACCGAACTTTTACATTTATTTCATCTTAATGTCTTTACATTTCCATATTCTAAATTTAAACGGAAATAGCCAC... |
Task1_train_47608 | This variant is present on Chromosome 19. Is the change likely to result in a pathogenic outcome? | Benign | GGTCTGGTATAGGGTCCAAGGCAGCATCTAAGAGGCGGGGCCTCTGCTCAGACACGCCTCTAATGAGGCAGTTTGGTTTCCAAGGGGTGTGTCCTATAAGATTGGTGACTTCTAAAGGGCGTGTCTAGTTTCTAGGGGGCGTGTCCGTCTGTTGGAGGTGGATCATGTATTTAAGGGACGGAACTCATTTTGATTGATACTGACTCTAATTGTATTTATTTATGAAACAGAGTCTCGCTCTGTTGCTCAGGCTGGAGTGCAGTGGTGCAATATCGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGAGATCCTCCTGCC... | GGTCTGGTATAGGGTCCAAGGCAGCATCTAAGAGGCGGGGCCTCTGCTCAGACACGCCTCTAATGAGGCAGTTTGGTTTCCAAGGGGTGTGTCCTATAAGATTGGTGACTTCTAAAGGGCGTGTCTAGTTTCTAGGGGGCGTGTCCGTCTGTTGGAGGTGGATCATGTATTTAAGGGACGGAACTCATTTTGATTGATACTGACTCTAATTGTATTTATTTATGAAACAGAGTCTCGCTCTGTTGCTCAGGCTGGAGTGCAGTGGTGCAATATCGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGAGATCCTCCTGCC... |
Task1_train_47609 | This variant is located on Chromosome 19. Evaluate its biological effect and specify any disease association. | Benign | AGCAGCGGTAGGGCCGCTCCCCGGTGTGCGAGCGCAGGTGGTTGGCTAGGTTGAAGCTGTGCTTGAAACCCTTGCCGCAGCGCGGACATGCGTGGGGCTTGAGCGCTGTGTGCCGGGCAAAGTGGCGCCGCAGGTCTGAGCGGTAGCGGAAGCTCTTGCCACATTCACTGCAGTGAAACGGGACCCTGGGGGCGGCAGCGGCGGGCGGTGCTGGTGCAGGGGTTGGGGCGGGGACGTCATCCATGGTGGCGGGGAATACAGTGGTATGTGGGGGCTCTCTCTGGAGTAGTGGGGAGACAGAGGAGCAGGTGAGGGGGTCG... | AGCAGCGGTAGGGCCGCTCCCCGGTGTGCGAGCGCAGGTGGTTGGCTAGGTTGAAGCTGTGCTTGAAACCCTTGCCGCAGCGCGGACATGCGTGGGGCTTGAGCGCTGTGTGCCGGGCAAAGTGGCGCCGCAGGTCTGAGCGGTAGCGGAAGCTCTTGCCACATTCACTGCAGTGAAACGGGACCCTGGGGGCGGCAGCGGCGGGCGGTGCTGGTGCAGGGGTTGGGGCGGGGACGTCATCCATGGTGGCGGGGAATACAGTGGTATGTGGGGGCTCTCTCTGGAGTAGTGGGGAGACAGAGGAGCAGGTGAGGGGGTCG... |
Task1_train_47610 | This is a variant located on Chromosome 19. Is this mutation a likely cause of disease or not? | Benign | GAAGCTCTTGCCACATTCACTGCAGTGAAACGGGACCCTGGGGGCGGCAGCGGCGGGCGGTGCTGGTGCAGGGGTTGGGGCGGGGACGTCATCCATGGTGGCGGGGAATACAGTGGTATGTGGGGGCTCTCTCTGGAGTAGTGGGGAGACAGAGGAGCAGGTGAGGGGGTCGGCTCCCCATCAGCTCTCTCCTCCCAGGTTCCCAGACCCACCACCTGTCCCCTGGGAGACCCTCCCACTGCCCACCTCTCTAAGCCACTCTCATTGTTCTTTAAAATCCTCCTACTCTCTTAGAAACCCTTCTCTCGCGGCTCCACGCC... | GAAGCTCTTGCCACATTCACTGCAGTGAAACGGGACCCTGGGGGCGGCAGCGGCGGGCGGTGCTGGTGCAGGGGTTGGGGCGGGGACGTCATCCATGGTGGCGGGGAATACAGTGGTATGTGGGGGCTCTCTCTGGAGTAGTGGGGAGACAGAGGAGCAGGTGAGGGGGTCGGCTCCCCATCAGCTCTCTCCTCCCAGGTTCCCAGACCCACCACCTGTCCCCTGGGAGACCCTCCCACTGCCCACCTCTCTAAGCCACTCTCATTGTTCTTTAAAATCCTCCTACTCTCTTAGAAACCCTTCTCTCGCGGCTCCACGCC... |
Task1_train_47611 | This alteration occurs on Chromosome 19. Is it associated with a disease or is it a benign variant? | Benign | CACTGCCCACCTCTCTAAGCCACTCTCATTGTTCTTTAAAATCCTCCTACTCTCTTAGAAACCCTTCTCTCGCGGCTCCACGCCTGTGGCAAAATCTTCCTAATCACTTCATAGTCTCCTCACTCCACGGAGTGTTTTTAAGCCTCTCCTCGCTCTTCGCCAATGCGCGGCCACTGCTCTCTGTGCCCCTCCCACTGTAATTTAAGCCTCTCCCACTCTTCCTTAAGTCCCACCTACTCCCTTCAAAGTCCCCCACAATGTTCCCTAAGGATCTTGTATTCTTTGCCAAGCCCTTTTCCTTCCAAAAGGCCCTCCCACTC... | CACTGCCCACCTCTCTAAGCCACTCTCATTGTTCTTTAAAATCCTCCTACTCTCTTAGAAACCCTTCTCTCGCGGCTCCACGCCTGTGGCAAAATCTTCCTAATCACTTCATAGTCTCCTCACTCCACGGAGTGTTTTTAAGCCTCTCCTCGCTCTTCGCCAATGCGCGGCCACTGCTCTCTGTGCCCCTCCCACTGTAATTTAAGCCTCTCCCACTCTTCCTTAAGTCCCACCTACTCCCTTCAAAGTCCCCCACAATGTTCCCTAAGGATCTTGTATTCTTTGCCAAGCCCTTTTCCTTCCAAAAGGCCCTCCCACTC... |
Task1_train_47612 | This is a variant located on Chromosome 19. Is this mutation a likely cause of disease or not? | Benign | GGAGGAGGCCAGGTGTGGTGGCTCAACCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGGATCACCTGAGGTCAGGAGTTGGAGACCAGGTGGCTAATATGGTGAAACCTGTCTCTACCAAAAATATAAAATTGTTATATTTTATATAATACAGCTGGGCGTGGTAGTGCATACCTGTAATCTCAGCTATTTGGGAGGTGGAAACAGGAGAATCACCTGAGCCCGGGAGTTGGAGGTTGCAGTGAGCCTAGAATTGCGCCACTGCACTTTAGCCTGGGCAACAGAGCAAGACTCCATCTCCAAAAAAAAAAAAAA... | GGAGGAGGCCAGGTGTGGTGGCTCAACCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGGATCACCTGAGGTCAGGAGTTGGAGACCAGGTGGCTAATATGGTGAAACCTGTCTCTACCAAAAATATAAAATTGTTATATTTTATATAATACAGCTGGGCGTGGTAGTGCATACCTGTAATCTCAGCTATTTGGGAGGTGGAAACAGGAGAATCACCTGAGCCCGGGAGTTGGAGGTTGCAGTGAGCCTAGAATTGCGCCACTGCACTTTAGCCTGGGCAACAGAGCAAGACTCCATCTCCAAAAAAAAAAAAAA... |
Task1_train_47613 | Chromosome 19 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TTTTTTTTTTTTTCCGCTATGCAGAAGATTCAGTTTTACCTGGTACGACTTATTTGTATTTTGTGTCTTGTCCTTTTGGTGTGCTATCAGGGTTTTCACCACATGCAGTTTGCACAGTTGGGGAAGTAGAAGGTCTTCAAATGGACTCCAGCACTGTCCAATAGAATCTTAAGATAACCCATATATGTAATTGTAAATTCATTTTCTGGTAGTCACATAAAATAGAACAAAACAAGCCTAATGAATTTTAACTCAGAATATAATCATTTAAGATGTGAGCAACTTGAAACCTTCTCAAGCAGATAGTTTACATTCTCTTT... | TTTTTTTTTTTTTCCGCTATGCAGAAGATTCAGTTTTACCTGGTACGACTTATTTGTATTTTGTGTCTTGTCCTTTTGGTGTGCTATCAGGGTTTTCACCACATGCAGTTTGCACAGTTGGGGAAGTAGAAGGTCTTCAAATGGACTCCAGCACTGTCCAATAGAATCTTAAGATAACCCATATATGTAATTGTAAATTCATTTTCTGGTAGTCACATAAAATAGAACAAAACAAGCCTAATGAATTTTAACTCAGAATATAATCATTTAAGATGTGAGCAACTTGAAACCTTCTCAAGCAGATAGTTTACATTCTCTTT... |
Task1_train_47614 | This variant lies on Chromosome 19. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TTTTTTTTTCCGCTATGCAGAAGATTCAGTTTTACCTGGTACGACTTATTTGTATTTTGTGTCTTGTCCTTTTGGTGTGCTATCAGGGTTTTCACCACATGCAGTTTGCACAGTTGGGGAAGTAGAAGGTCTTCAAATGGACTCCAGCACTGTCCAATAGAATCTTAAGATAACCCATATATGTAATTGTAAATTCATTTTCTGGTAGTCACATAAAATAGAACAAAACAAGCCTAATGAATTTTAACTCAGAATATAATCATTTAAGATGTGAGCAACTTGAAACCTTCTCAAGCAGATAGTTTACATTCTCTTTTCCC... | TTTTTTTTTCCGCTATGCAGAAGATTCAGTTTTACCTGGTACGACTTATTTGTATTTTGTGTCTTGTCCTTTTGGTGTGCTATCAGGGTTTTCACCACATGCAGTTTGCACAGTTGGGGAAGTAGAAGGTCTTCAAATGGACTCCAGCACTGTCCAATAGAATCTTAAGATAACCCATATATGTAATTGTAAATTCATTTTCTGGTAGTCACATAAAATAGAACAAAACAAGCCTAATGAATTTTAACTCAGAATATAATCATTTAAGATGTGAGCAACTTGAAACCTTCTCAAGCAGATAGTTTACATTCTCTTTTCCC... |
Task1_train_47615 | Given this context: Chromosome 19 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AGAAGATTCAGTTTTACCTGGTACGACTTATTTGTATTTTGTGTCTTGTCCTTTTGGTGTGCTATCAGGGTTTTCACCACATGCAGTTTGCACAGTTGGGGAAGTAGAAGGTCTTCAAATGGACTCCAGCACTGTCCAATAGAATCTTAAGATAACCCATATATGTAATTGTAAATTCATTTTCTGGTAGTCACATAAAATAGAACAAAACAAGCCTAATGAATTTTAACTCAGAATATAATCATTTAAGATGTGAGCAACTTGAAACCTTCTCAAGCAGATAGTTTACATTCTCTTTTCCCCATTACGTCTTCACAAAG... | AGAAGATTCAGTTTTACCTGGTACGACTTATTTGTATTTTGTGTCTTGTCCTTTTGGTGTGCTATCAGGGTTTTCACCACATGCAGTTTGCACAGTTGGGGAAGTAGAAGGTCTTCAAATGGACTCCAGCACTGTCCAATAGAATCTTAAGATAACCCATATATGTAATTGTAAATTCATTTTCTGGTAGTCACATAAAATAGAACAAAACAAGCCTAATGAATTTTAACTCAGAATATAATCATTTAAGATGTGAGCAACTTGAAACCTTCTCAAGCAGATAGTTTACATTCTCTTTTCCCCATTACGTCTTCACAAAG... |
Task1_train_47616 | A variant on Chromosome 19 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TTCAGTTTTACCTGGTACGACTTATTTGTATTTTGTGTCTTGTCCTTTTGGTGTGCTATCAGGGTTTTCACCACATGCAGTTTGCACAGTTGGGGAAGTAGAAGGTCTTCAAATGGACTCCAGCACTGTCCAATAGAATCTTAAGATAACCCATATATGTAATTGTAAATTCATTTTCTGGTAGTCACATAAAATAGAACAAAACAAGCCTAATGAATTTTAACTCAGAATATAATCATTTAAGATGTGAGCAACTTGAAACCTTCTCAAGCAGATAGTTTACATTCTCTTTTCCCCATTACGTCTTCACAAAGAGGAGT... | TTCAGTTTTACCTGGTACGACTTATTTGTATTTTGTGTCTTGTCCTTTTGGTGTGCTATCAGGGTTTTCACCACATGCAGTTTGCACAGTTGGGGAAGTAGAAGGTCTTCAAATGGACTCCAGCACTGTCCAATAGAATCTTAAGATAACCCATATATGTAATTGTAAATTCATTTTCTGGTAGTCACATAAAATAGAACAAAACAAGCCTAATGAATTTTAACTCAGAATATAATCATTTAAGATGTGAGCAACTTGAAACCTTCTCAAGCAGATAGTTTACATTCTCTTTTCCCCATTACGTCTTCACAAAGAGGAGT... |
Task1_train_47617 | A variant on Chromosome 19 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | ACTGAATATTTTAGTGCCATTTCCTATAGAGCTATTATAAACTCAGATAAATACTAATTTTCCCAGTGACTGTTTAGGCAAGTACAGCTGCTTTTCACCTGATTCTAACGCATTCTGTAGGAAAGAAACTGTTAGACTCCTACCCTGACCCATTTTTGCTTTCTTCCTTAGGATAAACCCACTTGTTACTATTTCTTCCTGATTCCAAGAGACTACTTTCCCAGTCCCCCTTTGTAGTTATATGAAGCCGTATGAAGACAAGGTAAACAGGCCAATGAGATGCAAGCAGAAGTGATACAAGAAAGAGTTTTGAAAAGACT... | ACTGAATATTTTAGTGCCATTTCCTATAGAGCTATTATAAACTCAGATAAATACTAATTTTCCCAGTGACTGTTTAGGCAAGTACAGCTGCTTTTCACCTGATTCTAACGCATTCTGTAGGAAAGAAACTGTTAGACTCCTACCCTGACCCATTTTTGCTTTCTTCCTTAGGATAAACCCACTTGTTACTATTTCTTCCTGATTCCAAGAGACTACTTTCCCAGTCCCCCTTTGTAGTTATATGAAGCCGTATGAAGACAAGGTAAACAGGCCAATGAGATGCAAGCAGAAGTGATACAAGAAAGAGTTTTGAAAAGACT... |
Task1_train_47618 | A genetic alteration is present on Chromosome 19. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GAGTTTTCGGCCTGGCTGAAGGATCAGCCTCTAGGCTGGTGCTCCAGAGATGACTGTAAGAACTATAGTATCAGGGAGCTGCTGCCTCTCCTGCAAAGAGGAAAGTGGGAGATGGGAAGCTCACTGTTAGAACTGTGGCTTTAGAAATACACCACGACAGCTATGATTCAGAAATCGGGAAGCTCACCAGTGTAGCAGCTGCTTAAAATCAATGACCACAGCAACTGGTTTTAGTTTTCGAGACAGTCTCGCTCTATTGCCAGGGCTAGATTACAGTGGTGCAATCTCTGCTCACTGCAACCTCCACCTCCCAGGTTCAA... | GAGTTTTCGGCCTGGCTGAAGGATCAGCCTCTAGGCTGGTGCTCCAGAGATGACTGTAAGAACTATAGTATCAGGGAGCTGCTGCCTCTCCTGCAAAGAGGAAAGTGGGAGATGGGAAGCTCACTGTTAGAACTGTGGCTTTAGAAATACACCACGACAGCTATGATTCAGAAATCGGGAAGCTCACCAGTGTAGCAGCTGCTTAAAATCAATGACCACAGCAACTGGTTTTAGTTTTCGAGACAGTCTCGCTCTATTGCCAGGGCTAGATTACAGTGGTGCAATCTCTGCTCACTGCAACCTCCACCTCCCAGGTTCAA... |
