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_40700 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | CAGGGACTGGCTCCAGGCTCTGAATTTGGCTCAGGTTTGCACCATGTACCTCCTTCTGGAAACCAGATTCAAGGGGAATTACCTACTAGGTTAGCACTACCCCAGTACAAGAAATCAAACCCTGCAGCAAAATCACACTGAAGCTCTTGCTTTTATCACATCCACTAACATCCTATTGACCAAAACAAGTCATGAGGACCACAATGGCCAGAGAAAATTATGTGTCTAAAGTGAGAGTGAATGTAAATACAATCCGTCCACTTTGTCCCTCCTGATGTGGATGTGAATGTATACTGCTGCTACTAGGAAGTAAAGAATTG... | CAGGGACTGGCTCCAGGCTCTGAATTTGGCTCAGGTTTGCACCATGTACCTCCTTCTGGAAACCAGATTCAAGGGGAATTACCTACTAGGTTAGCACTACCCCAGTACAAGAAATCAAACCCTGCAGCAAAATCACACTGAAGCTCTTGCTTTTATCACATCCACTAACATCCTATTGACCAAAACAAGTCATGAGGACCACAATGGCCAGAGAAAATTATGTGTCTAAAGTGAGAGTGAATGTAAATACAATCCGTCCACTTTGTCCCTCCTGATGTGGATGTGAATGTATACTGCTGCTACTAGGAAGTAAAGAATTG... |
Task1_train_40701 | A mutation on Chromosome 11 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | AAATCATTTTATGAGGCCAGCATCATCCTGATACCAAGGCCAGGCAGAGACACAACAAAAAAACAGAATTTCAGACCAATATCCCTGATGAACATCAATGCAAAAATACTCAATAAAATACTGGCAAACCGAATCCAGCAGCACATCAAAAAGCTTATCCGCCACGATCATGTTGGCTTCATCCCTGGGATGCAAGGCTGGTTCGACATATGCAAATCAATAAACGTAATCCATCATATAAACAGAACCAAAGACAAAAACCACATGATTATCTCAATAGATGCAGAAAAGGCTTTCGACAAAATTCAACAGCCCTTCAT... | AAATCATTTTATGAGGCCAGCATCATCCTGATACCAAGGCCAGGCAGAGACACAACAAAAAAACAGAATTTCAGACCAATATCCCTGATGAACATCAATGCAAAAATACTCAATAAAATACTGGCAAACCGAATCCAGCAGCACATCAAAAAGCTTATCCGCCACGATCATGTTGGCTTCATCCCTGGGATGCAAGGCTGGTTCGACATATGCAAATCAATAAACGTAATCCATCATATAAACAGAACCAAAGACAAAAACCACATGATTATCTCAATAGATGCAGAAAAGGCTTTCGACAAAATTCAACAGCCCTTCAT... |
Task1_train_40702 | A genomic change on Chromosome 11 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TAAAAAATTCTGGAGTGAGGATAGCTTGTCTTCTTCTCTCTAGCCTTCCATTGGCTCTACCTTCATCTTTTGTATTTTTGTTATTTTTAATTAAAATTATTAATTTCATAATTTTAATTTATGCATTTACTAAGGAAGCTTATTAAATATAGGCGGAATTTATAATGATTGTCTTAGAGATTTGTGTTTCTCTGACAGTTTTACCAATTTTTACCTGTTTACCTTGAAGGCCAAAAACTTGATGATAAGTTGCAAGATTGCATATTTTACTTCTGAAAGTAAACTTGTATGCTTTTTAAAAGAGACTCTAAAATAAAATC... | TAAAAAATTCTGGAGTGAGGATAGCTTGTCTTCTTCTCTCTAGCCTTCCATTGGCTCTACCTTCATCTTTTGTATTTTTGTTATTTTTAATTAAAATTATTAATTTCATAATTTTAATTTATGCATTTACTAAGGAAGCTTATTAAATATAGGCGGAATTTATAATGATTGTCTTAGAGATTTGTGTTTCTCTGACAGTTTTACCAATTTTTACCTGTTTACCTTGAAGGCCAAAAACTTGATGATAAGTTGCAAGATTGCATATTTTACTTCTGAAAGTAAACTTGTATGCTTTTTAAAAGAGACTCTAAAATAAAATC... |
Task1_train_40703 | A mutation located on Chromosome 11 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TCCACATACACTTCATAGTAGAAGACATTGTGTTCAGCCACACCCTTTCTTAATCTGCACTAAAACCATGCAGGAACATGACATTCTCATGCTTCTCTCTAGGTGTTCGAAGCTCCCCTTGGCAATATCACATTCAAGCTTGCTTTCCTCACAGTTACCTCCAAGCCCAAACTGCAAATACTATATTGACATGTATTACTCAAAATATAACTTTTATCTAGAATGTCTTGGGGGTACAATAACAATACAACATATAAAAGGGCATAACAAACTATCCTTGGTTCCTTGGCTTATAATCTCTTTCTGATACAGTCAGTACC... | TCCACATACACTTCATAGTAGAAGACATTGTGTTCAGCCACACCCTTTCTTAATCTGCACTAAAACCATGCAGGAACATGACATTCTCATGCTTCTCTCTAGGTGTTCGAAGCTCCCCTTGGCAATATCACATTCAAGCTTGCTTTCCTCACAGTTACCTCCAAGCCCAAACTGCAAATACTATATTGACATGTATTACTCAAAATATAACTTTTATCTAGAATGTCTTGGGGGTACAATAACAATACAACATATAAAAGGGCATAACAAACTATCCTTGGTTCCTTGGCTTATAATCTCTTTCTGATACAGTCAGTACC... |
Task1_train_40704 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TGATCATATGCACTTATTTAAAGTTATGCAAAAGCGGTTATGTTTGCAGTTGTTTTCTTTGGTGTCTTCTTCACAGGGAAAGAAGAGGCTCTAAAATAGATCTTTATTAATTTTTAAAAAGTTTTATTAAAAGTTATTGCTTTTAAAAAATTTGTATAATTTTAAAGGGTACAAGTGCAGTGTTGTTACATAGATATATTGCATAGTGGTGAAGTCTGGCCTTTTACTGTAACCATCACCTGAGTAATGTGTATTGTACCCATTAGGTAATTTCTCATGCCTTACTGCCCTCCCATTCTCCTACATTTCTGAGTCACCAG... | TGATCATATGCACTTATTTAAAGTTATGCAAAAGCGGTTATGTTTGCAGTTGTTTTCTTTGGTGTCTTCTTCACAGGGAAAGAAGAGGCTCTAAAATAGATCTTTATTAATTTTTAAAAAGTTTTATTAAAAGTTATTGCTTTTAAAAAATTTGTATAATTTTAAAGGGTACAAGTGCAGTGTTGTTACATAGATATATTGCATAGTGGTGAAGTCTGGCCTTTTACTGTAACCATCACCTGAGTAATGTGTATTGTACCCATTAGGTAATTTCTCATGCCTTACTGCCCTCCCATTCTCCTACATTTCTGAGTCACCAG... |
Task1_train_40705 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GAAGTCTGGCCTTTTACTGTAACCATCACCTGAGTAATGTGTATTGTACCCATTAGGTAATTTCTCATGCCTTACTGCCCTCCCATTCTCCTACATTTCTGAGTCACCAGTGTTTATTATTTCGAACACTATGTCCAGGTGTAAACATTATTTAGCTTTCACTTATAAGGGAGAACATGCAGTATTTGACTTTCTGTTTCTGAGATGTTTCACTTAATGGCCAACAAGCATATGAAAAAATGATCAACTTAATTGATAATTTTTAGTGTAGGTAACTTGCTTCTAGCTCTACTAGTTAAATTTACTTCTTCTTCATGGTG... | GAAGTCTGGCCTTTTACTGTAACCATCACCTGAGTAATGTGTATTGTACCCATTAGGTAATTTCTCATGCCTTACTGCCCTCCCATTCTCCTACATTTCTGAGTCACCAGTGTTTATTATTTCGAACACTATGTCCAGGTGTAAACATTATTTAGCTTTCACTTATAAGGGAGAACATGCAGTATTTGACTTTCTGTTTCTGAGATGTTTCACTTAATGGCCAACAAGCATATGAAAAAATGATCAACTTAATTGATAATTTTTAGTGTAGGTAACTTGCTTCTAGCTCTACTAGTTAAATTTACTTCTTCTTCATGGTG... |
Task1_train_40706 | Here is a genetic alteration on Chromosome 11. Based on the data, is it a benign variant or a cause of disease? | Benign | GTCTGGCCTTTTACTGTAACCATCACCTGAGTAATGTGTATTGTACCCATTAGGTAATTTCTCATGCCTTACTGCCCTCCCATTCTCCTACATTTCTGAGTCACCAGTGTTTATTATTTCGAACACTATGTCCAGGTGTAAACATTATTTAGCTTTCACTTATAAGGGAGAACATGCAGTATTTGACTTTCTGTTTCTGAGATGTTTCACTTAATGGCCAACAAGCATATGAAAAAATGATCAACTTAATTGATAATTTTTAGTGTAGGTAACTTGCTTCTAGCTCTACTAGTTAAATTTACTTCTTCTTCATGGTGAAT... | GTCTGGCCTTTTACTGTAACCATCACCTGAGTAATGTGTATTGTACCCATTAGGTAATTTCTCATGCCTTACTGCCCTCCCATTCTCCTACATTTCTGAGTCACCAGTGTTTATTATTTCGAACACTATGTCCAGGTGTAAACATTATTTAGCTTTCACTTATAAGGGAGAACATGCAGTATTTGACTTTCTGTTTCTGAGATGTTTCACTTAATGGCCAACAAGCATATGAAAAAATGATCAACTTAATTGATAATTTTTAGTGTAGGTAACTTGCTTCTAGCTCTACTAGTTAAATTTACTTCTTCTTCATGGTGAAT... |
Task1_train_40707 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | ACTGAGATGTTGCTACAGAGAGATGTTGCTGAAGTCTATGAGGCCCAGACTCTAAGGGACAAGGTAAGTAAATAATTTTCTCAGGGGCAGTTAATGGAACTAGACAGGGTTAAAATAAAGACCTAGGTAACAGAAGGGGCAGATAATCTCATAATGCTCAGCTGCTGTACCAAGTGCCATCAACACAGTATGATACAGCAAGGGCAACACTGGTTCAGCACAGGCAAGGAGGCTATTACAATAACAATTGCTGAGGGAAAGTAAAGCCAGATGTTAATATCATATTTTGAAACACTCAGAAGAGCTTGGTTGTTTCTAAG... | ACTGAGATGTTGCTACAGAGAGATGTTGCTGAAGTCTATGAGGCCCAGACTCTAAGGGACAAGGTAAGTAAATAATTTTCTCAGGGGCAGTTAATGGAACTAGACAGGGTTAAAATAAAGACCTAGGTAACAGAAGGGGCAGATAATCTCATAATGCTCAGCTGCTGTACCAAGTGCCATCAACACAGTATGATACAGCAAGGGCAACACTGGTTCAGCACAGGCAAGGAGGCTATTACAATAACAATTGCTGAGGGAAAGTAAAGCCAGATGTTAATATCATATTTTGAAACACTCAGAAGAGCTTGGTTGTTTCTAAG... |
Task1_train_40708 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | GAAAGTAAAGCCAGATGTTAATATCATATTTTGAAACACTCAGAAGAGCTTGGTTGTTTCTAAGAGGCACTGATAGTGAATATTTAAGGCCTAAATTCTGGATTGTCATGAGTTCACAGAAGTAGGTGCAAGTGGGTCAGAAAATTAAGAACCACTTAATATTTTGATTGATGATCTTTTAAAAATGATATTAAAAGCATCGTTTGGAAACAGAAATCAATCAATCAAAAAAATCAATAGAAATAAAGTGGAAAAGTACCTCTTTTACTGAAAACATGTAATAGATAACTGTTAAATGCATTGTTCTCATTTTGTGGAAG... | GAAAGTAAAGCCAGATGTTAATATCATATTTTGAAACACTCAGAAGAGCTTGGTTGTTTCTAAGAGGCACTGATAGTGAATATTTAAGGCCTAAATTCTGGATTGTCATGAGTTCACAGAAGTAGGTGCAAGTGGGTCAGAAAATTAAGAACCACTTAATATTTTGATTGATGATCTTTTAAAAATGATATTAAAAGCATCGTTTGGAAACAGAAATCAATCAATCAAAAAAATCAATAGAAATAAAGTGGAAAAGTACCTCTTTTACTGAAAACATGTAATAGATAACTGTTAAATGCATTGTTCTCATTTTGTGGAAG... |
Task1_train_40709 | A variant on Chromosome 11 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TACTCATCACTTTTCTTTGGGCTTCTATTCCCTAGATCAGAGTCAAAAATTTTGTTAACCATCTCAGAGGATTCAATCTCATGGTGCCAATTATAGTAGAAAACCCAGCTAACTCAATTTTCCTAATGTTCTAAGCAACTAAAGCCTTAATATAAAACGACTCTTCTTGGACTGTAAAAATGACAAGGCTATAGAGCCATGCTGCTTGATACTCCCCTTGAGCTTATATTTCTATGACATAATAAGGCAGGTGAATTTTCTCTTGACTTAGGTATGTATTACATTGAAATAAGTGAGAAATGATCAAGGGTTGCTGAGCT... | TACTCATCACTTTTCTTTGGGCTTCTATTCCCTAGATCAGAGTCAAAAATTTTGTTAACCATCTCAGAGGATTCAATCTCATGGTGCCAATTATAGTAGAAAACCCAGCTAACTCAATTTTCCTAATGTTCTAAGCAACTAAAGCCTTAATATAAAACGACTCTTCTTGGACTGTAAAAATGACAAGGCTATAGAGCCATGCTGCTTGATACTCCCCTTGAGCTTATATTTCTATGACATAATAAGGCAGGTGAATTTTCTCTTGACTTAGGTATGTATTACATTGAAATAAGTGAGAAATGATCAAGGGTTGCTGAGCT... |
Task1_train_40710 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | AAAACGACTCTTCTTGGACTGTAAAAATGACAAGGCTATAGAGCCATGCTGCTTGATACTCCCCTTGAGCTTATATTTCTATGACATAATAAGGCAGGTGAATTTTCTCTTGACTTAGGTATGTATTACATTGAAATAAGTGAGAAATGATCAAGGGTTGCTGAGCTTGCTGGGCTTGATATTGATCAGGTAGTACAATTTCTGACTCTAATGGAATAAAAATCCTTTGAAACTCTTAAATGGAGATTGAAAATTTAAAAACGATCTAGAAGACCCATGGAATAGATGTATTTATTCAAAGCAATTATATAGTTTATTGG... | AAAACGACTCTTCTTGGACTGTAAAAATGACAAGGCTATAGAGCCATGCTGCTTGATACTCCCCTTGAGCTTATATTTCTATGACATAATAAGGCAGGTGAATTTTCTCTTGACTTAGGTATGTATTACATTGAAATAAGTGAGAAATGATCAAGGGTTGCTGAGCTTGCTGGGCTTGATATTGATCAGGTAGTACAATTTCTGACTCTAATGGAATAAAAATCCTTTGAAACTCTTAAATGGAGATTGAAAATTTAAAAACGATCTAGAAGACCCATGGAATAGATGTATTTATTCAAAGCAATTATATAGTTTATTGG... |
Task1_train_40711 | A variant on Chromosome 11 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GAGCCATGCTGCTTGATACTCCCCTTGAGCTTATATTTCTATGACATAATAAGGCAGGTGAATTTTCTCTTGACTTAGGTATGTATTACATTGAAATAAGTGAGAAATGATCAAGGGTTGCTGAGCTTGCTGGGCTTGATATTGATCAGGTAGTACAATTTCTGACTCTAATGGAATAAAAATCCTTTGAAACTCTTAAATGGAGATTGAAAATTTAAAAACGATCTAGAAGACCCATGGAATAGATGTATTTATTCAAAGCAATTATATAGTTTATTGGTAAAATATATGTTCTGCCTTTCCTATGGGTTATAAGGAAT... | GAGCCATGCTGCTTGATACTCCCCTTGAGCTTATATTTCTATGACATAATAAGGCAGGTGAATTTTCTCTTGACTTAGGTATGTATTACATTGAAATAAGTGAGAAATGATCAAGGGTTGCTGAGCTTGCTGGGCTTGATATTGATCAGGTAGTACAATTTCTGACTCTAATGGAATAAAAATCCTTTGAAACTCTTAAATGGAGATTGAAAATTTAAAAACGATCTAGAAGACCCATGGAATAGATGTATTTATTCAAAGCAATTATATAGTTTATTGGTAAAATATATGTTCTGCCTTTCCTATGGGTTATAAGGAAT... |
Task1_train_40712 | This sequence change occurs on Chromosome 11. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CTGAGCTTGCTGGGCTTGATATTGATCAGGTAGTACAATTTCTGACTCTAATGGAATAAAAATCCTTTGAAACTCTTAAATGGAGATTGAAAATTTAAAAACGATCTAGAAGACCCATGGAATAGATGTATTTATTCAAAGCAATTATATAGTTTATTGGTAAAATATATGTTCTGCCTTTCCTATGGGTTATAAGGAATAAAATGGACTTCTGTAGAAATACAGCTTATTTCTTTCTCTCTCCTTTTCTCTCTCTTTCTTGCTCTCTATATCTCTACCCCCCTCCACACCTCAGAATGGGTATATTATTTATTTTATTT... | CTGAGCTTGCTGGGCTTGATATTGATCAGGTAGTACAATTTCTGACTCTAATGGAATAAAAATCCTTTGAAACTCTTAAATGGAGATTGAAAATTTAAAAACGATCTAGAAGACCCATGGAATAGATGTATTTATTCAAAGCAATTATATAGTTTATTGGTAAAATATATGTTCTGCCTTTCCTATGGGTTATAAGGAATAAAATGGACTTCTGTAGAAATACAGCTTATTTCTTTCTCTCTCCTTTTCTCTCTCTTTCTTGCTCTCTATATCTCTACCCCCCTCCACACCTCAGAATGGGTATATTATTTATTTTATTT... |
