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_38500 | Given this variant on Chromosome 7, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CAGCCACACTGCTATCACGCTGGACTCTGGCTCACCTGGCCTTCCTCTGGCACCTCCTGAGCTTTGGCACATGCTTCTCCGAGCTTCACCTGCATGGGTCTCAAATGCCTTCACTCCCAGCCTCAGGAGACCTTCTCTCCAGAGCTTCTGATCAGTCTCTCCTTGGTTCTCCTTCATATTCCTAAGAGACTTTCAAAAACCCCTCCACTCTCAGAACTTTCCCTGGCAACATAGTTAATTTCAACTGGGCTTTGAGTACACTGAGAGTGGGGCTGAGTCACCTCCACCTCTGTCCTCAGTAGCCCACAGTGTCTGGCACA... | CAGCCACACTGCTATCACGCTGGACTCTGGCTCACCTGGCCTTCCTCTGGCACCTCCTGAGCTTTGGCACATGCTTCTCCGAGCTTCACCTGCATGGGTCTCAAATGCCTTCACTCCCAGCCTCAGGAGACCTTCTCTCCAGAGCTTCTGATCAGTCTCTCCTTGGTTCTCCTTCATATTCCTAAGAGACTTTCAAAAACCCCTCCACTCTCAGAACTTTCCCTGGCAACATAGTTAATTTCAACTGGGCTTTGAGTACACTGAGAGTGGGGCTGAGTCACCTCCACCTCTGTCCTCAGTAGCCCACAGTGTCTGGCACA... |
Task1_train_38501 | Here is a genetic alteration on Chromosome 7. Based on the data, is it a benign variant or a cause of disease? | Benign | TGGCACCGAGTCCCAGCGAGCCAAGCAGCCCCACTACTCTGCAGAAGGGAACTTAAGCAAACGTTTGGCAGTGTTAGAATTTTGCAGCAAAAATATAAAATATTTGCTTAAAAAGTCTACAGACTATGTAAGGATGCTATATTATAAACAAATCTGTTGTGAATTTGAAAACCTACACTTAAGAGATACAGGGCAGAGAGTGTGGTGTTGGCGTGTTCTGTGTTGGCATGTTGGCCAACAGCAAGAAGCACATGTATGGAAGTAGAAGGCAGGATTCACAGCGATTGCACCTGACGTTTGCTCTTCCAAGTCGGGGGGGA... | TGGCACCGAGTCCCAGCGAGCCAAGCAGCCCCACTACTCTGCAGAAGGGAACTTAAGCAAACGTTTGGCAGTGTTAGAATTTTGCAGCAAAAATATAAAATATTTGCTTAAAAAGTCTACAGACTATGTAAGGATGCTATATTATAAACAAATCTGTTGTGAATTTGAAAACCTACACTTAAGAGATACAGGGCAGAGAGTGTGGTGTTGGCGTGTTCTGTGTTGGCATGTTGGCCAACAGCAAGAAGCACATGTATGGAAGTAGAAGGCAGGATTCACAGCGATTGCACCTGACGTTTGCTCTTCCAAGTCGGGGGGGA... |
Task1_train_38502 | A mutation is present on Chromosome 7. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | ATAAAATATTTGCTTAAAAAGTCTACAGACTATGTAAGGATGCTATATTATAAACAAATCTGTTGTGAATTTGAAAACCTACACTTAAGAGATACAGGGCAGAGAGTGTGGTGTTGGCGTGTTCTGTGTTGGCATGTTGGCCAACAGCAAGAAGCACATGTATGGAAGTAGAAGGCAGGATTCACAGCGATTGCACCTGACGTTTGCTCTTCCAAGTCGGGGGGGAGGGATCTGCTGAATCCTATGCACTCCCAGGCATGACTTATTCATGGGTATTCTAGAAAAAACTTGGGATGTATGGGGTTTCTCTTAATCCTCAC... | ATAAAATATTTGCTTAAAAAGTCTACAGACTATGTAAGGATGCTATATTATAAACAAATCTGTTGTGAATTTGAAAACCTACACTTAAGAGATACAGGGCAGAGAGTGTGGTGTTGGCGTGTTCTGTGTTGGCATGTTGGCCAACAGCAAGAAGCACATGTATGGAAGTAGAAGGCAGGATTCACAGCGATTGCACCTGACGTTTGCTCTTCCAAGTCGGGGGGGAGGGATCTGCTGAATCCTATGCACTCCCAGGCATGACTTATTCATGGGTATTCTAGAAAAAACTTGGGATGTATGGGGTTTCTCTTAATCCTCAC... |
Task1_train_38503 | This sequence change occurs on Chromosome 7. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TTTTCTTTTTTTTTTGAGATGGAGTCTTGCCCTGTCGCCCAGGCAGGAATGCAGTGGTGCGATCTCAGCTTACTGCAACCTCCACCTCCCGGGTTCAAGCAATTCTCCTGCCCCAGCCTCCTAAGTAGGGCGCGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACTATGTTGGTCAGGCTGGTCTCGAACTCTTGACCTCGTGATCCACCCGCCTCGGTCTCCCAAAGCACTAGTATTACAGGCGTGAGCCACCACATCCAGCCGACAAATTTTCTTAATAACAAAAGAGCTCATTGAAACC... | TTTTCTTTTTTTTTTGAGATGGAGTCTTGCCCTGTCGCCCAGGCAGGAATGCAGTGGTGCGATCTCAGCTTACTGCAACCTCCACCTCCCGGGTTCAAGCAATTCTCCTGCCCCAGCCTCCTAAGTAGGGCGCGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACTATGTTGGTCAGGCTGGTCTCGAACTCTTGACCTCGTGATCCACCCGCCTCGGTCTCCCAAAGCACTAGTATTACAGGCGTGAGCCACCACATCCAGCCGACAAATTTTCTTAATAACAAAAGAGCTCATTGAAACC... |
Task1_train_38504 | This genomic variant is located on Chromosome 7. Can you determine its pathogenicity and name any linked disease? | Benign | TATTCTGGAATGCTGGGGGTGGGGTGGATCAGAAAGAGGACATTCAGTGACTAGCCTCAGTCTAAGCCCACCTAGATCTAACTAGCTTCAGGACAAAGGGAAGTGCCATACTCCTGTCCAGTGTCAGGCAGTGTCAGGCAGAAGTTGGTGATAAAGGTTTATTTGCCATTTTATTTGTGCTTGAGATTCTCTTGGGGAAGTGTGGAGAATTTTTAGGACCTCATAGCTATAAAACTATTGTCTTAGTCTGTTTTCTGTTGCTATAACAGAATACCACAGCCTGGGTAATTTATAAACAACAGAAGTTTGTTTGGCTCACA... | TATTCTGGAATGCTGGGGGTGGGGTGGATCAGAAAGAGGACATTCAGTGACTAGCCTCAGTCTAAGCCCACCTAGATCTAACTAGCTTCAGGACAAAGGGAAGTGCCATACTCCTGTCCAGTGTCAGGCAGTGTCAGGCAGAAGTTGGTGATAAAGGTTTATTTGCCATTTTATTTGTGCTTGAGATTCTCTTGGGGAAGTGTGGAGAATTTTTAGGACCTCATAGCTATAAAACTATTGTCTTAGTCTGTTTTCTGTTGCTATAACAGAATACCACAGCCTGGGTAATTTATAAACAACAGAAGTTTGTTTGGCTCACA... |
Task1_train_38505 | A variant was discovered on Chromosome 7. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GTTTACTTTGGAATGCTCTTGGCTGAGTGGGGGGATTCATTCAGTCAGCTGGCGGGTGGTGGGGGGCTTAGAAGTTTATTTTTGGTTTACTCTGATAGGAGGAAGCCCACCCACATTATAGAGGACAGTCTACTTCACTCAAATTCTACCGTTTTTAATGTTATTTTCATCTAAAAAACTTCATAGACACAGCTAAAATAATGCTTTACCAATATCTGAGTACCATGGTCCAGCCAAGTTGACACATAAAATTAGACATTATACCTACCCAAGAAGAGGATATTGTGTTAGACTCTGAACATACTGCCCCTGTGACAGTA... | GTTTACTTTGGAATGCTCTTGGCTGAGTGGGGGGATTCATTCAGTCAGCTGGCGGGTGGTGGGGGGCTTAGAAGTTTATTTTTGGTTTACTCTGATAGGAGGAAGCCCACCCACATTATAGAGGACAGTCTACTTCACTCAAATTCTACCGTTTTTAATGTTATTTTCATCTAAAAAACTTCATAGACACAGCTAAAATAATGCTTTACCAATATCTGAGTACCATGGTCCAGCCAAGTTGACACATAAAATTAGACATTATACCTACCCAAGAAGAGGATATTGTGTTAGACTCTGAACATACTGCCCCTGTGACAGTA... |
Task1_train_38506 | A genomic variant on Chromosome 7 is under review. What is the biological outcome — benign or pathogenic? | Benign | CAGGCAATAGATGATTGACTATTTCTTTACCTCCCGCTTTTAGCCTAATTGGTATTTTAGTGAACGCTCTTTACTACCTGATTGGTCGGGTGTGAGCTGAGTTACAAGCCCCATGTTTAAAGGTGGGTGCGGTCGCCTTCCCCACCTAGGCTTAGGAATTCTTAGCTGGCCTAGGAAATCCAGCTAGTCCTGTCTCTCAGTAGGACTGACCACATCCTCCTGATGTAGAAATAGCAGCCTATCCCAAAGGGTTCTCATTAAAGACAAAAGGCACTAGGTAAAGCTAGAAATACATGAAATCCTAAATTTCTATGTTCAAT... | CAGGCAATAGATGATTGACTATTTCTTTACCTCCCGCTTTTAGCCTAATTGGTATTTTAGTGAACGCTCTTTACTACCTGATTGGTCGGGTGTGAGCTGAGTTACAAGCCCCATGTTTAAAGGTGGGTGCGGTCGCCTTCCCCACCTAGGCTTAGGAATTCTTAGCTGGCCTAGGAAATCCAGCTAGTCCTGTCTCTCAGTAGGACTGACCACATCCTCCTGATGTAGAAATAGCAGCCTATCCCAAAGGGTTCTCATTAAAGACAAAAGGCACTAGGTAAAGCTAGAAATACATGAAATCCTAAATTTCTATGTTCAAT... |
Task1_train_38507 | A variant was discovered on Chromosome 7. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GTCGGGTGTGAGCTGAGTTACAAGCCCCATGTTTAAAGGTGGGTGCGGTCGCCTTCCCCACCTAGGCTTAGGAATTCTTAGCTGGCCTAGGAAATCCAGCTAGTCCTGTCTCTCAGTAGGACTGACCACATCCTCCTGATGTAGAAATAGCAGCCTATCCCAAAGGGTTCTCATTAAAGACAAAAGGCACTAGGTAAAGCTAGAAATACATGAAATCCTAAATTTCTATGTTCAATATTGAGATATGGGGAGCCATCGTTCCCATAATATTTGAAATGTCTAAGAAATTTCTATTTGTGGACATGCAAACTTTATCTCCA... | GTCGGGTGTGAGCTGAGTTACAAGCCCCATGTTTAAAGGTGGGTGCGGTCGCCTTCCCCACCTAGGCTTAGGAATTCTTAGCTGGCCTAGGAAATCCAGCTAGTCCTGTCTCTCAGTAGGACTGACCACATCCTCCTGATGTAGAAATAGCAGCCTATCCCAAAGGGTTCTCATTAAAGACAAAAGGCACTAGGTAAAGCTAGAAATACATGAAATCCTAAATTTCTATGTTCAATATTGAGATATGGGGAGCCATCGTTCCCATAATATTTGAAATGTCTAAGAAATTTCTATTTGTGGACATGCAAACTTTATCTCCA... |
Task1_train_38508 | Here’s a variant located on Chromosome 7. What is the predicted biological effect — harmless or disease-causing? | Benign | CCTTTCTGTCTGACTGAAAGGTTGTATGCCACCCGCCTGGCCAAAACCTACTTGAAATTCCTCAAACTTTCAAAACATACCACTTCTTCTTTTCTGGCTTCCTGGATCCTTGATCTGCTTCATTCTTGGCTGCACATGCTAAGAAAAGCAGAGGAGTCTCTGGTGATTAGTCAATCCCAGCAAAACTGTGGCTTTGAGTGGTTACAAGCTTTAAAAGTCATATTCCTCTCATGTAACTGCCCAGGACAATGGGCTACCCCTGTTCAGCGCTCAAGTGGGACTGCAGAATGTTGAACGATTTGTTTGGAAAGATTATTTTG... | CCTTTCTGTCTGACTGAAAGGTTGTATGCCACCCGCCTGGCCAAAACCTACTTGAAATTCCTCAAACTTTCAAAACATACCACTTCTTCTTTTCTGGCTTCCTGGATCCTTGATCTGCTTCATTCTTGGCTGCACATGCTAAGAAAAGCAGAGGAGTCTCTGGTGATTAGTCAATCCCAGCAAAACTGTGGCTTTGAGTGGTTACAAGCTTTAAAAGTCATATTCCTCTCATGTAACTGCCCAGGACAATGGGCTACCCCTGTTCAGCGCTCAAGTGGGACTGCAGAATGTTGAACGATTTGTTTGGAAAGATTATTTTG... |
Task1_train_38509 | Given a variant located on Chromosome 7, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GATGGATCCTCTAGAGAATCAATTCCTTGCTTAGGTCAGATTTTTAATTCCTCTTTCCTGAAAGCCTCAAAAATTTAATAGCCCTAGAAAACCAGCACAAAACTAGTCTATATGTGCACAAGGACACATTTAATTTTATATTTGTGGACCCATAGCAGTTGGCACAGTGTCTTTCATCATGGATAGTGGTAGATAATTAGATGTTGATTTAATGAATGAAAAATCATTGAACATTAAGTGCAATTTATATTAAGAAAGCTGAACTTGAAATGACAAAACCTGGGTCGTCTCCTAGTCATGCCACATAATAACAGCTTGAA... | GATGGATCCTCTAGAGAATCAATTCCTTGCTTAGGTCAGATTTTTAATTCCTCTTTCCTGAAAGCCTCAAAAATTTAATAGCCCTAGAAAACCAGCACAAAACTAGTCTATATGTGCACAAGGACACATTTAATTTTATATTTGTGGACCCATAGCAGTTGGCACAGTGTCTTTCATCATGGATAGTGGTAGATAATTAGATGTTGATTTAATGAATGAAAAATCATTGAACATTAAGTGCAATTTATATTAAGAAAGCTGAACTTGAAATGACAAAACCTGGGTCGTCTCCTAGTCATGCCACATAATAACAGCTTGAA... |
Task1_train_38510 | Consider a variant on Chromosome 7. Determine its clinical classification and disease relevance. | Benign | TAAATTTTTCTGTTCCAGAAAATGAGATTCTGAGTACAAGTTTTAACTTTTCCCAGTTGTTCCATTCAGATTGGCCTAAATCACCAGCTATGAACATAGATTTTGTACGTTTAAGTGAGGCTATAATAACTAGTCTCCATGAATTTGGATTTTTGGAGCAGGAACAGATCTCAGAAGCTCTGAACACAGTCTACGCTATCAGGAATGCATCTGATCTTTTCTCAGCCCTTTCTGAACCACAAAAACAAGAAGTTGATAAAATTTTGACTCACATACACCTAAATGTCTTCCAGGACAAGGATTCAGCTTTACTTCTGCAA... | TAAATTTTTCTGTTCCAGAAAATGAGATTCTGAGTACAAGTTTTAACTTTTCCCAGTTGTTCCATTCAGATTGGCCTAAATCACCAGCTATGAACATAGATTTTGTACGTTTAAGTGAGGCTATAATAACTAGTCTCCATGAATTTGGATTTTTGGAGCAGGAACAGATCTCAGAAGCTCTGAACACAGTCTACGCTATCAGGAATGCATCTGATCTTTTCTCAGCCCTTTCTGAACCACAAAAACAAGAAGTTGATAAAATTTTGACTCACATACACCTAAATGTCTTCCAGGACAAGGATTCAGCTTTACTTCTGCAA... |
Task1_train_38511 | This mutation is located on Chromosome 7. Is it associated with a disease or is it a benign polymorphism? | Benign | TTCCACAAAGCAAGTAAGGATGAGTATCAACAACTTAACAACAGACTTTGATTTTGCATCTCAGTCCAATTGGAGATATTTTACTGAATTAATTCTAAGACCAATAGAAATGTCAGATGAAATTCCTAATCAGTTTCAAAATATTTGGCTTCATTTAATAACACTGGGGAAGGAATTTCAGAAGCTTGTAAAAGGTATTTACTTTAACATCCTGGAAAATAATTCCTCTTCTAAAACTGAAAACTTGTTAAACATATTTGCCACCAGTCCAAAAGAAAAGGATGTAAACAGTGTAGGCAATTCCATTTATCACTTAGCTA... | TTCCACAAAGCAAGTAAGGATGAGTATCAACAACTTAACAACAGACTTTGATTTTGCATCTCAGTCCAATTGGAGATATTTTACTGAATTAATTCTAAGACCAATAGAAATGTCAGATGAAATTCCTAATCAGTTTCAAAATATTTGGCTTCATTTAATAACACTGGGGAAGGAATTTCAGAAGCTTGTAAAAGGTATTTACTTTAACATCCTGGAAAATAATTCCTCTTCTAAAACTGAAAACTTGTTAAACATATTTGCCACCAGTCCAAAAGAAAAGGATGTAAACAGTGTAGGCAATTCCATTTATCACTTAGCTA... |