Task1_train_47619 | The following genetic variant occurs on Chromosome 19. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | AGATCTTGGCTCACTGCAAGCTCCGCCTCCCAGGTTCACGCCATTCTCCTGCCTCGGCCTCCCGAATAGCTGGGACTAGAGGGGCCCGCCACCACACCCAGCTAATTTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCAGGATGGTCTCGATCTCCTGACCTCGTGATCTGCCCACCTCGGCCTCTCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCCGGCCAAATCATATACATTTTAACTTACAGCTCATGCCTATAACCCCAACACTTTGAGAAGCTGAGCAGGAGGATGCTTGAAGCCAGG... | AGATCTTGGCTCACTGCAAGCTCCGCCTCCCAGGTTCACGCCATTCTCCTGCCTCGGCCTCCCGAATAGCTGGGACTAGAGGGGCCCGCCACCACACCCAGCTAATTTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCAGGATGGTCTCGATCTCCTGACCTCGTGATCTGCCCACCTCGGCCTCTCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCCGGCCAAATCATATACATTTTAACTTACAGCTCATGCCTATAACCCCAACACTTTGAGAAGCTGAGCAGGAGGATGCTTGAAGCCAGG... |
Task1_train_47620 | Here is a genetic alteration on Chromosome 19. Based on the data, is it a benign variant or a cause of disease? | Benign | TTGTTTTAATTCTTCAATAATTTCAATCTGCCACTAGTTGAATCTGTGGATATGGAGGACTGACGGTGCCTATCCACATGAATGACAAAGGCTGTCGTGCTTTGGTGTCTCTTTTCCTGATATTAGACTGAGGTGTAATAGCCTTTAAGCATGGTACCCTTACTCCTTTGCAGTTTGGTAAAATGTTTTATCACTGCTGCTGGCTGTGAAGACCTCGCCTCTGCTCTCATCAGCAATCAAAACCTGAAGATTCTGCAAATTGGGTGCAATGAAATCGGAGATGTGGGTGTGCAGCTGTTGTGTCGGGCTCTGACGCATAC... | TTGTTTTAATTCTTCAATAATTTCAATCTGCCACTAGTTGAATCTGTGGATATGGAGGACTGACGGTGCCTATCCACATGAATGACAAAGGCTGTCGTGCTTTGGTGTCTCTTTTCCTGATATTAGACTGAGGTGTAATAGCCTTTAAGCATGGTACCCTTACTCCTTTGCAGTTTGGTAAAATGTTTTATCACTGCTGCTGGCTGTGAAGACCTCGCCTCTGCTCTCATCAGCAATCAAAACCTGAAGATTCTGCAAATTGGGTGCAATGAAATCGGAGATGTGGGTGTGCAGCTGTTGTGTCGGGCTCTGACGCATAC... |
Task1_train_47621 | A mutation found on Chromosome 19 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TACTAAAAATACAAAAAGTAGCCGGGTGTGGTGGCGCATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACTCAGGAGGCGGAGGTTGCAGTGAGCCGAGATCGCACCACTGCACTCCAGCCTGAGCGACAGAGCGAGAGTGTCTTAAAAAAAAAAAAAAAAAAAAAAAAAAACTACAAAATAGTTGGAATTTCTGGAGTTTGAGCATGAAGGAGGCTTAGATACGGCAGAAGATACTGTCGTTGAAGATGCAGTCACACAGGGATGTCCGATCTTTTGGTTTCCCTGGGCCACGTTGGAAG... | TACTAAAAATACAAAAAGTAGCCGGGTGTGGTGGCGCATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACTCAGGAGGCGGAGGTTGCAGTGAGCCGAGATCGCACCACTGCACTCCAGCCTGAGCGACAGAGCGAGAGTGTCTTAAAAAAAAAAAAAAAAAAAAAAAAAAACTACAAAATAGTTGGAATTTCTGGAGTTTGAGCATGAAGGAGGCTTAGATACGGCAGAAGATACTGTCGTTGAAGATGCAGTCACACAGGGATGTCCGATCTTTTGGTTTCCCTGGGCCACGTTGGAAG... |
Task1_train_47622 | A genomic change on Chromosome 19 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TGCCAAATGTCCCCTGGGGGACAAAAATCAAATCATCCCCAGTTTCAACTAATTTAATAGAATCCAGTTGAAAACCCCTGGATTTGGGGAGAATCAAAGAAGCCTAAGGAAATTATGCAAAGAAAGGCTGCCGTGTGAGATAGCCATGATCAAAGTGAGGGGAAAACTGGCTGGAACTGAGACCTAAGGTGGTAGGAAGAAAGAAGAGGCCAGGCGTGGTGGCTCACGCCTGGAATCCCAGCACCTTGGGAGGCCAAGGCGAGTGGATCACCTGAGTTCAGGAGTTCGAGACCAGCCTGTCCAACATGGTGAAACCCCAT... | TGCCAAATGTCCCCTGGGGGACAAAAATCAAATCATCCCCAGTTTCAACTAATTTAATAGAATCCAGTTGAAAACCCCTGGATTTGGGGAGAATCAAAGAAGCCTAAGGAAATTATGCAAAGAAAGGCTGCCGTGTGAGATAGCCATGATCAAAGTGAGGGGAAAACTGGCTGGAACTGAGACCTAAGGTGGTAGGAAGAAAGAAGAGGCCAGGCGTGGTGGCTCACGCCTGGAATCCCAGCACCTTGGGAGGCCAAGGCGAGTGGATCACCTGAGTTCAGGAGTTCGAGACCAGCCTGTCCAACATGGTGAAACCCCAT... |
Task1_train_47623 | A variant on Chromosome 19 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TTCAACCTGGGAACCTACATCTGTCAGGGTGTGGGGGTTGCAAGACCACCCCTAGCTTCCATGATCCACTGGGAGGGCTGACAGCTCTCAGCATTGTAGCAGATGGAGACAGAGAAAGATGAGCAAAGGAAAATGTCCCTATGTTAGAGCCATGGTTCCCAAATATTAATGTATATCAGCCTCACCTTGGGGGAGGTTATTTTTTATTTTGTTTTGTTTTTGAGACAGGGTCTTACTCTGTTGCCCAGGCTGGAGTGCAGTGATGTGATCTCTGCTTGCTGCAACTTCTGCCTCCTTGGCTCAAGCAATCCTCCCACCGC... | TTCAACCTGGGAACCTACATCTGTCAGGGTGTGGGGGTTGCAAGACCACCCCTAGCTTCCATGATCCACTGGGAGGGCTGACAGCTCTCAGCATTGTAGCAGATGGAGACAGAGAAAGATGAGCAAAGGAAAATGTCCCTATGTTAGAGCCATGGTTCCCAAATATTAATGTATATCAGCCTCACCTTGGGGGAGGTTATTTTTTATTTTGTTTTGTTTTTGAGACAGGGTCTTACTCTGTTGCCCAGGCTGGAGTGCAGTGATGTGATCTCTGCTTGCTGCAACTTCTGCCTCCTTGGCTCAAGCAATCCTCCCACCGC... |
Task1_train_47624 | This variant lies on Chromosome 19. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GGTCAGCAATGGTCATGGAATAAGTAGAGGTAGAAAATGTGTGACTGTGTTAGGCTCCTCCATGCAGCGCCACCCACTGGACGGAAGGAGCACTAGCAAGAGTCAGCCACCCAGGAGCATATCACCTTTGTCCTGGGACCAAGCCCAGCTACTCTGGACCCAAGGGAGGACTGAGTCAATTAAACAAGTTTATCCAGATGTTTGGGTGTCACATAAGTTATAAGAGGGAGAAGTGTTAAAGAAGAAGCTATTGGCCAGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTGGATCACTTGA... | GGTCAGCAATGGTCATGGAATAAGTAGAGGTAGAAAATGTGTGACTGTGTTAGGCTCCTCCATGCAGCGCCACCCACTGGACGGAAGGAGCACTAGCAAGAGTCAGCCACCCAGGAGCATATCACCTTTGTCCTGGGACCAAGCCCAGCTACTCTGGACCCAAGGGAGGACTGAGTCAATTAAACAAGTTTATCCAGATGTTTGGGTGTCACATAAGTTATAAGAGGGAGAAGTGTTAAAGAAGAAGCTATTGGCCAGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTGGATCACTTGA... |
Task1_train_47625 | This variant lies on Chromosome 19. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GCATATCACCTTTGTCCTGGGACCAAGCCCAGCTACTCTGGACCCAAGGGAGGACTGAGTCAATTAAACAAGTTTATCCAGATGTTTGGGTGTCACATAAGTTATAAGAGGGAGAAGTGTTAAAGAAGAAGCTATTGGCCAGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTGGATCACTTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATAGTGAAACCCCATCTATACTAAAAATACAAAAAAATTAGCCAGGCATGGTGGCAGGTGCCTGTAATCCCAGCTACTCAGGGGGC... | GCATATCACCTTTGTCCTGGGACCAAGCCCAGCTACTCTGGACCCAAGGGAGGACTGAGTCAATTAAACAAGTTTATCCAGATGTTTGGGTGTCACATAAGTTATAAGAGGGAGAAGTGTTAAAGAAGAAGCTATTGGCCAGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTGGATCACTTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATAGTGAAACCCCATCTATACTAAAAATACAAAAAAATTAGCCAGGCATGGTGGCAGGTGCCTGTAATCCCAGCTACTCAGGGGGC... |
Task1_train_47626 | Here is a genetic alteration on Chromosome 19. Based on the data, is it a benign variant or a cause of disease? | Benign | ACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTGGATCACTTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATAGTGAAACCCCATCTATACTAAAAATACAAAAAAATTAGCCAGGCATGGTGGCAGGTGCCTGTAATCCCAGCTACTCAGGGGGCTGAGGCAAGGGAATTGCTTGAACCAGGGAAGTGGAGGTTGCAGTGAGCCGAGATCACACCACTGCACTCCAGCCTGGGAAACAGAGTGAGACTCTGTCTCTAAGTAAATAAATAAATAATAAATAAATAAACTATTATTGGAAGTTGGGGCAGGGG... | ACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTGGATCACTTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATAGTGAAACCCCATCTATACTAAAAATACAAAAAAATTAGCCAGGCATGGTGGCAGGTGCCTGTAATCCCAGCTACTCAGGGGGCTGAGGCAAGGGAATTGCTTGAACCAGGGAAGTGGAGGTTGCAGTGAGCCGAGATCACACCACTGCACTCCAGCCTGGGAAACAGAGTGAGACTCTGTCTCTAAGTAAATAAATAAATAATAAATAAATAAACTATTATTGGAAGTTGGGGCAGGGG... |
Task1_train_47627 | A sequence alteration has been identified on Chromosome 19. Is it disease-inducing or harmless? | Benign | CTACTTGGGAGGCTGAGTGAGAAGAATTGCTTGAACCCGGGAGGCGGAGGGTTGCAGTGAGGTGAGATCACGCCACTGCACTCTTGGGTGACAGATTGAGACTCCATCTCAAAAAAAATAATAAAATAAAAAAACAGACACAAACCATTGGCTCAGCGGTCCCCAACCCCCGGGCCATGGACTAGTACCAGTCTGTGGCCTGTTAGGAACTGGGCCACACAGCAGGAGGTGAGTGGCAGGGAGCAACCAAAGCTTCATCTGTATTTACAGCTGCTCCCTATTGCTCACATTACCTCCTGGGCTCTGCCTCCTGTCAGATC... | CTACTTGGGAGGCTGAGTGAGAAGAATTGCTTGAACCCGGGAGGCGGAGGGTTGCAGTGAGGTGAGATCACGCCACTGCACTCTTGGGTGACAGATTGAGACTCCATCTCAAAAAAAATAATAAAATAAAAAAACAGACACAAACCATTGGCTCAGCGGTCCCCAACCCCCGGGCCATGGACTAGTACCAGTCTGTGGCCTGTTAGGAACTGGGCCACACAGCAGGAGGTGAGTGGCAGGGAGCAACCAAAGCTTCATCTGTATTTACAGCTGCTCCCTATTGCTCACATTACCTCCTGGGCTCTGCCTCCTGTCAGATC... |
Task1_train_47628 | A variant has been detected on Chromosome 19. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | ACACGCACACACACACACTGTGATGAACATTCTAAGAAAAGAATTGCAGGGCCTTGGTGAGTGTTCATCTTCAGTTTTAGTAGGTTTGTTTCCAGAGTGTACGAATTGGCCAGAGCAATGGGTATGAAGGTGCTCCTAACTCCAGATCCCTATCCAAGTCTTACTATTATCAGTATTGTTGTTACTGTTATTGCCAATCTGTTGGGCAGGAAATGGTACCTTATGGTTTTAATTTGCATTTCCTTGATTACTAGCGACTATTTTTTTATCATCTGACTGTTCATCTTAGTTTATCTGATTTGCATGTCTTCCCATGTATT... | ACACGCACACACACACACTGTGATGAACATTCTAAGAAAAGAATTGCAGGGCCTTGGTGAGTGTTCATCTTCAGTTTTAGTAGGTTTGTTTCCAGAGTGTACGAATTGGCCAGAGCAATGGGTATGAAGGTGCTCCTAACTCCAGATCCCTATCCAAGTCTTACTATTATCAGTATTGTTGTTACTGTTATTGCCAATCTGTTGGGCAGGAAATGGTACCTTATGGTTTTAATTTGCATTTCCTTGATTACTAGCGACTATTTTTTTATCATCTGACTGTTCATCTTAGTTTATCTGATTTGCATGTCTTCCCATGTATT... |
Task1_train_47629 | This sequence variant lies on Chromosome 19. Is it clinically significant, and what condition might it cause if any? | Benign | TAAGGACAGGTTTATTTTAGAGAAAACAGACCTGAGAGGGGCTTCTGGCCGAGTTAGGTCAGAGCTACACTCTCTTATAGACTAAGAGTTTTTAAAGATTCAGGGTGGGAATATTTATCAGAGGCTTGGACTGCTTCTGTGACTCTTGGTTGTGCTTATCTGGGAGGGAGAGTTGTGTGTCTGTTCCCATACATCCTTCTGCAGCTGCAGGCATATCCCCTGAGTCTGCTTTTAGCTTCCCTATCTTAGTGCACCTGAAGGGAAAGGAATGTGCTATTAAGGCTCACTGTTTTGGGAGGCCTGTAATCCCAGCACTTTGG... | TAAGGACAGGTTTATTTTAGAGAAAACAGACCTGAGAGGGGCTTCTGGCCGAGTTAGGTCAGAGCTACACTCTCTTATAGACTAAGAGTTTTTAAAGATTCAGGGTGGGAATATTTATCAGAGGCTTGGACTGCTTCTGTGACTCTTGGTTGTGCTTATCTGGGAGGGAGAGTTGTGTGTCTGTTCCCATACATCCTTCTGCAGCTGCAGGCATATCCCCTGAGTCTGCTTTTAGCTTCCCTATCTTAGTGCACCTGAAGGGAAAGGAATGTGCTATTAAGGCTCACTGTTTTGGGAGGCCTGTAATCCCAGCACTTTGG... |
Task1_train_47630 | Consider a variant on Chromosome 19. Determine its clinical classification and disease relevance. | Benign | TGTCTGGCTAACTTTTTTTTTCGTATTTTTAGTAGAGACGGGGTTTCACTGTGTTAGCCAGGATGGTCTCAATCTCCTGACCTTGTGATCCACATGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGGGTGAGCCAGCACATCCGGCCATTCCCCTCTTTATGTACAGCAGGATTCCCCCATTGCGTGGGGGAAACCAAGGGATGGAACAGGAGGGGCACACCTGTCCTACAGGTGTAGAACTTGGGGCCATGGTACATGCATCCGTGGCTCCCTCAAGTTCCCCTCCCCCTCCCCAAGGCCACTTATGTTGGCATACAT... | TGTCTGGCTAACTTTTTTTTTCGTATTTTTAGTAGAGACGGGGTTTCACTGTGTTAGCCAGGATGGTCTCAATCTCCTGACCTTGTGATCCACATGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGGGTGAGCCAGCACATCCGGCCATTCCCCTCTTTATGTACAGCAGGATTCCCCCATTGCGTGGGGGAAACCAAGGGATGGAACAGGAGGGGCACACCTGTCCTACAGGTGTAGAACTTGGGGCCATGGTACATGCATCCGTGGCTCCCTCAAGTTCCCCTCCCCCTCCCCAAGGCCACTTATGTTGGCATACAT... |