Task1_train_40713 | With a mutation on Chromosome 11, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TTCAAAGCAATTATATAGTTTATTGGTAAAATATATGTTCTGCCTTTCCTATGGGTTATAAGGAATAAAATGGACTTCTGTAGAAATACAGCTTATTTCTTTCTCTCTCCTTTTCTCTCTCTTTCTTGCTCTCTATATCTCTACCCCCCTCCACACCTCAGAATGGGTATATTATTTATTTTATTTTTTATCTTGATGTATTTTCCACTTTGACATACTTGTCAGAAATATGGAGCTACATAAATGGTGAAACAGGAGTCTGTGCTACTTTCTTCTATCCTGAACCACTCTGCCACAAGTTGGAGACCCACAGAAGTTTG... | TTCAAAGCAATTATATAGTTTATTGGTAAAATATATGTTCTGCCTTTCCTATGGGTTATAAGGAATAAAATGGACTTCTGTAGAAATACAGCTTATTTCTTTCTCTCTCCTTTTCTCTCTCTTTCTTGCTCTCTATATCTCTACCCCCCTCCACACCTCAGAATGGGTATATTATTTATTTTATTTTTTATCTTGATGTATTTTCCACTTTGACATACTTGTCAGAAATATGGAGCTACATAAATGGTGAAACAGGAGTCTGTGCTACTTTCTTCTATCCTGAACCACTCTGCCACAAGTTGGAGACCCACAGAAGTTTG... |
Task1_train_40714 | A variant found on Chromosome 11 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GTATGCAGCCCGCTTTGGAGATCAGTATATCAAAACCTGGGAGGATTGTTGTTCAGACATAGTGAGTTTAAACATTTGTCCTTTCATATGTGGTAGCTAATAATCTCTAGAGCTCATTTAGCCATATTAAATATAATCATGAAGAAGAAACAGTAACTTGCATGCGTGTTCGTGTGTGTGTGCTATTGTGATATGTATGTTTCCGGTTGAACTATTAATTCACCAGCAGGCATCAATTGCTGTTAGTACATGTGGGGAAAGCATTAAGGAATTATGCTCCTGGTTTATAATTTCAGTTTCAGGGAAAAGAAGTGGAAACA... | GTATGCAGCCCGCTTTGGAGATCAGTATATCAAAACCTGGGAGGATTGTTGTTCAGACATAGTGAGTTTAAACATTTGTCCTTTCATATGTGGTAGCTAATAATCTCTAGAGCTCATTTAGCCATATTAAATATAATCATGAAGAAGAAACAGTAACTTGCATGCGTGTTCGTGTGTGTGTGCTATTGTGATATGTATGTTTCCGGTTGAACTATTAATTCACCAGCAGGCATCAATTGCTGTTAGTACATGTGGGGAAAGCATTAAGGAATTATGCTCCTGGTTTATAATTTCAGTTTCAGGGAAAAGAAGTGGAAACA... |
Task1_train_40715 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | AATTATGCTCCTGGTTTATAATTTCAGTTTCAGGGAAAAGAAGTGGAAACAGGCTGACAAAAAGTGTAATGAGTGATCAGGATGGGAGGAATTGAGTGTCATTGGAAAGGGACATACAAAACATAGACAAGCAGATATACGAATACAGTCAAAGATGGTTTAGAATGAAATAAACAAAATGCATTATGAAACAACTATTTCGAATAATAAAATTAATCCAGTTGTGTGAAATTAAATTCTAATTTTAAAAATTCTACTAGGACATATAATTTCAATTTTTCTCTCAACAAAGATATAAAAAATATTTGGGGGAATTACGG... | AATTATGCTCCTGGTTTATAATTTCAGTTTCAGGGAAAAGAAGTGGAAACAGGCTGACAAAAAGTGTAATGAGTGATCAGGATGGGAGGAATTGAGTGTCATTGGAAAGGGACATACAAAACATAGACAAGCAGATATACGAATACAGTCAAAGATGGTTTAGAATGAAATAAACAAAATGCATTATGAAACAACTATTTCGAATAATAAAATTAATCCAGTTGTGTGAAATTAAATTCTAATTTTAAAAATTCTACTAGGACATATAATTTCAATTTTTCTCTCAACAAAGATATAAAAAATATTTGGGGGAATTACGG... |
Task1_train_40716 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | TTCAGTTTCAGGGAAAAGAAGTGGAAACAGGCTGACAAAAAGTGTAATGAGTGATCAGGATGGGAGGAATTGAGTGTCATTGGAAAGGGACATACAAAACATAGACAAGCAGATATACGAATACAGTCAAAGATGGTTTAGAATGAAATAAACAAAATGCATTATGAAACAACTATTTCGAATAATAAAATTAATCCAGTTGTGTGAAATTAAATTCTAATTTTAAAAATTCTACTAGGACATATAATTTCAATTTTTCTCTCAACAAAGATATAAAAAATATTTGGGGGAATTACGGTGAAATGAAGAATGAGAGATAA... | TTCAGTTTCAGGGAAAAGAAGTGGAAACAGGCTGACAAAAAGTGTAATGAGTGATCAGGATGGGAGGAATTGAGTGTCATTGGAAAGGGACATACAAAACATAGACAAGCAGATATACGAATACAGTCAAAGATGGTTTAGAATGAAATAAACAAAATGCATTATGAAACAACTATTTCGAATAATAAAATTAATCCAGTTGTGTGAAATTAAATTCTAATTTTAAAAATTCTACTAGGACATATAATTTCAATTTTTCTCTCAACAAAGATATAAAAAATATTTGGGGGAATTACGGTGAAATGAAGAATGAGAGATAA... |
Task1_train_40717 | Assess the clinical impact of this variant found on Chromosome 11. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TCAATGCATTTGTATACTAAGTTCATTGACAGGGAGACTCAAGACTTTTTAAAAATAGGTTCTTCCCCAAAGGACCTATTTATTCATTGTGATTTTGAAAAATACCTCTTTTGTTTTAGAATAATTTTAGATATAACAGTAATTCGTGAGGATATTGCAGATAGTTCCCATATATCCCACATTTAATTCCCCTTATTGTAAACATCTTATATTAGTGTAGTCTATTTTCCAAAATTAATGAAGCAGGTAATTGATACATATTTATTGCTAAAGCTCATACTTTATTAAGATTTTCTTACTTTTTAGCCAATGTCCTTTTT... | TCAATGCATTTGTATACTAAGTTCATTGACAGGGAGACTCAAGACTTTTTAAAAATAGGTTCTTCCCCAAAGGACCTATTTATTCATTGTGATTTTGAAAAATACCTCTTTTGTTTTAGAATAATTTTAGATATAACAGTAATTCGTGAGGATATTGCAGATAGTTCCCATATATCCCACATTTAATTCCCCTTATTGTAAACATCTTATATTAGTGTAGTCTATTTTCCAAAATTAATGAAGCAGGTAATTGATACATATTTATTGCTAAAGCTCATACTTTATTAAGATTTTCTTACTTTTTAGCCAATGTCCTTTTT... |
Task1_train_40718 | A mutation on Chromosome 11 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TGGAATAATTATCTTAACTCAATTTCCTTTTCTTCTCCCTATACCTGATCAATTTCTACTTTCTAAGATTTCTTAAGAAATTTGCCCAACACCCAAGCTGCAGTGCACCCTTCCAAGACATACACACACACACACACACACACACACACACACACTAGTGTGTGAAAGAGTTTTTAATCACAGTGTGCTTGACCACAGTTTTATAAAGATAAGATACATCATAGCAACACAATATAGCAAGACAAATGCTAGACTCACTATCAGGAAGTGGTGTGTACAAATTAACTTACTTTGCCTGACAACTTTGTGATGTTTCATAA... | TGGAATAATTATCTTAACTCAATTTCCTTTTCTTCTCCCTATACCTGATCAATTTCTACTTTCTAAGATTTCTTAAGAAATTTGCCCAACACCCAAGCTGCAGTGCACCCTTCCAAGACATACACACACACACACACACACACACACACACACACTAGTGTGTGAAAGAGTTTTTAATCACAGTGTGCTTGACCACAGTTTTATAAAGATAAGATACATCATAGCAACACAATATAGCAAGACAAATGCTAGACTCACTATCAGGAAGTGGTGTGTACAAATTAACTTACTTTGCCTGACAACTTTGTGATGTTTCATAA... |
Task1_train_40719 | With a mutation on Chromosome 11, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TCTTAAGAAATTTGCCCAACACCCAAGCTGCAGTGCACCCTTCCAAGACATACACACACACACACACACACACACACACACACACTAGTGTGTGAAAGAGTTTTTAATCACAGTGTGCTTGACCACAGTTTTATAAAGATAAGATACATCATAGCAACACAATATAGCAAGACAAATGCTAGACTCACTATCAGGAAGTGGTGTGTACAAATTAACTTACTTTGCCTGACAACTTTGTGATGTTTCATAAACTTGAACACTAATGTTTGTGTGTGTACATGTTCGTAAATCTGTTTCTTTCTTGACAGTTATCAGCAGAA... | TCTTAAGAAATTTGCCCAACACCCAAGCTGCAGTGCACCCTTCCAAGACATACACACACACACACACACACACACACACACACACTAGTGTGTGAAAGAGTTTTTAATCACAGTGTGCTTGACCACAGTTTTATAAAGATAAGATACATCATAGCAACACAATATAGCAAGACAAATGCTAGACTCACTATCAGGAAGTGGTGTGTACAAATTAACTTACTTTGCCTGACAACTTTGTGATGTTTCATAAACTTGAACACTAATGTTTGTGTGTGTACATGTTCGTAAATCTGTTTCTTTCTTGACAGTTATCAGCAGAA... |
Task1_train_40720 | A mutation on Chromosome 11 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CTAAATCCTTTCAGAATCTGAGTGCTCAACTGAAAGTTTATTTAGAGATTGTAAATTCAATCATTTTTACTTCTACCATTTTAACTGTCAAAATGACATGTATATGTTACTGTGTAGCTATATATGTATATATGATTATATATATTCATATACCTATTTAAGATATCATGTTGCATGCATTTTGGATGTGAAATTGGCATTTTCTTAGCTCCCCACTGCTAAAATCAAGTATACAAAATCTTCCTACCTTTCAGTCAAATCCTCTGTCATCATACTGCAATCTATCTATTCCCTCATTTTCCATCATATTATTACTTTTA... | CTAAATCCTTTCAGAATCTGAGTGCTCAACTGAAAGTTTATTTAGAGATTGTAAATTCAATCATTTTTACTTCTACCATTTTAACTGTCAAAATGACATGTATATGTTACTGTGTAGCTATATATGTATATATGATTATATATATTCATATACCTATTTAAGATATCATGTTGCATGCATTTTGGATGTGAAATTGGCATTTTCTTAGCTCCCCACTGCTAAAATCAAGTATACAAAATCTTCCTACCTTTCAGTCAAATCCTCTGTCATCATACTGCAATCTATCTATTCCCTCATTTTCCATCATATTATTACTTTTA... |
Task1_train_40721 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AGACAATTCAAAATAGCACTTAAATATTTAGTGTAGTACTAGCAGAAACAAATTAATTAGATTTTTTAGAATGTTTTATGTATTCTCCCTTCCCAATAATGGAAATACTGTAGGAAGTCTATTTCTAACTTTCTTATTCTTTGGTGCACAAACGTGTGTGTGTGTGTGTGTGCATGCATATATATATGTGTGTGTGTGTGTGTGTGTACATATATATGAAGGTACATCCACATATAAATGTAGATAAATTAAGTGTGTGTATATGTAAATCTAAGTGTTAATACATGTATAAATTTCTATAAAAATCACAGAAAAAGCTA... | AGACAATTCAAAATAGCACTTAAATATTTAGTGTAGTACTAGCAGAAACAAATTAATTAGATTTTTTAGAATGTTTTATGTATTCTCCCTTCCCAATAATGGAAATACTGTAGGAAGTCTATTTCTAACTTTCTTATTCTTTGGTGCACAAACGTGTGTGTGTGTGTGTGTGCATGCATATATATATGTGTGTGTGTGTGTGTGTGTACATATATATGAAGGTACATCCACATATAAATGTAGATAAATTAAGTGTGTGTATATGTAAATCTAAGTGTTAATACATGTATAAATTTCTATAAAAATCACAGAAAAAGCTA... |
Task1_train_40722 | A variant has been detected on Chromosome 11. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GCACTTAAATATTTAGTGTAGTACTAGCAGAAACAAATTAATTAGATTTTTTAGAATGTTTTATGTATTCTCCCTTCCCAATAATGGAAATACTGTAGGAAGTCTATTTCTAACTTTCTTATTCTTTGGTGCACAAACGTGTGTGTGTGTGTGTGTGCATGCATATATATATGTGTGTGTGTGTGTGTGTGTACATATATATGAAGGTACATCCACATATAAATGTAGATAAATTAAGTGTGTGTATATGTAAATCTAAGTGTTAATACATGTATAAATTTCTATAAAAATCACAGAAAAAGCTAAGCATAAGCCAAGCA... | GCACTTAAATATTTAGTGTAGTACTAGCAGAAACAAATTAATTAGATTTTTTAGAATGTTTTATGTATTCTCCCTTCCCAATAATGGAAATACTGTAGGAAGTCTATTTCTAACTTTCTTATTCTTTGGTGCACAAACGTGTGTGTGTGTGTGTGTGCATGCATATATATATGTGTGTGTGTGTGTGTGTGTACATATATATGAAGGTACATCCACATATAAATGTAGATAAATTAAGTGTGTGTATATGTAAATCTAAGTGTTAATACATGTATAAATTTCTATAAAAATCACAGAAAAAGCTAAGCATAAGCCAAGCA... |
Task1_train_40723 | A variant has been detected on Chromosome 11. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GTGTAGTACTAGCAGAAACAAATTAATTAGATTTTTTAGAATGTTTTATGTATTCTCCCTTCCCAATAATGGAAATACTGTAGGAAGTCTATTTCTAACTTTCTTATTCTTTGGTGCACAAACGTGTGTGTGTGTGTGTGTGCATGCATATATATATGTGTGTGTGTGTGTGTGTGTACATATATATGAAGGTACATCCACATATAAATGTAGATAAATTAAGTGTGTGTATATGTAAATCTAAGTGTTAATACATGTATAAATTTCTATAAAAATCACAGAAAAAGCTAAGCATAAGCCAAGCATGAGTAGATTTCAAG... | GTGTAGTACTAGCAGAAACAAATTAATTAGATTTTTTAGAATGTTTTATGTATTCTCCCTTCCCAATAATGGAAATACTGTAGGAAGTCTATTTCTAACTTTCTTATTCTTTGGTGCACAAACGTGTGTGTGTGTGTGTGTGCATGCATATATATATGTGTGTGTGTGTGTGTGTGTACATATATATGAAGGTACATCCACATATAAATGTAGATAAATTAAGTGTGTGTATATGTAAATCTAAGTGTTAATACATGTATAAATTTCTATAAAAATCACAGAAAAAGCTAAGCATAAGCCAAGCATGAGTAGATTTCAAG... |
Task1_train_40724 | A mutation on Chromosome 11 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | ATGTTATTGAATGAAGTCCAAAGTGAAAGGAAAGGAAGGCATAATTACAGGAAGACAAATCTGGTTGTTTTAGTTGATATCTAAAAATAAAAATAAATATTTGCTTTTTGGTGTAAAATGACTCTTATGCATTAATTTGTCCAATTTTAACACTTACCTTCTTAGATACCTAATAGAATATAGGAAGATTAAAACAATTATTTTCTTGTTATCCATGCATAGTTTTGTACCTGATTTCCTTCCTTTCTTTCCTTCTTTGGAAAGCTGCACTAGCTTACTTAGAAAAGAACCGCTTTATGTTCTTTTATCTTTTTTCTTTT... | ATGTTATTGAATGAAGTCCAAAGTGAAAGGAAAGGAAGGCATAATTACAGGAAGACAAATCTGGTTGTTTTAGTTGATATCTAAAAATAAAAATAAATATTTGCTTTTTGGTGTAAAATGACTCTTATGCATTAATTTGTCCAATTTTAACACTTACCTTCTTAGATACCTAATAGAATATAGGAAGATTAAAACAATTATTTTCTTGTTATCCATGCATAGTTTTGTACCTGATTTCCTTCCTTTCTTTCCTTCTTTGGAAAGCTGCACTAGCTTACTTAGAAAAGAACCGCTTTATGTTCTTTTATCTTTTTTCTTTT... |