Task1_train_38512 | Mutation context: Chromosome 7. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TTCAAAATATTTGGCTTCATTTAATAACACTGGGGAAGGAATTTCAGAAGCTTGTAAAAGGTATTTACTTTAACATCCTGGAAAATAATTCCTCTTCTAAAACTGAAAACTTGTTAAACATATTTGCCACCAGTCCAAAAGAAAAGGATGTAAACAGTGTAGGCAATTCCATTTATCACTTAGCTAGTTACCTTGCCTTCAGCTTATCTCATGACCTCCAAAATTCACCAAAAATAATAATTTCACCTGAAATAATGAAAGCTACAGGTCTTGGTATTCAACTGATAAGGGATGTGTTCAACTCCTTAATGCCTGTAGTT... | TTCAAAATATTTGGCTTCATTTAATAACACTGGGGAAGGAATTTCAGAAGCTTGTAAAAGGTATTTACTTTAACATCCTGGAAAATAATTCCTCTTCTAAAACTGAAAACTTGTTAAACATATTTGCCACCAGTCCAAAAGAAAAGGATGTAAACAGTGTAGGCAATTCCATTTATCACTTAGCTAGTTACCTTGCCTTCAGCTTATCTCATGACCTCCAAAATTCACCAAAAATAATAATTTCACCTGAAATAATGAAAGCTACAGGTCTTGGTATTCAACTGATAAGGGATGTGTTCAACTCCTTAATGCCTGTAGTT... |
Task1_train_38513 | Given a variant located on Chromosome 7, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TATGCAAATGAGGATTACTCCAGAATGATAGAAACATTATTCATTCCTGTGACCAATGAGAGTTCAACTGAAGATATAGCTTTGTTAGCCAAAGCTATTGCTACTTTTTGGGGCTCTTTAAAAAATATATCTAGAGCAGGCAATTTTGATGTTGCCTTTCTTACCCATCTGCTAAATCAAGAACAGCTGACTAATTTCTCAGTTGTTCAGCTGCTTTTTGAAAACATCCTAATTAATTTGATCAATAACTTAGCTGGGAATTCTCAGGAAGCAGCTTGGAACTTAAATGATACTGACCTTCAAATAATGAATTTCATTAA... | TATGCAAATGAGGATTACTCCAGAATGATAGAAACATTATTCATTCCTGTGACCAATGAGAGTTCAACTGAAGATATAGCTTTGTTAGCCAAAGCTATTGCTACTTTTTGGGGCTCTTTAAAAAATATATCTAGAGCAGGCAATTTTGATGTTGCCTTTCTTACCCATCTGCTAAATCAAGAACAGCTGACTAATTTCTCAGTTGTTCAGCTGCTTTTTGAAAACATCCTAATTAATTTGATCAATAACTTAGCTGGGAATTCTCAGGAAGCAGCTTGGAACTTAAATGATACTGACCTTCAAATAATGAATTTCATTAA... |
Task1_train_38514 | Consider this mutation on Chromosome 7. Is this a benign change or a disease-causing variant? | Benign | CACAATTTTGGGGGCTGGCTGAGTAAGTCTGCAATCAGTAGGGCTGACTGTCAGGAAGGGAGGCCCACAGTAGGCAGGGGCGCCCACAGCAGGCAGGGGCGCTGCGGGCATGAGTGAAAGCTCCTTGTCCACAGTGGTCAGGAAGGAAGACCAGGGGAAGGGAGAGCCACTGACTATGAATACCCAGCAGTGGTTTTGTGCCTCTAAGTTACAGAGGTTCTATGCCCTCTTTCAGAGTTTTCCTGGCCCACTCAGGACAGTATCCCTTCTGACTAATTTAAAGTTAACTGATCAGGGATTTTAACTCCATCTGCAAAATC... | CACAATTTTGGGGGCTGGCTGAGTAAGTCTGCAATCAGTAGGGCTGACTGTCAGGAAGGGAGGCCCACAGTAGGCAGGGGCGCCCACAGCAGGCAGGGGCGCTGCGGGCATGAGTGAAAGCTCCTTGTCCACAGTGGTCAGGAAGGAAGACCAGGGGAAGGGAGAGCCACTGACTATGAATACCCAGCAGTGGTTTTGTGCCTCTAAGTTACAGAGGTTCTATGCCCTCTTTCAGAGTTTTCCTGGCCCACTCAGGACAGTATCCCTTCTGACTAATTTAAAGTTAACTGATCAGGGATTTTAACTCCATCTGCAAAATC... |
Task1_train_38515 | Located on Chromosome 7, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | GCGAGGGCTTGCATATCTCTCTTCTGCTTGATGATCAAAGTGCTATAATAGTCTTTATATCAGCCTTTTTAATTCTAATCAGTTGTAGAATTTAGGCCTTTAGGTAAGTTACGTTCATCAAACTTAAACTAGAATGGATGTGTTAAAAGAAAATTGGGAAATGTTAATAATGAAATCCCTTTTCATTTCAACATGTAATGAGGGCAAAGTGACTGTTAAATGGGCTGAAATGAATTTGGAGAATACTTTTGAAGAATGGTAACGTGTTTCATATGGAAATGTTAGCATTATGAATTATTCTTCTTTATGGAAATTTCAAT... | GCGAGGGCTTGCATATCTCTCTTCTGCTTGATGATCAAAGTGCTATAATAGTCTTTATATCAGCCTTTTTAATTCTAATCAGTTGTAGAATTTAGGCCTTTAGGTAAGTTACGTTCATCAAACTTAAACTAGAATGGATGTGTTAAAAGAAAATTGGGAAATGTTAATAATGAAATCCCTTTTCATTTCAACATGTAATGAGGGCAAAGTGACTGTTAAATGGGCTGAAATGAATTTGGAGAATACTTTTGAAGAATGGTAACGTGTTTCATATGGAAATGTTAGCATTATGAATTATTCTTCTTTATGGAAATTTCAAT... |
Task1_train_38516 | This variant is present on Chromosome 7. Is the change likely to result in a pathogenic outcome? | Benign | TTATGGAATCGGTGTTCCAACCAAGGTTTCCAGGCCAGGCTGGAGATGGCTTCCAATCAAGTGTCCAGGATATTGGAGATACCGAGACAGAGGGATCAGCACCCTCAAAAGCAGATCTGCCCAATCAAACAGTGGTTCTCCTGGTCTGGGCTGCGCTGGCTAGGCTGGGCTGGGTGCCGTGCTCAGGAAGAAATGGTGAGCAACAGGCCCTAGGATTGTGGAGGGATTCAAATACTATTTCAAAACGCATAGGTAACAAGAAGCCATTGATACATTTTGAGCAAAGAAAATGTCAGATTGGTATGTTAGAAGAGCTCACT... | TTATGGAATCGGTGTTCCAACCAAGGTTTCCAGGCCAGGCTGGAGATGGCTTCCAATCAAGTGTCCAGGATATTGGAGATACCGAGACAGAGGGATCAGCACCCTCAAAAGCAGATCTGCCCAATCAAACAGTGGTTCTCCTGGTCTGGGCTGCGCTGGCTAGGCTGGGCTGGGTGCCGTGCTCAGGAAGAAATGGTGAGCAACAGGCCCTAGGATTGTGGAGGGATTCAAATACTATTTCAAAACGCATAGGTAACAAGAAGCCATTGATACATTTTGAGCAAAGAAAATGTCAGATTGGTATGTTAGAAGAGCTCACT... |
Task1_train_38517 | Here is a genetic alteration on Chromosome 7. Based on the data, is it a benign variant or a cause of disease? | Benign | AGATACCGAGACAGAGGGATCAGCACCCTCAAAAGCAGATCTGCCCAATCAAACAGTGGTTCTCCTGGTCTGGGCTGCGCTGGCTAGGCTGGGCTGGGTGCCGTGCTCAGGAAGAAATGGTGAGCAACAGGCCCTAGGATTGTGGAGGGATTCAAATACTATTTCAAAACGCATAGGTAACAAGAAGCCATTGATACATTTTGAGCAAAGAAAATGTCAGATTGGTATGTTAGAAGAGCTCACTAAAGGAATTAGAGAAATTGGGAGTCTGTAATGTTCCATTCTATGTGTACGGTCACACTGAACAGTAGCCTAATGAG... | AGATACCGAGACAGAGGGATCAGCACCCTCAAAAGCAGATCTGCCCAATCAAACAGTGGTTCTCCTGGTCTGGGCTGCGCTGGCTAGGCTGGGCTGGGTGCCGTGCTCAGGAAGAAATGGTGAGCAACAGGCCCTAGGATTGTGGAGGGATTCAAATACTATTTCAAAACGCATAGGTAACAAGAAGCCATTGATACATTTTGAGCAAAGAAAATGTCAGATTGGTATGTTAGAAGAGCTCACTAAAGGAATTAGAGAAATTGGGAGTCTGTAATGTTCCATTCTATGTGTACGGTCACACTGAACAGTAGCCTAATGAG... |
Task1_train_38518 | Here is a genetic alteration on Chromosome 7. Based on the data, is it a benign variant or a cause of disease? | Benign | CCAGCCTGGGCAACGAGCAAAACTGTGTCTCAAAAAAAAAACAAAACAAAACAAAACAAAAAAAACAAACAAACACAAACAGAAGTCTCAGAATCTACAAAGGGTGAAACTAGGGAGGCTGAGCAGGCAGCCTCCTGTCTTTCCAGCTCCATTCAGCCAAAGAAGCTCTGTTTTTGTTTCTGTACTGTAGTGTGGTGTCATTTTTAAGTTTTTTTTTTAATCACTCTACTTTTAAAACAAAAATTAAAATAATAAAACAAATCAAAACAAAATTTAAAAAACCTTAATTCAGGGCAGGGACTATCCTTGTGTCTTCTATT... | CCAGCCTGGGCAACGAGCAAAACTGTGTCTCAAAAAAAAAACAAAACAAAACAAAACAAAAAAAACAAACAAACACAAACAGAAGTCTCAGAATCTACAAAGGGTGAAACTAGGGAGGCTGAGCAGGCAGCCTCCTGTCTTTCCAGCTCCATTCAGCCAAAGAAGCTCTGTTTTTGTTTCTGTACTGTAGTGTGGTGTCATTTTTAAGTTTTTTTTTTAATCACTCTACTTTTAAAACAAAAATTAAAATAATAAAACAAATCAAAACAAAATTTAAAAAACCTTAATTCAGGGCAGGGACTATCCTTGTGTCTTCTATT... |
Task1_train_38519 | Chromosome 7 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GAGAAGCGGCCATGGACATATCTTTTCAGATGTGTCAAAAGAGTCTGTTCCTGTGGCTACCTGAATAACAAAGACCTAGGCAGAAATCATTGAGTTGTAGATACAAACACTCTCAGACTAGCCAGACAATTGCAGGAGGACTGGGGAAGGAAGAATAAGATAGTATCTCCGGAACTTAAGGAGAAGATCTCTTGAGAAGCAAATGCCAATAACTAGAGGGAAACCACCTCAGGCTGAAAGGGTAGATAACAGTCTCCATCGTCTCTGGTGCCACGTGGTCAATCATTGTTGTTTCTCTCTAGGAGTCTGCTTTATTACTT... | GAGAAGCGGCCATGGACATATCTTTTCAGATGTGTCAAAAGAGTCTGTTCCTGTGGCTACCTGAATAACAAAGACCTAGGCAGAAATCATTGAGTTGTAGATACAAACACTCTCAGACTAGCCAGACAATTGCAGGAGGACTGGGGAAGGAAGAATAAGATAGTATCTCCGGAACTTAAGGAGAAGATCTCTTGAGAAGCAAATGCCAATAACTAGAGGGAAACCACCTCAGGCTGAAAGGGTAGATAACAGTCTCCATCGTCTCTGGTGCCACGTGGTCAATCATTGTTGTTTCTCTCTAGGAGTCTGCTTTATTACTT... |
Task1_train_38520 | Given a variant located on Chromosome 7, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CCAAACCAAAACTTAGGGATGAAGCTTCACGAAGCTCTCTTTTGTGAAGGAGAGAGGCCTGTTCCGTTGCCAAGGAGTGCAAAGCTGCACATTGGCTTTGGGATGACATTGGGTATAAAATTTATCACTTGTGATATCCCTGTGTGATCTTCTACACACATTGTTTAGCTTCTCCAAGACTTTTCTTTGGAAAGCCCACATAGAACAGAAAAAAGAAATGCCATCTTTTAAACTATCTATTTAACTATCTTGTGGCCCCATGTTTCCAAGGTTGGGGTATTGGGAGAGTTGGTGAAAGAGCAATATGTCAACATTAACTT... | CCAAACCAAAACTTAGGGATGAAGCTTCACGAAGCTCTCTTTTGTGAAGGAGAGAGGCCTGTTCCGTTGCCAAGGAGTGCAAAGCTGCACATTGGCTTTGGGATGACATTGGGTATAAAATTTATCACTTGTGATATCCCTGTGTGATCTTCTACACACATTGTTTAGCTTCTCCAAGACTTTTCTTTGGAAAGCCCACATAGAACAGAAAAAAGAAATGCCATCTTTTAAACTATCTATTTAACTATCTTGTGGCCCCATGTTTCCAAGGTTGGGGTATTGGGAGAGTTGGTGAAAGAGCAATATGTCAACATTAACTT... |
Task1_train_38521 | Located on Chromosome 7, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | ATGAGGAAAAAGTCTTGTTCATCAGCCATCTTAGAATCCAACTCTAAGGCTTAAAACATACCTGCTTGCTGAACATGGGATCCTTGTTGAACTTGCTGAACTTGCTGAACTTGGCATCCTCCATTCTTTTTCACCTCAATTTTCTCATCTTAAAAATGAAGGATGATAACCAAATGGCTCATAAATTCCTCTCTGACTTTTGGGTTTATTTCCCATTGTATTCTTATCTTGATTTTAATTTTAAAAATTCCAGTGATCATCTCAGAAACAGTTAATATTTTATTAAGGTTGTGATACTTCACTCAGAATGGAAAAGTTTT... | ATGAGGAAAAAGTCTTGTTCATCAGCCATCTTAGAATCCAACTCTAAGGCTTAAAACATACCTGCTTGCTGAACATGGGATCCTTGTTGAACTTGCTGAACTTGCTGAACTTGGCATCCTCCATTCTTTTTCACCTCAATTTTCTCATCTTAAAAATGAAGGATGATAACCAAATGGCTCATAAATTCCTCTCTGACTTTTGGGTTTATTTCCCATTGTATTCTTATCTTGATTTTAATTTTAAAAATTCCAGTGATCATCTCAGAAACAGTTAATATTTTATTAAGGTTGTGATACTTCACTCAGAATGGAAAAGTTTT... |
Task1_train_38522 | A variant was discovered on Chromosome 7. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GACTAGAGCGAGGCACCATCTCAAAAAAAAAAAAAAGAAAAAAAAAGATTCTTGTTCATATAGCAAGCTGAAGTTGATGATAATTCCATTTGAATACATTTTTTAAAATGTAATTTTTTTCTACTAATTCTTAACATGTGAATGTTAGTTCTAAAACTTTATTGGTATATTGGTATTTTTAATTTACATATCATGTGGTAAAATGGCAAATAGCTCAGGGAGATGATAATTTTTTTATTCCAGTTTACATAGATCCACTTAATTTGTTGATTATAAGTCAGCTGGCAAATGAAAAGCTATGTGGGTTAGTCAGCACTGCC... | GACTAGAGCGAGGCACCATCTCAAAAAAAAAAAAAAGAAAAAAAAAGATTCTTGTTCATATAGCAAGCTGAAGTTGATGATAATTCCATTTGAATACATTTTTTAAAATGTAATTTTTTTCTACTAATTCTTAACATGTGAATGTTAGTTCTAAAACTTTATTGGTATATTGGTATTTTTAATTTACATATCATGTGGTAAAATGGCAAATAGCTCAGGGAGATGATAATTTTTTTATTCCAGTTTACATAGATCCACTTAATTTGTTGATTATAAGTCAGCTGGCAAATGAAAAGCTATGTGGGTTAGTCAGCACTGCC... |
Task1_train_38523 | This variant lies on Chromosome 7. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ATATTACAGTATTCTTCATATTCAATGGCAATGTGTGAAGTGGGAAGTGTCTTGACAGAATTCGGTGTTTCAAGGCTTACACTTTGATGCCCAAGACTGCACAAGGCTACATTTTCTACTGGTGAGACAAATTCCAGACGCATTGCATTCAGATCTAATCTCTTAGCTCCTTAATCTTCAGGGTACTGGTAAACATGAAGACCTCCCCAGTGCTGTAGTCATCATGATATGTACAGCAGGTGGCTGAGCTCTGGATGTAGACTGCAGGGATATATTAGGAAGTTAATTCTCAAGGCAAGTCATCTTCAAGCACCATATCA... | ATATTACAGTATTCTTCATATTCAATGGCAATGTGTGAAGTGGGAAGTGTCTTGACAGAATTCGGTGTTTCAAGGCTTACACTTTGATGCCCAAGACTGCACAAGGCTACATTTTCTACTGGTGAGACAAATTCCAGACGCATTGCATTCAGATCTAATCTCTTAGCTCCTTAATCTTCAGGGTACTGGTAAACATGAAGACCTCCCCAGTGCTGTAGTCATCATGATATGTACAGCAGGTGGCTGAGCTCTGGATGTAGACTGCAGGGATATATTAGGAAGTTAATTCTCAAGGCAAGTCATCTTCAAGCACCATATCA... |
Task1_train_38524 | Here is a variant on Chromosome 7. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CTTAAATAACACTAAGCAATACTTTGTCCAAATGTAAACCATTATACTAGCTGACATTAAGAATTATGTGGCCATCAGAAGGCACTTTCTTCAATAAAAGATGAATATTAATCAGACACAACTTTATATGTAATCTTCAACTAAAAAAAATTTGAGCTCACTTTTCATGTTATATAGCTTCAAGATAAAGACTTCTTAGAAACAAAAGTTCATTCTCACTTTGTTCAAATAGGCTTACGTATCAGGTAATCACTGGAAAGCAAAACTTACATTAACATACACTATGTCAATCAGATGTAAAATCTGTGCTATTATTTGAA... | CTTAAATAACACTAAGCAATACTTTGTCCAAATGTAAACCATTATACTAGCTGACATTAAGAATTATGTGGCCATCAGAAGGCACTTTCTTCAATAAAAGATGAATATTAATCAGACACAACTTTATATGTAATCTTCAACTAAAAAAAATTTGAGCTCACTTTTCATGTTATATAGCTTCAAGATAAAGACTTCTTAGAAACAAAAGTTCATTCTCACTTTGTTCAAATAGGCTTACGTATCAGGTAATCACTGGAAAGCAAAACTTACATTAACATACACTATGTCAATCAGATGTAAAATCTGTGCTATTATTTGAA... |