Task1_train_47631 | Given a variant located on Chromosome 19, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CTCTGTTGCCCAGGCTGGAGTGCAGTGGTGCAATCTCGGCTCATTGCAAGCCCCACCTCCTGGGTTCACGCCATTCTCCTGCCTCAGCCTCCTAAGTAGCTAGGACTACAGGCGCCCGCCACCACGCCCGGCTAATTTTTTTGTATTTTTTTAAGTAGAGACAGGGTTTCACCAGGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCTTGAGCCACTGCGCCTGGCTGAGATTCTTTCATTCAATAACGACAGATGCTTGATTCTGTGTGTAGTAG... | CTCTGTTGCCCAGGCTGGAGTGCAGTGGTGCAATCTCGGCTCATTGCAAGCCCCACCTCCTGGGTTCACGCCATTCTCCTGCCTCAGCCTCCTAAGTAGCTAGGACTACAGGCGCCCGCCACCACGCCCGGCTAATTTTTTTGTATTTTTTTAAGTAGAGACAGGGTTTCACCAGGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCTTGAGCCACTGCGCCTGGCTGAGATTCTTTCATTCAATAACGACAGATGCTTGATTCTGTGTGTAGTAG... |
Task1_train_47632 | This sequence change occurs on Chromosome 19. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CAAGAAGCCAACTATGATCTGCACCAGTACACACTTCCTCCTGTAACAATAAAGAAAGCATGGCCGGGTGTGGTGGCTCATGACTGTCATCCCAGCACTATGGGAGGCTGAGGGGGGTGGATCACCTGAGGTCAAGAGTTCGAGACCAGTGTGCCAACATAGGAAAACCCCATCTCTACTAAAAATATAAAAGTTAGCCGGGCTTGGTGGCGTACGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTGGAACCTGGGAGGCGGAGGTTGCAGTGAACCGAGAACGTGCCACTGCACTCCAGCCTGGG... | CAAGAAGCCAACTATGATCTGCACCAGTACACACTTCCTCCTGTAACAATAAAGAAAGCATGGCCGGGTGTGGTGGCTCATGACTGTCATCCCAGCACTATGGGAGGCTGAGGGGGGTGGATCACCTGAGGTCAAGAGTTCGAGACCAGTGTGCCAACATAGGAAAACCCCATCTCTACTAAAAATATAAAAGTTAGCCGGGCTTGGTGGCGTACGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTGGAACCTGGGAGGCGGAGGTTGCAGTGAACCGAGAACGTGCCACTGCACTCCAGCCTGGG... |
Task1_train_47633 | A change on Chromosome 19 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GACTTCCCTGAGCATGAAGGAACACAGTTGTACTTGAAGGGAGTAAAATCTTGACCAGAGAAATGTACAGCTGGCAGCATTGATAGCCCATTTGAGGTTGGTTGTGGTATATTTATTTTATTTTAAGTTTTTTGAGATGGAGTCTCACTCTGTTGCCTCCAGGCTGGAGTGCAGGGGTGCAATCTTAGCTCACTGCAACCTCCGTCTCGCAGGTTCAAGCAATTCTGCTGCCTCAGCCTCCTGAGTGGCTGGGATTATAGGTACGTGCCACCACGCCCAGCTAATTTTTACATTTTTAGTAGAGAAGAGTTTTCACCAGG... | GACTTCCCTGAGCATGAAGGAACACAGTTGTACTTGAAGGGAGTAAAATCTTGACCAGAGAAATGTACAGCTGGCAGCATTGATAGCCCATTTGAGGTTGGTTGTGGTATATTTATTTTATTTTAAGTTTTTTGAGATGGAGTCTCACTCTGTTGCCTCCAGGCTGGAGTGCAGGGGTGCAATCTTAGCTCACTGCAACCTCCGTCTCGCAGGTTCAAGCAATTCTGCTGCCTCAGCCTCCTGAGTGGCTGGGATTATAGGTACGTGCCACCACGCCCAGCTAATTTTTACATTTTTAGTAGAGAAGAGTTTTCACCAGG... |
Task1_train_47634 | A variant on Chromosome 19 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TAAAATCTTGACCAGAGAAATGTACAGCTGGCAGCATTGATAGCCCATTTGAGGTTGGTTGTGGTATATTTATTTTATTTTAAGTTTTTTGAGATGGAGTCTCACTCTGTTGCCTCCAGGCTGGAGTGCAGGGGTGCAATCTTAGCTCACTGCAACCTCCGTCTCGCAGGTTCAAGCAATTCTGCTGCCTCAGCCTCCTGAGTGGCTGGGATTATAGGTACGTGCCACCACGCCCAGCTAATTTTTACATTTTTAGTAGAGAAGAGTTTTCACCAGGCTGGTCTCAAATTCCTGACCTCATATGATCCACCAGCTTCAGC... | TAAAATCTTGACCAGAGAAATGTACAGCTGGCAGCATTGATAGCCCATTTGAGGTTGGTTGTGGTATATTTATTTTATTTTAAGTTTTTTGAGATGGAGTCTCACTCTGTTGCCTCCAGGCTGGAGTGCAGGGGTGCAATCTTAGCTCACTGCAACCTCCGTCTCGCAGGTTCAAGCAATTCTGCTGCCTCAGCCTCCTGAGTGGCTGGGATTATAGGTACGTGCCACCACGCCCAGCTAATTTTTACATTTTTAGTAGAGAAGAGTTTTCACCAGGCTGGTCTCAAATTCCTGACCTCATATGATCCACCAGCTTCAGC... |
Task1_train_47635 | A mutation is present on Chromosome 19. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | AAGAGGCTGACCCGAGACTCAGTGTGCCCGACTTATGGGGCACCGAGCTGCCAATTCTACCAGACAGGGCACCTCCCATCCTCCCAGGCCTCCAGAAGTGCCCAAGGCCAGAGCTCCACAGAAGGACCCTAGGAGAAGTGAGCAATGCTTCCTCAGTCTTTGCTAACCCAGCCCACTCTGAACTGCCAAGGTTCACCCCCTCCTTTCGAGTGACCTGAAATTTCAAAAACTGACATGCAATACCAATTATCTAAGCAAGGCTCTGGCCACTTGAGAACACGCTTTTTTGATCCACAATCACTCCCTAGTCCTCTAACAAA... | AAGAGGCTGACCCGAGACTCAGTGTGCCCGACTTATGGGGCACCGAGCTGCCAATTCTACCAGACAGGGCACCTCCCATCCTCCCAGGCCTCCAGAAGTGCCCAAGGCCAGAGCTCCACAGAAGGACCCTAGGAGAAGTGAGCAATGCTTCCTCAGTCTTTGCTAACCCAGCCCACTCTGAACTGCCAAGGTTCACCCCCTCCTTTCGAGTGACCTGAAATTTCAAAAACTGACATGCAATACCAATTATCTAAGCAAGGCTCTGGCCACTTGAGAACACGCTTTTTTGATCCACAATCACTCCCTAGTCCTCTAACAAA... |
Task1_train_47636 | The following genetic variant occurs on Chromosome 19. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TGGGAGGTGGTTTCCCGGTGTGTTTTCAGGTGACGCTTGAATGTCCCCAGCTGACGGAAGGCCTTTTGACAGGTGGGACATTTGTAGGGCTTCTCTCCGGAGTGGGTGCGCTGGTGAACGTTCAGGTTCCCCTTGTGGCTGAAAACTTTGCTGCAGTATTTACATTTAAACGGCCTCTCCCCGGTGTGGATCCTCTTGTGGCCCTGTAAGGTGGACTCGTGGGCGAACCGCTTTTGGCAGACGTCACACATGTAGGGCCTCTCGCCAGTGTGGACTCGCTGGTGAACTCGGAGGTCTGAGGGCTGCAAGAAGCGCTTCCG... | TGGGAGGTGGTTTCCCGGTGTGTTTTCAGGTGACGCTTGAATGTCCCCAGCTGACGGAAGGCCTTTTGACAGGTGGGACATTTGTAGGGCTTCTCTCCGGAGTGGGTGCGCTGGTGAACGTTCAGGTTCCCCTTGTGGCTGAAAACTTTGCTGCAGTATTTACATTTAAACGGCCTCTCCCCGGTGTGGATCCTCTTGTGGCCCTGTAAGGTGGACTCGTGGGCGAACCGCTTTTGGCAGACGTCACACATGTAGGGCCTCTCGCCAGTGTGGACTCGCTGGTGAACTCGGAGGTCTGAGGGCTGCAAGAAGCGCTTCCG... |
Task1_train_47637 | Given this context: Chromosome 19 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GATACCCAAAACCTCAGCATCACTCAGTACACTCACGTAACAAATCTGCACAGGCACCCACCGAACCTAAAATAAAAGTGGAATTTTTTTTTAAAGTTATCTATTTTTGTTTTTAAACTTGCAGCAGTGTCTTGCTCTGTCACCCAGGCTGGAATGCAGTGGTGCATCCTGGCTTGCTGCAGCCTTGACTTCTTGGGTCCAAGTGATCCTCCTGCCTCTGCTTCCCAAAATTCTGGGATTACGTGTGAGCCACTATACCTGGCCTACTTAAAATTATTTTTATTTTTATTTCGTTTTATTGATTTATTTTTTGAGACAGA... | GATACCCAAAACCTCAGCATCACTCAGTACACTCACGTAACAAATCTGCACAGGCACCCACCGAACCTAAAATAAAAGTGGAATTTTTTTTTAAAGTTATCTATTTTTGTTTTTAAACTTGCAGCAGTGTCTTGCTCTGTCACCCAGGCTGGAATGCAGTGGTGCATCCTGGCTTGCTGCAGCCTTGACTTCTTGGGTCCAAGTGATCCTCCTGCCTCTGCTTCCCAAAATTCTGGGATTACGTGTGAGCCACTATACCTGGCCTACTTAAAATTATTTTTATTTTTATTTCGTTTTATTGATTTATTTTTTGAGACAGA... |
Task1_train_47638 | Given this variant on Chromosome 19, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GCACCCACCGAACCTAAAATAAAAGTGGAATTTTTTTTTAAAGTTATCTATTTTTGTTTTTAAACTTGCAGCAGTGTCTTGCTCTGTCACCCAGGCTGGAATGCAGTGGTGCATCCTGGCTTGCTGCAGCCTTGACTTCTTGGGTCCAAGTGATCCTCCTGCCTCTGCTTCCCAAAATTCTGGGATTACGTGTGAGCCACTATACCTGGCCTACTTAAAATTATTTTTATTTTTATTTCGTTTTATTGATTTATTTTTTGAGACAGAATCTCACTCTATCCCCCAGGCTGCAGTGCAGTGGCCGATCTGGGCTCACTGCC... | GCACCCACCGAACCTAAAATAAAAGTGGAATTTTTTTTTAAAGTTATCTATTTTTGTTTTTAAACTTGCAGCAGTGTCTTGCTCTGTCACCCAGGCTGGAATGCAGTGGTGCATCCTGGCTTGCTGCAGCCTTGACTTCTTGGGTCCAAGTGATCCTCCTGCCTCTGCTTCCCAAAATTCTGGGATTACGTGTGAGCCACTATACCTGGCCTACTTAAAATTATTTTTATTTTTATTTCGTTTTATTGATTTATTTTTTGAGACAGAATCTCACTCTATCCCCCAGGCTGCAGTGCAGTGGCCGATCTGGGCTCACTGCC... |
Task1_train_47639 | This variant is located on Chromosome 19. Evaluate its biological effect and specify any disease association. | Benign | TGGGATTACAGGCGTGAGCCACCACACTCAGCCTGAGTCCACTAGGTTTTTAATTATTGTTTACATTACCTACTTCTTTTATTTTAAAAACTATTTTATAATTTCAAGTTTTATTTTAAATTTGGGGTGTACCTGTGCAGATGTGTTACATGAGTATATTGAGTGATGCTGAGGTTTGAGGTATGACTCTACCCATCACCCAGGATGTGAGGATAGCAACCAATAGGTAGTTTTTCAACCCTCCCTCCCTCTATCCCTCCAGAGTTTCACTGTTTTGGAGTCCACGTCCTGATTTCCTTTCCTCTGTGTACCTGCCCCAG... | TGGGATTACAGGCGTGAGCCACCACACTCAGCCTGAGTCCACTAGGTTTTTAATTATTGTTTACATTACCTACTTCTTTTATTTTAAAAACTATTTTATAATTTCAAGTTTTATTTTAAATTTGGGGTGTACCTGTGCAGATGTGTTACATGAGTATATTGAGTGATGCTGAGGTTTGAGGTATGACTCTACCCATCACCCAGGATGTGAGGATAGCAACCAATAGGTAGTTTTTCAACCCTCCCTCCCTCTATCCCTCCAGAGTTTCACTGTTTTGGAGTCCACGTCCTGATTTCCTTTCCTCTGTGTACCTGCCCCAG... |
Task1_train_47640 | Given this context: Chromosome 19 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | ACCACACTCAGCCTGAGTCCACTAGGTTTTTAATTATTGTTTACATTACCTACTTCTTTTATTTTAAAAACTATTTTATAATTTCAAGTTTTATTTTAAATTTGGGGTGTACCTGTGCAGATGTGTTACATGAGTATATTGAGTGATGCTGAGGTTTGAGGTATGACTCTACCCATCACCCAGGATGTGAGGATAGCAACCAATAGGTAGTTTTTCAACCCTCCCTCCCTCTATCCCTCCAGAGTTTCACTGTTTTGGAGTCCACGTCCTGATTTCCTTTCCTCTGTGTACCTGCCCCAGAGCGGGATTGCCGGCTCATG... | ACCACACTCAGCCTGAGTCCACTAGGTTTTTAATTATTGTTTACATTACCTACTTCTTTTATTTTAAAAACTATTTTATAATTTCAAGTTTTATTTTAAATTTGGGGTGTACCTGTGCAGATGTGTTACATGAGTATATTGAGTGATGCTGAGGTTTGAGGTATGACTCTACCCATCACCCAGGATGTGAGGATAGCAACCAATAGGTAGTTTTTCAACCCTCCCTCCCTCTATCCCTCCAGAGTTTCACTGTTTTGGAGTCCACGTCCTGATTTCCTTTCCTCTGTGTACCTGCCCCAGAGCGGGATTGCCGGCTCATG... |
Task1_train_47641 | A mutation found on Chromosome 19 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GTTTTGGAGTCCACGTCCTGATTTCCTTTCCTCTGTGTACCTGCCCCAGAGCGGGATTGCCGGCTCATGCAGTTGTTGGACTTTCAATTTTCTGAGGAGCTTCTATACTGTCTCCCATATCGGCTGCTCTAATTTACATCCCAGCACAGGGCGCAGAGGACCCCTTTCCCCCGAATCCTCACCAACACTCGTTCCATGTGTCTTTTTGGGAACAGCCACTCTAGCAGGCGTGAGGGGTGCCTTGTGGTTTGGATTTGCATGTCCCTGATGATGAGTGATGACGAGCACCTTTTCCTAGACCTGCTGGCCATTCACATGTC... | GTTTTGGAGTCCACGTCCTGATTTCCTTTCCTCTGTGTACCTGCCCCAGAGCGGGATTGCCGGCTCATGCAGTTGTTGGACTTTCAATTTTCTGAGGAGCTTCTATACTGTCTCCCATATCGGCTGCTCTAATTTACATCCCAGCACAGGGCGCAGAGGACCCCTTTCCCCCGAATCCTCACCAACACTCGTTCCATGTGTCTTTTTGGGAACAGCCACTCTAGCAGGCGTGAGGGGTGCCTTGTGGTTTGGATTTGCATGTCCCTGATGATGAGTGATGACGAGCACCTTTTCCTAGACCTGCTGGCCATTCACATGTC... |
