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_41600 | An alteration has been detected on Chromosome 11. Is it pathogenic, and if so, what disease is involved? | Benign | CCGCTGTGTGGACTGTTGTGATCTCTGGCCAGACACTGAGCACTCATGCACAGCCCAGCTTGGGGCCACCTCCATCCAGAGGGGACACATTTCCCTAATTTGCATGAAGGTACTCCAAGGGATAGTGGTGGCTAGAGCACAGGGCCCCTGGGAAGGATATACCTTCTCTCTCATGTTTGGGACCAAACTGACTCCTGTCCTGCAGAGGAAGGCCCGGCTCTCCCAAGCTTTCATGCTGTGGGTGTCAACATCATCCCCCTGCTCTTCTGTCCCTATTCTTAACACGGGAACCAGCCATGAGTTAACATGGGGCTCCCCCA... | CCGCTGTGTGGACTGTTGTGATCTCTGGCCAGACACTGAGCACTCATGCACAGCCCAGCTTGGGGCCACCTCCATCCAGAGGGGACACATTTCCCTAATTTGCATGAAGGTACTCCAAGGGATAGTGGTGGCTAGAGCACAGGGCCCCTGGGAAGGATATACCTTCTCTCTCATGTTTGGGACCAAACTGACTCCTGTCCTGCAGAGGAAGGCCCGGCTCTCCCAAGCTTTCATGCTGTGGGTGTCAACATCATCCCCCTGCTCTTCTGTCCCTATTCTTAACACGGGAACCAGCCATGAGTTAACATGGGGCTCCCCCA... |
Task1_train_41601 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AGAGAAAATGGAGTCAAACCACACCCTTTCCCCATCCCCCTGGCCTCCCCCTCATCCCCAGGCCTATCACACATCCAGGGTTTAGGTGCCCTTTTCCAGCACCCAGCTGCATGTTCAGAAAGCACATGCCCTCAGGGAGCCTGGCTGCCTCCCTTTCAAGTCTGTGTCCTTGCAAGACGGAATTTTCCCTTTCCTGACCTGAAAGGTGGAGCATTGGTTCTCAAGGCTGGCTGCATGTTAGAATTGCTCGGGAAATTAAAAAAAAAAAAAAAAAAAAGCTTTGCCTTGGGCACACCCTAGACTAATTAAACCAGAATCTG... | AGAGAAAATGGAGTCAAACCACACCCTTTCCCCATCCCCCTGGCCTCCCCCTCATCCCCAGGCCTATCACACATCCAGGGTTTAGGTGCCCTTTTCCAGCACCCAGCTGCATGTTCAGAAAGCACATGCCCTCAGGGAGCCTGGCTGCCTCCCTTTCAAGTCTGTGTCCTTGCAAGACGGAATTTTCCCTTTCCTGACCTGAAAGGTGGAGCATTGGTTCTCAAGGCTGGCTGCATGTTAGAATTGCTCGGGAAATTAAAAAAAAAAAAAAAAAAAAGCTTTGCCTTGGGCACACCCTAGACTAATTAAACCAGAATCTG... |
Task1_train_41602 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | AAGGGAAAGGAACTGATTCACAGCATGGCTCTACACTAGCCAAGCGACTTTTATTTTAGTAAATCACTTAACCATGCAGGGCCTTGATTTTCACTTCTATCAAATGAGGCTAAAAATATCTGCTGCTCAAGATTTTTTGTAAGATTTCTTTGAGAAGATCAATACATACATTCCCTGTAAACTCCGAATGTATTATCTACCAACCCCCACCCCTGCCCAACCTTAGAGGAAGATGCTTTTCATGATCATGCCCTAAATTTGTAAAATACTTTAGGTAAATAATGTTTTTGTTTTGTTTTGTTTTTGAGACAGAGTCCTGC... | AAGGGAAAGGAACTGATTCACAGCATGGCTCTACACTAGCCAAGCGACTTTTATTTTAGTAAATCACTTAACCATGCAGGGCCTTGATTTTCACTTCTATCAAATGAGGCTAAAAATATCTGCTGCTCAAGATTTTTTGTAAGATTTCTTTGAGAAGATCAATACATACATTCCCTGTAAACTCCGAATGTATTATCTACCAACCCCCACCCCTGCCCAACCTTAGAGGAAGATGCTTTTCATGATCATGCCCTAAATTTGTAAAATACTTTAGGTAAATAATGTTTTTGTTTTGTTTTGTTTTTGAGACAGAGTCCTGC... |
Task1_train_41603 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | AGTTTTCTATTTTAACCATGTGTTTTTAAGCGTGGTCTACCATTCATTGTCACAGCAGCCCTGTGCAATGAGTACTGCCATCCTCTCCATTCTGCAGAAGGAGAACTAAGGCATGGAGTTTAAGCAACTTCCCCAAGATCACAGTGTCAGGAAATGATGGATCCAGGACTTAGATCCAGGTCTTCTGATTTCAAATCTTGTGATAATAATAATTACCAGTTGTTGAGTGTATGCTTTTTCCAGGCTATTATGGACTGACTCATGTCCCCGCCCCCAAACACACACACACAAATTCATATGTTAAAGCCCCAACCCTCAAT... | AGTTTTCTATTTTAACCATGTGTTTTTAAGCGTGGTCTACCATTCATTGTCACAGCAGCCCTGTGCAATGAGTACTGCCATCCTCTCCATTCTGCAGAAGGAGAACTAAGGCATGGAGTTTAAGCAACTTCCCCAAGATCACAGTGTCAGGAAATGATGGATCCAGGACTTAGATCCAGGTCTTCTGATTTCAAATCTTGTGATAATAATAATTACCAGTTGTTGAGTGTATGCTTTTTCCAGGCTATTATGGACTGACTCATGTCCCCGCCCCCAAACACACACACACAAATTCATATGTTAAAGCCCCAACCCTCAAT... |
Task1_train_41604 | A mutation is present on Chromosome 11. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CCATTGCCTAATTCAAAGTCATGAAGATTTACTTACTCCTATGGTTTCTTTTAAGAGTTTTATAGTTTAAGCTCTTACATTTGGGTGTATGATTCATTTTGAGTTAATGTTTATATACGGTGTGAGATATCCCTTTTTAAAAAATTCCTAAGAACATCTGAGTTTCAGAATGTTCTTTACTAGATTAGATATGAAAAAAATTGGTGAGGAGGGTTTTTTTTTCTTTTCTCTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTCTCTCTGTCACCTAGGCTGGAGTGCAGTGGCACAAACATGGCCCACTGCAATCTTGACC... | CCATTGCCTAATTCAAAGTCATGAAGATTTACTTACTCCTATGGTTTCTTTTAAGAGTTTTATAGTTTAAGCTCTTACATTTGGGTGTATGATTCATTTTGAGTTAATGTTTATATACGGTGTGAGATATCCCTTTTTAAAAAATTCCTAAGAACATCTGAGTTTCAGAATGTTCTTTACTAGATTAGATATGAAAAAAATTGGTGAGGAGGGTTTTTTTTTCTTTTCTCTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTCTCTCTGTCACCTAGGCTGGAGTGCAGTGGCACAAACATGGCCCACTGCAATCTTGACC... |
Task1_train_41605 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TATAATAAGCTCATTCAGTCTGTTTTATAAGCAGAGAAATCCAAACATACGGTAACTTAACAGGAATGGCTGCCAATAACAGTTGAGCTAACACTCATTGAAAGATTATGAATAATATCTTGATTACAAATCAAAGCTTGGTCTCATCTTTTTAGCCCAAAATTACTAAGACAACGTAACATTTTTTAGTCTGATTAATGGTAGAGTAACTAATTAGAGTGGGAAAGAGATTAGCAAATCATTCAAGATGTCAAGGGCAGGCAAAGTGCCGTTTTGTCATAGATAATATAGTAAAGCTCATAGCGACAGGTGTGCATAAT... | TATAATAAGCTCATTCAGTCTGTTTTATAAGCAGAGAAATCCAAACATACGGTAACTTAACAGGAATGGCTGCCAATAACAGTTGAGCTAACACTCATTGAAAGATTATGAATAATATCTTGATTACAAATCAAAGCTTGGTCTCATCTTTTTAGCCCAAAATTACTAAGACAACGTAACATTTTTTAGTCTGATTAATGGTAGAGTAACTAATTAGAGTGGGAAAGAGATTAGCAAATCATTCAAGATGTCAAGGGCAGGCAAAGTGCCGTTTTGTCATAGATAATATAGTAAAGCTCATAGCGACAGGTGTGCATAAT... |
Task1_train_41606 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | GGACATAATGACCAGTTGTCCTGCTGTTACAAAGCTTTAAAATTAATAAAGCTAAGTTTGAGCAGTGGATTCAGAAGTGACAGCCTGCTATATCCATAGTAAAGTTCCAATCAAACCTTTTAAAAAAGTTCATTCACTGATGATCTCTGCCTTATTTACTTATTTGAGTAGAAGTTTTTAAATGGTGCTTTCCTAATTCTGTCGTTCTTTCTGTATTCATTAGCTGTAATTCTTCCAAAAAGAAGAAATTTCCTTTATCTATTAGGGTTATTGATTTTCTCTTTAACAGGAAAGAGGATAAATGTTCATATATTTCCCTT... | GGACATAATGACCAGTTGTCCTGCTGTTACAAAGCTTTAAAATTAATAAAGCTAAGTTTGAGCAGTGGATTCAGAAGTGACAGCCTGCTATATCCATAGTAAAGTTCCAATCAAACCTTTTAAAAAAGTTCATTCACTGATGATCTCTGCCTTATTTACTTATTTGAGTAGAAGTTTTTAAATGGTGCTTTCCTAATTCTGTCGTTCTTTCTGTATTCATTAGCTGTAATTCTTCCAAAAAGAAGAAATTTCCTTTATCTATTAGGGTTATTGATTTTCTCTTTAACAGGAAAGAGGATAAATGTTCATATATTTCCCTT... |
Task1_train_41607 | A mutation on Chromosome 11 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | AGAAAGGATCAGCATGTTTTCATCCTTACTAGGATTTAGGCATAAGGATGGTTGATGGGTAGGAAGAGATTTGATGAGATGTACCATCAGAGATAAAAGGGAGGGAACAGAAACTTAACTGTGCTTTTACTTTTCAGAAGGGAGCCAGGGACTATAGATCAGGAGCCAAAACTTGGATAATGAGGTAAGATTCTGGAATGCATGTTATTTTGTCATGTTTGGTGCCTACTCTTAGCATATTTTTTTTGAAAGCTTATGGAAAAAAGACTCTAAACTTGACTTTGAAAACTGCTAGAAAGGGATTTCTGTGAACCTAGCAT... | AGAAAGGATCAGCATGTTTTCATCCTTACTAGGATTTAGGCATAAGGATGGTTGATGGGTAGGAAGAGATTTGATGAGATGTACCATCAGAGATAAAAGGGAGGGAACAGAAACTTAACTGTGCTTTTACTTTTCAGAAGGGAGCCAGGGACTATAGATCAGGAGCCAAAACTTGGATAATGAGGTAAGATTCTGGAATGCATGTTATTTTGTCATGTTTGGTGCCTACTCTTAGCATATTTTTTTTGAAAGCTTATGGAAAAAAGACTCTAAACTTGACTTTGAAAACTGCTAGAAAGGGATTTCTGTGAACCTAGCAT... |
Task1_train_41608 | A genetic alteration is present on Chromosome 11. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | ATTAAAATGTTAACCTACATGTGTAGATTATAGGGACCATTGTTATTGATTATCTACTTAATAGCTTTCAGACAATAGTGGCTCGCAAAGATGTTTTAAGCCGTGGAATTTTTTCAAACAAAAAGCTCACCCAGGATTCCATATACATATAGGTAAGAATGACTGATATTCTGGCTGAAGCAGTGGTATTGGAACTGGTACTCTGCCCCATGGGGCACCTCTCCTGACTCCTGCCCCTCAAGGTAGTGCCCAAAGTACCACATGAGACCCAGAGAGCTGAAGATACTTATCCAGTCTTTTGTTGTTGTTTTTTGAGGCTG... | ATTAAAATGTTAACCTACATGTGTAGATTATAGGGACCATTGTTATTGATTATCTACTTAATAGCTTTCAGACAATAGTGGCTCGCAAAGATGTTTTAAGCCGTGGAATTTTTTCAAACAAAAAGCTCACCCAGGATTCCATATACATATAGGTAAGAATGACTGATATTCTGGCTGAAGCAGTGGTATTGGAACTGGTACTCTGCCCCATGGGGCACCTCTCCTGACTCCTGCCCCTCAAGGTAGTGCCCAAAGTACCACATGAGACCCAGAGAGCTGAAGATACTTATCCAGTCTTTTGTTGTTGTTTTTTGAGGCTG... |
Task1_train_41609 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GATGAGTCGAAGAGGGTAGGTAACTCCATAACTCAGTCCTTTATATGACCCAAGAGAATCACTGTTACAGAATGTGATGCTAAAGGCTGTTACTAGACCCTGAATTTTGTAGATGAGGTAATTGAGGTTTCCCTAGGAGTTTAGTCATTTACCAGAGATCACAATTTAAAGCTCTTCCTTCCATTGAGAATTTTTCTTATAACTTAGAACTAAGGCCCTACCAATTTTCCCACTTTCATTGGATCAACTTTCCTTCTAAGTTTGAGATCATGAGTGGCCTCATTTTAGGAAGGCCAGGATGGAGCCACAGCTACTGCAAT... | GATGAGTCGAAGAGGGTAGGTAACTCCATAACTCAGTCCTTTATATGACCCAAGAGAATCACTGTTACAGAATGTGATGCTAAAGGCTGTTACTAGACCCTGAATTTTGTAGATGAGGTAATTGAGGTTTCCCTAGGAGTTTAGTCATTTACCAGAGATCACAATTTAAAGCTCTTCCTTCCATTGAGAATTTTTCTTATAACTTAGAACTAAGGCCCTACCAATTTTCCCACTTTCATTGGATCAACTTTCCTTCTAAGTTTGAGATCATGAGTGGCCTCATTTTAGGAAGGCCAGGATGGAGCCACAGCTACTGCAAT... |
Task1_train_41610 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | TGATGACAGTAATGATACCTTACACCAAAGAGAAGTTATGTAAGAAACAATATTCTAAATGCACTGTATGCATTACCTCATTTTACTAGGTAGAAACTCTTTTCATCTTCAGTTGACAGATGAGAAAACTGAGGGATGGAATGGTTATGTAACTTGTTCAAAGTCACCCAGATAGGAGGTAGAGAAGTCAGGTTTTGAACCCAGGTTGTCTGGTTCTAGAATCATACCCTTAATCATTTTGCTGGTTCTAGAAGCTGGACAATTTAATATCTTACATTATCTTTGGTTCCATCAATAGTTTTTGGAGCCTACTGGGTACA... | TGATGACAGTAATGATACCTTACACCAAAGAGAAGTTATGTAAGAAACAATATTCTAAATGCACTGTATGCATTACCTCATTTTACTAGGTAGAAACTCTTTTCATCTTCAGTTGACAGATGAGAAAACTGAGGGATGGAATGGTTATGTAACTTGTTCAAAGTCACCCAGATAGGAGGTAGAGAAGTCAGGTTTTGAACCCAGGTTGTCTGGTTCTAGAATCATACCCTTAATCATTTTGCTGGTTCTAGAAGCTGGACAATTTAATATCTTACATTATCTTTGGTTCCATCAATAGTTTTTGGAGCCTACTGGGTACA... |
Task1_train_41611 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | ATGAAAAATACAAAAATTAGCCAGGTGCTGGTGGCTCACACTACCTAGGTAGCTGAGGTGGGAGGATTACCTAAGCCTGGAGCCTGGTAGGTCAAGGATCCAGTGAGCTGTGATTGTGCCACTGCAATCCAGCCTAGGTGACAGAGTGAGACTCCATATCAAAAAAACCAAAAAAAAAAAAAAAAAAAGAAAGAAAAGAAAAGAAACCAACCATAAGCTAGCATCCATTTTAAATACAAAGATATAGGTAGGCTAAAAGTAAAATGACAAAAATAGATATACCATGCAAATCCTAACCAAAATAATGCTTGTATGAATTT... | ATGAAAAATACAAAAATTAGCCAGGTGCTGGTGGCTCACACTACCTAGGTAGCTGAGGTGGGAGGATTACCTAAGCCTGGAGCCTGGTAGGTCAAGGATCCAGTGAGCTGTGATTGTGCCACTGCAATCCAGCCTAGGTGACAGAGTGAGACTCCATATCAAAAAAACCAAAAAAAAAAAAAAAAAAAGAAAGAAAAGAAAAGAAACCAACCATAAGCTAGCATCCATTTTAAATACAAAGATATAGGTAGGCTAAAAGTAAAATGACAAAAATAGATATACCATGCAAATCCTAACCAAAATAATGCTTGTATGAATTT... |
Task1_train_41612 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | CCAGGATATCTTAAATATATCAAAATAAGGGGGGAAAGGCATTTGGAGAAGAGAGGTTTAATCCATCTAAACCAGTGATTCCTACTTTATTATCTGGGCAGATATTAAGCTAATTTATTTTCCCATTTCTTGCAGGTCCAACATAGGAGTTGAAATGATGAAGAACTTTACCCCCATTGAGGTCATACCATGCAACAGTAAGTCTGGAGTGTTGTTGTCTGCCATGATCACAATTTATCCACGGAAAGGACATGCTTACTTAGAGATATTTATTCCACATTAACGATTTGATCTCTCATTTCCTGGGACAAATTACATCA... | CCAGGATATCTTAAATATATCAAAATAAGGGGGGAAAGGCATTTGGAGAAGAGAGGTTTAATCCATCTAAACCAGTGATTCCTACTTTATTATCTGGGCAGATATTAAGCTAATTTATTTTCCCATTTCTTGCAGGTCCAACATAGGAGTTGAAATGATGAAGAACTTTACCCCCATTGAGGTCATACCATGCAACAGTAAGTCTGGAGTGTTGTTGTCTGCCATGATCACAATTTATCCACGGAAAGGACATGCTTACTTAGAGATATTTATTCCACATTAACGATTTGATCTCTCATTTCCTGGGACAAATTACATCA... |