Task1_train_38525 | A mutation on Chromosome 7 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TAAAATGCACAGTGTTGTTGTGAGAATTAAATGAGTTAATGCCTGGAAAATGCTTAGGCACAGTGGCCGGCGATGGGGAACCCCACACAAACGATAGTTGCTGTAGTTGTTACTTCCACGCACCTGCTGTGAGATAGCGGCTGTGCTACCTACCATAGCTAGGGGCCTGGGGAACTGAGTGCCCTGCCCTGGGGAAGCGAGTGAAAGACAGCACTGGGATCCTAATCCAGATCCTGCCAATCCCAAAGCCAGCATTTTCCCAAGAGCTCGGTTTTGTTTATTCTCCAGGAGAAATTTGAGGAACTAACAAGAAGCATGAG... | TAAAATGCACAGTGTTGTTGTGAGAATTAAATGAGTTAATGCCTGGAAAATGCTTAGGCACAGTGGCCGGCGATGGGGAACCCCACACAAACGATAGTTGCTGTAGTTGTTACTTCCACGCACCTGCTGTGAGATAGCGGCTGTGCTACCTACCATAGCTAGGGGCCTGGGGAACTGAGTGCCCTGCCCTGGGGAAGCGAGTGAAAGACAGCACTGGGATCCTAATCCAGATCCTGCCAATCCCAAAGCCAGCATTTTCCCAAGAGCTCGGTTTTGTTTATTCTCCAGGAGAAATTTGAGGAACTAACAAGAAGCATGAG... |
Task1_train_38526 | This alteration on Chromosome 7 may affect genome function. Does it lead to a disease or is it benign? | Benign | GCCGGAGGGCATAAATGATGGTGAGCAATGCAATGGGATCTGCTACATGTGTGGGTTTTGCTTGCACGGTTTCAGGGATTCACGCGTCCCCTCATAAGTAATTGAATGACAAGTTGAGAGTTCACTTAGGCGTACTGAAATGCATTTCTGTCGTCTGGGGCACTGCTGTGGCACACTGAGAAGACAGCTAGAAGCTCGGGTCCTGAGTCTAAACCCACTTTTTGTGATGTATTTGTCAATGACCTTGGAAGATGACTTTATCCTCCCTGGGCCTCAGGTTCCTTAAGAGCACATGTCTCGTGGTCACTCCTGATGAAGGC... | GCCGGAGGGCATAAATGATGGTGAGCAATGCAATGGGATCTGCTACATGTGTGGGTTTTGCTTGCACGGTTTCAGGGATTCACGCGTCCCCTCATAAGTAATTGAATGACAAGTTGAGAGTTCACTTAGGCGTACTGAAATGCATTTCTGTCGTCTGGGGCACTGCTGTGGCACACTGAGAAGACAGCTAGAAGCTCGGGTCCTGAGTCTAAACCCACTTTTTGTGATGTATTTGTCAATGACCTTGGAAGATGACTTTATCCTCCCTGGGCCTCAGGTTCCTTAAGAGCACATGTCTCGTGGTCACTCCTGATGAAGGC... |
Task1_train_38527 | A mutation is present on Chromosome 7. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GGAAGTAGGGGGTGCAGCCATCATGCCGCGTCCACAGGGGAAGTGGCAGGGAGGCGCAACTGCGGTGCCGCATTCAAATGGGAAGTGGGGGTGCAGCCATCATGCCACAACCACAGAAGTGGGGGGTGCAGCCGTGGTGCTGCATTCATGCAGGAAGGGAGGTAGGGCACAGCCATGGAGCCATGTCCATGCAGGAAGTGGGGTGGAGTGGACGTCCTGCCACGTTCACACGGCAAGAGGGGAGGCAGCCGTGGTGCAGATTTGACTGTCCTGAGCTCCAAGACACAGAGACATCAGCAGGGCCCCGCCTCCTCAGACAG... | GGAAGTAGGGGGTGCAGCCATCATGCCGCGTCCACAGGGGAAGTGGCAGGGAGGCGCAACTGCGGTGCCGCATTCAAATGGGAAGTGGGGGTGCAGCCATCATGCCACAACCACAGAAGTGGGGGGTGCAGCCGTGGTGCTGCATTCATGCAGGAAGGGAGGTAGGGCACAGCCATGGAGCCATGTCCATGCAGGAAGTGGGGTGGAGTGGACGTCCTGCCACGTTCACACGGCAAGAGGGGAGGCAGCCGTGGTGCAGATTTGACTGTCCTGAGCTCCAAGACACAGAGACATCAGCAGGGCCCCGCCTCCTCAGACAG... |
Task1_train_38528 | Here’s a variant located on Chromosome 7. What is the predicted biological effect — harmless or disease-causing? | Benign | GCAGTAATGTGCAGACCAGCACAAGACCAAAATGGAGAAGCCGGGGAAATCCAGAAAGTGCATGCTCTGCCCAAGGGACTTCAGATTCCGTAACTGTCCAACATTAGGCTGGAATGCAAGCATGTACGAGTGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATAAGACTGGCGGCTTCCGTGCCAGCTGAGGGCCATGAGTTTGTGATGTGTGCTCTGTGGGGCCCCAAATGGATGATCTTCCATCCTCTCCATGGACCAGTAGAAACTGTGGGTTAGGGTGGAACTGAGCTTGGGTTACAGTGGGGTTTAG... | GCAGTAATGTGCAGACCAGCACAAGACCAAAATGGAGAAGCCGGGGAAATCCAGAAAGTGCATGCTCTGCCCAAGGGACTTCAGATTCCGTAACTGTCCAACATTAGGCTGGAATGCAAGCATGTACGAGTGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATAAGACTGGCGGCTTCCGTGCCAGCTGAGGGCCATGAGTTTGTGATGTGTGCTCTGTGGGGCCCCAAATGGATGATCTTCCATCCTCTCCATGGACCAGTAGAAACTGTGGGTTAGGGTGGAACTGAGCTTGGGTTACAGTGGGGTTTAG... |
Task1_train_38529 | A mutation has occurred on Chromosome 7. What is the medical relevance of this mutation? | Benign | GAAGGAACTGTGCTTCAGCAAAGGCTGAGAGAGTGTCTGGAAGCTCTTGCTGCTCCTTGCCATGGCTGCCCCAGGCTCTTGGAGCAGGGTGTCCACCCCAGTGTCTCACACAGGCTGGGATGGCCACTCTAAAGACAGATGGTTCACCATCCAATCGGAAGGACAGAAGCTTCTGCAGCCACCACCCAAGTGCCTCGGAAGAAGGGGTGGGTGGGTTTGAGCTCCTGGCGCCATGGAAGGCCCTTCACCTCTTACCTTCCTCAGGCTGCAGGTGCCGCTGTGCCCGCGGATAGCTGCCAGCAGTGCAGATCGTTCGCCCT... | GAAGGAACTGTGCTTCAGCAAAGGCTGAGAGAGTGTCTGGAAGCTCTTGCTGCTCCTTGCCATGGCTGCCCCAGGCTCTTGGAGCAGGGTGTCCACCCCAGTGTCTCACACAGGCTGGGATGGCCACTCTAAAGACAGATGGTTCACCATCCAATCGGAAGGACAGAAGCTTCTGCAGCCACCACCCAAGTGCCTCGGAAGAAGGGGTGGGTGGGTTTGAGCTCCTGGCGCCATGGAAGGCCCTTCACCTCTTACCTTCCTCAGGCTGCAGGTGCCGCTGTGCCCGCGGATAGCTGCCAGCAGTGCAGATCGTTCGCCCT... |
Task1_train_38530 | Given this context: Chromosome 7 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CTTGTGGTGTGTTAAGTGCCTAGACAATGGGCAAGGCGTGTCCTACAATTACTCCTGTGTTACTGAAGAATGACAGTTCGCTGCTGCTACAAATGCATATGGGAAAGAAGTGGCCCTGCCTGAATTTTCTCCTCTGTTCCATTGTTCAAGGATAACCATATGGATGGGCCTGCCCCTGGCCTCTCCATTCCTCTGGCCCTGTGGATGGACATCACTGGCTGTTACCTTTCCCACAGGGCAGCCAGGGGCCTGAAGTCAGTGTGGACTAGCCTCACACCCATCCATTTTGTCCCTTTAATAGTTCAGTACAAATATCTGGA... | CTTGTGGTGTGTTAAGTGCCTAGACAATGGGCAAGGCGTGTCCTACAATTACTCCTGTGTTACTGAAGAATGACAGTTCGCTGCTGCTACAAATGCATATGGGAAAGAAGTGGCCCTGCCTGAATTTTCTCCTCTGTTCCATTGTTCAAGGATAACCATATGGATGGGCCTGCCCCTGGCCTCTCCATTCCTCTGGCCCTGTGGATGGACATCACTGGCTGTTACCTTTCCCACAGGGCAGCCAGGGGCCTGAAGTCAGTGTGGACTAGCCTCACACCCATCCATTTTGTCCCTTTAATAGTTCAGTACAAATATCTGGA... |
Task1_train_38531 | A mutation on Chromosome 7 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CAGGGGCCTGAAGTCAGTGTGGACTAGCCTCACACCCATCCATTTTGTCCCTTTAATAGTTCAGTACAAATATCTGGAGGCAGTATGATGGGAATTCTAGTTAAAATGAAACCTGTGTGGTAAGCCTCACTGTTATCCTAATCCCGTCTCTCTCTCTCCTCCGCTTTATTCTGAGACTCTGAGACCAGTGCACTGAAGTGGGCAGGTGTGGAAGGCCTGCCCCGGAAGCCGCCATCCTCACCTTGCGTAGTCTGTCCTTCCCTCCCGCAGAGTGGATGGCTTCCATCAGGGCAGAGTGCAGGGATGTGTCTTTTGGGACT... | CAGGGGCCTGAAGTCAGTGTGGACTAGCCTCACACCCATCCATTTTGTCCCTTTAATAGTTCAGTACAAATATCTGGAGGCAGTATGATGGGAATTCTAGTTAAAATGAAACCTGTGTGGTAAGCCTCACTGTTATCCTAATCCCGTCTCTCTCTCTCCTCCGCTTTATTCTGAGACTCTGAGACCAGTGCACTGAAGTGGGCAGGTGTGGAAGGCCTGCCCCGGAAGCCGCCATCCTCACCTTGCGTAGTCTGTCCTTCCCTCCCGCAGAGTGGATGGCTTCCATCAGGGCAGAGTGCAGGGATGTGTCTTTTGGGACT... |
Task1_train_38532 | A variant was discovered on Chromosome 7. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TTCACCAGTAGGAAGACTGTGGTTTTTTGAAGGATCTTTAACCAAAAACAAACCAAAATGGCACCCATTGGGTTGTACTTCAAATAGGACATGGAGAACTGTGTAGAAACTAAGAAAACATACATTAAAAAAAATCTAGACCCCCACTGCATTAACTGTCCACTCCAATGATAATACCATCTAAAGAGGCTTTTTAGCTATAAAAATTATTGTCATCTTTATCAAGAAATGACTTTTTAAGAAGACAGTTATGGCATAGGAAATTTGTTTTTAAAATCTTATACTGGAGGATTCTTAAGGAATCTGGGGAAATGAAAATG... | TTCACCAGTAGGAAGACTGTGGTTTTTTGAAGGATCTTTAACCAAAAACAAACCAAAATGGCACCCATTGGGTTGTACTTCAAATAGGACATGGAGAACTGTGTAGAAACTAAGAAAACATACATTAAAAAAAATCTAGACCCCCACTGCATTAACTGTCCACTCCAATGATAATACCATCTAAAGAGGCTTTTTAGCTATAAAAATTATTGTCATCTTTATCAAGAAATGACTTTTTAAGAAGACAGTTATGGCATAGGAAATTTGTTTTTAAAATCTTATACTGGAGGATTCTTAAGGAATCTGGGGAAATGAAAATG... |
Task1_train_38533 | The following genetic variant occurs on Chromosome 7. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | AAGAGGCTTTTTAGCTATAAAAATTATTGTCATCTTTATCAAGAAATGACTTTTTAAGAAGACAGTTATGGCATAGGAAATTTGTTTTTAAAATCTTATACTGGAGGATTCTTAAGGAATCTGGGGAAATGAAAATGAATGACTGACTGAGTGGAAAGTCCTGGGGCTTTCATCCTGCTGCTCCCCTTGGCTGAAAGTGCCTTTTTTCAGCTGATAATCAGCCCCTTTCTGAAGTACAGAACTTTCGTGAAGATTTCTTATTAAGCTTTTTTCAGTGTCCTCACCATTCACTTGTTTGTCTCTCAAATCCCAAAAGAAAA... | AAGAGGCTTTTTAGCTATAAAAATTATTGTCATCTTTATCAAGAAATGACTTTTTAAGAAGACAGTTATGGCATAGGAAATTTGTTTTTAAAATCTTATACTGGAGGATTCTTAAGGAATCTGGGGAAATGAAAATGAATGACTGACTGAGTGGAAAGTCCTGGGGCTTTCATCCTGCTGCTCCCCTTGGCTGAAAGTGCCTTTTTTCAGCTGATAATCAGCCCCTTTCTGAAGTACAGAACTTTCGTGAAGATTTCTTATTAAGCTTTTTTCAGTGTCCTCACCATTCACTTGTTTGTCTCTCAAATCCCAAAAGAAAA... |
Task1_train_38534 | This sequence change occurs on Chromosome 7. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TCATTAAAAGTCCTGTTCACTAAACATATCTGCTTATATCAAAGAGTAACTTGAAATATCTGAAAATATTTAATTTCAATATTTCCAACCAGTGAATACTGGATAATATTTTTATATACTTCTATCAACATTTTCTAATTTCGATTTCAGAAGCTGGGGCAGTCCAGTCACTCACTTTACTTATGTGTAAGTTCCTATACTTGCACAATTATTATATATGATTCAGTATCTGGGGTGGATATTTATATATTATATTCACTGTAATACCCACATCCTGATTTATGATTTTTGCCTCACGATTTTCAGATTATATTCAAATA... | TCATTAAAAGTCCTGTTCACTAAACATATCTGCTTATATCAAAGAGTAACTTGAAATATCTGAAAATATTTAATTTCAATATTTCCAACCAGTGAATACTGGATAATATTTTTATATACTTCTATCAACATTTTCTAATTTCGATTTCAGAAGCTGGGGCAGTCCAGTCACTCACTTTACTTATGTGTAAGTTCCTATACTTGCACAATTATTATATATGATTCAGTATCTGGGGTGGATATTTATATATTATATTCACTGTAATACCCACATCCTGATTTATGATTTTTGCCTCACGATTTTCAGATTATATTCAAATA... |
Task1_train_38535 | This mutation occurs on Chromosome 7. Does this change lead to a known medical condition, or is it benign? | Benign | ATAGCTTTTTGGAGGAAGGCCCCACTTCCCAGGCATCCCTCCCAGACCTGGTCAGAGGCCCCTGCTCTTTGCTTCCATGTTGCCCACACTCACTGTGCTCTTCACACCGGCTCAAAATGATCTGCTTACGGGGTTGTGTCACCACCAGATCAAGCGTCCTGGAGAGGAGGAAACATATTTAACCTGCACAGAATTTGGGACAGAGAACCTCTAGTGTTTGTTCAATAAATATATGAATGGATAGAGGGACAGGTTGGGTGGTGGATAGATGGATGAACCCACACCTTTGAAGTGTATTTGGCTGTTTGAGAGGTTAGAAT... | ATAGCTTTTTGGAGGAAGGCCCCACTTCCCAGGCATCCCTCCCAGACCTGGTCAGAGGCCCCTGCTCTTTGCTTCCATGTTGCCCACACTCACTGTGCTCTTCACACCGGCTCAAAATGATCTGCTTACGGGGTTGTGTCACCACCAGATCAAGCGTCCTGGAGAGGAGGAAACATATTTAACCTGCACAGAATTTGGGACAGAGAACCTCTAGTGTTTGTTCAATAAATATATGAATGGATAGAGGGACAGGTTGGGTGGTGGATAGATGGATGAACCCACACCTTTGAAGTGTATTTGGCTGTTTGAGAGGTTAGAAT... |
Task1_train_38536 | A mutation has occurred on Chromosome 7. What is the medical relevance of this mutation? | Benign | GCCAACAGTTGCCAGTTATCCACCAGCAGACTGCAGGAAGAAGAGACAATCTTCACCTCCCTCCTGGGTAGGGAGAGCTGAGAATTCACTAGGCTTAGCCTAACAAAGCCCGCAGTGGACGTTTCTGCTGTACCTGTCCAAGGCGTGATAGTTCCCCAGACTTTGGGGAATATCACCGTGGGTTATTTTGTCTAGTTAAGTCCCTGTGGTGGGATAAGGATGGCTCCTAGAGCATGTCGGCATCAGTAGTTCCTGGAGTGGATTTTCCTACACCGTCTAGGTATGAAAATTTGGTGGGAGAAAAGACCCCAGGAAAGGGG... | GCCAACAGTTGCCAGTTATCCACCAGCAGACTGCAGGAAGAAGAGACAATCTTCACCTCCCTCCTGGGTAGGGAGAGCTGAGAATTCACTAGGCTTAGCCTAACAAAGCCCGCAGTGGACGTTTCTGCTGTACCTGTCCAAGGCGTGATAGTTCCCCAGACTTTGGGGAATATCACCGTGGGTTATTTTGTCTAGTTAAGTCCCTGTGGTGGGATAAGGATGGCTCCTAGAGCATGTCGGCATCAGTAGTTCCTGGAGTGGATTTTCCTACACCGTCTAGGTATGAAAATTTGGTGGGAGAAAAGACCCCAGGAAAGGGG... |
Task1_train_38537 | A variant has been detected on Chromosome 7. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GCAGGAGGAGCTGGGCCTGGAGAGGCTGACTCGAGGAACTTTTGCACCCGGAGCGGCCGCCGAGAGGCCGGAGCTGGGCCTGGGGAGGCCGACTTGAGGACGACTTGGGCCTGCAGAGGGCGCCGGGAGGCTGGAGCTGGCCCTGGACAGGCCGACTTGACGACAGTCTGGGCCTGCAGAGGCCGCCGAGAGGAAGAGCTGGGCCTGGAGAGGCCGACTGGAGGAAGTCCAGAGCCTGGAGAGGATGCAAAGCAGCAAACGCTAGGCCTGGAAAGGCTGCCCTGAGGCACGGGCTTGGCCTACAGAGGCCACTGGGAGGC... | GCAGGAGGAGCTGGGCCTGGAGAGGCTGACTCGAGGAACTTTTGCACCCGGAGCGGCCGCCGAGAGGCCGGAGCTGGGCCTGGGGAGGCCGACTTGAGGACGACTTGGGCCTGCAGAGGGCGCCGGGAGGCTGGAGCTGGCCCTGGACAGGCCGACTTGACGACAGTCTGGGCCTGCAGAGGCCGCCGAGAGGAAGAGCTGGGCCTGGAGAGGCCGACTGGAGGAAGTCCAGAGCCTGGAGAGGATGCAAAGCAGCAAACGCTAGGCCTGGAAAGGCTGCCCTGAGGCACGGGCTTGGCCTACAGAGGCCACTGGGAGGC... |