Task1_train_40725 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | AGAATTTGACTGGGAGAGAGGACAAGGACCACTTGAGACTCATATTTTATTTCCAGAATCTAGCATCTACCTACCTAGGTATTGAATAAGAAAAATGAAGTTAAGGTGGTTGATGGTAACACTATGCTAATAACTGCAGAGCCAGAAGCACCATAAGGGACATGATAAGGGAGCCAGCAGACCTCTGATCTCTTCCTGAATGCTAATCTTAAACATCCTGAGGAAGAATGGGACTTCCATTTGGGGTGGGCCTATGACAGGGTAATAAGACAGTAGTGAATATCAAGCTACAAAAAGCCGCCTTTCAAATTCTTCTCAGT... | AGAATTTGACTGGGAGAGAGGACAAGGACCACTTGAGACTCATATTTTATTTCCAGAATCTAGCATCTACCTACCTAGGTATTGAATAAGAAAAATGAAGTTAAGGTGGTTGATGGTAACACTATGCTAATAACTGCAGAGCCAGAAGCACCATAAGGGACATGATAAGGGAGCCAGCAGACCTCTGATCTCTTCCTGAATGCTAATCTTAAACATCCTGAGGAAGAATGGGACTTCCATTTGGGGTGGGCCTATGACAGGGTAATAAGACAGTAGTGAATATCAAGCTACAAAAAGCCGCCTTTCAAATTCTTCTCAGT... |
Task1_train_40726 | Given this context: Chromosome 11 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TAAACTCTGTATGCCAACTTTGGAAAAACAAATAAATAAATTTTACACAGAGAATAACAACTAAAATGACAATGAATAAACCCCCCACGTCCTACTTTCAAAGAACTCTCACAAACAATTCGCACAATAACTGAATCCTTCAGGAGTAGTCATTTATTAGTTTTTATTTTTCCTGCATCCAAATGGGCCTTCTAATTTGGAGAAATACTGCATTATTTAGCTTTAGTTTTCAGTAAGTATTTTCTTATCAAATCTCTGGAATATTTTCAGAGTGCTCACTGTCCAGATGTAAAATAAATATGAAAGATTTCTTAAGTGAA... | TAAACTCTGTATGCCAACTTTGGAAAAACAAATAAATAAATTTTACACAGAGAATAACAACTAAAATGACAATGAATAAACCCCCCACGTCCTACTTTCAAAGAACTCTCACAAACAATTCGCACAATAACTGAATCCTTCAGGAGTAGTCATTTATTAGTTTTTATTTTTCCTGCATCCAAATGGGCCTTCTAATTTGGAGAAATACTGCATTATTTAGCTTTAGTTTTCAGTAAGTATTTTCTTATCAAATCTCTGGAATATTTTCAGAGTGCTCACTGTCCAGATGTAAAATAAATATGAAAGATTTCTTAAGTGAA... |
Task1_train_40727 | This is a variant located on Chromosome 11. Is this mutation a likely cause of disease or not? | Benign | GAATGGAATAATTATATACTGGGTTCTGAACATGGACTTTCAATCAGAAAAGAAAATATTAGAAGCAAGCTCAACGAGAACTTAAAAATTGGAAGAAACAGCAGTCTTCAGAGAGGAATGAATGCAACTTTTGAGATTAGTTTCCTATAAGGAGATCAGCTGCAAATACTAGCGCAGAACTAGCAGTAGATGAAGAAATTGTCATCCCCTGTTACACTAATAGCAAGTGGTAGACTGCGGTTCAGACCCAATGAACAGCATAAAGACTTACAAACACTTTGAAGAAGATTGAAGGAAGAAACTATTCCATCAGTGAAAAA... | GAATGGAATAATTATATACTGGGTTCTGAACATGGACTTTCAATCAGAAAAGAAAATATTAGAAGCAAGCTCAACGAGAACTTAAAAATTGGAAGAAACAGCAGTCTTCAGAGAGGAATGAATGCAACTTTTGAGATTAGTTTCCTATAAGGAGATCAGCTGCAAATACTAGCGCAGAACTAGCAGTAGATGAAGAAATTGTCATCCCCTGTTACACTAATAGCAAGTGGTAGACTGCGGTTCAGACCCAATGAACAGCATAAAGACTTACAAACACTTTGAAGAAGATTGAAGGAAGAAACTATTCCATCAGTGAAAAA... |
Task1_train_40728 | A genetic alteration is present on Chromosome 11. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | AAGAGTGATAGCTGGTTTGGTTTAATGAAGTATTGGCTTGTGCCCTCAGAAGGGACTGTGTATCTTTTATCATGAAAGTTGATATTTCAGAGCACTAATAACTTAGTTTCCTTCTATGTAAAAGATGAAAAGTCTCAATGAAATAAAATGCTAGTGGATTCAGATCACCCTCTTAGAATCAATTTGAAAAATATTTTCTTTAAACAACCATGAAGGCACCAAGAACAGAGAATTCAACGTCTAAACCAGTTTAAGGACAACGTCATTAATAATAAACATATTTCCCAATAATTTGGGCTTCTTTCATCTTGGAAACAACA... | AAGAGTGATAGCTGGTTTGGTTTAATGAAGTATTGGCTTGTGCCCTCAGAAGGGACTGTGTATCTTTTATCATGAAAGTTGATATTTCAGAGCACTAATAACTTAGTTTCCTTCTATGTAAAAGATGAAAAGTCTCAATGAAATAAAATGCTAGTGGATTCAGATCACCCTCTTAGAATCAATTTGAAAAATATTTTCTTTAAACAACCATGAAGGCACCAAGAACAGAGAATTCAACGTCTAAACCAGTTTAAGGACAACGTCATTAATAATAAACATATTTCCCAATAATTTGGGCTTCTTTCATCTTGGAAACAACA... |
Task1_train_40729 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | GAGCACTAATAACTTAGTTTCCTTCTATGTAAAAGATGAAAAGTCTCAATGAAATAAAATGCTAGTGGATTCAGATCACCCTCTTAGAATCAATTTGAAAAATATTTTCTTTAAACAACCATGAAGGCACCAAGAACAGAGAATTCAACGTCTAAACCAGTTTAAGGACAACGTCATTAATAATAAACATATTTCCCAATAATTTGGGCTTCTTTCATCTTGGAAACAACACTGCTTATCCAAAGTAAGCACCTCCTTATACCTATTCAGTGAGGCTGCAATATTGCCATATCCTCAACCCACCATATACACAAAAGGCA... | GAGCACTAATAACTTAGTTTCCTTCTATGTAAAAGATGAAAAGTCTCAATGAAATAAAATGCTAGTGGATTCAGATCACCCTCTTAGAATCAATTTGAAAAATATTTTCTTTAAACAACCATGAAGGCACCAAGAACAGAGAATTCAACGTCTAAACCAGTTTAAGGACAACGTCATTAATAATAAACATATTTCCCAATAATTTGGGCTTCTTTCATCTTGGAAACAACACTGCTTATCCAAAGTAAGCACCTCCTTATACCTATTCAGTGAGGCTGCAATATTGCCATATCCTCAACCCACCATATACACAAAAGGCA... |
Task1_train_40730 | This sequence change occurs on Chromosome 11. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GGAAACAACACTGCTTATCCAAAGTAAGCACCTCCTTATACCTATTCAGTGAGGCTGCAATATTGCCATATCCTCAACCCACCATATACACAAAAGGCATGCCAGTGATGCTGCTCCATCATGGTTTGAAACTTCCTTATTTCTCACACATGTGGCAGGTAATTAAACTATGGCTTGAAGTCCTGGCCTTGGCCAGTTAAACTAAGAGTCCTTCCATCAAATGTATCACTGTAAAACAGATAGCCTATCCTCAAAATTTAGATATCAGATGGGGATATAATATCGCAGTAACTTGTGATTACCACAGCAACTTGTGATGT... | GGAAACAACACTGCTTATCCAAAGTAAGCACCTCCTTATACCTATTCAGTGAGGCTGCAATATTGCCATATCCTCAACCCACCATATACACAAAAGGCATGCCAGTGATGCTGCTCCATCATGGTTTGAAACTTCCTTATTTCTCACACATGTGGCAGGTAATTAAACTATGGCTTGAAGTCCTGGCCTTGGCCAGTTAAACTAAGAGTCCTTCCATCAAATGTATCACTGTAAAACAGATAGCCTATCCTCAAAATTTAGATATCAGATGGGGATATAATATCGCAGTAACTTGTGATTACCACAGCAACTTGTGATGT... |
Task1_train_40731 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | CACTGTAAAACAGATAGCCTATCCTCAAAATTTAGATATCAGATGGGGATATAATATCGCAGTAACTTGTGATTACCACAGCAACTTGTGATGTCCCACAGCTTCTGTTCTACAAAGATGGGAAACAAAGGCAGGCTTTCCTCAGCTACAAGAGGTTCTGCATCAAGATAGCAAATCAAGATGGGAATTATCCGAAATGAGATTTTTCCATTAAGATGCCTAGATGTATTATAGACCTCATGGTCACATATAAGGAACAGAGAAAGTCTTTGGTAGATAACTGACTTTTAGGATTTGAGTTTATATTCAGCATCAATAAC... | CACTGTAAAACAGATAGCCTATCCTCAAAATTTAGATATCAGATGGGGATATAATATCGCAGTAACTTGTGATTACCACAGCAACTTGTGATGTCCCACAGCTTCTGTTCTACAAAGATGGGAAACAAAGGCAGGCTTTCCTCAGCTACAAGAGGTTCTGCATCAAGATAGCAAATCAAGATGGGAATTATCCGAAATGAGATTTTTCCATTAAGATGCCTAGATGTATTATAGACCTCATGGTCACATATAAGGAACAGAGAAAGTCTTTGGTAGATAACTGACTTTTAGGATTTGAGTTTATATTCAGCATCAATAAC... |
Task1_train_40732 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | ATGGGGATATAATATCGCAGTAACTTGTGATTACCACAGCAACTTGTGATGTCCCACAGCTTCTGTTCTACAAAGATGGGAAACAAAGGCAGGCTTTCCTCAGCTACAAGAGGTTCTGCATCAAGATAGCAAATCAAGATGGGAATTATCCGAAATGAGATTTTTCCATTAAGATGCCTAGATGTATTATAGACCTCATGGTCACATATAAGGAACAGAGAAAGTCTTTGGTAGATAACTGACTTTTAGGATTTGAGTTTATATTCAGCATCAATAACTTGAACATTATACTCTGAGATAGGTTTTCCCCTTTTGAAATT... | ATGGGGATATAATATCGCAGTAACTTGTGATTACCACAGCAACTTGTGATGTCCCACAGCTTCTGTTCTACAAAGATGGGAAACAAAGGCAGGCTTTCCTCAGCTACAAGAGGTTCTGCATCAAGATAGCAAATCAAGATGGGAATTATCCGAAATGAGATTTTTCCATTAAGATGCCTAGATGTATTATAGACCTCATGGTCACATATAAGGAACAGAGAAAGTCTTTGGTAGATAACTGACTTTTAGGATTTGAGTTTATATTCAGCATCAATAACTTGAACATTATACTCTGAGATAGGTTTTCCCCTTTTGAAATT... |
Task1_train_40733 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | AAACAGTGATAATATCTACCCCACAATATTTTTATGAATAAAATAAGTTGTGGATGTAGTAGAGCATAATTAAGGGACACATGTTTGGTTTTATGAATGATTGAAAACAGGACAAAAACCTACCATCACATATATGCACTCACACTCACAATTTAGTATTCAGACTGTGTTGCTCAGGTGACATGGCGTGACAAGGATAAAAAACATGATAAAGCTGATTTTTTTATATGTTCAGTTCTTTCACAATTACATCTCTTAATGAAACAGAATATAAATAAGGATTGCAGTTTTTCTTAAGTTGGACTCTCTATGAGCAATAC... | AAACAGTGATAATATCTACCCCACAATATTTTTATGAATAAAATAAGTTGTGGATGTAGTAGAGCATAATTAAGGGACACATGTTTGGTTTTATGAATGATTGAAAACAGGACAAAAACCTACCATCACATATATGCACTCACACTCACAATTTAGTATTCAGACTGTGTTGCTCAGGTGACATGGCGTGACAAGGATAAAAAACATGATAAAGCTGATTTTTTTATATGTTCAGTTCTTTCACAATTACATCTCTTAATGAAACAGAATATAAATAAGGATTGCAGTTTTTCTTAAGTTGGACTCTCTATGAGCAATAC... |
Task1_train_40734 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GACATGGCGTGACAAGGATAAAAAACATGATAAAGCTGATTTTTTTATATGTTCAGTTCTTTCACAATTACATCTCTTAATGAAACAGAATATAAATAAGGATTGCAGTTTTTCTTAAGTTGGACTCTCTATGAGCAATACCTGAGATAGGGATTCAAATGTGTGCAATTTATTAATGAATGCTCTCAGGAGACAGGGAGCAAGTAAAAGCAGTGTGGACAGGGGAAGGAGGTAAGCAAGTGCATACTGAAGCTGGAGCTTAGCTTCAGAAGGCAAGAGGGTCAGTATTTGCCTATGGCCTGCTACCTAAGGAGCAGGGG... | GACATGGCGTGACAAGGATAAAAAACATGATAAAGCTGATTTTTTTATATGTTCAGTTCTTTCACAATTACATCTCTTAATGAAACAGAATATAAATAAGGATTGCAGTTTTTCTTAAGTTGGACTCTCTATGAGCAATACCTGAGATAGGGATTCAAATGTGTGCAATTTATTAATGAATGCTCTCAGGAGACAGGGAGCAAGTAAAAGCAGTGTGGACAGGGGAAGGAGGTAAGCAAGTGCATACTGAAGCTGGAGCTTAGCTTCAGAAGGCAAGAGGGTCAGTATTTGCCTATGGCCTGCTACCTAAGGAGCAGGGG... |
Task1_train_40735 | A variant found on Chromosome 11 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | AAAAAACATGATAAAGCTGATTTTTTTATATGTTCAGTTCTTTCACAATTACATCTCTTAATGAAACAGAATATAAATAAGGATTGCAGTTTTTCTTAAGTTGGACTCTCTATGAGCAATACCTGAGATAGGGATTCAAATGTGTGCAATTTATTAATGAATGCTCTCAGGAGACAGGGAGCAAGTAAAAGCAGTGTGGACAGGGGAAGGAGGTAAGCAAGTGCATACTGAAGCTGGAGCTTAGCTTCAGAAGGCAAGAGGGTCAGTATTTGCCTATGGCCTGCTACCTAAGGAGCAGGGGCCATTTTCTTCATAAGACA... | AAAAAACATGATAAAGCTGATTTTTTTATATGTTCAGTTCTTTCACAATTACATCTCTTAATGAAACAGAATATAAATAAGGATTGCAGTTTTTCTTAAGTTGGACTCTCTATGAGCAATACCTGAGATAGGGATTCAAATGTGTGCAATTTATTAATGAATGCTCTCAGGAGACAGGGAGCAAGTAAAAGCAGTGTGGACAGGGGAAGGAGGTAAGCAAGTGCATACTGAAGCTGGAGCTTAGCTTCAGAAGGCAAGAGGGTCAGTATTTGCCTATGGCCTGCTACCTAAGGAGCAGGGGCCATTTTCTTCATAAGACA... |
Task1_train_40736 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | AATGAATGCTCTCAGGAGACAGGGAGCAAGTAAAAGCAGTGTGGACAGGGGAAGGAGGTAAGCAAGTGCATACTGAAGCTGGAGCTTAGCTTCAGAAGGCAAGAGGGTCAGTATTTGCCTATGGCCTGCTACCTAAGGAGCAGGGGCCATTTTCTTCATAAGACATTTCCTGCTGAGTTGAGAACAACAACCTGCAGAAAGCAGAAACATGAACAATGAGCAGCCAACATTCACAGGTGCACAATTCTGTAAAATGATCGGGGTAAAACACCAAAGACATAAACAATATCTTCTATATAGTCCCCTCTCTTGTCTCACTG... | AATGAATGCTCTCAGGAGACAGGGAGCAAGTAAAAGCAGTGTGGACAGGGGAAGGAGGTAAGCAAGTGCATACTGAAGCTGGAGCTTAGCTTCAGAAGGCAAGAGGGTCAGTATTTGCCTATGGCCTGCTACCTAAGGAGCAGGGGCCATTTTCTTCATAAGACATTTCCTGCTGAGTTGAGAACAACAACCTGCAGAAAGCAGAAACATGAACAATGAGCAGCCAACATTCACAGGTGCACAATTCTGTAAAATGATCGGGGTAAAACACCAAAGACATAAACAATATCTTCTATATAGTCCCCTCTCTTGTCTCACTG... |
Task1_train_40737 | Here is a genetic alteration on Chromosome 11. Based on the data, is it a benign variant or a cause of disease? | Benign | GACAGGGGAAGGAGGTAAGCAAGTGCATACTGAAGCTGGAGCTTAGCTTCAGAAGGCAAGAGGGTCAGTATTTGCCTATGGCCTGCTACCTAAGGAGCAGGGGCCATTTTCTTCATAAGACATTTCCTGCTGAGTTGAGAACAACAACCTGCAGAAAGCAGAAACATGAACAATGAGCAGCCAACATTCACAGGTGCACAATTCTGTAAAATGATCGGGGTAAAACACCAAAGACATAAACAATATCTTCTATATAGTCCCCTCTCTTGTCTCACTGAAGTATTATTTTTGCTCTGATTAAAGTATAATTAAGACATAAC... | GACAGGGGAAGGAGGTAAGCAAGTGCATACTGAAGCTGGAGCTTAGCTTCAGAAGGCAAGAGGGTCAGTATTTGCCTATGGCCTGCTACCTAAGGAGCAGGGGCCATTTTCTTCATAAGACATTTCCTGCTGAGTTGAGAACAACAACCTGCAGAAAGCAGAAACATGAACAATGAGCAGCCAACATTCACAGGTGCACAATTCTGTAAAATGATCGGGGTAAAACACCAAAGACATAAACAATATCTTCTATATAGTCCCCTCTCTTGTCTCACTGAAGTATTATTTTTGCTCTGATTAAAGTATAATTAAGACATAAC... |
