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_41200 | 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 | ACACCCATGAATAACTATACTTGAATTGATGTGCACACTTTCTGGCATTTATCCAGAAATAAATAAAAAGAATGAAAGCAGCCAGGTGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGCGGATCACCTAAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAGCCCCGTCTCTACTAAAGATACAAAAAATTAGCTAGGCATGCAGCATGCACCTGTAATCCCAGCTCGGGAGGCTGGGGCAGGAAAATTGCTTGAACCTGGGAGGCAGAGGTTGCAGTGTGCTGAGATGGCACCAC... | ACACCCATGAATAACTATACTTGAATTGATGTGCACACTTTCTGGCATTTATCCAGAAATAAATAAAAAGAATGAAAGCAGCCAGGTGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGCGGATCACCTAAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAGCCCCGTCTCTACTAAAGATACAAAAAATTAGCTAGGCATGCAGCATGCACCTGTAATCCCAGCTCGGGAGGCTGGGGCAGGAAAATTGCTTGAACCTGGGAGGCAGAGGTTGCAGTGTGCTGAGATGGCACCAC... |
Task1_train_41201 | This genomic variant is located on Chromosome 11. Can you determine its pathogenicity and name any linked disease? | Benign | TTGGGAGGCCAAGGTGGGCGGATCACCTAAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAGCCCCGTCTCTACTAAAGATACAAAAAATTAGCTAGGCATGCAGCATGCACCTGTAATCCCAGCTCGGGAGGCTGGGGCAGGAAAATTGCTTGAACCTGGGAGGCAGAGGTTGCAGTGTGCTGAGATGGCACCACTGCACTCCAGCCTGGGCAACAGGGCAAGATTCCATCTCCAAAAATAAAAAAGAATGAAAGCTAGAGACAGTAGGAGTGACAGAGAGTTTAGTTTTTTCAAGGAGTCCACAATTTACA... | TTGGGAGGCCAAGGTGGGCGGATCACCTAAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAGCCCCGTCTCTACTAAAGATACAAAAAATTAGCTAGGCATGCAGCATGCACCTGTAATCCCAGCTCGGGAGGCTGGGGCAGGAAAATTGCTTGAACCTGGGAGGCAGAGGTTGCAGTGTGCTGAGATGGCACCACTGCACTCCAGCCTGGGCAACAGGGCAAGATTCCATCTCCAAAAATAAAAAAGAATGAAAGCTAGAGACAGTAGGAGTGACAGAGAGTTTAGTTTTTTCAAGGAGTCCACAATTTACA... |
Task1_train_41202 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GGAACAGCCTGGGAGGCAATCTGTTCTGAAGCAAGCAAGGAGCAAGCGGGGATTCCAGGAGGAGGGAGGGAGACCCGCGTCTGCCGCAGATTGATGGCTGTGTCCTTGGAACGGAGTGAGTAGGCTCCTGGGGCCTGTGGGAGTGCGAGGGGGAGACCTGGGGCTTAGAAAAATGAGTCTGCATGAAGGGGAGCTGGGGTGATTTCCAGGTGGGCGGGATTGAGGCTTGAAGCGGTAGGAAAATAGGCAGCGCCAGGCCGAGGGTGAGGGGAGGACCGAGGACAGCAGGTGGGCAAGGGAGAAGCGAGAGGGCGCGGGGC... | GGAACAGCCTGGGAGGCAATCTGTTCTGAAGCAAGCAAGGAGCAAGCGGGGATTCCAGGAGGAGGGAGGGAGACCCGCGTCTGCCGCAGATTGATGGCTGTGTCCTTGGAACGGAGTGAGTAGGCTCCTGGGGCCTGTGGGAGTGCGAGGGGGAGACCTGGGGCTTAGAAAAATGAGTCTGCATGAAGGGGAGCTGGGGTGATTTCCAGGTGGGCGGGATTGAGGCTTGAAGCGGTAGGAAAATAGGCAGCGCCAGGCCGAGGGTGAGGGGAGGACCGAGGACAGCAGGTGGGCAAGGGAGAAGCGAGAGGGCGCGGGGC... |
Task1_train_41203 | An alteration has been detected on Chromosome 11. Is it pathogenic, and if so, what disease is involved? | Benign | AGTCCTGCGCCCTCCCCTCGTCCCTGCAGTCCTCAATGCAGCCTCAGTGGTTCCCTGTGCTCCGTCACCACCCCGTCAACAGCCTGAGTCGTCAGGAAGCTCCACTTCCTCAAATCCCCCTGGGCATCTCACTGGGCCCATCTTCCTCTCTCCCTTCTCCTCCTCCATCCCAAATGCCTCTCCAGAGTCCCCAAGACCACCATGATATGCTCTAGCCCCTTCCTGCTCCTCTCCTCCCACCACCAACCCCTTCCACTTATAAAAGCCCCTGCCCCACACTTCCCTTGCCTTCCCCACATACCCAGTGAGAAGCTCCCACT... | AGTCCTGCGCCCTCCCCTCGTCCCTGCAGTCCTCAATGCAGCCTCAGTGGTTCCCTGTGCTCCGTCACCACCCCGTCAACAGCCTGAGTCGTCAGGAAGCTCCACTTCCTCAAATCCCCCTGGGCATCTCACTGGGCCCATCTTCCTCTCTCCCTTCTCCTCCTCCATCCCAAATGCCTCTCCAGAGTCCCCAAGACCACCATGATATGCTCTAGCCCCTTCCTGCTCCTCTCCTCCCACCACCAACCCCTTCCACTTATAAAAGCCCCTGCCCCACACTTCCCTTGCCTTCCCCACATACCCAGTGAGAAGCTCCCACT... |
Task1_train_41204 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | GCAGCCCCCAGAGGCCCCCTGGCTCCTCCTTTCCTGCAGCCCCGCCCCTTGCAGCCCAGGCCCGGCTTGAGAAATAAATTTCGAAAGCCACCTGGCCCCCGGCCCTTAAATTCAGAGGCAGCCTGGTAGGAGAAAGGGCACTGGGCCGGGAAACGGCGCTGGCCCGGGCCCAGCCACCAACTTGCTGGATAACTGCACAAGGCTAACCTCCTCTGAGGCCCAGCTGCCTGTCTACAAAGCAGGTCTGGAGCTCAATGTTAATAACGTTTGTAAAAGCCAACACTTCTTAAGCACTTAGGATGAGCCAGGCACTATTCTTA... | GCAGCCCCCAGAGGCCCCCTGGCTCCTCCTTTCCTGCAGCCCCGCCCCTTGCAGCCCAGGCCCGGCTTGAGAAATAAATTTCGAAAGCCACCTGGCCCCCGGCCCTTAAATTCAGAGGCAGCCTGGTAGGAGAAAGGGCACTGGGCCGGGAAACGGCGCTGGCCCGGGCCCAGCCACCAACTTGCTGGATAACTGCACAAGGCTAACCTCCTCTGAGGCCCAGCTGCCTGTCTACAAAGCAGGTCTGGAGCTCAATGTTAATAACGTTTGTAAAAGCCAACACTTCTTAAGCACTTAGGATGAGCCAGGCACTATTCTTA... |
Task1_train_41205 | Assess the clinical impact of this variant found on Chromosome 11. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CAGCCCAGGCCCGGCTTGAGAAATAAATTTCGAAAGCCACCTGGCCCCCGGCCCTTAAATTCAGAGGCAGCCTGGTAGGAGAAAGGGCACTGGGCCGGGAAACGGCGCTGGCCCGGGCCCAGCCACCAACTTGCTGGATAACTGCACAAGGCTAACCTCCTCTGAGGCCCAGCTGCCTGTCTACAAAGCAGGTCTGGAGCTCAATGTTAATAACGTTTGTAAAAGCCAACACTTCTTAAGCACTTAGGATGAGCCAGGCACTATTCTTAGCACTTTAGACATTACAGCTCATTGAACCCTTGCCAACACCCTTGGAGGTA... | CAGCCCAGGCCCGGCTTGAGAAATAAATTTCGAAAGCCACCTGGCCCCCGGCCCTTAAATTCAGAGGCAGCCTGGTAGGAGAAAGGGCACTGGGCCGGGAAACGGCGCTGGCCCGGGCCCAGCCACCAACTTGCTGGATAACTGCACAAGGCTAACCTCCTCTGAGGCCCAGCTGCCTGTCTACAAAGCAGGTCTGGAGCTCAATGTTAATAACGTTTGTAAAAGCCAACACTTCTTAAGCACTTAGGATGAGCCAGGCACTATTCTTAGCACTTTAGACATTACAGCTCATTGAACCCTTGCCAACACCCTTGGAGGTA... |
Task1_train_41206 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TTCCAGGATTTTTCCGAACTGGAGTAATCCCCAAAGTGAGCAATAAAGAAACGAGAGTCAGGAAATGCTGTGGGAAGTCTGGATTTATGAGCAGGAGAGGTTGGGGGACGGGAGGGAGCTGCTGGCAGGGTCTCCGTGCCGCTGGCTTAGAAGGAGCAGACGAAGGGCAGTTGCTTGTCGCATTGAGCTCGTCGCCAATAACCTCCTAGCAGCACAGAGCACAGTGAAGTCCACCGCCCTGCGGGGTCTGGCCTGGGCTTCACCTCTTTCCCTCCTCAGGGGCCCCCTATGTCCCCATCTATGGCCATCGTCATCTGCCA... | TTCCAGGATTTTTCCGAACTGGAGTAATCCCCAAAGTGAGCAATAAAGAAACGAGAGTCAGGAAATGCTGTGGGAAGTCTGGATTTATGAGCAGGAGAGGTTGGGGGACGGGAGGGAGCTGCTGGCAGGGTCTCCGTGCCGCTGGCTTAGAAGGAGCAGACGAAGGGCAGTTGCTTGTCGCATTGAGCTCGTCGCCAATAACCTCCTAGCAGCACAGAGCACAGTGAAGTCCACCGCCCTGCGGGGTCTGGCCTGGGCTTCACCTCTTTCCCTCCTCAGGGGCCCCCTATGTCCCCATCTATGGCCATCGTCATCTGCCA... |
Task1_train_41207 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | AAAGTGCTGGGATTACAGACATGAGCCACCGTGCCCGGCCAAGAAAAATTTTTCAATGGATGTACAATGTGCTCCTATAAAGCACACTATAGAGTGGACTGCTCAGGGAAACTTCACAGTGAATGCACCAATGTAAACATGCCTAGGTCGAGATACAGGATGGGACTAGGAGCCCTGCAGCTTCCTTCGTGCCCCTTCTTGATATTACTCCCCCAAAGAAGATCTCTGTGGACTGGAAGTCAAACTTCTGTCAAAGTACACACCCACAGCGGCAGAGATTTATGAGGAACAAGACAAAGTTCACCTAACATTTAGCACAG... | AAAGTGCTGGGATTACAGACATGAGCCACCGTGCCCGGCCAAGAAAAATTTTTCAATGGATGTACAATGTGCTCCTATAAAGCACACTATAGAGTGGACTGCTCAGGGAAACTTCACAGTGAATGCACCAATGTAAACATGCCTAGGTCGAGATACAGGATGGGACTAGGAGCCCTGCAGCTTCCTTCGTGCCCCTTCTTGATATTACTCCCCCAAAGAAGATCTCTGTGGACTGGAAGTCAAACTTCTGTCAAAGTACACACCCACAGCGGCAGAGATTTATGAGGAACAAGACAAAGTTCACCTAACATTTAGCACAG... |
Task1_train_41208 | 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 | AATCCCAGCACTTTGGGAGGCTGAGGTGGGTGGATCACCTGAGGTCAGGAGTTCGAGACTAGCCTGACCAACATGGAGAAACCCCGTCTCTACTAAAAATACAAAATTAGCCAGGCGTGATGGTGCCTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAGCCTGGGAGGCGGAGGTTGCGGTGAGCTGAGATGGCACCATTGCACTCCAGCCTGGGCAACAAGAGTGAAACTCCATCTTAAGGAAGGAAGGAAGGAAAGAAAGGGAGAGAGAAAGAAAGAAGGAAAGAAATAGAAACAACAAA... | AATCCCAGCACTTTGGGAGGCTGAGGTGGGTGGATCACCTGAGGTCAGGAGTTCGAGACTAGCCTGACCAACATGGAGAAACCCCGTCTCTACTAAAAATACAAAATTAGCCAGGCGTGATGGTGCCTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAGCCTGGGAGGCGGAGGTTGCGGTGAGCTGAGATGGCACCATTGCACTCCAGCCTGGGCAACAAGAGTGAAACTCCATCTTAAGGAAGGAAGGAAGGAAAGAAAGGGAGAGAGAAAGAAAGAAGGAAAGAAATAGAAACAACAAA... |
Task1_train_41209 | 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 | GTGCGATCTCTGCTCACTGCAAGATCCGCCTCCCAGATTCACGCCATGCCATTCTCTCGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCCCGCCACCACGCCTGGCTAATTTTGTTTTTGTATTTTTAGTAGAGACGGGGTTTCACTGTGTTAACCAGGATGGTCACAATCTCCGGACCTTGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGTCACCGCGCCCAGCCCAGAGACTCCATTTTCTAACCTTTGTTTTTTTGTTTGTTTGTTTTTGAGACGGAGCCTCACTCTGTCACCC... | GTGCGATCTCTGCTCACTGCAAGATCCGCCTCCCAGATTCACGCCATGCCATTCTCTCGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCCCGCCACCACGCCTGGCTAATTTTGTTTTTGTATTTTTAGTAGAGACGGGGTTTCACTGTGTTAACCAGGATGGTCACAATCTCCGGACCTTGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGTCACCGCGCCCAGCCCAGAGACTCCATTTTCTAACCTTTGTTTTTTTGTTTGTTTGTTTTTGAGACGGAGCCTCACTCTGTCACCC... |
Task1_train_41210 | Assess the clinical impact of this variant found on Chromosome 11. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | ATCTATTTCTCAGACAGCTTATTCATCCGGCTGGTACGCTGCTGCTGGCTGTCAGTGGAAGCTTGGCCAGGCTGAGGCCTGAGGGACTTAGTTCCTCTCCACCTAGGCCTTTCCACAGGCTGGATAGGCTTCCTCACACTACTGTCACTGGGTTTCAAGAAGCAAGAAGAGGAAACTGGGGTTTCCAAGTCCCGGGCCTGGAACCTGGCACAGCATCACTTCCCCCTTATTCTGTTGTTAAGCAGTCACAGAACCCAGATTCAATGGGAATAGCCATAGACCTCACTTTTGGATGGGAAGAGTGTTCAAGAATTTGGGGC... | ATCTATTTCTCAGACAGCTTATTCATCCGGCTGGTACGCTGCTGCTGGCTGTCAGTGGAAGCTTGGCCAGGCTGAGGCCTGAGGGACTTAGTTCCTCTCCACCTAGGCCTTTCCACAGGCTGGATAGGCTTCCTCACACTACTGTCACTGGGTTTCAAGAAGCAAGAAGAGGAAACTGGGGTTTCCAAGTCCCGGGCCTGGAACCTGGCACAGCATCACTTCCCCCTTATTCTGTTGTTAAGCAGTCACAGAACCCAGATTCAATGGGAATAGCCATAGACCTCACTTTTGGATGGGAAGAGTGTTCAAGAATTTGGGGC... |
Task1_train_41211 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TTCCCCCTTATTCTGTTGTTAAGCAGTCACAGAACCCAGATTCAATGGGAATAGCCATAGACCTCACTTTTGGATGGGAAGAGTGTTCAAGAATTTGGGGCTGTATTTTAAAACTGGCACAAAAATGGAGATATTATATTTTCTCATTTAATTCTAAAATGAGATAGGAAGTAATCTCTTTGGAACTCTTGTATTATCTGTTTTTTAAAAAATGGGATTATTTAGTGATTCACTCATGGTCACATATTTCAAGTTGATATTGGAGCTTAAATTCAAACCCAGTGTGGATTCAAACCCAATTATGTTGATTCTATCTCTTA... | TTCCCCCTTATTCTGTTGTTAAGCAGTCACAGAACCCAGATTCAATGGGAATAGCCATAGACCTCACTTTTGGATGGGAAGAGTGTTCAAGAATTTGGGGCTGTATTTTAAAACTGGCACAAAAATGGAGATATTATATTTTCTCATTTAATTCTAAAATGAGATAGGAAGTAATCTCTTTGGAACTCTTGTATTATCTGTTTTTTAAAAAATGGGATTATTTAGTGATTCACTCATGGTCACATATTTCAAGTTGATATTGGAGCTTAAATTCAAACCCAGTGTGGATTCAAACCCAATTATGTTGATTCTATCTCTTA... |
