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_43200 | A mutation on Chromosome 14 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CAATCAAGAATGCAATCCTAGTCAAAATTGCCACAAAAAGAATAAAATACCTAAGAATACTGCTAACTAGGGAGGTGCAAGATCTCTACAAGGGGAATTACAAAACACTGCTCAAAGAAATCAGAGATGACACAAACAAATGGAAAAACACTCCAGGCTCATGGGTAGGAAGAATCAGTATCATTAAAATGGCCATAGTGCCCAAAGCAATCTACAGATTCTATGCTATTCCCATCAAACTACCGATGACATTCTTCACAGAACTAGAAAAAACTGATTTAAAATTCATACAGAATCAGAAAAAAGCCTGAATAGCCAAA... | CAATCAAGAATGCAATCCTAGTCAAAATTGCCACAAAAAGAATAAAATACCTAAGAATACTGCTAACTAGGGAGGTGCAAGATCTCTACAAGGGGAATTACAAAACACTGCTCAAAGAAATCAGAGATGACACAAACAAATGGAAAAACACTCCAGGCTCATGGGTAGGAAGAATCAGTATCATTAAAATGGCCATAGTGCCCAAAGCAATCTACAGATTCTATGCTATTCCCATCAAACTACCGATGACATTCTTCACAGAACTAGAAAAAACTGATTTAAAATTCATACAGAATCAGAAAAAAGCCTGAATAGCCAAA... |
Task1_train_43201 | This sequence change occurs on Chromosome 14. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GTGAGATATTCTGAGTGGGGAGAAGTGTTTTCTATCGATGACACAGGGTGGGCCCTATGGGAGCAGCAGCATGGCCCCACCTTCGACCCAATGCTGAGAGGAAAGGGGCCTCAGGAAGGGGAGACTGAAGCCAGGACAGGGTGGGATGCTCAGGAAGAATGACAGTGGAGCTGCTGCCCTCCCCGGACACCCTCCATCAGGACAAAAGAGCTGGGCCTCCACTCCCTCAGTAGAGAGGACAGCAGCCACGGGCTCTTCACCTGCCCCATGAACTCAGGATTAGGGAGCTGAGAGTTGCCTTGAAAATCCTTACCCTGACA... | GTGAGATATTCTGAGTGGGGAGAAGTGTTTTCTATCGATGACACAGGGTGGGCCCTATGGGAGCAGCAGCATGGCCCCACCTTCGACCCAATGCTGAGAGGAAAGGGGCCTCAGGAAGGGGAGACTGAAGCCAGGACAGGGTGGGATGCTCAGGAAGAATGACAGTGGAGCTGCTGCCCTCCCCGGACACCCTCCATCAGGACAAAAGAGCTGGGCCTCCACTCCCTCAGTAGAGAGGACAGCAGCCACGGGCTCTTCACCTGCCCCATGAACTCAGGATTAGGGAGCTGAGAGTTGCCTTGAAAATCCTTACCCTGACA... |
Task1_train_43202 | A variant on Chromosome 14 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GGTAACCTCTATTCCACCTTCCCTCTCTATCTATCCATTTTTGTAGTTTATCACGTGCTGTACCTTTATTTAGGAAACTCAGGACTTGAAGCTACAGTGCTATCACCAACAGACAGAAAACAACCTCCTTCTAAATAAAAGGAGTGGGAATTGCAGTTTGGAAAAGGATGAACATATATCTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTTGTTTCCCAGGCTGGAGTGCAATGGCACAATATCGGCTCTCTGCAACCTCTGCCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGA... | GGTAACCTCTATTCCACCTTCCCTCTCTATCTATCCATTTTTGTAGTTTATCACGTGCTGTACCTTTATTTAGGAAACTCAGGACTTGAAGCTACAGTGCTATCACCAACAGACAGAAAACAACCTCCTTCTAAATAAAAGGAGTGGGAATTGCAGTTTGGAAAAGGATGAACATATATCTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTTGTTTCCCAGGCTGGAGTGCAATGGCACAATATCGGCTCTCTGCAACCTCTGCCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGA... |