Task1_train_41613 | A variant was discovered on Chromosome 11. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CTGGAGTGCAGTGGCATGATCTCAGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCAATTATTGTGCCTCAGCCTCCCAAGTAGCTGGAATTACAGGTGTGTGCCACCACGCCCAGCTAATTTTTGTGTTTTTAGTAGAGATGGGGTTTCGCTATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTGAGGTGATCTGCCCACCTCGGCCTCCAAAGTGCTGGGATTATAGGCTTGAGCCACCATGCCTGGCCAAAGAGTTCTTTAATCCCCTTGGAAGAATCTAAAAAGATAACTTACCAAGCTAATGTACAATATTTA... | CTGGAGTGCAGTGGCATGATCTCAGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCAATTATTGTGCCTCAGCCTCCCAAGTAGCTGGAATTACAGGTGTGTGCCACCACGCCCAGCTAATTTTTGTGTTTTTAGTAGAGATGGGGTTTCGCTATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTGAGGTGATCTGCCCACCTCGGCCTCCAAAGTGCTGGGATTATAGGCTTGAGCCACCATGCCTGGCCAAAGAGTTCTTTAATCCCCTTGGAAGAATCTAAAAAGATAACTTACCAAGCTAATGTACAATATTTA... |
Task1_train_41614 | With a mutation on Chromosome 11, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | ATTAGGATGTCTGAAGTCTTCCAGTCCCTCTTCACACAGCCAAATTGCTCAAAGGTGGTTTACACACTACTCAAGTGACTCACCAGTTCCCGGATGTCTTTCAGCAGCCCTTCCAGTGTGGTGAACTTGCCCCCGAGGACTGCCATTCCCAGTTCAAATTCTAGCTCTGGGATTTCCACACTGCAAGTCTCAGACTGTGAAATGAGAGGTCAGTTTAAGCTTTAAGTCAGAAGCAAAGAAAGCCAACCAGAGGCCTCCTGCCCAATTAATACCAGCAGTGATAGACTGCGGACAAGGGCAGCTGTCTCAGTTTTCTCTGA... | ATTAGGATGTCTGAAGTCTTCCAGTCCCTCTTCACACAGCCAAATTGCTCAAAGGTGGTTTACACACTACTCAAGTGACTCACCAGTTCCCGGATGTCTTTCAGCAGCCCTTCCAGTGTGGTGAACTTGCCCCCGAGGACTGCCATTCCCAGTTCAAATTCTAGCTCTGGGATTTCCACACTGCAAGTCTCAGACTGTGAAATGAGAGGTCAGTTTAAGCTTTAAGTCAGAAGCAAAGAAAGCCAACCAGAGGCCTCCTGCCCAATTAATACCAGCAGTGATAGACTGCGGACAAGGGCAGCTGTCTCAGTTTTCTCTGA... |
Task1_train_41615 | Given this context: Chromosome 11 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AGACCAGCCTGCAGGCATGATGAGCCTACATATGTGTGGGGTCTGTGCTATGGGGTTGGGGAGCAGGCAGGTGCTGAGAACCCGGGGACAGTAGGCTGAGCTGGGAGGAAAGGGGGCCGGACAGGGAAGTCCAAAGACAAGGAGCTGTGTTTACCCTTTCCACGTCCTCCACCACACCCCAGTTTCAGTTCCCAGGGGATCTATAGGGAGCATTGGTGCCCCTGAGTGAGGGGAGTCCCCAGAAGAGAGTCCGGCATAAAAAGAGGCCATTCAAACTCTAGAACAGCAGGAACAAAGGAGGCAGCCCACCTCAGGAATCT... | AGACCAGCCTGCAGGCATGATGAGCCTACATATGTGTGGGGTCTGTGCTATGGGGTTGGGGAGCAGGCAGGTGCTGAGAACCCGGGGACAGTAGGCTGAGCTGGGAGGAAAGGGGGCCGGACAGGGAAGTCCAAAGACAAGGAGCTGTGTTTACCCTTTCCACGTCCTCCACCACACCCCAGTTTCAGTTCCCAGGGGATCTATAGGGAGCATTGGTGCCCCTGAGTGAGGGGAGTCCCCAGAAGAGAGTCCGGCATAAAAAGAGGCCATTCAAACTCTAGAACAGCAGGAACAAAGGAGGCAGCCCACCTCAGGAATCT... |
Task1_train_41616 | A mutation on Chromosome 11 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | AGCTCTTCCAGACACAGCCTGCATTCCATGCACAGTGTCCTGTGGGGGAGCAGGCTAGTGAACAGTGCAGGTGCAGAGGAAGGGCCCGTAACCCAGGCCCTCCTGCCAGGTGTGACAGACAGCCGTTGTCTAGCCAGGATCCCTGAAGCAGAGCCCAGCCAGACCCCCTTTGACAGACCTGGACTGGGAGTGGGTGGATGAGAAAGAGCAGCAAGGGAATGGAGTGGGTGATGGGTGTGCTTTGGGGATAGTGGTGAGGCCACTGCTTTCAGACATGGTCCAAATGAGAGTCACGCCAGGCAAACTTCTATCATAAACAT... | AGCTCTTCCAGACACAGCCTGCATTCCATGCACAGTGTCCTGTGGGGGAGCAGGCTAGTGAACAGTGCAGGTGCAGAGGAAGGGCCCGTAACCCAGGCCCTCCTGCCAGGTGTGACAGACAGCCGTTGTCTAGCCAGGATCCCTGAAGCAGAGCCCAGCCAGACCCCCTTTGACAGACCTGGACTGGGAGTGGGTGGATGAGAAAGAGCAGCAAGGGAATGGAGTGGGTGATGGGTGTGCTTTGGGGATAGTGGTGAGGCCACTGCTTTCAGACATGGTCCAAATGAGAGTCACGCCAGGCAAACTTCTATCATAAACAT... |
Task1_train_41617 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TTCACCTCATGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGCCCGGCCCAGGGTTCATATTAAGAACCAAGTTCTGGGAGACACTGAGGCCCCCAGGGGTTCTGGAGTCAGCACTAAACCAGGCAGCCCTCAGGTGAGGTCTGAGAGCATCTCAGAAGCTTCCAGACCCTCTTGGAACCCGGCCCACCCTGCATCTCACTTCCTTTTGGTGACTCGTTGCTCTGTTTGGCCTCATTGGCCCTTTCCTAAAGCCATCCAGTAAACCTCCAGGTGCCTGGTGGGTTTGTCAAGGTGTT... | TTCACCTCATGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGCCCGGCCCAGGGTTCATATTAAGAACCAAGTTCTGGGAGACACTGAGGCCCCCAGGGGTTCTGGAGTCAGCACTAAACCAGGCAGCCCTCAGGTGAGGTCTGAGAGCATCTCAGAAGCTTCCAGACCCTCTTGGAACCCGGCCCACCCTGCATCTCACTTCCTTTTGGTGACTCGTTGCTCTGTTTGGCCTCATTGGCCCTTTCCTAAAGCCATCCAGTAAACCTCCAGGTGCCTGGTGGGTTTGTCAAGGTGTT... |
Task1_train_41618 | This sequence change occurs on Chromosome 11. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TGTCTGATTCCCAAGCATACATCCCTCCCACCAGGCCAGCACCAGGGGCCAGAGGGGTATAGGCCTGGGCCAGACCATGCTGGGGGCCACTACCCTGAGGGCACCTTGAGAGGGAAGGAGGAGGCCCCAGGACACCCTCCAAGGGGACTTCCCCCTCCTCCTTAGCATGTTCCAGGCCTCTTCCAGGAAAGCCCTGAAGGGCCTGCATCCCCCTGTGGCGAGGAAAGGGAGGTGGCTAGACTCGCAGGGCTGGGGTCCACGGGTAACAGGCTGTGGAGTCGTTTGAGACAAACGCTTGAACTGGCTCTTTCCTTGTGAGG... | TGTCTGATTCCCAAGCATACATCCCTCCCACCAGGCCAGCACCAGGGGCCAGAGGGGTATAGGCCTGGGCCAGACCATGCTGGGGGCCACTACCCTGAGGGCACCTTGAGAGGGAAGGAGGAGGCCCCAGGACACCCTCCAAGGGGACTTCCCCCTCCTCCTTAGCATGTTCCAGGCCTCTTCCAGGAAAGCCCTGAAGGGCCTGCATCCCCCTGTGGCGAGGAAAGGGAGGTGGCTAGACTCGCAGGGCTGGGGTCCACGGGTAACAGGCTGTGGAGTCGTTTGAGACAAACGCTTGAACTGGCTCTTTCCTTGTGAGG... |
Task1_train_41619 | 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 | ATACTTTTTTGAATGTATCATGTCTTCATTAACAACAGAAAATCCACATGGTGTTTACTAAACTTGTTTACGACATTAAAAATTTCCTTTTTATTTTTAGTAGCCCAGGTTGAGTTTTTCACAAGAGATTTTTTTCTTAGCTGAGGTATAGTTGTATAGCAAGAAGAATTAAGCCAGATTTTTGTGTGTGGAAAGACAGTTTTCTATCCACGTCTTTTTCTGTTTGTCAGAAGGTGGGAGTATGGTCCAAATAAATCCATTAGGTTACTCCTGCAGCATGCGCTTTTAGCTTCTCTCTTGACTGAGGATCAAATATCCCT... | ATACTTTTTTGAATGTATCATGTCTTCATTAACAACAGAAAATCCACATGGTGTTTACTAAACTTGTTTACGACATTAAAAATTTCCTTTTTATTTTTAGTAGCCCAGGTTGAGTTTTTCACAAGAGATTTTTTTCTTAGCTGAGGTATAGTTGTATAGCAAGAAGAATTAAGCCAGATTTTTGTGTGTGGAAAGACAGTTTTCTATCCACGTCTTTTTCTGTTTGTCAGAAGGTGGGAGTATGGTCCAAATAAATCCATTAGGTTACTCCTGCAGCATGCGCTTTTAGCTTCTCTCTTGACTGAGGATCAAATATCCCT... |
Task1_train_41620 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TCAATGACACAATCTCGGCTCACTGCAACCTTCACCTCCTGGGTTCAAGTGATTCTCCTGCCTTAGCCTCCTGAGTAGCTGGGATTACAGGCACACGCCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGAGTTTCACCATGTTGGTCAGGCTGGTCTCAAACTCCTGACCTCGTGATCTGCCTGCCTTGGCCTCGCAAAGTGCTGGGATTACAGGCATGAGCCACCATGCCCGGCCAATTTTTGTATTTTTTAGTAGAGATGGGATTTCACCATGTTGATCAGGCTGGTCTTGAACTCCTGACGTCAGGTG... | TCAATGACACAATCTCGGCTCACTGCAACCTTCACCTCCTGGGTTCAAGTGATTCTCCTGCCTTAGCCTCCTGAGTAGCTGGGATTACAGGCACACGCCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGAGTTTCACCATGTTGGTCAGGCTGGTCTCAAACTCCTGACCTCGTGATCTGCCTGCCTTGGCCTCGCAAAGTGCTGGGATTACAGGCATGAGCCACCATGCCCGGCCAATTTTTGTATTTTTTAGTAGAGATGGGATTTCACCATGTTGATCAGGCTGGTCTTGAACTCCTGACGTCAGGTG... |
Task1_train_41621 | A variant has been detected on Chromosome 11. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TTTTGTTTCCCTCCAGAGCCTTGTGCTTCCTCTTGTCCAAGCTCCACAGACACTTCTTTTTTCCCTCCCCTCCCTGACATGTTACTCACGGTTCTGAGAAACATGGTAACAAGCCCATTCCTCCAGATGGAGAAAAGAGGGCAGATAATTTCCAGCTAGGCTGGATTTTCCAATGTCATGTGTTTGAATGGCAAAAGGTGGCCACAGGGCTTTTCATGGACCCAGGATTATTTGAAGTGGTAGTCAGGCATCTGGGCAGGCTGTGGCTTGACGAAAGGCAGGAGACGGAATGAAGTGAGGGTTCTGGGGTGGAGAGCTGG... | TTTTGTTTCCCTCCAGAGCCTTGTGCTTCCTCTTGTCCAAGCTCCACAGACACTTCTTTTTTCCCTCCCCTCCCTGACATGTTACTCACGGTTCTGAGAAACATGGTAACAAGCCCATTCCTCCAGATGGAGAAAAGAGGGCAGATAATTTCCAGCTAGGCTGGATTTTCCAATGTCATGTGTTTGAATGGCAAAAGGTGGCCACAGGGCTTTTCATGGACCCAGGATTATTTGAAGTGGTAGTCAGGCATCTGGGCAGGCTGTGGCTTGACGAAAGGCAGGAGACGGAATGAAGTGAGGGTTCTGGGGTGGAGAGCTGG... |
Task1_train_41622 | A genomic change on Chromosome 11 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TGGATCACTGCAACCTCCGCCCCCTGGGTTCAAGCAATTCTCGTCCCTCAGCCTTCCGAGGAGCAGGGACTACAGGCGCCCACCACCGTGCCCGGCTAATTTTTTGTATTTTTAGTAGACATGGGGTTTCACCATGATGGCCAGGCTGGTCTCGAACTCCTGACCTCAAGTGATCCGCCCGCCGCAGCCTCCTAAAGTGCTGGGATTACAGGTGTGAGCCACCACACACGGCTCAAGGTTGGTGCATTTTATAAAACTAATCAATCACAGAATCTGAGAGCTGGATAGTATCTTAGGGATAATCTGGTTGGCGAGTTTCA... | TGGATCACTGCAACCTCCGCCCCCTGGGTTCAAGCAATTCTCGTCCCTCAGCCTTCCGAGGAGCAGGGACTACAGGCGCCCACCACCGTGCCCGGCTAATTTTTTGTATTTTTAGTAGACATGGGGTTTCACCATGATGGCCAGGCTGGTCTCGAACTCCTGACCTCAAGTGATCCGCCCGCCGCAGCCTCCTAAAGTGCTGGGATTACAGGTGTGAGCCACCACACACGGCTCAAGGTTGGTGCATTTTATAAAACTAATCAATCACAGAATCTGAGAGCTGGATAGTATCTTAGGGATAATCTGGTTGGCGAGTTTCA... |
Task1_train_41623 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CAAGCCACAAAGATGGGGCTGCACGGAGCAGCCCCGTCCCCTACTCTTATGACAGCACGGTTTCCCTCGGCATTGATTAATGCCATAAATATTTACTCGGCACCTCGTGTGTGTTAGGCACAGGGCCAGGCGCTGAAGACACAGGGGTGAATCGGGAGCCGGGTTGTTGCCCTCCCAGCTCCTGATCTCCTGGCCTTGCCCCACATGTGACAGACAAGTGGAAGTGGTCCTGGAGAGAGTCTCTGTGGGTCAGGGCAGAGCTCATCACCAAACCACCAAACTCAGGGCAGAGCTCTGAGCGGCAGAGGCACACAGAATCA... | CAAGCCACAAAGATGGGGCTGCACGGAGCAGCCCCGTCCCCTACTCTTATGACAGCACGGTTTCCCTCGGCATTGATTAATGCCATAAATATTTACTCGGCACCTCGTGTGTGTTAGGCACAGGGCCAGGCGCTGAAGACACAGGGGTGAATCGGGAGCCGGGTTGTTGCCCTCCCAGCTCCTGATCTCCTGGCCTTGCCCCACATGTGACAGACAAGTGGAAGTGGTCCTGGAGAGAGTCTCTGTGGGTCAGGGCAGAGCTCATCACCAAACCACCAAACTCAGGGCAGAGCTCTGAGCGGCAGAGGCACACAGAATCA... |
Task1_train_41624 | Located on Chromosome 11, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TGCAAACACTTACTGTAAATCCGGCCCTTAGGTCAAACAACCTTGATGTTATCATACTTCAACTGTCCTACACATCTTTTCTGAATCACCCTTCCCCTGTGGTCTATAAGCCCTGGTCCTGGGGGTGAATCATGGAGACACAAACGTAGCTTCTGTTTATAAGTCCTTATTAAATGTTTTTTTCGAAGAAACTGGATGTGTCAGCCTGTAACCTGCAAAAGGATCTGGCTGCTCTCTGCTTGTAGAAAGAATGGATAATAAAGGAAAATCTGCTAGCTGCCATGCTAGCAGGGGAAGAGCAGCAAACAATTCCACTCTTC... | TGCAAACACTTACTGTAAATCCGGCCCTTAGGTCAAACAACCTTGATGTTATCATACTTCAACTGTCCTACACATCTTTTCTGAATCACCCTTCCCCTGTGGTCTATAAGCCCTGGTCCTGGGGGTGAATCATGGAGACACAAACGTAGCTTCTGTTTATAAGTCCTTATTAAATGTTTTTTTCGAAGAAACTGGATGTGTCAGCCTGTAACCTGCAAAAGGATCTGGCTGCTCTCTGCTTGTAGAAAGAATGGATAATAAAGGAAAATCTGCTAGCTGCCATGCTAGCAGGGGAAGAGCAGCAAACAATTCCACTCTTC... |