Task1_train_38538 | This sequence variant lies on Chromosome 7. Is it clinically significant, and what condition might it cause if any? | Benign | AACTTTTGCACCCGGAGCGGCCGCCGAGAGGCCGGAGCTGGGCCTGGGGAGGCCGACTTGAGGACGACTTGGGCCTGCAGAGGGCGCCGGGAGGCTGGAGCTGGCCCTGGACAGGCCGACTTGACGACAGTCTGGGCCTGCAGAGGCCGCCGAGAGGAAGAGCTGGGCCTGGAGAGGCCGACTGGAGGAAGTCCAGAGCCTGGAGAGGATGCAAAGCAGCAAACGCTAGGCCTGGAAAGGCTGCCCTGAGGCACGGGCTTGGCCTACAGAGGCCACTGGGAGGCAGGAGCTGGGCCCGCAGAGGCTCCCGAGAGCGGGGA... | AACTTTTGCACCCGGAGCGGCCGCCGAGAGGCCGGAGCTGGGCCTGGGGAGGCCGACTTGAGGACGACTTGGGCCTGCAGAGGGCGCCGGGAGGCTGGAGCTGGCCCTGGACAGGCCGACTTGACGACAGTCTGGGCCTGCAGAGGCCGCCGAGAGGAAGAGCTGGGCCTGGAGAGGCCGACTGGAGGAAGTCCAGAGCCTGGAGAGGATGCAAAGCAGCAAACGCTAGGCCTGGAAAGGCTGCCCTGAGGCACGGGCTTGGCCTACAGAGGCCACTGGGAGGCAGGAGCTGGGCCCGCAGAGGCTCCCGAGAGCGGGGA... |
Task1_train_38539 | Consider a variant on Chromosome 7. Determine its clinical classification and disease relevance. | Benign | GTTTATCTACTCTAGGTATCCATGTATATTTTTTCTGTGTCAAAAATTGCTTTGAAAAACACATAGTGCAAATTGCAAAGATAAATGTGGGCTCTCTTATAGGAGTGCCACACATTTTACATTTTTCTTTGCTTCTGCTTCTTGGAGTGCATGCTGTTGTCATGGAAAGCAGGCATTCTTTGGTAGCCCAGGTTCTGGAACGGTGCCTAGAATAGCTGCTCACTGTGTTTGCCAGATTAACTGATGGATATATGAAAACAGTATACTGCGTGACAACACCTTTGTTATTCCATAGGACATGGACATCTTCCAGCAACAGA... | GTTTATCTACTCTAGGTATCCATGTATATTTTTTCTGTGTCAAAAATTGCTTTGAAAAACACATAGTGCAAATTGCAAAGATAAATGTGGGCTCTCTTATAGGAGTGCCACACATTTTACATTTTTCTTTGCTTCTGCTTCTTGGAGTGCATGCTGTTGTCATGGAAAGCAGGCATTCTTTGGTAGCCCAGGTTCTGGAACGGTGCCTAGAATAGCTGCTCACTGTGTTTGCCAGATTAACTGATGGATATATGAAAACAGTATACTGCGTGACAACACCTTTGTTATTCCATAGGACATGGACATCTTCCAGCAACAGA... |
Task1_train_38540 | This mutation occurs on Chromosome 7. Does this change lead to a known medical condition, or is it benign? | Benign | GGTATTGCTGTGTGGTGGGAACACCCACTTCCCTTGTGCACAGCCTTTGAGAGGGGATCGTGGCCTCAGTTCCAGGGGTTCCTGGCCAGGGCCAAGTGCTCCTTCTGCAGAGGCCTGCACGCATCTCACCCCTTTGACTTGTATTTCCATGGCTTCCCCTCCCCACCTGCCCCCTAGCCCTCCCTGACTGGCCAGCCCCTCAGTAGTCCTCCTCGGCCAGGGAGAGGAGCACGGCCTTGGGTGTGTTCTCGAAAAGGGCTGCCCGGTTCTGCTGCTGCCCCTTCTTCACCCAGTGGCCATAGATTCGGAAAGCGTAGGCG... | GGTATTGCTGTGTGGTGGGAACACCCACTTCCCTTGTGCACAGCCTTTGAGAGGGGATCGTGGCCTCAGTTCCAGGGGTTCCTGGCCAGGGCCAAGTGCTCCTTCTGCAGAGGCCTGCACGCATCTCACCCCTTTGACTTGTATTTCCATGGCTTCCCCTCCCCACCTGCCCCCTAGCCCTCCCTGACTGGCCAGCCCCTCAGTAGTCCTCCTCGGCCAGGGAGAGGAGCACGGCCTTGGGTGTGTTCTCGAAAAGGGCTGCCCGGTTCTGCTGCTGCCCCTTCTTCACCCAGTGGCCATAGATTCGGAAAGCGTAGGCG... |
Task1_train_38541 | Chromosome 7 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | ATGGAAGTAAAGGTACAGCAATCCTCTTTAAGTTTGTATGTTTGTCTTCAGAATAACTGGTCTTTACTTTAAAGGCCTATATTTTCCAAAAGGTCTTTTTACAGTAATCACATTTATAATTTTTTTTTTGAGACAGAGTCTTGCTCTGTCACCCAGGCTGTAGTGTAGTGGCTCTATCTCAGCTCACTGCAACCTCTGCCTCCCCGGTTCAAGCAATTCTCCTACCTCTGCCTGCCAAGTAGCTGGGATTACAAGTGCACGCCACCACACCCAGCTAGTTTTTCTATTTTTAGTAGAGATGGAGTTTCACCATGTTGGCC... | ATGGAAGTAAAGGTACAGCAATCCTCTTTAAGTTTGTATGTTTGTCTTCAGAATAACTGGTCTTTACTTTAAAGGCCTATATTTTCCAAAAGGTCTTTTTACAGTAATCACATTTATAATTTTTTTTTTGAGACAGAGTCTTGCTCTGTCACCCAGGCTGTAGTGTAGTGGCTCTATCTCAGCTCACTGCAACCTCTGCCTCCCCGGTTCAAGCAATTCTCCTACCTCTGCCTGCCAAGTAGCTGGGATTACAAGTGCACGCCACCACACCCAGCTAGTTTTTCTATTTTTAGTAGAGATGGAGTTTCACCATGTTGGCC... |
Task1_train_38542 | This sequence variant lies on Chromosome 7. Is it clinically significant, and what condition might it cause if any? | Benign | TGCTTTCCTGTACCATAAGGTGTGAGAATTTGTTAAAAGTTTTGCCACATTCTTCATATTTGTAGGAGTCTTCTTCAGTATAAACTATCTTACCTACCATAACGTGTGACTACCATTTAAAGTCCTTGCCACATTTAACACATTTCTAGAGTTTCTCACCAGTATGATTTCTCTTTTTTAGAAAAGTTTGAGGTGTGCTTAAATGCTCTGTCACATTTTTATGTAAGCAGAGTTTCTCTCCAGTATAAAATTTTTTAGTGAGTAAGCATGGAGAACCAGTTAAAGGGTTTGCCACATTTTTTTCTGCAATTGCAGGGTTT... | TGCTTTCCTGTACCATAAGGTGTGAGAATTTGTTAAAAGTTTTGCCACATTCTTCATATTTGTAGGAGTCTTCTTCAGTATAAACTATCTTACCTACCATAACGTGTGACTACCATTTAAAGTCCTTGCCACATTTAACACATTTCTAGAGTTTCTCACCAGTATGATTTCTCTTTTTTAGAAAAGTTTGAGGTGTGCTTAAATGCTCTGTCACATTTTTATGTAAGCAGAGTTTCTCTCCAGTATAAAATTTTTTAGTGAGTAAGCATGGAGAACCAGTTAAAGGGTTTGCCACATTTTTTTCTGCAATTGCAGGGTTT... |
Task1_train_38543 | Here is a genetic alteration on Chromosome 7. Based on the data, is it a benign variant or a cause of disease? | Benign | GTGTGCTTAAATGCTCTGTCACATTTTTATGTAAGCAGAGTTTCTCTCCAGTATAAAATTTTTTAGTGAGTAAGCATGGAGAACCAGTTAAAGGGTTTGCCACATTTTTTTCTGCAATTGCAGGGTTTCTCTCCAATATCAATTATCTTACATTTATTCAGGTTTGAGGACTTTTTAAAGACATTACCATATTCCTTATTGTAGGGTTTCTCTTCAGTATTAATTCTCTTATGTATAATAAGGGTTCAAGACTAGTTAACAGCTTTACCACATTCTTTGCTTTTGTAGAGTTTCTCTCTAGAATGAATGATCAGATAATA... | GTGTGCTTAAATGCTCTGTCACATTTTTATGTAAGCAGAGTTTCTCTCCAGTATAAAATTTTTTAGTGAGTAAGCATGGAGAACCAGTTAAAGGGTTTGCCACATTTTTTTCTGCAATTGCAGGGTTTCTCTCCAATATCAATTATCTTACATTTATTCAGGTTTGAGGACTTTTTAAAGACATTACCATATTCCTTATTGTAGGGTTTCTCTTCAGTATTAATTCTCTTATGTATAATAAGGGTTCAAGACTAGTTAACAGCTTTACCACATTCTTTGCTTTTGTAGAGTTTCTCTCTAGAATGAATGATCAGATAATA... |
Task1_train_38544 | Located on Chromosome 7, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | GATTATCTTCTAGTTTGTGACTTTTGAAACTTTGCATGAATATGTGTTATGGACCTTTCTGTGTATATCCTAGTTTGTTTGTTTAGCTTCTTCATTAAATGTTTTCAGCTATTTTCTTTTACCTACACGTTTGTTTATTTTTATTATTCCAAGCTTTTGTTGATATTCTTATTTTTCTGATATTATTTAGGTATCTAGTTTTGCATTTCTCTCACTGAGCATAATATGGATTATCTTATATTTTTAAAATTAATATATAAATCTTTAGCTTAATAGTTTCTTTTTCAAAATTTTTTATTTTTTTGATTGGACCGTGTTGC... | GATTATCTTCTAGTTTGTGACTTTTGAAACTTTGCATGAATATGTGTTATGGACCTTTCTGTGTATATCCTAGTTTGTTTGTTTAGCTTCTTCATTAAATGTTTTCAGCTATTTTCTTTTACCTACACGTTTGTTTATTTTTATTATTCCAAGCTTTTGTTGATATTCTTATTTTTCTGATATTATTTAGGTATCTAGTTTTGCATTTCTCTCACTGAGCATAATATGGATTATCTTATATTTTTAAAATTAATATATAAATCTTTAGCTTAATAGTTTCTTTTTCAAAATTTTTTATTTTTTTGATTGGACCGTGTTGC... |
Task1_train_38545 | This is a variant located on Chromosome 7. Is this mutation a likely cause of disease or not? | Benign | TCATATCCTCACCAGAAGCAGATGCTGGCATATACTTCTTTTACAGTCTACTGAACTGTGAACCAAAGAAATCTTTTTCTTTATAAATTACCCAGTCTCAGGTTATTTTCTGTAGCATTGCAAAATGAATTCATACACAGTATAATGTTATTCAGGCTTTCTGTTTTTTAATTGATATTTTATTTAAATTTTTTATTCATTATTGAAAGTGAGGTCTTAATGTTTATAATTTTATGTTGCTATTTTATTTCTTGCTTCATTTTTGTCAATATTTGCTTTATATATTTTGAAGCCGTGATGTTATATATGCCTATACATAT... | TCATATCCTCACCAGAAGCAGATGCTGGCATATACTTCTTTTACAGTCTACTGAACTGTGAACCAAAGAAATCTTTTTCTTTATAAATTACCCAGTCTCAGGTTATTTTCTGTAGCATTGCAAAATGAATTCATACACAGTATAATGTTATTCAGGCTTTCTGTTTTTTAATTGATATTTTATTTAAATTTTTTATTCATTATTGAAAGTGAGGTCTTAATGTTTATAATTTTATGTTGCTATTTTATTTCTTGCTTCATTTTTGTCAATATTTGCTTTATATATTTTGAAGCCGTGATGTTATATATGCCTATACATAT... |
Task1_train_38546 | This is a variant located on Chromosome 7. Is this mutation a likely cause of disease or not? | Benign | GCTGTCACTATATACTAGTGATTCAAACTTCATTGTCTTCAATAGCAACAACCTGAAATCAATCTAGTTGCCTATCAGTGGTGGATTGGATAAAGAATATGTGGTGCCTATACACTATGAAATAGTACACAGCCAAAAAAAAATTATGCTCTTTGTAGCAACACTGATGCAGCTGAAAGCCATTATCTTAAGTAAATTAATGCAAAAACAGAAAGCCAAATACTACATGTTCTTACTTACAAGTGAGAGCTAAATATTGGGTATACATGGATATAAAGATGGAAACAATAGATGCTGGAGACCACTAGTGGAGGAAGGGA... | GCTGTCACTATATACTAGTGATTCAAACTTCATTGTCTTCAATAGCAACAACCTGAAATCAATCTAGTTGCCTATCAGTGGTGGATTGGATAAAGAATATGTGGTGCCTATACACTATGAAATAGTACACAGCCAAAAAAAAATTATGCTCTTTGTAGCAACACTGATGCAGCTGAAAGCCATTATCTTAAGTAAATTAATGCAAAAACAGAAAGCCAAATACTACATGTTCTTACTTACAAGTGAGAGCTAAATATTGGGTATACATGGATATAAAGATGGAAACAATAGATGCTGGAGACCACTAGTGGAGGAAGGGA... |
Task1_train_38547 | This variant is found on Chromosome 7. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | AGAAACAGATGCTGGCATATACTTCTTGTACAGTCTACTGAACTGTGAACCAAAGAAGTCTTTTTCATTATAAAAGTTTTCTATAGCATTGTTTTCTCAGGTTGTTTTCTATAGCATTGCAAAATGAATTCATATACAATACAATGTTCTTCAGGTTTTCTGTTTTTTTTAATTGATTTTTTATTTAAATTTTTTATTTATTATTGAAAGTGAGGTCTTAATGTTTATAATTTTATGTTGCTATTTTATTTCTTGCTTCATTTTTGTCAATATTTGCTTTATATATTTTGAAGTCCTGATGTTATATATGCATATGCATA... | AGAAACAGATGCTGGCATATACTTCTTGTACAGTCTACTGAACTGTGAACCAAAGAAGTCTTTTTCATTATAAAAGTTTTCTATAGCATTGTTTTCTCAGGTTGTTTTCTATAGCATTGCAAAATGAATTCATATACAATACAATGTTCTTCAGGTTTTCTGTTTTTTTTAATTGATTTTTTATTTAAATTTTTTATTTATTATTGAAAGTGAGGTCTTAATGTTTATAATTTTATGTTGCTATTTTATTTCTTGCTTCATTTTTGTCAATATTTGCTTTATATATTTTGAAGTCCTGATGTTATATATGCATATGCATA... |
Task1_train_38548 | Chromosome 7 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | ACTATTATATAATATCAGTCTTTGTCTCATGCTAGTAATGGACTCATTTTCTTTTGTGTGTCTATAAAGATTTTTTCTTTGTGCTACATTGGAGATTTTATAAAACCTCTTAATGTTACAATAGTATATTTTACATTGGTAAAAAAAAATGACTTCAGTTGCATAGAAAAATTTGTCCTCATTATATCTACCCTGTGCTTCTTACTGATCTTGCTAATTGTATCTTTTTATGTTTTATGATTATTTTTATGCTTATATCTTTCAAATTTTAAAGAATAACTAAAAATGTTTTCTGTACAATCACAATAATGCCACAGAAT... | ACTATTATATAATATCAGTCTTTGTCTCATGCTAGTAATGGACTCATTTTCTTTTGTGTGTCTATAAAGATTTTTTCTTTGTGCTACATTGGAGATTTTATAAAACCTCTTAATGTTACAATAGTATATTTTACATTGGTAAAAAAAAATGACTTCAGTTGCATAGAAAAATTTGTCCTCATTATATCTACCCTGTGCTTCTTACTGATCTTGCTAATTGTATCTTTTTATGTTTTATGATTATTTTTATGCTTATATCTTTCAAATTTTAAAGAATAACTAAAAATGTTTTCTGTACAATCACAATAATGCCACAGAAT... |
Task1_train_38549 | This mutation on Chromosome 7 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TATTTTTATGATAGTCCAGGGGTTCTGAAAAAAAATTTTTCTATATAGCATAGTCTTCTTTTTTTGTTGTTTTTGTTTTGTTTTGTTTTGTTTTGTTTGTTTTGAGACCGAGTTTTCACTCTTGTCCCCCAGGCTGGAGTGAAATGGCACAATCTCAGCCCACTGCAACCTCCGCCTTGTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCTCTAGTATCTGGGATTACAGGTGCCTGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACAT... | TATTTTTATGATAGTCCAGGGGTTCTGAAAAAAAATTTTTCTATATAGCATAGTCTTCTTTTTTTGTTGTTTTTGTTTTGTTTTGTTTTGTTTTGTTTGTTTTGAGACCGAGTTTTCACTCTTGTCCCCCAGGCTGGAGTGAAATGGCACAATCTCAGCCCACTGCAACCTCCGCCTTGTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCTCTAGTATCTGGGATTACAGGTGCCTGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACAT... |