Task1_train_43203 | This genomic variant is located on Chromosome 14. Can you determine its pathogenicity and name any linked disease? | Benign | CCCAGGCCCCTGAGGCATGATCACTCGTGTTCCGTGTTCCGGGGAGAGCTTAAGAAATCACAGTGGCCAGAAGCCCAGCCTCTCTCTCTCCCAGGCAGGACCAATGGGGCAGTAACCATCTGGGGAGGGCGGTGGGGGAATGAAATGTCAGAGAACATTTCTCAATCTGACGGTGTGAGAAATACTTATGTATCTTAGAGTTTGGAAAGCCCTTTTTTCAGTTAATCCTTAAAACAACCTTGTGAGTTAGGCATTAGATAACATTTTGTCAAACAGTCATAGGTTTCGTTTTACCTAAATCCTTCAAACTTCAGTTTCAT... | CCCAGGCCCCTGAGGCATGATCACTCGTGTTCCGTGTTCCGGGGAGAGCTTAAGAAATCACAGTGGCCAGAAGCCCAGCCTCTCTCTCTCCCAGGCAGGACCAATGGGGCAGTAACCATCTGGGGAGGGCGGTGGGGGAATGAAATGTCAGAGAACATTTCTCAATCTGACGGTGTGAGAAATACTTATGTATCTTAGAGTTTGGAAAGCCCTTTTTTCAGTTAATCCTTAAAACAACCTTGTGAGTTAGGCATTAGATAACATTTTGTCAAACAGTCATAGGTTTCGTTTTACCTAAATCCTTCAAACTTCAGTTTCAT... |
Task1_train_43204 | This mutation on Chromosome 14 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GGGGGCAGGGTGGAAGCAGAATGCAGCAGAGGCTGCTGGGGCCCTCAGCACAAGACATAGGCAGTAGCTGCCTGAAGTGAGGGGTCCCTAGAGCTGGGGGATGGGGGCAGGGGGCGTGGGCTGGGGGGGTGTACAGTTATGGAGTCAGACACACAGACCCCACAAGGAAGGAAGGAGGGAGCCCAGAGAGCTCCTGGAATACCAGCAATGGCCAGTTACTGAGAGCCTACTGTGGCCCACCAGGCCCCATGAAGAGTTTTCCATATATGACTTTGTTTTATCACCTGGAATACTAACGCAAGCTAACATTTATTGAACTC... | GGGGGCAGGGTGGAAGCAGAATGCAGCAGAGGCTGCTGGGGCCCTCAGCACAAGACATAGGCAGTAGCTGCCTGAAGTGAGGGGTCCCTAGAGCTGGGGGATGGGGGCAGGGGGCGTGGGCTGGGGGGGTGTACAGTTATGGAGTCAGACACACAGACCCCACAAGGAAGGAAGGAGGGAGCCCAGAGAGCTCCTGGAATACCAGCAATGGCCAGTTACTGAGAGCCTACTGTGGCCCACCAGGCCCCATGAAGAGTTTTCCATATATGACTTTGTTTTATCACCTGGAATACTAACGCAAGCTAACATTTATTGAACTC... |
Task1_train_43205 | This variant is located on Chromosome 14. Evaluate its biological effect and specify any disease association. | Benign | ATTAGCCAGGTGTCCCAACTACTTGGGAGGTTGAGGCTGCAGTGAGCCATGATTGTGCCACTGCACTGTTATAATGCTGTCAACTAGATACATAAAGCAGTTTGCTTAATTTATAGGGTGGCAATAGTCTGGAAACATAAGTCATGTATATATTTCTAATAGTGCAAACTTTGATGACCACTTCTGGGATATGCTAAAGGTGCAGGTTTAGTCAGTGGAAATCAGAGACAAATCAGGAACACAGGTCCATGTGCAGGAAATGATGGAAATGCTACAGTAATACACCTGTTGGTTGCAGTTTGGCACTGTACACTCAACTA... | ATTAGCCAGGTGTCCCAACTACTTGGGAGGTTGAGGCTGCAGTGAGCCATGATTGTGCCACTGCACTGTTATAATGCTGTCAACTAGATACATAAAGCAGTTTGCTTAATTTATAGGGTGGCAATAGTCTGGAAACATAAGTCATGTATATATTTCTAATAGTGCAAACTTTGATGACCACTTCTGGGATATGCTAAAGGTGCAGGTTTAGTCAGTGGAAATCAGAGACAAATCAGGAACACAGGTCCATGTGCAGGAAATGATGGAAATGCTACAGTAATACACCTGTTGGTTGCAGTTTGGCACTGTACACTCAACTA... |