Task1_train_40738 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | CTATATAGTCCCCTCTCTTGTCTCACTGAAGTATTATTTTTGCTCTGATTAAAGTATAATTAAGACATAACCTCCCTCTTTTTAGGATATTTTAAATTGAGTTATGGGTCCCTTCCTAACTCATCAGACAATTTTAATCAAATGAGAATGACATTGTTGTATTCTTTGGGAAATTTACACTTATTACATGGAATCAGAATGTATGTACAGAAAGCAATCATTCTTCAAAAAAATGCAGAAACCTATTTTTTTTTGTTCCTTCAGACCTTTTTCATAGCAAAAGGAGGGTGAAGGAACTGTCTCTTCCACTAATTTGGACT... | CTATATAGTCCCCTCTCTTGTCTCACTGAAGTATTATTTTTGCTCTGATTAAAGTATAATTAAGACATAACCTCCCTCTTTTTAGGATATTTTAAATTGAGTTATGGGTCCCTTCCTAACTCATCAGACAATTTTAATCAAATGAGAATGACATTGTTGTATTCTTTGGGAAATTTACACTTATTACATGGAATCAGAATGTATGTACAGAAAGCAATCATTCTTCAAAAAAATGCAGAAACCTATTTTTTTTTGTTCCTTCAGACCTTTTTCATAGCAAAAGGAGGGTGAAGGAACTGTCTCTTCCACTAATTTGGACT... |
Task1_train_40739 | A mutation on Chromosome 11 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | AGGTGATAGATATATTAATTAGTTTGATTATGGTAATCATTTAACAATGAATACCTATAATAAAACAATAAGTTATATACCTATGTACAATTTTTATTTGCCATACTGCTTCTTTAATCCTGCATAAGCTGAGTATTGTCTGAACCTCTCACTGGCAGGCAGATTGAGCAATAATACCTCCTTTTCTCACTTTTTGAGGACAGAGTTGCTTTCCCCTCTACTTCCCTCAGTCCCAATGCCCCAGGCTCAACGTTACTTTTAGCTATGTCAGAAGTTCCCACATTGGCTCATCAATCTTTTCTCCTTTCCCTTTCCCACCC... | AGGTGATAGATATATTAATTAGTTTGATTATGGTAATCATTTAACAATGAATACCTATAATAAAACAATAAGTTATATACCTATGTACAATTTTTATTTGCCATACTGCTTCTTTAATCCTGCATAAGCTGAGTATTGTCTGAACCTCTCACTGGCAGGCAGATTGAGCAATAATACCTCCTTTTCTCACTTTTTGAGGACAGAGTTGCTTTCCCCTCTACTTCCCTCAGTCCCAATGCCCCAGGCTCAACGTTACTTTTAGCTATGTCAGAAGTTCCCACATTGGCTCATCAATCTTTTCTCCTTTCCCTTTCCCACCC... |
Task1_train_40740 | A variant on Chromosome 11 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | ACTGGCAGGCAGATTGAGCAATAATACCTCCTTTTCTCACTTTTTGAGGACAGAGTTGCTTTCCCCTCTACTTCCCTCAGTCCCAATGCCCCAGGCTCAACGTTACTTTTAGCTATGTCAGAAGTTCCCACATTGGCTCATCAATCTTTTCTCCTTTCCCTTTCCCACCCAGACATATCACATTTTATCTGCTGATTAGAGAAACTATAGTTTAATATCTTTATTTAAAGTCAAACACAGGCTCCTAAAAACCCCATCATCATCTTATATCTGTTCCCAAGGCTTCCACAGAAAAAAAGGAAATCATTTGACACACCTCT... | ACTGGCAGGCAGATTGAGCAATAATACCTCCTTTTCTCACTTTTTGAGGACAGAGTTGCTTTCCCCTCTACTTCCCTCAGTCCCAATGCCCCAGGCTCAACGTTACTTTTAGCTATGTCAGAAGTTCCCACATTGGCTCATCAATCTTTTCTCCTTTCCCTTTCCCACCCAGACATATCACATTTTATCTGCTGATTAGAGAAACTATAGTTTAATATCTTTATTTAAAGTCAAACACAGGCTCCTAAAAACCCCATCATCATCTTATATCTGTTCCCAAGGCTTCCACAGAAAAAAAGGAAATCATTTGACACACCTCT... |
Task1_train_40741 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | CCCAGGCTCAACGTTACTTTTAGCTATGTCAGAAGTTCCCACATTGGCTCATCAATCTTTTCTCCTTTCCCTTTCCCACCCAGACATATCACATTTTATCTGCTGATTAGAGAAACTATAGTTTAATATCTTTATTTAAAGTCAAACACAGGCTCCTAAAAACCCCATCATCATCTTATATCTGTTCCCAAGGCTTCCACAGAAAAAAAGGAAATCATTTGACACACCTCTGGGTGAATAATCCTGACATGTACTCACTAGAGAAAGAGAAAGGAGGTACTTCTCTGAAACAATAACAAAAACACAAAAATAAAAAAATT... | CCCAGGCTCAACGTTACTTTTAGCTATGTCAGAAGTTCCCACATTGGCTCATCAATCTTTTCTCCTTTCCCTTTCCCACCCAGACATATCACATTTTATCTGCTGATTAGAGAAACTATAGTTTAATATCTTTATTTAAAGTCAAACACAGGCTCCTAAAAACCCCATCATCATCTTATATCTGTTCCCAAGGCTTCCACAGAAAAAAAGGAAATCATTTGACACACCTCTGGGTGAATAATCCTGACATGTACTCACTAGAGAAAGAGAAAGGAGGTACTTCTCTGAAACAATAACAAAAACACAAAAATAAAAAAATT... |
Task1_train_40742 | A mutation has occurred on Chromosome 11. What is the medical relevance of this mutation? | Benign | AACGTTACTTTTAGCTATGTCAGAAGTTCCCACATTGGCTCATCAATCTTTTCTCCTTTCCCTTTCCCACCCAGACATATCACATTTTATCTGCTGATTAGAGAAACTATAGTTTAATATCTTTATTTAAAGTCAAACACAGGCTCCTAAAAACCCCATCATCATCTTATATCTGTTCCCAAGGCTTCCACAGAAAAAAAGGAAATCATTTGACACACCTCTGGGTGAATAATCCTGACATGTACTCACTAGAGAAAGAGAAAGGAGGTACTTCTCTGAAACAATAACAAAAACACAAAAATAAAAAAATTATCCACTCT... | AACGTTACTTTTAGCTATGTCAGAAGTTCCCACATTGGCTCATCAATCTTTTCTCCTTTCCCTTTCCCACCCAGACATATCACATTTTATCTGCTGATTAGAGAAACTATAGTTTAATATCTTTATTTAAAGTCAAACACAGGCTCCTAAAAACCCCATCATCATCTTATATCTGTTCCCAAGGCTTCCACAGAAAAAAAGGAAATCATTTGACACACCTCTGGGTGAATAATCCTGACATGTACTCACTAGAGAAAGAGAAAGGAGGTACTTCTCTGAAACAATAACAAAAACACAAAAATAAAAAAATTATCCACTCT... |
Task1_train_40743 | A mutation on Chromosome 11 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CTTTTAGCTATGTCAGAAGTTCCCACATTGGCTCATCAATCTTTTCTCCTTTCCCTTTCCCACCCAGACATATCACATTTTATCTGCTGATTAGAGAAACTATAGTTTAATATCTTTATTTAAAGTCAAACACAGGCTCCTAAAAACCCCATCATCATCTTATATCTGTTCCCAAGGCTTCCACAGAAAAAAAGGAAATCATTTGACACACCTCTGGGTGAATAATCCTGACATGTACTCACTAGAGAAAGAGAAAGGAGGTACTTCTCTGAAACAATAACAAAAACACAAAAATAAAAAAATTATCCACTCTTTACAAA... | CTTTTAGCTATGTCAGAAGTTCCCACATTGGCTCATCAATCTTTTCTCCTTTCCCTTTCCCACCCAGACATATCACATTTTATCTGCTGATTAGAGAAACTATAGTTTAATATCTTTATTTAAAGTCAAACACAGGCTCCTAAAAACCCCATCATCATCTTATATCTGTTCCCAAGGCTTCCACAGAAAAAAAGGAAATCATTTGACACACCTCTGGGTGAATAATCCTGACATGTACTCACTAGAGAAAGAGAAAGGAGGTACTTCTCTGAAACAATAACAAAAACACAAAAATAAAAAAATTATCCACTCTTTACAAA... |
Task1_train_40744 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | TTAGCTATGTCAGAAGTTCCCACATTGGCTCATCAATCTTTTCTCCTTTCCCTTTCCCACCCAGACATATCACATTTTATCTGCTGATTAGAGAAACTATAGTTTAATATCTTTATTTAAAGTCAAACACAGGCTCCTAAAAACCCCATCATCATCTTATATCTGTTCCCAAGGCTTCCACAGAAAAAAAGGAAATCATTTGACACACCTCTGGGTGAATAATCCTGACATGTACTCACTAGAGAAAGAGAAAGGAGGTACTTCTCTGAAACAATAACAAAAACACAAAAATAAAAAAATTATCCACTCTTTACAAAACA... | TTAGCTATGTCAGAAGTTCCCACATTGGCTCATCAATCTTTTCTCCTTTCCCTTTCCCACCCAGACATATCACATTTTATCTGCTGATTAGAGAAACTATAGTTTAATATCTTTATTTAAAGTCAAACACAGGCTCCTAAAAACCCCATCATCATCTTATATCTGTTCCCAAGGCTTCCACAGAAAAAAAGGAAATCATTTGACACACCTCTGGGTGAATAATCCTGACATGTACTCACTAGAGAAAGAGAAAGGAGGTACTTCTCTGAAACAATAACAAAAACACAAAAATAAAAAAATTATCCACTCTTTACAAAACA... |
Task1_train_40745 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | GTTCCCACATTGGCTCATCAATCTTTTCTCCTTTCCCTTTCCCACCCAGACATATCACATTTTATCTGCTGATTAGAGAAACTATAGTTTAATATCTTTATTTAAAGTCAAACACAGGCTCCTAAAAACCCCATCATCATCTTATATCTGTTCCCAAGGCTTCCACAGAAAAAAAGGAAATCATTTGACACACCTCTGGGTGAATAATCCTGACATGTACTCACTAGAGAAAGAGAAAGGAGGTACTTCTCTGAAACAATAACAAAAACACAAAAATAAAAAAATTATCCACTCTTTACAAAACATTTCCCCTTACTTTG... | GTTCCCACATTGGCTCATCAATCTTTTCTCCTTTCCCTTTCCCACCCAGACATATCACATTTTATCTGCTGATTAGAGAAACTATAGTTTAATATCTTTATTTAAAGTCAAACACAGGCTCCTAAAAACCCCATCATCATCTTATATCTGTTCCCAAGGCTTCCACAGAAAAAAAGGAAATCATTTGACACACCTCTGGGTGAATAATCCTGACATGTACTCACTAGAGAAAGAGAAAGGAGGTACTTCTCTGAAACAATAACAAAAACACAAAAATAAAAAAATTATCCACTCTTTACAAAACATTTCCCCTTACTTTG... |
Task1_train_40746 | A mutation has occurred on Chromosome 11. What is the medical relevance of this mutation? | Benign | ACAGGCTCCTAAAAACCCCATCATCATCTTATATCTGTTCCCAAGGCTTCCACAGAAAAAAAGGAAATCATTTGACACACCTCTGGGTGAATAATCCTGACATGTACTCACTAGAGAAAGAGAAAGGAGGTACTTCTCTGAAACAATAACAAAAACACAAAAATAAAAAAATTATCCACTCTTTACAAAACATTTCCCCTTACTTTGTGTCAAGAGAATGACTGAGAAGACAGAAATCACTAGTAGTCTTTACAGGTTATGTAACCAAATCTCAAGATTAAATTACTTTCCCAAGATCATTATTGTTAGAAAGAGCAGAG... | ACAGGCTCCTAAAAACCCCATCATCATCTTATATCTGTTCCCAAGGCTTCCACAGAAAAAAAGGAAATCATTTGACACACCTCTGGGTGAATAATCCTGACATGTACTCACTAGAGAAAGAGAAAGGAGGTACTTCTCTGAAACAATAACAAAAACACAAAAATAAAAAAATTATCCACTCTTTACAAAACATTTCCCCTTACTTTGTGTCAAGAGAATGACTGAGAAGACAGAAATCACTAGTAGTCTTTACAGGTTATGTAACCAAATCTCAAGATTAAATTACTTTCCCAAGATCATTATTGTTAGAAAGAGCAGAG... |
Task1_train_40747 | This sequence change occurs on Chromosome 11. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TAAAAACCCCATCATCATCTTATATCTGTTCCCAAGGCTTCCACAGAAAAAAAGGAAATCATTTGACACACCTCTGGGTGAATAATCCTGACATGTACTCACTAGAGAAAGAGAAAGGAGGTACTTCTCTGAAACAATAACAAAAACACAAAAATAAAAAAATTATCCACTCTTTACAAAACATTTCCCCTTACTTTGTGTCAAGAGAATGACTGAGAAGACAGAAATCACTAGTAGTCTTTACAGGTTATGTAACCAAATCTCAAGATTAAATTACTTTCCCAAGATCATTATTGTTAGAAAGAGCAGAGCTGAAACTT... | TAAAAACCCCATCATCATCTTATATCTGTTCCCAAGGCTTCCACAGAAAAAAAGGAAATCATTTGACACACCTCTGGGTGAATAATCCTGACATGTACTCACTAGAGAAAGAGAAAGGAGGTACTTCTCTGAAACAATAACAAAAACACAAAAATAAAAAAATTATCCACTCTTTACAAAACATTTCCCCTTACTTTGTGTCAAGAGAATGACTGAGAAGACAGAAATCACTAGTAGTCTTTACAGGTTATGTAACCAAATCTCAAGATTAAATTACTTTCCCAAGATCATTATTGTTAGAAAGAGCAGAGCTGAAACTT... |
Task1_train_40748 | A variant was discovered on Chromosome 11. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | ATTTGACACACCTCTGGGTGAATAATCCTGACATGTACTCACTAGAGAAAGAGAAAGGAGGTACTTCTCTGAAACAATAACAAAAACACAAAAATAAAAAAATTATCCACTCTTTACAAAACATTTCCCCTTACTTTGTGTCAAGAGAATGACTGAGAAGACAGAAATCACTAGTAGTCTTTACAGGTTATGTAACCAAATCTCAAGATTAAATTACTTTCCCAAGATCATTATTGTTAGAAAGAGCAGAGCTGAAACTTCAACAAATTCTTCTGAAAATGAAAGTCCAGTAATCTTGGATGCATTCTTTTCATGGACAG... | ATTTGACACACCTCTGGGTGAATAATCCTGACATGTACTCACTAGAGAAAGAGAAAGGAGGTACTTCTCTGAAACAATAACAAAAACACAAAAATAAAAAAATTATCCACTCTTTACAAAACATTTCCCCTTACTTTGTGTCAAGAGAATGACTGAGAAGACAGAAATCACTAGTAGTCTTTACAGGTTATGTAACCAAATCTCAAGATTAAATTACTTTCCCAAGATCATTATTGTTAGAAAGAGCAGAGCTGAAACTTCAACAAATTCTTCTGAAAATGAAAGTCCAGTAATCTTGGATGCATTCTTTTCATGGACAG... |
Task1_train_40749 | An alteration has been detected on Chromosome 11. Is it pathogenic, and if so, what disease is involved? | Benign | GTTATGTAACCAAATCTCAAGATTAAATTACTTTCCCAAGATCATTATTGTTAGAAAGAGCAGAGCTGAAACTTCAACAAATTCTTCTGAAAATGAAAGTCCAGTAATCTTGGATGCATTCTTTTCATGGACAGAAAGAGGTCTTGTAAATCGTGCATAAATTTACATCAATATGCTCTTTCAATAGTATATGAGATGTATAGTCCAAACCAACCATAAGAGAAGGTGGGCCTATTTTCTCTGGCTCATGCCACCAACACACAATTTATGTATTCTCAGAGGTTGGCTGCCTGCACCAGCTGAAATCTTAGAATTCTAAT... | GTTATGTAACCAAATCTCAAGATTAAATTACTTTCCCAAGATCATTATTGTTAGAAAGAGCAGAGCTGAAACTTCAACAAATTCTTCTGAAAATGAAAGTCCAGTAATCTTGGATGCATTCTTTTCATGGACAGAAAGAGGTCTTGTAAATCGTGCATAAATTTACATCAATATGCTCTTTCAATAGTATATGAGATGTATAGTCCAAACCAACCATAAGAGAAGGTGGGCCTATTTTCTCTGGCTCATGCCACCAACACACAATTTATGTATTCTCAGAGGTTGGCTGCCTGCACCAGCTGAAATCTTAGAATTCTAAT... |