Task1_train_41212 | This is a variant located on Chromosome 11. Is this mutation a likely cause of disease or not? | Benign | TTTTTTTTTGACATTAAGTCTTGCTCTGTTGCCCAGGCTAGAGTGCAGTGGCATAATCTCAGCTCACTGCAACCTCTGCCTCCTGGATTCAAGTGATTCTCCTGCCTCAGCCTCTTGAGTAGCTGGGATTACAGGTGCCCACCACCACGCTGGGCTAACTTTTGTACTTTTAATAGAGACAGGGTTTCACAATGTTGGCCAGGCTGATCTTGAACACCCAACCTCAGGTGAGCTGCCTGCCTTAGACTCCCAAAGTGCTGGGATTACACATATGAGCCACCGGGCCCGGCCTCTGGCTCTTATCTTGTTCCCCTCCAAAC... | TTTTTTTTTGACATTAAGTCTTGCTCTGTTGCCCAGGCTAGAGTGCAGTGGCATAATCTCAGCTCACTGCAACCTCTGCCTCCTGGATTCAAGTGATTCTCCTGCCTCAGCCTCTTGAGTAGCTGGGATTACAGGTGCCCACCACCACGCTGGGCTAACTTTTGTACTTTTAATAGAGACAGGGTTTCACAATGTTGGCCAGGCTGATCTTGAACACCCAACCTCAGGTGAGCTGCCTGCCTTAGACTCCCAAAGTGCTGGGATTACACATATGAGCCACCGGGCCCGGCCTCTGGCTCTTATCTTGTTCCCCTCCAAAC... |
Task1_train_41213 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | CTGGAGAATCACCTCAGGAACCAATTAGGGTGTAATACTGGGACAGCGAATATAAGAAGCACATCAGCAAGGTTTCATGATAGATTGGAAGCTCAGGGAGAAAGGCTGGTCCCCTAGTCTTGTTATCTCAAAGTAAGTCTAGAAAAATCTAAGGAAACACTAGTGTCAGGGATATATTGTTTTGTCAAGGGGTAGAGGAAAGAGAGAGACTCCTAGAAGTGAGACTAAAACACAGAAGTATTGGAAGTGACCCCATCTCATCAGGTTGCTATGATTATGGGGTTATCTGCAATTTTATTTACGGAAAGGGAACAAAGGCA... | CTGGAGAATCACCTCAGGAACCAATTAGGGTGTAATACTGGGACAGCGAATATAAGAAGCACATCAGCAAGGTTTCATGATAGATTGGAAGCTCAGGGAGAAAGGCTGGTCCCCTAGTCTTGTTATCTCAAAGTAAGTCTAGAAAAATCTAAGGAAACACTAGTGTCAGGGATATATTGTTTTGTCAAGGGGTAGAGGAAAGAGAGAGACTCCTAGAAGTGAGACTAAAACACAGAAGTATTGGAAGTGACCCCATCTCATCAGGTTGCTATGATTATGGGGTTATCTGCAATTTTATTTACGGAAAGGGAACAAAGGCA... |
Task1_train_41214 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | AAATTCTGTTTTACAAAAAATGGGTTTTTATGATACATGCTGTTATAAAACTTTCTTTGTTCATATTAGACCAATTGCAAGATCACAGAAAAAAGAAGCTGAGAGATTAGCAACATGACTTGCCTTGCAGTGAATTAGCTGCAGAGTTGGTCTAGATTCCATGTCTCTTGATTACAAATCTGGGACCCTTTCTACTGCTCCACATGGAATAATGAAGGCAGAGTTCTGTGCTGTTCCATGTTGGAGCTACGGATGAAACAGGATGGGTATTGAGGTACTTGAGGAAGGCTAGAACTGTTGAGAGGTTTATTTGGTAGCCC... | AAATTCTGTTTTACAAAAAATGGGTTTTTATGATACATGCTGTTATAAAACTTTCTTTGTTCATATTAGACCAATTGCAAGATCACAGAAAAAAGAAGCTGAGAGATTAGCAACATGACTTGCCTTGCAGTGAATTAGCTGCAGAGTTGGTCTAGATTCCATGTCTCTTGATTACAAATCTGGGACCCTTTCTACTGCTCCACATGGAATAATGAAGGCAGAGTTCTGTGCTGTTCCATGTTGGAGCTACGGATGAAACAGGATGGGTATTGAGGTACTTGAGGAAGGCTAGAACTGTTGAGAGGTTTATTTGGTAGCCC... |
Task1_train_41215 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | AATTCTGTTTTACAAAAAATGGGTTTTTATGATACATGCTGTTATAAAACTTTCTTTGTTCATATTAGACCAATTGCAAGATCACAGAAAAAAGAAGCTGAGAGATTAGCAACATGACTTGCCTTGCAGTGAATTAGCTGCAGAGTTGGTCTAGATTCCATGTCTCTTGATTACAAATCTGGGACCCTTTCTACTGCTCCACATGGAATAATGAAGGCAGAGTTCTGTGCTGTTCCATGTTGGAGCTACGGATGAAACAGGATGGGTATTGAGGTACTTGAGGAAGGCTAGAACTGTTGAGAGGTTTATTTGGTAGCCCA... | AATTCTGTTTTACAAAAAATGGGTTTTTATGATACATGCTGTTATAAAACTTTCTTTGTTCATATTAGACCAATTGCAAGATCACAGAAAAAAGAAGCTGAGAGATTAGCAACATGACTTGCCTTGCAGTGAATTAGCTGCAGAGTTGGTCTAGATTCCATGTCTCTTGATTACAAATCTGGGACCCTTTCTACTGCTCCACATGGAATAATGAAGGCAGAGTTCTGTGCTGTTCCATGTTGGAGCTACGGATGAAACAGGATGGGTATTGAGGTACTTGAGGAAGGCTAGAACTGTTGAGAGGTTTATTTGGTAGCCCA... |
Task1_train_41216 | A mutation is present on Chromosome 11. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TTGGCAGGGCAGGTAGGTCGGAGTTGGAAGCCAGGAAGGTGGGCAGTTAAAAAAAAGTATCACTTTGTTTTTAGTGTCTACTATATACTACATAGCTGTTGGGGACAGAGTCAGAACTCTAACTGATACATTTATACATAAACTCTGTGGTTTTCCACTGAAATAATTGAAGTCATCTGGAGTCATATTTCCTAAAACATATTTGTGCAATGCTAGTTCCGCGAACAACTGTGATGAATTGGGTTCTGTATGATGGAAATAATTGAATTTCAATTATTTCAAGTTTAGTCTTGAGAAATGCTGTGTACCATCTTACCCTC... | TTGGCAGGGCAGGTAGGTCGGAGTTGGAAGCCAGGAAGGTGGGCAGTTAAAAAAAAGTATCACTTTGTTTTTAGTGTCTACTATATACTACATAGCTGTTGGGGACAGAGTCAGAACTCTAACTGATACATTTATACATAAACTCTGTGGTTTTCCACTGAAATAATTGAAGTCATCTGGAGTCATATTTCCTAAAACATATTTGTGCAATGCTAGTTCCGCGAACAACTGTGATGAATTGGGTTCTGTATGATGGAAATAATTGAATTTCAATTATTTCAAGTTTAGTCTTGAGAAATGCTGTGTACCATCTTACCCTC... |
Task1_train_41217 | Consider this mutation on Chromosome 11. Is this a benign change or a disease-causing variant? | Benign | AATGCCTTTCAGTTTTCAGGAATTTCAGAGACGAAGATTGTCTCTTTTCTGGCCTCTGAATGGAAAGAAAATCTTTGAGAGATAAGTGATGTTGGAGATAGGTAGAAGAGAGGGATAAAGTGAGAGGGAGACAAATGTCTCTTTGTTCCCAAGCTGATATTATTTCCAATAAATCACAAGGAAAATCATACTAGGTCCAGTCTCTCTTCCCTTCTCCTGGATGACACCTTGTGAGAGCCGTTTACCTTTCTGGCCACTTAAGGTTTTAAAAATGTTTAACTGATACTGAAGACCCATTTCCAGGTATTAAAAAACCAAGT... | AATGCCTTTCAGTTTTCAGGAATTTCAGAGACGAAGATTGTCTCTTTTCTGGCCTCTGAATGGAAAGAAAATCTTTGAGAGATAAGTGATGTTGGAGATAGGTAGAAGAGAGGGATAAAGTGAGAGGGAGACAAATGTCTCTTTGTTCCCAAGCTGATATTATTTCCAATAAATCACAAGGAAAATCATACTAGGTCCAGTCTCTCTTCCCTTCTCCTGGATGACACCTTGTGAGAGCCGTTTACCTTTCTGGCCACTTAAGGTTTTAAAAATGTTTAACTGATACTGAAGACCCATTTCCAGGTATTAAAAAACCAAGT... |
Task1_train_41218 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TGTTCCCAAGCTGATATTATTTCCAATAAATCACAAGGAAAATCATACTAGGTCCAGTCTCTCTTCCCTTCTCCTGGATGACACCTTGTGAGAGCCGTTTACCTTTCTGGCCACTTAAGGTTTTAAAAATGTTTAACTGATACTGAAGACCCATTTCCAGGTATTAAAAAACCAAGTCCAGCCCAATTTTAAACTTCAGCTTCACTATCAATTCAAAGCATGGGTCCTCCCTTGTGAGCTCAGATCTGATGTGTAGCTTGGGTCATACAGTGGAAAGGTGGGAGCATATGTTCTTCCCTTGCTCTTTGGCCTCTCTTCCC... | TGTTCCCAAGCTGATATTATTTCCAATAAATCACAAGGAAAATCATACTAGGTCCAGTCTCTCTTCCCTTCTCCTGGATGACACCTTGTGAGAGCCGTTTACCTTTCTGGCCACTTAAGGTTTTAAAAATGTTTAACTGATACTGAAGACCCATTTCCAGGTATTAAAAAACCAAGTCCAGCCCAATTTTAAACTTCAGCTTCACTATCAATTCAAAGCATGGGTCCTCCCTTGTGAGCTCAGATCTGATGTGTAGCTTGGGTCATACAGTGGAAAGGTGGGAGCATATGTTCTTCCCTTGCTCTTTGGCCTCTCTTCCC... |
Task1_train_41219 | A genetic alteration is present on Chromosome 11. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TCTCCTGGATGACACCTTGTGAGAGCCGTTTACCTTTCTGGCCACTTAAGGTTTTAAAAATGTTTAACTGATACTGAAGACCCATTTCCAGGTATTAAAAAACCAAGTCCAGCCCAATTTTAAACTTCAGCTTCACTATCAATTCAAAGCATGGGTCCTCCCTTGTGAGCTCAGATCTGATGTGTAGCTTGGGTCATACAGTGGAAAGGTGGGAGCATATGTTCTTCCCTTGCTCTTTGGCCTCTCTTCCCACAAACCCGTTGTTGTTACTATTGTTGTTGTTGTTTTAGTCATTTTGGTCTTTCCTTCTTTTTCAGTTT... | TCTCCTGGATGACACCTTGTGAGAGCCGTTTACCTTTCTGGCCACTTAAGGTTTTAAAAATGTTTAACTGATACTGAAGACCCATTTCCAGGTATTAAAAAACCAAGTCCAGCCCAATTTTAAACTTCAGCTTCACTATCAATTCAAAGCATGGGTCCTCCCTTGTGAGCTCAGATCTGATGTGTAGCTTGGGTCATACAGTGGAAAGGTGGGAGCATATGTTCTTCCCTTGCTCTTTGGCCTCTCTTCCCACAAACCCGTTGTTGTTACTATTGTTGTTGTTGTTTTAGTCATTTTGGTCTTTCCTTCTTTTTCAGTTT... |
Task1_train_41220 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TAACTGATACTGAAGACCCATTTCCAGGTATTAAAAAACCAAGTCCAGCCCAATTTTAAACTTCAGCTTCACTATCAATTCAAAGCATGGGTCCTCCCTTGTGAGCTCAGATCTGATGTGTAGCTTGGGTCATACAGTGGAAAGGTGGGAGCATATGTTCTTCCCTTGCTCTTTGGCCTCTCTTCCCACAAACCCGTTGTTGTTACTATTGTTGTTGTTGTTTTAGTCATTTTGGTCTTTCCTTCTTTTTCAGTTTTATCAGGTCAAGGAGGAAGAACAGGAGTGGGAAAAAAGGCAAAAGTGTTCATATCTGTTGCCAT... | TAACTGATACTGAAGACCCATTTCCAGGTATTAAAAAACCAAGTCCAGCCCAATTTTAAACTTCAGCTTCACTATCAATTCAAAGCATGGGTCCTCCCTTGTGAGCTCAGATCTGATGTGTAGCTTGGGTCATACAGTGGAAAGGTGGGAGCATATGTTCTTCCCTTGCTCTTTGGCCTCTCTTCCCACAAACCCGTTGTTGTTACTATTGTTGTTGTTGTTTTAGTCATTTTGGTCTTTCCTTCTTTTTCAGTTTTATCAGGTCAAGGAGGAAGAACAGGAGTGGGAAAAAAGGCAAAAGTGTTCATATCTGTTGCCAT... |
Task1_train_41221 | Chromosome 11 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AGGAGGAAGAACAGGAGTGGGAAAAAAGGCAAAAGTGTTCATATCTGTTGCCATAGATACTAGCAGCTTGTGCCTTATATGTGGCAGGCCTGGTGTCTCTTGAGACCATTTTGGGGTTCGTCAGGGGCTCCCGTTTGGGACTGCCTCATTATGCGGTTCCCTGACAAGGGCAATGAATTATGTCCCTGATCTCTTTAAGATCTCTCTTTCATAAGAGACCCACCTCATGGTTTCTTATTGCTACAGCCTCCTCTGCCCTGATAGGCTGTTTCTGGATTGGAATCTCAACAAGGTGACTTGACTCCAATGACCTCCTATAG... | AGGAGGAAGAACAGGAGTGGGAAAAAAGGCAAAAGTGTTCATATCTGTTGCCATAGATACTAGCAGCTTGTGCCTTATATGTGGCAGGCCTGGTGTCTCTTGAGACCATTTTGGGGTTCGTCAGGGGCTCCCGTTTGGGACTGCCTCATTATGCGGTTCCCTGACAAGGGCAATGAATTATGTCCCTGATCTCTTTAAGATCTCTCTTTCATAAGAGACCCACCTCATGGTTTCTTATTGCTACAGCCTCCTCTGCCCTGATAGGCTGTTTCTGGATTGGAATCTCAACAAGGTGACTTGACTCCAATGACCTCCTATAG... |
Task1_train_41222 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | GCTCAAAATTGAGGATCTTGTACTTAGCATCAACTCCATATTTACATGAGAATAGACACCTCCATTCAAAAGGGTGAGAAACAGGAGGCACAATGCAGTCACTATTCCGTAGCAATTTTGAATCCAATTTGGCACATTATTGGTATCCTCCACTCTGGCAGCAGAGAATCTTCCTTTATTACAGCTCAATTATGTTCCCTAGGACTGGTTTCCTGATCCATAGTTATGTACAGATACAATAGTCCCCCCTTACCTTGTCCAAGGGGGATACAGTCCACGACTCCTGCAGTAGATGCCTGAAGCTGTGGATAGTACTGAAC... | GCTCAAAATTGAGGATCTTGTACTTAGCATCAACTCCATATTTACATGAGAATAGACACCTCCATTCAAAAGGGTGAGAAACAGGAGGCACAATGCAGTCACTATTCCGTAGCAATTTTGAATCCAATTTGGCACATTATTGGTATCCTCCACTCTGGCAGCAGAGAATCTTCCTTTATTACAGCTCAATTATGTTCCCTAGGACTGGTTTCCTGATCCATAGTTATGTACAGATACAATAGTCCCCCCTTACCTTGTCCAAGGGGGATACAGTCCACGACTCCTGCAGTAGATGCCTGAAGCTGTGGATAGTACTGAAC... |
Task1_train_41223 | With a mutation on Chromosome 11, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | ATCAGTGGTTTGAGACTTTCTTCTTTGCTGCCATAAGCATTTAGTGCGATGAATTTCCCCCTCAGAGTTGCAGAAGGCTTCTAAAGACAAACATGTTTCAGCAAGCTGTGGCCAGCTGATTCCCATTCTTCTCATAATATTACCTCTACCCCCTGCCAAGTGATGTGGGTTAGGAGAGAGTTTGGAGGAGGGTTGTGATGAGATTTTTGAAACTCAGACATCTCTTGCAAAAAGTGGACTGTTTTAAATGGACTCTAGGGTCCCTGTTGCTTCTCTCTCATGTGGGTGGCTGTTGGGTTTTGCTTTTGTTTTTTCAAAAG... | ATCAGTGGTTTGAGACTTTCTTCTTTGCTGCCATAAGCATTTAGTGCGATGAATTTCCCCCTCAGAGTTGCAGAAGGCTTCTAAAGACAAACATGTTTCAGCAAGCTGTGGCCAGCTGATTCCCATTCTTCTCATAATATTACCTCTACCCCCTGCCAAGTGATGTGGGTTAGGAGAGAGTTTGGAGGAGGGTTGTGATGAGATTTTTGAAACTCAGACATCTCTTGCAAAAAGTGGACTGTTTTAAATGGACTCTAGGGTCCCTGTTGCTTCTCTCTCATGTGGGTGGCTGTTGGGTTTTGCTTTTGTTTTTTCAAAAG... |
Task1_train_41224 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | AGGGTTTATTTCCGGGTTCACAATTCTATTCCATTAGTCTATATGTCTATTCTTATGCCATTACCATACTATCTTGATTACTACAGTTTTTGTTGTAACTTTTGAAATTGTGGTGTGAGAGGACTCCAACTCTGTTCTCTTTTTAAAATATTATTCTGGGCTTTTAAATTTCCTTATGAATTTTAGGATAAGTTTACCAATTTCTGCAAATAAGCCAGCTGGGATTTGAGAGGAAGTGTATTTAATCTGAATATCAATTAGGGAATGTGGCCAGCTGTACAATGTTGGTTCATAATCAAGTAATGTTTTCCTTTATTTAG... | AGGGTTTATTTCCGGGTTCACAATTCTATTCCATTAGTCTATATGTCTATTCTTATGCCATTACCATACTATCTTGATTACTACAGTTTTTGTTGTAACTTTTGAAATTGTGGTGTGAGAGGACTCCAACTCTGTTCTCTTTTTAAAATATTATTCTGGGCTTTTAAATTTCCTTATGAATTTTAGGATAAGTTTACCAATTTCTGCAAATAAGCCAGCTGGGATTTGAGAGGAAGTGTATTTAATCTGAATATCAATTAGGGAATGTGGCCAGCTGTACAATGTTGGTTCATAATCAAGTAATGTTTTCCTTTATTTAG... |