Task1_train_43206 | This mutation is located on Chromosome 14. Is it associated with a disease or is it a benign polymorphism? | Benign | CAATATGTTCACTCTACCGTTGAAGGATGGCTGGGAGAATGAATGCTCTGTCCCCCAGTCCCAAGCTCACTTACTATACCTCCTTTATAGCCTAGGATATGAACATACTGCTCTTTTTTTGTCTTGGACCCAGGAGCCCGAGTCTATATTGCCTGCAGAGATGTACTGAAGGGGGAGTCTGCTGCCAGTGAAATCCGAGTGGATACAAAGAACTCCCAGGTGCTGGTGCGGAAATTGGACCTATCCGACACCAAATCTATCCGAGCCTTTGCTGAGGGCTTTCTGGCAGGTGAGGTCCTGATGGGTAGGTAGAAAAGCAG... | CAATATGTTCACTCTACCGTTGAAGGATGGCTGGGAGAATGAATGCTCTGTCCCCCAGTCCCAAGCTCACTTACTATACCTCCTTTATAGCCTAGGATATGAACATACTGCTCTTTTTTTGTCTTGGACCCAGGAGCCCGAGTCTATATTGCCTGCAGAGATGTACTGAAGGGGGAGTCTGCTGCCAGTGAAATCCGAGTGGATACAAAGAACTCCCAGGTGCTGGTGCGGAAATTGGACCTATCCGACACCAAATCTATCCGAGCCTTTGCTGAGGGCTTTCTGGCAGGTGAGGTCCTGATGGGTAGGTAGAAAAGCAG... |
Task1_train_43207 | This genomic variant is located on Chromosome 14. Can you determine its pathogenicity and name any linked disease? | Benign | AAATCTATTATCCAGAATTCACTGAAGTCACAGTTTGAATTTGGTCAGGATTGGAGTAGAGTTTTGTTCAAGGCTAATCACTGGACATTCAAGGAGGACACATTTTCTTTAAAAGCCAGAAAGTCCCACAGAGACTAAAGGTGGTTCCCTACATTGACTTTAATGACAAATCAACTAATGAAAGTCTTTACTCTCTTTCTGACTGGTATAGCTAGAGTAAACTCTGCTTTGAGGGTCTGCTCTGAAAAAGAAAAGGACACAGGGTGTCAGGTAGGATGGGGAAGAACACTTGAGATCTGGCAACACCGTTTCATCAACAT... | AAATCTATTATCCAGAATTCACTGAAGTCACAGTTTGAATTTGGTCAGGATTGGAGTAGAGTTTTGTTCAAGGCTAATCACTGGACATTCAAGGAGGACACATTTTCTTTAAAAGCCAGAAAGTCCCACAGAGACTAAAGGTGGTTCCCTACATTGACTTTAATGACAAATCAACTAATGAAAGTCTTTACTCTCTTTCTGACTGGTATAGCTAGAGTAAACTCTGCTTTGAGGGTCTGCTCTGAAAAAGAAAAGGACACAGGGTGTCAGGTAGGATGGGGAAGAACACTTGAGATCTGGCAACACCGTTTCATCAACAT... |
Task1_train_43208 | Chromosome 14 