Task1_train_40750 | A genomic change on Chromosome 11 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CTGAAACTTCAACAAATTCTTCTGAAAATGAAAGTCCAGTAATCTTGGATGCATTCTTTTCATGGACAGAAAGAGGTCTTGTAAATCGTGCATAAATTTACATCAATATGCTCTTTCAATAGTATATGAGATGTATAGTCCAAACCAACCATAAGAGAAGGTGGGCCTATTTTCTCTGGCTCATGCCACCAACACACAATTTATGTATTCTCAGAGGTTGGCTGCCTGCACCAGCTGAAATCTTAGAATTCTAATGAGTCACAGAGCCTTCTCACTTTTGTCAAATCCCATCAGATTCCATAGTTTTAAAAAAAAAATTC... | CTGAAACTTCAACAAATTCTTCTGAAAATGAAAGTCCAGTAATCTTGGATGCATTCTTTTCATGGACAGAAAGAGGTCTTGTAAATCGTGCATAAATTTACATCAATATGCTCTTTCAATAGTATATGAGATGTATAGTCCAAACCAACCATAAGAGAAGGTGGGCCTATTTTCTCTGGCTCATGCCACCAACACACAATTTATGTATTCTCAGAGGTTGGCTGCCTGCACCAGCTGAAATCTTAGAATTCTAATGAGTCACAGAGCCTTCTCACTTTTGTCAAATCCCATCAGATTCCATAGTTTTAAAAAAAAAATTC... |
Task1_train_40751 | A mutation is present on Chromosome 11. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GCCTTCTTTTGTCTTTTAAACTTGTCAAGCTGCTCTCTGCTTCAGGAACTTTCACTTGTTCTTCCTCCTTCCTTGAATGTTTTTCCCTAAGATAGCCACACACTTGCCCTCTGATTTTGATTTCTTCTCTAAAATTACCTACTCAGAGAGGTCTTCTCTGACTACCCTATATAAAATGCATCACTCTTACCTTCCTCCTTTGCTCCCTACTTCTTTATTGCATTACATTACCTTGCATTGCAGTATGTATGTATGTGTTTATTTTTGTCTCTGTTCTGTTTCTGTTCATTGTATTTTCAGTACCTAGGTGTAAAAGTAAT... | GCCTTCTTTTGTCTTTTAAACTTGTCAAGCTGCTCTCTGCTTCAGGAACTTTCACTTGTTCTTCCTCCTTCCTTGAATGTTTTTCCCTAAGATAGCCACACACTTGCCCTCTGATTTTGATTTCTTCTCTAAAATTACCTACTCAGAGAGGTCTTCTCTGACTACCCTATATAAAATGCATCACTCTTACCTTCCTCCTTTGCTCCCTACTTCTTTATTGCATTACATTACCTTGCATTGCAGTATGTATGTATGTGTTTATTTTTGTCTCTGTTCTGTTTCTGTTCATTGTATTTTCAGTACCTAGGTGTAAAAGTAAT... |
Task1_train_40752 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ACACACTTGCCCTCTGATTTTGATTTCTTCTCTAAAATTACCTACTCAGAGAGGTCTTCTCTGACTACCCTATATAAAATGCATCACTCTTACCTTCCTCCTTTGCTCCCTACTTCTTTATTGCATTACATTACCTTGCATTGCAGTATGTATGTATGTGTTTATTTTTGTCTCTGTTCTGTTTCTGTTCATTGTATTTTCAGTACCTAGGTGTAAAAGTAATTGCAGTTCTTGCCATTGAAAGTAATGGTAAAAACCACAATTACTTTTGCACCAACCTAATAGAATTATGTCTGCCATGTAATACAATTTCAATATGT... | ACACACTTGCCCTCTGATTTTGATTTCTTCTCTAAAATTACCTACTCAGAGAGGTCTTCTCTGACTACCCTATATAAAATGCATCACTCTTACCTTCCTCCTTTGCTCCCTACTTCTTTATTGCATTACATTACCTTGCATTGCAGTATGTATGTATGTGTTTATTTTTGTCTCTGTTCTGTTTCTGTTCATTGTATTTTCAGTACCTAGGTGTAAAAGTAATTGCAGTTCTTGCCATTGAAAGTAATGGTAAAAACCACAATTACTTTTGCACCAACCTAATAGAATTATGTCTGCCATGTAATACAATTTCAATATGT... |
Task1_train_40753 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | AGGTGTAAAAGTAATTGCAGTTCTTGCCATTGAAAGTAATGGTAAAAACCACAATTACTTTTGCACCAACCTAATAGAATTATGTCTGCCATGTAATACAATTTCAATATGTATTTATTGAATCAATTAATGAATAATTATTGAAATAATTGAATATTGAAATAATTATTGAAATAAGATTAATGGTAATGATACATATTTAATAATTTATTCAAATAATATTTAAAGGATTCCAATGATATGGTGGCTAAAAAAGTCAATCCCTAGAGCTAATATTAAAATTAAAAAAGAGACAGTCATGGTTTATGTCCACAAGGAAT... | AGGTGTAAAAGTAATTGCAGTTCTTGCCATTGAAAGTAATGGTAAAAACCACAATTACTTTTGCACCAACCTAATAGAATTATGTCTGCCATGTAATACAATTTCAATATGTATTTATTGAATCAATTAATGAATAATTATTGAAATAATTGAATATTGAAATAATTATTGAAATAAGATTAATGGTAATGATACATATTTAATAATTTATTCAAATAATATTTAAAGGATTCCAATGATATGGTGGCTAAAAAAGTCAATCCCTAGAGCTAATATTAAAATTAAAAAAGAGACAGTCATGGTTTATGTCCACAAGGAAT... |
Task1_train_40754 | With a mutation on Chromosome 11, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GAAATTGACAATGCTGCAGGGAAAATATCATGGTAATTAGTGCATAGTGAACTACAGGAACACATAGGAGAGGGTATTCAAACTAAACTTGGGGAATTTAAGAAGGCCTTCTGAAGGACATCATATCTAAGCTAAGGTGGGTTATATTAGTAGAAGTTAACTAGACAAAGATTAAGGGAAAGCTATTTCAGGAAAAAATGTTTTTATTCCAGGAAGAATGAAAATACAAATGTTTACCTATGAGCAAGCATACTAGATAAACTGGAAGAATTGTTTAGTGTCATTAACACCGTGAATATACAGAGGAAATTAGGATAGAT... | GAAATTGACAATGCTGCAGGGAAAATATCATGGTAATTAGTGCATAGTGAACTACAGGAACACATAGGAGAGGGTATTCAAACTAAACTTGGGGAATTTAAGAAGGCCTTCTGAAGGACATCATATCTAAGCTAAGGTGGGTTATATTAGTAGAAGTTAACTAGACAAAGATTAAGGGAAAGCTATTTCAGGAAAAAATGTTTTTATTCCAGGAAGAATGAAAATACAAATGTTTACCTATGAGCAAGCATACTAGATAAACTGGAAGAATTGTTTAGTGTCATTAACACCGTGAATATACAGAGGAAATTAGGATAGAT... |
Task1_train_40755 | A mutation is present on Chromosome 11. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CCTTGGTCCTGCAAGGTCCTTGACATAGAGGTGTGCTCACTGGTTATAGATCTGCAGAGCAAAGAAGAACTTCATAATAACCATTACGGAATAGTGAGGTCCCTGTTGATGCGTAAGTTCAGCAGTGGCTGAATGGAAAGTTCATACAAGAATCAGATTTTCAGCACATGCGGGAAGCATGTTTGTTCGTGTGTGAATAGGTAAGCAGGTGTGTCTGTGTGTGTTTGTGTGCATTTGGGTGAATGAGTTGAAAACAATCTTCAGAGGTCCTTCCTACCATGCTAGTCTAGGATTCTAATGTTATAACTGCTGACCTAGAC... | CCTTGGTCCTGCAAGGTCCTTGACATAGAGGTGTGCTCACTGGTTATAGATCTGCAGAGCAAAGAAGAACTTCATAATAACCATTACGGAATAGTGAGGTCCCTGTTGATGCGTAAGTTCAGCAGTGGCTGAATGGAAAGTTCATACAAGAATCAGATTTTCAGCACATGCGGGAAGCATGTTTGTTCGTGTGTGAATAGGTAAGCAGGTGTGTCTGTGTGTGTTTGTGTGCATTTGGGTGAATGAGTTGAAAACAATCTTCAGAGGTCCTTCCTACCATGCTAGTCTAGGATTCTAATGTTATAACTGCTGACCTAGAC... |
Task1_train_40756 | A mutation has occurred on Chromosome 11. What is the medical relevance of this mutation? | Benign | AGCAGTGGCTGAATGGAAAGTTCATACAAGAATCAGATTTTCAGCACATGCGGGAAGCATGTTTGTTCGTGTGTGAATAGGTAAGCAGGTGTGTCTGTGTGTGTTTGTGTGCATTTGGGTGAATGAGTTGAAAACAATCTTCAGAGGTCCTTCCTACCATGCTAGTCTAGGATTCTAATGTTATAACTGCTGACCTAGACAATGCTTATCTCAAAACACACCCAATCCAGGCAGGTGGTTTTCTCTTTCCCTCTATTGCCTTCCTCTCCTCCCCAGGAAAAGAACATCCTTGAAAATCTGTTTAGATTTCCACTGTTGTT... | AGCAGTGGCTGAATGGAAAGTTCATACAAGAATCAGATTTTCAGCACATGCGGGAAGCATGTTTGTTCGTGTGTGAATAGGTAAGCAGGTGTGTCTGTGTGTGTTTGTGTGCATTTGGGTGAATGAGTTGAAAACAATCTTCAGAGGTCCTTCCTACCATGCTAGTCTAGGATTCTAATGTTATAACTGCTGACCTAGACAATGCTTATCTCAAAACACACCCAATCCAGGCAGGTGGTTTTCTCTTTCCCTCTATTGCCTTCCTCTCCTCCCCAGGAAAAGAACATCCTTGAAAATCTGTTTAGATTTCCACTGTTGTT... |
Task1_train_40757 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TTGTTCGTGTGTGAATAGGTAAGCAGGTGTGTCTGTGTGTGTTTGTGTGCATTTGGGTGAATGAGTTGAAAACAATCTTCAGAGGTCCTTCCTACCATGCTAGTCTAGGATTCTAATGTTATAACTGCTGACCTAGACAATGCTTATCTCAAAACACACCCAATCCAGGCAGGTGGTTTTCTCTTTCCCTCTATTGCCTTCCTCTCCTCCCCAGGAAAAGAACATCCTTGAAAATCTGTTTAGATTTCCACTGTTGTTGCCGTAGTGTATTCAGCAGTGTGTCTGAGCTAGAAAGAAAAAGTCCCAATGGATAAGGTAAG... | TTGTTCGTGTGTGAATAGGTAAGCAGGTGTGTCTGTGTGTGTTTGTGTGCATTTGGGTGAATGAGTTGAAAACAATCTTCAGAGGTCCTTCCTACCATGCTAGTCTAGGATTCTAATGTTATAACTGCTGACCTAGACAATGCTTATCTCAAAACACACCCAATCCAGGCAGGTGGTTTTCTCTTTCCCTCTATTGCCTTCCTCTCCTCCCCAGGAAAAGAACATCCTTGAAAATCTGTTTAGATTTCCACTGTTGTTGCCGTAGTGTATTCAGCAGTGTGTCTGAGCTAGAAAGAAAAAGTCCCAATGGATAAGGTAAG... |
Task1_train_40758 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | TTCCTCTCCTCCCCAGGAAAAGAACATCCTTGAAAATCTGTTTAGATTTCCACTGTTGTTGCCGTAGTGTATTCAGCAGTGTGTCTGAGCTAGAAAGAAAAAGTCCCAATGGATAAGGTAAGTTTCTTTGAGAACTGTTGAGTCAACAGATTGTGGATGTGATCGTTGACAGAATATTTTCATGAACCTTAAAGTCTGCACACACATCCACGAACGTAGGTTCCTTCTCCTTCCTGAATCTTCCATGCCTTTGCACATAATCTTTCTAGTTGACTCCTAGAATTTTCAAAACATGGGACAGCTAGCCCAGTGTGGGTCCA... | TTCCTCTCCTCCCCAGGAAAAGAACATCCTTGAAAATCTGTTTAGATTTCCACTGTTGTTGCCGTAGTGTATTCAGCAGTGTGTCTGAGCTAGAAAGAAAAAGTCCCAATGGATAAGGTAAGTTTCTTTGAGAACTGTTGAGTCAACAGATTGTGGATGTGATCGTTGACAGAATATTTTCATGAACCTTAAAGTCTGCACACACATCCACGAACGTAGGTTCCTTCTCCTTCCTGAATCTTCCATGCCTTTGCACATAATCTTTCTAGTTGACTCCTAGAATTTTCAAAACATGGGACAGCTAGCCCAGTGTGGGTCCA... |
Task1_train_40759 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | CTACTTGTCTTTCTCTGTGATTCTTGTCTATTGCTGCTATTTACAAAGTCTTCACAAAGGAAAGATTTAAATGCTTATATTATTTTCTCTATTTTATTTTTTGTCACTGATTTTCATTTAGTTACTTAATTCATTTTGAAATTAGTTTTGTGGGAATTGAGAGATGAACCACCAAATAGCTAACTATTGAATAATTTTTTTTCTAATTCAGTTTTGATTTCTGTCTTCATTTCCTTATTTCTTGTACATATATATAAACATTTCTTTTTTCTTAGTGTTTCCAGAGGCTCAGGTTAAGATGAATGCCCCTTGAAATTGAT... | CTACTTGTCTTTCTCTGTGATTCTTGTCTATTGCTGCTATTTACAAAGTCTTCACAAAGGAAAGATTTAAATGCTTATATTATTTTCTCTATTTTATTTTTTGTCACTGATTTTCATTTAGTTACTTAATTCATTTTGAAATTAGTTTTGTGGGAATTGAGAGATGAACCACCAAATAGCTAACTATTGAATAATTTTTTTTCTAATTCAGTTTTGATTTCTGTCTTCATTTCCTTATTTCTTGTACATATATATAAACATTTCTTTTTTCTTAGTGTTTCCAGAGGCTCAGGTTAAGATGAATGCCCCTTGAAATTGAT... |
Task1_train_40760 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GTCTTTCTCTGTGATTCTTGTCTATTGCTGCTATTTACAAAGTCTTCACAAAGGAAAGATTTAAATGCTTATATTATTTTCTCTATTTTATTTTTTGTCACTGATTTTCATTTAGTTACTTAATTCATTTTGAAATTAGTTTTGTGGGAATTGAGAGATGAACCACCAAATAGCTAACTATTGAATAATTTTTTTTCTAATTCAGTTTTGATTTCTGTCTTCATTTCCTTATTTCTTGTACATATATATAAACATTTCTTTTTTCTTAGTGTTTCCAGAGGCTCAGGTTAAGATGAATGCCCCTTGAAATTGATGCACAA... | GTCTTTCTCTGTGATTCTTGTCTATTGCTGCTATTTACAAAGTCTTCACAAAGGAAAGATTTAAATGCTTATATTATTTTCTCTATTTTATTTTTTGTCACTGATTTTCATTTAGTTACTTAATTCATTTTGAAATTAGTTTTGTGGGAATTGAGAGATGAACCACCAAATAGCTAACTATTGAATAATTTTTTTTCTAATTCAGTTTTGATTTCTGTCTTCATTTCCTTATTTCTTGTACATATATATAAACATTTCTTTTTTCTTAGTGTTTCCAGAGGCTCAGGTTAAGATGAATGCCCCTTGAAATTGATGCACAA... |
Task1_train_40761 | A mutation located on Chromosome 11 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | ATATTATTTTCTCTATTTTATTTTTTGTCACTGATTTTCATTTAGTTACTTAATTCATTTTGAAATTAGTTTTGTGGGAATTGAGAGATGAACCACCAAATAGCTAACTATTGAATAATTTTTTTTCTAATTCAGTTTTGATTTCTGTCTTCATTTCCTTATTTCTTGTACATATATATAAACATTTCTTTTTTCTTAGTGTTTCCAGAGGCTCAGGTTAAGATGAATGCCCCTTGAAATTGATGCACAATATTTCTTTCAACTACAGCTCTCTTGCCCCTGTAAACTCTATCCCAGCTTCGGAGTACTTATAGAAGGAA... | ATATTATTTTCTCTATTTTATTTTTTGTCACTGATTTTCATTTAGTTACTTAATTCATTTTGAAATTAGTTTTGTGGGAATTGAGAGATGAACCACCAAATAGCTAACTATTGAATAATTTTTTTTCTAATTCAGTTTTGATTTCTGTCTTCATTTCCTTATTTCTTGTACATATATATAAACATTTCTTTTTTCTTAGTGTTTCCAGAGGCTCAGGTTAAGATGAATGCCCCTTGAAATTGATGCACAATATTTCTTTCAACTACAGCTCTCTTGCCCCTGTAAACTCTATCCCAGCTTCGGAGTACTTATAGAAGGAA... |
Task1_train_40762 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | AATAGCTAACTATTGAATAATTTTTTTTCTAATTCAGTTTTGATTTCTGTCTTCATTTCCTTATTTCTTGTACATATATATAAACATTTCTTTTTTCTTAGTGTTTCCAGAGGCTCAGGTTAAGATGAATGCCCCTTGAAATTGATGCACAATATTTCTTTCAACTACAGCTCTCTTGCCCCTGTAAACTCTATCCCAGCTTCGGAGTACTTATAGAAGGAAGTCTTTTAGAACTAATTTTTGAGAGATTGTACAGTTCAAGCTTAAGCATGCAGTTTCAAATCACATTCAACAAGCTAATGAAACTGTGATTCAATATG... | AATAGCTAACTATTGAATAATTTTTTTTCTAATTCAGTTTTGATTTCTGTCTTCATTTCCTTATTTCTTGTACATATATATAAACATTTCTTTTTTCTTAGTGTTTCCAGAGGCTCAGGTTAAGATGAATGCCCCTTGAAATTGATGCACAATATTTCTTTCAACTACAGCTCTCTTGCCCCTGTAAACTCTATCCCAGCTTCGGAGTACTTATAGAAGGAAGTCTTTTAGAACTAATTTTTGAGAGATTGTACAGTTCAAGCTTAAGCATGCAGTTTCAAATCACATTCAACAAGCTAATGAAACTGTGATTCAATATG... |