Task1_train_41625 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CTACATGTTTATGAGGTACAGTGTTATGTATACATAATACATGTATACCTTGTGGAATGATCAAATCAAGGTAATTAGAATATCTATCACCTCAAATATTTAGCATTTCTTTGTGCCAAAAACATTTAAAATATTATCTTTCAGCTATTTTGAAATATACAGTCCATTATTATTACTACAGTCACCTTGCCGTGCAATAGGCACCAGAACTTATTCCTCCTGTCTCACTGTAACTTGGTACCCCTCTCCTTGTTCCCTATCCACTTCTCCCACCTGCCTCCTTCCAGCTTCTGGTAACCACTTCTACTCTCTACTTCTAT... | CTACATGTTTATGAGGTACAGTGTTATGTATACATAATACATGTATACCTTGTGGAATGATCAAATCAAGGTAATTAGAATATCTATCACCTCAAATATTTAGCATTTCTTTGTGCCAAAAACATTTAAAATATTATCTTTCAGCTATTTTGAAATATACAGTCCATTATTATTACTACAGTCACCTTGCCGTGCAATAGGCACCAGAACTTATTCCTCCTGTCTCACTGTAACTTGGTACCCCTCTCCTTGTTCCCTATCCACTTCTCCCACCTGCCTCCTTCCAGCTTCTGGTAACCACTTCTACTCTCTACTTCTAT... |
Task1_train_41626 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TACAGTGTTATGTATACATAATACATGTATACCTTGTGGAATGATCAAATCAAGGTAATTAGAATATCTATCACCTCAAATATTTAGCATTTCTTTGTGCCAAAAACATTTAAAATATTATCTTTCAGCTATTTTGAAATATACAGTCCATTATTATTACTACAGTCACCTTGCCGTGCAATAGGCACCAGAACTTATTCCTCCTGTCTCACTGTAACTTGGTACCCCTCTCCTTGTTCCCTATCCACTTCTCCCACCTGCCTCCTTCCAGCTTCTGGTAACCACTTCTACTCTCTACTTCTATGAATTGAATTCTAAAA... | TACAGTGTTATGTATACATAATACATGTATACCTTGTGGAATGATCAAATCAAGGTAATTAGAATATCTATCACCTCAAATATTTAGCATTTCTTTGTGCCAAAAACATTTAAAATATTATCTTTCAGCTATTTTGAAATATACAGTCCATTATTATTACTACAGTCACCTTGCCGTGCAATAGGCACCAGAACTTATTCCTCCTGTCTCACTGTAACTTGGTACCCCTCTCCTTGTTCCCTATCCACTTCTCCCACCTGCCTCCTTCCAGCTTCTGGTAACCACTTCTACTCTCTACTTCTATGAATTGAATTCTAAAA... |
Task1_train_41627 | A mutation found on Chromosome 11 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | ACCACATTTAAAAAACCCATTCATCCATTGGTGGGCATTTCCATATCTTGGCTGTTATGAATAATACTGCAATGAACGGGGGATACAGGTATCTCTTCAATACACTAATTTCAATATCTTTCGATATATACCCAGTAGTGGGAATTGCTGGATCACATGGTAGCTCTATTTTTAGATTTTCGAGGAACATCCATACTGTTTTCCATAATGGCTGAGAAATTCACCACCAGCGACATGCAAGGGTTTCCCTTTTCACCACATCCTTGCCAATGCTTGTTACTTCCATCTTTTGGATAATAGCCAATCTAACAGGTGTGGAG... | ACCACATTTAAAAAACCCATTCATCCATTGGTGGGCATTTCCATATCTTGGCTGTTATGAATAATACTGCAATGAACGGGGGATACAGGTATCTCTTCAATACACTAATTTCAATATCTTTCGATATATACCCAGTAGTGGGAATTGCTGGATCACATGGTAGCTCTATTTTTAGATTTTCGAGGAACATCCATACTGTTTTCCATAATGGCTGAGAAATTCACCACCAGCGACATGCAAGGGTTTCCCTTTTCACCACATCCTTGCCAATGCTTGTTACTTCCATCTTTTGGATAATAGCCAATCTAACAGGTGTGGAG... |
Task1_train_41628 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | ACTGACTTGTCCTTGAGGGTTTTTTCTCTTCAGGATAAATATAGCTCAATCCCTTCATCTGATGATCGTAGTCATTACCACATGAATAAATTATAATGCACAGAGCACTGACACATTCATTAGTTTGTTCTCATTCATTAGCTTGTTTGATTTGATCTTTCAACAGTTCATCAAGGTAAGTATTATTGGACAAGGAAGGGATTTCAAATCAGGACAGTTGAGGATGAATTCCAGATGTGTTCTTTACTGTTGTGCCACTTTGTGCAAGTCATTTAACTTCTCTGAGCTTCAGTTTTCTCCTCTAGGAAATAGAGGTAATA... | ACTGACTTGTCCTTGAGGGTTTTTTCTCTTCAGGATAAATATAGCTCAATCCCTTCATCTGATGATCGTAGTCATTACCACATGAATAAATTATAATGCACAGAGCACTGACACATTCATTAGTTTGTTCTCATTCATTAGCTTGTTTGATTTGATCTTTCAACAGTTCATCAAGGTAAGTATTATTGGACAAGGAAGGGATTTCAAATCAGGACAGTTGAGGATGAATTCCAGATGTGTTCTTTACTGTTGTGCCACTTTGTGCAAGTCATTTAACTTCTCTGAGCTTCAGTTTTCTCCTCTAGGAAATAGAGGTAATA... |
Task1_train_41629 | A variant was discovered on Chromosome 11. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TCTTAGGACCTTACTTGGACATCAGGCTCACTCGGCAGCTCTCCCAACTCCAACTCACCTCCCCAGGGCTTCACAAGTTGCTGTCTCTGCATCAGACTAGCCCGTTGGAGAACTTCATGTAGCCACCATCTGTGCTGCTGATGTGACCACTGATGGTGAAGGGTGGACCCATCTCCAGATCCTTCAGGTTCCTGAAAAAGATGATCCAATCAGGCTACTGGAGCTGATAACCTAGCCTCTCCCTGGGTCCCCATCTCCCTTGACTCCAGGGCACCAACTCACTGACTTGTCTTCCAGAAAAGGAAGTGGGCCACTTACCA... | TCTTAGGACCTTACTTGGACATCAGGCTCACTCGGCAGCTCTCCCAACTCCAACTCACCTCCCCAGGGCTTCACAAGTTGCTGTCTCTGCATCAGACTAGCCCGTTGGAGAACTTCATGTAGCCACCATCTGTGCTGCTGATGTGACCACTGATGGTGAAGGGTGGACCCATCTCCAGATCCTTCAGGTTCCTGAAAAAGATGATCCAATCAGGCTACTGGAGCTGATAACCTAGCCTCTCCCTGGGTCCCCATCTCCCTTGACTCCAGGGCACCAACTCACTGACTTGTCTTCCAGAAAAGGAAGTGGGCCACTTACCA... |
Task1_train_41630 | A mutation located on Chromosome 11 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GACTGGCCTGGAAGCATAGCCAGAAATTAGAACGCCTAAGGGAAGAAGGTCACAACGCTGCCTCTGCAATTTAGGAGTGTATATGCTTTCCTGCAGGATGTTGAGAGTTTCATTCATTATCGTATGCCCCCTACCCCGGCCCCACAATACCTAGTGCGTGGGATCTGACACGTGGTGGCTGGTCAATGAATGAATGAATGAATGGTCACACCATCTGAGGTTCTGCACTGAGTAGCCCTGAAGGCTTGAAGCAGCATAAGTGACAGGTCCTCCCTTGAGGGGCCTCTGTTTTACCAATAAGCCAAGACCTAAGCTCAACA... | GACTGGCCTGGAAGCATAGCCAGAAATTAGAACGCCTAAGGGAAGAAGGTCACAACGCTGCCTCTGCAATTTAGGAGTGTATATGCTTTCCTGCAGGATGTTGAGAGTTTCATTCATTATCGTATGCCCCCTACCCCGGCCCCACAATACCTAGTGCGTGGGATCTGACACGTGGTGGCTGGTCAATGAATGAATGAATGAATGGTCACACCATCTGAGGTTCTGCACTGAGTAGCCCTGAAGGCTTGAAGCAGCATAAGTGACAGGTCCTCCCTTGAGGGGCCTCTGTTTTACCAATAAGCCAAGACCTAAGCTCAACA... |
Task1_train_41631 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | AGATCTAATTTCCAGTGTACAGGAAATACAAGAATTAGAGGAACAAAACATAAGAATTAGAGGAACAAATTAAATGACACCACTAAAAGACAAATCCAGAAGGTGGGACATTCCACCACAGGACATTCCCATCTCTTCAACAAATCAATGTCATGTAATTACTGTTATGTCTTTTTTTTTGAGACGGAGTCTTGCACTGTCACCCAGGCTGGAGTGCAGTGCAGTGGCACCATCTCGGCTCACTGCGAGCTCCGTCTCCTGGGTTCATGCCATTCTCTTGCCTTAGCCTCCCAAGTAGCTGGGACTACAGGCGCCCGCCA... | AGATCTAATTTCCAGTGTACAGGAAATACAAGAATTAGAGGAACAAAACATAAGAATTAGAGGAACAAATTAAATGACACCACTAAAAGACAAATCCAGAAGGTGGGACATTCCACCACAGGACATTCCCATCTCTTCAACAAATCAATGTCATGTAATTACTGTTATGTCTTTTTTTTTGAGACGGAGTCTTGCACTGTCACCCAGGCTGGAGTGCAGTGCAGTGGCACCATCTCGGCTCACTGCGAGCTCCGTCTCCTGGGTTCATGCCATTCTCTTGCCTTAGCCTCCCAAGTAGCTGGGACTACAGGCGCCCGCCA... |
Task1_train_41632 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GGAACTACAAGGACAGTGAGGATGCCCCCTCTTCCCATCCACCCTTTTCCTGGGGAAGAGAGGCAGTTACCTCTGTGAGGCACCTGGATGCGCAGCACACCTTGTTTCAAGAGCCTCCAGAGCACGCAGCCCACCCAGGGTCCTCTGGGGCCCTAGCGCAGTGCCGGGGCCGGTGGTGGGACCAGGGGCTTCATGCCATGGGGCTCCTACCTCCTCCCCTGCCCCTGCCTTCAGCCCAGGACTCACCATCTCCTCAGAGCAGTTGTTGCACTCCTGGTAAGTCCAGTTCAGGGAGAACTGTTTGTGGTTCACTGTGTAGC... | GGAACTACAAGGACAGTGAGGATGCCCCCTCTTCCCATCCACCCTTTTCCTGGGGAAGAGAGGCAGTTACCTCTGTGAGGCACCTGGATGCGCAGCACACCTTGTTTCAAGAGCCTCCAGAGCACGCAGCCCACCCAGGGTCCTCTGGGGCCCTAGCGCAGTGCCGGGGCCGGTGGTGGGACCAGGGGCTTCATGCCATGGGGCTCCTACCTCCTCCCCTGCCCCTGCCTTCAGCCCAGGACTCACCATCTCCTCAGAGCAGTTGTTGCACTCCTGGTAAGTCCAGTTCAGGGAGAACTGTTTGTGGTTCACTGTGTAGC... |
Task1_train_41633 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GCCTGGCTAATTTTTTTGTATTTTTAGTAAGACAGTGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAAGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTAGGTTTACAGGTGTGAGCCACCATGCTCGGCCTTTTTTTTTTTTTTTGAAACAGAGTCTTACTCTGTCTCCCAGGCTGGAGTGTAGTGGTGGATCTCGGCTCATGTAACCAACGCCTTCCAGGTCCAAGCAATTCTCGTGCCTCAGCCTCCCAAGTAGCTGGGATTATAGGCACGCATCTCCACACCTGGCCAATTTTTGTATTTTTA... | GCCTGGCTAATTTTTTTGTATTTTTAGTAAGACAGTGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAAGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTAGGTTTACAGGTGTGAGCCACCATGCTCGGCCTTTTTTTTTTTTTTTGAAACAGAGTCTTACTCTGTCTCCCAGGCTGGAGTGTAGTGGTGGATCTCGGCTCATGTAACCAACGCCTTCCAGGTCCAAGCAATTCTCGTGCCTCAGCCTCCCAAGTAGCTGGGATTATAGGCACGCATCTCCACACCTGGCCAATTTTTGTATTTTTA... |
Task1_train_41634 | A genomic variant on Chromosome 11 is under review. What is the biological outcome — benign or pathogenic? | Benign | AACATTGAAAGATTATTAGCAGTGGAAGAGAAAGTTCTTAATGTGATTTAGAAAGATGGCACCAAGAGCCGCGTGAAGAATGAGGAGCAGTGGCTGAGAGAGAAAGCAGAGACTGGTTAGAGGCCTACAGTTCAAGACAGAGATGAAGACAGCCAGAACTAAGGCGGCAGTGACAGACTGGAAGGAAGACAACTTCAAGAGTCTGTAGTAGGAGTCAAGGACTTGTTGACCTGACCTGTTAGATTAGGGGTCTAGGAAAGGGAAAGAATCAAGCACACCCCCAGGCATCTAGTTAGACAACTGAGGTTGGGGAGATGGGC... | AACATTGAAAGATTATTAGCAGTGGAAGAGAAAGTTCTTAATGTGATTTAGAAAGATGGCACCAAGAGCCGCGTGAAGAATGAGGAGCAGTGGCTGAGAGAGAAAGCAGAGACTGGTTAGAGGCCTACAGTTCAAGACAGAGATGAAGACAGCCAGAACTAAGGCGGCAGTGACAGACTGGAAGGAAGACAACTTCAAGAGTCTGTAGTAGGAGTCAAGGACTTGTTGACCTGACCTGTTAGATTAGGGGTCTAGGAAAGGGAAAGAATCAAGCACACCCCCAGGCATCTAGTTAGACAACTGAGGTTGGGGAGATGGGC... |
Task1_train_41635 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | GGAGGCTAAGGACCTAAGCTAGCTGCAGGCGGGAAATGGCCCCAGATTCTAGTTCCCTAACTACATTGCAAGCTCTCCTGGGGTCACAGACTGTTCCTTCTATTCCACACTCTTAAAGAATGCATCTAGTTCTGTGGCTTGCAAACTTTTACTTTCATTTATGTATTTTTATTTGTAAGTTTTATATCAATAAGCAAAACTAAATTTTAGAGACACTGGCTAACGTTAGTTTGGATATCATTAGTTTATTATAAAAGAGAGACATGGAAATTATTTACACAATGAAAGATTTCAGAACTCCAGTGGAATCAGTGTCTTCA... | GGAGGCTAAGGACCTAAGCTAGCTGCAGGCGGGAAATGGCCCCAGATTCTAGTTCCCTAACTACATTGCAAGCTCTCCTGGGGTCACAGACTGTTCCTTCTATTCCACACTCTTAAAGAATGCATCTAGTTCTGTGGCTTGCAAACTTTTACTTTCATTTATGTATTTTTATTTGTAAGTTTTATATCAATAAGCAAAACTAAATTTTAGAGACACTGGCTAACGTTAGTTTGGATATCATTAGTTTATTATAAAAGAGAGACATGGAAATTATTTACACAATGAAAGATTTCAGAACTCCAGTGGAATCAGTGTCTTCA... |
Task1_train_41636 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | TGATTGAATCATTGGCCGCTTGACTGATCTCAATCTCTAGGATCCCTTCCTGGGGCTGATACCACTAGTTTCAAAGCTGCAATCCTCTTACCATATGGTTGGTCTTGACCAGCACCATCCTGAGTCATTGCCATGCATAAACTCAGGTATGGTCTAAGGATCCACCACAGATAACAAAGCCACTCCTGTCACTCATGAAATTCCAACGGTTAGAAACACCCTCCCAGGATACCAGGACAAAGATGAGACAAATTGTTTATTATCACCTTGAATTCAATTGAGTGATTTAGTCTACAATCCGGAAAACTAAGTATAGATAC... | TGATTGAATCATTGGCCGCTTGACTGATCTCAATCTCTAGGATCCCTTCCTGGGGCTGATACCACTAGTTTCAAAGCTGCAATCCTCTTACCATATGGTTGGTCTTGACCAGCACCATCCTGAGTCATTGCCATGCATAAACTCAGGTATGGTCTAAGGATCCACCACAGATAACAAAGCCACTCCTGTCACTCATGAAATTCCAACGGTTAGAAACACCCTCCCAGGATACCAGGACAAAGATGAGACAAATTGTTTATTATCACCTTGAATTCAATTGAGTGATTTAGTCTACAATCCGGAAAACTAAGTATAGATAC... |
Task1_train_41637 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CTCTCTGTACCATCCCACCCTCTCAAGTACATGAGAAGGGGTCTGGTGGCACTTGAGACTTGCAGGGGCAGGTGGAACAGGGTCCATGTCTTTGCCTCTGTGGCCTGGAGCCTGTGGCATGCCCTCCCTTAGGACCTGAAGGATGACCAATTGGCCCCCTTTAAAAGTAGGTTTTCAAAACTTGGTTTCTATATACCGTATGGCTTATACTGAGGTTAACACGTTTGATTCCAGTTGTTTAAAATTAATTTGTTTTTATGGTAAAGCAGCTATTGGCACACAAAATTGTGACACGTTACAGGACACCAAAAACTGCTTTT... | CTCTCTGTACCATCCCACCCTCTCAAGTACATGAGAAGGGGTCTGGTGGCACTTGAGACTTGCAGGGGCAGGTGGAACAGGGTCCATGTCTTTGCCTCTGTGGCCTGGAGCCTGTGGCATGCCCTCCCTTAGGACCTGAAGGATGACCAATTGGCCCCCTTTAAAAGTAGGTTTTCAAAACTTGGTTTCTATATACCGTATGGCTTATACTGAGGTTAACACGTTTGATTCCAGTTGTTTAAAATTAATTTGTTTTTATGGTAAAGCAGCTATTGGCACACAAAATTGTGACACGTTACAGGACACCAAAAACTGCTTTT... |