Task1_train_38550 | A mutation is present on Chromosome 7. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CCTCTAAATGTTACCACAATATTTTTTAAACTGGTAAAAAAAAATGACTTCAGTTGCATAGAAAAATTTGTCCTCATTATATCTACCCTATACATCTTATTGATGTTGATAATTATATCTTTTTATGTTTTATGATTATTTTTATGCTTATATCTTTGAAATTTTAAAGAATAACTAAAAATGTTTTCTGCATGATCACAATAATACCACAGATTTTTATTTTTTGTATATGCATATGTTTTTCAGAAAGTTATATATTTTCATATGATTATGTATTTTTTTCATCATGTTATTTTAAGCGGCAGGACCTCTTTTCAGCA... | CCTCTAAATGTTACCACAATATTTTTTAAACTGGTAAAAAAAAATGACTTCAGTTGCATAGAAAAATTTGTCCTCATTATATCTACCCTATACATCTTATTGATGTTGATAATTATATCTTTTTATGTTTTATGATTATTTTTATGCTTATATCTTTGAAATTTTAAAGAATAACTAAAAATGTTTTCTGCATGATCACAATAATACCACAGATTTTTATTTTTTGTATATGCATATGTTTTTCAGAAAGTTATATATTTTCATATGATTATGTATTTTTTTCATCATGTTATTTTAAGCGGCAGGACCTCTTTTCAGCA... |
Task1_train_38551 | A mutation on Chromosome 7 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TAAACCAGCAAGAAATAAAAACAATCTCATTTAAAAGTAGGCTAAGGATATGAATAGACAATTCTCAAAAGAAGATATACGAATGGCCAAGAAACATATGGAAACTTGCTCAACATCTCTAATTATCAGAGTAATGCAAATGAAAATCACAATATGATACCACCTCACTCCTGCAAGAATGGCCATAATTAAAAAATAAAAAAATATAGTGTTGGTGGGGATGTGGTGCAAAGGGAACAATTTTACACTTCTGGTGTGAATGTAAATTAGCACCATTATGAAAAATAGTGTGGAGATTTTTTTAAAGAACTAAAAGTTGA... | TAAACCAGCAAGAAATAAAAACAATCTCATTTAAAAGTAGGCTAAGGATATGAATAGACAATTCTCAAAAGAAGATATACGAATGGCCAAGAAACATATGGAAACTTGCTCAACATCTCTAATTATCAGAGTAATGCAAATGAAAATCACAATATGATACCACCTCACTCCTGCAAGAATGGCCATAATTAAAAAATAAAAAAATATAGTGTTGGTGGGGATGTGGTGCAAAGGGAACAATTTTACACTTCTGGTGTGAATGTAAATTAGCACCATTATGAAAAATAGTGTGGAGATTTTTTTAAAGAACTAAAAGTTGA... |
Task1_train_38552 | A mutation found on Chromosome 7 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CTCAAATACTTACAGCCAACTGATCTTTCAGAAAGCAAACAAAAACATAAGTGGGAAAAGGAAACCCTTTTCAACAAAAGGTGCTGGGAAAATTGGCTAGCCACATGTAGGAGAATAAAACTGGATCTTTATCTCTCACCTTATACAAAAATAAACTCAAGATAGATTAAGGACTTAAATGTAAGACCTGAAACTATAAAAATTCTGTAAGATAACATTGGAAAAACCCTTCTAAACATTGGCTTAGGCAAGGATTTCATGACCAAGAACCCAAAAGCAAATGCAATAAAAACAAAGATAAATAGCTGGAACTTAATTAA... | CTCAAATACTTACAGCCAACTGATCTTTCAGAAAGCAAACAAAAACATAAGTGGGAAAAGGAAACCCTTTTCAACAAAAGGTGCTGGGAAAATTGGCTAGCCACATGTAGGAGAATAAAACTGGATCTTTATCTCTCACCTTATACAAAAATAAACTCAAGATAGATTAAGGACTTAAATGTAAGACCTGAAACTATAAAAATTCTGTAAGATAACATTGGAAAAACCCTTCTAAACATTGGCTTAGGCAAGGATTTCATGACCAAGAACCCAAAAGCAAATGCAATAAAAACAAAGATAAATAGCTGGAACTTAATTAA... |
Task1_train_38553 | A mutation on Chromosome 7 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TAATATTATTAATATATTTTAACCTGGTAAAAAATAAACTTCAGTTGCATTCAACAATTCTTTCTCATTACATTTGTTCTCAATTTTGTTGGTGATGTTGCTAATTGTATTTTTCTATGTGGTATGTTAGCAGATGTTTATAAAAATTTTTATGCTTTTATCTTTCACATTTTAGAGAATAATTAGAAATGTTTTCTGCACTATTATGATAATGCTAAGGAATTCCATTTTTGTGTATGTGCATGTCTTCCCTAGAAAGTTATGTTATAATGGTAAGGAATTCCATTTTGTGTATATGCATGTCTTTCCCAGAAATTTAT... | TAATATTATTAATATATTTTAACCTGGTAAAAAATAAACTTCAGTTGCATTCAACAATTCTTTCTCATTACATTTGTTCTCAATTTTGTTGGTGATGTTGCTAATTGTATTTTTCTATGTGGTATGTTAGCAGATGTTTATAAAAATTTTTATGCTTTTATCTTTCACATTTTAGAGAATAATTAGAAATGTTTTCTGCACTATTATGATAATGCTAAGGAATTCCATTTTTGTGTATGTGCATGTCTTCCCTAGAAAGTTATGTTATAATGGTAAGGAATTCCATTTTGTGTATATGCATGTCTTTCCCAGAAATTTAT... |
Task1_train_38554 | A mutation found on Chromosome 7 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | ATATATTTTAACCTGGTAAAAAATAAACTTCAGTTGCATTCAACAATTCTTTCTCATTACATTTGTTCTCAATTTTGTTGGTGATGTTGCTAATTGTATTTTTCTATGTGGTATGTTAGCAGATGTTTATAAAAATTTTTATGCTTTTATCTTTCACATTTTAGAGAATAATTAGAAATGTTTTCTGCACTATTATGATAATGCTAAGGAATTCCATTTTTGTGTATGTGCATGTCTTCCCTAGAAAGTTATGTTATAATGGTAAGGAATTCCATTTTGTGTATATGCATGTCTTTCCCAGAAATTTATGTATTTTCATA... | ATATATTTTAACCTGGTAAAAAATAAACTTCAGTTGCATTCAACAATTCTTTCTCATTACATTTGTTCTCAATTTTGTTGGTGATGTTGCTAATTGTATTTTTCTATGTGGTATGTTAGCAGATGTTTATAAAAATTTTTATGCTTTTATCTTTCACATTTTAGAGAATAATTAGAAATGTTTTCTGCACTATTATGATAATGCTAAGGAATTCCATTTTTGTGTATGTGCATGTCTTCCCTAGAAAGTTATGTTATAATGGTAAGGAATTCCATTTTGTGTATATGCATGTCTTTCCCAGAAATTTATGTATTTTCATA... |
Task1_train_38555 | This mutation is located on Chromosome 7. Is it associated with a disease or is it a benign polymorphism? | Benign | CCTTAAAGTGGGGTGGGGTAGACATGTCAGGATGCAGAATGGAGCTGGACAGAATGTAGGCATTTCTGCTGCATCTGGAAAGTAAGATAAGTGAGCTCACTGTCACAAAAGGCACAGAAGAGGAAACTAAATTTGCACTTGGTGGAGAAAATTTAACTCTACTAATATAAACTGACCATCGCTACATGTTTACTGGGCACCTGGTGCAGGGCTAAGAAATCTGCCATTATAATCTGATGCAGTGGCACTGAGCCTGCAGAGTCAATGTGCACTCACAAACTCAACCACTGTCATCTCACTTAACCCTCACACATCACCTG... | CCTTAAAGTGGGGTGGGGTAGACATGTCAGGATGCAGAATGGAGCTGGACAGAATGTAGGCATTTCTGCTGCATCTGGAAAGTAAGATAAGTGAGCTCACTGTCACAAAAGGCACAGAAGAGGAAACTAAATTTGCACTTGGTGGAGAAAATTTAACTCTACTAATATAAACTGACCATCGCTACATGTTTACTGGGCACCTGGTGCAGGGCTAAGAAATCTGCCATTATAATCTGATGCAGTGGCACTGAGCCTGCAGAGTCAATGTGCACTCACAAACTCAACCACTGTCATCTCACTTAACCCTCACACATCACCTG... |
Task1_train_38556 | This sequence change occurs on Chromosome 7. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | AAAGGAACTCACACCTGGGCACACCTGCATGAGGTGACCTACGATGCTTTTTACTTTCCATCAAAACAGTAATTGATGCTCATATCACCTTCTTGTGGTACAAGAAGGAAACCACAGAAGAGAATGAAAATGGAAAACATACATCATCACCAATGTTGCCTCCCAGAGATGAGCATGGTCCCCATGTGGAAGTCTTCTGTCCATTTCTCCCTTGGCCTGCACACATTATGATAGTGGCAGCAGATCTGTGCTGGGCATTTACCAGGCTGGGCACGACACCAAGAACTTTACAGATGTCCCTTCACTTATTCCTCACAAAG... | AAAGGAACTCACACCTGGGCACACCTGCATGAGGTGACCTACGATGCTTTTTACTTTCCATCAAAACAGTAATTGATGCTCATATCACCTTCTTGTGGTACAAGAAGGAAACCACAGAAGAGAATGAAAATGGAAAACATACATCATCACCAATGTTGCCTCCCAGAGATGAGCATGGTCCCCATGTGGAAGTCTTCTGTCCATTTCTCCCTTGGCCTGCACACATTATGATAGTGGCAGCAGATCTGTGCTGGGCATTTACCAGGCTGGGCACGACACCAAGAACTTTACAGATGTCCCTTCACTTATTCCTCACAAAG... |
Task1_train_38557 | A mutation found on Chromosome 7 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GGGCCAGTGTCCTCTGGATGAAGGACAACTGCTCCATTGTGCAGTGTTTTTGTTGTTGTTTGTTTGTTTTTGAGATGGAGTCTAGCTCTGTTGCACAGGCTGGAGTGCAGTGGTGGGATCTCAGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGAGATTACAGGCGCCCGCCACTACATGCAGCTAATCTTTTTGTATTTTTAGTAGAGACAAGGTTTCACTGTGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCATGATCTGCCCGCCTCGACCTCCCAGAGTGC... | GGGCCAGTGTCCTCTGGATGAAGGACAACTGCTCCATTGTGCAGTGTTTTTGTTGTTGTTTGTTTGTTTTTGAGATGGAGTCTAGCTCTGTTGCACAGGCTGGAGTGCAGTGGTGGGATCTCAGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGAGATTACAGGCGCCCGCCACTACATGCAGCTAATCTTTTTGTATTTTTAGTAGAGACAAGGTTTCACTGTGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCATGATCTGCCCGCCTCGACCTCCCAGAGTGC... |
Task1_train_38558 | A mutation on Chromosome 7 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | ACACTATGTACCCACAAAAGTTAAGAAAAATATGTTTAAATAAGAAAAAGAATAAAAATTTAACCTATGGGAACAATGTTCTTTAATTAAGTTCTTTAGTTTAAAGTCACTGGCAAGAGAAATTATTAGAGATGTTAGTCCACTCTGTTATTAAATAGTACATTGTTACTATCTTTTACCAACACCCTTGAGTAAGGTGGGATAGGTTGAAGTTAGTGGCATGATAATACTTCACTGAATGCACAATTGGTCTTAACATGTTAAAAAAAAAGTTTAATTAAAAAATTAAGTTCACAATAATCTAAAATTTTTTAAATGTG... | ACACTATGTACCCACAAAAGTTAAGAAAAATATGTTTAAATAAGAAAAAGAATAAAAATTTAACCTATGGGAACAATGTTCTTTAATTAAGTTCTTTAGTTTAAAGTCACTGGCAAGAGAAATTATTAGAGATGTTAGTCCACTCTGTTATTAAATAGTACATTGTTACTATCTTTTACCAACACCCTTGAGTAAGGTGGGATAGGTTGAAGTTAGTGGCATGATAATACTTCACTGAATGCACAATTGGTCTTAACATGTTAAAAAAAAAGTTTAATTAAAAAATTAAGTTCACAATAATCTAAAATTTTTTAAATGTG... |
Task1_train_38559 | A mutation on Chromosome 7 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TAAGAAAAATATGTTTAAATAAGAAAAAGAATAAAAATTTAACCTATGGGAACAATGTTCTTTAATTAAGTTCTTTAGTTTAAAGTCACTGGCAAGAGAAATTATTAGAGATGTTAGTCCACTCTGTTATTAAATAGTACATTGTTACTATCTTTTACCAACACCCTTGAGTAAGGTGGGATAGGTTGAAGTTAGTGGCATGATAATACTTCACTGAATGCACAATTGGTCTTAACATGTTAAAAAAAAAGTTTAATTAAAAAATTAAGTTCACAATAATCTAAAATTTTTTAAATGTGCTGCATTTTATTACATAAAAG... | TAAGAAAAATATGTTTAAATAAGAAAAAGAATAAAAATTTAACCTATGGGAACAATGTTCTTTAATTAAGTTCTTTAGTTTAAAGTCACTGGCAAGAGAAATTATTAGAGATGTTAGTCCACTCTGTTATTAAATAGTACATTGTTACTATCTTTTACCAACACCCTTGAGTAAGGTGGGATAGGTTGAAGTTAGTGGCATGATAATACTTCACTGAATGCACAATTGGTCTTAACATGTTAAAAAAAAAGTTTAATTAAAAAATTAAGTTCACAATAATCTAAAATTTTTTAAATGTGCTGCATTTTATTACATAAAAG... |
Task1_train_38560 | The following genetic variant occurs on Chromosome 7. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | AAGATCGGTTAAAAACTTTGCCACATTCTTCACATTTGTAGCATTTCTCTCCAGTGTGAATTATCTTATATGTAGAAAGGGTTGAAGACTGGCTAAAAGCTTTAGCACATTTTTCACATTTGTAAGGTTTCTCTCCTGTATGAATTTTCTTATGTGTAGTAAGTTTTGAGCATCGACTGAAAGTTTTGCCACATTCCTCACATTTGTAAGGTTTCTCTCCAGTATGAATTCTTTTATGTATAGTAAGAGTTGACACTTGGTTAAAAGCTTTGCCACATTCTTCACACTTGTAGGGTTTCTCTCCAGTATGAATTCTTTTA... | AAGATCGGTTAAAAACTTTGCCACATTCTTCACATTTGTAGCATTTCTCTCCAGTGTGAATTATCTTATATGTAGAAAGGGTTGAAGACTGGCTAAAAGCTTTAGCACATTTTTCACATTTGTAAGGTTTCTCTCCTGTATGAATTTTCTTATGTGTAGTAAGTTTTGAGCATCGACTGAAAGTTTTGCCACATTCCTCACATTTGTAAGGTTTCTCTCCAGTATGAATTCTTTTATGTATAGTAAGAGTTGACACTTGGTTAAAAGCTTTGCCACATTCTTCACACTTGTAGGGTTTCTCTCCAGTATGAATTCTTTTA... |
Task1_train_38561 | A mutation has occurred on Chromosome 7. What is the medical relevance of this mutation? | Benign | TGATCTTCAACAAAGCTTACAAGAGCAATGCAGGAAGAATTCCCTATTTAATAAATGAGGTTGGAATAACTAGCTAGCACTATGCAGAAGATTGAAACTGGATGCCTTTCTTACATGATATATAAAAATCAATTCAAGATGAATTAAAGACTTAAATGTAGAACTTAAAATTATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAACCTGAAAATAATCTAGAAAATAACCTAGAAAATTCTAAGACATAAAAACTGGCAAAGATTTTATGATGAAGATACCAAAAGCAATTGCAA... | TGATCTTCAACAAAGCTTACAAGAGCAATGCAGGAAGAATTCCCTATTTAATAAATGAGGTTGGAATAACTAGCTAGCACTATGCAGAAGATTGAAACTGGATGCCTTTCTTACATGATATATAAAAATCAATTCAAGATGAATTAAAGACTTAAATGTAGAACTTAAAATTATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAACCTGAAAATAATCTAGAAAATAACCTAGAAAATTCTAAGACATAAAAACTGGCAAAGATTTTATGATGAAGATACCAAAAGCAATTGCAA... |
Task1_train_38562 | Assess the clinical impact of this variant found on Chromosome 7. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CTAAGACATAAAAACTGGCAAAGATTTTATGATGAAGATACCAAAAGCAATTGCAACAGAAGCAAAAATTGACAAATGGGACCTAATTAAACTAAAGAGCTATTTTGCAGCAATGGAAACAATCAACTGAATAAACAGACAACCTACAGACTAGAAGAAAATATTTGCAAACTATGCTTCTGACAAAGGTCTAAAATCTAGCATCCATAAGAAACTTAAACAAATTTATTTTAAAAAAAAAGAAGAAGAAGAATAAGCCAGGATCTGTGGCTCATGCTTGTAATCCCAGCACTTTGGGAAGCTGAGGCAGATGGATCATG... | CTAAGACATAAAAACTGGCAAAGATTTTATGATGAAGATACCAAAAGCAATTGCAACAGAAGCAAAAATTGACAAATGGGACCTAATTAAACTAAAGAGCTATTTTGCAGCAATGGAAACAATCAACTGAATAAACAGACAACCTACAGACTAGAAGAAAATATTTGCAAACTATGCTTCTGACAAAGGTCTAAAATCTAGCATCCATAAGAAACTTAAACAAATTTATTTTAAAAAAAAAGAAGAAGAAGAATAAGCCAGGATCTGTGGCTCATGCTTGTAATCCCAGCACTTTGGGAAGCTGAGGCAGATGGATCATG... |