Task1_train_41225 | A mutation found on Chromosome 11 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GCTGAGGGCCATGGGCAAAAAAGATTTGGCTCTAGAATTCACTAAGTTTCAAAGGTAAAAGAAGCATGAGAACGTGCCACTATTCATCACCTTCACTTTAACCCAGCATCTCTTATTAAACCATAACATAGCCTCAAGATTTCTTGAAAGCTCACTTCTTTTTCTGATACAATGCACTGTCAGCGACCATAAACTATCAGAAAGGTACTAAAGATTTTATAAACAACAAAAAATTAACTGCTTTAATGAAGTTTGCATTCTGGTTGGATAGAAGGATATAAAGTAAACAAGTGAATAAATATACAGGAGAGTGTGAATAA... | GCTGAGGGCCATGGGCAAAAAAGATTTGGCTCTAGAATTCACTAAGTTTCAAAGGTAAAAGAAGCATGAGAACGTGCCACTATTCATCACCTTCACTTTAACCCAGCATCTCTTATTAAACCATAACATAGCCTCAAGATTTCTTGAAAGCTCACTTCTTTTTCTGATACAATGCACTGTCAGCGACCATAAACTATCAGAAAGGTACTAAAGATTTTATAAACAACAAAAAATTAACTGCTTTAATGAAGTTTGCATTCTGGTTGGATAGAAGGATATAAAGTAAACAAGTGAATAAATATACAGGAGAGTGTGAATAA... |
Task1_train_41226 | An alteration has been detected on Chromosome 11. Is it pathogenic, and if so, what disease is involved? | Benign | AAGCTCACTTCTTTTTCTGATACAATGCACTGTCAGCGACCATAAACTATCAGAAAGGTACTAAAGATTTTATAAACAACAAAAAATTAACTGCTTTAATGAAGTTTGCATTCTGGTTGGATAGAAGGATATAAAGTAAACAAGTGAATAAATATACAGGAGAGTGTGAATAAAAACGAGGAAGAATAACACGAGATGAGGGGTAGTGTACATGGGGTGGGGAGAGGGATTATTTTATAAAGGTGGTGAAGGAAGGACTCTATGACTGGGTCACATTTAAGGAAAGACCTGAATGGAGTGAGGAAATATTATGCACAGAG... | AAGCTCACTTCTTTTTCTGATACAATGCACTGTCAGCGACCATAAACTATCAGAAAGGTACTAAAGATTTTATAAACAACAAAAAATTAACTGCTTTAATGAAGTTTGCATTCTGGTTGGATAGAAGGATATAAAGTAAACAAGTGAATAAATATACAGGAGAGTGTGAATAAAAACGAGGAAGAATAACACGAGATGAGGGGTAGTGTACATGGGGTGGGGAGAGGGATTATTTTATAAAGGTGGTGAAGGAAGGACTCTATGACTGGGTCACATTTAAGGAAAGACCTGAATGGAGTGAGGAAATATTATGCACAGAG... |
Task1_train_41227 | A genomic variant on Chromosome 11 is under review. What is the biological outcome — benign or pathogenic? | Benign | TAAATATACAGGAGAGTGTGAATAAAAACGAGGAAGAATAACACGAGATGAGGGGTAGTGTACATGGGGTGGGGAGAGGGATTATTTTATAAAGGTGGTGAAGGAAGGACTCTATGACTGGGTCACATTTAAGGAAAGACCTGAATGGAGTGAGGAAATATTATGCACAGAGAACAGCAAGTGCACAGGCCCTGAGGTTGGAGCATGCTTGGAATTGTGAAAAACAGCAAGGAGAGCAGCCTGGACAAAATGGAGTAAAACACAGGTGAAGCTGCAAAAGGTGGTGTATGTCAACTAAAATAAGAATGAAGGAGCAGAAT... | TAAATATACAGGAGAGTGTGAATAAAAACGAGGAAGAATAACACGAGATGAGGGGTAGTGTACATGGGGTGGGGAGAGGGATTATTTTATAAAGGTGGTGAAGGAAGGACTCTATGACTGGGTCACATTTAAGGAAAGACCTGAATGGAGTGAGGAAATATTATGCACAGAGAACAGCAAGTGCACAGGCCCTGAGGTTGGAGCATGCTTGGAATTGTGAAAAACAGCAAGGAGAGCAGCCTGGACAAAATGGAGTAAAACACAGGTGAAGCTGCAAAAGGTGGTGTATGTCAACTAAAATAAGAATGAAGGAGCAGAAT... |
Task1_train_41228 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | GGGGTAGTGTACATGGGGTGGGGAGAGGGATTATTTTATAAAGGTGGTGAAGGAAGGACTCTATGACTGGGTCACATTTAAGGAAAGACCTGAATGGAGTGAGGAAATATTATGCACAGAGAACAGCAAGTGCACAGGCCCTGAGGTTGGAGCATGCTTGGAATTGTGAAAAACAGCAAGGAGAGCAGCCTGGACAAAATGGAGTAAAACACAGGTGAAGCTGCAAAAGGTGGTGTATGTCAACTAAAATAAGAATGAAGGAGCAGAATTAACCATTTCAAAGCATTTGCAGAAAGAAAAATGTACACTTTTTGTTTCTT... | GGGGTAGTGTACATGGGGTGGGGAGAGGGATTATTTTATAAAGGTGGTGAAGGAAGGACTCTATGACTGGGTCACATTTAAGGAAAGACCTGAATGGAGTGAGGAAATATTATGCACAGAGAACAGCAAGTGCACAGGCCCTGAGGTTGGAGCATGCTTGGAATTGTGAAAAACAGCAAGGAGAGCAGCCTGGACAAAATGGAGTAAAACACAGGTGAAGCTGCAAAAGGTGGTGTATGTCAACTAAAATAAGAATGAAGGAGCAGAATTAACCATTTCAAAGCATTTGCAGAAAGAAAAATGTACACTTTTTGTTTCTT... |
Task1_train_41229 | The following genetic variant occurs on Chromosome 11. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | ATTTTATAAAGGTGGTGAAGGAAGGACTCTATGACTGGGTCACATTTAAGGAAAGACCTGAATGGAGTGAGGAAATATTATGCACAGAGAACAGCAAGTGCACAGGCCCTGAGGTTGGAGCATGCTTGGAATTGTGAAAAACAGCAAGGAGAGCAGCCTGGACAAAATGGAGTAAAACACAGGTGAAGCTGCAAAAGGTGGTGTATGTCAACTAAAATAAGAATGAAGGAGCAGAATTAACCATTTCAAAGCATTTGCAGAAAGAAAAATGTACACTTTTTGTTTCTTAGTACATTTTTTAAACAATGTAAAAGTTGGTA... | ATTTTATAAAGGTGGTGAAGGAAGGACTCTATGACTGGGTCACATTTAAGGAAAGACCTGAATGGAGTGAGGAAATATTATGCACAGAGAACAGCAAGTGCACAGGCCCTGAGGTTGGAGCATGCTTGGAATTGTGAAAAACAGCAAGGAGAGCAGCCTGGACAAAATGGAGTAAAACACAGGTGAAGCTGCAAAAGGTGGTGTATGTCAACTAAAATAAGAATGAAGGAGCAGAATTAACCATTTCAAAGCATTTGCAGAAAGAAAAATGTACACTTTTTGTTTCTTAGTACATTTTTTAAACAATGTAAAAGTTGGTA... |
Task1_train_41230 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | TACTCTAGTTATTTTATCCTTTTAAAATTTAAAACATGAACATGTTGCTTCTATAAATCAGTAATGACACAAATAAAAAAATTCATATGAGATGCTATATTTACATATTCTTGATAAAATGTGCTAAGGAAAAGCATATACTTTCATTTAATAATATGTTTTTTTAAATAAAATGAGGACTCCTAAAACAGTATTCAGCTAAATAAATTTAAAAGCATTAGGCTTAACTTTATATTCCACTACCCAAATTAAGTATTTAAATTATTTTTATCAAATATTAGTGTATTAGCGTTCTACAGAGAAACAGAACAGAGAGATGG... | TACTCTAGTTATTTTATCCTTTTAAAATTTAAAACATGAACATGTTGCTTCTATAAATCAGTAATGACACAAATAAAAAAATTCATATGAGATGCTATATTTACATATTCTTGATAAAATGTGCTAAGGAAAAGCATATACTTTCATTTAATAATATGTTTTTTTAAATAAAATGAGGACTCCTAAAACAGTATTCAGCTAAATAAATTTAAAAGCATTAGGCTTAACTTTATATTCCACTACCCAAATTAAGTATTTAAATTATTTTTATCAAATATTAGTGTATTAGCGTTCTACAGAGAAACAGAACAGAGAGATGG... |
Task1_train_41231 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | GATCTGCTTACAACATAGTACCTATAATTAACAATACTATATTGTACACTTAAAAATTATTAAAAGAGTAGATCTTATTATAAGAGTTCTTATCACAATTAAAAGAAAAGAAGCCATGATGCTGAAATAGAGGCTAATGGACATGGGAGATCATAATTTTAGATGCTTAGTTAAATTGGGCTCTCTGAGTATATCGTATTTAAAATGACATATAAGGAAAGAACATGGCAGGCAAAGAGGCCAAGATGGACAGCATTCTGCAGTGTGAATGTGAATGTGCTTCTTGTGTTCAATAAATGAACAAAGATTAATTTGCTGGA... | GATCTGCTTACAACATAGTACCTATAATTAACAATACTATATTGTACACTTAAAAATTATTAAAAGAGTAGATCTTATTATAAGAGTTCTTATCACAATTAAAAGAAAAGAAGCCATGATGCTGAAATAGAGGCTAATGGACATGGGAGATCATAATTTTAGATGCTTAGTTAAATTGGGCTCTCTGAGTATATCGTATTTAAAATGACATATAAGGAAAGAACATGGCAGGCAAAGAGGCCAAGATGGACAGCATTCTGCAGTGTGAATGTGAATGTGCTTCTTGTGTTCAATAAATGAACAAAGATTAATTTGCTGGA... |
Task1_train_41232 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TAATTAACAATACTATATTGTACACTTAAAAATTATTAAAAGAGTAGATCTTATTATAAGAGTTCTTATCACAATTAAAAGAAAAGAAGCCATGATGCTGAAATAGAGGCTAATGGACATGGGAGATCATAATTTTAGATGCTTAGTTAAATTGGGCTCTCTGAGTATATCGTATTTAAAATGACATATAAGGAAAGAACATGGCAGGCAAAGAGGCCAAGATGGACAGCATTCTGCAGTGTGAATGTGAATGTGCTTCTTGTGTTCAATAAATGAACAAAGATTAATTTGCTGGATCATAGAGAGCAAGGAGAAATTTG... | TAATTAACAATACTATATTGTACACTTAAAAATTATTAAAAGAGTAGATCTTATTATAAGAGTTCTTATCACAATTAAAAGAAAAGAAGCCATGATGCTGAAATAGAGGCTAATGGACATGGGAGATCATAATTTTAGATGCTTAGTTAAATTGGGCTCTCTGAGTATATCGTATTTAAAATGACATATAAGGAAAGAACATGGCAGGCAAAGAGGCCAAGATGGACAGCATTCTGCAGTGTGAATGTGAATGTGCTTCTTGTGTTCAATAAATGAACAAAGATTAATTTGCTGGATCATAGAGAGCAAGGAGAAATTTG... |
Task1_train_41233 | A genomic change on Chromosome 11 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | ATCGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATCACTTGAGGCCAGGAATTCAAGACCAGCCTGGCCAACTTGGTGAAACACCATCTCTACTAAAAATATTATACAAAAATTTAGCCAGGCATGGTGGTGCATGCCTGTAATTCCAGCTACTCAGGCGGCTGAGGCATGAGAATATCTTGAAGCCAGGAGGTGAAGGTTTCAGTGAGCTGAGATGGTGCCACTGCACTTTTCCCTGGGCAACAGAGCAAGACTCTGTATCAAAAATAAAAAATAAATAAATAAAAATTTAAAGGATAGAA... | ATCGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATCACTTGAGGCCAGGAATTCAAGACCAGCCTGGCCAACTTGGTGAAACACCATCTCTACTAAAAATATTATACAAAAATTTAGCCAGGCATGGTGGTGCATGCCTGTAATTCCAGCTACTCAGGCGGCTGAGGCATGAGAATATCTTGAAGCCAGGAGGTGAAGGTTTCAGTGAGCTGAGATGGTGCCACTGCACTTTTCCCTGGGCAACAGAGCAAGACTCTGTATCAAAAATAAAAAATAAATAAATAAAAATTTAAAGGATAGAA... |
Task1_train_41234 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TGTTAGTTCCTATTTTTCTATTGGGTTATTAGACTTTGTTTATGGTTGATTTTTGCCATGAGGAAAATTGTTTTTATGTGTATCTTATGACCTGAAATTTTGTTTTATTATTGGGCCTTTCCCGTTCTGAGTTTATTAAAGAATCTTCTATTGTTAAAATGGGCTCAATTCTAATGTACTTTTTTTTTATATAGGTCTAAGTATTTAGCTACGCCAGGTATGAAAGCCAGTTTCTGAGATTAACTTTTTATTACTTACTACTCAAGAGAGGATGACCTACCGTACTTCACCCTTAAAACATGACAAAATATAGGATAACA... | TGTTAGTTCCTATTTTTCTATTGGGTTATTAGACTTTGTTTATGGTTGATTTTTGCCATGAGGAAAATTGTTTTTATGTGTATCTTATGACCTGAAATTTTGTTTTATTATTGGGCCTTTCCCGTTCTGAGTTTATTAAAGAATCTTCTATTGTTAAAATGGGCTCAATTCTAATGTACTTTTTTTTTATATAGGTCTAAGTATTTAGCTACGCCAGGTATGAAAGCCAGTTTCTGAGATTAACTTTTTATTACTTACTACTCAAGAGAGGATGACCTACCGTACTTCACCCTTAAAACATGACAAAATATAGGATAACA... |
Task1_train_41235 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TTTATATATTTTAGGGAGATATGAGGCCTCGATCAATATATGTAAGAAGTACTTTGGTTCGGTTTGGAAAGGTGGGACATATTGAAGAAGGGACATTTTGAAGCAATGGCAGGAAGACTTGAAGCAGGGAGAAAGCTTTCAGGTCACAGATATGTGAGACAAACAATTCATTCTTTTGAGTTTCTGATTAGCCTTTCCAAAGAGGCAATCAGATATGCATCTATCTTAGCAACTTTGAATAAATAGAATGGGAGGCAAGTTTGCCCTAAGCAGTTTCCAGCTTGAGTTTTCTTTAGTGATTTTGGGGGCCCAAGATATTT... | TTTATATATTTTAGGGAGATATGAGGCCTCGATCAATATATGTAAGAAGTACTTTGGTTCGGTTTGGAAAGGTGGGACATATTGAAGAAGGGACATTTTGAAGCAATGGCAGGAAGACTTGAAGCAGGGAGAAAGCTTTCAGGTCACAGATATGTGAGACAAACAATTCATTCTTTTGAGTTTCTGATTAGCCTTTCCAAAGAGGCAATCAGATATGCATCTATCTTAGCAACTTTGAATAAATAGAATGGGAGGCAAGTTTGCCCTAAGCAGTTTCCAGCTTGAGTTTTCTTTAGTGATTTTGGGGGCCCAAGATATTT... |
Task1_train_41236 | The following genetic variant occurs on Chromosome 11. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CGCCCCCAAATCCCTTCTATGAATGTGCTCTGATTACTTTTTCTTTTTTCTTTTTTTTGAGACGAGGTCTTGCTCTGTTGCCAGGCTGGACTACAGTGGCACAGTCTTGGCTCACTGCAACCTCCGACTCCCTGGTTCAAGCGACTCCCCTGCCTCAGCCTCCTGAGTAGCTGAGACTACAGGCACCTGCCACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACTGGGTTTTACCCTGTTGGCCAGGTTGGTCTCCATCTCGGGACCTCGCGATCTGCCAGCCTTGGCCTCCCAATGTGCTGGGATTACAGGTGTG... | CGCCCCCAAATCCCTTCTATGAATGTGCTCTGATTACTTTTTCTTTTTTCTTTTTTTTGAGACGAGGTCTTGCTCTGTTGCCAGGCTGGACTACAGTGGCACAGTCTTGGCTCACTGCAACCTCCGACTCCCTGGTTCAAGCGACTCCCCTGCCTCAGCCTCCTGAGTAGCTGAGACTACAGGCACCTGCCACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACTGGGTTTTACCCTGTTGGCCAGGTTGGTCTCCATCTCGGGACCTCGCGATCTGCCAGCCTTGGCCTCCCAATGTGCTGGGATTACAGGTGTG... |