Task1_train_41638 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | GAGAGTGGAGGACCAGGCCTCCAGCTGTCTGGCCTCGCCCTTCACGCCTTAACACTAAGCCCACCTCCCCTGCTCTCCTTCCCAGCATTGAGCCCTTGGTTGCCTGGGCCCAGGCTGGGGGTTTTCAGTATTTGTAAGCATTTCAGCAGAACAATAAAGCCTTTGGACTACGGAAGTGAGTGGAAGGCCGGTGTGGGGCTTGGCGCTGAGGCACTTGGGGATAGGTCTTCCCTCCAGAGCAGGATTTCCACCCTATTCAAGGTTCCAGGAGGGAGCTAGGCCCCTACCCATGACCTCCAGGTCGTGACCCTGCCCTCCAC... | GAGAGTGGAGGACCAGGCCTCCAGCTGTCTGGCCTCGCCCTTCACGCCTTAACACTAAGCCCACCTCCCCTGCTCTCCTTCCCAGCATTGAGCCCTTGGTTGCCTGGGCCCAGGCTGGGGGTTTTCAGTATTTGTAAGCATTTCAGCAGAACAATAAAGCCTTTGGACTACGGAAGTGAGTGGAAGGCCGGTGTGGGGCTTGGCGCTGAGGCACTTGGGGATAGGTCTTCCCTCCAGAGCAGGATTTCCACCCTATTCAAGGTTCCAGGAGGGAGCTAGGCCCCTACCCATGACCTCCAGGTCGTGACCCTGCCCTCCAC... |
Task1_train_41639 | With a mutation on Chromosome 11, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TGTTTGTTTGTGGGGTTTTTTTTGTTGATGTTTTTTTTTTTTTTTTTTTTTTTGAGACTGAGCTTCACTCTTAACCACCCAGGCTGGAATGCAATGGTGCCATCACGGCTCACCACAACCTCTGCCTTCCGGGTTCAGGCGATTCTTTTGTCTCAGCCTCCGGAGTAGCTGGGATTACAGGCACCTGCCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATATTGGCCAGGCTAGTCTCAAAGTCCTGACCTCAGCTGATCCGCCCACCTCAGCCTTCCATGATATATGTTGTTCTTCAAGC... | TGTTTGTTTGTGGGGTTTTTTTTGTTGATGTTTTTTTTTTTTTTTTTTTTTTTGAGACTGAGCTTCACTCTTAACCACCCAGGCTGGAATGCAATGGTGCCATCACGGCTCACCACAACCTCTGCCTTCCGGGTTCAGGCGATTCTTTTGTCTCAGCCTCCGGAGTAGCTGGGATTACAGGCACCTGCCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATATTGGCCAGGCTAGTCTCAAAGTCCTGACCTCAGCTGATCCGCCCACCTCAGCCTTCCATGATATATGTTGTTCTTCAAGC... |
Task1_train_41640 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GAGAGGCATCCACACCACATTCATTCCTTCAACCAAACATGGAACTTCTACCAGGCTCTGCTAGGCCTCGTTCACAGTTACGGTACAAGATGTAGCCCCCGCTCTCAGGGAACTCTGGCTGGTGGAAATACAGCATCAAATATTCTGAAATAAGTTGGGGGAGGGCCGGGTGCGGTGGCTCACGCCTGTAATTCCAGTACTTGGGAGGCCGAGGCGGGTGGATCACCCGAGGTCAGGAGTTCGAGACCAGCCTGGCCAAAATGGCAAAACCCCAACTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGCAGGCAGC... | GAGAGGCATCCACACCACATTCATTCCTTCAACCAAACATGGAACTTCTACCAGGCTCTGCTAGGCCTCGTTCACAGTTACGGTACAAGATGTAGCCCCCGCTCTCAGGGAACTCTGGCTGGTGGAAATACAGCATCAAATATTCTGAAATAAGTTGGGGGAGGGCCGGGTGCGGTGGCTCACGCCTGTAATTCCAGTACTTGGGAGGCCGAGGCGGGTGGATCACCCGAGGTCAGGAGTTCGAGACCAGCCTGGCCAAAATGGCAAAACCCCAACTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGCAGGCAGC... |
Task1_train_41641 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GAGGCATCCACACCACATTCATTCCTTCAACCAAACATGGAACTTCTACCAGGCTCTGCTAGGCCTCGTTCACAGTTACGGTACAAGATGTAGCCCCCGCTCTCAGGGAACTCTGGCTGGTGGAAATACAGCATCAAATATTCTGAAATAAGTTGGGGGAGGGCCGGGTGCGGTGGCTCACGCCTGTAATTCCAGTACTTGGGAGGCCGAGGCGGGTGGATCACCCGAGGTCAGGAGTTCGAGACCAGCCTGGCCAAAATGGCAAAACCCCAACTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGCAGGCAGCTG... | GAGGCATCCACACCACATTCATTCCTTCAACCAAACATGGAACTTCTACCAGGCTCTGCTAGGCCTCGTTCACAGTTACGGTACAAGATGTAGCCCCCGCTCTCAGGGAACTCTGGCTGGTGGAAATACAGCATCAAATATTCTGAAATAAGTTGGGGGAGGGCCGGGTGCGGTGGCTCACGCCTGTAATTCCAGTACTTGGGAGGCCGAGGCGGGTGGATCACCCGAGGTCAGGAGTTCGAGACCAGCCTGGCCAAAATGGCAAAACCCCAACTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGCAGGCAGCTG... |
Task1_train_41642 | Chromosome 11 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TTCTTCAAGTTGTGTTTTAATTGAGGAATTCCAAAAAATGGTTTATTACATAGATCATTATTTATTGGGCTTTGGATGATATTATTTTGTAGCAGGTACTTTTTGTTCTTTATATGCCTGTATTCTACCACTTCTAAACACATCCGTATTGTGGTTGGAAGCCGTTCTGGTGTTTTTCTTTTTTGAGACAGGATCTTGTCACTGAGGCTGGAGTGGAGGGGTGTGATCACGGCTCACTGCAGCTTTGATCTCCTGGGCTCAAGTGATTCTCCCGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCGTGTGCCACCAAGC... | TTCTTCAAGTTGTGTTTTAATTGAGGAATTCCAAAAAATGGTTTATTACATAGATCATTATTTATTGGGCTTTGGATGATATTATTTTGTAGCAGGTACTTTTTGTTCTTTATATGCCTGTATTCTACCACTTCTAAACACATCCGTATTGTGGTTGGAAGCCGTTCTGGTGTTTTTCTTTTTTGAGACAGGATCTTGTCACTGAGGCTGGAGTGGAGGGGTGTGATCACGGCTCACTGCAGCTTTGATCTCCTGGGCTCAAGTGATTCTCCCGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCGTGTGCCACCAAGC... |
Task1_train_41643 | A variant was discovered on Chromosome 11. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TCACTGAGGCTGGAGTGGAGGGGTGTGATCACGGCTCACTGCAGCTTTGATCTCCTGGGCTCAAGTGATTCTCCCGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCGTGTGCCACCAAGCCCAGCTAATTTTTGGATTTTTAGTAGAGATGGGGTTTATAATGTTGGCCAGGCTGGTCTCGAACTCCTGGCCTCAAGTGATCCTCCGGCCTTGACCTCCCAAAGTGCTGGGATGAGCCACGGTGCCCGGCCATAATCCCAACTCTGAAATCTTACCTGCCCTTAACATTCTGTAAAATATTTATTAGAGAACAACAGT... | TCACTGAGGCTGGAGTGGAGGGGTGTGATCACGGCTCACTGCAGCTTTGATCTCCTGGGCTCAAGTGATTCTCCCGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCGTGTGCCACCAAGCCCAGCTAATTTTTGGATTTTTAGTAGAGATGGGGTTTATAATGTTGGCCAGGCTGGTCTCGAACTCCTGGCCTCAAGTGATCCTCCGGCCTTGACCTCCCAAAGTGCTGGGATGAGCCACGGTGCCCGGCCATAATCCCAACTCTGAAATCTTACCTGCCCTTAACATTCTGTAAAATATTTATTAGAGAACAACAGT... |
Task1_train_41644 | Here is a genetic alteration on Chromosome 11. Based on the data, is it a benign variant or a cause of disease? | Benign | CCCGAGGGCGCCTTCGGCCCCACGGTGGCGCTGGTCTTCTTGGGCAGCAGCACGGCCTGGATGTTGGGCAGGACGCCTCCCTGGGCGATCGTCACGCCGCCCAGCAGCTTGTTGAGCTCCTCGTCGTTGCGGATGGCCAGCTGCAGGTGGCGGGGGATGATTCGCGTCTTCTTGTTGTCGCGGGCCGCATTGCCCGCCAGCTCCAGGATCTCAGCGGTGAGGTACTCCAGCACTGCCGCCAGGTACACTGGCGCGCCGGCGCCAACGCGCTCGGCGTAGTGGCCCTTCCGCAGCAGCCGGTGTACACGGCCCACTGGGAA... | CCCGAGGGCGCCTTCGGCCCCACGGTGGCGCTGGTCTTCTTGGGCAGCAGCACGGCCTGGATGTTGGGCAGGACGCCTCCCTGGGCGATCGTCACGCCGCCCAGCAGCTTGTTGAGCTCCTCGTCGTTGCGGATGGCCAGCTGCAGGTGGCGGGGGATGATTCGCGTCTTCTTGTTGTCGCGGGCCGCATTGCCCGCCAGCTCCAGGATCTCAGCGGTGAGGTACTCCAGCACTGCCGCCAGGTACACTGGCGCGCCGGCGCCAACGCGCTCGGCGTAGTGGCCCTTCCGCAGCAGCCGGTGTACACGGCCCACTGGGAA... |
Task1_train_41645 | A mutation located on Chromosome 11 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CACAGGTAGAAGGGGATGTGGGAAACTGAGTTGGGCAGGGGCGGTTCCATTGGCTCAGCTTCTTCCATTTGTTTCCTCTCTGGGATGGAATTCAGGAAGGGAGAGTCCTCGAATTAGGAGTCCTTGGGTAAATGGGGCAAGTCAGCCCAGTCACTTTGTTCCTGTCTGTAGTTGGAAGTCAACCTGGAGGAAATCCCTGGTGAGGGGCTGCTCATATCCTGGGCCTTCACTGATCGCCCAGATCTCAGCCTAACGGTGCTTCCCAAGCTTCAGGCCAGGGAGGTAAGGAGGCAGAGCTGGCAGAGAAGAGGCAGAACGGG... | CACAGGTAGAAGGGGATGTGGGAAACTGAGTTGGGCAGGGGCGGTTCCATTGGCTCAGCTTCTTCCATTTGTTTCCTCTCTGGGATGGAATTCAGGAAGGGAGAGTCCTCGAATTAGGAGTCCTTGGGTAAATGGGGCAAGTCAGCCCAGTCACTTTGTTCCTGTCTGTAGTTGGAAGTCAACCTGGAGGAAATCCCTGGTGAGGGGCTGCTCATATCCTGGGCCTTCACTGATCGCCCAGATCTCAGCCTAACGGTGCTTCCCAAGCTTCAGGCCAGGGAGGTAAGGAGGCAGAGCTGGCAGAGAAGAGGCAGAACGGG... |
Task1_train_41646 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | TTTGCCAACAATACCAAGTTCTTAGATCACATCCGTCGCCAGACCTCATTGGATCGTAAGTAGTCAGAGGAAGTGGGGTGGATGCAGGCTGTCCTGCTTGGAATGGGTTAGGGGCATGTTTCTAGTGGGGGTGGCCACTGAAGAGACCTGCCTTTTGGCTGCCTCTTCTTTTTGGGCTCAGGCACCTCCCATAGTCTCTTTGCTGATTCAGATTCGTAGGCATTGTTATTCAGTACTTACTGTACCTCGTATCAGTTACTTAGGGAATCCTCACAACAGCCCCATGAGGTAGGCTTCTTATCCCCCTTTTTGCAGATGAG... | TTTGCCAACAATACCAAGTTCTTAGATCACATCCGTCGCCAGACCTCATTGGATCGTAAGTAGTCAGAGGAAGTGGGGTGGATGCAGGCTGTCCTGCTTGGAATGGGTTAGGGGCATGTTTCTAGTGGGGGTGGCCACTGAAGAGACCTGCCTTTTGGCTGCCTCTTCTTTTTGGGCTCAGGCACCTCCCATAGTCTCTTTGCTGATTCAGATTCGTAGGCATTGTTATTCAGTACTTACTGTACCTCGTATCAGTTACTTAGGGAATCCTCACAACAGCCCCATGAGGTAGGCTTCTTATCCCCCTTTTTGCAGATGAG... |
Task1_train_41647 | Consider this mutation on Chromosome 11. Is this a benign change or a disease-causing variant? | Benign | GCTCCCTAAGCTCTCCTTTTCTCCTTGGGTGGTTCCCTTCTGCCTGGGATGGTTCCCCTCTCCTTTCTGTGCCTCTCCACTATCACCTACAGCCCTCCTTTCTTCTGCCTGCCCCACCCCAGAGCAGCACTTCCAGTGTTCTCACTGTTCCAAGAGATTTGCCACAGAGCGGCTATTGCGGGACCACATGCGCAACCATGGTGAGTGGCCTGCGGCCCACAGCCTCCCTCCTGCCCTCCAAGGTTCCACAAGTTCTCACATCACAGCCTCCTCTCTGCTTCTCTCAGTGAATCACTATAAGTGCCCTCTGTGTGACATGA... | GCTCCCTAAGCTCTCCTTTTCTCCTTGGGTGGTTCCCTTCTGCCTGGGATGGTTCCCCTCTCCTTTCTGTGCCTCTCCACTATCACCTACAGCCCTCCTTTCTTCTGCCTGCCCCACCCCAGAGCAGCACTTCCAGTGTTCTCACTGTTCCAAGAGATTTGCCACAGAGCGGCTATTGCGGGACCACATGCGCAACCATGGTGAGTGGCCTGCGGCCCACAGCCTCCCTCCTGCCCTCCAAGGTTCCACAAGTTCTCACATCACAGCCTCCTCTCTGCTTCTCTCAGTGAATCACTATAAGTGCCCTCTGTGTGACATGA... |
Task1_train_41648 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | TTTGCAAGGCCAAGGCAGGCAGATTACCTGAGGTCAGAAGTTCAAGACCAGCTTAACCAACATGGTAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCCAGTGTGGTGGTGGGCGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGGGCCCGGGAGGCATAGGCTTCAATGAGCCACAATCATGCCTGGGCAACAGAGGGGCACTCCATCTCAAAAAAGAAAAAAGAAAAAAAAGGTGGTAGGAGATAAAATGGGATTCCTCAAGCTGGAGTTTGGGAGAGGGACGAGAGCTGAAAACCAGG... | TTTGCAAGGCCAAGGCAGGCAGATTACCTGAGGTCAGAAGTTCAAGACCAGCTTAACCAACATGGTAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCCAGTGTGGTGGTGGGCGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGGGCCCGGGAGGCATAGGCTTCAATGAGCCACAATCATGCCTGGGCAACAGAGGGGCACTCCATCTCAAAAAAGAAAAAAGAAAAAAAAGGTGGTAGGAGATAAAATGGGATTCCTCAAGCTGGAGTTTGGGAGAGGGACGAGAGCTGAAAACCAGG... |
Task1_train_41649 | Consider this mutation on Chromosome 11. Is this a benign change or a disease-causing variant? | Benign | ATGAGTTCCAGAACCAGCGCTTCTCCGCTGAGGTGCTCAGCTCCCTGCGTCAGCTCAACCTGGCAGGTGTGCGCATGACACCAGTCAAGTGCACAGTGGTGGCAGCTGTGCTGGGCAGCGGAAGGCATGCCCTGGATGAGGTGAACTTGGCCTCCTGCCAGCTAGATCCTGCTGGGCTGCGCACACTCCTGCCTGTCTTCCTGCGTGCCCGGAAGCTGGGGTGAGGACCTATCCTCATGCACAGGCATGAAGAGGGAAGAGGGTTGGAGGTGAAGAAGTGGGAAAAGAAAGTGCCAGGGAAACCAGAGGTACCGATGAGT... | ATGAGTTCCAGAACCAGCGCTTCTCCGCTGAGGTGCTCAGCTCCCTGCGTCAGCTCAACCTGGCAGGTGTGCGCATGACACCAGTCAAGTGCACAGTGGTGGCAGCTGTGCTGGGCAGCGGAAGGCATGCCCTGGATGAGGTGAACTTGGCCTCCTGCCAGCTAGATCCTGCTGGGCTGCGCACACTCCTGCCTGTCTTCCTGCGTGCCCGGAAGCTGGGGTGAGGACCTATCCTCATGCACAGGCATGAAGAGGGAAGAGGGTTGGAGGTGAAGAAGTGGGAAAAGAAAGTGCCAGGGAAACCAGAGGTACCGATGAGT... |