Task1_train_38563 | A genetic alteration is present on Chromosome 7. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TAACATCCAAAGGCTGAGCCCTGAACAAAGACAGGGCTTGACTTTTATACATGCATCAGGCAGGGGCAAGTCGGGTTTTTGGCGCAAAACCTGCGAGGTGAGAAAGCAGTCTTACAGAAGCAGAACAAAGGCAGTTAATCATACCGTGACAGGTTTTACAACAGGATTTGCAACATGAGCCTACCTTACTTAAACATGTCTTGTGACCTTGCCATGCTACAGAAAGAAAAACAAGAACTTACAAAATCTTTACAGACTTGCAGAAATAGTTACAAAAATAGTTGTGAGAGCAGAACAAAGAATAATGTTATGGGGAGAGA... | TAACATCCAAAGGCTGAGCCCTGAACAAAGACAGGGCTTGACTTTTATACATGCATCAGGCAGGGGCAAGTCGGGTTTTTGGCGCAAAACCTGCGAGGTGAGAAAGCAGTCTTACAGAAGCAGAACAAAGGCAGTTAATCATACCGTGACAGGTTTTACAACAGGATTTGCAACATGAGCCTACCTTACTTAAACATGTCTTGTGACCTTGCCATGCTACAGAAAGAAAAACAAGAACTTACAAAATCTTTACAGACTTGCAGAAATAGTTACAAAAATAGTTGTGAGAGCAGAACAAAGAATAATGTTATGGGGAGAGA... |
Task1_train_38564 | A variant on Chromosome 7 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GTTATGGGGAGAGAATTTCAAACAGGGAAACTGATAAGGAGAACTTGTTTTTCTCATCCCTGCTCCTGGAGCCCACTCCTTCGGAGCCCCTGCCTGGCCTTGCAGATAATTATCATAGCTCCAGCAGGACTTTGGAGTGAGTCAGACTGGTCAGGAAAGGACTTGTTTTCCCTTTACTTGTTTTTCCTTTTATATTTCCTGCTTCATTCCCCCCTTTGATGCTTTTTATAAGTAAAGTTTAAGAGAAAGCATCACTATCTTCATTTACTTCAAGAGGAAGTAGCTCTTTTCTTGGCAGGGGTTAATACTTAGTTAGGGCC... | GTTATGGGGAGAGAATTTCAAACAGGGAAACTGATAAGGAGAACTTGTTTTTCTCATCCCTGCTCCTGGAGCCCACTCCTTCGGAGCCCCTGCCTGGCCTTGCAGATAATTATCATAGCTCCAGCAGGACTTTGGAGTGAGTCAGACTGGTCAGGAAAGGACTTGTTTTCCCTTTACTTGTTTTTCCTTTTATATTTCCTGCTTCATTCCCCCCTTTGATGCTTTTTATAAGTAAAGTTTAAGAGAAAGCATCACTATCTTCATTTACTTCAAGAGGAAGTAGCTCTTTTCTTGGCAGGGGTTAATACTTAGTTAGGGCC... |
Task1_train_38565 | A mutation on Chromosome 7 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GTTAAAACATTTTCTAGTTTGTTACTAATACTACAAATTATATTGTGTTTCTATTAACAGATTTATTCAGATTTATATTTTGTTTCTCATATTCTATAGGAGAACTTTAAGGGTTTGATGCTCCATCATTATGATAGTAAAGAATTCTGTGTGTGTCTATATTTACATTTAATAGAGAGCTTTATATTTATATATGGTTTTATGATGCTGTGCAGCATTATTTTATTTTTCAACATAATGGAGTCATTTTAGCATTTCTCTTTTTGTATATGCAATGTCTCACTATGTTGCTCAGGCTGATCTTGAACTCCTGGTCTCAA... | GTTAAAACATTTTCTAGTTTGTTACTAATACTACAAATTATATTGTGTTTCTATTAACAGATTTATTCAGATTTATATTTTGTTTCTCATATTCTATAGGAGAACTTTAAGGGTTTGATGCTCCATCATTATGATAGTAAAGAATTCTGTGTGTGTCTATATTTACATTTAATAGAGAGCTTTATATTTATATATGGTTTTATGATGCTGTGCAGCATTATTTTATTTTTCAACATAATGGAGTCATTTTAGCATTTCTCTTTTTGTATATGCAATGTCTCACTATGTTGCTCAGGCTGATCTTGAACTCCTGGTCTCAA... |
Task1_train_38566 | Here’s a variant located on Chromosome 7. What is the predicted biological effect — harmless or disease-causing? | Benign | TAGTCTTAAACCAATTGTCTTGGCTAGAGATTCCGGGAGTCTCTCAAACATGTTCTTAGGATGTGCCTTGTCTGAAATTTTGTGTTTACTTTTTAGTTAAAGGAGTTCATTTGTGTTTTTTGTTAAGTCGGTAATCAGTTGCTACACGTGTTCGCTGTCTGTGGTGCTGCTGCATTCTCTCTGCTGCTGTAATGTTTACCTTTGGTCTCAGCAGACAAACTGTCATTCCAAAGTATACCACCATTTCCTTCAGCACTTTATGGCATGGGAGACAGAAACCAGTGTCTTGAAAGGCCCCTAGAGGCCAAAAATAAAGATGT... | TAGTCTTAAACCAATTGTCTTGGCTAGAGATTCCGGGAGTCTCTCAAACATGTTCTTAGGATGTGCCTTGTCTGAAATTTTGTGTTTACTTTTTAGTTAAAGGAGTTCATTTGTGTTTTTTGTTAAGTCGGTAATCAGTTGCTACACGTGTTCGCTGTCTGTGGTGCTGCTGCATTCTCTCTGCTGCTGTAATGTTTACCTTTGGTCTCAGCAGACAAACTGTCATTCCAAAGTATACCACCATTTCCTTCAGCACTTTATGGCATGGGAGACAGAAACCAGTGTCTTGAAAGGCCCCTAGAGGCCAAAAATAAAGATGT... |
Task1_train_38567 | Mutation context: Chromosome 7. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | AGTTTTACTTTAGCTTACCTTGAATACTCCCTGTATAATCCTCTAAAAAGGTAGCATCGGCAAGAAAGATGAATCCGTTGGAAATACAGCTGAGCCATACTTCACGGAATAGAACAAGTGTGTTCTGTGCTGGAGCTCAAGACCTGTGGAAAGGGACTGCCCCCACTGGGTGCAATGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGTAGAGGCGGGTGGATCACTTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCTGCCTCTACTGAAAAATACAGAAAAATTAGCCAGGATTGTGGTGTGCG... | AGTTTTACTTTAGCTTACCTTGAATACTCCCTGTATAATCCTCTAAAAAGGTAGCATCGGCAAGAAAGATGAATCCGTTGGAAATACAGCTGAGCCATACTTCACGGAATAGAACAAGTGTGTTCTGTGCTGGAGCTCAAGACCTGTGGAAAGGGACTGCCCCCACTGGGTGCAATGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGTAGAGGCGGGTGGATCACTTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCTGCCTCTACTGAAAAATACAGAAAAATTAGCCAGGATTGTGGTGTGCG... |
Task1_train_38568 | A mutation on Chromosome 7 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | AGGGCACAGTTTCAGCTTGAACTCCGTTTAATGAATTCTCTAAATCACCGGGCAAACTGAGAAGATTCTCTTGTTTATTGTAATTAAGCTGGGTGGCTGTGGTTTATATTCCACAAAGGCCATCACAGTTTAGTGCACCAGTCATCTGTTTGAACAGCTGTCTTGAGTAGAGTGTTTGGCAAAGCTCATGTGAGTCTTCATCCAAGTCCCAGCTCTGTCATCAGGGTCAGGGTCACTCTGCTCATTTGTTGGTTTTTAAAAATTAAGTGTTGGCCAGGCGTGTTGGCTCACATCTGTAATCCCAGCACATAGGAGGCCGA... | AGGGCACAGTTTCAGCTTGAACTCCGTTTAATGAATTCTCTAAATCACCGGGCAAACTGAGAAGATTCTCTTGTTTATTGTAATTAAGCTGGGTGGCTGTGGTTTATATTCCACAAAGGCCATCACAGTTTAGTGCACCAGTCATCTGTTTGAACAGCTGTCTTGAGTAGAGTGTTTGGCAAAGCTCATGTGAGTCTTCATCCAAGTCCCAGCTCTGTCATCAGGGTCAGGGTCACTCTGCTCATTTGTTGGTTTTTAAAAATTAAGTGTTGGCCAGGCGTGTTGGCTCACATCTGTAATCCCAGCACATAGGAGGCCGA... |
Task1_train_38569 | Assess the clinical impact of this variant found on Chromosome 7. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CTTGTTTAGATGTGTCCTCGTACATACCACTTTCTCAGTTCACCTTTGTTTCTGGCACTCCCAGCTGTTCCTGCTGGCACAGTTTCCTTCTTACTGAACTCAGTGGTAAACTTAGCCTTCTTTTTTCTCCCCAAAACATCTTTATTTCACTTTCTTGAATAATAGATCATCAGAGTAGAAACTCTAAATCGAGGTATTTCCTATTAGCACTTTGAAGATATTCCTCTATTGCCTTCCAACATAATTATTTCATTATCTTCTAGTGTCTTTCATCACCACGAAGAAAATGTCTGGTGTCATTCCTTAGTTTCGGAGTCTGC... | CTTGTTTAGATGTGTCCTCGTACATACCACTTTCTCAGTTCACCTTTGTTTCTGGCACTCCCAGCTGTTCCTGCTGGCACAGTTTCCTTCTTACTGAACTCAGTGGTAAACTTAGCCTTCTTTTTTCTCCCCAAAACATCTTTATTTCACTTTCTTGAATAATAGATCATCAGAGTAGAAACTCTAAATCGAGGTATTTCCTATTAGCACTTTGAAGATATTCCTCTATTGCCTTCCAACATAATTATTTCATTATCTTCTAGTGTCTTTCATCACCACGAAGAAAATGTCTGGTGTCATTCCTTAGTTTCGGAGTCTGC... |
Task1_train_38570 | This sequence change occurs on Chromosome 7. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GGGGTCAGAACATTGATCTTCTAATATTTGAAAGCCTGTTAACTAGGAAAGAGAGAGCAAACGATTTTGTTGTAGGAGGACCCACCCAGCTCTGACGGTTTAAAGCGTCATGAATGCGAATTTGAACTCCAGAAAAGCAGAGCTTCCTAACAATGGGACTTCCACAGCAATGGGATCGGCTTCCTCTTTCAGTGTGTGCCTTTTCTATGAGCGAGAGACTCCTAGGAAAGCAGCAGCCCATTAGGAAAACGTGTGGGAACTCACTCGCAGGTTCTTTATTTTTTTTGAGATGGAGTTTTGCTCTTGTTGCCCAGGCTGGA... | GGGGTCAGAACATTGATCTTCTAATATTTGAAAGCCTGTTAACTAGGAAAGAGAGAGCAAACGATTTTGTTGTAGGAGGACCCACCCAGCTCTGACGGTTTAAAGCGTCATGAATGCGAATTTGAACTCCAGAAAAGCAGAGCTTCCTAACAATGGGACTTCCACAGCAATGGGATCGGCTTCCTCTTTCAGTGTGTGCCTTTTCTATGAGCGAGAGACTCCTAGGAAAGCAGCAGCCCATTAGGAAAACGTGTGGGAACTCACTCGCAGGTTCTTTATTTTTTTTGAGATGGAGTTTTGCTCTTGTTGCCCAGGCTGGA... |
Task1_train_38571 | A mutation is present on Chromosome 7. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GTCTCTTGGACTCAAAATTGCCTTAGGGCAGAGGACGTGTGTACCCCCAGTATAGAATCTGGGACAGTGAATGTGAGTAAACATTCGGCAGAAAAGCTCTGCCAAACTGAGTGCTCTGATGTGACTTTTTCATCAAGTCAGTATTCCTGGGATCTCTTGTACATGATAATCTCACTCTTGCACATGATAATCTCACTCTTGTACATGATAATCTCACTCTTGCACATGATAATCTCACTCTTGTACATGATAATCTCACTCTTATAAGGTTTCATCGTTTCTGCTTACCCTAGTTTTCTTTCCCACTCTGTTCCCTCTCC... | GTCTCTTGGACTCAAAATTGCCTTAGGGCAGAGGACGTGTGTACCCCCAGTATAGAATCTGGGACAGTGAATGTGAGTAAACATTCGGCAGAAAAGCTCTGCCAAACTGAGTGCTCTGATGTGACTTTTTCATCAAGTCAGTATTCCTGGGATCTCTTGTACATGATAATCTCACTCTTGCACATGATAATCTCACTCTTGTACATGATAATCTCACTCTTGCACATGATAATCTCACTCTTGTACATGATAATCTCACTCTTATAAGGTTTCATCGTTTCTGCTTACCCTAGTTTTCTTTCCCACTCTGTTCCCTCTCC... |
Task1_train_38572 | With a mutation on Chromosome 7, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GTTCGAGACCAGCCTGGCCAACATGGCCAAACCCCGTCTCTACTAAAACTAGAAAAATTAGCTGGGCGTGGTGGTGTGCATCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAAGAGAACCCTTTGAACCCAGGAGGTGGAGGTTGCAGTAAGCTAAGGTCGAGCCACTGCACTCCAGCCTGGGTGACAGAGTGAGACTTTTTCTCAAAAAAAAAAAAAAAAAAAGCCAAAAAAACAAACTCCAATGCCAGTGTACAAATAAAAGAATAAAACAAAAGGAACCATAAACCGCTCCTAAGGGGAAAAGAAAAGGAGTGGAG... | GTTCGAGACCAGCCTGGCCAACATGGCCAAACCCCGTCTCTACTAAAACTAGAAAAATTAGCTGGGCGTGGTGGTGTGCATCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAAGAGAACCCTTTGAACCCAGGAGGTGGAGGTTGCAGTAAGCTAAGGTCGAGCCACTGCACTCCAGCCTGGGTGACAGAGTGAGACTTTTTCTCAAAAAAAAAAAAAAAAAAAGCCAAAAAAACAAACTCCAATGCCAGTGTACAAATAAAAGAATAAAACAAAAGGAACCATAAACCGCTCCTAAGGGGAAAAGAAAAGGAGTGGAG... |
Task1_train_38573 | This alteration on Chromosome 7 may affect genome function. Does it lead to a disease or is it benign? | Benign | CCCCCTTCTGACAACCAGCAAACACTGCATAGGTGGTCAATACAAGAATGTGGTAAAAGACACCACTGCACACACCACAACAGAAGGAAGGACCAGCCACAGATATCCCACCCTGGCTGGTGACCCTCAAGAGACCAGTTTCTATGAAAAAGAAATTTCTAAATGCGACCCCAGCCCTGCCCAATATTTATGAACGGATCAGAAGCTACCCACTGGAGAGATAAATGTAAAACTCAACAATGAACAGTTGTCATCCACCCCTCAACCTGTACCCCCCCTCCCCTTACAGAGGAAAGGGCATCATGTGTGTCAATCAAGTC... | CCCCCTTCTGACAACCAGCAAACACTGCATAGGTGGTCAATACAAGAATGTGGTAAAAGACACCACTGCACACACCACAACAGAAGGAAGGACCAGCCACAGATATCCCACCCTGGCTGGTGACCCTCAAGAGACCAGTTTCTATGAAAAAGAAATTTCTAAATGCGACCCCAGCCCTGCCCAATATTTATGAACGGATCAGAAGCTACCCACTGGAGAGATAAATGTAAAACTCAACAATGAACAGTTGTCATCCACCCCTCAACCTGTACCCCCCCTCCCCTTACAGAGGAAAGGGCATCATGTGTGTCAATCAAGTC... |
Task1_train_38574 | A variant was discovered on Chromosome 7. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GTGCTGGGATTACAGGCGTGAGTCACTGCGCCCTGCCCCTTTAATTCTTACAATCTTATACTTTATTGGCCAGTGTTTACGAAACAAACTTGAATTCAAAAAGATCTTTTTTTTTTCCTATTTCCCCAATATTTCACTACCCATGTACTGAGCACCTTTAGGGCACCAGGCAAAAAATGCACTGAGATAAATAAGCAGAGGTCTTGACCTCAAGGAACTTGCAGTCTAATCGGGGAAAACACCAATACATAACAGATGAGTAAATGTAATAATAGTTTTGGTGTTACAGCATGTGCCTAGTCCCAGTATGACACAAAAAC... | GTGCTGGGATTACAGGCGTGAGTCACTGCGCCCTGCCCCTTTAATTCTTACAATCTTATACTTTATTGGCCAGTGTTTACGAAACAAACTTGAATTCAAAAAGATCTTTTTTTTTTCCTATTTCCCCAATATTTCACTACCCATGTACTGAGCACCTTTAGGGCACCAGGCAAAAAATGCACTGAGATAAATAAGCAGAGGTCTTGACCTCAAGGAACTTGCAGTCTAATCGGGGAAAACACCAATACATAACAGATGAGTAAATGTAATAATAGTTTTGGTGTTACAGCATGTGCCTAGTCCCAGTATGACACAAAAAC... |