Task1_train_41237 | A variant has been detected on Chromosome 11. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GCTCAAATTCTGTGACTCACTTCTCTGTGTCTCGGTTGGAAATGAATGGGTATCCTGGTTCCCACCTTCCCACACACTGTGATACTTCAAACTCCTTGGGTGAAGGGCCTCTTCTCAGCCCAAGATCTTGATTGTGAACATTAACAAAGAGAACAGTCATCCTCCACAGAAGATAACTCATTAATGACATTTGATTCAGTGAATAAATATATCATTTAAAAAAATATTGTAGGGGGATCATGAAAGTAGTGGAGGTAATTACAATCAGGAGAGATTGGTATTAAAATTGAGCAAAGTCCCAACTCTCACCAGATGACAAT... | GCTCAAATTCTGTGACTCACTTCTCTGTGTCTCGGTTGGAAATGAATGGGTATCCTGGTTCCCACCTTCCCACACACTGTGATACTTCAAACTCCTTGGGTGAAGGGCCTCTTCTCAGCCCAAGATCTTGATTGTGAACATTAACAAAGAGAACAGTCATCCTCCACAGAAGATAACTCATTAATGACATTTGATTCAGTGAATAAATATATCATTTAAAAAAATATTGTAGGGGGATCATGAAAGTAGTGGAGGTAATTACAATCAGGAGAGATTGGTATTAAAATTGAGCAAAGTCCCAACTCTCACCAGATGACAAT... |
Task1_train_41238 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | ATTGTCCTTACATTATTAGTAGTAAATTAAGCTTAATGTTTTTATGTCACTGGTACAAGTTAATAGAAGAAGAAGGTATTGGAAATAAACTCCAAAGTCTGAACCCTTAGCCACATTACTATGCTGTTTCCCAGATACTCTAAAATTGAGACAATAGTTGGGGCCAAGAGTGAGCTGCACTAGCCTCCTTCTGGAATGCTTTGTATTAAGGCTTCCCTGAGAAAACTTATTCCAAAACTTTATTGGACACCCACGCTCTGTCTGCCTCAAAATATTATCAGAATTTATGATATTATTGTTAAGGCCAGTTTGGATATGTT... | ATTGTCCTTACATTATTAGTAGTAAATTAAGCTTAATGTTTTTATGTCACTGGTACAAGTTAATAGAAGAAGAAGGTATTGGAAATAAACTCCAAAGTCTGAACCCTTAGCCACATTACTATGCTGTTTCCCAGATACTCTAAAATTGAGACAATAGTTGGGGCCAAGAGTGAGCTGCACTAGCCTCCTTCTGGAATGCTTTGTATTAAGGCTTCCCTGAGAAAACTTATTCCAAAACTTTATTGGACACCCACGCTCTGTCTGCCTCAAAATATTATCAGAATTTATGATATTATTGTTAAGGCCAGTTTGGATATGTT... |
Task1_train_41239 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | CTCTTCTATTTCTTCTATTTGGATAATGATTAAGCATTATATAATAATAATAATAGTAATAGCACCTCTGGGACATTTTCTATTCACAATGCAGTATTCTAAGTATTTACATGTACTGACTCATTTAATTCTTCACAATAGTCCTAGGATAAAATTACTATTATAATTTCCATTTTATGGTTAGGATCTGAGGCACCTAGAGTCCAAGCAACTTGCCTAAAGACACACAGGCAGATATTATTTACTCACTTATTTATAGCCTACCCAAGAAAGGCCACAGCTGAATGAATTTATTCTAGTTCTTTAATGCCAGTTCAAGG... | CTCTTCTATTTCTTCTATTTGGATAATGATTAAGCATTATATAATAATAATAATAGTAATAGCACCTCTGGGACATTTTCTATTCACAATGCAGTATTCTAAGTATTTACATGTACTGACTCATTTAATTCTTCACAATAGTCCTAGGATAAAATTACTATTATAATTTCCATTTTATGGTTAGGATCTGAGGCACCTAGAGTCCAAGCAACTTGCCTAAAGACACACAGGCAGATATTATTTACTCACTTATTTATAGCCTACCCAAGAAAGGCCACAGCTGAATGAATTTATTCTAGTTCTTTAATGCCAGTTCAAGG... |
Task1_train_41240 | A variant was discovered on Chromosome 11. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GCTGTGTGAGGGGGCAATGGGAGTCCTTACTGGTGTGGATTTAATAAAATCAAGTCCCTGATCTTGAAAGATGCTTCATGCACTAAAAATTCAAATAATTTGATTGAGGATACTTTGTAACTTAGGTTTAAAATAACAACAGCAACAACAACAAATACTTATAGAACAGTTACTATGGGCCAGGCATGATCTAAGAAGATTAGATGATACATGATGATGATGATAGATGGTAGATAGATGATAGACAGATAGATAAAGATGGATAGAGAGATGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATA... | GCTGTGTGAGGGGGCAATGGGAGTCCTTACTGGTGTGGATTTAATAAAATCAAGTCCCTGATCTTGAAAGATGCTTCATGCACTAAAAATTCAAATAATTTGATTGAGGATACTTTGTAACTTAGGTTTAAAATAACAACAGCAACAACAACAAATACTTATAGAACAGTTACTATGGGCCAGGCATGATCTAAGAAGATTAGATGATACATGATGATGATGATAGATGGTAGATAGATGATAGACAGATAGATAAAGATGGATAGAGAGATGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATA... |
Task1_train_41241 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TCTTTTGTTTCACATGCCTGCTGTATCAAATGGTTTGGGGGCGGGGTTGTTGTTTTGTAGAGACAGGGACTTGCTCTGTCACCCAGGCTGCAGTACAATGGCACAATCATAGCTCACTGCAGCCTCGAATTCCTGGGCTCAAGCGATCCCCCCACTTCAGCCTCCTGAGTAGCTGGGACTGCAGGTGCACACCACCATGCCTGGCTAATTTTTTTTTAATTTGTTGTTGTTGTTAAGACAGGGTCTCACTATTGTCCTGGCTGGTCTCAAACTCCTGAACTCAAGCAATCTGCCTGCCTTGACCTCCCAAAGTGCTGGGA... | TCTTTTGTTTCACATGCCTGCTGTATCAAATGGTTTGGGGGCGGGGTTGTTGTTTTGTAGAGACAGGGACTTGCTCTGTCACCCAGGCTGCAGTACAATGGCACAATCATAGCTCACTGCAGCCTCGAATTCCTGGGCTCAAGCGATCCCCCCACTTCAGCCTCCTGAGTAGCTGGGACTGCAGGTGCACACCACCATGCCTGGCTAATTTTTTTTTAATTTGTTGTTGTTGTTAAGACAGGGTCTCACTATTGTCCTGGCTGGTCTCAAACTCCTGAACTCAAGCAATCTGCCTGCCTTGACCTCCCAAAGTGCTGGGA... |
Task1_train_41242 | Consider this mutation on Chromosome 11. Is this a benign change or a disease-causing variant? | Benign | CTCACTGCAGCCTCGAATTCCTGGGCTCAAGCGATCCCCCCACTTCAGCCTCCTGAGTAGCTGGGACTGCAGGTGCACACCACCATGCCTGGCTAATTTTTTTTTAATTTGTTGTTGTTGTTAAGACAGGGTCTCACTATTGTCCTGGCTGGTCTCAAACTCCTGAACTCAAGCAATCTGCCTGCCTTGACCTCCCAAAGTGCTGGGATTACAGGCATTAGCCACTGCACCTGGTTCATACAGATATTCTTACTGAAAGAAGTTTGTCCTCATATGACTGAATTTCTGATTTGGGAAAAAGAAGTATCAATATAGTAAAT... | CTCACTGCAGCCTCGAATTCCTGGGCTCAAGCGATCCCCCCACTTCAGCCTCCTGAGTAGCTGGGACTGCAGGTGCACACCACCATGCCTGGCTAATTTTTTTTTAATTTGTTGTTGTTGTTAAGACAGGGTCTCACTATTGTCCTGGCTGGTCTCAAACTCCTGAACTCAAGCAATCTGCCTGCCTTGACCTCCCAAAGTGCTGGGATTACAGGCATTAGCCACTGCACCTGGTTCATACAGATATTCTTACTGAAAGAAGTTTGTCCTCATATGACTGAATTTCTGATTTGGGAAAAAGAAGTATCAATATAGTAAAT... |
Task1_train_41243 | An alteration has been detected on Chromosome 11. Is it pathogenic, and if so, what disease is involved? | Benign | TCCTGGGCTCAAGCGATCCCCCCACTTCAGCCTCCTGAGTAGCTGGGACTGCAGGTGCACACCACCATGCCTGGCTAATTTTTTTTTAATTTGTTGTTGTTGTTAAGACAGGGTCTCACTATTGTCCTGGCTGGTCTCAAACTCCTGAACTCAAGCAATCTGCCTGCCTTGACCTCCCAAAGTGCTGGGATTACAGGCATTAGCCACTGCACCTGGTTCATACAGATATTCTTACTGAAAGAAGTTTGTCCTCATATGACTGAATTTCTGATTTGGGAAAAAGAAGTATCAATATAGTAAATTGCTATTATATAGCAATA... | TCCTGGGCTCAAGCGATCCCCCCACTTCAGCCTCCTGAGTAGCTGGGACTGCAGGTGCACACCACCATGCCTGGCTAATTTTTTTTTAATTTGTTGTTGTTGTTAAGACAGGGTCTCACTATTGTCCTGGCTGGTCTCAAACTCCTGAACTCAAGCAATCTGCCTGCCTTGACCTCCCAAAGTGCTGGGATTACAGGCATTAGCCACTGCACCTGGTTCATACAGATATTCTTACTGAAAGAAGTTTGTCCTCATATGACTGAATTTCTGATTTGGGAAAAAGAAGTATCAATATAGTAAATTGCTATTATATAGCAATA... |
Task1_train_41244 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | TCAGTTTTTCTGTGATACTAAAACATGCCCTGAACAATGACTGTGGCTCTATACAAAGAGCCCTGTGTGTCAATAGCAAGGTCCAGGCTTCCCAGAGTGCCAAAGAGGAGTACTTATGAGGGCCTGACCCTTCTCTTTTTATAAGGGATGAGATAAGGATTAGGTAGTCAAACTACTTAATAAACTGTTTAAGCCTTATATACACACTAGAATTCCGGTAAGCCAAAGTAAGCCCCAGACTCTCTGATTTCTCAGAGTTGTACAGTGGAAAAACCTCTGGAGACTGTTATGTTAAAGAAAAATTATTCACCAGACAATTA... | TCAGTTTTTCTGTGATACTAAAACATGCCCTGAACAATGACTGTGGCTCTATACAAAGAGCCCTGTGTGTCAATAGCAAGGTCCAGGCTTCCCAGAGTGCCAAAGAGGAGTACTTATGAGGGCCTGACCCTTCTCTTTTTATAAGGGATGAGATAAGGATTAGGTAGTCAAACTACTTAATAAACTGTTTAAGCCTTATATACACACTAGAATTCCGGTAAGCCAAAGTAAGCCCCAGACTCTCTGATTTCTCAGAGTTGTACAGTGGAAAAACCTCTGGAGACTGTTATGTTAAAGAAAAATTATTCACCAGACAATTA... |
Task1_train_41245 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | AGCAGCTTTATGAGTAATATTCAGAAGCCACAAATAACCCAAATGTTCACCTACAAGTGAGTGGATAAGCAAACTGTGGTATATTCATACAATAGAAAGGAACAAAATAGCAGTACACACAAAACAACGGATGAATTTCATGGTTGAAAGAAGGCAGACAAGAAGAAAATACAAATAGTAGAATTTCACTTATAGAATATTATAGAAAATACAAACTAATGTATAATGACAGAAAGCAGATCAGTTGTTGCCTGAAGAAGGAAGGGTAAAGGGGACAGGCTACAAAGGGGCACAAGGACATTTTCTGGGTGATAGATATA... | AGCAGCTTTATGAGTAATATTCAGAAGCCACAAATAACCCAAATGTTCACCTACAAGTGAGTGGATAAGCAAACTGTGGTATATTCATACAATAGAAAGGAACAAAATAGCAGTACACACAAAACAACGGATGAATTTCATGGTTGAAAGAAGGCAGACAAGAAGAAAATACAAATAGTAGAATTTCACTTATAGAATATTATAGAAAATACAAACTAATGTATAATGACAGAAAGCAGATCAGTTGTTGCCTGAAGAAGGAAGGGTAAAGGGGACAGGCTACAAAGGGGCACAAGGACATTTTCTGGGTGATAGATATA... |
Task1_train_41246 | This genomic variant is located on Chromosome 11. Can you determine its pathogenicity and name any linked disease? | Benign | ATGCTACTAAAATAAATTATGGTCAGGCAGAATTGAAAACTATTTTAAAGCTATATGAAGGTTTTATGTGATATCAAATTTTGTGGCTAAAGTGATCAAAATTATTTAATGAAAACATAGTGTCCAGGTGTGGTGGTTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATCACTTGAGGTGAGGAGTTCGAGACCCACCTGGCCAACATGGTGAAACCCCTTCTCTACTAAAAATACAAAAATTCGCTGGGCGTGGTGGTGTGCACCTGTAATCCCAGTTACTCAGGAGGCTGAAGTGGGGGAATTGC... | ATGCTACTAAAATAAATTATGGTCAGGCAGAATTGAAAACTATTTTAAAGCTATATGAAGGTTTTATGTGATATCAAATTTTGTGGCTAAAGTGATCAAAATTATTTAATGAAAACATAGTGTCCAGGTGTGGTGGTTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATCACTTGAGGTGAGGAGTTCGAGACCCACCTGGCCAACATGGTGAAACCCCTTCTCTACTAAAAATACAAAAATTCGCTGGGCGTGGTGGTGTGCACCTGTAATCCCAGTTACTCAGGAGGCTGAAGTGGGGGAATTGC... |
Task1_train_41247 | Here is a genetic alteration on Chromosome 11. Based on the data, is it a benign variant or a cause of disease? | Benign | TAACTTGATGACTCTAGTATTTGGTATTTGAGAATCCCTGGTATTTGATTAGAAAAGCAGCAAAATACTCATATAGATTTATATACAGAAATTTACAGTTGCAAAATAATTTAAACTTTATCTAACTTGAGCCTGCAGGCAGCTCCTGGGAGATAGGCAGAACAGAGATTTTATTATTATTATCATTGCTATTAGTAGTAGTAGGGTTATTGTTACTACAATCATCTGCAAGGTGAGGCTGAGCAGTATCCAGTGACTTGTCTCAGATCCCAGAGTTATGACGTGGCAGAGCCAGAACCAGAAGGCTGCTCTTTCGACGT... | TAACTTGATGACTCTAGTATTTGGTATTTGAGAATCCCTGGTATTTGATTAGAAAAGCAGCAAAATACTCATATAGATTTATATACAGAAATTTACAGTTGCAAAATAATTTAAACTTTATCTAACTTGAGCCTGCAGGCAGCTCCTGGGAGATAGGCAGAACAGAGATTTTATTATTATTATCATTGCTATTAGTAGTAGTAGGGTTATTGTTACTACAATCATCTGCAAGGTGAGGCTGAGCAGTATCCAGTGACTTGTCTCAGATCCCAGAGTTATGACGTGGCAGAGCCAGAACCAGAAGGCTGCTCTTTCGACGT... |
Task1_train_41248 | A mutation is present on Chromosome 11. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CTTTATAATGTATATTATATTATTATTCTGATTTTCTTTATAGCATCCTACACTGTGTTGTTAGATATGATAAATAACTGTCAACTAGAGTTAAGGAGCCAAATAAGTCATACTTTTCAGAGGCAAAGCCATTATTTTAATTTTAATACTTGACCTCCTTGACCAGTTACTTTAGTTTGGGGATCTATGAGTTTTCTGAAAGCGAGGGCAGGGAGAAGCTTCAGGGTATCTGTGAAACCCTCAGTTGAAATGCTAAATTTGGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGCAGATCTCTTG... | CTTTATAATGTATATTATATTATTATTCTGATTTTCTTTATAGCATCCTACACTGTGTTGTTAGATATGATAAATAACTGTCAACTAGAGTTAAGGAGCCAAATAAGTCATACTTTTCAGAGGCAAAGCCATTATTTTAATTTTAATACTTGACCTCCTTGACCAGTTACTTTAGTTTGGGGATCTATGAGTTTTCTGAAAGCGAGGGCAGGGAGAAGCTTCAGGGTATCTGTGAAACCCTCAGTTGAAATGCTAAATTTGGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGCAGATCTCTTG... |
Task1_train_41249 | The following genetic variant occurs on Chromosome 11. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GATAGACTTTAGTCTACAATTCTCAGAGTCTAGAATCTCTAGAATTTCACATTGGAACACTGCAATGTGGTGAGAGCCACCATCTATCTCCACTGTACTACCATCCCCTGCCCATGGCCCATGGCCAAATCCTTCCTCTTGCTAACCCCACTCTGATCTGCATTGTAGGGGGCCTCAAGTGCACGTGTGTGGACACTCCAGGTGTTGTGTCCAAGCTCCGTCCATATTTCCAGCAGACAACTGCCTCTTGGCCACCATTAGGCCCAGGGCTATATACACCTGAGAGAACTGACTCAGGGAAGGGGCTCAAGCAGCCCTTG... | GATAGACTTTAGTCTACAATTCTCAGAGTCTAGAATCTCTAGAATTTCACATTGGAACACTGCAATGTGGTGAGAGCCACCATCTATCTCCACTGTACTACCATCCCCTGCCCATGGCCCATGGCCAAATCCTTCCTCTTGCTAACCCCACTCTGATCTGCATTGTAGGGGGCCTCAAGTGCACGTGTGTGGACACTCCAGGTGTTGTGTCCAAGCTCCGTCCATATTTCCAGCAGACAACTGCCTCTTGGCCACCATTAGGCCCAGGGCTATATACACCTGAGAGAACTGACTCAGGGAAGGGGCTCAAGCAGCCCTTG... |