Task1_train_47642 | This mutation is located on Chromosome 19. Is it associated with a disease or is it a benign polymorphism? | Benign | TTGGAGTCCACGTCCTGATTTCCTTTCCTCTGTGTACCTGCCCCAGAGCGGGATTGCCGGCTCATGCAGTTGTTGGACTTTCAATTTTCTGAGGAGCTTCTATACTGTCTCCCATATCGGCTGCTCTAATTTACATCCCAGCACAGGGCGCAGAGGACCCCTTTCCCCCGAATCCTCACCAACACTCGTTCCATGTGTCTTTTTGGGAACAGCCACTCTAGCAGGCGTGAGGGGTGCCTTGTGGTTTGGATTTGCATGTCCCTGATGATGAGTGATGACGAGCACCTTTTCCTAGACCTGCTGGCCATTCACATGTCTTC... | TTGGAGTCCACGTCCTGATTTCCTTTCCTCTGTGTACCTGCCCCAGAGCGGGATTGCCGGCTCATGCAGTTGTTGGACTTTCAATTTTCTGAGGAGCTTCTATACTGTCTCCCATATCGGCTGCTCTAATTTACATCCCAGCACAGGGCGCAGAGGACCCCTTTCCCCCGAATCCTCACCAACACTCGTTCCATGTGTCTTTTTGGGAACAGCCACTCTAGCAGGCGTGAGGGGTGCCTTGTGGTTTGGATTTGCATGTCCCTGATGATGAGTGATGACGAGCACCTTTTCCTAGACCTGCTGGCCATTCACATGTCTTC... |
Task1_train_47643 | A variant affecting Chromosome 19 has been observed. Determine if it's benign or associated with disease. | Benign | TGCACAACATGGTGCATGTCTTAGTCCCATGAAATTGTTCACCTGAAGAGGGTAAAAATGATGAAATTATGAATGTGCATTTCACCAAAATAACAAAATATCTGTGTAGGAGCTTAATCCTCATAGGATTCTTTAGTGCTGTCCCTTCTCTGGAGCGAATAATTCTGGGATTAAGAGGGTTTGTTGTGGGACAATATCTTACGTTGTAACTATTTTTATTTGTCTTATTGCATAATTATGACTAAGGATTTGCCTTGGATCTTATCTTGATAAGAAAACATAAAGAATTGACATGATTGTTATATCAGATTTTAGGCGCT... | TGCACAACATGGTGCATGTCTTAGTCCCATGAAATTGTTCACCTGAAGAGGGTAAAAATGATGAAATTATGAATGTGCATTTCACCAAAATAACAAAATATCTGTGTAGGAGCTTAATCCTCATAGGATTCTTTAGTGCTGTCCCTTCTCTGGAGCGAATAATTCTGGGATTAAGAGGGTTTGTTGTGGGACAATATCTTACGTTGTAACTATTTTTATTTGTCTTATTGCATAATTATGACTAAGGATTTGCCTTGGATCTTATCTTGATAAGAAAACATAAAGAATTGACATGATTGTTATATCAGATTTTAGGCGCT... |
Task1_train_47644 | A mutation on Chromosome 19 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | AGTTCATCGCTCCAGTCAGTTCAAAGGTGCCATCCTAATGAACCATGTTGGCAATGGGGGAAGCCATGTGGGGCATTAGGGAGCTCCATGGACTTTAGAAAGCTATTCTAAAATGAATTATATATTTTAATGCACACTCTCAGGCCCCATGCCCGGTCTGCTCAATCAGAAGCTGAGTCTGGGGCCCACCCACCTGAGGATTAACCACGCCTTCAGGGGATGGTAGTATCACTAAGACCAACTAGTCACCAGAGACTCCCAATGCCTCTGTAGTTCAAGAGTCAAATCGGGAATTTAGAGGTTGCCAAATTTAGGCCACA... | AGTTCATCGCTCCAGTCAGTTCAAAGGTGCCATCCTAATGAACCATGTTGGCAATGGGGGAAGCCATGTGGGGCATTAGGGAGCTCCATGGACTTTAGAAAGCTATTCTAAAATGAATTATATATTTTAATGCACACTCTCAGGCCCCATGCCCGGTCTGCTCAATCAGAAGCTGAGTCTGGGGCCCACCCACCTGAGGATTAACCACGCCTTCAGGGGATGGTAGTATCACTAAGACCAACTAGTCACCAGAGACTCCCAATGCCTCTGTAGTTCAAGAGTCAAATCGGGAATTTAGAGGTTGCCAAATTTAGGCCACA... |
Task1_train_47645 | This variant is located on Chromosome 19. Evaluate its biological effect and specify any disease association. | Benign | GGCTCAGAGCCCTATAATGGACTTCACAATTCTATTTTGTTGTATGTGACCAATAAATTATCTTTAAAACTATGCTGGAAGTAAAATATCGGTAATTTTTTTTTTTTTTGACACAGAGTCTTGCTCTGTTGCCCAGACTGGAGTGCAGTGGTGCAATCTCTGCTCGGTGCAACCCCCACCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCTCCAGTAGCTGAGATTACAGGTGCGCACCACCACGCCCAGCTAATTTTGTATTTTTTAGTAGAGACAGGGTTTCACCGTGGTCTCAAACTCTTGACCTCGTGATCC... | GGCTCAGAGCCCTATAATGGACTTCACAATTCTATTTTGTTGTATGTGACCAATAAATTATCTTTAAAACTATGCTGGAAGTAAAATATCGGTAATTTTTTTTTTTTTTGACACAGAGTCTTGCTCTGTTGCCCAGACTGGAGTGCAGTGGTGCAATCTCTGCTCGGTGCAACCCCCACCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCTCCAGTAGCTGAGATTACAGGTGCGCACCACCACGCCCAGCTAATTTTGTATTTTTTAGTAGAGACAGGGTTTCACCGTGGTCTCAAACTCTTGACCTCGTGATCC... |
Task1_train_47646 | Given this variant on Chromosome 19, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CTTGAAACCACCTTTTCCCTCAGGTTTTCTCTCAGTATCATCTCTTCAATACAAATTTCTTTATATTTTACTGATAACTTTGTATATATGCCCAGATTTCTTCTATCTATGGTAAGTGATGTAGCAATATATTTTTTCTTTTTTTCTTTTTTTTTTTTTGAGATGGAGTTTCATTCTTGTCACCCAGGCTGGAGTGCAATGGCACAGTCTTGGCTCACTGCAACCTATGCCTCCTGGGTTCAAGCAATTTTCCTGCTTTAGCCTCCCAGGTAGCTGGGATTACAGGCAGGTGACACCATGCCCCGCTAATTTTGTGTTTT... | CTTGAAACCACCTTTTCCCTCAGGTTTTCTCTCAGTATCATCTCTTCAATACAAATTTCTTTATATTTTACTGATAACTTTGTATATATGCCCAGATTTCTTCTATCTATGGTAAGTGATGTAGCAATATATTTTTTCTTTTTTTCTTTTTTTTTTTTTGAGATGGAGTTTCATTCTTGTCACCCAGGCTGGAGTGCAATGGCACAGTCTTGGCTCACTGCAACCTATGCCTCCTGGGTTCAAGCAATTTTCCTGCTTTAGCCTCCCAGGTAGCTGGGATTACAGGCAGGTGACACCATGCCCCGCTAATTTTGTGTTTT... |
Task1_train_47647 | With a mutation on Chromosome 19, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CAGTGGCTCACACCTGTAATCCTAGCTACTCAAGAGAAGGTGGGAAGATTGCTTAAGCCCAGGAGTTAGTGAGCCATGATCATGCCACTGCACTCCAGCCCGGACAACTGAGTGAAACCCTCTTTTTTTTTTTTTTTTATAAAAAGGTGGTCTAAGAGGTGATAATTTTACCAGGCTGTTGAAAGTAAGATGAAAGGGAAAATCTCTTAATATGCAGATTAAAGTTCAGGGAACTCTGAGAATTGGAGAGTTTGCTGTATTGAAACATGTAGATGATTTCATAGGAACACCATTTTCACATTATGAAAAGATAACCATAG... | CAGTGGCTCACACCTGTAATCCTAGCTACTCAAGAGAAGGTGGGAAGATTGCTTAAGCCCAGGAGTTAGTGAGCCATGATCATGCCACTGCACTCCAGCCCGGACAACTGAGTGAAACCCTCTTTTTTTTTTTTTTTTATAAAAAGGTGGTCTAAGAGGTGATAATTTTACCAGGCTGTTGAAAGTAAGATGAAAGGGAAAATCTCTTAATATGCAGATTAAAGTTCAGGGAACTCTGAGAATTGGAGAGTTTGCTGTATTGAAACATGTAGATGATTTCATAGGAACACCATTTTCACATTATGAAAAGATAACCATAG... |
Task1_train_47648 | Chromosome 19 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AACCAATTACAAGTGGAAGAGAGTAGATGAAGAGAGCTTAATTTATAGTCTGTTAGGTCAATACAGGCATGAAATATTACCATTGCAGACTACTTCTCTAGGATTTCATCCTACATTGAGGTTTTTGTTTTTGTTTTTTGTTTTTGTTTTTGTTTTGAGACAGGGTCTTGCTCTGTTGCCTAAGCTGGAGTGCAGTAGGGCAATCATGGCTCACTGCAGTCTCAACCTCCTGGGCTCAAGTGATCCTCTGACCTCAGCCTCCTGAGTAACTGGGAATATAGGCATGTACCACCATGCTTGACTAATTTTTGTGTTTTTTG... | AACCAATTACAAGTGGAAGAGAGTAGATGAAGAGAGCTTAATTTATAGTCTGTTAGGTCAATACAGGCATGAAATATTACCATTGCAGACTACTTCTCTAGGATTTCATCCTACATTGAGGTTTTTGTTTTTGTTTTTTGTTTTTGTTTTTGTTTTGAGACAGGGTCTTGCTCTGTTGCCTAAGCTGGAGTGCAGTAGGGCAATCATGGCTCACTGCAGTCTCAACCTCCTGGGCTCAAGTGATCCTCTGACCTCAGCCTCCTGAGTAACTGGGAATATAGGCATGTACCACCATGCTTGACTAATTTTTGTGTTTTTTG... |
Task1_train_47649 | This variant is present on Chromosome 19. Is the change likely to result in a pathogenic outcome? | Benign | CTTTGTGAGCTCCCTTATCTCTTGATTTTTAATTGCTTTTTCCAGTCTTCTGCTAAAAACATAATGTGAACTCTTATTCAACTTTTAGGTGGGAAAGGTCTTATTGTGGCCTTTAGGACTATGGCTACACAAATTTAGGAATGTAGGGTTGGTTGAATATTGCTAGTAATATAAGAAAGCTTTCAAAATGATATGCTTTTCATTTTCTTCCATAAAAATAAATGACTATATGCTTTTTTGTGGCTTTTAATTTAACGGTTGCATTTTGGAATTTTTCTTCATACTAACACATGATAAAAGATAAATTTACCTTCTTTACG... | CTTTGTGAGCTCCCTTATCTCTTGATTTTTAATTGCTTTTTCCAGTCTTCTGCTAAAAACATAATGTGAACTCTTATTCAACTTTTAGGTGGGAAAGGTCTTATTGTGGCCTTTAGGACTATGGCTACACAAATTTAGGAATGTAGGGTTGGTTGAATATTGCTAGTAATATAAGAAAGCTTTCAAAATGATATGCTTTTCATTTTCTTCCATAAAAATAAATGACTATATGCTTTTTTGTGGCTTTTAATTTAACGGTTGCATTTTGGAATTTTTCTTCATACTAACACATGATAAAAGATAAATTTACCTTCTTTACG... |
Task1_train_47650 | Given a variant located on Chromosome 19, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TTTTAATTGCTTTTTCCAGTCTTCTGCTAAAAACATAATGTGAACTCTTATTCAACTTTTAGGTGGGAAAGGTCTTATTGTGGCCTTTAGGACTATGGCTACACAAATTTAGGAATGTAGGGTTGGTTGAATATTGCTAGTAATATAAGAAAGCTTTCAAAATGATATGCTTTTCATTTTCTTCCATAAAAATAAATGACTATATGCTTTTTTGTGGCTTTTAATTTAACGGTTGCATTTTGGAATTTTTCTTCATACTAACACATGATAAAAGATAAATTTACCTTCTTTACGTCTTTCAGACTTGAAGGCTGTGTGGA... | TTTTAATTGCTTTTTCCAGTCTTCTGCTAAAAACATAATGTGAACTCTTATTCAACTTTTAGGTGGGAAAGGTCTTATTGTGGCCTTTAGGACTATGGCTACACAAATTTAGGAATGTAGGGTTGGTTGAATATTGCTAGTAATATAAGAAAGCTTTCAAAATGATATGCTTTTCATTTTCTTCCATAAAAATAAATGACTATATGCTTTTTTGTGGCTTTTAATTTAACGGTTGCATTTTGGAATTTTTCTTCATACTAACACATGATAAAAGATAAATTTACCTTCTTTACGTCTTTCAGACTTGAAGGCTGTGTGGA... |
Task1_train_47651 | This mutation on Chromosome 19 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | AAAAAAAAAAAAAAAAAAAAATATATATATATATATATAAATTAGCCAGGTGTGGTGGTGCATGCCTGTAATCCCAGCTATTCAAGAGGCTGAGGCATGAGAATCACTTGAACCTGGGAGGTGGAGGTTGCCGTGAGCCAAGATTGTACCACTGCACTCCAGTCTGGGCAACAGAACAAGACCCTGTCTCAAAAAAAAAAAAAAAAAAAGTAGCAGTCAGATTGGGGAAAAAGCCCCAGATTTGAAGTACCACCAGACCATGGTGCGTTTACCTTCAAGAGACTCAAAACCTGCAAGTGGGTAATGATGTGGACAGAAAG... | AAAAAAAAAAAAAAAAAAAAATATATATATATATATATAAATTAGCCAGGTGTGGTGGTGCATGCCTGTAATCCCAGCTATTCAAGAGGCTGAGGCATGAGAATCACTTGAACCTGGGAGGTGGAGGTTGCCGTGAGCCAAGATTGTACCACTGCACTCCAGTCTGGGCAACAGAACAAGACCCTGTCTCAAAAAAAAAAAAAAAAAAAGTAGCAGTCAGATTGGGGAAAAAGCCCCAGATTTGAAGTACCACCAGACCATGGTGCGTTTACCTTCAAGAGACTCAAAACCTGCAAGTGGGTAATGATGTGGACAGAAAG... |
Task1_train_47652 | This mutation is located on Chromosome 19. Is it associated with a disease or is it a benign polymorphism? | Benign | TTTTATTTTACTTTTTAAAATTAGAGACAGGATCTTGCTATGTTACCCAGGCTGGAGTTGAACTTTTGGGCTCAAGCAATACTCCCACCACAGCTTCTTGAGTAGCTAGGACTACAGGAATGCATCACCACACCTGGCCCTACTTTCAGTTCTTATAGTTTCAACAAGAGGATTGTGGGTTACTTGTGGTCCTATGTACATTAATAAATAAGAAATAATGAAAATCAGTAAGCATCTGATTCACAATATTAGAAAAAGAACAAAATGAATTTAAGGAAAGCCCAGATAAGTTATATGTAGTGATTTATACGTCTACAAAT... | TTTTATTTTACTTTTTAAAATTAGAGACAGGATCTTGCTATGTTACCCAGGCTGGAGTTGAACTTTTGGGCTCAAGCAATACTCCCACCACAGCTTCTTGAGTAGCTAGGACTACAGGAATGCATCACCACACCTGGCCCTACTTTCAGTTCTTATAGTTTCAACAAGAGGATTGTGGGTTACTTGTGGTCCTATGTACATTAATAAATAAGAAATAATGAAAATCAGTAAGCATCTGATTCACAATATTAGAAAAAGAACAAAATGAATTTAAGGAAAGCCCAGATAAGTTATATGTAGTGATTTATACGTCTACAAAT... |
Task1_train_47653 | Here is a variant on Chromosome 19. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GGGCTTTTTTGAACAGTTTGGACATAGCCCAGAAAGCAGGTCTGGGCTGAAGGTGTATGTTTGAGCAGCATCAGCCTGTGGATAACGTTTAGATCCAGACTCACTTTGTGTGGCTTTGAAGGTCCAGTGTGATTCAGGAGAGTGGTCTCAAACTCAGGTGGCCTCAGGAACTACCAGGTGGATCATTTATGTGGAGGAGGGGGACAGCTGCTGCCCCATGCAATGTCTTGTTGCCCATAAGAATGAGGCTCCACGTGGCCATATCTTCATGTTTTTTATGAGCTAGCAGCCACATGGACAGCAACTTTTAAATGCTGGGA... | GGGCTTTTTTGAACAGTTTGGACATAGCCCAGAAAGCAGGTCTGGGCTGAAGGTGTATGTTTGAGCAGCATCAGCCTGTGGATAACGTTTAGATCCAGACTCACTTTGTGTGGCTTTGAAGGTCCAGTGTGATTCAGGAGAGTGGTCTCAAACTCAGGTGGCCTCAGGAACTACCAGGTGGATCATTTATGTGGAGGAGGGGGACAGCTGCTGCCCCATGCAATGTCTTGTTGCCCATAAGAATGAGGCTCCACGTGGCCATATCTTCATGTTTTTTATGAGCTAGCAGCCACATGGACAGCAACTTTTAAATGCTGGGA... |