Task1_train_40763 | A mutation on Chromosome 11 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CAAGCTAATGAAACTGTGATTCAATATGGCTTTCTAACTTATTGCTCTGTGAGGACACCAGGGGCAGCAAAGGCTGTCACCACCAGAGTTGATTTACTGGGCTCCCTGTGGGACCCAGGTCCCAAGATGCGATGCCTCCGTGTAATCCTGAAGCGACCTGCCACACCTTCCACCCTCCAGACTAGAGATCTGCAAGGGGCTTATACCGCACCTGCTCTCTGAGCTAAGCTGAGAAAACAGAAGCCACAGATGGTGACGAGGGTACCTCCAAGGCAGGAGAAACCACAGGTAAGACTCCTCTGTGAATCATCAGGAAAAAG... | CAAGCTAATGAAACTGTGATTCAATATGGCTTTCTAACTTATTGCTCTGTGAGGACACCAGGGGCAGCAAAGGCTGTCACCACCAGAGTTGATTTACTGGGCTCCCTGTGGGACCCAGGTCCCAAGATGCGATGCCTCCGTGTAATCCTGAAGCGACCTGCCACACCTTCCACCCTCCAGACTAGAGATCTGCAAGGGGCTTATACCGCACCTGCTCTCTGAGCTAAGCTGAGAAAACAGAAGCCACAGATGGTGACGAGGGTACCTCCAAGGCAGGAGAAACCACAGGTAAGACTCCTCTGTGAATCATCAGGAAAAAG... |
Task1_train_40764 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TTTTAGCTTGGACTGCCATTATCTATTGCTCTTTTTTAGATATTTAAAATGTCTTTTTCCAAACTCAGTTTCTGCCTCCATTAAATGAGGGCATAAGTCAAGAAAAACTCTAAATATTTGTTCACTCTGATAATGGTAATACTAAACAAAACATCCATGCAAATCTCAAGACGAGGGCTTATTGTATTAAACGTCATTTGTGGGGAAATTTTGAAGCTTTCCTCCCCACAACAAAGCTTAAATAGAGAAATAAATATATCCTGTGGAGTGGAAGTTAAACTTTTAACAATGGAGCAAAGCAGAGATAGACGCAATCTGCA... | TTTTAGCTTGGACTGCCATTATCTATTGCTCTTTTTTAGATATTTAAAATGTCTTTTTCCAAACTCAGTTTCTGCCTCCATTAAATGAGGGCATAAGTCAAGAAAAACTCTAAATATTTGTTCACTCTGATAATGGTAATACTAAACAAAACATCCATGCAAATCTCAAGACGAGGGCTTATTGTATTAAACGTCATTTGTGGGGAAATTTTGAAGCTTTCCTCCCCACAACAAAGCTTAAATAGAGAAATAAATATATCCTGTGGAGTGGAAGTTAAACTTTTAACAATGGAGCAAAGCAGAGATAGACGCAATCTGCA... |
Task1_train_40765 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TGCAAATCTCAAGACGAGGGCTTATTGTATTAAACGTCATTTGTGGGGAAATTTTGAAGCTTTCCTCCCCACAACAAAGCTTAAATAGAGAAATAAATATATCCTGTGGAGTGGAAGTTAAACTTTTAACAATGGAGCAAAGCAGAGATAGACGCAATCTGCAGGTAAACGCTTGGTAAACAAAAATACAACCAGATTAAACATATCCCATCTAAAGAGGGAAGAAGTTAATAGACTGCAGAAAAGAAAAAGAGTTAATAGATTTGCAGAAAAGTCTCCGAAGACTTCCTGATCAGGAGACTTGTGTACAGTGAAGTTCC... | TGCAAATCTCAAGACGAGGGCTTATTGTATTAAACGTCATTTGTGGGGAAATTTTGAAGCTTTCCTCCCCACAACAAAGCTTAAATAGAGAAATAAATATATCCTGTGGAGTGGAAGTTAAACTTTTAACAATGGAGCAAAGCAGAGATAGACGCAATCTGCAGGTAAACGCTTGGTAAACAAAAATACAACCAGATTAAACATATCCCATCTAAAGAGGGAAGAAGTTAATAGACTGCAGAAAAGAAAAAGAGTTAATAGATTTGCAGAAAAGTCTCCGAAGACTTCCTGATCAGGAGACTTGTGTACAGTGAAGTTCC... |
Task1_train_40766 | A genetic alteration is present on Chromosome 11. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TGCAGAAAAGTCTCCGAAGACTTCCTGATCAGGAGACTTGTGTACAGTGAAGTTCCATTGACAAATTTCTCTTGCCTAACCATCTCAGTATGACAATCAACTGTTCTTTCTCTCTCTCTCGTCCTCTCTCTCTCTCTCTCTCTTCCAGTTCTATTTGCCTGAATGGGAGCCCTAAAGTTGGAGTTTGCCTGAATTTTCAATGTCAAGTAGTTTGGCATGACAGGAGGTAGGAATTGAGGGAAAAGAAGGAAAGCACAATATGGGATTATGACTGTGGGGTGGCTGGAAATTGTGTATCAAATTCTCCTCTGAAGCTATTT... | TGCAGAAAAGTCTCCGAAGACTTCCTGATCAGGAGACTTGTGTACAGTGAAGTTCCATTGACAAATTTCTCTTGCCTAACCATCTCAGTATGACAATCAACTGTTCTTTCTCTCTCTCTCGTCCTCTCTCTCTCTCTCTCTCTTCCAGTTCTATTTGCCTGAATGGGAGCCCTAAAGTTGGAGTTTGCCTGAATTTTCAATGTCAAGTAGTTTGGCATGACAGGAGGTAGGAATTGAGGGAAAAGAAGGAAAGCACAATATGGGATTATGACTGTGGGGTGGCTGGAAATTGTGTATCAAATTCTCCTCTGAAGCTATTT... |
Task1_train_40767 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TTGAAATGTCTGCTTAGTGAAAAGCCTTCTAGCCTTCTGTATCCTCATCCACGATGAGGCAATGAACACAAAAGTGTGTCAAAAACAGAATAAACAATACAATCACTGTGACAGAGAAATGGCTGTAAGAAATAATATGTGAATGCCAGCATAAGAAAAATGGTAAATAAATACAAGCCATTAAGGGTTTAAAAAGTGCCTGTGTGGGTTAGTAGATTAATATCAGTGGGCAGTCCCCAAGCATGTAGATAGAAGTGTTGTGTGAGTATACAAATCTATGTGTCTATGAGTGTGTATACATGTATAAATCCTGCATATAT... | TTGAAATGTCTGCTTAGTGAAAAGCCTTCTAGCCTTCTGTATCCTCATCCACGATGAGGCAATGAACACAAAAGTGTGTCAAAAACAGAATAAACAATACAATCACTGTGACAGAGAAATGGCTGTAAGAAATAATATGTGAATGCCAGCATAAGAAAAATGGTAAATAAATACAAGCCATTAAGGGTTTAAAAAGTGCCTGTGTGGGTTAGTAGATTAATATCAGTGGGCAGTCCCCAAGCATGTAGATAGAAGTGTTGTGTGAGTATACAAATCTATGTGTCTATGAGTGTGTATACATGTATAAATCCTGCATATAT... |
Task1_train_40768 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | GGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCGGATCACGAGGTCAGGAGATCGAGATCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAACTACAAAAAAAATTAGCCGGGCATGGTGGCGGGAGCCTGTAGTCCCAACTACTCGGGAGGCTGAGGCAGAAGAATGGCGTGAACCCGGGAGGTGGAGTTGCAGTGAGCCGAGATTGCACCACTGCACTCCAGCCTGGGCAAAAGAGAGAGACTCTGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATCA... | GGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCGGATCACGAGGTCAGGAGATCGAGATCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAACTACAAAAAAAATTAGCCGGGCATGGTGGCGGGAGCCTGTAGTCCCAACTACTCGGGAGGCTGAGGCAGAAGAATGGCGTGAACCCGGGAGGTGGAGTTGCAGTGAGCCGAGATTGCACCACTGCACTCCAGCCTGGGCAAAAGAGAGAGACTCTGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATCA... |
Task1_train_40769 | A genetic alteration is present on Chromosome 11. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | ATTCCATGAATAGTCATCTTTTGTCAACCACAAAATTTTGTGAAGTTAGGTCAGATGGTGTCATTCCCAATTTAAAGATAAAAACTAAGCCACAAAAAGGCTTTGGAATTTTTTTCAATGCCACATAGTGAGCAGACAGAAAATCAGAGAATGACTACATTCATTGCCCTTTCTAAATTGAGACTGTCCAGATAAGTAAGAGATTTGTTCAAAGTCACAAATCAATAATGTTACAGAATCGGGGCTAAAATTCAGATTTCCTGGCATTTCTACTCAGAATTCTTTTAGGGATACATGTTACTGAGACAATGTGTATAATA... | ATTCCATGAATAGTCATCTTTTGTCAACCACAAAATTTTGTGAAGTTAGGTCAGATGGTGTCATTCCCAATTTAAAGATAAAAACTAAGCCACAAAAAGGCTTTGGAATTTTTTTCAATGCCACATAGTGAGCAGACAGAAAATCAGAGAATGACTACATTCATTGCCCTTTCTAAATTGAGACTGTCCAGATAAGTAAGAGATTTGTTCAAAGTCACAAATCAATAATGTTACAGAATCGGGGCTAAAATTCAGATTTCCTGGCATTTCTACTCAGAATTCTTTTAGGGATACATGTTACTGAGACAATGTGTATAATA... |
Task1_train_40770 | An alteration has been detected on Chromosome 11. Is it pathogenic, and if so, what disease is involved? | Benign | CACAAAAAGGCTTTGGAATTTTTTTCAATGCCACATAGTGAGCAGACAGAAAATCAGAGAATGACTACATTCATTGCCCTTTCTAAATTGAGACTGTCCAGATAAGTAAGAGATTTGTTCAAAGTCACAAATCAATAATGTTACAGAATCGGGGCTAAAATTCAGATTTCCTGGCATTTCTACTCAGAATTCTTTTAGGGATACATGTTACTGAGACAATGTGTATAATACTAGCTATCCCTCTACAGCAAGAACAGAATCCCCTTCCAGTCCCTTTATGGGTGGTAAATCCAGAATACCTCACTTTTTATATCTGTCTC... | CACAAAAAGGCTTTGGAATTTTTTTCAATGCCACATAGTGAGCAGACAGAAAATCAGAGAATGACTACATTCATTGCCCTTTCTAAATTGAGACTGTCCAGATAAGTAAGAGATTTGTTCAAAGTCACAAATCAATAATGTTACAGAATCGGGGCTAAAATTCAGATTTCCTGGCATTTCTACTCAGAATTCTTTTAGGGATACATGTTACTGAGACAATGTGTATAATACTAGCTATCCCTCTACAGCAAGAACAGAATCCCCTTCCAGTCCCTTTATGGGTGGTAAATCCAGAATACCTCACTTTTTATATCTGTCTC... |
Task1_train_40771 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | CAGGCAAAAAGAGAGCTTGTGTAGAGCAACTCCGGTTTTTAAAACCATCAGATCTCGTGAGACCCATTCACTGTCACGAGAACAGCATGGGAAAGACCCACCCCCATGATTCAATCATCTCACACCAGGTCCCTCCCACAACAGGTGGGAATTATGGGAGCTACAAGATGAGATTTGGGTGGGGCCACAGAGCCAAATCATATCAGGAACCTTGTGCTCCACCTAAACATTGAAACCTAAATCGCTAGAATAAATGTTTTCCCAAAGGCTGCTTTTATCTCCTTTAAACCGTGTGCTAGCAGCTCTAAGTTACACAGGCT... | CAGGCAAAAAGAGAGCTTGTGTAGAGCAACTCCGGTTTTTAAAACCATCAGATCTCGTGAGACCCATTCACTGTCACGAGAACAGCATGGGAAAGACCCACCCCCATGATTCAATCATCTCACACCAGGTCCCTCCCACAACAGGTGGGAATTATGGGAGCTACAAGATGAGATTTGGGTGGGGCCACAGAGCCAAATCATATCAGGAACCTTGTGCTCCACCTAAACATTGAAACCTAAATCGCTAGAATAAATGTTTTCCCAAAGGCTGCTTTTATCTCCTTTAAACCGTGTGCTAGCAGCTCTAAGTTACACAGGCT... |
Task1_train_40772 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | ACCTAAATCGCTAGAATAAATGTTTTCCCAAAGGCTGCTTTTATCTCCTTTAAACCGTGTGCTAGCAGCTCTAAGTTACACAGGCTGATCAAAATATCCTGAGCTCCAAGTAGAGGTTCCCTCTCTCCCAGTACTGAGTCTCTGACATCTAAACACACACCACAGCCACTTTTAGGTATCCCCCATCAAGACCTCTTTACTTCCTTGATAGGAAAATACTGTGAATGTTTCTTAGGTTTACACTTCCATTTTGCGATGAAACTCTGATTTAACAGACTGTGTTTTGTATGTATGCTTGTACATATGTACATAGAATATAC... | ACCTAAATCGCTAGAATAAATGTTTTCCCAAAGGCTGCTTTTATCTCCTTTAAACCGTGTGCTAGCAGCTCTAAGTTACACAGGCTGATCAAAATATCCTGAGCTCCAAGTAGAGGTTCCCTCTCTCCCAGTACTGAGTCTCTGACATCTAAACACACACCACAGCCACTTTTAGGTATCCCCCATCAAGACCTCTTTACTTCCTTGATAGGAAAATACTGTGAATGTTTCTTAGGTTTACACTTCCATTTTGCGATGAAACTCTGATTTAACAGACTGTGTTTTGTATGTATGCTTGTACATATGTACATAGAATATAC... |
Task1_train_40773 | This genomic variant is located on Chromosome 11. Can you determine its pathogenicity and name any linked disease? | Benign | AATTATATATAATGTGAATTATATAGTCACAATTTGCACAATTCTTGCTATAAGATCATAAATTCATTGAGGCAGGGCAGTGAGTAAAACTCTTTTGCTCATATTGAATTCCTAATAGCTAGCAAAATGCTATACACAAAGTATGTCTTCAGTTTTGAGCTTGAAGTTGCAAAAAATTAACTCTCTGGATCTGGCTACAAGGGACTGTATAAAGTCGGTAAGATTCAGGAATCTGAGAAGTCACCCTGACTCCTTTGCTGCTCTATCTCTATCTGCTTAGAGATCAGCATCAAATCCTGGAAGTGCAAGCTGCTTGGGGG... | AATTATATATAATGTGAATTATATAGTCACAATTTGCACAATTCTTGCTATAAGATCATAAATTCATTGAGGCAGGGCAGTGAGTAAAACTCTTTTGCTCATATTGAATTCCTAATAGCTAGCAAAATGCTATACACAAAGTATGTCTTCAGTTTTGAGCTTGAAGTTGCAAAAAATTAACTCTCTGGATCTGGCTACAAGGGACTGTATAAAGTCGGTAAGATTCAGGAATCTGAGAAGTCACCCTGACTCCTTTGCTGCTCTATCTCTATCTGCTTAGAGATCAGCATCAAATCCTGGAAGTGCAAGCTGCTTGGGGG... |
Task1_train_40774 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | GGTGGGATACTCTAGGTGAGGCAGAAAGAGAAAAAGGTGGGGCATTGGCAACCATGGAAAATGTAAACTACAAACATAAGATAGATATACTGAAGGAGGTGATATTCTTGGAAGGTGCTGTGCCCCATGGAGGGCTGGATTTGTGGTGACTGGGATATACAGTGGAGATGGCAGCAGCTGCATCTCTGTGTGCTAAAGAGACAGTAGAGACAGCCCATCACCATCTTATAATGGTGGCAAAATCAACGAGCAGGAGGTTCCAATGATGATAACTATTCATCCGGACTTGGTTAATATGTGAATTCACCCTACTCTGGCCC... | GGTGGGATACTCTAGGTGAGGCAGAAAGAGAAAAAGGTGGGGCATTGGCAACCATGGAAAATGTAAACTACAAACATAAGATAGATATACTGAAGGAGGTGATATTCTTGGAAGGTGCTGTGCCCCATGGAGGGCTGGATTTGTGGTGACTGGGATATACAGTGGAGATGGCAGCAGCTGCATCTCTGTGTGCTAAAGAGACAGTAGAGACAGCCCATCACCATCTTATAATGGTGGCAAAATCAACGAGCAGGAGGTTCCAATGATGATAACTATTCATCCGGACTTGGTTAATATGTGAATTCACCCTACTCTGGCCC... |