Task1_train_41250 | The following genetic variant occurs on Chromosome 11. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | AGATGAGATCTTGCTATATTGCCCAGGCTGGTCTCCTGAGCTCAAGCGATCCTCCTGCTTCTGCCTCACCTTCCCAAAGTGGTGGGATTAGAGGTGTGAGCCACCATGCTGGACCAACATAGTGTTTTTGACATCTCCACAATGAGCATGTGTTCAGAAAAGGCAAATCTCCAATTGGTTCAATATTTTCAGACATCTGGGATACAGCACTGTGATAATGTTTAAGAGCTAAATATGAGAAAAAAAAACTTGTTAAGTAGAAGCTGTAGCCCTTGTTCCTAGTCTGGCAATTCAAGATTACAATCTTGTTATTTTATTTC... | AGATGAGATCTTGCTATATTGCCCAGGCTGGTCTCCTGAGCTCAAGCGATCCTCCTGCTTCTGCCTCACCTTCCCAAAGTGGTGGGATTAGAGGTGTGAGCCACCATGCTGGACCAACATAGTGTTTTTGACATCTCCACAATGAGCATGTGTTCAGAAAAGGCAAATCTCCAATTGGTTCAATATTTTCAGACATCTGGGATACAGCACTGTGATAATGTTTAAGAGCTAAATATGAGAAAAAAAAACTTGTTAAGTAGAAGCTGTAGCCCTTGTTCCTAGTCTGGCAATTCAAGATTACAATCTTGTTATTTTATTTC... |
Task1_train_41251 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | AGACTAAGATTCTGGGTCCTAATGTAAGTAAGAAGCCCTCTTCTCCTGTTCCATGAACACCATCCTTTTCTGTAACTTCTATTACACAGTATAGTGGTTCTGTAAGTTCACACAGCCCAGGGAGATGCTGGCTGCCCACTCCCCTCAACCCAGGCAAATTCCTCGGGGTTAAAGTTATCTACTGCAAGTGACGATCTCTGGGTTTTTCTGTGCCTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTCACTTTAAAAGGACTGGTCAGATGGTAGGGAGATGAAAACAGGAGATGCTATAAGAAAA... | AGACTAAGATTCTGGGTCCTAATGTAAGTAAGAAGCCCTCTTCTCCTGTTCCATGAACACCATCCTTTTCTGTAACTTCTATTACACAGTATAGTGGTTCTGTAAGTTCACACAGCCCAGGGAGATGCTGGCTGCCCACTCCCCTCAACCCAGGCAAATTCCTCGGGGTTAAAGTTATCTACTGCAAGTGACGATCTCTGGGTTTTTCTGTGCCTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTCACTTTAAAAGGACTGGTCAGATGGTAGGGAGATGAAAACAGGAGATGCTATAAGAAAA... |
Task1_train_41252 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CAGTAGGTAAATAAATAAAAGAAATGGTGTGTGTCAGTGGGGGGTGCAATGGACAGGGAGAAGACATAATGAACGAGAGTTTGAAGATAAAGCTAAAATCAAAGAATCTGACAGTCCAGTTTCAGCCTGGAAAAGAAAACAGCAGAAAAGCTGAGTATCAGGATATCTGATACAGTGGGTATGACCCCTGCTACAGTGGGTAAAAGCAAGGGAAACATGACCAGTTCTTTCAATGAAATGGAGCTCATGTAAAATTGAAATACTTTTCTACGTGTGTGTGTGTACACACATGCTGAAACTTAATATTTATACACAAACAA... | CAGTAGGTAAATAAATAAAAGAAATGGTGTGTGTCAGTGGGGGGTGCAATGGACAGGGAGAAGACATAATGAACGAGAGTTTGAAGATAAAGCTAAAATCAAAGAATCTGACAGTCCAGTTTCAGCCTGGAAAAGAAAACAGCAGAAAAGCTGAGTATCAGGATATCTGATACAGTGGGTATGACCCCTGCTACAGTGGGTAAAAGCAAGGGAAACATGACCAGTTCTTTCAATGAAATGGAGCTCATGTAAAATTGAAATACTTTTCTACGTGTGTGTGTGTACACACATGCTGAAACTTAATATTTATACACAAACAA... |
Task1_train_41253 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | AAGGAAAATCTGAGAAAGTCTAAAGGAACCTGAGGAGACATCAGGCCTAAATGTAATGTAGTATACTGTAGTAGCCTCTGTGTCTACTTTGGATACCTCACATGAACAACACTTTGACTCATTTTTTTTTCAAGGGTTGTAACACCTGGGCTTAAAGAATGGACCCCAACCAATAGACCGCTTTATAACACTGTCAGCTTCCTTGCCACTGAAAACCTGAATTTGAAGGCCAGTTATCACCGAAAGAACCTCATAAACAGGCACAATTTCTCTGTGATACATTCTTCGGCATGGGCAGAGGGAATATTATAATCCCCTGA... | AAGGAAAATCTGAGAAAGTCTAAAGGAACCTGAGGAGACATCAGGCCTAAATGTAATGTAGTATACTGTAGTAGCCTCTGTGTCTACTTTGGATACCTCACATGAACAACACTTTGACTCATTTTTTTTTCAAGGGTTGTAACACCTGGGCTTAAAGAATGGACCCCAACCAATAGACCGCTTTATAACACTGTCAGCTTCCTTGCCACTGAAAACCTGAATTTGAAGGCCAGTTATCACCGAAAGAACCTCATAAACAGGCACAATTTCTCTGTGATACATTCTTCGGCATGGGCAGAGGGAATATTATAATCCCCTGA... |
Task1_train_41254 | 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 | AGATTTTGTCTCTATCATTGTGCCATTAAAGTCTATGAATGAAGAGAGCCTCATAAACTAAAAGTAAGGTTCTTCTTCGGGATAGCAATAGCAAATAAGAGGGAAATTAGAGACAAGAAGTTCTACAATTGAATCTTGCTTTTGCCAATTTCTAACTGAGTGACATTGGGAAAATTTGTCAAATTCTCAAAAGAAACTTTCTTTTCTTATCTTGAGTGAGTGGCAAGAAATAAAATTACTTACTATAAAAAGCATTAGATATCTCAAGGGAAGTAAATTAGTTTCGCAAAGACACCTCAAGCGGTTATTTTGGTGTGACT... | AGATTTTGTCTCTATCATTGTGCCATTAAAGTCTATGAATGAAGAGAGCCTCATAAACTAAAAGTAAGGTTCTTCTTCGGGATAGCAATAGCAAATAAGAGGGAAATTAGAGACAAGAAGTTCTACAATTGAATCTTGCTTTTGCCAATTTCTAACTGAGTGACATTGGGAAAATTTGTCAAATTCTCAAAAGAAACTTTCTTTTCTTATCTTGAGTGAGTGGCAAGAAATAAAATTACTTACTATAAAAAGCATTAGATATCTCAAGGGAAGTAAATTAGTTTCGCAAAGACACCTCAAGCGGTTATTTTGGTGTGACT... |
Task1_train_41255 | With a mutation on Chromosome 11, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GTGAGGTGTGGAGTGGGGGAAGTTGATTGGGTCTAGACCAAAGAACTTTGAGGAACTTGCCCAGAGCCCTGCATGCATCAGACCTACAGCAGACATTGCAGGCCTGAAGAAAGGTAGGTCCAGGGACTTGCCTTCCTAGGCTTTCGGGCTGATGGCTTGTTTCACTTCCTGGGTTAAGAATTTCTGGGAGGGGAATGAGAAGAATAATGAGGCCACTTCCCATGACCCAAGCTGGTATTCAGGGTTGGGGTGGGTTGAGTGCACCTTTAAATGTGCATTCGGTGGGGGGATGAGGAACAGTTTTTGCTACAGTCGATAGG... | GTGAGGTGTGGAGTGGGGGAAGTTGATTGGGTCTAGACCAAAGAACTTTGAGGAACTTGCCCAGAGCCCTGCATGCATCAGACCTACAGCAGACATTGCAGGCCTGAAGAAAGGTAGGTCCAGGGACTTGCCTTCCTAGGCTTTCGGGCTGATGGCTTGTTTCACTTCCTGGGTTAAGAATTTCTGGGAGGGGAATGAGAAGAATAATGAGGCCACTTCCCATGACCCAAGCTGGTATTCAGGGTTGGGGTGGGTTGAGTGCACCTTTAAATGTGCATTCGGTGGGGGGATGAGGAACAGTTTTTGCTACAGTCGATAGG... |
Task1_train_41256 | A mutation on Chromosome 11 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GTATACTCTGAAATCTGTGGCCATGGTGTCCTGTTTCTTTCATACTCTCACTACACTTCTCCCCAAATTTATCATCATGTAATCTTTGTTTCTAACACTCATTTCACCTGATTTATAGAAATGTTAGTTGTTTCCCACTTTCATAAAAAAAATGGAGTTCTAATTCTGTTTGTCCAAATTGTTTTCGGAACTTTTCTAAAAGTGAAAAGAATAAGAACATTGATTTTTTGGTTACATTCTTATATATAATTCCTTATCTTAACTACTTCATTCACATTTACATTATATATTTCTTATTTATTATATTTGTCTTTCTTTTT... | GTATACTCTGAAATCTGTGGCCATGGTGTCCTGTTTCTTTCATACTCTCACTACACTTCTCCCCAAATTTATCATCATGTAATCTTTGTTTCTAACACTCATTTCACCTGATTTATAGAAATGTTAGTTGTTTCCCACTTTCATAAAAAAAATGGAGTTCTAATTCTGTTTGTCCAAATTGTTTTCGGAACTTTTCTAAAAGTGAAAAGAATAAGAACATTGATTTTTTGGTTACATTCTTATATATAATTCCTTATCTTAACTACTTCATTCACATTTACATTATATATTTCTTATTTATTATATTTGTCTTTCTTTTT... |
Task1_train_41257 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | AATAATTTTAGTGTATTTTTTGTTTAAATATAGTCATCAATTTTGGTACCATGTAAGAATTACTTTGTATCAGGAGTTTGGAAACTATCTTTTAGTGCCCTCAAACAGTTTTAATATCATTTCAGTTAGATATTTGAAAAACTTGATAAATTCTCCCATGGATTTATCTGGTATTATTTCTCTGTTCTTTCTGGGAAAAGGGAAAATAATGTGCAAACCTTTGTGGTTTTCTTTAAGATAATTGGTCTGATTAACATATCTATCTAATTTAGAATTAAGTTTAGTAAGTTATGACTCCCAATACTGGCTTAAAGTTTTTT... | AATAATTTTAGTGTATTTTTTGTTTAAATATAGTCATCAATTTTGGTACCATGTAAGAATTACTTTGTATCAGGAGTTTGGAAACTATCTTTTAGTGCCCTCAAACAGTTTTAATATCATTTCAGTTAGATATTTGAAAAACTTGATAAATTCTCCCATGGATTTATCTGGTATTATTTCTCTGTTCTTTCTGGGAAAAGGGAAAATAATGTGCAAACCTTTGTGGTTTTCTTTAAGATAATTGGTCTGATTAACATATCTATCTAATTTAGAATTAAGTTTAGTAAGTTATGACTCCCAATACTGGCTTAAAGTTTTTT... |
Task1_train_41258 | A mutation is present on Chromosome 11. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TCTTGTTAAAACACCCGCATGCCCGCATAAATCAGTCAGAACCAGATGACTCTTTCTAGCTGTTGATTCCTCCTCCTCACAAAGAGCCCACACGCTTCATTTTGCTTAATTGTCACTTTGAGGAAAATGTTTCTTCCTTTCTTTCCTTCACACTTCCCTCTTTTCCTTCATTATAGGAAGAAACTTCTCACTTACATATGAGAAATCACAGTCACTTTTGTGAAATAGCTTATGCTGAACATTAGCCCTTCCTTCTCTGGATCCCTTGAATGCTGGAATAGTTACCAGGCTGTGTTTTCAACTGAGGACTTCCTGTTGCC... | TCTTGTTAAAACACCCGCATGCCCGCATAAATCAGTCAGAACCAGATGACTCTTTCTAGCTGTTGATTCCTCCTCCTCACAAAGAGCCCACACGCTTCATTTTGCTTAATTGTCACTTTGAGGAAAATGTTTCTTCCTTTCTTTCCTTCACACTTCCCTCTTTTCCTTCATTATAGGAAGAAACTTCTCACTTACATATGAGAAATCACAGTCACTTTTGTGAAATAGCTTATGCTGAACATTAGCCCTTCCTTCTCTGGATCCCTTGAATGCTGGAATAGTTACCAGGCTGTGTTTTCAACTGAGGACTTCCTGTTGCC... |
Task1_train_41259 | Chromosome 11 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | ACCCGCATGCCCGCATAAATCAGTCAGAACCAGATGACTCTTTCTAGCTGTTGATTCCTCCTCCTCACAAAGAGCCCACACGCTTCATTTTGCTTAATTGTCACTTTGAGGAAAATGTTTCTTCCTTTCTTTCCTTCACACTTCCCTCTTTTCCTTCATTATAGGAAGAAACTTCTCACTTACATATGAGAAATCACAGTCACTTTTGTGAAATAGCTTATGCTGAACATTAGCCCTTCCTTCTCTGGATCCCTTGAATGCTGGAATAGTTACCAGGCTGTGTTTTCAACTGAGGACTTCCTGTTGCCCAATACTAATGT... | ACCCGCATGCCCGCATAAATCAGTCAGAACCAGATGACTCTTTCTAGCTGTTGATTCCTCCTCCTCACAAAGAGCCCACACGCTTCATTTTGCTTAATTGTCACTTTGAGGAAAATGTTTCTTCCTTTCTTTCCTTCACACTTCCCTCTTTTCCTTCATTATAGGAAGAAACTTCTCACTTACATATGAGAAATCACAGTCACTTTTGTGAAATAGCTTATGCTGAACATTAGCCCTTCCTTCTCTGGATCCCTTGAATGCTGGAATAGTTACCAGGCTGTGTTTTCAACTGAGGACTTCCTGTTGCCCAATACTAATGT... |
Task1_train_41260 | A variant was discovered on Chromosome 11. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GAAGGAGAGGGTTGGAGAGTGGGAGATGAAAGCTGAGATGCAGATGGGACCTGGGAAACAGGGCTAGCTGAGAAACAAAAACTCGGATAGTTGTTTTGGGTCCAAAGAGTTAAGGCCTTCTTATTCTCTAAGGAGGGATCCCTAGAACTAGAAATGCCAGGGAGACAGTTTTGCCCATGGACCTGCAGGAACAAGAGATATTTTATGGAGAATGTGCACAGAGAGTTGTATATATTGTTAGAGAAACACCAAAATTTATCTCCAACTCCTTTGTTGTCAAACATAAATATCTGTTTCTGAGCTCTGCCACGGGAACTTGG... | GAAGGAGAGGGTTGGAGAGTGGGAGATGAAAGCTGAGATGCAGATGGGACCTGGGAAACAGGGCTAGCTGAGAAACAAAAACTCGGATAGTTGTTTTGGGTCCAAAGAGTTAAGGCCTTCTTATTCTCTAAGGAGGGATCCCTAGAACTAGAAATGCCAGGGAGACAGTTTTGCCCATGGACCTGCAGGAACAAGAGATATTTTATGGAGAATGTGCACAGAGAGTTGTATATATTGTTAGAGAAACACCAAAATTTATCTCCAACTCCTTTGTTGTCAAACATAAATATCTGTTTCTGAGCTCTGCCACGGGAACTTGG... |
Task1_train_41261 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GAGTGGGAGATGAAAGCTGAGATGCAGATGGGACCTGGGAAACAGGGCTAGCTGAGAAACAAAAACTCGGATAGTTGTTTTGGGTCCAAAGAGTTAAGGCCTTCTTATTCTCTAAGGAGGGATCCCTAGAACTAGAAATGCCAGGGAGACAGTTTTGCCCATGGACCTGCAGGAACAAGAGATATTTTATGGAGAATGTGCACAGAGAGTTGTATATATTGTTAGAGAAACACCAAAATTTATCTCCAACTCCTTTGTTGTCAAACATAAATATCTGTTTCTGAGCTCTGCCACGGGAACTTGGGAGCACTTCAGGTGAG... | GAGTGGGAGATGAAAGCTGAGATGCAGATGGGACCTGGGAAACAGGGCTAGCTGAGAAACAAAAACTCGGATAGTTGTTTTGGGTCCAAAGAGTTAAGGCCTTCTTATTCTCTAAGGAGGGATCCCTAGAACTAGAAATGCCAGGGAGACAGTTTTGCCCATGGACCTGCAGGAACAAGAGATATTTTATGGAGAATGTGCACAGAGAGTTGTATATATTGTTAGAGAAACACCAAAATTTATCTCCAACTCCTTTGTTGTCAAACATAAATATCTGTTTCTGAGCTCTGCCACGGGAACTTGGGAGCACTTCAGGTGAG... |