Task1_train_47654 | This is a variant located on Chromosome 19. Is this mutation a likely cause of disease or not? | Benign | ACTTGAAAGCATGCCTGTGTGTCCACTCCCTCTCAGACTCCTGCCACCTCCCTGAGAACACACCCAGGTGAGATGTGAGTCAGGAGAAGAAGATCAAATTGGCCCAGCTGAGCCCTCCTGGTCCAGGTCCAGACCAAGCCTGGTCCAGACCAACAGAACCAGCAGCTGACCTCCAGATGCATGAGAAATAGTAAATGGATAAATGAGGGCTGGATGGTTTGTTACACAGCAAGAGCTGACTGATACAAGCATTAAAGTCAGGTCTTTGAGTTAGGGGGAAAAATGGTGGAGATGGGTAGGTGTTTCCTCATACTGAAAAA... | ACTTGAAAGCATGCCTGTGTGTCCACTCCCTCTCAGACTCCTGCCACCTCCCTGAGAACACACCCAGGTGAGATGTGAGTCAGGAGAAGAAGATCAAATTGGCCCAGCTGAGCCCTCCTGGTCCAGGTCCAGACCAAGCCTGGTCCAGACCAACAGAACCAGCAGCTGACCTCCAGATGCATGAGAAATAGTAAATGGATAAATGAGGGCTGGATGGTTTGTTACACAGCAAGAGCTGACTGATACAAGCATTAAAGTCAGGTCTTTGAGTTAGGGGGAAAAATGGTGGAGATGGGTAGGTGTTTCCTCATACTGAAAAA... |
Task1_train_47655 | A mutation on Chromosome 19 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGTGGATAACGAAGTCAGGAGATCGAGACCATCCTAGCCAACATGGTGAAACCCCGCCTCTACTAAAATACAAAAAAACTAGTCCGGGTGTGGTGGCCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTAGGGGAATCACTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCGAGATTGCATCACTGCACTCCAGCCTGGGCGACAGAGCAAGACTCCGTCTCAGAAAAAAAAAAAAAAAAAAATTAGCCAGACTCCTGTAATTTTAACT... | GGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGTGGATAACGAAGTCAGGAGATCGAGACCATCCTAGCCAACATGGTGAAACCCCGCCTCTACTAAAATACAAAAAAACTAGTCCGGGTGTGGTGGCCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTAGGGGAATCACTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCGAGATTGCATCACTGCACTCCAGCCTGGGCGACAGAGCAAGACTCCGTCTCAGAAAAAAAAAAAAAAAAAAATTAGCCAGACTCCTGTAATTTTAACT... |
Task1_train_47656 | A change on Chromosome 19 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TAGGGGAATCACTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCGAGATTGCATCACTGCACTCCAGCCTGGGCGACAGAGCAAGACTCCGTCTCAGAAAAAAAAAAAAAAAAAAATTAGCCAGACTCCTGTAATTTTAACTACTCGGGAGGTTGAGGCAGGAGAATCACTTGTACCCGGGAGGCAGAAGTTTCAGTGAGCCGAGATCGCTCCACTGCACTCTAGCCTGGGTGACAGAGAGAGACACTGTCTCAAAGAAAAAAAGAAAGAAATTAAAGGCCAGCCATAGGTGTTTCTGCAGGTCTACTTGCCCGTGCCCC... | TAGGGGAATCACTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCGAGATTGCATCACTGCACTCCAGCCTGGGCGACAGAGCAAGACTCCGTCTCAGAAAAAAAAAAAAAAAAAAATTAGCCAGACTCCTGTAATTTTAACTACTCGGGAGGTTGAGGCAGGAGAATCACTTGTACCCGGGAGGCAGAAGTTTCAGTGAGCCGAGATCGCTCCACTGCACTCTAGCCTGGGTGACAGAGAGAGACACTGTCTCAAAGAAAAAAAGAAAGAAATTAAAGGCCAGCCATAGGTGTTTCTGCAGGTCTACTTGCCCGTGCCCC... |
Task1_train_47657 | This mutation is located on Chromosome 19. Is it associated with a disease or is it a benign polymorphism? | Benign | CGTTTCAAGAGTCCTTTTCCCATGTAGTAAACCTCACTGCCCCTCAGCTTTCCCGATGTCCGTTCCAACCTCAGTCCTTCCTATGCAGCCAGCCCTCACCTACACCATACCATCAAAAACTCCTTTTCCAAACTGCTCAGGACACCCCGCTCAATTCATTCTCAGAAACCTGGCCTTCTACAGTTCTTGCCTCTGGTGTTTTCTTCTGTCTGTCTCCTCTCCCCTCCTAGATCTGGTGATATATTAGGACTCCCTTCTTTGACTCACTCATTTCTGCTTCTTGCTCTCAGCTCTACAATCTTCCTAAACTTTGACACTCC... | CGTTTCAAGAGTCCTTTTCCCATGTAGTAAACCTCACTGCCCCTCAGCTTTCCCGATGTCCGTTCCAACCTCAGTCCTTCCTATGCAGCCAGCCCTCACCTACACCATACCATCAAAAACTCCTTTTCCAAACTGCTCAGGACACCCCGCTCAATTCATTCTCAGAAACCTGGCCTTCTACAGTTCTTGCCTCTGGTGTTTTCTTCTGTCTGTCTCCTCTCCCCTCCTAGATCTGGTGATATATTAGGACTCCCTTCTTTGACTCACTCATTTCTGCTTCTTGCTCTCAGCTCTACAATCTTCCTAAACTTTGACACTCC... |
Task1_train_47658 | This variant is present on Chromosome 19. Is the change likely to result in a pathogenic outcome? | Benign | CTGCTGAGTGAGATCACTTGGCCCCCTGGCTTCAGCCCCCTTTCCAGGGGAGTGAATGGTTCTGTCTCACTGGGGTTTCAGGCACCACTGGTGTACAAAAAAAAATCAACTCTTGCAACTAGCTCGGTGTCTCCCCGAACAGCTGGCTAGTTTTGTGCTTGAAACCCAGGGCCCTGGTGGTGTAGGCACACAAGGGAATCTCCTGATCTGCAGATTGCAAAAACTGTGGGAAAAGCGTAGTAACCGGGCGAGTAGCATAGTTCTTCACGGCTTCCCTTGGCTGGGGGAGGGAGGTCCCTGGCTCCTTGCATTTCCCAGGT... | CTGCTGAGTGAGATCACTTGGCCCCCTGGCTTCAGCCCCCTTTCCAGGGGAGTGAATGGTTCTGTCTCACTGGGGTTTCAGGCACCACTGGTGTACAAAAAAAAATCAACTCTTGCAACTAGCTCGGTGTCTCCCCGAACAGCTGGCTAGTTTTGTGCTTGAAACCCAGGGCCCTGGTGGTGTAGGCACACAAGGGAATCTCCTGATCTGCAGATTGCAAAAACTGTGGGAAAAGCGTAGTAACCGGGCGAGTAGCATAGTTCTTCACGGCTTCCCTTGGCTGGGGGAGGGAGGTCCCTGGCTCCTTGCATTTCCCAGGT... |
Task1_train_47659 | A genomic change on Chromosome 19 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TTCTCGATGAGCAGTGATGCTGAGCACCTGTTCATATCTCTGTTGGCCATTTGTATATTCTTTCTCGCCTAACAGCTCCCTTGAAAATGCGTGTGCCTCAGTCTATGTCTTCTGGAGAACTGGCACAGCTTCAGAATATTAGCACCCCAAAAGAGTATTTTACTTAGAGCATAAGAAGACTAAAAATAAATCATTATTATATGTGGATGAGGTTTTTCATAAAATATAACTGTTAATATATTCTTGGTTAAAATGCATGTGTGCTTTTCTTCTTTAGGTTACATAAAGAAAGGATGATATCTCTAAAGGTATGTGGATTC... | TTCTCGATGAGCAGTGATGCTGAGCACCTGTTCATATCTCTGTTGGCCATTTGTATATTCTTTCTCGCCTAACAGCTCCCTTGAAAATGCGTGTGCCTCAGTCTATGTCTTCTGGAGAACTGGCACAGCTTCAGAATATTAGCACCCCAAAAGAGTATTTTACTTAGAGCATAAGAAGACTAAAAATAAATCATTATTATATGTGGATGAGGTTTTTCATAAAATATAACTGTTAATATATTCTTGGTTAAAATGCATGTGTGCTTTTCTTCTTTAGGTTACATAAAGAAAGGATGATATCTCTAAAGGTATGTGGATTC... |
Task1_train_47660 | A variant on Chromosome 19 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | ACCATTTTCCAGGAATTTCAGGGCATAACATTAGGGTTATATGCAAAATGCAGTATACTAAATATCCGTGTGATTTTGTGAATTCAAAAGCACTGCAAGATGTTGCTCATGTTATTAATATGAATAAGACGATAAACCCATCCTCATAAATGTACAACATTTCCTGGTGGCCAAGCCTTAAACAGCTTATAATGTACCCAGTATCAGTGGGTGATGTGTTAGACTGTGAATTCAGCAAGGAGTAAAGAACGATTTTTTTAAATGGCCATGTGAGTAGACAAATGGAAATTGAGAGGATTTTTTGGGTAAAAAGAGATAAG... | ACCATTTTCCAGGAATTTCAGGGCATAACATTAGGGTTATATGCAAAATGCAGTATACTAAATATCCGTGTGATTTTGTGAATTCAAAAGCACTGCAAGATGTTGCTCATGTTATTAATATGAATAAGACGATAAACCCATCCTCATAAATGTACAACATTTCCTGGTGGCCAAGCCTTAAACAGCTTATAATGTACCCAGTATCAGTGGGTGATGTGTTAGACTGTGAATTCAGCAAGGAGTAAAGAACGATTTTTTTAAATGGCCATGTGAGTAGACAAATGGAAATTGAGAGGATTTTTTGGGTAAAAAGAGATAAG... |
Task1_train_47661 | Given this context: Chromosome 19 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AGGAGAATCACCTGAACCAGGGAGGCGGAGATTGCAGTGAGCTGAGATCACACCACCGTACTCCAGCCTGGGTGACAAGAGTAAAACTCTGTCTCCAAAAAAAGAAAAAGAAAAGAAAGAAACGAGGCTGAGTGCCATGGCTCATGCCTGTAATCAAAGCACTTTGGGAGCCTGAGGTGGAAGGATTGCCTGAGCCCAAGAGTTTGAGGCTGCAGTGAGCTATGACTACACCACTGCCCTCCAGCCTGGGCAACAGGTGACACCCTATCTCAAAAGGAAAAACAAAAAAGGCAAATGGCAATTGCAGTGAAGAAATGCCA... | AGGAGAATCACCTGAACCAGGGAGGCGGAGATTGCAGTGAGCTGAGATCACACCACCGTACTCCAGCCTGGGTGACAAGAGTAAAACTCTGTCTCCAAAAAAAGAAAAAGAAAAGAAAGAAACGAGGCTGAGTGCCATGGCTCATGCCTGTAATCAAAGCACTTTGGGAGCCTGAGGTGGAAGGATTGCCTGAGCCCAAGAGTTTGAGGCTGCAGTGAGCTATGACTACACCACTGCCCTCCAGCCTGGGCAACAGGTGACACCCTATCTCAAAAGGAAAAACAAAAAAGGCAAATGGCAATTGCAGTGAAGAAATGCCA... |
Task1_train_47662 | This variant is found on Chromosome 19. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GAAACCCTGTCTCTACTAAAAATACAAAAAATTCGCCGGGCATGGTGGCAAGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGTTCGAACTCGGGAGGCGGAGGTTGCAGTGAGCCCAGATCGCGCCACTGCACTCCAGCCTGGGCGACAGAGACTCCGTTTCCAGAAAAAAAAAAAAAAGAAAAAAAAAAGAGTTTGCCTGCAAAGGAAAACCCAGATAAGAATGTAAAGAAATTTCTGAGTGGAGAAAAATACCTGGAGATTTCTTCCAGCACTCCCAGGAAGTCACAGCTGGCTGCCAAACGAC... | GAAACCCTGTCTCTACTAAAAATACAAAAAATTCGCCGGGCATGGTGGCAAGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGTTCGAACTCGGGAGGCGGAGGTTGCAGTGAGCCCAGATCGCGCCACTGCACTCCAGCCTGGGCGACAGAGACTCCGTTTCCAGAAAAAAAAAAAAAAGAAAAAAAAAAGAGTTTGCCTGCAAAGGAAAACCCAGATAAGAATGTAAAGAAATTTCTGAGTGGAGAAAAATACCTGGAGATTTCTTCCAGCACTCCCAGGAAGTCACAGCTGGCTGCCAAACGAC... |
Task1_train_47663 | Given a variant located on Chromosome 19, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGTTCGAACTCGGGAGGCGGAGGTTGCAGTGAGCCCAGATCGCGCCACTGCACTCCAGCCTGGGCGACAGAGACTCCGTTTCCAGAAAAAAAAAAAAAAGAAAAAAAAAAGAGTTTGCCTGCAAAGGAAAACCCAGATAAGAATGTAAAGAAATTTCTGAGTGGAGAAAAATACCTGGAGATTTCTTCCAGCACTCCCAGGAAGTCACAGCTGGCTGCCAAACGACTTCCTCATTTAGAAAAGCTGAATTGGCTTCCATGCACCATTGACCCACAGTGCTCTCCTGGT... | CCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGTTCGAACTCGGGAGGCGGAGGTTGCAGTGAGCCCAGATCGCGCCACTGCACTCCAGCCTGGGCGACAGAGACTCCGTTTCCAGAAAAAAAAAAAAAAGAAAAAAAAAAGAGTTTGCCTGCAAAGGAAAACCCAGATAAGAATGTAAAGAAATTTCTGAGTGGAGAAAAATACCTGGAGATTTCTTCCAGCACTCCCAGGAAGTCACAGCTGGCTGCCAAACGACTTCCTCATTTAGAAAAGCTGAATTGGCTTCCATGCACCATTGACCCACAGTGCTCTCCTGGT... |
Task1_train_47664 | A mutation found on Chromosome 19 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AGAAAAGGTCTTGCTCTGTTGCCCAAGCTGGGTGCAGTGGCACAGTCATACTTTGCTGCAGTCTTGAATTTTGCGGCTGAAGCAATCCTCCCATGTCAGCCTCCCGAGTAGTTGGGACTACACAGGCTTGCACCACCATGCCTGGCTAATGTGTTTTTAGTTTTGTTTTTAAAAAATTTTTTTTAGAGATGGGAGCTTGCCGTGTTTCTCAGAGTGGTCTAAAACTTCTGGGCTCGAGTAATCTGCTCACCTCGGCCTCCCAAAGCACTAGGATTACAGGCTTTGGGGGGCTGAGGTGAAAAGATGAGCACCATACACAG... | AGAAAAGGTCTTGCTCTGTTGCCCAAGCTGGGTGCAGTGGCACAGTCATACTTTGCTGCAGTCTTGAATTTTGCGGCTGAAGCAATCCTCCCATGTCAGCCTCCCGAGTAGTTGGGACTACACAGGCTTGCACCACCATGCCTGGCTAATGTGTTTTTAGTTTTGTTTTTAAAAAATTTTTTTTAGAGATGGGAGCTTGCCGTGTTTCTCAGAGTGGTCTAAAACTTCTGGGCTCGAGTAATCTGCTCACCTCGGCCTCCCAAAGCACTAGGATTACAGGCTTTGGGGGGCTGAGGTGAAAAGATGAGCACCATACACAG... |
Task1_train_47665 | This mutation is located on Chromosome 19. Is it associated with a disease or is it a benign polymorphism? | Benign | CCCGTCTGTACTAAATATACAAAAATTAGCTGGGTGTGGTAGCGCATGCCTGTAATCCCAGCTACTCAGGAGGTGGAGGCAGGAGAATCACTTGAACCAGGGAGTTGGAGGTTGCAGTGAGCTGAGATCGCGCTACTGCACTCCAGCCTGATGACAGAGCGAGACTTCGTCTCAAAAAAAAAAAAAAAAAAAGAAAAGCAGTTAACAGTCCAGATCCCCAGAGCACTGATTGGGTGTCTCAGGCCTGTTCCAGGCAGTGTTCATGCTCCATTTATTCTCACAGGATCCCTGTCCTCAGCAAAGTAAGGAAAATTTAGCCA... | CCCGTCTGTACTAAATATACAAAAATTAGCTGGGTGTGGTAGCGCATGCCTGTAATCCCAGCTACTCAGGAGGTGGAGGCAGGAGAATCACTTGAACCAGGGAGTTGGAGGTTGCAGTGAGCTGAGATCGCGCTACTGCACTCCAGCCTGATGACAGAGCGAGACTTCGTCTCAAAAAAAAAAAAAAAAAAAGAAAAGCAGTTAACAGTCCAGATCCCCAGAGCACTGATTGGGTGTCTCAGGCCTGTTCCAGGCAGTGTTCATGCTCCATTTATTCTCACAGGATCCCTGTCCTCAGCAAAGTAAGGAAAATTTAGCCA... |