Task1_train_41650 | A genomic variant on Chromosome 11 is under review. What is the biological outcome — benign or pathogenic? | Benign | AGTGCAGTGGCGCGATCTCAGCTCACTGCAACTGCCACCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACATGCCACCATGCCCAGCTAATCTTCGAATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGATGGTCCCTATCTCTTAACCTTGTGATCCGCCCGCCTCGGCCTCCCAAAGTGGTGGGATTACAAGTGTGAGCCACCGCGGCTGGCTGGTGTCTTCATCTGTAAAGAGAGAATGACACATCCCTCAGGGGCATGCTGTGACCTTTAAACATGATAAATG... | AGTGCAGTGGCGCGATCTCAGCTCACTGCAACTGCCACCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACATGCCACCATGCCCAGCTAATCTTCGAATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGATGGTCCCTATCTCTTAACCTTGTGATCCGCCCGCCTCGGCCTCCCAAAGTGGTGGGATTACAAGTGTGAGCCACCGCGGCTGGCTGGTGTCTTCATCTGTAAAGAGAGAATGACACATCCCTCAGGGGCATGCTGTGACCTTTAAACATGATAAATG... |
Task1_train_41651 | A variant was discovered on Chromosome 11. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CCGACATGGAAGCCGGGGGTGGCAGACAGTGAGGATGGAGTTATCCATGGCTCTTCCCTGGCTCCTGTACCTGCCCAGGAGGCTGAAGGCCCCTGAGCTGCTGGTCTCATACACCTCCACGTAGTCAAACTTGCACTCGTCCTGAGCCTCCAGGCTGAAGTTGTGGAACTGTAGTTCTATGCTGTGTCCGGCAGGCACCGAGATATGCCAGGTGCAGAGCTGGGGGAGGGCATAGGTGGAGCAATTCATGGCCCCTTCTCCTGTCTCATCCCGGGCACCCAGAAGGGTCTTCTTCCCCCACTGCTGGCTGGGGGGATGGG... | CCGACATGGAAGCCGGGGGTGGCAGACAGTGAGGATGGAGTTATCCATGGCTCTTCCCTGGCTCCTGTACCTGCCCAGGAGGCTGAAGGCCCCTGAGCTGCTGGTCTCATACACCTCCACGTAGTCAAACTTGCACTCGTCCTGAGCCTCCAGGCTGAAGTTGTGGAACTGTAGTTCTATGCTGTGTCCGGCAGGCACCGAGATATGCCAGGTGCAGAGCTGGGGGAGGGCATAGGTGGAGCAATTCATGGCCCCTTCTCCTGTCTCATCCCGGGCACCCAGAAGGGTCTTCTTCCCCCACTGCTGGCTGGGGGGATGGG... |
Task1_train_41652 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GAACAGGAAGAAGCCATACAGTTAGCCCCACTCTTAATTTTGAGATAGAGTAGACCTAGAGAAAGAAAGCAGCTTGCTCAAGGGCATGTGCAGATAGCGAGAAGCAGAAAGGGGACTAGTACTCAGGTTTCAGTCCAATATTCTTTTCTAATGGACTTCTAGGCCTGGGATTGGAGGCTAGTTCTTTCCCTTATTGGCTCTGAAATAGTGGATAAGTCACTTAAGTTCTCTGAACCTTAGCTATTTAATCTGCAAAACGGGACTAATAGTAATAATAGTGGTCTATCTCAGTTGTGAGGATTAAATAAAATAATATTTGT... | GAACAGGAAGAAGCCATACAGTTAGCCCCACTCTTAATTTTGAGATAGAGTAGACCTAGAGAAAGAAAGCAGCTTGCTCAAGGGCATGTGCAGATAGCGAGAAGCAGAAAGGGGACTAGTACTCAGGTTTCAGTCCAATATTCTTTTCTAATGGACTTCTAGGCCTGGGATTGGAGGCTAGTTCTTTCCCTTATTGGCTCTGAAATAGTGGATAAGTCACTTAAGTTCTCTGAACCTTAGCTATTTAATCTGCAAAACGGGACTAATAGTAATAATAGTGGTCTATCTCAGTTGTGAGGATTAAATAAAATAATATTTGT... |
Task1_train_41653 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AGGGAGAGGTGGGCACCAAGCTGGGGGGCCAGACTCATTGGAAATGCCAGTCTTCCAGAATGGTCTGTCCAGCATCCAGTCACCCTTTGCCCAGGGTGCCTGCAGTGCTTGGGTGGGCCTCCCTGTGCCCCCCTGCCCTCACCTCCTCCACCTCATCTGTCTGGTTTCCCTCTAAGGCAGCTGGGCTCATGGCCAGGCTGGGTGGTCCTGGGCTAGGGGCACTCTCCTCGAGGTTCGGTTGTCCTTACCGAGGGGTGGTAGGAGGGGGAGACCCCCAGATCATAGTAGGGGGGCTGCAGGGACAGCTTCTGCAAGTCCTC... | AGGGAGAGGTGGGCACCAAGCTGGGGGGCCAGACTCATTGGAAATGCCAGTCTTCCAGAATGGTCTGTCCAGCATCCAGTCACCCTTTGCCCAGGGTGCCTGCAGTGCTTGGGTGGGCCTCCCTGTGCCCCCCTGCCCTCACCTCCTCCACCTCATCTGTCTGGTTTCCCTCTAAGGCAGCTGGGCTCATGGCCAGGCTGGGTGGTCCTGGGCTAGGGGCACTCTCCTCGAGGTTCGGTTGTCCTTACCGAGGGGTGGTAGGAGGGGGAGACCCCCAGATCATAGTAGGGGGGCTGCAGGGACAGCTTCTGCAAGTCCTC... |
Task1_train_41654 | An alteration has been detected on Chromosome 11. Is it pathogenic, and if so, what disease is involved? | Benign | GGGCCCTGCTGAGCCCCCATCTCCACAACGTGTGTGCCGAGGCCGTGGATGCCATCTACACCCGCCAGGAGGATGTCCGGTTCTGGCTGGAGCAAGGTCAGCTGGGAGCTGGGCACTGCCCGCTGCTGGGCGGAGGGAAGGGGACAGGGAGACAGCACAGAGCAGTGGAGGAGGGCAGGGGCATCATTAGTTGAGTCTCATCATTAGCCAAGTCTCATCATTAGCCTTTCCTTTGTTCAGGAGACATTTACTGAACACCTACAGAGATGTACTGGCGCAGGAATCAGAGATGTAGACACTCAGTTCCTGTCCCCCAGCAG... | GGGCCCTGCTGAGCCCCCATCTCCACAACGTGTGTGCCGAGGCCGTGGATGCCATCTACACCCGCCAGGAGGATGTCCGGTTCTGGCTGGAGCAAGGTCAGCTGGGAGCTGGGCACTGCCCGCTGCTGGGCGGAGGGAAGGGGACAGGGAGACAGCACAGAGCAGTGGAGGAGGGCAGGGGCATCATTAGTTGAGTCTCATCATTAGCCAAGTCTCATCATTAGCCTTTCCTTTGTTCAGGAGACATTTACTGAACACCTACAGAGATGTACTGGCGCAGGAATCAGAGATGTAGACACTCAGTTCCTGTCCCCCAGCAG... |
Task1_train_41655 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TCCACAACGTGTGTGCCGAGGCCGTGGATGCCATCTACACCCGCCAGGAGGATGTCCGGTTCTGGCTGGAGCAAGGTCAGCTGGGAGCTGGGCACTGCCCGCTGCTGGGCGGAGGGAAGGGGACAGGGAGACAGCACAGAGCAGTGGAGGAGGGCAGGGGCATCATTAGTTGAGTCTCATCATTAGCCAAGTCTCATCATTAGCCTTTCCTTTGTTCAGGAGACATTTACTGAACACCTACAGAGATGTACTGGCGCAGGAATCAGAGATGTAGACACTCAGTTCCTGTCCCCCAGCAGGGTAGATCTGCACAGAGTTAA... | TCCACAACGTGTGTGCCGAGGCCGTGGATGCCATCTACACCCGCCAGGAGGATGTCCGGTTCTGGCTGGAGCAAGGTCAGCTGGGAGCTGGGCACTGCCCGCTGCTGGGCGGAGGGAAGGGGACAGGGAGACAGCACAGAGCAGTGGAGGAGGGCAGGGGCATCATTAGTTGAGTCTCATCATTAGCCAAGTCTCATCATTAGCCTTTCCTTTGTTCAGGAGACATTTACTGAACACCTACAGAGATGTACTGGCGCAGGAATCAGAGATGTAGACACTCAGTTCCTGTCCCCCAGCAGGGTAGATCTGCACAGAGTTAA... |
Task1_train_41656 | This sequence change occurs on Chromosome 11. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | AGCTGTATCTTAGCTGCCATTCCTCCCCTGATCTGGGTGCCCCTGTACAGTTAATAACCTGCACAGCTGCATGAGATGGCTCTGCACAGATGGTTGGGCAGAATGGTTGGGAATGACTGCAGAGATCTCTGTGCTAAGATCCCCATGGCTCACCAAGAGCCCGGCCTTCAGAGAGGGCTGAGGCCACTAAAAGTACCTGGAGGGGAAGCTCGCCATCTAGTGGTTGAAATGGGGACACCAGCATCATAAGCTGCTCTTCCGCCTCCTCCTGGCTGCCCTCTCCAGAATCTCATAGCCATGGGCTTACAGCTGGAAGAGAT... | AGCTGTATCTTAGCTGCCATTCCTCCCCTGATCTGGGTGCCCCTGTACAGTTAATAACCTGCACAGCTGCATGAGATGGCTCTGCACAGATGGTTGGGCAGAATGGTTGGGAATGACTGCAGAGATCTCTGTGCTAAGATCCCCATGGCTCACCAAGAGCCCGGCCTTCAGAGAGGGCTGAGGCCACTAAAAGTACCTGGAGGGGAAGCTCGCCATCTAGTGGTTGAAATGGGGACACCAGCATCATAAGCTGCTCTTCCGCCTCCTCCTGGCTGCCCTCTCCAGAATCTCATAGCCATGGGCTTACAGCTGGAAGAGAT... |
Task1_train_41657 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | AAAGGAGGATGGCATGTAGGCTAGGAAATCACCAAGGAAGCCAAGCCCTGGTCTCTGTAGAGTCTGGGGCCTACTGTCTTTGGAGAGTGATCTGAAGTTGGAGAAGGGAGCAGAAATGGACATTTACAAGCTTCTGTTGTTTTTCAGGTATCTCCCTCAGGGTCTCTGGGCCCCCTCTCTGTCCCTCCTGTCCACAGTACCATGCCTGGAACAGGTGAGCTTTAAAATGAGATTTCTGAAGAACACCAGAATTCTTTTAAAAAATGGGATATTAGAACTGAAAGGTATCTACCTAAGTCAGGCTTCCCTAAATGCATTTC... | AAAGGAGGATGGCATGTAGGCTAGGAAATCACCAAGGAAGCCAAGCCCTGGTCTCTGTAGAGTCTGGGGCCTACTGTCTTTGGAGAGTGATCTGAAGTTGGAGAAGGGAGCAGAAATGGACATTTACAAGCTTCTGTTGTTTTTCAGGTATCTCCCTCAGGGTCTCTGGGCCCCCTCTCTGTCCCTCCTGTCCACAGTACCATGCCTGGAACAGGTGAGCTTTAAAATGAGATTTCTGAAGAACACCAGAATTCTTTTAAAAAATGGGATATTAGAACTGAAAGGTATCTACCTAAGTCAGGCTTCCCTAAATGCATTTC... |
Task1_train_41658 | A genetic alteration is present on Chromosome 11. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TTTCAATATCCTTATATAGACTGCTATGCATTTTTATGTGCCTCCGGACATATATCAATCTAATGAGACTGGGATTTGGCCTGGGGTATAGCAGGGGAAGTGTTCTGTAGAGCTGGTTTATTATATCATCATTCCACAAACAAAATTATCTCAAAGAGTCTACCTTTTGGTCCAAACCTCCTCTATTCAAAGGCATTTTCCTCTCACTTATTGAAAGCCTGAAAAAGCAGGGCCTGGAAATGATGCTGAGTGGAGGCTGTCACAATACATACAGCCCTGAACTAGTGCCAAGGAGTGCTGAGGATTAGGACCTGTTTTCA... | TTTCAATATCCTTATATAGACTGCTATGCATTTTTATGTGCCTCCGGACATATATCAATCTAATGAGACTGGGATTTGGCCTGGGGTATAGCAGGGGAAGTGTTCTGTAGAGCTGGTTTATTATATCATCATTCCACAAACAAAATTATCTCAAAGAGTCTACCTTTTGGTCCAAACCTCCTCTATTCAAAGGCATTTTCCTCTCACTTATTGAAAGCCTGAAAAAGCAGGGCCTGGAAATGATGCTGAGTGGAGGCTGTCACAATACATACAGCCCTGAACTAGTGCCAAGGAGTGCTGAGGATTAGGACCTGTTTTCA... |
Task1_train_41659 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CGGGGACGTCTACTGCTTCAACAAGACCTGCGGCAGCGGGGAGGTGTGCGCCGTGGAGGACGGCTACCAGGGCTGCTTCCCCAAGCGGGAGACCGTGTGCCTGCTCAGCCAGAACCAGGTGCTGCACACCTTTGACGGCGCCTCCTACGCCTTCCCCTCCGAGTTCTCCTACACCCTCCTGAAGACCTGCCCTGAGCGCCCAGAGTACTTGGAAATCGACATCAACAAGAAGAAGCCCGATGCAGGACCTGCTTGGCTGCGGGGACTTCGGATCCTGGTGGCCGACCAGGAGGTCAAGATAGGAGGCATCGGGGCTTCGG... | CGGGGACGTCTACTGCTTCAACAAGACCTGCGGCAGCGGGGAGGTGTGCGCCGTGGAGGACGGCTACCAGGGCTGCTTCCCCAAGCGGGAGACCGTGTGCCTGCTCAGCCAGAACCAGGTGCTGCACACCTTTGACGGCGCCTCCTACGCCTTCCCCTCCGAGTTCTCCTACACCCTCCTGAAGACCTGCCCTGAGCGCCCAGAGTACTTGGAAATCGACATCAACAAGAAGAAGCCCGATGCAGGACCTGCTTGGCTGCGGGGACTTCGGATCCTGGTGGCCGACCAGGAGGTCAAGATAGGAGGCATCGGGGCTTCGG... |
Task1_train_41660 | A genomic change on Chromosome 11 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TATTTATTGAAAAAATACAAGATCACATGGTATTCTATTAATATCACATGGAGCAGACTTCTATTTGTGTTGCTACACTTGCAGTTCCCAAACTCTGCTCCAAGGTCTTGCTACCACTTCTGGGCAGAAGCAACTCAGAAAAAAAAAAAAAAAAGTAGTATTCGTTTTTAGTACTACTTGTTTAGTTAGACCATTACTTGGTCTTTTGGATTTTTGAATTTTGTTTGTCCATGGTGGGCTATGTGGACACTCCCCTATATAATGTATCTGTGGCCCTTGGGAAAATTCTTTTGGAGACTCTTACCTTAGAATTTACTTCT... | TATTTATTGAAAAAATACAAGATCACATGGTATTCTATTAATATCACATGGAGCAGACTTCTATTTGTGTTGCTACACTTGCAGTTCCCAAACTCTGCTCCAAGGTCTTGCTACCACTTCTGGGCAGAAGCAACTCAGAAAAAAAAAAAAAAAAGTAGTATTCGTTTTTAGTACTACTTGTTTAGTTAGACCATTACTTGGTCTTTTGGATTTTTGAATTTTGTTTGTCCATGGTGGGCTATGTGGACACTCCCCTATATAATGTATCTGTGGCCCTTGGGAAAATTCTTTTGGAGACTCTTACCTTAGAATTTACTTCT... |
Task1_train_41661 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | TTGAACTCCAGGGCTCAAGAGATCTCCTACCTCCACCTCCCAAATAGCTGGGATTACAGGTGTGAGCCACTGTGCCCAGTAAGCAAAAGATTTCTATACCTATATTTCCAGAACATCCTCCTCAGCATTGCTCCCAATTTCTTTCCATTTTCTATGTATCTGTAGCTGAATTTTCTGTGATTTCCCCAAACTCAACATTGCTAAATACCAAACAGCACCTTCTCCCACAAAATCAGCTTGTCCAAAGCATCACACAGGCCCCAAAGCAACACACGGGTCCCAAACCTTGGTGTTATCTATCACTCCTATGTATGTGTACA... | TTGAACTCCAGGGCTCAAGAGATCTCCTACCTCCACCTCCCAAATAGCTGGGATTACAGGTGTGAGCCACTGTGCCCAGTAAGCAAAAGATTTCTATACCTATATTTCCAGAACATCCTCCTCAGCATTGCTCCCAATTTCTTTCCATTTTCTATGTATCTGTAGCTGAATTTTCTGTGATTTCCCCAAACTCAACATTGCTAAATACCAAACAGCACCTTCTCCCACAAAATCAGCTTGTCCAAAGCATCACACAGGCCCCAAAGCAACACACGGGTCCCAAACCTTGGTGTTATCTATCACTCCTATGTATGTGTACA... |