Task1_train_40775 | A variant has been detected on Chromosome 11. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TAATTTTACTTTTGCTTTTAAGTTCTAGGATGCATGTGCAGGTTTGTTACGTAGGTAAACTTGTGTCATGGGGGTTTGTTGTACAGATTATTTCATCATCCAGATATTAAGCCTAGTACCCATTAGTTATTTTTCCTAATCCTCTCCCTTCTCTCATCCTCTACCCTCTGATAGGCCCCAGTATGTGTTGTTCCCCTCTATGTGTCCATGTGTTCTCATTATTTAGTTCCTACTTATAAGTAAGAACATACAGTATTTGGTTTTCTGTTCCTGTGTTAGTTTGCTAAGGATAATGGCCTCCAGCTCCATCCATGTTCCTG... | TAATTTTACTTTTGCTTTTAAGTTCTAGGATGCATGTGCAGGTTTGTTACGTAGGTAAACTTGTGTCATGGGGGTTTGTTGTACAGATTATTTCATCATCCAGATATTAAGCCTAGTACCCATTAGTTATTTTTCCTAATCCTCTCCCTTCTCTCATCCTCTACCCTCTGATAGGCCCCAGTATGTGTTGTTCCCCTCTATGTGTCCATGTGTTCTCATTATTTAGTTCCTACTTATAAGTAAGAACATACAGTATTTGGTTTTCTGTTCCTGTGTTAGTTTGCTAAGGATAATGGCCTCCAGCTCCATCCATGTTCCTG... |
Task1_train_40776 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | AGTTATTTTTCCTAATCCTCTCCCTTCTCTCATCCTCTACCCTCTGATAGGCCCCAGTATGTGTTGTTCCCCTCTATGTGTCCATGTGTTCTCATTATTTAGTTCCTACTTATAAGTAAGAACATACAGTATTTGGTTTTCTGTTCCTGTGTTAGTTTGCTAAGGATAATGGCCTCCAGCTCCATCCATGTTCCTGCAAAGGACATGATCTCATTGTTTTTTATGGCTGCATAGTGTTCCATGGTGTATATGTACCACGTTTTTTTATCCAGTGTAACATTGATGGGCATTTGGGTTGATTCCATGTCTTTGCTATTGTA... | AGTTATTTTTCCTAATCCTCTCCCTTCTCTCATCCTCTACCCTCTGATAGGCCCCAGTATGTGTTGTTCCCCTCTATGTGTCCATGTGTTCTCATTATTTAGTTCCTACTTATAAGTAAGAACATACAGTATTTGGTTTTCTGTTCCTGTGTTAGTTTGCTAAGGATAATGGCCTCCAGCTCCATCCATGTTCCTGCAAAGGACATGATCTCATTGTTTTTTATGGCTGCATAGTGTTCCATGGTGTATATGTACCACGTTTTTTTATCCAGTGTAACATTGATGGGCATTTGGGTTGATTCCATGTCTTTGCTATTGTA... |
Task1_train_40777 | A variant found on Chromosome 11 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CCCTTCTCTCATCCTCTACCCTCTGATAGGCCCCAGTATGTGTTGTTCCCCTCTATGTGTCCATGTGTTCTCATTATTTAGTTCCTACTTATAAGTAAGAACATACAGTATTTGGTTTTCTGTTCCTGTGTTAGTTTGCTAAGGATAATGGCCTCCAGCTCCATCCATGTTCCTGCAAAGGACATGATCTCATTGTTTTTTATGGCTGCATAGTGTTCCATGGTGTATATGTACCACGTTTTTTTATCCAGTGTAACATTGATGGGCATTTGGGTTGATTCCATGTCTTTGCTATTGTAAATATTGATGCAATGAACATA... | CCCTTCTCTCATCCTCTACCCTCTGATAGGCCCCAGTATGTGTTGTTCCCCTCTATGTGTCCATGTGTTCTCATTATTTAGTTCCTACTTATAAGTAAGAACATACAGTATTTGGTTTTCTGTTCCTGTGTTAGTTTGCTAAGGATAATGGCCTCCAGCTCCATCCATGTTCCTGCAAAGGACATGATCTCATTGTTTTTTATGGCTGCATAGTGTTCCATGGTGTATATGTACCACGTTTTTTTATCCAGTGTAACATTGATGGGCATTTGGGTTGATTCCATGTCTTTGCTATTGTAAATATTGATGCAATGAACATA... |
Task1_train_40778 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | AACATATGCATGCATGTGTCTTTATAATAGAACCATTTATATTCCTTTGTATATACCCAGTAATGGGATTGTTGGGTCAAATGATATTTCTGTCTTTAGGTCTTTGAGAAATTGCCACACTGTCTTCTACAATGGTTGAACTAATTTACACTCCCACTCTCAGTGTATAAGTGTTCCTTTTTCTCCATAACCTCACCAGCACCTGTTTTTCTTTTCACATTTTAATAACAGCCAAAGAATGGATGATTTTCAAAACAGGATTTATTGGAGAAACTTTATTGTTCAAGTAGAATCTTACCTAAGTGCTTGATACACAAGCA... | AACATATGCATGCATGTGTCTTTATAATAGAACCATTTATATTCCTTTGTATATACCCAGTAATGGGATTGTTGGGTCAAATGATATTTCTGTCTTTAGGTCTTTGAGAAATTGCCACACTGTCTTCTACAATGGTTGAACTAATTTACACTCCCACTCTCAGTGTATAAGTGTTCCTTTTTCTCCATAACCTCACCAGCACCTGTTTTTCTTTTCACATTTTAATAACAGCCAAAGAATGGATGATTTTCAAAACAGGATTTATTGGAGAAACTTTATTGTTCAAGTAGAATCTTACCTAAGTGCTTGATACACAAGCA... |
Task1_train_40779 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TTCTACAATGGTTGAACTAATTTACACTCCCACTCTCAGTGTATAAGTGTTCCTTTTTCTCCATAACCTCACCAGCACCTGTTTTTCTTTTCACATTTTAATAACAGCCAAAGAATGGATGATTTTCAAAACAGGATTTATTGGAGAAACTTTATTGTTCAAGTAGAATCTTACCTAAGTGCTTGATACACAAGCAAAACTAGATAATATCAGATCTGCTGTGATTGTGGAAAAATAAGACAAGAAACTTCCTTCACATAAGCCTTGAGATGCACCTTAAAGCAACCTCTCAGAGTCCAGCTCTTTAGGATTACCTCGGA... | TTCTACAATGGTTGAACTAATTTACACTCCCACTCTCAGTGTATAAGTGTTCCTTTTTCTCCATAACCTCACCAGCACCTGTTTTTCTTTTCACATTTTAATAACAGCCAAAGAATGGATGATTTTCAAAACAGGATTTATTGGAGAAACTTTATTGTTCAAGTAGAATCTTACCTAAGTGCTTGATACACAAGCAAAACTAGATAATATCAGATCTGCTGTGATTGTGGAAAAATAAGACAAGAAACTTCCTTCACATAAGCCTTGAGATGCACCTTAAAGCAACCTCTCAGAGTCCAGCTCTTTAGGATTACCTCGGA... |
Task1_train_40780 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AAAAAGTCGTATATTCATTGTGAGAATAGTTCAATAGGACTAAGGAGGAATCATGTGTCCTAATATGTACTAAAGACTACTTATGTGATTGTGTCATTTTTTCACATCCTGACTATGTAAGCTGAGGATAACACTAGTTAGATTTAGTTGAAGTCTGAGAATTTACAGATGCAGGGGAAACCAATGGATACTAAAAGGTAATGATCCTGGTGGAACTGATAGACATCTAGAGTAGATAGGGAAGAAAGTTCAAAAAGTTCTTACATCAGTGGCTCACAAACTTCAGCATGAATCAGAATCACCTAGAGAGCTTGCTAAAA... | AAAAAGTCGTATATTCATTGTGAGAATAGTTCAATAGGACTAAGGAGGAATCATGTGTCCTAATATGTACTAAAGACTACTTATGTGATTGTGTCATTTTTTCACATCCTGACTATGTAAGCTGAGGATAACACTAGTTAGATTTAGTTGAAGTCTGAGAATTTACAGATGCAGGGGAAACCAATGGATACTAAAAGGTAATGATCCTGGTGGAACTGATAGACATCTAGAGTAGATAGGGAAGAAAGTTCAAAAAGTTCTTACATCAGTGGCTCACAAACTTCAGCATGAATCAGAATCACCTAGAGAGCTTGCTAAAA... |
Task1_train_40781 | Assess the clinical impact of this variant found on Chromosome 11. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TATCCCAACTCTAGGTTTTCTCATCCGTAGGTTTGTGGTAGGGCCGAAGAATTTACAAGTTCCCTGATGGTGCTGTGGAGACCAAGCTTCAGAAGCATTGTTCTACACCTTCCTTTCTGCTCTGGATGACAGTGCCACATTTCACAGCCACAGAGGTGACTCAGGAAGTCACACGCAATTTAATAAGCTTTCCACAGAGAAAATTTAGCTTAATATACCAACAAAACAACAATTATGCTCATTTTAAAAATTAGAAAATTGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCCAGGTGGGTGGATCACGAGGTCAGGA... | TATCCCAACTCTAGGTTTTCTCATCCGTAGGTTTGTGGTAGGGCCGAAGAATTTACAAGTTCCCTGATGGTGCTGTGGAGACCAAGCTTCAGAAGCATTGTTCTACACCTTCCTTTCTGCTCTGGATGACAGTGCCACATTTCACAGCCACAGAGGTGACTCAGGAAGTCACACGCAATTTAATAAGCTTTCCACAGAGAAAATTTAGCTTAATATACCAACAAAACAACAATTATGCTCATTTTAAAAATTAGAAAATTGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCCAGGTGGGTGGATCACGAGGTCAGGA... |
Task1_train_40782 | An alteration has been detected on Chromosome 11. Is it pathogenic, and if so, what disease is involved? | Benign | CTAGGTTTTCTCATCCGTAGGTTTGTGGTAGGGCCGAAGAATTTACAAGTTCCCTGATGGTGCTGTGGAGACCAAGCTTCAGAAGCATTGTTCTACACCTTCCTTTCTGCTCTGGATGACAGTGCCACATTTCACAGCCACAGAGGTGACTCAGGAAGTCACACGCAATTTAATAAGCTTTCCACAGAGAAAATTTAGCTTAATATACCAACAAAACAACAATTATGCTCATTTTAAAAATTAGAAAATTGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCCAGGTGGGTGGATCACGAGGTCAGGAGATCGAGACC... | CTAGGTTTTCTCATCCGTAGGTTTGTGGTAGGGCCGAAGAATTTACAAGTTCCCTGATGGTGCTGTGGAGACCAAGCTTCAGAAGCATTGTTCTACACCTTCCTTTCTGCTCTGGATGACAGTGCCACATTTCACAGCCACAGAGGTGACTCAGGAAGTCACACGCAATTTAATAAGCTTTCCACAGAGAAAATTTAGCTTAATATACCAACAAAACAACAATTATGCTCATTTTAAAAATTAGAAAATTGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCCAGGTGGGTGGATCACGAGGTCAGGAGATCGAGACC... |
Task1_train_40783 | Assess the clinical impact of this variant found on Chromosome 11. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CAAAAATACAAAAAAATTAGCCGGGCGTGGTGGAGGGCGCCTGTAGTCCCAGCTCCTTGGGAGGCTGAGGCAGGAGAATGGCGTGAGCCTGGGAGGCGGAGCTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAAAGAAAGAAAGAAAGAAAATTGTTACTCAGAGAAGACAGTGACTTGTCCAAGATCAAGCAGCCAATAGTTAACAGGGCAGACCTCTGACCCAGGTTTTTTCACACCCTCTGCGGTGTTCTTTCTAAATGCCGTAGCTACCT... | CAAAAATACAAAAAAATTAGCCGGGCGTGGTGGAGGGCGCCTGTAGTCCCAGCTCCTTGGGAGGCTGAGGCAGGAGAATGGCGTGAGCCTGGGAGGCGGAGCTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAAAGAAAGAAAGAAAGAAAATTGTTACTCAGAGAAGACAGTGACTTGTCCAAGATCAAGCAGCCAATAGTTAACAGGGCAGACCTCTGACCCAGGTTTTTTCACACCCTCTGCGGTGTTCTTTCTAAATGCCGTAGCTACCT... |
Task1_train_40784 | A genomic change on Chromosome 11 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AGAGCTACAGCCAAAAAGGATATTAAGGATGAGAGCTTTTACTGTCAGACTTCGGTGACTTCACTCATTTAATTCATCCTCTGTCCCTGCATCCAGCCCTGGATCTTTTATTTTATATGTGTTTGTCATACACATGGAGGGCCTTGTCAAATCCTAAAATAGGGCATGGAGACAGCTTCTTTATATGTACTTTGCTTACTTAGAAATAGAAGGTACCGGATCATTATGCAAGGTTCTCTTTAGATTTCCAAAAGTAGACTCGAGCCTCAGGACGGTAGCTGTGACTCTGGTGATGATAATTAATCTCTGCCAGTTCACAC... | AGAGCTACAGCCAAAAAGGATATTAAGGATGAGAGCTTTTACTGTCAGACTTCGGTGACTTCACTCATTTAATTCATCCTCTGTCCCTGCATCCAGCCCTGGATCTTTTATTTTATATGTGTTTGTCATACACATGGAGGGCCTTGTCAAATCCTAAAATAGGGCATGGAGACAGCTTCTTTATATGTACTTTGCTTACTTAGAAATAGAAGGTACCGGATCATTATGCAAGGTTCTCTTTAGATTTCCAAAAGTAGACTCGAGCCTCAGGACGGTAGCTGTGACTCTGGTGATGATAATTAATCTCTGCCAGTTCACAC... |
Task1_train_40785 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | AGCGTCGGACATCTGTCAGCTCTGAAATGATAAAAATGCACAATATTGAATACAAACAAAGGAGTCAGCACTGAAATTCATTTTCTCTCCAGATTAGGGAAAGAGTAGGTATGCCCTATGGTAGGGCAGTAAATTGCTGAATGATGAGATGAAACAGCCACCTAGCCATTTCCCATTAAATATAATCCCATCAGCAGCAGACAATATCTATCCTCCCCTATCCCCTCTATCCATATTTGGAAACTGCACCCTCTTCCCTATTTAGCACCCTAACACCACTTGAATTCCATAACCCTGTTGTTGATCTAGCTCTCCTCACC... | AGCGTCGGACATCTGTCAGCTCTGAAATGATAAAAATGCACAATATTGAATACAAACAAAGGAGTCAGCACTGAAATTCATTTTCTCTCCAGATTAGGGAAAGAGTAGGTATGCCCTATGGTAGGGCAGTAAATTGCTGAATGATGAGATGAAACAGCCACCTAGCCATTTCCCATTAAATATAATCCCATCAGCAGCAGACAATATCTATCCTCCCCTATCCCCTCTATCCATATTTGGAAACTGCACCCTCTTCCCTATTTAGCACCCTAACACCACTTGAATTCCATAACCCTGTTGTTGATCTAGCTCTCCTCACC... |
Task1_train_40786 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | TATCTATCCTCCCCTATCCCCTCTATCCATATTTGGAAACTGCACCCTCTTCCCTATTTAGCACCCTAACACCACTTGAATTCCATAACCCTGTTGTTGATCTAGCTCTCCTCACCTCTAAACACTTCTAGCATTCCTTTCAGATCAGGAGCTCGAAACACTCTCCTTTGATTTTTTGGAAAAGTTTCTGGCTTCTTCAAGGTCACGTTCTCCGTCCTAAGAATTAAAAAAAAAAAAAAAAACTTCCAAACCTTTGACCTTGTGTCCGTGGAACACCCCTGACTTCCTATCATTTCAACCCATTGAGGCACTTGAACTCT... | TATCTATCCTCCCCTATCCCCTCTATCCATATTTGGAAACTGCACCCTCTTCCCTATTTAGCACCCTAACACCACTTGAATTCCATAACCCTGTTGTTGATCTAGCTCTCCTCACCTCTAAACACTTCTAGCATTCCTTTCAGATCAGGAGCTCGAAACACTCTCCTTTGATTTTTTGGAAAAGTTTCTGGCTTCTTCAAGGTCACGTTCTCCGTCCTAAGAATTAAAAAAAAAAAAAAAAACTTCCAAACCTTTGACCTTGTGTCCGTGGAACACCCCTGACTTCCTATCATTTCAACCCATTGAGGCACTTGAACTCT... |