Task1_train_47666 | This variant is located on Chromosome 19. Evaluate its biological effect and specify any disease association. | Benign | TAGCGCATGCCTGTAATCCCAGCTACTCAGGAGGTGGAGGCAGGAGAATCACTTGAACCAGGGAGTTGGAGGTTGCAGTGAGCTGAGATCGCGCTACTGCACTCCAGCCTGATGACAGAGCGAGACTTCGTCTCAAAAAAAAAAAAAAAAAAAGAAAAGCAGTTAACAGTCCAGATCCCCAGAGCACTGATTGGGTGTCTCAGGCCTGTTCCAGGCAGTGTTCATGCTCCATTTATTCTCACAGGATCCCTGTCCTCAGCAAAGTAAGGAAAATTTAGCCACTCCTGTGAGTCCCTCATCCAGTTTAACTTACTCAGCAC... | TAGCGCATGCCTGTAATCCCAGCTACTCAGGAGGTGGAGGCAGGAGAATCACTTGAACCAGGGAGTTGGAGGTTGCAGTGAGCTGAGATCGCGCTACTGCACTCCAGCCTGATGACAGAGCGAGACTTCGTCTCAAAAAAAAAAAAAAAAAAAGAAAAGCAGTTAACAGTCCAGATCCCCAGAGCACTGATTGGGTGTCTCAGGCCTGTTCCAGGCAGTGTTCATGCTCCATTTATTCTCACAGGATCCCTGTCCTCAGCAAAGTAAGGAAAATTTAGCCACTCCTGTGAGTCCCTCATCCAGTTTAACTTACTCAGCAC... |
Task1_train_47667 | A mutation on Chromosome 19 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | ATTTGCATTTTCCTCATTGGTAGGGTGGTTTAGTGTCTTTCATGATTCTGAGCCAATCTATATTTTCTTCTGTGAGATGTTATTTGGTGATAAATGCCTTTTTTTCAATTAACTTCTTTGGCTTTCTCTTTTTGATTTTATTTTTGTACATTATAGATACCTATCTTTTATCAGTTACATTTGCTGCCGGTATATTCTTCTAGTTTTTAATTTTGTCCTTCCACTCTTTTTAAAGTATCTTTTGTTCAATGAGTTCCTTACATAGCGTAGTCTGATTTATGTTTTTTTTTTACGTGATTAATGATTTTGTACCTTGTGGA... | ATTTGCATTTTCCTCATTGGTAGGGTGGTTTAGTGTCTTTCATGATTCTGAGCCAATCTATATTTTCTTCTGTGAGATGTTATTTGGTGATAAATGCCTTTTTTTCAATTAACTTCTTTGGCTTTCTCTTTTTGATTTTATTTTTGTACATTATAGATACCTATCTTTTATCAGTTACATTTGCTGCCGGTATATTCTTCTAGTTTTTAATTTTGTCCTTCCACTCTTTTTAAAGTATCTTTTGTTCAATGAGTTCCTTACATAGCGTAGTCTGATTTATGTTTTTTTTTTACGTGATTAATGATTTTGTACCTTGTGGA... |
Task1_train_47668 | Consider this mutation on Chromosome 19. Is this a benign change or a disease-causing variant? | Benign | TGACTAGACTCAGGTGTACATTTTGGCTTGGCCATTCGCCATTTCCCAGATTTTGGCAAGTCACTTTATCTGCCTGAGCCTCGATCTCTTCATCTATAATGTGGTCCTGATTGCAGTACATTCTTAATGTGCATCCTGTGAAGAAATCCTAAAATAGAATTTTTCATGCAGGGACCATAGGAGTAGCAATGTAATGCTTTGCTTAGAATGTAAAAAAAAAGCCTTAGGTCAGTGAAGAAACTTACCTTTCTCCTGAATGGAGACTCAGTATCTCAAATATGTTATTTCTTTTCTAAACTAATGACTAAATTTAATTGAGT... | TGACTAGACTCAGGTGTACATTTTGGCTTGGCCATTCGCCATTTCCCAGATTTTGGCAAGTCACTTTATCTGCCTGAGCCTCGATCTCTTCATCTATAATGTGGTCCTGATTGCAGTACATTCTTAATGTGCATCCTGTGAAGAAATCCTAAAATAGAATTTTTCATGCAGGGACCATAGGAGTAGCAATGTAATGCTTTGCTTAGAATGTAAAAAAAAAGCCTTAGGTCAGTGAAGAAACTTACCTTTCTCCTGAATGGAGACTCAGTATCTCAAATATGTTATTTCTTTTCTAAACTAATGACTAAATTTAATTGAGT... |
Task1_train_47669 | Consider this mutation on Chromosome 19. Is this a benign change or a disease-causing variant? | Benign | TGCTTACAGTCTTTGGGGCCCAATGAGGATGTTTTTTTTCTCTTTTTTTGAGACGGAGCTTCGCTCTTGTCGCCCAGGCTGGAGTGCAGTGGCATGATCTCGGTTCACTACAACCTCCGCCTCCTGGGTTCAGCCTCCCGAGTAGCTGGGACTACAGGTACCCGCCACCACACCTGGCTAACTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGGCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGACCCACTGTGCCCTGCCAGATG... | TGCTTACAGTCTTTGGGGCCCAATGAGGATGTTTTTTTTCTCTTTTTTTGAGACGGAGCTTCGCTCTTGTCGCCCAGGCTGGAGTGCAGTGGCATGATCTCGGTTCACTACAACCTCCGCCTCCTGGGTTCAGCCTCCCGAGTAGCTGGGACTACAGGTACCCGCCACCACACCTGGCTAACTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGGCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGACCCACTGTGCCCTGCCAGATG... |
Task1_train_47670 | Chromosome 19 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CTGGGTTCAGCCTCCCGAGTAGCTGGGACTACAGGTACCCGCCACCACACCTGGCTAACTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGGCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGACCCACTGTGCCCTGCCAGATGGTGTTTTTGTGGTTGTTTTATGGTCACGGTTCAACGTTTTCTTTGCTTGGCTGAGAATAGCTTCACTTCATGGTCTTCCCCATCCTGCAGTCCCAGATCAGATTGACAGGTTTCTTTCTTCTA... | CTGGGTTCAGCCTCCCGAGTAGCTGGGACTACAGGTACCCGCCACCACACCTGGCTAACTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGGCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGACCCACTGTGCCCTGCCAGATGGTGTTTTTGTGGTTGTTTTATGGTCACGGTTCAACGTTTTCTTTGCTTGGCTGAGAATAGCTTCACTTCATGGTCTTCCCCATCCTGCAGTCCCAGATCAGATTGACAGGTTTCTTTCTTCTA... |
Task1_train_47671 | This alteration on Chromosome 19 may affect genome function. Does it lead to a disease or is it benign? | Benign | TGCTGAGCCACCAAGCCTGGCCTCTTACATCTTAAATTTAAGTACTTCCAAGTTAGGTCCCAGATGTATATATTTCACTAACGCATAATAAAAAATTATGGCTAACATGTATTTATTTCTTACTCAGTGCCTTGCTCTCTGCCGACGATAGTATATGTAGTGTTTCACTTCATCTTCACTATAGTCTTACAAGGCAGACTCTATTTTTGGCCCTTTTTGTTTGTTTGTTTCCGAGATGGAGCCTCCCACTGTTGCCCTGGCAGGAGTGCGATGGTGCAGTCTTGGCTCACTACAACCTCCGTCTCCTGGGTTCAAGTGAT... | TGCTGAGCCACCAAGCCTGGCCTCTTACATCTTAAATTTAAGTACTTCCAAGTTAGGTCCCAGATGTATATATTTCACTAACGCATAATAAAAAATTATGGCTAACATGTATTTATTTCTTACTCAGTGCCTTGCTCTCTGCCGACGATAGTATATGTAGTGTTTCACTTCATCTTCACTATAGTCTTACAAGGCAGACTCTATTTTTGGCCCTTTTTGTTTGTTTGTTTCCGAGATGGAGCCTCCCACTGTTGCCCTGGCAGGAGTGCGATGGTGCAGTCTTGGCTCACTACAACCTCCGTCTCCTGGGTTCAAGTGAT... |
Task1_train_47672 | This mutation occurs on Chromosome 19. Does this change lead to a known medical condition, or is it benign? | Benign | TGGAGAACTTTGCACTTTTGTCCTCAGTAGGTAAGGCCCTGACACCTACGTCAGTGTCTTGTGCTGGGCAATGTTTTTTCACTTTTTTCCTTGGCATCTCCGTCTCACACCAGGTCATGGATGCTGCATCCTCTCCTGGTTTCCTGGCATATGTGTTGTGGCAGCTACAGCTGGGCTGTGTGATCTGTATCAATTTTCCTTAAGAAGCTTAGCTCTTGTCACTCTGAAGCCTTATAAGGCTCAAAAGTCAGAAGTCCTCAGGTTTCTCAAGAATATCCTAATGACCTTGCCTGTCCCTGGTTAGTTTACTCTGTCCAAAT... | TGGAGAACTTTGCACTTTTGTCCTCAGTAGGTAAGGCCCTGACACCTACGTCAGTGTCTTGTGCTGGGCAATGTTTTTTCACTTTTTTCCTTGGCATCTCCGTCTCACACCAGGTCATGGATGCTGCATCCTCTCCTGGTTTCCTGGCATATGTGTTGTGGCAGCTACAGCTGGGCTGTGTGATCTGTATCAATTTTCCTTAAGAAGCTTAGCTCTTGTCACTCTGAAGCCTTATAAGGCTCAAAAGTCAGAAGTCCTCAGGTTTCTCAAGAATATCCTAATGACCTTGCCTGTCCCTGGTTAGTTTACTCTGTCCAAAT... |
Task1_train_47673 | This genomic variant is located on Chromosome 19. Can you determine its pathogenicity and name any linked disease? | Benign | CTAAGGAAACACAGAATAAGAAGTTGTTCATAGACTGAAGTGTCATAATTTTGGCAGGATTGTATGGTCTTTGAGGATGTGGCCATATATTTCTCCCAAGAGGAATGGGGGATCCTTAATGATGCTCAGAGACACCTGCACAGCAATGTGATGTTGGAGAACTTTGCGCTTTTGTCATCAGTAGGTAAGGCCTTCATACCTACTCTGGTGTCTTGTGCTGGGTGCTGTTTTTTTGCTCTTTTCCATGACAACTCTGTCTTTCCCACACCAGATTGTGAGTGCTACGTCCTGTCCTCTCCTGGTTTCCTGGCAAATGTGAT... | CTAAGGAAACACAGAATAAGAAGTTGTTCATAGACTGAAGTGTCATAATTTTGGCAGGATTGTATGGTCTTTGAGGATGTGGCCATATATTTCTCCCAAGAGGAATGGGGGATCCTTAATGATGCTCAGAGACACCTGCACAGCAATGTGATGTTGGAGAACTTTGCGCTTTTGTCATCAGTAGGTAAGGCCTTCATACCTACTCTGGTGTCTTGTGCTGGGTGCTGTTTTTTTGCTCTTTTCCATGACAACTCTGTCTTTCCCACACCAGATTGTGAGTGCTACGTCCTGTCCTCTCCTGGTTTCCTGGCAAATGTGAT... |
Task1_train_47674 | A genetic alteration is present on Chromosome 19. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GTGTAGCTCAATTCTGAAGGACATTCTGCACCTGGCTGAGCACGATGGAACACACCCTGAGCAAGGGCTGTACACATGTGCAGCAGAGCATGACCTGCACCAAAAGGAGCAGATTAGAGAGAAGCTCACCAGAAGTGATGAGTGGAGGCCTTCATTTGTGAACCACAGTGCTCACGTGGGAGAGAGGAACTTCACATGCACGCAGGGTGGCAAGGATTTTACTGCCAGCTCAGACCTTCTCCAGCAACAGGTCTTAAACAGTGGGTGGAAGCTGTACAGGGATACCCAGGATGGGGAAGCCTTTCAAGGTGAACAGAATG... | GTGTAGCTCAATTCTGAAGGACATTCTGCACCTGGCTGAGCACGATGGAACACACCCTGAGCAAGGGCTGTACACATGTGCAGCAGAGCATGACCTGCACCAAAAGGAGCAGATTAGAGAGAAGCTCACCAGAAGTGATGAGTGGAGGCCTTCATTTGTGAACCACAGTGCTCACGTGGGAGAGAGGAACTTCACATGCACGCAGGGTGGCAAGGATTTTACTGCCAGCTCAGACCTTCTCCAGCAACAGGTCTTAAACAGTGGGTGGAAGCTGTACAGGGATACCCAGGATGGGGAAGCCTTTCAAGGTGAACAGAATG... |
Task1_train_47675 | A mutation located on Chromosome 19 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TCATTTTTTGTTGATGAAGAGTATTGCATTGAATATACCACAATTTATTAATCTATTAATAAATATTTTGATTGTTTCTAGTGTTGGACTAAAAAACTAACAAAGACCCATGAACATTCATATACAAGTGTTTATATGAATATATTTAGCAGAATTGCATTTGTTATACCTCCTTGTCCATGATGGTTATGGTGTATTTTAAAGATTAACCATTTTCATAGATGTGTTGTGGTCAGTGTGGTTTTTAAATTTGCATTTCTCTAATAATTAATGATGCTGAATAAGTTTTTATATGCTTATTTGTTATCTGTATATTTGGC... | TCATTTTTTGTTGATGAAGAGTATTGCATTGAATATACCACAATTTATTAATCTATTAATAAATATTTTGATTGTTTCTAGTGTTGGACTAAAAAACTAACAAAGACCCATGAACATTCATATACAAGTGTTTATATGAATATATTTAGCAGAATTGCATTTGTTATACCTCCTTGTCCATGATGGTTATGGTGTATTTTAAAGATTAACCATTTTCATAGATGTGTTGTGGTCAGTGTGGTTTTTAAATTTGCATTTCTCTAATAATTAATGATGCTGAATAAGTTTTTATATGCTTATTTGTTATCTGTATATTTGGC... |
Task1_train_47676 | A mutation on Chromosome 19 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TTAGAAGGGTCATATTCCCTATAGTTTGCTGCAGTTTTCTCATTCCTTTATTAATCTGGGTTTCTGCACCAACTATGATTCCTACCTGGGCCTTCTGGAGGACAGCCAATATCAACTGCCTACTGAAAAATAGACTTCAGAGATCTTGACATGTCCACTGAGTTCAAATTCTCCTCAAGAAGCCTTGGGAATATGAAGTATCTTCTGGGAACAAGGGACGTAATTCATGTTGCTCCCAGACACATTAGAGATTATCACAACAAATGCCCACTGCTTAGGGTGACCTCAATTACACAAAAAATCTTAACATATAGACCAAA... | TTAGAAGGGTCATATTCCCTATAGTTTGCTGCAGTTTTCTCATTCCTTTATTAATCTGGGTTTCTGCACCAACTATGATTCCTACCTGGGCCTTCTGGAGGACAGCCAATATCAACTGCCTACTGAAAAATAGACTTCAGAGATCTTGACATGTCCACTGAGTTCAAATTCTCCTCAAGAAGCCTTGGGAATATGAAGTATCTTCTGGGAACAAGGGACGTAATTCATGTTGCTCCCAGACACATTAGAGATTATCACAACAAATGCCCACTGCTTAGGGTGACCTCAATTACACAAAAAATCTTAACATATAGACCAAA... |