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TACTTTGCTGATTTTTCTTTGTATCCATTTGCTGAAATAAATCTTAGCTCTATGACGATAAGCTGATTCTTGAGAGTTCTCCTAGAGAATCACTGAACCTGGGGGTGGACTTGGGGACCCCAGACACATGGGGCTACTCATATCATAACCTATTCACCACTCCTCCCTCTATATTACTAAGGCAGAACAGGTTCCTTTCTCCTCCACTGCTCAGTCCTTCCAATGTTTGGTGCAAGTAGCAAGGACAGGTGTGGGGAGTAGAACGTTGCCTAATTCTACCTTCATATACTGATGCCTTCACATACCTGATTTCTCTAAGA... | TACTTTGCTGATTTTTCTTTGTATCCATTTGCTGAAATAAATCTTAGCTCTATGACGATAAGCTGATTCTTGAGAGTTCTCCTAGAGAATCACTGAACCTGGGGGTGGACTTGGGGACCCCAGACACATGGGGCTACTCATATCATAACCTATTCACCACTCCTCCCTCTATATTACTAAGGCAGAACAGGTTCCTTTCTCCTCCACTGCTCAGTCCTTCCAATGTTTGGTGCAAGTAGCAAGGACAGGTGTGGGGAGTAGAACGTTGCCTAATTCTACCTTCATATACTGATGCCTTCACATACCTGATTTCTCTAAGA... |
Task1_train_43209 | A variant on Chromosome 14 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TTGGGGTAAGTTATGTAGCCTCCTTGGGACTCAATTTCCTCATTACTACAATGACAGTGTTGGGCCAGATGCTCACCAAGCCTCTTCCTGCACTGACATTTTGTGATGGCGATGACCCTGTGGGGAGTATCAGGTTATGGGAGAAACAGATCTACATGTCAGTCAGCAGGGCAACTCTGTTATTAGAAATCAAGCAGAGTGCAGTCCTAGGACTGATGACCAAGAGTCCAGTGTGCACAATCCTGGCTGTCTCCAGAGGCAACCCTCGCATGTCATAGCAATGGAACATGAAGAGGTGGAGATCTTTTGGAGTGATCAGA... | TTGGGGTAAGTTATGTAGCCTCCTTGGGACTCAATTTCCTCATTACTACAATGACAGTGTTGGGCCAGATGCTCACCAAGCCTCTTCCTGCACTGACATTTTGTGATGGCGATGACCCTGTGGGGAGTATCAGGTTATGGGAGAAACAGATCTACATGTCAGTCAGCAGGGCAACTCTGTTATTAGAAATCAAGCAGAGTGCAGTCCTAGGACTGATGACCAAGAGTCCAGTGTGCACAATCCTGGCTGTCTCCAGAGGCAACCCTCGCATGTCATAGCAATGGAACATGAAGAGGTGGAGATCTTTTGGAGTGATCAGA... |
Task1_train_43210 | Consider a variant on Chromosome 14. Determine its clinical classification and disease relevance. | Benign | GGAGGCCCACGGGTGCCCTCTGGCGCTGAAGAGGTAATGTAGTCACAGTGACAAAGTTAGATTACAAGGCACTAAGTTGCTTCTGTAAACTGTTACTGCTTTTTCTCTTGTGATTTGGCACTTAAGGCTTAAGCCGGAAAAAAAAAGGCATCTACTGACAAAATATGGGACTTGTCTGTTATGCATGGTAAGTGGGCTATAAAATCCAGGGAGGGGGTTTCAAGCCAGAAGAAGCTACTGACAAATTGACTTGTCCTTATGTTAGGTGGGGTTATGAGGGGGAGAGGGAGGGCACATTCTGAGGTGCTGGGGGAAAGGGG... | GGAGGCCCACGGGTGCCCTCTGGCGCTGAAGAGGTAATGTAGTCACAGTGACAAAGTTAGATTACAAGGCACTAAGTTGCTTCTGTAAACTGTTACTGCTTTTTCTCTTGTGATTTGGCACTTAAGGCTTAAGCCGGAAAAAAAAAGGCATCTACTGACAAAATATGGGACTTGTCTGTTATGCATGGTAAGTGGGCTATAAAATCCAGGGAGGGGGTTTCAAGCCAGAAGAAGCTACTGACAAATTGACTTGTCCTTATGTTAGGTGGGGTTATGAGGGGGAGAGGGAGGGCACATTCTGAGGTGCTGGGGGAAAGGGG... |