Task1_train_41262 | With a mutation on Chromosome 11, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TAGGTTTTTTACAGAGTAAATTTACCCTGTTGCGCAGATTTTTTAAAATCATGAATGGGTATTGGCTTTTGTCATTTTTCATCTCATGCTTTCATCTTTATCGTATTATCTGTATATTACACAACTAGAGGAGAGTACAAACCCTGTTTTAAGCCCTTTAGAAACAATACTAAAATAAGTTACACTAAATAACTCTTCAATTGAATTTAGTGAATACAGATCTTTAATCCACTAATGGCACAGTAATGTGCAAAGTACAACAGGGGATTCAAAAATAATAAAATATGTACCTTGATCTCAAGAAAAGGAAAGGGAAAGTG... | TAGGTTTTTTACAGAGTAAATTTACCCTGTTGCGCAGATTTTTTAAAATCATGAATGGGTATTGGCTTTTGTCATTTTTCATCTCATGCTTTCATCTTTATCGTATTATCTGTATATTACACAACTAGAGGAGAGTACAAACCCTGTTTTAAGCCCTTTAGAAACAATACTAAAATAAGTTACACTAAATAACTCTTCAATTGAATTTAGTGAATACAGATCTTTAATCCACTAATGGCACAGTAATGTGCAAAGTACAACAGGGGATTCAAAAATAATAAAATATGTACCTTGATCTCAAGAAAAGGAAAGGGAAAGTG... |
Task1_train_41263 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AAAGTCCAAATTTCCTAGCCTAGCATACCATCTAATAATATCAGTAATATCTAACTGCTTACCATCTGCCATCACACCATGCTATATCACAACCTTGTGTTTTTGTACCCGCTATTCCACTGCTGCTTCTACCTGGATTCTGACTCCTGTCTTATTTCATCTTACCGTCTATGCCTGAGTAATTCCTACTCAGCTGTTAAGATATAGATTAAATATTGCCTCTTCTGTAAAGCATTTCCAGGTTGTCTCAGAATTAGGTCATCTTCTATGTTCCCATAAAGCACTAAGTACCTATTTATGTAATTGCATTTGCTGAATTG... | AAAGTCCAAATTTCCTAGCCTAGCATACCATCTAATAATATCAGTAATATCTAACTGCTTACCATCTGCCATCACACCATGCTATATCACAACCTTGTGTTTTTGTACCCGCTATTCCACTGCTGCTTCTACCTGGATTCTGACTCCTGTCTTATTTCATCTTACCGTCTATGCCTGAGTAATTCCTACTCAGCTGTTAAGATATAGATTAAATATTGCCTCTTCTGTAAAGCATTTCCAGGTTGTCTCAGAATTAGGTCATCTTCTATGTTCCCATAAAGCACTAAGTACCTATTTATGTAATTGCATTTGCTGAATTG... |
Task1_train_41264 | A mutation on Chromosome 11 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TTGGACTTACAGTTTCTCATGGCTGGGAAGGCCTCACAATTGTGGCAGAAGGCAAGGAGGAGCAAGTCACATCTTACATGAATGGCAGCAGGCAAAGAGAGAGGGCTTGTGCAGGGAAACTCCCATTTTTAAAACCATCAGATCTCATAGGACTTATTCACTATCACAAGAACAGCATGGGAAGGACCCGCTCCCATGATTCAATTATCTCCCACTGGGTCCCGCCCACAACACATGGGAATTATGGAAGCTACAAGATGAGATTTGGGTGGGGACACAGAGCCAAACCATATCAAAAGATCAGACAGATAGATAGATAG... | TTGGACTTACAGTTTCTCATGGCTGGGAAGGCCTCACAATTGTGGCAGAAGGCAAGGAGGAGCAAGTCACATCTTACATGAATGGCAGCAGGCAAAGAGAGAGGGCTTGTGCAGGGAAACTCCCATTTTTAAAACCATCAGATCTCATAGGACTTATTCACTATCACAAGAACAGCATGGGAAGGACCCGCTCCCATGATTCAATTATCTCCCACTGGGTCCCGCCCACAACACATGGGAATTATGGAAGCTACAAGATGAGATTTGGGTGGGGACACAGAGCCAAACCATATCAAAAGATCAGACAGATAGATAGATAG... |
Task1_train_41265 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | TGGCAATTATACCCTCTGTTTCCATAATAATGTTACTGACATAGTTGTGATTTGTACTACGCACTCTTATATACTTTTGTTTGGGCAAAGTGTTCCTAATATAGAGCAGAATCAATCCTTTTATAGTAGTAAAGTCTCTTCCAGTAGTTAGTATGCTACATGCCTGTCTCATCGAAATGTTACATAGTTAAATATAACCTATGTCATGATCTTAAAATGGCGTGCAGAATTTTGGCTGCCTGTAAATTTAGCCTGGAGCTGGGAAGGAGATTCAACCCTGCAGCTGTTTAGAAAAGCACTGTCTCATACTCAGAAAAAAA... | TGGCAATTATACCCTCTGTTTCCATAATAATGTTACTGACATAGTTGTGATTTGTACTACGCACTCTTATATACTTTTGTTTGGGCAAAGTGTTCCTAATATAGAGCAGAATCAATCCTTTTATAGTAGTAAAGTCTCTTCCAGTAGTTAGTATGCTACATGCCTGTCTCATCGAAATGTTACATAGTTAAATATAACCTATGTCATGATCTTAAAATGGCGTGCAGAATTTTGGCTGCCTGTAAATTTAGCCTGGAGCTGGGAAGGAGATTCAACCCTGCAGCTGTTTAGAAAAGCACTGTCTCATACTCAGAAAAAAA... |
Task1_train_41266 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | AGCCTCCCAAGTAGCTGGGACTACAGGCATGTGCCACCATACCTGGCTAATTTTTGTATTTTTTTAAGTATAGATGAGGTTTTGCCATCCTGGCCAGGCTGGTCTCAAACTCCTGACCTCAAGTGATCCACCACCCATGGCCTCCCAAAGTGCTGGGATTACAGGCATCAGCCATCATGCCCAGCCCTCAACAACCCTTTGAGGTACTTACATTCTCATACTACAGACTAGCAAGCTGAGGTCCAGAGAGGTCACATCACTTCTCAAGGCGAAGCAGCCAATTAGGAAATCCAGGACTCAGCCTGAGCTATGTCCAACCC... | AGCCTCCCAAGTAGCTGGGACTACAGGCATGTGCCACCATACCTGGCTAATTTTTGTATTTTTTTAAGTATAGATGAGGTTTTGCCATCCTGGCCAGGCTGGTCTCAAACTCCTGACCTCAAGTGATCCACCACCCATGGCCTCCCAAAGTGCTGGGATTACAGGCATCAGCCATCATGCCCAGCCCTCAACAACCCTTTGAGGTACTTACATTCTCATACTACAGACTAGCAAGCTGAGGTCCAGAGAGGTCACATCACTTCTCAAGGCGAAGCAGCCAATTAGGAAATCCAGGACTCAGCCTGAGCTATGTCCAACCC... |
Task1_train_41267 | A mutation on Chromosome 11 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | ATGATCCAATCGGCACTGGAGAGTGATCCCTCCAGCTGGGGACAAGAGCTTAGGAGGCAGGGCAAGCCAAGGGGGACTGGAGCAGGGCAGAGGGGCATACAGTCTCCTCCAGCACTCTGGCAACACCTGCCGGGCTTGGTTCTGAGTGTCAGATCATTGGGGTCTCCAGGCAGGGGCAGGGCATTTAAGGAACTGAATGGAACTCACTCCTCTGACAGTTGGGGGGTGGAAGAGCTGGGCAAGGAGGTGTCCCGGCTGCTTCTGCTGTGGACAGCTGCATGGCCGGAGAGGAGCAGTGAGGCAGGCAAAGCCCCCCTGCA... | ATGATCCAATCGGCACTGGAGAGTGATCCCTCCAGCTGGGGACAAGAGCTTAGGAGGCAGGGCAAGCCAAGGGGGACTGGAGCAGGGCAGAGGGGCATACAGTCTCCTCCAGCACTCTGGCAACACCTGCCGGGCTTGGTTCTGAGTGTCAGATCATTGGGGTCTCCAGGCAGGGGCAGGGCATTTAAGGAACTGAATGGAACTCACTCCTCTGACAGTTGGGGGGTGGAAGAGCTGGGCAAGGAGGTGTCCCGGCTGCTTCTGCTGTGGACAGCTGCATGGCCGGAGAGGAGCAGTGAGGCAGGCAAAGCCCCCCTGCA... |
Task1_train_41268 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CTCCAGCCCGACCCTGGCCTCCCAGGCCTCCGGCACAGCTACGACTGTGGGATCAAGGGAATGCAGCTGCTGGTGTTCCCCAGGCCAGGCCAGACTCTCCGCTTCAAGGTGGTGGGTGAGTGCTGGCAGAGTCCTGGCCCCTGCCTCCCTGGCCACGGGCTGCTGCCAGAAGGGAGCTGGGACCCTTCCCCTGAAGGAGCAAGAACAGAGGCCTCCCTCCAGCCTGGGGGTGTCCAGCCCCCCACCCCCTCACCACAGAAAAGGGCAAGGAGGAGAATCATCACCCAGGGCAGCTTCTCCCACGTTAGTGTGCATGGGAA... | CTCCAGCCCGACCCTGGCCTCCCAGGCCTCCGGCACAGCTACGACTGTGGGATCAAGGGAATGCAGCTGCTGGTGTTCCCCAGGCCAGGCCAGACTCTCCGCTTCAAGGTGGTGGGTGAGTGCTGGCAGAGTCCTGGCCCCTGCCTCCCTGGCCACGGGCTGCTGCCAGAAGGGAGCTGGGACCCTTCCCCTGAAGGAGCAAGAACAGAGGCCTCCCTCCAGCCTGGGGGTGTCCAGCCCCCCACCCCCTCACCACAGAAAAGGGCAAGGAGGAGAATCATCACCCAGGGCAGCTTCTCCCACGTTAGTGTGCATGGGAA... |
Task1_train_41269 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | CCCTGGGCCGCCCAGCCAATGATCGCTTTCTGTGAAATTGCTGACTTCCGCATCCCTCTCCTCCTTCCCTGCCTCACTTCTCCCGTAGCACCCTCCACTTCCTAATCTACGTCAGTACTGGTTAATGTTGCCTGTCCATCCTTTCCACGCTCCTCCCCCGAGAATGTCAGCCCCTTGAAGCTGCGGTCTGTCTATGCTGGTCGTACCCTCAGAGCCTAAGATGACACAGAGCTCAGGAAATGAACACCCTCGGAGGGGGCTCCCCAAAACCCAGGGAGAGGTGGCCCACGCCTCTGGAATCTAGCTTCCAGGCCCTTCAG... | CCCTGGGCCGCCCAGCCAATGATCGCTTTCTGTGAAATTGCTGACTTCCGCATCCCTCTCCTCCTTCCCTGCCTCACTTCTCCCGTAGCACCCTCCACTTCCTAATCTACGTCAGTACTGGTTAATGTTGCCTGTCCATCCTTTCCACGCTCCTCCCCCGAGAATGTCAGCCCCTTGAAGCTGCGGTCTGTCTATGCTGGTCGTACCCTCAGAGCCTAAGATGACACAGAGCTCAGGAAATGAACACCCTCGGAGGGGGCTCCCCAAAACCCAGGGAGAGGTGGCCCACGCCTCTGGAATCTAGCTTCCAGGCCCTTCAG... |
Task1_train_41270 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GGGAGCAAGAGCGGTGATCGAGGCACAGCGCCAGTCGGGAGTGGGCTGGGGCGGCTCGCCTGCAGGTGGAAGGGCCTGACCCCAAGAGGGGCGGATGTCTGCGTTTGAGAAACAGGAGCTGCTGGTGATTAGGAGCCGCCGGGGACGAGCTGCGGGTCTCCAGCAGCTGGGCCCTGGGCAGGCTGGGGCCGCTCAGCGCTGACGGCCAGTCCCGGCCTCCCCGCCCTGCAGGCCTGCGGAACCCGCTGCAGAGGCGTCGGATGAGGCCGAGCGGCGCGCCCGTGGCTGCCACCTGCAGTACCAGCGGGCCGGTGTGCGCT... | GGGAGCAAGAGCGGTGATCGAGGCACAGCGCCAGTCGGGAGTGGGCTGGGGCGGCTCGCCTGCAGGTGGAAGGGCCTGACCCCAAGAGGGGCGGATGTCTGCGTTTGAGAAACAGGAGCTGCTGGTGATTAGGAGCCGCCGGGGACGAGCTGCGGGTCTCCAGCAGCTGGGCCCTGGGCAGGCTGGGGCCGCTCAGCGCTGACGGCCAGTCCCGGCCTCCCCGCCCTGCAGGCCTGCGGAACCCGCTGCAGAGGCGTCGGATGAGGCCGAGCGGCGCGCCCGTGGCTGCCACCTGCAGTACCAGCGGGCCGGTGTGCGCT... |
Task1_train_41271 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | GACTCGCGTGTAGCCTCTCTGGAGGGTGGCCGTGTCGTGGTGGGCCGGGAGCCCGGTGTCACCTCCATTGAGGTAAGCAGCTGGGGACCAGGAGAGTAGACCCCCTGAGAAGGGTGGAGGGGCCCCCAAAATGTTCGTGGGTGGGAGTGAAGAGTGTGCCAGGAGCCCAGAGTGTGTGGGGGAGTTGTGCGGTCTAGGTCTGAGTGCAGTGGGATTGGGGATAGGCTCAGAATGGGGTGGCCGCATAAGGGGGGAAGCCCTCTAGCTATGAAGGGCTGAGGTGTGGGTAGTGTGGGGACCGGGTCTTGAGGGAAAAGGGA... | GACTCGCGTGTAGCCTCTCTGGAGGGTGGCCGTGTCGTGGTGGGCCGGGAGCCCGGTGTCACCTCCATTGAGGTAAGCAGCTGGGGACCAGGAGAGTAGACCCCCTGAGAAGGGTGGAGGGGCCCCCAAAATGTTCGTGGGTGGGAGTGAAGAGTGTGCCAGGAGCCCAGAGTGTGTGGGGGAGTTGTGCGGTCTAGGTCTGAGTGCAGTGGGATTGGGGATAGGCTCAGAATGGGGTGGCCGCATAAGGGGGGAAGCCCTCTAGCTATGAAGGGCTGAGGTGTGGGTAGTGTGGGGACCGGGTCTTGAGGGAAAAGGGA... |
Task1_train_41272 | Chromosome 11 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GGTTGCAGTGATCTGAGATCGCACCTCTGCACTCCAGCGTAGGCAACAGAGCGAGACTCCGTCAAAAGAAAGGAAGAAAGAAAGGAAAGAAGGAAAGAAAGAGAAAGAAAGAGAGAGAGAGAAAGAGAAAGAAAGGAAGAAAGAAAGAAAGAAGGAAAGAAAGAAAGAAAGAAAGAAAGAGAAAGAAAGAGAGAGAGAGAAAGAGAAAGAAAGGAAGAAAGAAAGAAAGAAGGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAAGAGATGGCCAGGGCTGGCC... | GGTTGCAGTGATCTGAGATCGCACCTCTGCACTCCAGCGTAGGCAACAGAGCGAGACTCCGTCAAAAGAAAGGAAGAAAGAAAGGAAAGAAGGAAAGAAAGAGAAAGAAAGAGAGAGAGAGAAAGAGAAAGAAAGGAAGAAAGAAAGAAAGAAGGAAAGAAAGAAAGAAAGAAAGAAAGAGAAAGAAAGAGAGAGAGAGAAAGAGAAAGAAAGGAAGAAAGAAAGAAAGAAGGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAAGAGATGGCCAGGGCTGGCC... |
Task1_train_41273 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GTCCATGATCAGCTTTCTGTAGGTGGTCCCCCAGGGTAATAAAGAAGGGAAATGGACATTTAGGATACCAGGGAGGCTCCCTGACTTCAGACAACACTTCTTCCTGACCCATCACCTGAAGTTCCACTATCAATTCACTTTGAGGTCGTAGAACTACCATTTTTGAGAGGACACTGATAAGTCACATACAGGTGGGCAGGTATGCCTGGAGCATTTTAAGGGGATTTGTTGAGAACAGGCTAGAGTTCTTGGTGGGGGAGGCAGGGTCCTTGATTTACTCAGCAGACGTTTATTAAGGACCTACTGTATGCAAAGATGCA... | GTCCATGATCAGCTTTCTGTAGGTGGTCCCCCAGGGTAATAAAGAAGGGAAATGGACATTTAGGATACCAGGGAGGCTCCCTGACTTCAGACAACACTTCTTCCTGACCCATCACCTGAAGTTCCACTATCAATTCACTTTGAGGTCGTAGAACTACCATTTTTGAGAGGACACTGATAAGTCACATACAGGTGGGCAGGTATGCCTGGAGCATTTTAAGGGGATTTGTTGAGAACAGGCTAGAGTTCTTGGTGGGGGAGGCAGGGTCCTTGATTTACTCAGCAGACGTTTATTAAGGACCTACTGTATGCAAAGATGCA... |
Task1_train_41274 | A variant has been detected on Chromosome 11. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TGGTCCCCCAGGGTAATAAAGAAGGGAAATGGACATTTAGGATACCAGGGAGGCTCCCTGACTTCAGACAACACTTCTTCCTGACCCATCACCTGAAGTTCCACTATCAATTCACTTTGAGGTCGTAGAACTACCATTTTTGAGAGGACACTGATAAGTCACATACAGGTGGGCAGGTATGCCTGGAGCATTTTAAGGGGATTTGTTGAGAACAGGCTAGAGTTCTTGGTGGGGGAGGCAGGGTCCTTGATTTACTCAGCAGACGTTTATTAAGGACCTACTGTATGCAAAGATGCATGCTAGCACTGGGGGTACAATCC... | TGGTCCCCCAGGGTAATAAAGAAGGGAAATGGACATTTAGGATACCAGGGAGGCTCCCTGACTTCAGACAACACTTCTTCCTGACCCATCACCTGAAGTTCCACTATCAATTCACTTTGAGGTCGTAGAACTACCATTTTTGAGAGGACACTGATAAGTCACATACAGGTGGGCAGGTATGCCTGGAGCATTTTAAGGGGATTTGTTGAGAACAGGCTAGAGTTCTTGGTGGGGGAGGCAGGGTCCTTGATTTACTCAGCAGACGTTTATTAAGGACCTACTGTATGCAAAGATGCATGCTAGCACTGGGGGTACAATCC... |