Task1_train_47677 | Consider a variant on Chromosome 19. Determine its clinical classification and disease relevance. | Benign | CTCACTACAAATATGTGTCTAACACAACTAAGACCAAGGTCATAGGACTGTTGTTAGGACAAGGGTCCAAACTCAAGTTCAGCAAATGTGTACTATACGGTAGTTGGCATCTAAATGTCATAGAATGGAGAAGGCCTCAACTGGGAGAGGACAAAGATGTGGGGTACAGCACAAAAAAGAGGCAGGTCTCAAAGTCATTCACAATCAGATTTTCTTGGCTGCTGGGGACAGGTGAGAGTTGTGCAGAAGGTTATGGTCCATACCAAAGAAAATCAAATTGCTACTCAGTAGTTGGTGTTTAAGGACTATTTGGGCTACAC... | CTCACTACAAATATGTGTCTAACACAACTAAGACCAAGGTCATAGGACTGTTGTTAGGACAAGGGTCCAAACTCAAGTTCAGCAAATGTGTACTATACGGTAGTTGGCATCTAAATGTCATAGAATGGAGAAGGCCTCAACTGGGAGAGGACAAAGATGTGGGGTACAGCACAAAAAAGAGGCAGGTCTCAAAGTCATTCACAATCAGATTTTCTTGGCTGCTGGGGACAGGTGAGAGTTGTGCAGAAGGTTATGGTCCATACCAAAGAAAATCAAATTGCTACTCAGTAGTTGGTGTTTAAGGACTATTTGGGCTACAC... |
Task1_train_47678 | An alteration has been detected on Chromosome 19. Is it pathogenic, and if so, what disease is involved? | Benign | CTTGCTTACAGACCATGAGGAGGTAAGTGGAGGATGTCTCAGGTCCTCACACTCCTGCACTCCTACCTACATGGTCTTCAGAATTATGGTGTCTTGAGGCTCCTTGCTGGCTATTCTCCCTACCCTTCCATTTGAGTTCCCTGGAAGATGGTCACACACAGTCAGGGCCCTGAGTCCAGACTATATATTATTTTTATTATTTTCTTTTAAGACAGAGTTTTGCTCTTGTTGCCCAGGCTGGAGTGCAAAGGCGCGATCTCGGCTCACTGCAACTTCTGGCTCCTGGGTTCAAGCAATTCTCCTGTCTGAGCCTCCCGAGT... | CTTGCTTACAGACCATGAGGAGGTAAGTGGAGGATGTCTCAGGTCCTCACACTCCTGCACTCCTACCTACATGGTCTTCAGAATTATGGTGTCTTGAGGCTCCTTGCTGGCTATTCTCCCTACCCTTCCATTTGAGTTCCCTGGAAGATGGTCACACACAGTCAGGGCCCTGAGTCCAGACTATATATTATTTTTATTATTTTCTTTTAAGACAGAGTTTTGCTCTTGTTGCCCAGGCTGGAGTGCAAAGGCGCGATCTCGGCTCACTGCAACTTCTGGCTCCTGGGTTCAAGCAATTCTCCTGTCTGAGCCTCCCGAGT... |
Task1_train_47679 | Chromosome 19 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GTGGGGCTGAGGATTGGCCCTGGCAGTCAGTGCCATTGGGGGTCTGGGATGGCACGGAGTTCTGATTGCATTTGGTAAGTGCCCTCTGGATGCCATGTGTAGACTGGCATGTGGTGACACTAGGGGAAGCACATGAGGTGATGTAGAGGGTAGTGGTTGTGGTACAAAGTATGTGCACATTCTAATAAGTGTAAACAGATGTCCCCAGGACCTTGTACTGGGGGCTTCAGGGAGAACACTGACACAAATTTGATTGTATTTGAGAAACACAGTCTAGGGGATCCAAGGTAAATTGTCTGGCAAGAGAAGAGTAGGACTCT... | GTGGGGCTGAGGATTGGCCCTGGCAGTCAGTGCCATTGGGGGTCTGGGATGGCACGGAGTTCTGATTGCATTTGGTAAGTGCCCTCTGGATGCCATGTGTAGACTGGCATGTGGTGACACTAGGGGAAGCACATGAGGTGATGTAGAGGGTAGTGGTTGTGGTACAAAGTATGTGCACATTCTAATAAGTGTAAACAGATGTCCCCAGGACCTTGTACTGGGGGCTTCAGGGAGAACACTGACACAAATTTGATTGTATTTGAGAAACACAGTCTAGGGGATCCAAGGTAAATTGTCTGGCAAGAGAAGAGTAGGACTCT... |
Task1_train_47680 | This mutation is located on Chromosome 19. Is it associated with a disease or is it a benign polymorphism? | Benign | TGGGTGCTTCAGGGAGAACACTGACACAAATTTGATTGTATTTGGGAAACACAATCTGGGGGATCCAAGGTGAGTTGTCTGGCAAGAGAAGAGTAGGACTCTGCATACCATGCCCAGAGCTGAGATGGACTTTATCTGCCTACCTGCCTCTGCTTGCTCAGTGGGAACATGAGGAGAGAGTGGGCATCAGTGGTTCTGGGGCAGGGTCTCTCTTCTGAGATGGGGATTAAGGAAGAGGGTGAGCAGGGGTGGATGTTTAGGGGGATGCCTAAATTCCCCAGTAAGGAGACCGCAGATAAACTCAACTCTGTCCATCTTAG... | TGGGTGCTTCAGGGAGAACACTGACACAAATTTGATTGTATTTGGGAAACACAATCTGGGGGATCCAAGGTGAGTTGTCTGGCAAGAGAAGAGTAGGACTCTGCATACCATGCCCAGAGCTGAGATGGACTTTATCTGCCTACCTGCCTCTGCTTGCTCAGTGGGAACATGAGGAGAGAGTGGGCATCAGTGGTTCTGGGGCAGGGTCTCTCTTCTGAGATGGGGATTAAGGAAGAGGGTGAGCAGGGGTGGATGTTTAGGGGGATGCCTAAATTCCCCAGTAAGGAGACCGCAGATAAACTCAACTCTGTCCATCTTAG... |
Task1_train_47681 | A genetic alteration is present on Chromosome 19. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GGGTGCTTCAGGGAGAACACTGACACAAATTTGATTGTATTTGGGAAACACAATCTGGGGGATCCAAGGTGAGTTGTCTGGCAAGAGAAGAGTAGGACTCTGCATACCATGCCCAGAGCTGAGATGGACTTTATCTGCCTACCTGCCTCTGCTTGCTCAGTGGGAACATGAGGAGAGAGTGGGCATCAGTGGTTCTGGGGCAGGGTCTCTCTTCTGAGATGGGGATTAAGGAAGAGGGTGAGCAGGGGTGGATGTTTAGGGGGATGCCTAAATTCCCCAGTAAGGAGACCGCAGATAAACTCAACTCTGTCCATCTTAGC... | GGGTGCTTCAGGGAGAACACTGACACAAATTTGATTGTATTTGGGAAACACAATCTGGGGGATCCAAGGTGAGTTGTCTGGCAAGAGAAGAGTAGGACTCTGCATACCATGCCCAGAGCTGAGATGGACTTTATCTGCCTACCTGCCTCTGCTTGCTCAGTGGGAACATGAGGAGAGAGTGGGCATCAGTGGTTCTGGGGCAGGGTCTCTCTTCTGAGATGGGGATTAAGGAAGAGGGTGAGCAGGGGTGGATGTTTAGGGGGATGCCTAAATTCCCCAGTAAGGAGACCGCAGATAAACTCAACTCTGTCCATCTTAGC... |
Task1_train_47682 | Located on Chromosome 19, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TGGGTGGCTGAGGTTGATGAAAGGAGTAGACTCAGGTAGGAAGGGCTTCAGAGCAGGATATGGGGCTGCCTGTGGCAGTAGGGACCATCATAGGTCTGGGTAGTCCTGGAACTTGTTTGAATTTGCAAGCACTTTCTAGATGTCTTGTGCTGAGTAACATATAGGAAGGCAGGAGAGATGCCTGTGTTGTGGGATCGGGGTGGAGGTGGCTGAGGGAGTGAGTTGGGTAAGAGAGGTGTGGTGGAAAGAGTGATGCACATATGAAGACGGAGTGTGAGCTTTTGTTTCATGAGTCTGGACATTGAGGACATGAGGGTGAA... | TGGGTGGCTGAGGTTGATGAAAGGAGTAGACTCAGGTAGGAAGGGCTTCAGAGCAGGATATGGGGCTGCCTGTGGCAGTAGGGACCATCATAGGTCTGGGTAGTCCTGGAACTTGTTTGAATTTGCAAGCACTTTCTAGATGTCTTGTGCTGAGTAACATATAGGAAGGCAGGAGAGATGCCTGTGTTGTGGGATCGGGGTGGAGGTGGCTGAGGGAGTGAGTTGGGTAAGAGAGGTGTGGTGGAAAGAGTGATGCACATATGAAGACGGAGTGTGAGCTTTTGTTTCATGAGTCTGGACATTGAGGACATGAGGGTGAA... |
Task1_train_47683 | The following genetic variant occurs on Chromosome 19. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GGCTGAGTTTATCTGGGATCTGCACATGGTTCTGGATTGCTGAATTGACCCATGAAATAGAGCCAGGAGGGGAAGATTTAATAGGTGGATTCAGGGCAACCCATGGCAGTGTGGCCGTTGATCAGGACCAGATGTAATCCTGGATGCATTATCCAAGCATTCTCTGGATGCTGTGTGCAGATTTGCATGTGGGGAAGCCATGGAGGTACCAGTGTTGTGGGTGTCCATAGATGTAAAGGAGGTATAGCCAAAAGGGTGATGTGCACATGGAGATGGAGTGTGAATTCATGAGCCCAGAGCTTTGGTATGGAGGGTTTCTG... | GGCTGAGTTTATCTGGGATCTGCACATGGTTCTGGATTGCTGAATTGACCCATGAAATAGAGCCAGGAGGGGAAGATTTAATAGGTGGATTCAGGGCAACCCATGGCAGTGTGGCCGTTGATCAGGACCAGATGTAATCCTGGATGCATTATCCAAGCATTCTCTGGATGCTGTGTGCAGATTTGCATGTGGGGAAGCCATGGAGGTACCAGTGTTGTGGGTGTCCATAGATGTAAAGGAGGTATAGCCAAAAGGGTGATGTGCACATGGAGATGGAGTGTGAATTCATGAGCCCAGAGCTTTGGTATGGAGGGTTTCTG... |
Task1_train_47684 | A mutation has occurred on Chromosome 19. What is the medical relevance of this mutation? | Benign | TGTGACAAGGAGTCCTGGAGAGAGAGGCTGTCCTTAAGCTCAGTTGTCCACCTCACACAGGGCTATGTGACCTTCAAGGATTTATTTGTTTACTTCTCTTAGGAGGAATGGGAGCTGCTGGATGAGGCTCAGAGACTCTTCTATTATGAAATAATGGCTTCTGTGCTTCGCATTTATAGTCTCCCTGGGTAAGGCCCCAGTATCCCATTTTTCTGGGCTGGGTCCTACTCTTCCTTTTTGCCCTAGGGGTTGCTCTTTCCTTTCCATAGCTAGAGCATGGGTACTGCTCTCTTCTCTGATTCCCTCACATAGGTCCCCTG... | TGTGACAAGGAGTCCTGGAGAGAGAGGCTGTCCTTAAGCTCAGTTGTCCACCTCACACAGGGCTATGTGACCTTCAAGGATTTATTTGTTTACTTCTCTTAGGAGGAATGGGAGCTGCTGGATGAGGCTCAGAGACTCTTCTATTATGAAATAATGGCTTCTGTGCTTCGCATTTATAGTCTCCCTGGGTAAGGCCCCAGTATCCCATTTTTCTGGGCTGGGTCCTACTCTTCCTTTTTGCCCTAGGGGTTGCTCTTTCCTTTCCATAGCTAGAGCATGGGTACTGCTCTCTTCTCTGATTCCCTCACATAGGTCCCCTG... |
Task1_train_47685 | A mutation found on Chromosome 19 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GAAACTTCCCTTGTCATTTCCTTTATGTACTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTAATGGTGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGGGCGATCTCGGCTCACTGCAACCTCTGCCTCCCATAATCAAGCGATTATCCTGCCTCAGCCTCCTGAGTAATCCCTCCTGGGATTACAAACGCACACCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCATACTGGTCCCAAACTCCTGACCTCAGTTGATCCACCCACCTCAGCCTCCCAAAGTGCTGAGAT... | GAAACTTCCCTTGTCATTTCCTTTATGTACTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTAATGGTGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGGGCGATCTCGGCTCACTGCAACCTCTGCCTCCCATAATCAAGCGATTATCCTGCCTCAGCCTCCTGAGTAATCCCTCCTGGGATTACAAACGCACACCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCATACTGGTCCCAAACTCCTGACCTCAGTTGATCCACCCACCTCAGCCTCCCAAAGTGCTGAGAT... |
Task1_train_47686 | Located on Chromosome 19, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | AAGATACACAATTCTGTAGGTCCTGAGGATTTCTGTACCTGCTCATCCTTAAGAGCCATAATAACGAACATCATGGAAACCTCTGTAAAAGGGGCACATTCTATTTATTGCAGTGTTATTGCAGTTTTCCACTCTCTATCAATCCAGTACTTCTATAACAATTATAATTCCTACTATAATCTTACCACCTGTGGTGCTACCCTGTGGAATTCAGGATATCAAGGCATACAGGACCTGGGGAACAGATTTCCCCCACTGGCACTGAACACGATGCAGTATTCCTTGTGAACAAGAGAACAATTTCATGTTGCTTTCAGAAA... | AAGATACACAATTCTGTAGGTCCTGAGGATTTCTGTACCTGCTCATCCTTAAGAGCCATAATAACGAACATCATGGAAACCTCTGTAAAAGGGGCACATTCTATTTATTGCAGTGTTATTGCAGTTTTCCACTCTCTATCAATCCAGTACTTCTATAACAATTATAATTCCTACTATAATCTTACCACCTGTGGTGCTACCCTGTGGAATTCAGGATATCAAGGCATACAGGACCTGGGGAACAGATTTCCCCCACTGGCACTGAACACGATGCAGTATTCCTTGTGAACAAGAGAACAATTTCATGTTGCTTTCAGAAA... |
Task1_train_47687 | This mutation is located on Chromosome 19. Is it associated with a disease or is it a benign polymorphism? | Benign | ACACAAATTAGGTCAAAGCTGTAATCAGAGCTGTTCTCTGCCATTTGCTCTAAGGGACAGAAAACAAGGACTCCCACAAAAGCTGTTAACTTGTTCATGCTGAGAACACACCTGTTTCCTCAATAGACTCCAAACAATAAACAGAACCCACAACATTAATGGTGGCTTAAAGAACAGGCCTTTATTATCATGAGCAATGTGAAGCAGGCAGTTCCAGAGCTGGGTGACTTGGATATTGGATATATCCATAACGAGCATCATATGAAATCAATCAACACAGGTAAGTCTCTGCAGGCTATTTGCAGAATCCTTCTGTGTCC... | ACACAAATTAGGTCAAAGCTGTAATCAGAGCTGTTCTCTGCCATTTGCTCTAAGGGACAGAAAACAAGGACTCCCACAAAAGCTGTTAACTTGTTCATGCTGAGAACACACCTGTTTCCTCAATAGACTCCAAACAATAAACAGAACCCACAACATTAATGGTGGCTTAAAGAACAGGCCTTTATTATCATGAGCAATGTGAAGCAGGCAGTTCCAGAGCTGGGTGACTTGGATATTGGATATATCCATAACGAGCATCATATGAAATCAATCAACACAGGTAAGTCTCTGCAGGCTATTTGCAGAATCCTTCTGTGTCC... |
Task1_train_47688 | This is a variant located on Chromosome 19. Is this mutation a likely cause of disease or not? | Benign | GTGGCTGTACCCCATGACCAGTGGGCCTAGTTTCTCCTATGTTTGAGGACCTTGAGAGGAGGATGTGCGAGAGTAGATGTGTGGGAGAGATGGATTGTGATACCTCAGCATAGGGGTGGTTTGTGGTTTCATCTGTCAACATCATAACAGGGCACAGTGACTTTTGAAGACGTGGCTGTGAAATTTACCCAGGAGGAATGGAATCTCCTTAGTGAGGCTCAGAGATGCCTGTACCGTGATGTGACTCTGGAGAACCTGGCACTTATGTCCTCCCTGGGTAAGTTGCTCACACTCACCCTGTGACTTGAGCTAGTCTCTGT... | GTGGCTGTACCCCATGACCAGTGGGCCTAGTTTCTCCTATGTTTGAGGACCTTGAGAGGAGGATGTGCGAGAGTAGATGTGTGGGAGAGATGGATTGTGATACCTCAGCATAGGGGTGGTTTGTGGTTTCATCTGTCAACATCATAACAGGGCACAGTGACTTTTGAAGACGTGGCTGTGAAATTTACCCAGGAGGAATGGAATCTCCTTAGTGAGGCTCAGAGATGCCTGTACCGTGATGTGACTCTGGAGAACCTGGCACTTATGTCCTCCCTGGGTAAGTTGCTCACACTCACCCTGTGACTTGAGCTAGTCTCTGT... |