Task1_train_41662 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GAGTTGCCTGGCCAATCGTTGCCCTGAGAAAGTTTGGTTTGTGATCCTATTTCAGTAGGCTGATTGGAGCAGCCTTTACTTGGAGGTCGAGTCCCTCCCCGAGGGAATCCGTGTACAGTTACACTAGCGGTCGCTGCCAGTGCTAGCCCATTCAGGATAGCCCCCCTCACCCCGCCCCCAGCCCCCGCTCCTCCTCCTCCTTTTTTGTTTTTATCCAGTGTCTCGCTTCCTCTCTCTCTCTCTCTCTCTGTCTCTCTCTCCCTTTCCCTCCTACCACTGCCTCTTCCTCCCGCTCTCTACCTCCCTGCAGCGCCAAGCCG... | GAGTTGCCTGGCCAATCGTTGCCCTGAGAAAGTTTGGTTTGTGATCCTATTTCAGTAGGCTGATTGGAGCAGCCTTTACTTGGAGGTCGAGTCCCTCCCCGAGGGAATCCGTGTACAGTTACACTAGCGGTCGCTGCCAGTGCTAGCCCATTCAGGATAGCCCCCCTCACCCCGCCCCCAGCCCCCGCTCCTCCTCCTCCTTTTTTGTTTTTATCCAGTGTCTCGCTTCCTCTCTCTCTCTCTCTCTCTGTCTCTCTCTCCCTTTCCCTCCTACCACTGCCTCTTCCTCCCGCTCTCTACCTCCCTGCAGCGCCAAGCCG... |
Task1_train_41663 | The following genetic variant occurs on Chromosome 11. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TCATCTCTTTAGTTTGTGTACTTTTAACCAAGGACTGCGTATCTCTTGCCTTTCTTGTGGTTTTCACCTGCAACTTAATAATTATACCATTGTACACCTTATCCTCTTTTCCCATATTCAAGAAAGATTATCTCCAACTCTTACTGTTTTAAAACTCATGTGCTTACTTCAAATATTTCTGCACTAAAGCTGTCATATTACAAGTTTGTTTTCCTATTAGAGGTTTCCATTTCCATCCATTTATCTTTTACTTGAAAGGACACCATATTTTTCACCTAATCCCTCAATTTTATTGGTGGGGAAGGCATAAGAGAAGTTCA... | TCATCTCTTTAGTTTGTGTACTTTTAACCAAGGACTGCGTATCTCTTGCCTTTCTTGTGGTTTTCACCTGCAACTTAATAATTATACCATTGTACACCTTATCCTCTTTTCCCATATTCAAGAAAGATTATCTCCAACTCTTACTGTTTTAAAACTCATGTGCTTACTTCAAATATTTCTGCACTAAAGCTGTCATATTACAAGTTTGTTTTCCTATTAGAGGTTTCCATTTCCATCCATTTATCTTTTACTTGAAAGGACACCATATTTTTCACCTAATCCCTCAATTTTATTGGTGGGGAAGGCATAAGAGAAGTTCA... |
Task1_train_41664 | A genomic change on Chromosome 11 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TGGCTTTTCCTGAATTCCAAAAGGGAGGAGGGCATAATGAGGTGTGTCTGACCCCTTCTTCCCGTCATGACCCAAACCAGTCTTTCAGGTTAACTTTGGAGTGCCCTGGCCAAGAGGAGGAGTCCATTCAGATGGTTGAGAGGCCCTTAGAATTTGGTTTACAGCAGTAATTTTTTTTTTTAGTCATAGTTTTAATGGTCTTTTAATGCTAGTTTTTCTTTACTGTTGGGAAGAGACATATCTAATACTCATTATCACAAACTGAATCACCTGCATCATCATTCCCTAAAAAGATATCTTGCCTGAAGACAAGGGTCAGA... | TGGCTTTTCCTGAATTCCAAAAGGGAGGAGGGCATAATGAGGTGTGTCTGACCCCTTCTTCCCGTCATGACCCAAACCAGTCTTTCAGGTTAACTTTGGAGTGCCCTGGCCAAGAGGAGGAGTCCATTCAGATGGTTGAGAGGCCCTTAGAATTTGGTTTACAGCAGTAATTTTTTTTTTTAGTCATAGTTTTAATGGTCTTTTAATGCTAGTTTTTCTTTACTGTTGGGAAGAGACATATCTAATACTCATTATCACAAACTGAATCACCTGCATCATCATTCCCTAAAAAGATATCTTGCCTGAAGACAAGGGTCAGA... |
Task1_train_41665 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | CATAAAATTTTCTAGTATATTCTTTTCTGTCAAGCTAAAATGTGAATAACTTAGGAGTGGAGATCATGTCCTGTTTCTCTTTGTATCATCAGCATCTCCCATTGAATTTTACACAGGGCCCTAAAAAAGATAAATAATATTCATTCAGCATTTCTGTATCATACAATTGGTATAAGTGCTTTTAGGTTAATCCTACTTTAGCCCCGCACCGTTGAAATTCTCATTTTGTAGATAAGTAAGAAACTGAGATACAGAAAGTTTCGATAACTTGCCCAGGATCATAATTCAGGTGTGCTCAGCACATCTTCTATGAATAAATG... | CATAAAATTTTCTAGTATATTCTTTTCTGTCAAGCTAAAATGTGAATAACTTAGGAGTGGAGATCATGTCCTGTTTCTCTTTGTATCATCAGCATCTCCCATTGAATTTTACACAGGGCCCTAAAAAAGATAAATAATATTCATTCAGCATTTCTGTATCATACAATTGGTATAAGTGCTTTTAGGTTAATCCTACTTTAGCCCCGCACCGTTGAAATTCTCATTTTGTAGATAAGTAAGAAACTGAGATACAGAAAGTTTCGATAACTTGCCCAGGATCATAATTCAGGTGTGCTCAGCACATCTTCTATGAATAAATG... |
Task1_train_41666 | 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 | ATCATACAATTGGTATAAGTGCTTTTAGGTTAATCCTACTTTAGCCCCGCACCGTTGAAATTCTCATTTTGTAGATAAGTAAGAAACTGAGATACAGAAAGTTTCGATAACTTGCCCAGGATCATAATTCAGGTGTGCTCAGCACATCTTCTATGAATAAATGCCTGACTGCCTAATGAGTTCTGGGGAAAAATGACCATAATATATACAATGGTAATTAAACCATACAGTTAAACTAAAACTTTTTTATTTATTTATTTATTTTTAGAGCCAGAAAGAGCCAGAGAGATTTAAATCACAAAAGATTTAGGTGACCGAGA... | ATCATACAATTGGTATAAGTGCTTTTAGGTTAATCCTACTTTAGCCCCGCACCGTTGAAATTCTCATTTTGTAGATAAGTAAGAAACTGAGATACAGAAAGTTTCGATAACTTGCCCAGGATCATAATTCAGGTGTGCTCAGCACATCTTCTATGAATAAATGCCTGACTGCCTAATGAGTTCTGGGGAAAAATGACCATAATATATACAATGGTAATTAAACCATACAGTTAAACTAAAACTTTTTTATTTATTTATTTATTTTTAGAGCCAGAAAGAGCCAGAGAGATTTAAATCACAAAAGATTTAGGTGACCGAGA... |
Task1_train_41667 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | AAATCAAATAACTCAGTAAATGGATATATATTACATATTCATGGATAGGGAGACTCAATATTGTCAAGATGTCAATTTTGCCTAACTTATTCTACAGTTTCAACACATTCCAATAAAAATCTCAGCAAGTTATTTTGTGGACATTGACAACTGGATTCTCAAGTTTATAGAGAGATGAAAAAGACCCAGAATAGCCAACATAATATTTCAGAAGAACAAAGTCAGAGGACTGACATTACCTGATCTCAGGACTTACTATGAAGCTGTAGTGATGAAGACAATGTGGTTTTGGTGAAAAAAAAAAGACAAATAGATCAACG... | AAATCAAATAACTCAGTAAATGGATATATATTACATATTCATGGATAGGGAGACTCAATATTGTCAAGATGTCAATTTTGCCTAACTTATTCTACAGTTTCAACACATTCCAATAAAAATCTCAGCAAGTTATTTTGTGGACATTGACAACTGGATTCTCAAGTTTATAGAGAGATGAAAAAGACCCAGAATAGCCAACATAATATTTCAGAAGAACAAAGTCAGAGGACTGACATTACCTGATCTCAGGACTTACTATGAAGCTGTAGTGATGAAGACAATGTGGTTTTGGTGAAAAAAAAAAGACAAATAGATCAACG... |
Task1_train_41668 | This is a variant located on Chromosome 11. Is this mutation a likely cause of disease or not? | Benign | GGATATATATTACATATTCATGGATAGGGAGACTCAATATTGTCAAGATGTCAATTTTGCCTAACTTATTCTACAGTTTCAACACATTCCAATAAAAATCTCAGCAAGTTATTTTGTGGACATTGACAACTGGATTCTCAAGTTTATAGAGAGATGAAAAAGACCCAGAATAGCCAACATAATATTTCAGAAGAACAAAGTCAGAGGACTGACATTACCTGATCTCAGGACTTACTATGAAGCTGTAGTGATGAAGACAATGTGGTTTTGGTGAAAAAAAAAAGACAAATAGATCAACGGAATAGAACAGAGAGTCCAGA... | GGATATATATTACATATTCATGGATAGGGAGACTCAATATTGTCAAGATGTCAATTTTGCCTAACTTATTCTACAGTTTCAACACATTCCAATAAAAATCTCAGCAAGTTATTTTGTGGACATTGACAACTGGATTCTCAAGTTTATAGAGAGATGAAAAAGACCCAGAATAGCCAACATAATATTTCAGAAGAACAAAGTCAGAGGACTGACATTACCTGATCTCAGGACTTACTATGAAGCTGTAGTGATGAAGACAATGTGGTTTTGGTGAAAAAAAAAAGACAAATAGATCAACGGAATAGAACAGAGAGTCCAGA... |
Task1_train_41669 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | ACTCCGGGTATTTCTGTAACAGGCAAAGAGCAATTGGACACTCACTTTTGCACGTGATCTTCCATCTCCATCATTTAGGATGAGAGAGGAGCAGATACAAAAGACACAGGTTCTGAAGAATGGGGAAGCCTGCTCAGAGAATAGCTGTTCAGTGCTCATGCAGCTTATTTGTTTTAAACTGTGAGAAGGATTTGGGAAATAAGGAGTCACCTGCATCCTGGGAACTCAAGCTGCCTACGGAAGTTTGGCTTGTCCTATTACAGCAGTAATATATTGGAAACAAGAAGACATGAACAGCTTATTAAATAGCCAGGTAGCTG... | ACTCCGGGTATTTCTGTAACAGGCAAAGAGCAATTGGACACTCACTTTTGCACGTGATCTTCCATCTCCATCATTTAGGATGAGAGAGGAGCAGATACAAAAGACACAGGTTCTGAAGAATGGGGAAGCCTGCTCAGAGAATAGCTGTTCAGTGCTCATGCAGCTTATTTGTTTTAAACTGTGAGAAGGATTTGGGAAATAAGGAGTCACCTGCATCCTGGGAACTCAAGCTGCCTACGGAAGTTTGGCTTGTCCTATTACAGCAGTAATATATTGGAAACAAGAAGACATGAACAGCTTATTAAATAGCCAGGTAGCTG... |
Task1_train_41670 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TTCTGAAGAATGGGGAAGCCTGCTCAGAGAATAGCTGTTCAGTGCTCATGCAGCTTATTTGTTTTAAACTGTGAGAAGGATTTGGGAAATAAGGAGTCACCTGCATCCTGGGAACTCAAGCTGCCTACGGAAGTTTGGCTTGTCCTATTACAGCAGTAATATATTGGAAACAAGAAGACATGAACAGCTTATTAAATAGCCAGGTAGCTGGGCAGAATGAGAAAATGCAACCCTAGACAATTGAGCCATTTGGGCAAATATGAGAGTCTGGAGTGAGCTCTGGGAGAGGCCCAACACTAAATAAAGGGTCAGCTTTCTCA... | TTCTGAAGAATGGGGAAGCCTGCTCAGAGAATAGCTGTTCAGTGCTCATGCAGCTTATTTGTTTTAAACTGTGAGAAGGATTTGGGAAATAAGGAGTCACCTGCATCCTGGGAACTCAAGCTGCCTACGGAAGTTTGGCTTGTCCTATTACAGCAGTAATATATTGGAAACAAGAAGACATGAACAGCTTATTAAATAGCCAGGTAGCTGGGCAGAATGAGAAAATGCAACCCTAGACAATTGAGCCATTTGGGCAAATATGAGAGTCTGGAGTGAGCTCTGGGAGAGGCCCAACACTAAATAAAGGGTCAGCTTTCTCA... |
Task1_train_41671 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | GAAATAAGGAGTCACCTGCATCCTGGGAACTCAAGCTGCCTACGGAAGTTTGGCTTGTCCTATTACAGCAGTAATATATTGGAAACAAGAAGACATGAACAGCTTATTAAATAGCCAGGTAGCTGGGCAGAATGAGAAAATGCAACCCTAGACAATTGAGCCATTTGGGCAAATATGAGAGTCTGGAGTGAGCTCTGGGAGAGGCCCAACACTAAATAAAGGGTCAGCTTTCTCAGAGATAAGGCCATGATTGACCCCAGAATAGACGATTCCAAGATGTGTGCTATGTGGGAGCCTCCAAGTGGCAACAAAAACATCTG... | GAAATAAGGAGTCACCTGCATCCTGGGAACTCAAGCTGCCTACGGAAGTTTGGCTTGTCCTATTACAGCAGTAATATATTGGAAACAAGAAGACATGAACAGCTTATTAAATAGCCAGGTAGCTGGGCAGAATGAGAAAATGCAACCCTAGACAATTGAGCCATTTGGGCAAATATGAGAGTCTGGAGTGAGCTCTGGGAGAGGCCCAACACTAAATAAAGGGTCAGCTTTCTCAGAGATAAGGCCATGATTGACCCCAGAATAGACGATTCCAAGATGTGTGCTATGTGGGAGCCTCCAAGTGGCAACAAAAACATCTG... |
Task1_train_41672 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CTACGGAAGTTTGGCTTGTCCTATTACAGCAGTAATATATTGGAAACAAGAAGACATGAACAGCTTATTAAATAGCCAGGTAGCTGGGCAGAATGAGAAAATGCAACCCTAGACAATTGAGCCATTTGGGCAAATATGAGAGTCTGGAGTGAGCTCTGGGAGAGGCCCAACACTAAATAAAGGGTCAGCTTTCTCAGAGATAAGGCCATGATTGACCCCAGAATAGACGATTCCAAGATGTGTGCTATGTGGGAGCCTCCAAGTGGCAACAAAAACATCTGGGTTGCTTGCATTGCCAGTAGTGGCAGCACTAGTGTGTT... | CTACGGAAGTTTGGCTTGTCCTATTACAGCAGTAATATATTGGAAACAAGAAGACATGAACAGCTTATTAAATAGCCAGGTAGCTGGGCAGAATGAGAAAATGCAACCCTAGACAATTGAGCCATTTGGGCAAATATGAGAGTCTGGAGTGAGCTCTGGGAGAGGCCCAACACTAAATAAAGGGTCAGCTTTCTCAGAGATAAGGCCATGATTGACCCCAGAATAGACGATTCCAAGATGTGTGCTATGTGGGAGCCTCCAAGTGGCAACAAAAACATCTGGGTTGCTTGCATTGCCAGTAGTGGCAGCACTAGTGTGTT... |
Task1_train_41673 | Consider this mutation on Chromosome 11. Is this a benign change or a disease-causing variant? | Benign | TAAGGCCATGATTGACCCCAGAATAGACGATTCCAAGATGTGTGCTATGTGGGAGCCTCCAAGTGGCAACAAAAACATCTGGGTTGCTTGCATTGCCAGTAGTGGCAGCACTAGTGTGTTATATTGGACTCCATGGCCTTGGCGAGAGATGTAGCCTTAGCCTGGAGGATGGCCAGAGATCCAGAAGGTAGAAACAGTTTTGGGAAGTCTGCCATTCTACTATCATCCAGCTTTTTACTCAAGTGTACGAATTAATTTCCCACCTGGAAATCAATGTATGATTAGATTAAAAATAGAACAAACACACAAATGAAAATATA... | TAAGGCCATGATTGACCCCAGAATAGACGATTCCAAGATGTGTGCTATGTGGGAGCCTCCAAGTGGCAACAAAAACATCTGGGTTGCTTGCATTGCCAGTAGTGGCAGCACTAGTGTGTTATATTGGACTCCATGGCCTTGGCGAGAGATGTAGCCTTAGCCTGGAGGATGGCCAGAGATCCAGAAGGTAGAAACAGTTTTGGGAAGTCTGCCATTCTACTATCATCCAGCTTTTTACTCAAGTGTACGAATTAATTTCCCACCTGGAAATCAATGTATGATTAGATTAAAAATAGAACAAACACACAAATGAAAATATA... |
Task1_train_41674 | With a mutation on Chromosome 11, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | ATTAATTTCCCACCTGGAAATCAATGTATGATTAGATTAAAAATAGAACAAACACACAAATGAAAATATAGTTTTCTAAAATACATTCTGAGCCATGCTTGTGCTATAAAATGTTTTTAAAAAGTGTGAAGTTGGCCTATCACCAAGTAAGTTTGATAAATATTGTATTTATATAGTCCTTCAGGAGGACTGAGGCATCCTCCAGTTACAAAACCAGTTTAACTATGTAATTCAGGATGTCTGAAGTCATATGATCCTCAGATACTTATTTAATGTAACACCTTTTAACATCTCCCTGGAATTATTCTTTTGCTGAACAC... | ATTAATTTCCCACCTGGAAATCAATGTATGATTAGATTAAAAATAGAACAAACACACAAATGAAAATATAGTTTTCTAAAATACATTCTGAGCCATGCTTGTGCTATAAAATGTTTTTAAAAAGTGTGAAGTTGGCCTATCACCAAGTAAGTTTGATAAATATTGTATTTATATAGTCCTTCAGGAGGACTGAGGCATCCTCCAGTTACAAAACCAGTTTAACTATGTAATTCAGGATGTCTGAAGTCATATGATCCTCAGATACTTATTTAATGTAACACCTTTTAACATCTCCCTGGAATTATTCTTTTGCTGAACAC... |