Task1_train_41275 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | GTTCCACTATCAATTCACTTTGAGGTCGTAGAACTACCATTTTTGAGAGGACACTGATAAGTCACATACAGGTGGGCAGGTATGCCTGGAGCATTTTAAGGGGATTTGTTGAGAACAGGCTAGAGTTCTTGGTGGGGGAGGCAGGGTCCTTGATTTACTCAGCAGACGTTTATTAAGGACCTACTGTATGCAAAGATGCATGCTAGCACTGGGGGTACAATCCTGGGCTAAAAGGGGCAGGTGGTTCCCATAGAAGGGGTTCTGGGGAAGTGAGGACCACCATCAGCTGAAGCAGCCCATCATCAACCCCATGGCCAGCC... | GTTCCACTATCAATTCACTTTGAGGTCGTAGAACTACCATTTTTGAGAGGACACTGATAAGTCACATACAGGTGGGCAGGTATGCCTGGAGCATTTTAAGGGGATTTGTTGAGAACAGGCTAGAGTTCTTGGTGGGGGAGGCAGGGTCCTTGATTTACTCAGCAGACGTTTATTAAGGACCTACTGTATGCAAAGATGCATGCTAGCACTGGGGGTACAATCCTGGGCTAAAAGGGGCAGGTGGTTCCCATAGAAGGGGTTCTGGGGAAGTGAGGACCACCATCAGCTGAAGCAGCCCATCATCAACCCCATGGCCAGCC... |
Task1_train_41276 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | CTTCCAGGGGAGCGGCTTCCGGTCCGTCTGACAAACGGGAGCAGCAGCTGCAGCGGGACGGTGGAGGTGCGGCTCGAGGCGTCCTGGGAGCCCGCGTGCGGGGCGCTCTGGGACAGCCGCGCCGCCGAGGCCGTGTGCCGAGCACTGGGCTGCGGCGGGGCGGAGGCCGCCTCTCAGCTCGCCCCGCCGACCCCTGAGCTGCCGCCCCCGCCTGCAGCCGGGAACACCAGCGTAGCAGCTAATGCCACTCTGGCCGGGGCGCCCGCCCTCCTGTGCAGCGGCGCCGAGTGGCGGCTCTGCGAGGTGGTGGAGCACGCGTG... | CTTCCAGGGGAGCGGCTTCCGGTCCGTCTGACAAACGGGAGCAGCAGCTGCAGCGGGACGGTGGAGGTGCGGCTCGAGGCGTCCTGGGAGCCCGCGTGCGGGGCGCTCTGGGACAGCCGCGCCGCCGAGGCCGTGTGCCGAGCACTGGGCTGCGGCGGGGCGGAGGCCGCCTCTCAGCTCGCCCCGCCGACCCCTGAGCTGCCGCCCCCGCCTGCAGCCGGGAACACCAGCGTAGCAGCTAATGCCACTCTGGCCGGGGCGCCCGCCCTCCTGTGCAGCGGCGCCGAGTGGCGGCTCTGCGAGGTGGTGGAGCACGCGTG... |
Task1_train_41277 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | ACAGAATCCCCCTGGTTACCCACTGGATTGACTGTAAATGGTCCTACACTGACGTTTGCACCGTGCTTTGTGACCCTGGGGTCATCTCGATGTCTCAGGACATCTCCACTCTGACCTCTGTCTCTCCCATGTTTGTCTCTGGCCACGTAAGGTCTTAAGACCAGGCCTTTGACATTCACCTGAAGATGGCTCTCTGTGTGAGAGCGGGGGAGTGCGGATGAGAGACACAGTTGGCAGGGGTTCTCGCATGCCATATCCCTCCGTGTCCCATCCTGCCCTGTCTGACCCCATCAGCCCCACTCACTTCCTCACCTCCACGC... | ACAGAATCCCCCTGGTTACCCACTGGATTGACTGTAAATGGTCCTACACTGACGTTTGCACCGTGCTTTGTGACCCTGGGGTCATCTCGATGTCTCAGGACATCTCCACTCTGACCTCTGTCTCTCCCATGTTTGTCTCTGGCCACGTAAGGTCTTAAGACCAGGCCTTTGACATTCACCTGAAGATGGCTCTCTGTGTGAGAGCGGGGGAGTGCGGATGAGAGACACAGTTGGCAGGGGTTCTCGCATGCCATATCCCTCCGTGTCCCATCCTGCCCTGTCTGACCCCATCAGCCCCACTCACTTCCTCACCTCCACGC... |
Task1_train_41278 | A variant was discovered on Chromosome 11. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | ATTATGGTGGTGGTTACATGCATGTATACATTTGTCAAATTCCATCGAACAGTATCCTTAAAATGAGTGCATTTCACTGTATGTAAAATTACCTCAATAAAATTTTTTTTTTTTGAGATGGAATCTTGATCTGTTACCCAGGCTGGAGTGCAGTGGCGCGATCTTGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTAGGATTACAGGCGCCTGCCACCACACCCAGCTAATTTTTGGTATTTTTTCTTTTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCT... | ATTATGGTGGTGGTTACATGCATGTATACATTTGTCAAATTCCATCGAACAGTATCCTTAAAATGAGTGCATTTCACTGTATGTAAAATTACCTCAATAAAATTTTTTTTTTTTGAGATGGAATCTTGATCTGTTACCCAGGCTGGAGTGCAGTGGCGCGATCTTGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTAGGATTACAGGCGCCTGCCACCACACCCAGCTAATTTTTGGTATTTTTTCTTTTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCT... |
Task1_train_41279 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | CTGCACTAGAGTCCTCCGGAGGAGGGGTCATGCCTCCAGAGAGCTGGGCACGCAGGACACCTCTGCTTCACCACCCAGCCTTCCCCTCTCCTGCCCATTAGCCATTTTCTGCCCCAAGTAACAGAAACACAAAGTAAACAAAATTGCAATTGCTGATTTGTCCATCTCTGGAGCCCAGCTGAGACCCACTCCAGGTCAGAGAGAAGGTGTGGCCATTCCCAAGGCTGTGGCAGGCCCAGAGGGTGTTCAGTACAGCCTCTGATGGTAGGAGACACACATCCCAGGCCTAGCCCCACCACTTACCACTGCCCAAGATGCTG... | CTGCACTAGAGTCCTCCGGAGGAGGGGTCATGCCTCCAGAGAGCTGGGCACGCAGGACACCTCTGCTTCACCACCCAGCCTTCCCCTCTCCTGCCCATTAGCCATTTTCTGCCCCAAGTAACAGAAACACAAAGTAAACAAAATTGCAATTGCTGATTTGTCCATCTCTGGAGCCCAGCTGAGACCCACTCCAGGTCAGAGAGAAGGTGTGGCCATTCCCAAGGCTGTGGCAGGCCCAGAGGGTGTTCAGTACAGCCTCTGATGGTAGGAGACACACATCCCAGGCCTAGCCCCACCACTTACCACTGCCCAAGATGCTG... |
Task1_train_41280 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GAAACTGAGGCCTACGAGAGACTCCAGGGGGCAGAGCCCAGCAGCCCTGCCCTCAGCTGCACCTGCCGCCACCATCTCCCTCCCAGGCCCAGCCCCATCCCCACCCCTGCCTGCCCCCACCCATACCTGCCCCCACCACTCTGATGTGCCTTTCTTGTCTCTTGCCCAGTCCGCCAGAAGAAGCAGCGCCAGTGGATTGGCCCAACGGGAATGAACCAAAACAGTAAGTGTCCCCGGAGGCAGGAGCCTCCCTCAGGCCCTGGACAGAGGCCATGGAGGCAGAGTCGAGGCTCTCTGCTGACCACAGACGGAGCCTGTGG... | GAAACTGAGGCCTACGAGAGACTCCAGGGGGCAGAGCCCAGCAGCCCTGCCCTCAGCTGCACCTGCCGCCACCATCTCCCTCCCAGGCCCAGCCCCATCCCCACCCCTGCCTGCCCCCACCCATACCTGCCCCCACCACTCTGATGTGCCTTTCTTGTCTCTTGCCCAGTCCGCCAGAAGAAGCAGCGCCAGTGGATTGGCCCAACGGGAATGAACCAAAACAGTAAGTGTCCCCGGAGGCAGGAGCCTCCCTCAGGCCCTGGACAGAGGCCATGGAGGCAGAGTCGAGGCTCTCTGCTGACCACAGACGGAGCCTGTGG... |
Task1_train_41281 | A mutation has occurred on Chromosome 11. What is the medical relevance of this mutation? | Benign | CCACACCACATGTGACTCATCAAAGTTTATTATGGCAATTAATTACACAAACATACAGGCGGTCGGTCATCCAGCTCAGAAGCACTCAAACCAGTAGAGTCCATTAGTGATTTCTCTTTATAAATAACTTAGGAGAAGCAAGCACATTTGGTAAAGAACCGGCAGCGCTGACCTAGCGTCACGCGGATGGCACATAGGCCGGGGAGGGGCAGGCACCAGAAGGTCAAGGTCCCTCCTTGGCCCCAGCAGCCCCGGGCCCACCAGATGCTGCGTCCTCAGGTAGTGGACATTTCAAGGCACGTACAACTTCCTAAGCAATA... | CCACACCACATGTGACTCATCAAAGTTTATTATGGCAATTAATTACACAAACATACAGGCGGTCGGTCATCCAGCTCAGAAGCACTCAAACCAGTAGAGTCCATTAGTGATTTCTCTTTATAAATAACTTAGGAGAAGCAAGCACATTTGGTAAAGAACCGGCAGCGCTGACCTAGCGTCACGCGGATGGCACATAGGCCGGGGAGGGGCAGGCACCAGAAGGTCAAGGTCCCTCCTTGGCCCCAGCAGCCCCGGGCCCACCAGATGCTGCGTCCTCAGGTAGTGGACATTTCAAGGCACGTACAACTTCCTAAGCAATA... |
Task1_train_41282 | An alteration has been detected on Chromosome 11. Is it pathogenic, and if so, what disease is involved? | Benign | AAACATACAGGCGGTCGGTCATCCAGCTCAGAAGCACTCAAACCAGTAGAGTCCATTAGTGATTTCTCTTTATAAATAACTTAGGAGAAGCAAGCACATTTGGTAAAGAACCGGCAGCGCTGACCTAGCGTCACGCGGATGGCACATAGGCCGGGGAGGGGCAGGCACCAGAAGGTCAAGGTCCCTCCTTGGCCCCAGCAGCCCCGGGCCCACCAGATGCTGCGTCCTCAGGTAGTGGACATTTCAAGGCACGTACAACTTCCTAAGCAATAGCAGCTCCAGGCTCTTCCCTGAGACCTGGTTTACCTCTGGAACAACCA... | AAACATACAGGCGGTCGGTCATCCAGCTCAGAAGCACTCAAACCAGTAGAGTCCATTAGTGATTTCTCTTTATAAATAACTTAGGAGAAGCAAGCACATTTGGTAAAGAACCGGCAGCGCTGACCTAGCGTCACGCGGATGGCACATAGGCCGGGGAGGGGCAGGCACCAGAAGGTCAAGGTCCCTCCTTGGCCCCAGCAGCCCCGGGCCCACCAGATGCTGCGTCCTCAGGTAGTGGACATTTCAAGGCACGTACAACTTCCTAAGCAATAGCAGCTCCAGGCTCTTCCCTGAGACCTGGTTTACCTCTGGAACAACCA... |
Task1_train_41283 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | GTCACTCAGGCTGGAGTGCAGTGGCGCGAACTTGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCAATTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACCCGCCACCACACCCACCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGTCATGGCTGGTCTCGAACCCCTGACCTCGTGATCCACCCACCTCGGCCTCCCAAAGTACTGAGATTACAGCGGTGAGCCACCGTGCCCGGCCCTATGGCAGCATTATTTATACTGGTGAAACACTGCAAACCTCTTAAATAAGGGACAA... | GTCACTCAGGCTGGAGTGCAGTGGCGCGAACTTGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCAATTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACCCGCCACCACACCCACCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGTCATGGCTGGTCTCGAACCCCTGACCTCGTGATCCACCCACCTCGGCCTCCCAAAGTACTGAGATTACAGCGGTGAGCCACCGTGCCCGGCCCTATGGCAGCATTATTTATACTGGTGAAACACTGCAAACCTCTTAAATAAGGGACAA... |
Task1_train_41284 | 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 | TTCATGCAATTCTCCTGCCTCGGCCTCCTGAGTAGCCGGGATTACAGGCATGTACCACTACACCAGCTAGTTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAAGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCAAGCCTAGCGAAAAAAAAAATTATGTTGCAAGGAATTGTTAGTGATGCCTACAACATAAAGTTAGATGGGAAAAATAATAAAAGCTACAGATAAGATATAATCCCAGTTTTATAAAGCATACATATA... | TTCATGCAATTCTCCTGCCTCGGCCTCCTGAGTAGCCGGGATTACAGGCATGTACCACTACACCAGCTAGTTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAAGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCAAGCCTAGCGAAAAAAAAAATTATGTTGCAAGGAATTGTTAGTGATGCCTACAACATAAAGTTAGATGGGAAAAATAATAAAAGCTACAGATAAGATATAATCCCAGTTTTATAAAGCATACATATA... |
Task1_train_41285 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | CGTGGAGACTGGCCAGCCCTTTCCAGCCTTCCCTTGCCTGGCAGCACCCAGTAACTGGACCTTTCCAGCCCTTCCCCAAGAAGCTAGTTCTTTTTCTCCAGTGTTCCCTGATCTCAGAAGGCCCCGCCATCCCCTCAGCTACCTAAGCCCAGATACAGGCATTTTCCCAGACTCGTCCCCTTTTCTTCTCCACACCCAATCAGTTGCCCGGTCCTGGTGCTTCTCCTCCCAAATGTACAACACACATCCTTCTCAGACCCCGCCCTCCTGCTTTGCCTTGGTTCAGGGGTCATCTACTCATGCCTGATGGCTGCAGCCAC... | CGTGGAGACTGGCCAGCCCTTTCCAGCCTTCCCTTGCCTGGCAGCACCCAGTAACTGGACCTTTCCAGCCCTTCCCCAAGAAGCTAGTTCTTTTTCTCCAGTGTTCCCTGATCTCAGAAGGCCCCGCCATCCCCTCAGCTACCTAAGCCCAGATACAGGCATTTTCCCAGACTCGTCCCCTTTTCTTCTCCACACCCAATCAGTTGCCCGGTCCTGGTGCTTCTCCTCCCAAATGTACAACACACATCCTTCTCAGACCCCGCCCTCCTGCTTTGCCTTGGTTCAGGGGTCATCTACTCATGCCTGATGGCTGCAGCCAC... |
Task1_train_41286 | Here is a genetic alteration on Chromosome 11. Based on the data, is it a benign variant or a cause of disease? | Benign | CCCTGGGGGTGAGCTTATCCTCCTGCAGCGTCCCTGGTTCCAAACCCACCTTCGAGCTCTCAGCCGACGAGGTGGAGCTGGGCCTGGGTAAGCTTGTGGCCATCCATCCCAGCCCTGCCTGCTCCTTGGCCCTGGACTTTGCCCACCTTGCATACCCTTAGAGCCATCAACCTGGTCCTCTCCCCAGGTGGTCTTAGTATTTTTACCTGGTCATTTGAGGCCCAGCCTGGGCCAACCTGCCTGATTTCTACCTGCTTTGCTGTCTATACCCACAGCTTTGGCCATGTGGAGCTCTGTGCACTGCCCACCTCCTAGCCTTT... | CCCTGGGGGTGAGCTTATCCTCCTGCAGCGTCCCTGGTTCCAAACCCACCTTCGAGCTCTCAGCCGACGAGGTGGAGCTGGGCCTGGGTAAGCTTGTGGCCATCCATCCCAGCCCTGCCTGCTCCTTGGCCCTGGACTTTGCCCACCTTGCATACCCTTAGAGCCATCAACCTGGTCCTCTCCCCAGGTGGTCTTAGTATTTTTACCTGGTCATTTGAGGCCCAGCCTGGGCCAACCTGCCTGATTTCTACCTGCTTTGCTGTCTATACCCACAGCTTTGGCCATGTGGAGCTCTGTGCACTGCCCACCTCCTAGCCTTT... |