Task1_train_47689 | Given this variant on Chromosome 19, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TTAGTCCTGTGGATGTTTGGGTGTCCTTGTCCAGATTTCAGGTTCCTGTGTACCCACAGTCTACTTCCTTTCTCTAGCTGCTATTTTCTTATGCCTTCCTGTGGCAGGAATTGCCTTCACAGACTACATCACTGCCTATATAGACCAGAGGCTGTTCTTGCAAGATCTTCTTTAGAAATTCTCCTTCAAATACTCAGTTTTTTTCTCTCATGGGCTGAGTTGTTCTGAGACAATGTTGGCTGTTCCCTTGTTCTGTCTTTCCCTTAGTCTGTGCATCATTCATGTCCCATGTATTTGGTCATCATTGTGGTGGGAGGCAC... | TTAGTCCTGTGGATGTTTGGGTGTCCTTGTCCAGATTTCAGGTTCCTGTGTACCCACAGTCTACTTCCTTTCTCTAGCTGCTATTTTCTTATGCCTTCCTGTGGCAGGAATTGCCTTCACAGACTACATCACTGCCTATATAGACCAGAGGCTGTTCTTGCAAGATCTTCTTTAGAAATTCTCCTTCAAATACTCAGTTTTTTTCTCTCATGGGCTGAGTTGTTCTGAGACAATGTTGGCTGTTCCCTTGTTCTGTCTTTCCCTTAGTCTGTGCATCATTCATGTCCCATGTATTTGGTCATCATTGTGGTGGGAGGCAC... |
Task1_train_47690 | A mutation on Chromosome 19 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TTCATTGTTCATAAGAGAGTTCACACTGGTCAGAAGCCTTATGAGTGCAGTGAATGTGGGAAATCTTTTGCTGCAAGCTCCTATCTCACTAGTCACAGGAGAGTTCACACTGGTCAGAAGCCTTATGAGTGCAGTGAATGTGGGAAATCTTTTGCTGGAATCTCCAGTCTCACTAATCACAGGAGAGTTCACACTGGAGAAAAGCCTTATGGGTGTAGTGAATGTGAAAAAAAATTTAGGAAAAGCTCTTCACTTCGTTACCATCAGAGAGTTCATGAAAGAAAGGCCTTATGAGTGCAGAGAATGAGTCCAGTCTCATT... | TTCATTGTTCATAAGAGAGTTCACACTGGTCAGAAGCCTTATGAGTGCAGTGAATGTGGGAAATCTTTTGCTGCAAGCTCCTATCTCACTAGTCACAGGAGAGTTCACACTGGTCAGAAGCCTTATGAGTGCAGTGAATGTGGGAAATCTTTTGCTGGAATCTCCAGTCTCACTAATCACAGGAGAGTTCACACTGGAGAAAAGCCTTATGGGTGTAGTGAATGTGAAAAAAAATTTAGGAAAAGCTCTTCACTTCGTTACCATCAGAGAGTTCATGAAAGAAAGGCCTTATGAGTGCAGAGAATGAGTCCAGTCTCATT... |
Task1_train_47691 | A mutation on Chromosome 19 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TTTCTCCCCATTGTTGAGAGTTTCACATGTGTTAGTTCTGTACCTTTTCATTTCTGCAGTGATATCCACCCCAGCACTAATACTCACATTTCTGGACTCCACATCTCACCCATTTTTCTTTTGCTTTCATCTGCAGTTGTCTCTGATATTGGTGTATTGATTACGTATTAGGAAGTGTATGCCCATGGTTAAACCATCTATGACCACCCCTGCTGTGTTGTACTCATGTTTTCTTGGTCTTCACATGTTTCTATATATATATAGATGTATATATATGTGTGTATGTGTATATATATATATGTGTGTGTGTATATGTATAT... | TTTCTCCCCATTGTTGAGAGTTTCACATGTGTTAGTTCTGTACCTTTTCATTTCTGCAGTGATATCCACCCCAGCACTAATACTCACATTTCTGGACTCCACATCTCACCCATTTTTCTTTTGCTTTCATCTGCAGTTGTCTCTGATATTGGTGTATTGATTACGTATTAGGAAGTGTATGCCCATGGTTAAACCATCTATGACCACCCCTGCTGTGTTGTACTCATGTTTTCTTGGTCTTCACATGTTTCTATATATATATAGATGTATATATATGTGTGTATGTGTATATATATATATGTGTGTGTGTATATGTATAT... |
Task1_train_47692 | This alteration occurs on Chromosome 19. Is it associated with a disease or is it a benign variant? | Benign | CTAAAAGGGCGAACAGATCGAACCGCATTAGGGTATCATTTTTAGGAGCGGCTATTGCTGAGCCTCCAGCTCCCATTCCTCTTGTTTGGTTAACTGCCAAACCAGTTTGGGTGGAGCAATGGCCGCTGAAACAGGAAAAAACTGGAGGCTTTAAAAGAATTAGTACAGGAACAATTGCAAAAGGGACACATAGAGCCTACTTTCTCTCCTTGGAATTCTCCTGTTTGTTATTAAGAAAAAAATCAGACGGACGCGGTGGCTCACGCCTGTAATCCCAGAACTTGGGAGGCCGAGGCGGGTGGATGGCAAGGTCAAGAGAT... | CTAAAAGGGCGAACAGATCGAACCGCATTAGGGTATCATTTTTAGGAGCGGCTATTGCTGAGCCTCCAGCTCCCATTCCTCTTGTTTGGTTAACTGCCAAACCAGTTTGGGTGGAGCAATGGCCGCTGAAACAGGAAAAAACTGGAGGCTTTAAAAGAATTAGTACAGGAACAATTGCAAAAGGGACACATAGAGCCTACTTTCTCTCCTTGGAATTCTCCTGTTTGTTATTAAGAAAAAAATCAGACGGACGCGGTGGCTCACGCCTGTAATCCCAGAACTTGGGAGGCCGAGGCGGGTGGATGGCAAGGTCAAGAGAT... |
Task1_train_47693 | Here is a genetic alteration on Chromosome 19. Based on the data, is it a benign variant or a cause of disease? | Benign | GTGAGACTCTGTCTCAAAAAAAAAAAAAAAAAAAAATTTAGGGATAATATCTAAGCCCATATAACCTGCTGTTATAAAAGGTAACATTTAGGGATTGAGATTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCACCAGGCTGGAGTGCAGTGGTGCAATCTCGGCTCACTGCAACCTATGCCTCCCAGGTTTAACGAATTCTCCTGCCTCAGCCTCCCAAGCAGCTGGGACTACAGGCACCCACCACTATGCTTGGGTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATATTGTCCAGG... | GTGAGACTCTGTCTCAAAAAAAAAAAAAAAAAAAAATTTAGGGATAATATCTAAGCCCATATAACCTGCTGTTATAAAAGGTAACATTTAGGGATTGAGATTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCACCAGGCTGGAGTGCAGTGGTGCAATCTCGGCTCACTGCAACCTATGCCTCCCAGGTTTAACGAATTCTCCTGCCTCAGCCTCCCAAGCAGCTGGGACTACAGGCACCCACCACTATGCTTGGGTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATATTGTCCAGG... |
Task1_train_47694 | A mutation has occurred on Chromosome 19. What is the medical relevance of this mutation? | Benign | CTTAATGAAAAATGTCCCCTCTTGATTATGTTTATAGGGTTTTCCTCAATGTGTTGTCAAATGTACAAGAAACGAAAAACTCGCATAAATTCAATTCAGTTTCTCTTCACTGTGATTTCTCTGGTGTTGAAGTAGGGCTGAGTGACCACTAAAGGCTTTTCCACATTCACTGCATATAAAGCGTTTCTCTCCACTATGCATTCTCTGATGAATAATAAGGGAAGAATTCTTACAAAATGCTTTTTCACAATGATTACATTTGTAGGGCTTTTCTCCAGTATGGTTTCTTAGGTGTACAATAAGGGATGAACTCTCATTAA... | CTTAATGAAAAATGTCCCCTCTTGATTATGTTTATAGGGTTTTCCTCAATGTGTTGTCAAATGTACAAGAAACGAAAAACTCGCATAAATTCAATTCAGTTTCTCTTCACTGTGATTTCTCTGGTGTTGAAGTAGGGCTGAGTGACCACTAAAGGCTTTTCCACATTCACTGCATATAAAGCGTTTCTCTCCACTATGCATTCTCTGATGAATAATAAGGGAAGAATTCTTACAAAATGCTTTTTCACAATGATTACATTTGTAGGGCTTTTCTCCAGTATGGTTTCTTAGGTGTACAATAAGGGATGAACTCTCATTAA... |
Task1_train_47695 | This sequence variant lies on Chromosome 19. Is it clinically significant, and what condition might it cause if any? | Benign | CTCTCAGCTCCCCTCTCCCCTGACAGGGCTTTGTCCTTCTGCATCTTTGCCCCTGTGACCCCACGTCGAGATTCCATCCACCCAGGGCCCAGTCCCATGAGTGGGGCTCTTTCTTTCCTAGTGACAAAAGTGCAGGGATTGGACACTGGGAGGCCAAAAGAGGCAGCCACGGATGGTGAGAGCAGTCGTGGCACTGTGGCCTCGGGAGGGCTTCCCCAGCAGGGCCCCAGCAAGGAGGGTGCCAGGCAGCCACGCTGCAGGAGCAAAGGCTGGGAGTGAGAAGGGTTGCATCAGAGCTCACAGAAAAGAGGGGTGGAGCA... | CTCTCAGCTCCCCTCTCCCCTGACAGGGCTTTGTCCTTCTGCATCTTTGCCCCTGTGACCCCACGTCGAGATTCCATCCACCCAGGGCCCAGTCCCATGAGTGGGGCTCTTTCTTTCCTAGTGACAAAAGTGCAGGGATTGGACACTGGGAGGCCAAAAGAGGCAGCCACGGATGGTGAGAGCAGTCGTGGCACTGTGGCCTCGGGAGGGCTTCCCCAGCAGGGCCCCAGCAAGGAGGGTGCCAGGCAGCCACGCTGCAGGAGCAAAGGCTGGGAGTGAGAAGGGTTGCATCAGAGCTCACAGAAAAGAGGGGTGGAGCA... |
Task1_train_47696 | This alteration occurs on Chromosome 19. Is it associated with a disease or is it a benign variant? | Benign | CGGCCCCTGAGGGAACGCGCGCCCCGCCCCTGGCCCCACCTCTGCCCCACACCGGGCACTGGGCCGCCACCTTTGTTGATGGAAGAGAGAAACTGAGGCATAGTGCCCAGGGCCAGGGGACCGCAACCACCCGGCCCTTGTCACTGTAGCGTTAAGGCTCAGAGTCTGCGCAGCAGATATGTGTCCGCACCCGCCAGGCCTTCAGCTTCCCTCAGACAGGCGGGAAAACCCTAGGCTGCCCTTCTCCGAGCGGAGGGCCGCCCCACACACAGCAGGCGCTTAAACGGGTACGCGGGGCCCTGGACGGCTCTCCGCGGAGC... | CGGCCCCTGAGGGAACGCGCGCCCCGCCCCTGGCCCCACCTCTGCCCCACACCGGGCACTGGGCCGCCACCTTTGTTGATGGAAGAGAGAAACTGAGGCATAGTGCCCAGGGCCAGGGGACCGCAACCACCCGGCCCTTGTCACTGTAGCGTTAAGGCTCAGAGTCTGCGCAGCAGATATGTGTCCGCACCCGCCAGGCCTTCAGCTTCCCTCAGACAGGCGGGAAAACCCTAGGCTGCCCTTCTCCGAGCGGAGGGCCGCCCCACACACAGCAGGCGCTTAAACGGGTACGCGGGGCCCTGGACGGCTCTCCGCGGAGC... |
Task1_train_47697 | This alteration occurs on Chromosome 19. Is it associated with a disease or is it a benign variant? | Benign | GGAACTAAGCTTGTAACTGTTGCGGAGACAGGCACTCCAGGTGACAGTTCACAGGCCCTTTCAAGTGACTGGAGCCATGGGATCATTTCTCTCCAAGGATTTGTGAGTAGAAGTGATGTGTGTCATCTCCCAGGTGAACAGGTTCGGCCTTCCCTACATGCTCCAAGGGTACAGTGAAGAGCAGAGCTACAACAGAGATGGGGCCTGGATCCCTGAATCACTGTATGGAGCAGAGTGCAAACCAATATATAAGCAACAGCAACACCAACACAGGACAATCGACTGTTAGTAAATAATTTTTTTTTCTTTTTTTCTTTTTT... | GGAACTAAGCTTGTAACTGTTGCGGAGACAGGCACTCCAGGTGACAGTTCACAGGCCCTTTCAAGTGACTGGAGCCATGGGATCATTTCTCTCCAAGGATTTGTGAGTAGAAGTGATGTGTGTCATCTCCCAGGTGAACAGGTTCGGCCTTCCCTACATGCTCCAAGGGTACAGTGAAGAGCAGAGCTACAACAGAGATGGGGCCTGGATCCCTGAATCACTGTATGGAGCAGAGTGCAAACCAATATATAAGCAACAGCAACACCAACACAGGACAATCGACTGTTAGTAAATAATTTTTTTTTCTTTTTTTCTTTTTT... |
Task1_train_47698 | A genetic alteration is present on Chromosome 19. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GTATAGTAGGGAGCCAGCCACGGTCCCTTGTGTTCTGTAGAGAGAGTCAAAGGCAGGTAGGGAGTGAGAAGACGTGCATTCATAAGGAAGGGTTCTGAGTGGAGAACCCTATTGGCTTGGCGGGGAGCAGTAAAAGGGTATATTGGCAGTCATCTAAGTCCTGAGCTGTGCTTGTTGCCAGAGGTTGTGGGTCAGTGCTGTGTTAACTATATTTGGTTTGGCTGTTGTGTTTTTATTCATTCCTTTGGTGCCTCTATACCTATCTTCATCTCCGAATAGCTCCAGTAGATTCATCCCGTGAAAGTAGCTGTGGTTCCTTG... | GTATAGTAGGGAGCCAGCCACGGTCCCTTGTGTTCTGTAGAGAGAGTCAAAGGCAGGTAGGGAGTGAGAAGACGTGCATTCATAAGGAAGGGTTCTGAGTGGAGAACCCTATTGGCTTGGCGGGGAGCAGTAAAAGGGTATATTGGCAGTCATCTAAGTCCTGAGCTGTGCTTGTTGCCAGAGGTTGTGGGTCAGTGCTGTGTTAACTATATTTGGTTTGGCTGTTGTGTTTTTATTCATTCCTTTGGTGCCTCTATACCTATCTTCATCTCCGAATAGCTCCAGTAGATTCATCCCGTGAAAGTAGCTGTGGTTCCTTG... |
Task1_train_47699 | Here’s a variant located on Chromosome 19. What is the predicted biological effect — harmless or disease-causing? | Benign | TGTTCTTGGAGGACTTGAGTGCTTGATTTGCCTGAAGAATGTTATGTGTCTGTTCAGAAGAGAGATTAGGACCTGCGAAGCTCATGCCTAGAGGGGAGAGTATTCCTGCAGAATTCAGCGTAGGAAAGGAGGCCTCAGGCACCAGAAGTGTTTGAGAGCAGGAGAGTTCTCAGAAGAGATTGCCTGGGAAATGAGAGCATCGCTGGGGTGAAGTCCCAGCAGCTGCGAGTGTTGAGGCTGCTGTGAGGTGGCCCATGCTTAGGCTCTGTGTTCCTGGCCAGAGTGAGTCCCCAGCACCGCAACATCTGCAGGAGATGATG... | TGTTCTTGGAGGACTTGAGTGCTTGATTTGCCTGAAGAATGTTATGTGTCTGTTCAGAAGAGAGATTAGGACCTGCGAAGCTCATGCCTAGAGGGGAGAGTATTCCTGCAGAATTCAGCGTAGGAAAGGAGGCCTCAGGCACCAGAAGTGTTTGAGAGCAGGAGAGTTCTCAGAAGAGATTGCCTGGGAAATGAGAGCATCGCTGGGGTGAAGTCCCAGCAGCTGCGAGTGTTGAGGCTGCTGTGAGGTGGCCCATGCTTAGGCTCTGTGTTCCTGGCCAGAGTGAGTCCCCAGCACCGCAACATCTGCAGGAGATGATG... |
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