Task1_train_41675 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | GAACAAACACACAAATGAAAATATAGTTTTCTAAAATACATTCTGAGCCATGCTTGTGCTATAAAATGTTTTTAAAAAGTGTGAAGTTGGCCTATCACCAAGTAAGTTTGATAAATATTGTATTTATATAGTCCTTCAGGAGGACTGAGGCATCCTCCAGTTACAAAACCAGTTTAACTATGTAATTCAGGATGTCTGAAGTCATATGATCCTCAGATACTTATTTAATGTAACACCTTTTAACATCTCCCTGGAATTATTCTTTTGCTGAACACCCTTGGAAACCTTGATGTAGAAAATTATAATTCACCTTAACAGTA... | GAACAAACACACAAATGAAAATATAGTTTTCTAAAATACATTCTGAGCCATGCTTGTGCTATAAAATGTTTTTAAAAAGTGTGAAGTTGGCCTATCACCAAGTAAGTTTGATAAATATTGTATTTATATAGTCCTTCAGGAGGACTGAGGCATCCTCCAGTTACAAAACCAGTTTAACTATGTAATTCAGGATGTCTGAAGTCATATGATCCTCAGATACTTATTTAATGTAACACCTTTTAACATCTCCCTGGAATTATTCTTTTGCTGAACACCCTTGGAAACCTTGATGTAGAAAATTATAATTCACCTTAACAGTA... |
Task1_train_41676 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | ACCAAGCAACTAGTACAGTGCCTTGTACATACATATGTCAAAAATGATTATAATTATGATTCCCATTCTAATAGTCTTATAATTTTTTCTCTTCAAAACACTTCTGATCTAATTCTATAAAGTGTCTCTTCATCTAGGTTTAGCAATACTTTTATTATCTTATGTCTCTGATGTTATAATAGTTTATTAACTGGCCATTCTACCATTTCTCCTTTTTTTGTCTCTCTTTTCTAATTTATCTCATGGTTTAGCATTTAAAGAAGTGGCTTCTCAGGATAAAGGTATTTCTATAGATGACAAGGAGGAGGAAAAGTAAACAG... | ACCAAGCAACTAGTACAGTGCCTTGTACATACATATGTCAAAAATGATTATAATTATGATTCCCATTCTAATAGTCTTATAATTTTTTCTCTTCAAAACACTTCTGATCTAATTCTATAAAGTGTCTCTTCATCTAGGTTTAGCAATACTTTTATTATCTTATGTCTCTGATGTTATAATAGTTTATTAACTGGCCATTCTACCATTTCTCCTTTTTTTGTCTCTCTTTTCTAATTTATCTCATGGTTTAGCATTTAAAGAAGTGGCTTCTCAGGATAAAGGTATTTCTATAGATGACAAGGAGGAGGAAAAGTAAACAG... |
Task1_train_41677 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TTCAAAACACTTCTGATCTAATTCTATAAAGTGTCTCTTCATCTAGGTTTAGCAATACTTTTATTATCTTATGTCTCTGATGTTATAATAGTTTATTAACTGGCCATTCTACCATTTCTCCTTTTTTTGTCTCTCTTTTCTAATTTATCTCATGGTTTAGCATTTAAAGAAGTGGCTTCTCAGGATAAAGGTATTTCTATAGATGACAAGGAGGAGGAAAAGTAAACAGGTAGGATGCCTAGGGCATAATCTGAATTCTTTAGGTTGGCATTCAAGGACATTTTCATCTTATAGAATAGGTTAGGTGAATACAACACAAC... | TTCAAAACACTTCTGATCTAATTCTATAAAGTGTCTCTTCATCTAGGTTTAGCAATACTTTTATTATCTTATGTCTCTGATGTTATAATAGTTTATTAACTGGCCATTCTACCATTTCTCCTTTTTTTGTCTCTCTTTTCTAATTTATCTCATGGTTTAGCATTTAAAGAAGTGGCTTCTCAGGATAAAGGTATTTCTATAGATGACAAGGAGGAGGAAAAGTAAACAGGTAGGATGCCTAGGGCATAATCTGAATTCTTTAGGTTGGCATTCAAGGACATTTTCATCTTATAGAATAGGTTAGGTGAATACAACACAAC... |
Task1_train_41678 | A mutation located on Chromosome 11 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TAATGTAGCTTCAGCTGCATTTCCTGGTGGTAATGTCAGGATACATTTTACCTGGGTTCTGTAAACTGCAGATATCCTGGTTTCTTCCATATCAGTGAATCAGTTTCATAGTCTTCCCCACAGAACAATTCATAACAAGCCTAGACTAAGAAAACATTTTGTATGCAGTTAAAAACATCATTTCAACCTGAATACCAATTGTACAGAATCTCAGCTTTTCTGGACATCACGCCAATATATATCCTTCCTCTTGCATTGGTTCTGTTTTCCTGTCTTAGGTGGCAGGTATTAAAAAAGAAACATAGACTTGAAAGAATTGT... | TAATGTAGCTTCAGCTGCATTTCCTGGTGGTAATGTCAGGATACATTTTACCTGGGTTCTGTAAACTGCAGATATCCTGGTTTCTTCCATATCAGTGAATCAGTTTCATAGTCTTCCCCACAGAACAATTCATAACAAGCCTAGACTAAGAAAACATTTTGTATGCAGTTAAAAACATCATTTCAACCTGAATACCAATTGTACAGAATCTCAGCTTTTCTGGACATCACGCCAATATATATCCTTCCTCTTGCATTGGTTCTGTTTTCCTGTCTTAGGTGGCAGGTATTAAAAAAGAAACATAGACTTGAAAGAATTGT... |
Task1_train_41679 | A mutation is present on Chromosome 11. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TTTTACCTGGGTTCTGTAAACTGCAGATATCCTGGTTTCTTCCATATCAGTGAATCAGTTTCATAGTCTTCCCCACAGAACAATTCATAACAAGCCTAGACTAAGAAAACATTTTGTATGCAGTTAAAAACATCATTTCAACCTGAATACCAATTGTACAGAATCTCAGCTTTTCTGGACATCACGCCAATATATATCCTTCCTCTTGCATTGGTTCTGTTTTCCTGTCTTAGGTGGCAGGTATTAAAAAAGAAACATAGACTTGAAAGAATTGTCTTTTATTATGCATTGCCTGGGGTTATGAATATGTGGAGGAGGGG... | TTTTACCTGGGTTCTGTAAACTGCAGATATCCTGGTTTCTTCCATATCAGTGAATCAGTTTCATAGTCTTCCCCACAGAACAATTCATAACAAGCCTAGACTAAGAAAACATTTTGTATGCAGTTAAAAACATCATTTCAACCTGAATACCAATTGTACAGAATCTCAGCTTTTCTGGACATCACGCCAATATATATCCTTCCTCTTGCATTGGTTCTGTTTTCCTGTCTTAGGTGGCAGGTATTAAAAAAGAAACATAGACTTGAAAGAATTGTCTTTTATTATGCATTGCCTGGGGTTATGAATATGTGGAGGAGGGG... |
Task1_train_41680 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TGTATGCAGTTAAAAACATCATTTCAACCTGAATACCAATTGTACAGAATCTCAGCTTTTCTGGACATCACGCCAATATATATCCTTCCTCTTGCATTGGTTCTGTTTTCCTGTCTTAGGTGGCAGGTATTAAAAAAGAAACATAGACTTGAAAGAATTGTCTTTTATTATGCATTGCCTGGGGTTATGAATATGTGGAGGAGGGGAAGATCATGGGGGGCAAAATGTTATCTCTAACGAAGCCAATATTAGGAAACATTTACACATCTAGGATAGAGTGATGTACAACAGAAAGCTAGCCCCTATCTAGTAGATTGTAG... | TGTATGCAGTTAAAAACATCATTTCAACCTGAATACCAATTGTACAGAATCTCAGCTTTTCTGGACATCACGCCAATATATATCCTTCCTCTTGCATTGGTTCTGTTTTCCTGTCTTAGGTGGCAGGTATTAAAAAAGAAACATAGACTTGAAAGAATTGTCTTTTATTATGCATTGCCTGGGGTTATGAATATGTGGAGGAGGGGAAGATCATGGGGGGCAAAATGTTATCTCTAACGAAGCCAATATTAGGAAACATTTACACATCTAGGATAGAGTGATGTACAACAGAAAGCTAGCCCCTATCTAGTAGATTGTAG... |
Task1_train_41681 | A mutation found on Chromosome 11 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GGGGGCAAAATGTTATCTCTAACGAAGCCAATATTAGGAAACATTTACACATCTAGGATAGAGTGATGTACAACAGAAAGCTAGCCCCTATCTAGTAGATTGTAGTTGGGAGAGCACATATGAACATCATGTTCTTAGAACCTCCCAGGGGATGGCCTAGTGTAAGAGAAACAGGGCCAGTCATGTATGAAGCTTGGTGCTCTCTGGATAATTTGGGAGGTGGGAGGTTGTAGGAATCCCACTATAGAGTTGTGCTGAGATTCTTACCTTCTCTAAGAGACCTAGGAGAAGCCCTTTAAAAGCAGGCAATAGTAAGGACA... | GGGGGCAAAATGTTATCTCTAACGAAGCCAATATTAGGAAACATTTACACATCTAGGATAGAGTGATGTACAACAGAAAGCTAGCCCCTATCTAGTAGATTGTAGTTGGGAGAGCACATATGAACATCATGTTCTTAGAACCTCCCAGGGGATGGCCTAGTGTAAGAGAAACAGGGCCAGTCATGTATGAAGCTTGGTGCTCTCTGGATAATTTGGGAGGTGGGAGGTTGTAGGAATCCCACTATAGAGTTGTGCTGAGATTCTTACCTTCTCTAAGAGACCTAGGAGAAGCCCTTTAAAAGCAGGCAATAGTAAGGACA... |
Task1_train_41682 | A mutation on Chromosome 11 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GGAAACATTTACACATCTAGGATAGAGTGATGTACAACAGAAAGCTAGCCCCTATCTAGTAGATTGTAGTTGGGAGAGCACATATGAACATCATGTTCTTAGAACCTCCCAGGGGATGGCCTAGTGTAAGAGAAACAGGGCCAGTCATGTATGAAGCTTGGTGCTCTCTGGATAATTTGGGAGGTGGGAGGTTGTAGGAATCCCACTATAGAGTTGTGCTGAGATTCTTACCTTCTCTAAGAGACCTAGGAGAAGCCCTTTAAAAGCAGGCAATAGTAAGGACATCAGTAACAATATTGGGCATGAAATAGTCCACAAAG... | GGAAACATTTACACATCTAGGATAGAGTGATGTACAACAGAAAGCTAGCCCCTATCTAGTAGATTGTAGTTGGGAGAGCACATATGAACATCATGTTCTTAGAACCTCCCAGGGGATGGCCTAGTGTAAGAGAAACAGGGCCAGTCATGTATGAAGCTTGGTGCTCTCTGGATAATTTGGGAGGTGGGAGGTTGTAGGAATCCCACTATAGAGTTGTGCTGAGATTCTTACCTTCTCTAAGAGACCTAGGAGAAGCCCTTTAAAAGCAGGCAATAGTAAGGACATCAGTAACAATATTGGGCATGAAATAGTCCACAAAG... |
Task1_train_41683 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GTATGAAGCTTGGTGCTCTCTGGATAATTTGGGAGGTGGGAGGTTGTAGGAATCCCACTATAGAGTTGTGCTGAGATTCTTACCTTCTCTAAGAGACCTAGGAGAAGCCCTTTAAAAGCAGGCAATAGTAAGGACATCAGTAACAATATTGGGCATGAAATAGTCCACAAAGACATAGCTCTTAGATTAAGGACTCTCTGAAAACACTCAGAGAATATATGAACTCTATCTAAGACAAAGAATGGCAAATCCATAACACTGCTGCGAGGCACAATGTCATAAAACTCACTATCATTTATCAAGCAGTTATTACCTGCCAG... | GTATGAAGCTTGGTGCTCTCTGGATAATTTGGGAGGTGGGAGGTTGTAGGAATCCCACTATAGAGTTGTGCTGAGATTCTTACCTTCTCTAAGAGACCTAGGAGAAGCCCTTTAAAAGCAGGCAATAGTAAGGACATCAGTAACAATATTGGGCATGAAATAGTCCACAAAGACATAGCTCTTAGATTAAGGACTCTCTGAAAACACTCAGAGAATATATGAACTCTATCTAAGACAAAGAATGGCAAATCCATAACACTGCTGCGAGGCACAATGTCATAAAACTCACTATCATTTATCAAGCAGTTATTACCTGCCAG... |
Task1_train_41684 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AGGCAATAGTAAGGACATCAGTAACAATATTGGGCATGAAATAGTCCACAAAGACATAGCTCTTAGATTAAGGACTCTCTGAAAACACTCAGAGAATATATGAACTCTATCTAAGACAAAGAATGGCAAATCCATAACACTGCTGCGAGGCACAATGTCATAAAACTCACTATCATTTATCAAGCAGTTATTACCTGCCAGGGATAGTATTTAGTCAGGGAATTCCCTGATCCCTTGCGCTTCCCAGATGAAGCGATGCCTCGCCCTGCTTCGGCTCACACATGGTGTGCTGCACCCACTGTCCTGCACCCACTTTCCGG... | AGGCAATAGTAAGGACATCAGTAACAATATTGGGCATGAAATAGTCCACAAAGACATAGCTCTTAGATTAAGGACTCTCTGAAAACACTCAGAGAATATATGAACTCTATCTAAGACAAAGAATGGCAAATCCATAACACTGCTGCGAGGCACAATGTCATAAAACTCACTATCATTTATCAAGCAGTTATTACCTGCCAGGGATAGTATTTAGTCAGGGAATTCCCTGATCCCTTGCGCTTCCCAGATGAAGCGATGCCTCGCCCTGCTTCGGCTCACACATGGTGTGCTGCACCCACTGTCCTGCACCCACTTTCCGG... |
Task1_train_41685 | A genomic variant on Chromosome 11 is under review. What is the biological outcome — benign or pathogenic? | Benign | ATACTGGTTCCATTTTAAAAGTTCTGATATGCATGCTGGTGATTACAGTAGCCTCCTTTCTGCAATTTATTTACATATTTGACAAACCTTCCTTTAACGTAGCTTAAGCCACATTCCCTGGAGGTATCTTAACTGGGCTTTGAGAAGAGTAGAGACTATAATTTCTCTCATATCGATGAACAAGTTTCATAGTGTTCTCCCACTGAACAATTAGTAAGAATCCTGAACTAATACAACATTTTGTATTAAGTAAAAAATCTTACTTCTGCCTCAATTTCCATTATACAGAATCCCAGCTTCTCTTGACATCAAGGTGGCAT... | ATACTGGTTCCATTTTAAAAGTTCTGATATGCATGCTGGTGATTACAGTAGCCTCCTTTCTGCAATTTATTTACATATTTGACAAACCTTCCTTTAACGTAGCTTAAGCCACATTCCCTGGAGGTATCTTAACTGGGCTTTGAGAAGAGTAGAGACTATAATTTCTCTCATATCGATGAACAAGTTTCATAGTGTTCTCCCACTGAACAATTAGTAAGAATCCTGAACTAATACAACATTTTGTATTAAGTAAAAAATCTTACTTCTGCCTCAATTTCCATTATACAGAATCCCAGCTTCTCTTGACATCAAGGTGGCAT... |
Task1_train_41686 | Located on Chromosome 11, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TATTAAGTAAAAAATCTTACTTCTGCCTCAATTTCCATTATACAGAATCCCAGCTTCTCTTGACATCAAGGTGGCATAGGCCTCTCTTCTTGCATTGGTCCCATTTTTTTCCTGTCTCATGTTCTAGGTCTTAATTGAGAGGCACAGACTTCATGGAATTGTCTTCTCTTGTGAGATGATTCATTACCTGGATTTATGAGAATAAGGAGTAGAGGAAGATGGTGAGGGGCCAACATGTGATATCTAACAAAGTTAATATTAGAATATATTTAGAAACCTAGGATAGAAGGAGAATGCAAGACAGCTGGCACCTACCCAGT... | TATTAAGTAAAAAATCTTACTTCTGCCTCAATTTCCATTATACAGAATCCCAGCTTCTCTTGACATCAAGGTGGCATAGGCCTCTCTTCTTGCATTGGTCCCATTTTTTTCCTGTCTCATGTTCTAGGTCTTAATTGAGAGGCACAGACTTCATGGAATTGTCTTCTCTTGTGAGATGATTCATTACCTGGATTTATGAGAATAAGGAGTAGAGGAAGATGGTGAGGGGCCAACATGTGATATCTAACAAAGTTAATATTAGAATATATTTAGAAACCTAGGATAGAAGGAGAATGCAAGACAGCTGGCACCTACCCAGT... |
Task1_train_41687 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | TAATTGAGAGGCACAGACTTCATGGAATTGTCTTCTCTTGTGAGATGATTCATTACCTGGATTTATGAGAATAAGGAGTAGAGGAAGATGGTGAGGGGCCAACATGTGATATCTAACAAAGTTAATATTAGAATATATTTAGAAACCTAGGATAGAAGGAGAATGCAAGACAGCTGGCACCTACCCAGTAGATTGTGTTTGGGAGAGCACATATGAATGCCATGTTCTCAGAACCACATAGGAAGTGTTCTAGGGTAACAGAAATGGGGGTGGGGGCAGTCACGTAAGAAGCTTGGTGCTCTCTGGATGATTTGGGAGGA... | TAATTGAGAGGCACAGACTTCATGGAATTGTCTTCTCTTGTGAGATGATTCATTACCTGGATTTATGAGAATAAGGAGTAGAGGAAGATGGTGAGGGGCCAACATGTGATATCTAACAAAGTTAATATTAGAATATATTTAGAAACCTAGGATAGAAGGAGAATGCAAGACAGCTGGCACCTACCCAGTAGATTGTGTTTGGGAGAGCACATATGAATGCCATGTTCTCAGAACCACATAGGAAGTGTTCTAGGGTAACAGAAATGGGGGTGGGGGCAGTCACGTAAGAAGCTTGGTGCTCTCTGGATGATTTGGGAGGA... |