Task1_train_38575 | This mutation is located on Chromosome 7. Is it associated with a disease or is it a benign polymorphism? | Benign | GCAAAACCCCATCTCTACAAAAAATACAAAAATTAGCTGGGTATGGTGGCATGCACCTATAGTCCCAGATACTCAGGAGGCTGAGGTGGGAGGATGCCTTGAGCCCGAGAGGCAGAGGTTGCAGTGAGTGAAGATGGCACAACTGCACTCCAGCCTGGGCAACAGAGAGACCCTGTCTCCAAAAAAAAAAAAAAAAGCAAAAAGGAGAAATCAAAGTACATACCAGATAATCTCACTAAATCCTCACAGTGACCCTGAGATAACCACACTATTACCATCTGCAATTTACCATTTCACAGATAAGCAACTGAAGCTTAGAT... | GCAAAACCCCATCTCTACAAAAAATACAAAAATTAGCTGGGTATGGTGGCATGCACCTATAGTCCCAGATACTCAGGAGGCTGAGGTGGGAGGATGCCTTGAGCCCGAGAGGCAGAGGTTGCAGTGAGTGAAGATGGCACAACTGCACTCCAGCCTGGGCAACAGAGAGACCCTGTCTCCAAAAAAAAAAAAAAAAGCAAAAAGGAGAAATCAAAGTACATACCAGATAATCTCACTAAATCCTCACAGTGACCCTGAGATAACCACACTATTACCATCTGCAATTTACCATTTCACAGATAAGCAACTGAAGCTTAGAT... |
Task1_train_38576 | A variant on Chromosome 7 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | AGCCCTGGGGCCCTTTCCCTTCTGGAGGAAGCACAAGCCTCAGGGAAGGGGAAGCAGGATGCGGAGGGCCAAAGCCCGGGACCTCTACTTGAACAGTTCTACTGGGGAGGCTGGAGAACTAAGGAAACACCTGTACATAGTGTCCGCTGCCCTGACTCCCGCTTAGCACACCCTTAGGCAGGCGCCCCTTCCACCTTTCCCCGAGACCGTCGTCGCTGGAGGGGGCAGGGTCCAGCCCGCCTGGATCGGTGGTGTGCACCTGATGGGATTTGGGAAATGGGCTATCCGTAAAGCTTTATCTTGCTTGGCTTAGCTGTGAG... | AGCCCTGGGGCCCTTTCCCTTCTGGAGGAAGCACAAGCCTCAGGGAAGGGGAAGCAGGATGCGGAGGGCCAAAGCCCGGGACCTCTACTTGAACAGTTCTACTGGGGAGGCTGGAGAACTAAGGAAACACCTGTACATAGTGTCCGCTGCCCTGACTCCCGCTTAGCACACCCTTAGGCAGGCGCCCCTTCCACCTTTCCCCGAGACCGTCGTCGCTGGAGGGGGCAGGGTCCAGCCCGCCTGGATCGGTGGTGTGCACCTGATGGGATTTGGGAAATGGGCTATCCGTAAAGCTTTATCTTGCTTGGCTTAGCTGTGAG... |
Task1_train_38577 | This sequence variant lies on Chromosome 7. Is it clinically significant, and what condition might it cause if any? | Benign | AGCACAAGCCTCAGGGAAGGGGAAGCAGGATGCGGAGGGCCAAAGCCCGGGACCTCTACTTGAACAGTTCTACTGGGGAGGCTGGAGAACTAAGGAAACACCTGTACATAGTGTCCGCTGCCCTGACTCCCGCTTAGCACACCCTTAGGCAGGCGCCCCTTCCACCTTTCCCCGAGACCGTCGTCGCTGGAGGGGGCAGGGTCCAGCCCGCCTGGATCGGTGGTGTGCACCTGATGGGATTTGGGAAATGGGCTATCCGTAAAGCTTTATCTTGCTTGGCTTAGCTGTGAGAAGTGGTTCTCTTCCTCTGGTCCCTTCTG... | AGCACAAGCCTCAGGGAAGGGGAAGCAGGATGCGGAGGGCCAAAGCCCGGGACCTCTACTTGAACAGTTCTACTGGGGAGGCTGGAGAACTAAGGAAACACCTGTACATAGTGTCCGCTGCCCTGACTCCCGCTTAGCACACCCTTAGGCAGGCGCCCCTTCCACCTTTCCCCGAGACCGTCGTCGCTGGAGGGGGCAGGGTCCAGCCCGCCTGGATCGGTGGTGTGCACCTGATGGGATTTGGGAAATGGGCTATCCGTAAAGCTTTATCTTGCTTGGCTTAGCTGTGAGAAGTGGTTCTCTTCCTCTGGTCCCTTCTG... |
Task1_train_38578 | Given this context: Chromosome 7 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AGGGAGAAGCTCTTGGAGCAGGCAGGATGCCCACCGCTGCTTCAGCTGCCTCCTCGCCCAGCTACCCTTTGGCCCCATTGGGCCCTCGTCTGCCTCTCCAGGATTGTATGTTTCAAGCCTTGCCCTGTGTTCCTTTGTCTGACGCTCTGTGTATTGCTCTTTGAATCGAGTTTGGAGGAAGAGTTGAGTTGTATGAGTGGCGGCATGTTGGTAGTGCCGGACTTCCTGTTTCAAGTTTTCTGGGGCCTCGCTAATTGAATGTGGAAAGTAGCACCACTTGACGGCTACAAGTGCCGACTCCTGAATTTTCCCATGGTGTT... | AGGGAGAAGCTCTTGGAGCAGGCAGGATGCCCACCGCTGCTTCAGCTGCCTCCTCGCCCAGCTACCCTTTGGCCCCATTGGGCCCTCGTCTGCCTCTCCAGGATTGTATGTTTCAAGCCTTGCCCTGTGTTCCTTTGTCTGACGCTCTGTGTATTGCTCTTTGAATCGAGTTTGGAGGAAGAGTTGAGTTGTATGAGTGGCGGCATGTTGGTAGTGCCGGACTTCCTGTTTCAAGTTTTCTGGGGCCTCGCTAATTGAATGTGGAAAGTAGCACCACTTGACGGCTACAAGTGCCGACTCCTGAATTTTCCCATGGTGTT... |
Task1_train_38579 | Consider a variant on Chromosome 7. Determine its clinical classification and disease relevance. | Benign | ACGGGTTCGGACGTAGTCATCAAACATGTCTCGCATCTGGTCAAAACGCTGGTGTGTGATGGGTACCCCTGTGGCGGGCAGCTGCTGCTGGCACAGGCTGGGGGCAGGGCAGGGGTCAGGGGCTGGGGGTAAGGCGGCATGGCCCCCTGGTCCCAGCACCCGCCTGGACCCTGCCTACTTAATGGCGGCATTGAGCTCCTCAATCTCATCCCGCAGCTGCTGGGCCTCCTCCTGCAAGCCCGCACGCTCCTGCTGTAGCATAAGGATGTACTCAGCTGTCTTCTGCAGCGTGGTAGCTTTGCTCACCTGCAGACGCCACC... | ACGGGTTCGGACGTAGTCATCAAACATGTCTCGCATCTGGTCAAAACGCTGGTGTGTGATGGGTACCCCTGTGGCGGGCAGCTGCTGCTGGCACAGGCTGGGGGCAGGGCAGGGGTCAGGGGCTGGGGGTAAGGCGGCATGGCCCCCTGGTCCCAGCACCCGCCTGGACCCTGCCTACTTAATGGCGGCATTGAGCTCCTCAATCTCATCCCGCAGCTGCTGGGCCTCCTCCTGCAAGCCCGCACGCTCCTGCTGTAGCATAAGGATGTACTCAGCTGTCTTCTGCAGCGTGGTAGCTTTGCTCACCTGCAGACGCCACC... |
Task1_train_38580 | A variant was discovered on Chromosome 7. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TAATCCCAGCACTTTGGGAGTCCGAGGTGGGAGGATCGCTTGAGGTCAGGAGTTCAAAACCAGCCTGGCCAACATGGCAAAACCCCGTCTCTACTAAAAATACAAAAAGTAGCTGGGTGTGGTGGCACATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCACAAGAATCGCTTGAACCTGGGAGGCGGAAGCTGCAGTGAGCTGAGATGGACTCACTGCATTCCAACCTGGGTGACAGAGTGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAGCTTTACAAGATATGATGCATGCCTGGGATTTTCT... | TAATCCCAGCACTTTGGGAGTCCGAGGTGGGAGGATCGCTTGAGGTCAGGAGTTCAAAACCAGCCTGGCCAACATGGCAAAACCCCGTCTCTACTAAAAATACAAAAAGTAGCTGGGTGTGGTGGCACATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCACAAGAATCGCTTGAACCTGGGAGGCGGAAGCTGCAGTGAGCTGAGATGGACTCACTGCATTCCAACCTGGGTGACAGAGTGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAGCTTTACAAGATATGATGCATGCCTGGGATTTTCT... |
Task1_train_38581 | A mutation is present on Chromosome 7. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | AAGTCTCCACCATGAACACCAAGCCACCAACTCCCCGTCCCTCAGTAGTCCTGTGTACTCCCAAAGCCCCAAAATTTACCCCAGCCTCAAGCAGCCTTGTTTAAAAAATTAAGGAAGGGCCTGTGATAAGCACTGCAAGTTAAACAGAAACAGGGGACTTAAGTGCAGAGTTTGTCACTCTATTTCTGGGAGGGGATGGGCTGCACAGTGTGCAATGGGGCTGGCTGGTAAAGGGAGGACCAGGTGACAGCCAGCCACACTGTCTCAAGGATGAACCTGGCCCTGCTAGCATTATGCTGTAATCCCTGTGGATTAGAACT... | AAGTCTCCACCATGAACACCAAGCCACCAACTCCCCGTCCCTCAGTAGTCCTGTGTACTCCCAAAGCCCCAAAATTTACCCCAGCCTCAAGCAGCCTTGTTTAAAAAATTAAGGAAGGGCCTGTGATAAGCACTGCAAGTTAAACAGAAACAGGGGACTTAAGTGCAGAGTTTGTCACTCTATTTCTGGGAGGGGATGGGCTGCACAGTGTGCAATGGGGCTGGCTGGTAAAGGGAGGACCAGGTGACAGCCAGCCACACTGTCTCAAGGATGAACCTGGCCCTGCTAGCATTATGCTGTAATCCCTGTGGATTAGAACT... |
Task1_train_38582 | A genomic variant on Chromosome 7 is under review. What is the biological outcome — benign or pathogenic? | Benign | TAAGCCCTGCAGTGGGGTTTCCTGCAGGTGTCAGATTCCAGGCCTTGAGAGTGGCCTCTGGGCCTGTTCTCAGGGAATAAGGCCTGGATGTTTTCCACTGCACGGCCAGAGACAGGTCTGAGGAAGTTGAAGGCCCAGGGTGGGGTTGAGGCTGAGTTGGGATCCTCGCCTCTGAGCCCTTCCTCTTAGTGCCACATTCATTCATCCTCAGGTTCTAAGACTGTGACACTGCAGATGGCAAGAAGTCTAGAGCAGCCAGGCCAGGCACAACCTGTGGTCCCAGCTCTGTGGGAGGCTGAGGTGGGAGGCCAGCTTGGGCA... | TAAGCCCTGCAGTGGGGTTTCCTGCAGGTGTCAGATTCCAGGCCTTGAGAGTGGCCTCTGGGCCTGTTCTCAGGGAATAAGGCCTGGATGTTTTCCACTGCACGGCCAGAGACAGGTCTGAGGAAGTTGAAGGCCCAGGGTGGGGTTGAGGCTGAGTTGGGATCCTCGCCTCTGAGCCCTTCCTCTTAGTGCCACATTCATTCATCCTCAGGTTCTAAGACTGTGACACTGCAGATGGCAAGAAGTCTAGAGCAGCCAGGCCAGGCACAACCTGTGGTCCCAGCTCTGTGGGAGGCTGAGGTGGGAGGCCAGCTTGGGCA... |
Task1_train_38583 | A genetic alteration is present on Chromosome 7. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GGGCAGGTACAGAGCACCTCAGCCGCCTCTCCACCTGACAGCAACATCAAAGCCGAGGCCAAGGCGGGAGGGCCCAGAGTGAGACACCTCTTCCAGACAAGACTTGGTCGCTGCCTCCTCCTCTGTCACCCTGCGACACAGCCCAGAGTACCAGGCGGCTGGAGCACTGGGGGACACCCGGACAGAACCCTCCCTGGACCAAGTCCTCCAGGAACGGGATGAAGCCATTGCCAAGTAAGGGGAAGCTGCTTTTGGGGGCTGGGAGGGGAGTTGGGGGCTCCCCTGCAGGGCCTTGTCCTGCTAATGGAGGAGCGGGGGGC... | GGGCAGGTACAGAGCACCTCAGCCGCCTCTCCACCTGACAGCAACATCAAAGCCGAGGCCAAGGCGGGAGGGCCCAGAGTGAGACACCTCTTCCAGACAAGACTTGGTCGCTGCCTCCTCCTCTGTCACCCTGCGACACAGCCCAGAGTACCAGGCGGCTGGAGCACTGGGGGACACCCGGACAGAACCCTCCCTGGACCAAGTCCTCCAGGAACGGGATGAAGCCATTGCCAAGTAAGGGGAAGCTGCTTTTGGGGGCTGGGAGGGGAGTTGGGGGCTCCCCTGCAGGGCCTTGTCCTGCTAATGGAGGAGCGGGGGGC... |
Task1_train_38584 | This mutation is located on Chromosome 7. Is it associated with a disease or is it a benign polymorphism? | Benign | TGTTTTGGCCGGGACATAAACACTTAAAAAAAAAAAAAAAAAACGAGATCCAGGGAATTGTGAAAAATTGGAGCTGGGCCGGGTGCGGTAGTGAGCACCTGCAATCCCAGCACTTTAAAAGGTCGAGGTGGGAGGATCGCTCGAGGCAGGAGTTTGAGACCAGCCTGGGGAACATAGTGGCACCATCTCTACAAAAAGTTAAAAAAATTAGCTGGGTGTGGTGGCTCATGCCTGTAATCCCTGTACTTGGGGAGGTCGAGGTAGGCGAATTGCTTGAGCCCAGGAGTTTGAGGCTGCAGTGAGCTTTGATCGCACCACTG... | TGTTTTGGCCGGGACATAAACACTTAAAAAAAAAAAAAAAAAACGAGATCCAGGGAATTGTGAAAAATTGGAGCTGGGCCGGGTGCGGTAGTGAGCACCTGCAATCCCAGCACTTTAAAAGGTCGAGGTGGGAGGATCGCTCGAGGCAGGAGTTTGAGACCAGCCTGGGGAACATAGTGGCACCATCTCTACAAAAAGTTAAAAAAATTAGCTGGGTGTGGTGGCTCATGCCTGTAATCCCTGTACTTGGGGAGGTCGAGGTAGGCGAATTGCTTGAGCCCAGGAGTTTGAGGCTGCAGTGAGCTTTGATCGCACCACTG... |
Task1_train_38585 | Chromosome 7 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GATCGCTCGAGGCAGGAGTTTGAGACCAGCCTGGGGAACATAGTGGCACCATCTCTACAAAAAGTTAAAAAAATTAGCTGGGTGTGGTGGCTCATGCCTGTAATCCCTGTACTTGGGGAGGTCGAGGTAGGCGAATTGCTTGAGCCCAGGAGTTTGAGGCTGCAGTGAGCTTTGATCGCACCACTGCACTCCAGCCTGGGTGACAGGGCGAGACCTTATCTCTTAACGAAAAAAAAAAAAAAATCGAAACGGGCCTCCAAGGTATCACCTTAAAAAAGAAATTAAATGGGCCCCCAAGGTATCACCTTGTCCACTGTATA... | GATCGCTCGAGGCAGGAGTTTGAGACCAGCCTGGGGAACATAGTGGCACCATCTCTACAAAAAGTTAAAAAAATTAGCTGGGTGTGGTGGCTCATGCCTGTAATCCCTGTACTTGGGGAGGTCGAGGTAGGCGAATTGCTTGAGCCCAGGAGTTTGAGGCTGCAGTGAGCTTTGATCGCACCACTGCACTCCAGCCTGGGTGACAGGGCGAGACCTTATCTCTTAACGAAAAAAAAAAAAAAATCGAAACGGGCCTCCAAGGTATCACCTTAAAAAAGAAATTAAATGGGCCCCCAAGGTATCACCTTGTCCACTGTATA... |
Task1_train_38586 | Chromosome 7 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GGATTCCTTTTTGCTGTCCCTACCCCAGAGTCCTCTGCCTTAGTTTCCATGCACACTGCTTGAGCCGCCTGCTGCAAGACCCCCACCCGACCATCTGCTGGAGGGCTTTCTCTGGTGTTTGTGCTGGTAAGATTGGAGGTTCAGCGGGAGTTAATGTCCAACAGGAAGCAGACAGGTCATGGAAGATAAATACCCCAGTATTCATGCTCCTTGGGTGGGGTGACTCTGAGGTGCGTTCTGCACCATTTTCCAGGGGATTTTGGGGATCAGCCCCGGTTGTCTGAACTCAAACCCTGCTCATGAACTCATCTGTCCTTGCC... | GGATTCCTTTTTGCTGTCCCTACCCCAGAGTCCTCTGCCTTAGTTTCCATGCACACTGCTTGAGCCGCCTGCTGCAAGACCCCCACCCGACCATCTGCTGGAGGGCTTTCTCTGGTGTTTGTGCTGGTAAGATTGGAGGTTCAGCGGGAGTTAATGTCCAACAGGAAGCAGACAGGTCATGGAAGATAAATACCCCAGTATTCATGCTCCTTGGGTGGGGTGACTCTGAGGTGCGTTCTGCACCATTTTCCAGGGGATTTTGGGGATCAGCCCCGGTTGTCTGAACTCAAACCCTGCTCATGAACTCATCTGTCCTTGCC... |
Task1_train_38587 | This sequence change occurs on Chromosome 7. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TTTGGTCTCAGCATAGCTCCACCCTCCACGTCCCAAGCTCTGCAAATCCAGCCCGTGAGTGGGGGGTCTTGCAGCCAATCTCAGATGGTGGGGCCTGTGGACACGGGGATGGGGGGTCCAGGTGGGTGGATTGGTGTCACTCAAGGGCTGGGGGCTTTCCAGCTCTGATGAAGGGTCTCCAGGACTCAAGAACAGCTTTCCCCCACCTCACCCCAGTCCTGCAGCTTCATCTCAGTGAATGGGAGACACCGTTGTCCAACTCACCACCCAGATCAGAAATCTGGAATTCTTTTTTTTTTTTTTTGAGATGGAGTCTCACT... | TTTGGTCTCAGCATAGCTCCACCCTCCACGTCCCAAGCTCTGCAAATCCAGCCCGTGAGTGGGGGGTCTTGCAGCCAATCTCAGATGGTGGGGCCTGTGGACACGGGGATGGGGGGTCCAGGTGGGTGGATTGGTGTCACTCAAGGGCTGGGGGCTTTCCAGCTCTGATGAAGGGTCTCCAGGACTCAAGAACAGCTTTCCCCCACCTCACCCCAGTCCTGCAGCTTCATCTCAGTGAATGGGAGACACCGTTGTCCAACTCACCACCCAGATCAGAAATCTGGAATTCTTTTTTTTTTTTTTTGAGATGGAGTCTCACT... |