Task1_train_41287 | 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 | TGGACCGCAGTTTCCTTCTCTGTACAATGGAGATGAGCACCTATCTCAGAAGGTGGTTATGTGGCTAAGGAAATATGTAGAGCCCCGCACACTGCCTGGGATGTGACAGGGCCTCAGTGAATGGTGACCCTTTTCCCTGCTGGAAGTAGATGAGAAGTGACTTTCCATTTGGTGACAGAGCAGAGGGTGCTGGCAGAGCCAGGGCAAGGGCGTGCAGGGCCAGGCTGCACGGCAGAGACGTTCTGCCCATGGCAGGAAGGAGGCGGCCTGGTGATCTGCCCTTGAACCTGCTCCCACACCCCATCCCCCAGAGTGCCGAA... | TGGACCGCAGTTTCCTTCTCTGTACAATGGAGATGAGCACCTATCTCAGAAGGTGGTTATGTGGCTAAGGAAATATGTAGAGCCCCGCACACTGCCTGGGATGTGACAGGGCCTCAGTGAATGGTGACCCTTTTCCCTGCTGGAAGTAGATGAGAAGTGACTTTCCATTTGGTGACAGAGCAGAGGGTGCTGGCAGAGCCAGGGCAAGGGCGTGCAGGGCCAGGCTGCACGGCAGAGACGTTCTGCCCATGGCAGGAAGGAGGCGGCCTGGTGATCTGCCCTTGAACCTGCTCCCACACCCCATCCCCCAGAGTGCCGAA... |
Task1_train_41288 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | TCTCTCTTAAAAAAAAAAAAGAGCATTTACTACCTGTCAGGTGCTGAATCCATGCTCTTGCTAAATCTGCCAGCAGCCCTGTGAGGTGGGTGCAGTCACGTCCCTTGCGAAGATGGGGATTTGGGGGCGTGAAGAGGATAAGTACCTCATCAAAGGTGACAGATCAGATTTGAACCACACTCTTAACTGCTGCGGTTTATTGGCCCTACAATAATAGTGCCCAGTTCACAGGGTGGTTTGGGGGATTACACGACGTAATGTGTGTTAAAGGGCTTAGCACAGATTCAGCTCCAGAGGAACATAGTAAATGTTGATTTACC... | TCTCTCTTAAAAAAAAAAAAGAGCATTTACTACCTGTCAGGTGCTGAATCCATGCTCTTGCTAAATCTGCCAGCAGCCCTGTGAGGTGGGTGCAGTCACGTCCCTTGCGAAGATGGGGATTTGGGGGCGTGAAGAGGATAAGTACCTCATCAAAGGTGACAGATCAGATTTGAACCACACTCTTAACTGCTGCGGTTTATTGGCCCTACAATAATAGTGCCCAGTTCACAGGGTGGTTTGGGGGATTACACGACGTAATGTGTGTTAAAGGGCTTAGCACAGATTCAGCTCCAGAGGAACATAGTAAATGTTGATTTACC... |
Task1_train_41289 | Consider this mutation on Chromosome 11. Is this a benign change or a disease-causing variant? | Benign | AGGGTGGGCTGTGGCAATGGCCCATCCAGAAGAGAAGACAGCTGGGGCCAGTCTTCCTGGGGGGGGGAAGATGGAAGGAGGGCAGTGGAGGGCCAGACACACAGGGGCCTGGTGGGCAGGGAGAAGGGGAGAGGTGGGGAGGCCCAAGGTGACCAGATCTAGGATGTGGAAAATCTGATGCTCTAATGTGGATTCAAGAAAACCACAGGATAGACCGGGCGCAGTGGCTCATGCCTGTAATCACAGCACTTTGGGAGGCCGAGGCAGGTGGATCACTTGAGGCTAAGAGTTTGAGACTGGCCTGGCCAACATGGTGAAAC... | AGGGTGGGCTGTGGCAATGGCCCATCCAGAAGAGAAGACAGCTGGGGCCAGTCTTCCTGGGGGGGGGAAGATGGAAGGAGGGCAGTGGAGGGCCAGACACACAGGGGCCTGGTGGGCAGGGAGAAGGGGAGAGGTGGGGAGGCCCAAGGTGACCAGATCTAGGATGTGGAAAATCTGATGCTCTAATGTGGATTCAAGAAAACCACAGGATAGACCGGGCGCAGTGGCTCATGCCTGTAATCACAGCACTTTGGGAGGCCGAGGCAGGTGGATCACTTGAGGCTAAGAGTTTGAGACTGGCCTGGCCAACATGGTGAAAC... |
Task1_train_41290 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TTGAAGCTTACACACATACATGTGCACACAATTATTAGTTATAAGTACACAGGTCACCCCCTACAGACATGCACATGTACAAGACACACACCAAGACAAAGGTGGAGACACATATACAAGGACACATGTGGACAGGCAGGTGCTCATGGAAATGCATGAATACACCTGTGCACAGACCCAGACACACAAGCCAGCTGACATACACAGACGTCTGGTCTACACACTCATACACATGAACAGAGGCGTGCACACATGCTCACAGGGGCACGCACATGGGGGCCACAGCGCCCTTGCTATTCACACACTCTTTGAGGGGTGCG... | TTGAAGCTTACACACATACATGTGCACACAATTATTAGTTATAAGTACACAGGTCACCCCCTACAGACATGCACATGTACAAGACACACACCAAGACAAAGGTGGAGACACATATACAAGGACACATGTGGACAGGCAGGTGCTCATGGAAATGCATGAATACACCTGTGCACAGACCCAGACACACAAGCCAGCTGACATACACAGACGTCTGGTCTACACACTCATACACATGAACAGAGGCGTGCACACATGCTCACAGGGGCACGCACATGGGGGCCACAGCGCCCTTGCTATTCACACACTCTTTGAGGGGTGCG... |
Task1_train_41291 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GCCTCTTAAGGCCAAGGAAGTGTGTGTCTCAGTGGAGGCCCCAGATCCTCAGGGCCAAAGCCAGCCTCAGGTGCAGAGACCACTACCTACTGCTTGGAGTCAGTGGGGCAGGGAGGGGGCCTCAGGTCCCCAGATGGTATACCCTGGAGGCTGCAGGCCAAGTGCCTCAGATCACAGGAGGTTGGAGAGAAAGGACCTGCCCAGCCCTCACATCCCAGAGAGGCGCAGGACAGGCTCCAGGTCACACAGCATGGGGCAGGCTGGTCCTCACTGGGCTCGGACCCTGCCTACCGCAGGCACTGCCACCCTTCCCCGTGCCC... | GCCTCTTAAGGCCAAGGAAGTGTGTGTCTCAGTGGAGGCCCCAGATCCTCAGGGCCAAAGCCAGCCTCAGGTGCAGAGACCACTACCTACTGCTTGGAGTCAGTGGGGCAGGGAGGGGGCCTCAGGTCCCCAGATGGTATACCCTGGAGGCTGCAGGCCAAGTGCCTCAGATCACAGGAGGTTGGAGAGAAAGGACCTGCCCAGCCCTCACATCCCAGAGAGGCGCAGGACAGGCTCCAGGTCACACAGCATGGGGCAGGCTGGTCCTCACTGGGCTCGGACCCTGCCTACCGCAGGCACTGCCACCCTTCCCCGTGCCC... |
Task1_train_41292 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GTGCAGAGACCACTACCTACTGCTTGGAGTCAGTGGGGCAGGGAGGGGGCCTCAGGTCCCCAGATGGTATACCCTGGAGGCTGCAGGCCAAGTGCCTCAGATCACAGGAGGTTGGAGAGAAAGGACCTGCCCAGCCCTCACATCCCAGAGAGGCGCAGGACAGGCTCCAGGTCACACAGCATGGGGCAGGCTGGTCCTCACTGGGCTCGGACCCTGCCTACCGCAGGCACTGCCACCCTTCCCCGTGCCCAGAGCCCGCTTCCCACCCTCACCTCCTTGCCCTCTCTGTCTGGGGTGAGGGTGTGTCCCGCAGCGGGACA... | GTGCAGAGACCACTACCTACTGCTTGGAGTCAGTGGGGCAGGGAGGGGGCCTCAGGTCCCCAGATGGTATACCCTGGAGGCTGCAGGCCAAGTGCCTCAGATCACAGGAGGTTGGAGAGAAAGGACCTGCCCAGCCCTCACATCCCAGAGAGGCGCAGGACAGGCTCCAGGTCACACAGCATGGGGCAGGCTGGTCCTCACTGGGCTCGGACCCTGCCTACCGCAGGCACTGCCACCCTTCCCCGTGCCCAGAGCCCGCTTCCCACCCTCACCTCCTTGCCCTCTCTGTCTGGGGTGAGGGTGTGTCCCGCAGCGGGACA... |
Task1_train_41293 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | TTAAACGGAGTTTCACTCTTGTTGCCCAGAGCTGGAGTGCAGTGGCATAATCTCGGCTCACTGCAACCTCCGCCTCCCAGATTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTATAGGTGCCAGCCACCAAGCCCGGCTAATTTTTGTATTTTTAGTAGAGACAGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCACCCTCCTCAGCCTCCCAAAGTGCTGGGATTACATGTGTGAGCCACTGTGCCTGGCTGCTTGTTCTTTTAAGAACCAAATATCCTACTAGACTG... | TTAAACGGAGTTTCACTCTTGTTGCCCAGAGCTGGAGTGCAGTGGCATAATCTCGGCTCACTGCAACCTCCGCCTCCCAGATTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTATAGGTGCCAGCCACCAAGCCCGGCTAATTTTTGTATTTTTAGTAGAGACAGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCACCCTCCTCAGCCTCCCAAAGTGCTGGGATTACATGTGTGAGCCACTGTGCCTGGCTGCTTGTTCTTTTAAGAACCAAATATCCTACTAGACTG... |
Task1_train_41294 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | TCTAGGCGAGAGTGCTCCTCCAGTTAGGCTCAGAAGCCAAGGAGAAATCGATAGTAACCAGTACAGGAAGAGGGGGAAGCTATTGGACACTGTGCCTAAAGGTGGGAGTCTACTGGGAGCCAGGTTGGGGTGATGGGTGTGGGGCTTCCCTCTGGGTCCCAGCCTCCACCCAGCCCCAGACTGTTCAAGGGGAAAGCACTAGCCTTGTCCTTGGCCAGGGAGGGCTTAGAGCCCCTGCCCATCCCTGCTGGCTGCCCATTGCTGTGGCTGTGCCCCTGGGACTTTCTGTGTCTGCCCAGGAGGGGGTGCCAGCATCAATC... | TCTAGGCGAGAGTGCTCCTCCAGTTAGGCTCAGAAGCCAAGGAGAAATCGATAGTAACCAGTACAGGAAGAGGGGGAAGCTATTGGACACTGTGCCTAAAGGTGGGAGTCTACTGGGAGCCAGGTTGGGGTGATGGGTGTGGGGCTTCCCTCTGGGTCCCAGCCTCCACCCAGCCCCAGACTGTTCAAGGGGAAAGCACTAGCCTTGTCCTTGGCCAGGGAGGGCTTAGAGCCCCTGCCCATCCCTGCTGGCTGCCCATTGCTGTGGCTGTGCCCCTGGGACTTTCTGTGTCTGCCCAGGAGGGGGTGCCAGCATCAATC... |
Task1_train_41295 | A mutation found on Chromosome 11 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | ACAGCTAGATTTGAAGTGGAAAACTTGAGCCTAGAGGTTGGGGGGAAGTGACCACTCACCCTGATCATCTGTCTCTTCTTTTCCATCTTCTTCCCCTCCTGGAGCCCCAGAGCAAAGAACTCTCAGTACCTGTCCGATGCATGATTGGCTCTGGACACTCCAAAAGCTACTTGGAAAAAGTTAGGCTATGTAATCATCAGGTCAACCCATCAACATGTGGGTGGCTACACATCACAGAAAGCTTGCTCCTCGTAGAGAGAAAATGTGAGTCTTGGCCATATTTATAGCTGCACTCATAAACAAGACTCAGGTTTGGGAGT... | ACAGCTAGATTTGAAGTGGAAAACTTGAGCCTAGAGGTTGGGGGGAAGTGACCACTCACCCTGATCATCTGTCTCTTCTTTTCCATCTTCTTCCCCTCCTGGAGCCCCAGAGCAAAGAACTCTCAGTACCTGTCCGATGCATGATTGGCTCTGGACACTCCAAAAGCTACTTGGAAAAAGTTAGGCTATGTAATCATCAGGTCAACCCATCAACATGTGGGTGGCTACACATCACAGAAAGCTTGCTCCTCGTAGAGAGAAAATGTGAGTCTTGGCCATATTTATAGCTGCACTCATAAACAAGACTCAGGTTTGGGAGT... |
Task1_train_41296 | 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 | TCAATCCGTCTAACCAGGTAAGGATTGCTGGAAGAGTTCTCAAAATAGACGTAATCTGTAAGGGAAGGGAGGGGGGAGAACCACGAAGATCAGAGGAGATGGGAGACGCAGAGCACCAGGGTAGGAGAGAAAGTTGGCCTGAGTGGATCAAAAGGAGATAAGGATTCAGGTAGAAAGGGCGCTGAGATGTGAAAGTGGACAGACTAAGAGAAAATAAGGATGTCCCCCATCCCCACCGCACCTAGTTCTAAAATTAGATCCTTTACTCAAAAGAGAGCCTTAAGGAACAGGCAAGAAGCAGGGGTTCCCCTGCAGTCCCC... | TCAATCCGTCTAACCAGGTAAGGATTGCTGGAAGAGTTCTCAAAATAGACGTAATCTGTAAGGGAAGGGAGGGGGGAGAACCACGAAGATCAGAGGAGATGGGAGACGCAGAGCACCAGGGTAGGAGAGAAAGTTGGCCTGAGTGGATCAAAAGGAGATAAGGATTCAGGTAGAAAGGGCGCTGAGATGTGAAAGTGGACAGACTAAGAGAAAATAAGGATGTCCCCCATCCCCACCGCACCTAGTTCTAAAATTAGATCCTTTACTCAAAAGAGAGCCTTAAGGAACAGGCAAGAAGCAGGGGTTCCCCTGCAGTCCCC... |
Task1_train_41297 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | GCGACCGGAGGAACTGTGGAGGATGCTCGGAGCCCCTGGGGCGGAGGAGCACGCGGGGACGCCTCCAGACAGCCGTCCAGCTCTGGCATAACCCGACGAGCCGGGCGCTCCGGGAAGGGGCACGCCGCCCGCCCCGCCCCGTACTCACCGGGCCCCGCGGCCCCGTCCATCCGGCCCCCGGGTTGCTCCGAGCGGCGGCGGCGGAGGAGGCGTCTAAGCCGCGGGGGCCACGGCCGGGGAGAGGGGAAGGGGAAGCACCCCGGGGCGCGCGCGAAGGGCGCCGTACCACCACCCCGAGGGGGCGCTGTCGGGCGCGGGGA... | GCGACCGGAGGAACTGTGGAGGATGCTCGGAGCCCCTGGGGCGGAGGAGCACGCGGGGACGCCTCCAGACAGCCGTCCAGCTCTGGCATAACCCGACGAGCCGGGCGCTCCGGGAAGGGGCACGCCGCCCGCCCCGCCCCGTACTCACCGGGCCCCGCGGCCCCGTCCATCCGGCCCCCGGGTTGCTCCGAGCGGCGGCGGCGGAGGAGGCGTCTAAGCCGCGGGGGCCACGGCCGGGGAGAGGGGAAGGGGAAGCACCCCGGGGCGCGCGCGAAGGGCGCCGTACCACCACCCCGAGGGGGCGCTGTCGGGCGCGGGGA... |
Task1_train_41298 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | CCAAAACCCAAAGAAAGGTTGTCTGCTACAGGTATTGTGAGAGGCTATCAGAGCTTAGGAACTAACAGCCGACAGACATTCCCCGCATAAGCGTCAGTGCACAAGGTGAGCTGAGAGGTGAAGCTGCTCCGGAGCTCTGCAGGGAGGAAGGAAGACTCGGTGGGGACGACCAACAGGAAGAGGGTCTAGTACTTACGCCCGCTTCTTGAGGTGGTGCCGCGTGATCAGCCCTTGGTCTATCACAGCCCCGACCACCCGGTGCCTCAGACGCCGCTCCCGATTCAACACCCGCCGGCGTTTGAACAGCTTCTTCTTCAGCT... | CCAAAACCCAAAGAAAGGTTGTCTGCTACAGGTATTGTGAGAGGCTATCAGAGCTTAGGAACTAACAGCCGACAGACATTCCCCGCATAAGCGTCAGTGCACAAGGTGAGCTGAGAGGTGAAGCTGCTCCGGAGCTCTGCAGGGAGGAAGGAAGACTCGGTGGGGACGACCAACAGGAAGAGGGTCTAGTACTTACGCCCGCTTCTTGAGGTGGTGCCGCGTGATCAGCCCTTGGTCTATCACAGCCCCGACCACCCGGTGCCTCAGACGCCGCTCCCGATTCAACACCCGCCGGCGTTTGAACAGCTTCTTCTTCAGCT... |
Task1_train_41299 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CTTTCAAAATGTTTACATTGCTGCAGGAAAAGATAAAATTACCCCAAGACTGGCCGGCTTGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCAGGAGGCGGAGCTTGCAGTGAGCTGAGATCGCGCCACTGCACTCCAGTCTGGGTGACAGAGCGAGACTCAGTCTCAAAAAAAAAAAAAAGAAGAAAAAGAAAGTACAGATTAAAGGATGGCACCCATTCTGATACCAAAACTGCTCTCTACAATTCATCAACTTTGCCAGCTGCCTTTTCTCTCCCACATCTTCACATTTATTGAGCACCTGCTGTGTGCCTGGCACT... | CTTTCAAAATGTTTACATTGCTGCAGGAAAAGATAAAATTACCCCAAGACTGGCCGGCTTGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCAGGAGGCGGAGCTTGCAGTGAGCTGAGATCGCGCCACTGCACTCCAGTCTGGGTGACAGAGCGAGACTCAGTCTCAAAAAAAAAAAAAAGAAGAAAAAGAAAGTACAGATTAAAGGATGGCACCCATTCTGATACCAAAACTGCTCTCTACAATTCATCAACTTTGCCAGCTGCCTTTTCTCTCCCACATCTTCACATTTATTGAGCACCTGCTGTGTGCCTGGCACT... |
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