Task1_train_41688 | An alteration has been detected on Chromosome 11. Is it pathogenic, and if so, what disease is involved? | Benign | ACAAAGTTAATATTAGAATATATTTAGAAACCTAGGATAGAAGGAGAATGCAAGACAGCTGGCACCTACCCAGTAGATTGTGTTTGGGAGAGCACATATGAATGCCATGTTCTCAGAACCACATAGGAAGTGTTCTAGGGTAACAGAAATGGGGGTGGGGGCAGTCACGTAAGAAGCTTGGTGCTCTCTGGATGATTTGGGAGGACATGGGAATCCTACTATAGAGTTATGCTGAGATTCTTACCTGCTCTGAGAGACCTAGGAGAAGCCCTTTAAAAGCAGGCAGTAGTGAGGACATCAGTAACTGTATCAGGGATACA... | ACAAAGTTAATATTAGAATATATTTAGAAACCTAGGATAGAAGGAGAATGCAAGACAGCTGGCACCTACCCAGTAGATTGTGTTTGGGAGAGCACATATGAATGCCATGTTCTCAGAACCACATAGGAAGTGTTCTAGGGTAACAGAAATGGGGGTGGGGGCAGTCACGTAAGAAGCTTGGTGCTCTCTGGATGATTTGGGAGGACATGGGAATCCTACTATAGAGTTATGCTGAGATTCTTACCTGCTCTGAGAGACCTAGGAGAAGCCCTTTAAAAGCAGGCAGTAGTGAGGACATCAGTAACTGTATCAGGGATACA... |
Task1_train_41689 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TTAGAATATATTTAGAAACCTAGGATAGAAGGAGAATGCAAGACAGCTGGCACCTACCCAGTAGATTGTGTTTGGGAGAGCACATATGAATGCCATGTTCTCAGAACCACATAGGAAGTGTTCTAGGGTAACAGAAATGGGGGTGGGGGCAGTCACGTAAGAAGCTTGGTGCTCTCTGGATGATTTGGGAGGACATGGGAATCCTACTATAGAGTTATGCTGAGATTCTTACCTGCTCTGAGAGACCTAGGAGAAGCCCTTTAAAAGCAGGCAGTAGTGAGGACATCAGTAACTGTATCAGGGATACAATAGTACAAAAA... | TTAGAATATATTTAGAAACCTAGGATAGAAGGAGAATGCAAGACAGCTGGCACCTACCCAGTAGATTGTGTTTGGGAGAGCACATATGAATGCCATGTTCTCAGAACCACATAGGAAGTGTTCTAGGGTAACAGAAATGGGGGTGGGGGCAGTCACGTAAGAAGCTTGGTGCTCTCTGGATGATTTGGGAGGACATGGGAATCCTACTATAGAGTTATGCTGAGATTCTTACCTGCTCTGAGAGACCTAGGAGAAGCCCTTTAAAAGCAGGCAGTAGTGAGGACATCAGTAACTGTATCAGGGATACAATAGTACAAAAA... |
Task1_train_41690 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | TTGGGAGAGCACATATGAATGCCATGTTCTCAGAACCACATAGGAAGTGTTCTAGGGTAACAGAAATGGGGGTGGGGGCAGTCACGTAAGAAGCTTGGTGCTCTCTGGATGATTTGGGAGGACATGGGAATCCTACTATAGAGTTATGCTGAGATTCTTACCTGCTCTGAGAGACCTAGGAGAAGCCCTTTAAAAGCAGGCAGTAGTGAGGACATCAGTAACTGTATCAGGGATACAATAGTACAAAAAGACCTAGCTCTTAGATTCAGAACTCTCTGAAAACACTGAAAGAATATATGTACTCTCTTTCTCTCTAAGAT... | TTGGGAGAGCACATATGAATGCCATGTTCTCAGAACCACATAGGAAGTGTTCTAGGGTAACAGAAATGGGGGTGGGGGCAGTCACGTAAGAAGCTTGGTGCTCTCTGGATGATTTGGGAGGACATGGGAATCCTACTATAGAGTTATGCTGAGATTCTTACCTGCTCTGAGAGACCTAGGAGAAGCCCTTTAAAAGCAGGCAGTAGTGAGGACATCAGTAACTGTATCAGGGATACAATAGTACAAAAAGACCTAGCTCTTAGATTCAGAACTCTCTGAAAACACTGAAAGAATATATGTACTCTCTTTCTCTCTAAGAT... |
Task1_train_41691 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GTAAGAAGCTTGGTGCTCTCTGGATGATTTGGGAGGACATGGGAATCCTACTATAGAGTTATGCTGAGATTCTTACCTGCTCTGAGAGACCTAGGAGAAGCCCTTTAAAAGCAGGCAGTAGTGAGGACATCAGTAACTGTATCAGGGATACAATAGTACAAAAAGACCTAGCTCTTAGATTCAGAACTCTCTGAAAACACTGAAAGAATATATGTACTCTCTTTCTCTCTAAGATCAAAAACAGCAATTCCATAATACTGCTGCAAGGCACAATGTGGTAAGACTCACTGTGATTTATTGAGCAGTTATTACCTGCCAGT... | GTAAGAAGCTTGGTGCTCTCTGGATGATTTGGGAGGACATGGGAATCCTACTATAGAGTTATGCTGAGATTCTTACCTGCTCTGAGAGACCTAGGAGAAGCCCTTTAAAAGCAGGCAGTAGTGAGGACATCAGTAACTGTATCAGGGATACAATAGTACAAAAAGACCTAGCTCTTAGATTCAGAACTCTCTGAAAACACTGAAAGAATATATGTACTCTCTTTCTCTCTAAGATCAAAAACAGCAATTCCATAATACTGCTGCAAGGCACAATGTGGTAAGACTCACTGTGATTTATTGAGCAGTTATTACCTGCCAGT... |
Task1_train_41692 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | TTGGCACAAAGGAGCATTCTTGCTAAAGCATCTTTGAAATGCAGCTGCTGCAAATCTGAGGAGTTTGAGAAATGCTTTTCAGTTCTAGCAGCTGCCTTCTAGTTTTCTTTTACTCTTCATGCTATGCTAGGCAGAGTTGGCATGACCAGGATACCTGTGGTATTTAAATTAAACATTTATTTTGAGAAAAATTTATTTACACTTTAAATATATGTATTTATTTGGATGACAGATTATAAGGTTCATGGTCTGAGCCTTACCTACCCAGAGAGTGTACAGAGTCCATTTCATATACTTTAAGTCAAACAAACGAATGTGAC... | TTGGCACAAAGGAGCATTCTTGCTAAAGCATCTTTGAAATGCAGCTGCTGCAAATCTGAGGAGTTTGAGAAATGCTTTTCAGTTCTAGCAGCTGCCTTCTAGTTTTCTTTTACTCTTCATGCTATGCTAGGCAGAGTTGGCATGACCAGGATACCTGTGGTATTTAAATTAAACATTTATTTTGAGAAAAATTTATTTACACTTTAAATATATGTATTTATTTGGATGACAGATTATAAGGTTCATGGTCTGAGCCTTACCTACCCAGAGAGTGTACAGAGTCCATTTCATATACTTTAAGTCAAACAAACGAATGTGAC... |
Task1_train_41693 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | TAAAGCATCTTTGAAATGCAGCTGCTGCAAATCTGAGGAGTTTGAGAAATGCTTTTCAGTTCTAGCAGCTGCCTTCTAGTTTTCTTTTACTCTTCATGCTATGCTAGGCAGAGTTGGCATGACCAGGATACCTGTGGTATTTAAATTAAACATTTATTTTGAGAAAAATTTATTTACACTTTAAATATATGTATTTATTTGGATGACAGATTATAAGGTTCATGGTCTGAGCCTTACCTACCCAGAGAGTGTACAGAGTCCATTTCATATACTTTAAGTCAAACAAACGAATGTGACTTGCAGACATAGTCTAATTACAT... | TAAAGCATCTTTGAAATGCAGCTGCTGCAAATCTGAGGAGTTTGAGAAATGCTTTTCAGTTCTAGCAGCTGCCTTCTAGTTTTCTTTTACTCTTCATGCTATGCTAGGCAGAGTTGGCATGACCAGGATACCTGTGGTATTTAAATTAAACATTTATTTTGAGAAAAATTTATTTACACTTTAAATATATGTATTTATTTGGATGACAGATTATAAGGTTCATGGTCTGAGCCTTACCTACCCAGAGAGTGTACAGAGTCCATTTCATATACTTTAAGTCAAACAAACGAATGTGACTTGCAGACATAGTCTAATTACAT... |
Task1_train_41694 | This sequence change occurs on Chromosome 11. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | AGCATCTTTGAAATGCAGCTGCTGCAAATCTGAGGAGTTTGAGAAATGCTTTTCAGTTCTAGCAGCTGCCTTCTAGTTTTCTTTTACTCTTCATGCTATGCTAGGCAGAGTTGGCATGACCAGGATACCTGTGGTATTTAAATTAAACATTTATTTTGAGAAAAATTTATTTACACTTTAAATATATGTATTTATTTGGATGACAGATTATAAGGTTCATGGTCTGAGCCTTACCTACCCAGAGAGTGTACAGAGTCCATTTCATATACTTTAAGTCAAACAAACGAATGTGACTTGCAGACATAGTCTAATTACATGGG... | AGCATCTTTGAAATGCAGCTGCTGCAAATCTGAGGAGTTTGAGAAATGCTTTTCAGTTCTAGCAGCTGCCTTCTAGTTTTCTTTTACTCTTCATGCTATGCTAGGCAGAGTTGGCATGACCAGGATACCTGTGGTATTTAAATTAAACATTTATTTTGAGAAAAATTTATTTACACTTTAAATATATGTATTTATTTGGATGACAGATTATAAGGTTCATGGTCTGAGCCTTACCTACCCAGAGAGTGTACAGAGTCCATTTCATATACTTTAAGTCAAACAAACGAATGTGACTTGCAGACATAGTCTAATTACATGGG... |
Task1_train_41695 | A genomic variant on Chromosome 11 is under review. What is the biological outcome — benign or pathogenic? | Benign | ATCTTTGAAATGCAGCTGCTGCAAATCTGAGGAGTTTGAGAAATGCTTTTCAGTTCTAGCAGCTGCCTTCTAGTTTTCTTTTACTCTTCATGCTATGCTAGGCAGAGTTGGCATGACCAGGATACCTGTGGTATTTAAATTAAACATTTATTTTGAGAAAAATTTATTTACACTTTAAATATATGTATTTATTTGGATGACAGATTATAAGGTTCATGGTCTGAGCCTTACCTACCCAGAGAGTGTACAGAGTCCATTTCATATACTTTAAGTCAAACAAACGAATGTGACTTGCAGACATAGTCTAATTACATGGGAAA... | ATCTTTGAAATGCAGCTGCTGCAAATCTGAGGAGTTTGAGAAATGCTTTTCAGTTCTAGCAGCTGCCTTCTAGTTTTCTTTTACTCTTCATGCTATGCTAGGCAGAGTTGGCATGACCAGGATACCTGTGGTATTTAAATTAAACATTTATTTTGAGAAAAATTTATTTACACTTTAAATATATGTATTTATTTGGATGACAGATTATAAGGTTCATGGTCTGAGCCTTACCTACCCAGAGAGTGTACAGAGTCCATTTCATATACTTTAAGTCAAACAAACGAATGTGACTTGCAGACATAGTCTAATTACATGGGAAA... |
Task1_train_41696 | With a mutation on Chromosome 11, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CTGCTGCAAATCTGAGGAGTTTGAGAAATGCTTTTCAGTTCTAGCAGCTGCCTTCTAGTTTTCTTTTACTCTTCATGCTATGCTAGGCAGAGTTGGCATGACCAGGATACCTGTGGTATTTAAATTAAACATTTATTTTGAGAAAAATTTATTTACACTTTAAATATATGTATTTATTTGGATGACAGATTATAAGGTTCATGGTCTGAGCCTTACCTACCCAGAGAGTGTACAGAGTCCATTTCATATACTTTAAGTCAAACAAACGAATGTGACTTGCAGACATAGTCTAATTACATGGGAAATATTATCTAGTACTT... | CTGCTGCAAATCTGAGGAGTTTGAGAAATGCTTTTCAGTTCTAGCAGCTGCCTTCTAGTTTTCTTTTACTCTTCATGCTATGCTAGGCAGAGTTGGCATGACCAGGATACCTGTGGTATTTAAATTAAACATTTATTTTGAGAAAAATTTATTTACACTTTAAATATATGTATTTATTTGGATGACAGATTATAAGGTTCATGGTCTGAGCCTTACCTACCCAGAGAGTGTACAGAGTCCATTTCATATACTTTAAGTCAAACAAACGAATGTGACTTGCAGACATAGTCTAATTACATGGGAAATATTATCTAGTACTT... |
Task1_train_41697 | A mutation on Chromosome 11 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GAAATGCTTTTCAGTTCTAGCAGCTGCCTTCTAGTTTTCTTTTACTCTTCATGCTATGCTAGGCAGAGTTGGCATGACCAGGATACCTGTGGTATTTAAATTAAACATTTATTTTGAGAAAAATTTATTTACACTTTAAATATATGTATTTATTTGGATGACAGATTATAAGGTTCATGGTCTGAGCCTTACCTACCCAGAGAGTGTACAGAGTCCATTTCATATACTTTAAGTCAAACAAACGAATGTGACTTGCAGACATAGTCTAATTACATGGGAAATATTATCTAGTACTTTATTCTAAATTAAGGGATACTCTT... | GAAATGCTTTTCAGTTCTAGCAGCTGCCTTCTAGTTTTCTTTTACTCTTCATGCTATGCTAGGCAGAGTTGGCATGACCAGGATACCTGTGGTATTTAAATTAAACATTTATTTTGAGAAAAATTTATTTACACTTTAAATATATGTATTTATTTGGATGACAGATTATAAGGTTCATGGTCTGAGCCTTACCTACCCAGAGAGTGTACAGAGTCCATTTCATATACTTTAAGTCAAACAAACGAATGTGACTTGCAGACATAGTCTAATTACATGGGAAATATTATCTAGTACTTTATTCTAAATTAAGGGATACTCTT... |
Task1_train_41698 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | CCTAATGCTGATGCCACTAGACTTGGGGATGATGGCTCACACTAAGAAAGACTGATACATAAACCAAAATTGCAGGGTATTAATTTACAATGAAAACTCTGTCTGTCATGCCTTCCAAAAGCGCCTGTGCTAGTACTACCAATGTATTCTTTGTTTATATATAATTCTATTTGGGAAATCGCATTATGTTTAAGAAGTTACTTGGTGCACATGGACTAAGGCAGGGCAAGAACTCTCCATTTAGAAGTGCAGGAGGCACACTTCCTTTCTCTAAGAATAGTCTTGCTAGGGGAGATATGGTACCAGCACATCATTAGGTA... | CCTAATGCTGATGCCACTAGACTTGGGGATGATGGCTCACACTAAGAAAGACTGATACATAAACCAAAATTGCAGGGTATTAATTTACAATGAAAACTCTGTCTGTCATGCCTTCCAAAAGCGCCTGTGCTAGTACTACCAATGTATTCTTTGTTTATATATAATTCTATTTGGGAAATCGCATTATGTTTAAGAAGTTACTTGGTGCACATGGACTAAGGCAGGGCAAGAACTCTCCATTTAGAAGTGCAGGAGGCACACTTCCTTTCTCTAAGAATAGTCTTGCTAGGGGAGATATGGTACCAGCACATCATTAGGTA... |
Task1_train_41699 | This sequence change occurs on Chromosome 11. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CTTGGGGATGATGGCTCACACTAAGAAAGACTGATACATAAACCAAAATTGCAGGGTATTAATTTACAATGAAAACTCTGTCTGTCATGCCTTCCAAAAGCGCCTGTGCTAGTACTACCAATGTATTCTTTGTTTATATATAATTCTATTTGGGAAATCGCATTATGTTTAAGAAGTTACTTGGTGCACATGGACTAAGGCAGGGCAAGAACTCTCCATTTAGAAGTGCAGGAGGCACACTTCCTTTCTCTAAGAATAGTCTTGCTAGGGGAGATATGGTACCAGCACATCATTAGGTAGGAACTGGTGTTAGTTTCTAT... | CTTGGGGATGATGGCTCACACTAAGAAAGACTGATACATAAACCAAAATTGCAGGGTATTAATTTACAATGAAAACTCTGTCTGTCATGCCTTCCAAAAGCGCCTGTGCTAGTACTACCAATGTATTCTTTGTTTATATATAATTCTATTTGGGAAATCGCATTATGTTTAAGAAGTTACTTGGTGCACATGGACTAAGGCAGGGCAAGAACTCTCCATTTAGAAGTGCAGGAGGCACACTTCCTTTCTCTAAGAATAGTCTTGCTAGGGGAGATATGGTACCAGCACATCATTAGGTAGGAACTGGTGTTAGTTTCTAT... |
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