Task1_train_38588 | This is a variant located on Chromosome 7. Is this mutation a likely cause of disease or not? | Benign | GTCTCACTCCAGGCTGGAGTACAGTGGTGCTGTCTCGGCTCACTGTAGCCTCCACCTTCCAGGTTTAAACGATTCTCCTGCCTCAGCCTCCCGAGTAACTGGGATTACAGGCGTGAGCCACCATGCCTGGCCATGAGCATTTGTTTTAAGAGACAAGTCTTTCTTTAGCCCAGGCTGGAGTGTAGTGGCACAATCATAACTCACTGCAGCCTTAAACTCCTGGGCTCAAGCAATCCTGCTTCAGCCTCCTGAGTAGCTGGGACTGCAGGGGCACGCCACCACACCTGGCTAATTTTTACATTTTTTGTAGAGAAGGGGTC... | GTCTCACTCCAGGCTGGAGTACAGTGGTGCTGTCTCGGCTCACTGTAGCCTCCACCTTCCAGGTTTAAACGATTCTCCTGCCTCAGCCTCCCGAGTAACTGGGATTACAGGCGTGAGCCACCATGCCTGGCCATGAGCATTTGTTTTAAGAGACAAGTCTTTCTTTAGCCCAGGCTGGAGTGTAGTGGCACAATCATAACTCACTGCAGCCTTAAACTCCTGGGCTCAAGCAATCCTGCTTCAGCCTCCTGAGTAGCTGGGACTGCAGGGGCACGCCACCACACCTGGCTAATTTTTACATTTTTTGTAGAGAAGGGGTC... |
Task1_train_38589 | This sequence variant lies on Chromosome 7. Is it clinically significant, and what condition might it cause if any? | Benign | TGCATTCCAGCCTGGGTGACAGAATAAGACTCTGTCTCAAAAACAAAACAAAACAAAACAAAACAAAAAACACCACCATCTCTTAGCGCGGTAGGTAAGTTGACAGATCTCCTTAGTTTTGAATCCTGGCCCCATCCTTACCAACTGTGTGATCTGAGATAGATTACTTTACCTCTATATCTGTTTCTCCTTCTCTAAAAAGTAAAGATGATAATAGTACCATCTCTCTCACTAAGCTGTTGTGAAGACTAAACGAGTTAATATAGCTAAAGCCCTTATAGGGAATAGTACCCATCTCAAGGTAAGAGCTATATTTTGAG... | TGCATTCCAGCCTGGGTGACAGAATAAGACTCTGTCTCAAAAACAAAACAAAACAAAACAAAACAAAAAACACCACCATCTCTTAGCGCGGTAGGTAAGTTGACAGATCTCCTTAGTTTTGAATCCTGGCCCCATCCTTACCAACTGTGTGATCTGAGATAGATTACTTTACCTCTATATCTGTTTCTCCTTCTCTAAAAAGTAAAGATGATAATAGTACCATCTCTCTCACTAAGCTGTTGTGAAGACTAAACGAGTTAATATAGCTAAAGCCCTTATAGGGAATAGTACCCATCTCAAGGTAAGAGCTATATTTTGAG... |
Task1_train_38590 | This alteration occurs on Chromosome 7. Is it associated with a disease or is it a benign variant? | Benign | CGAGGAGCCGGGCAGGAGCCTGTGCTCTGCAGGGCACTTCCCACGGGACCCTCAGCCCCACTTCTGCTTCTGGGGCACTCCTCCATCAGCAGCTGAGCCAGACAACCGAGTCTTCATGCCTGGTGCCCCAGCTCAGCCTGCTTCTCCCACCCGCTAATGGCCACGCCAGGGCAGAGAAAAAGCCCCCCTGCCCCGCAGCCACCTCGTGGGCCTCCTGACCATCGCTGCAGAGGGGAGTACTCTGGGGCCCCCGCCTCCTAGCGTACCTGGGTTGGCTACCTCCTCTGTTCAGGCCTTTTCCCCCTAGCCACCGTCCCCTC... | CGAGGAGCCGGGCAGGAGCCTGTGCTCTGCAGGGCACTTCCCACGGGACCCTCAGCCCCACTTCTGCTTCTGGGGCACTCCTCCATCAGCAGCTGAGCCAGACAACCGAGTCTTCATGCCTGGTGCCCCAGCTCAGCCTGCTTCTCCCACCCGCTAATGGCCACGCCAGGGCAGAGAAAAAGCCCCCCTGCCCCGCAGCCACCTCGTGGGCCTCCTGACCATCGCTGCAGAGGGGAGTACTCTGGGGCCCCCGCCTCCTAGCGTACCTGGGTTGGCTACCTCCTCTGTTCAGGCCTTTTCCCCCTAGCCACCGTCCCCTC... |
Task1_train_38591 | This mutation is located on Chromosome 7. Is it associated with a disease or is it a benign polymorphism? | Benign | ACCGTAACTCAGGTTCAAATCACTTTAATCTGCCATGTCCTCATGTCACCTGTCAACTGCCAGGTCACTCCCTGATTCACAGAGGACCCTTGGCTCACTGGCTTCCTCCCCATCACCACTCACGGTGACTTCGCCCTGTGGGGCTGACTGATGGTCCTCTCAGCCCCTCGGCCCTGCCACCCCCATGACCTCCTCTCCCCGACCCCTGCCACCACTCCTGCAGCCACACTGTCACCACAACTGCTCCGGCTCCCGAATCTCCTGCAGGCACCACCCCTCCTGCAGCTGACTTCACCCGCTCTCCACTCCTGCACCCCCTG... | ACCGTAACTCAGGTTCAAATCACTTTAATCTGCCATGTCCTCATGTCACCTGTCAACTGCCAGGTCACTCCCTGATTCACAGAGGACCCTTGGCTCACTGGCTTCCTCCCCATCACCACTCACGGTGACTTCGCCCTGTGGGGCTGACTGATGGTCCTCTCAGCCCCTCGGCCCTGCCACCCCCATGACCTCCTCTCCCCGACCCCTGCCACCACTCCTGCAGCCACACTGTCACCACAACTGCTCCGGCTCCCGAATCTCCTGCAGGCACCACCCCTCCTGCAGCTGACTTCACCCGCTCTCCACTCCTGCACCCCCTG... |
Task1_train_38592 | This mutation is located on Chromosome 7. Is it associated with a disease or is it a benign polymorphism? | Benign | CCACAAAAGAGAAATTTTAATGGGGTCAGAACATTGATCTTCTAATATTTGAAAGCCTGTTAACTAGGAGAGAGAGAGCAAACGATTTTGTTGTAGAAGGACCCACCCAGCTCTGACGGTTTAAAGCATCATGAATGCGAATTTGAACTCCAGAAAAGCAGAGCTTCCTAACAATGGGACTTCCACAGCAATGGGATCTGCTTCCTCTTTCAGTGTGTGCCTTTTCTATGAGCGAGAGACTCCTAGGAAAGCAGCAGCCCATTAGGAAAACGTGTGGGAACTCACTCGCAGGTTCTTTATTTTTTTTGAGATGGAGTTTT... | CCACAAAAGAGAAATTTTAATGGGGTCAGAACATTGATCTTCTAATATTTGAAAGCCTGTTAACTAGGAGAGAGAGAGCAAACGATTTTGTTGTAGAAGGACCCACCCAGCTCTGACGGTTTAAAGCATCATGAATGCGAATTTGAACTCCAGAAAAGCAGAGCTTCCTAACAATGGGACTTCCACAGCAATGGGATCTGCTTCCTCTTTCAGTGTGTGCCTTTTCTATGAGCGAGAGACTCCTAGGAAAGCAGCAGCCCATTAGGAAAACGTGTGGGAACTCACTCGCAGGTTCTTTATTTTTTTTGAGATGGAGTTTT... |
Task1_train_38593 | A mutation located on Chromosome 7 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | AGGTACTCGGGAGGCTGAGGCACGAGAATCACTTGAACCCAGGAGGCGGAGGTTGCAGTGAACCGAGATTGTGCCACTGCACTCCAGCCTGGGTGACAGAGCGAGACTCCGTCTCAGAAAAAAAAAAAAAAGAAAAAGCATCAGAACCAGGTCAGGAGGAGAAGGCAAAGAGTTGCCACTGCTCTCCTTCTGGGATCTTCTCACCCAGCTCCAGAAAGGCAAGGGGCCTTGGATGCTTGGAGCCATTGCTCAGCCCCCGGGAACCACATCACCTGCTCCCTCGGGTTTTTCATAGAAGAGACACATCCCTGGAGAGTGTT... | AGGTACTCGGGAGGCTGAGGCACGAGAATCACTTGAACCCAGGAGGCGGAGGTTGCAGTGAACCGAGATTGTGCCACTGCACTCCAGCCTGGGTGACAGAGCGAGACTCCGTCTCAGAAAAAAAAAAAAAAGAAAAAGCATCAGAACCAGGTCAGGAGGAGAAGGCAAAGAGTTGCCACTGCTCTCCTTCTGGGATCTTCTCACCCAGCTCCAGAAAGGCAAGGGGCCTTGGATGCTTGGAGCCATTGCTCAGCCCCCGGGAACCACATCACCTGCTCCCTCGGGTTTTTCATAGAAGAGACACATCCCTGGAGAGTGTT... |
Task1_train_38594 | Mutation context: Chromosome 7. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CCAGCTGCCACTGTCACCCCCTGAACCCTCACTCTGGGCCTCCTGACCTGGGGCAGGGCCAGCCTTCCGCCCCTCCCGAGCCTCACATCTCCCTCCAGGTATGAATCTGGGGACCACGTGGCTGTGTACCCAGCCAACGACTCTGCTCTCGTCAACCAGCTGGGCAAAATCCTGGGTGCCGACCTGGACGTCGTCATGTCCCTGAACAACCTGGATGGTGAGTGCCACAGTCAGGGCGCCCTGCCGGGCTCAGGCAGCCGCGGGATTGGGCCTGTAGGAAGGCCCTGGGTTGAGCTTCTGCTTAGGCCTGAAGCCCCGGT... | CCAGCTGCCACTGTCACCCCCTGAACCCTCACTCTGGGCCTCCTGACCTGGGGCAGGGCCAGCCTTCCGCCCCTCCCGAGCCTCACATCTCCCTCCAGGTATGAATCTGGGGACCACGTGGCTGTGTACCCAGCCAACGACTCTGCTCTCGTCAACCAGCTGGGCAAAATCCTGGGTGCCGACCTGGACGTCGTCATGTCCCTGAACAACCTGGATGGTGAGTGCCACAGTCAGGGCGCCCTGCCGGGCTCAGGCAGCCGCGGGATTGGGCCTGTAGGAAGGCCCTGGGTTGAGCTTCTGCTTAGGCCTGAAGCCCCGGT... |
Task1_train_38595 | A variant was discovered on Chromosome 7. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | AGGGCCGGCACTGCCCTGCCAGCCACACGCTGGAGGCCCAGCCCTGCTCACAGCAGGCAGAGTGCAAGGCGGCACAGGAGCTCCGAGATCTGAGCCCTGAGCTCCAGTTCCAGCCCCAGCGCAGCTCCAAATGCCTCCCCAGGCTGTGGACTCAGTCGGGCTGGCTTGTGAGATTCTCAGCATCTGTCCAGCCCCGGTCCCCAGAACCAGTCCGGGAAGCCGCTGGGGAGGGGGCCTCTGAGGTTTGGGTGCCAGGTGGGCTGGAAGAGGCCCTGGGTGAGTGGGGCTGGCCTGCAGAACGGGACTTGGGGCCGGGGCTG... | AGGGCCGGCACTGCCCTGCCAGCCACACGCTGGAGGCCCAGCCCTGCTCACAGCAGGCAGAGTGCAAGGCGGCACAGGAGCTCCGAGATCTGAGCCCTGAGCTCCAGTTCCAGCCCCAGCGCAGCTCCAAATGCCTCCCCAGGCTGTGGACTCAGTCGGGCTGGCTTGTGAGATTCTCAGCATCTGTCCAGCCCCGGTCCCCAGAACCAGTCCGGGAAGCCGCTGGGGAGGGGGCCTCTGAGGTTTGGGTGCCAGGTGGGCTGGAAGAGGCCCTGGGTGAGTGGGGCTGGCCTGCAGAACGGGACTTGGGGCCGGGGCTG... |
Task1_train_38596 | This variant is found on Chromosome 7. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TCCCATTGTTAAATGCTCAGGCCCTAGTGCCCCTCCTTTGAGAATTCTGATTCCAAGGCAAGGGATCTTTCCCTCCTCTGGAGTTGAATGTTCCATTGAGAAACACCTACTCTTCCAGCATGTCTCAGCTTATCTGCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCGCGCGCGCGCGCGCGCTTTTGAGCCGGAGTTTAGCTCTTATCACCCAGGATGGAGTACAATGGCACAATCTTGGCTCACAGCAACCTCCACCTCCTGGGTTCAAGGGATTCTCC... | TCCCATTGTTAAATGCTCAGGCCCTAGTGCCCCTCCTTTGAGAATTCTGATTCCAAGGCAAGGGATCTTTCCCTCCTCTGGAGTTGAATGTTCCATTGAGAAACACCTACTCTTCCAGCATGTCTCAGCTTATCTGCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCGCGCGCGCGCGCGCGCTTTTGAGCCGGAGTTTAGCTCTTATCACCCAGGATGGAGTACAATGGCACAATCTTGGCTCACAGCAACCTCCACCTCCTGGGTTCAAGGGATTCTCC... |
Task1_train_38597 | A genetic alteration is present on Chromosome 7. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | ATTCAAGACCACCCTGGGCAAAATAACAAGAACGTGACTCTACAAAAAAAAATTCTTTGTTTTAATTAGCTGGGTATGGTGGCACATGCCTGTAGTTCCAGCTACTGGGGAGACTGAGGTGGGAGGATATCGCTTGAGCTCAGGAGTTCAAGGCTGCAGTGAGCTATGACTGTGCCACTGCACTCCAGCCTGGGTGATAGAGTGAGACCCTGTCTCAAAAAATGAACAAAGAAGAAGGGATGAGGGACCCAACTTGATGACAGGTGAACTGTTGTGGGTCAGGTCAATAGGGGTCTCCAAGCTCCACACATGTCCCTGGC... | ATTCAAGACCACCCTGGGCAAAATAACAAGAACGTGACTCTACAAAAAAAAATTCTTTGTTTTAATTAGCTGGGTATGGTGGCACATGCCTGTAGTTCCAGCTACTGGGGAGACTGAGGTGGGAGGATATCGCTTGAGCTCAGGAGTTCAAGGCTGCAGTGAGCTATGACTGTGCCACTGCACTCCAGCCTGGGTGATAGAGTGAGACCCTGTCTCAAAAAATGAACAAAGAAGAAGGGATGAGGGACCCAACTTGATGACAGGTGAACTGTTGTGGGTCAGGTCAATAGGGGTCTCCAAGCTCCACACATGTCCCTGGC... |
Task1_train_38598 | A mutation on Chromosome 7 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | ATACACTGGGAATGATAGCCCTTAGTTTGCTATGAGTTATGAGTTGTGGGCAACCACTTTATCTCTTACAGAGCAGAGTCCATCTGTGAAATAGCATTATTGGCCCTATTATTCCTCTTTGCTGAGAAACCCTCCCAAATTGGAGAGGGCCTAGGTGGGGAGAAAATACTATTATTAGAGCATCAGGATGACAGAGGGGTGTGCTAGGTAATGCTGTGAGCATCAGAGAATGCTGGAATATCTCTGGGGCAATTCTAGAGTGTTACTCCGAGTGTTATCCTAGAGTGTTACTCTAAAGTGGTCCAGGAACAGTACTTGCT... | ATACACTGGGAATGATAGCCCTTAGTTTGCTATGAGTTATGAGTTGTGGGCAACCACTTTATCTCTTACAGAGCAGAGTCCATCTGTGAAATAGCATTATTGGCCCTATTATTCCTCTTTGCTGAGAAACCCTCCCAAATTGGAGAGGGCCTAGGTGGGGAGAAAATACTATTATTAGAGCATCAGGATGACAGAGGGGTGTGCTAGGTAATGCTGTGAGCATCAGAGAATGCTGGAATATCTCTGGGGCAATTCTAGAGTGTTACTCCGAGTGTTATCCTAGAGTGTTACTCTAAAGTGGTCCAGGAACAGTACTTGCT... |
Task1_train_38599 | Given this variant on Chromosome 7, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GACAGGGTCTCACTGTGTCCCCCAGGCTAGAGTACAGTGGCATGATCTTACTGCAACCTCTGCCTCCCGGGTTCAAGTGATCCCCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGAATATGCCACCACGCCTGGCTAATTTTTGTATTTTTTGTAGAGACAGGGTTTCACCATGTTGGCCAGTCTGGTCTGGAGCTCCCAACCTCAAGTGATCCGCTGGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCATGCCCAGCCATTTTCTCTAACTTTACATCTTCAATTTGTAATCCCTGTCTTCCC... | GACAGGGTCTCACTGTGTCCCCCAGGCTAGAGTACAGTGGCATGATCTTACTGCAACCTCTGCCTCCCGGGTTCAAGTGATCCCCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGAATATGCCACCACGCCTGGCTAATTTTTGTATTTTTTGTAGAGACAGGGTTTCACCATGTTGGCCAGTCTGGTCTGGAGCTCCCAACCTCAAGTGATCCGCTGGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCATGCCCAGCCATTTTCTCTAACTTTACATCTTCAATTTGTAATCCCTGTCTTCCC... |
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