Task1_train_40787 | A mutation on Chromosome 11 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CCAGCCTTTACTAGTGAATTCTATTGAGCATATAAAGAAGAAATGATAGCAGTTATTTAATTCTTTTCAGAAAATTAAAAAAAAAGGAAAAAGTCTCAATTAATTCCATGAAGGAAAAAAATAAAAAGCATCTTGTATTTTGACGTGTATTTGTTTGCCAGTGGCTAAGCTGAGCAATGAAAAGCTGCACTGGTAAGTCTCAACACTAGAATACAGAGAATAGGAACCTATCAAACATGACTAGAGCTAATTGATCATCTCCACTACGTCAAATTTTTCTACTGCTCTGGATAAATTAATAAAAATGGGATTATCTCTTG... | CCAGCCTTTACTAGTGAATTCTATTGAGCATATAAAGAAGAAATGATAGCAGTTATTTAATTCTTTTCAGAAAATTAAAAAAAAAGGAAAAAGTCTCAATTAATTCCATGAAGGAAAAAAATAAAAAGCATCTTGTATTTTGACGTGTATTTGTTTGCCAGTGGCTAAGCTGAGCAATGAAAAGCTGCACTGGTAAGTCTCAACACTAGAATACAGAGAATAGGAACCTATCAAACATGACTAGAGCTAATTGATCATCTCCACTACGTCAAATTTTTCTACTGCTCTGGATAAATTAATAAAAATGGGATTATCTCTTG... |
Task1_train_40788 | A genomic change on Chromosome 11 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | ATTAAAAAAAAAGGAAAAAGTCTCAATTAATTCCATGAAGGAAAAAAATAAAAAGCATCTTGTATTTTGACGTGTATTTGTTTGCCAGTGGCTAAGCTGAGCAATGAAAAGCTGCACTGGTAAGTCTCAACACTAGAATACAGAGAATAGGAACCTATCAAACATGACTAGAGCTAATTGATCATCTCCACTACGTCAAATTTTTCTACTGCTCTGGATAAATTAATAAAAATGGGATTATCTCTTGCTACTTCTACATTCAATTATTCTTATAACTTCAGCAATTGATTCAGAAAAGCGGTCCTGCAGAGAACATTGTT... | ATTAAAAAAAAAGGAAAAAGTCTCAATTAATTCCATGAAGGAAAAAAATAAAAAGCATCTTGTATTTTGACGTGTATTTGTTTGCCAGTGGCTAAGCTGAGCAATGAAAAGCTGCACTGGTAAGTCTCAACACTAGAATACAGAGAATAGGAACCTATCAAACATGACTAGAGCTAATTGATCATCTCCACTACGTCAAATTTTTCTACTGCTCTGGATAAATTAATAAAAATGGGATTATCTCTTGCTACTTCTACATTCAATTATTCTTATAACTTCAGCAATTGATTCAGAAAAGCGGTCCTGCAGAGAACATTGTT... |
Task1_train_40789 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | ACTGCTCTGGATAAATTAATAAAAATGGGATTATCTCTTGCTACTTCTACATTCAATTATTCTTATAACTTCAGCAATTGATTCAGAAAAGCGGTCCTGCAGAGAACATTGTTAATATTAGAAAAAGCACAGCAACGCAGAGAAGGAAATAGCCTTCACTTTTCTTTAATCTCAGTGCTCAGGCTTCTTTCCACTTTTTACCTGAAGCAGCTCCATCACTGACCCCTGCAGCCGATGCTCCAGATCTGAGATGAGCTCTCTCAGGGACTGGGTCTGCTGCACCATCTCAGTTTCAGAGTTCGTAAGGCTTTTCAGAATGT... | ACTGCTCTGGATAAATTAATAAAAATGGGATTATCTCTTGCTACTTCTACATTCAATTATTCTTATAACTTCAGCAATTGATTCAGAAAAGCGGTCCTGCAGAGAACATTGTTAATATTAGAAAAAGCACAGCAACGCAGAGAAGGAAATAGCCTTCACTTTTCTTTAATCTCAGTGCTCAGGCTTCTTTCCACTTTTTACCTGAAGCAGCTCCATCACTGACCCCTGCAGCCGATGCTCCAGATCTGAGATGAGCTCTCTCAGGGACTGGGTCTGCTGCACCATCTCAGTTTCAGAGTTCGTAAGGCTTTTCAGAATGT... |
Task1_train_40790 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TGTCCTTCTAAGAAGAGGACTTCTAAGAGGAGACTGAATTAAATGTAAGAGTGAGTCTTGCTAACATCAGGGGGAGGATCATTTTATGCAGAGAGAGGAGCAAGTGCAAAAGCCTTGAGGAGCCATAGATTTGATAGTTTAATTGAGGAGGTATTTTTTACATGGGGAAAAAAGTCAGAGGAGATAAACCTTAACAGTATAAGTAAAATAATTCAGACACCAAAGACATATATTATGATTCTATTTTTATCAACTGATTAAAAACCCAAAGGATATTAGTAGTGGTTGCCTGGAGCTTGGGATCAGAATAGGAGTGATGG... | TGTCCTTCTAAGAAGAGGACTTCTAAGAGGAGACTGAATTAAATGTAAGAGTGAGTCTTGCTAACATCAGGGGGAGGATCATTTTATGCAGAGAGAGGAGCAAGTGCAAAAGCCTTGAGGAGCCATAGATTTGATAGTTTAATTGAGGAGGTATTTTTTACATGGGGAAAAAAGTCAGAGGAGATAAACCTTAACAGTATAAGTAAAATAATTCAGACACCAAAGACATATATTATGATTCTATTTTTATCAACTGATTAAAAACCCAAAGGATATTAGTAGTGGTTGCCTGGAGCTTGGGATCAGAATAGGAGTGATGG... |
Task1_train_40791 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | ACAAAGCCAGTCAGCAAGTCTGGGAACATGTGTAGTAAATTCTCTACAGTATTAGAGTCTTAGGAAAAAGTAAACATAGCAGAATGCGCCAGAGATAATCACAGAAAAGAGTGGAGGGGAAAGAAAGCATGTCCTGGAATCCTTTGGGTGGTAGAACTGCCTTCAAGTAACCACAGTATTTGTATCCTCAATGACTCTAAAATGTTAGCTGCCCTTATGGAAATGGTGCCAGTACTGATATGTGGGGAGTTAAAACCAAACCAAAACAACAGGAAAAGAACTCCAAGGGAACAGACTACAAATATGTCTTCCCTGAATCT... | ACAAAGCCAGTCAGCAAGTCTGGGAACATGTGTAGTAAATTCTCTACAGTATTAGAGTCTTAGGAAAAAGTAAACATAGCAGAATGCGCCAGAGATAATCACAGAAAAGAGTGGAGGGGAAAGAAAGCATGTCCTGGAATCCTTTGGGTGGTAGAACTGCCTTCAAGTAACCACAGTATTTGTATCCTCAATGACTCTAAAATGTTAGCTGCCCTTATGGAAATGGTGCCAGTACTGATATGTGGGGAGTTAAAACCAAACCAAAACAACAGGAAAAGAACTCCAAGGGAACAGACTACAAATATGTCTTCCCTGAATCT... |
Task1_train_40792 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | ACTACAAATATGTCTTCCCTGAATCTTTAACAAAAGCCTCTGGCTTCACCTTCACATTCTGATCTGGACTGCATTCAGAAGAGTAGGGCGTGAATGCCCAATTTCCTAGGGAACACAGAGGCTCCCTAGGCAGCTCTAGCCTTAAACTCAGTGCAAGCCAGTACACTCCCAGGGGGCTGTGAAATGTATTTCAGATAGTTGAGGGTGAGCAGAGACTTGTAATGTTCTTGCAATCTTCTGAGGATGCTTCTACACTGTGGTGCCTTCTCTTTTCTGCTCTCCTGGAATCCTGTGAGTTTGGCTAGGAAAAGACTCTGGAA... | ACTACAAATATGTCTTCCCTGAATCTTTAACAAAAGCCTCTGGCTTCACCTTCACATTCTGATCTGGACTGCATTCAGAAGAGTAGGGCGTGAATGCCCAATTTCCTAGGGAACACAGAGGCTCCCTAGGCAGCTCTAGCCTTAAACTCAGTGCAAGCCAGTACACTCCCAGGGGGCTGTGAAATGTATTTCAGATAGTTGAGGGTGAGCAGAGACTTGTAATGTTCTTGCAATCTTCTGAGGATGCTTCTACACTGTGGTGCCTTCTCTTTTCTGCTCTCCTGGAATCCTGTGAGTTTGGCTAGGAAAAGACTCTGGAA... |
Task1_train_40793 | A variant on Chromosome 11 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GCGTGAATGCCCAATTTCCTAGGGAACACAGAGGCTCCCTAGGCAGCTCTAGCCTTAAACTCAGTGCAAGCCAGTACACTCCCAGGGGGCTGTGAAATGTATTTCAGATAGTTGAGGGTGAGCAGAGACTTGTAATGTTCTTGCAATCTTCTGAGGATGCTTCTACACTGTGGTGCCTTCTCTTTTCTGCTCTCCTGGAATCCTGTGAGTTTGGCTAGGAAAAGACTCTGGAAAAGGCATTTCTTAGCCCTCAAGAGAAGTTTTTCTGTGCAAACTGGTTATGGAAAGTTTGCTTGAAAGCATGGAGAATAAGATTTAAA... | GCGTGAATGCCCAATTTCCTAGGGAACACAGAGGCTCCCTAGGCAGCTCTAGCCTTAAACTCAGTGCAAGCCAGTACACTCCCAGGGGGCTGTGAAATGTATTTCAGATAGTTGAGGGTGAGCAGAGACTTGTAATGTTCTTGCAATCTTCTGAGGATGCTTCTACACTGTGGTGCCTTCTCTTTTCTGCTCTCCTGGAATCCTGTGAGTTTGGCTAGGAAAAGACTCTGGAAAAGGCATTTCTTAGCCCTCAAGAGAAGTTTTTCTGTGCAAACTGGTTATGGAAAGTTTGCTTGAAAGCATGGAGAATAAGATTTAAA... |
Task1_train_40794 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TGTATTTCAGATAGTTGAGGGTGAGCAGAGACTTGTAATGTTCTTGCAATCTTCTGAGGATGCTTCTACACTGTGGTGCCTTCTCTTTTCTGCTCTCCTGGAATCCTGTGAGTTTGGCTAGGAAAAGACTCTGGAAAAGGCATTTCTTAGCCCTCAAGAGAAGTTTTTCTGTGCAAACTGGTTATGGAAAGTTTGCTTGAAAGCATGGAGAATAAGATTTAAAATAAAGATTTAAAGATTTGCTTGAAAGCATGGAGAATATCCAGGAAAGGAAATTTCCCCGAGTAACACCTCTGTAGAGTCTAATTTGGAATTTTAGT... | TGTATTTCAGATAGTTGAGGGTGAGCAGAGACTTGTAATGTTCTTGCAATCTTCTGAGGATGCTTCTACACTGTGGTGCCTTCTCTTTTCTGCTCTCCTGGAATCCTGTGAGTTTGGCTAGGAAAAGACTCTGGAAAAGGCATTTCTTAGCCCTCAAGAGAAGTTTTTCTGTGCAAACTGGTTATGGAAAGTTTGCTTGAAAGCATGGAGAATAAGATTTAAAATAAAGATTTAAAGATTTGCTTGAAAGCATGGAGAATATCCAGGAAAGGAAATTTCCCCGAGTAACACCTCTGTAGAGTCTAATTTGGAATTTTAGT... |
Task1_train_40795 | A genomic change on Chromosome 11 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GGAAAAGGCATTTCTTAGCCCTCAAGAGAAGTTTTTCTGTGCAAACTGGTTATGGAAAGTTTGCTTGAAAGCATGGAGAATAAGATTTAAAATAAAGATTTAAAGATTTGCTTGAAAGCATGGAGAATATCCAGGAAAGGAAATTTCCCCGAGTAACACCTCTGTAGAGTCTAATTTGGAATTTTAGTTAGCAGGCATCCTGAAACAGAAATTATAGTTTGGCGTTAAGCTGAGTAGTTGGAAAGGGGAACACAGTGGGGAACTACCTGGAAAGGAAGAAGCAAGTGATATGTTAACCAGATGAAAGACATGCGAGGCAT... | GGAAAAGGCATTTCTTAGCCCTCAAGAGAAGTTTTTCTGTGCAAACTGGTTATGGAAAGTTTGCTTGAAAGCATGGAGAATAAGATTTAAAATAAAGATTTAAAGATTTGCTTGAAAGCATGGAGAATATCCAGGAAAGGAAATTTCCCCGAGTAACACCTCTGTAGAGTCTAATTTGGAATTTTAGTTAGCAGGCATCCTGAAACAGAAATTATAGTTTGGCGTTAAGCTGAGTAGTTGGAAAGGGGAACACAGTGGGGAACTACCTGGAAAGGAAGAAGCAAGTGATATGTTAACCAGATGAAAGACATGCGAGGCAT... |
Task1_train_40796 | This is a variant located on Chromosome 11. Is this mutation a likely cause of disease or not? | Benign | TATGTTAACCAGATGAAAGACATGCGAGGCATTGTGAAGAAAGTTTATGGCATTCACTATAATATTCCTGAAATTACTAACAAGCAGTAATTTCTCATGAAGCATGGAAGGGGGAATTTGTGTGCCTAGTGAGATGGACAGACGCTATAAAGATGAACAGCATGAAACTAGGCAGAGGGAATCAGCAGAACCTTAGATTTCCTTGAGCTTTTTTTGCCCCTAGTATTCTGACATCAGGCACATTAGTCATCACTGTCCAGGTAAAGTCAAAGTACTCTTGTAAAATCGCTTCTTGCCACTGTGGAATGGTAACATTGAGA... | TATGTTAACCAGATGAAAGACATGCGAGGCATTGTGAAGAAAGTTTATGGCATTCACTATAATATTCCTGAAATTACTAACAAGCAGTAATTTCTCATGAAGCATGGAAGGGGGAATTTGTGTGCCTAGTGAGATGGACAGACGCTATAAAGATGAACAGCATGAAACTAGGCAGAGGGAATCAGCAGAACCTTAGATTTCCTTGAGCTTTTTTTGCCCCTAGTATTCTGACATCAGGCACATTAGTCATCACTGTCCAGGTAAAGTCAAAGTACTCTTGTAAAATCGCTTCTTGCCACTGTGGAATGGTAACATTGAGA... |
Task1_train_40797 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | GGCATTGTGAAGAAAGTTTATGGCATTCACTATAATATTCCTGAAATTACTAACAAGCAGTAATTTCTCATGAAGCATGGAAGGGGGAATTTGTGTGCCTAGTGAGATGGACAGACGCTATAAAGATGAACAGCATGAAACTAGGCAGAGGGAATCAGCAGAACCTTAGATTTCCTTGAGCTTTTTTTGCCCCTAGTATTCTGACATCAGGCACATTAGTCATCACTGTCCAGGTAAAGTCAAAGTACTCTTGTAAAATCGCTTCTTGCCACTGTGGAATGGTAACATTGAGAAGGATTTGACTATGCCCTTTCTTAGAA... | GGCATTGTGAAGAAAGTTTATGGCATTCACTATAATATTCCTGAAATTACTAACAAGCAGTAATTTCTCATGAAGCATGGAAGGGGGAATTTGTGTGCCTAGTGAGATGGACAGACGCTATAAAGATGAACAGCATGAAACTAGGCAGAGGGAATCAGCAGAACCTTAGATTTCCTTGAGCTTTTTTTGCCCCTAGTATTCTGACATCAGGCACATTAGTCATCACTGTCCAGGTAAAGTCAAAGTACTCTTGTAAAATCGCTTCTTGCCACTGTGGAATGGTAACATTGAGAAGGATTTGACTATGCCCTTTCTTAGAA... |
Task1_train_40798 | A variant on Chromosome 11 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TATGTCACTACATACCAAAAAAAGGTGCTTTGTCATGAGAGATACAATTTTTACTTATTTTTCTGATTAATATAAAAGTTTGTGCCTATTTACCTGTTCATTGGCAATTTTATTTCTCTTTTGAAGTGTATGTTTCTTCCTGCAACTTTTTCTTACTGATGTTGTTGAAGTACTTTATATATTTTCTGTATGTATGCATTTGGATATCTTCTAGTTTGCGTTGACTAGATACATAAAGAACAAGAAAGATATCTTGAAAAGTGAAAAAATTGAATCAAAACTTCATTGACTTTTTTAATTTTAAATTTTTGTGGGCACAT... | TATGTCACTACATACCAAAAAAAGGTGCTTTGTCATGAGAGATACAATTTTTACTTATTTTTCTGATTAATATAAAAGTTTGTGCCTATTTACCTGTTCATTGGCAATTTTATTTCTCTTTTGAAGTGTATGTTTCTTCCTGCAACTTTTTCTTACTGATGTTGTTGAAGTACTTTATATATTTTCTGTATGTATGCATTTGGATATCTTCTAGTTTGCGTTGACTAGATACATAAAGAACAAGAAAGATATCTTGAAAAGTGAAAAAATTGAATCAAAACTTCATTGACTTTTTTAATTTTAAATTTTTGTGGGCACAT... |
Task1_train_40799 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | TTTGTCATGAGAGATACAATTTTTACTTATTTTTCTGATTAATATAAAAGTTTGTGCCTATTTACCTGTTCATTGGCAATTTTATTTCTCTTTTGAAGTGTATGTTTCTTCCTGCAACTTTTTCTTACTGATGTTGTTGAAGTACTTTATATATTTTCTGTATGTATGCATTTGGATATCTTCTAGTTTGCGTTGACTAGATACATAAAGAACAAGAAAGATATCTTGAAAAGTGAAAAAATTGAATCAAAACTTCATTGACTTTTTTAATTTTAAATTTTTGTGGGCACATAGTAGGTGTATATATTTATGGGTGTATG... | TTTGTCATGAGAGATACAATTTTTACTTATTTTTCTGATTAATATAAAAGTTTGTGCCTATTTACCTGTTCATTGGCAATTTTATTTCTCTTTTGAAGTGTATGTTTCTTCCTGCAACTTTTTCTTACTGATGTTGTTGAAGTACTTTATATATTTTCTGTATGTATGCATTTGGATATCTTCTAGTTTGCGTTGACTAGATACATAAAGAACAAGAAAGATATCTTGAAAAGTGAAAAAATTGAATCAAAACTTCATTGACTTTTTTAATTTTAAATTTTTGTGGGCACATAGTAGGTGTATATATTTATGGGTGTATG... |
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