Task1_train_43211 | This variant is located on Chromosome 14. Evaluate its biological effect and specify any disease association. | Benign | CTTATACTAATCCTGTGTCCTGACACCTTAGCTGAGCCCAAGACATTACAGAAATGAGTAGAAGTGGCAAACAAGGAGAGGCCAAAGGACCCTGGAAGAAGGGGCGGTTGAGGAGTTCATGTTCCAGCTCTCACCCCTTTAGATCACAGTCCAGCCAGTGCCTGCCACCCCAGCACAGTGCCCACCCATAGGACACCCACCTTGTCCCCAGCCAGGATCTTGAAGGAAGCCATGACTTGGTCTGCTGTATCTGTGTCGGCTGTCTCGCGGGACATGAAGTCAATGAAGGCCTGGAATGTCACTACCCCCAGGCGGTTGGG... | CTTATACTAATCCTGTGTCCTGACACCTTAGCTGAGCCCAAGACATTACAGAAATGAGTAGAAGTGGCAAACAAGGAGAGGCCAAAGGACCCTGGAAGAAGGGGCGGTTGAGGAGTTCATGTTCCAGCTCTCACCCCTTTAGATCACAGTCCAGCCAGTGCCTGCCACCCCAGCACAGTGCCCACCCATAGGACACCCACCTTGTCCCCAGCCAGGATCTTGAAGGAAGCCATGACTTGGTCTGCTGTATCTGTGTCGGCTGTCTCGCGGGACATGAAGTCAATGAAGGCCTGGAATGTCACTACCCCCAGGCGGTTGGG... |
Task1_train_43212 | Consider a variant on Chromosome 14. Determine its clinical classification and disease relevance. | Benign | CACTCCAGTAACTGAACTGATTAGGATTTTTTGCTGTTTTACAGTTGTCTGTAAATGTGGTTGGTTGTGGGCTTTGTTTTTGTTTTTTTTTAAGATGGAGTTTTGCTCTTGTTGCCCAGGCTGGAGTGCAATGGCACAATCTCCGCTCACTGCAACCTCCATCTCTCAGGTTCAAGCTATTCTCCTGCCTTACCCTCCCCCGACTAGCTGGGATTACAGGCATGTGCCACCACACCCAACTAATTTTGTATTTTTAGTAGAGATGGGGTTTCTCCATATTGGTCAGGCTGGTCTCGAACTCCTGAGCTCAGGTGATCCAC... | CACTCCAGTAACTGAACTGATTAGGATTTTTTGCTGTTTTACAGTTGTCTGTAAATGTGGTTGGTTGTGGGCTTTGTTTTTGTTTTTTTTTAAGATGGAGTTTTGCTCTTGTTGCCCAGGCTGGAGTGCAATGGCACAATCTCCGCTCACTGCAACCTCCATCTCTCAGGTTCAAGCTATTCTCCTGCCTTACCCTCCCCCGACTAGCTGGGATTACAGGCATGTGCCACCACACCCAACTAATTTTGTATTTTTAGTAGAGATGGGGTTTCTCCATATTGGTCAGGCTGGTCTCGAACTCCTGAGCTCAGGTGATCCAC... |
Task1_train_43213 | Here is a mutation located on Chromosome 14. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | ACTTGACACACTCCCTAATGTCCTAGTCCATAAGTGTAAAAACTAGAGGCATAAACTCATTCATTTTTAGTTCTGTTTCCTAGCCCAGTGCAGGTGAGGATTAAACATGGTTTCTCACTCTGTTTTTTCCATAGTGGTGTGTTTGACCTTAGTGTTGAGAATAGTTTTGAGTCACTCAGAAGAGAGCATGGGAAGGCAACAGACATTTTGACCCACAGTTAGCTTCCGGTTTGAGATTTCTCTTTCCTTTCCCTGCAGAAAATCACCTCTTTATGATAACTGCTTTCTCCATGCTCCTGATGGACAGCCCCTCTGCACTT... | ACTTGACACACTCCCTAATGTCCTAGTCCATAAGTGTAAAAACTAGAGGCATAAACTCATTCATTTTTAGTTCTGTTTCCTAGCCCAGTGCAGGTGAGGATTAAACATGGTTTCTCACTCTGTTTTTTCCATAGTGGTGTGTTTGACCTTAGTGTTGAGAATAGTTTTGAGTCACTCAGAAGAGAGCATGGGAAGGCAACAGACATTTTGACCCACAGTTAGCTTCCGGTTTGAGATTTCTCTTTCCTTTCCCTGCAGAAAATCACCTCTTTATGATAACTGCTTTCTCCATGCTCCTGATGGACAGCCCCTCTGCACTT... |
Task1_train_43214 | This mutation on Chromosome 14 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | AGGGGACACGAAGGAAGTACAAAGCATAGTCCCTGCCCTCGGAGAGCTACTACATAGCCAAGGGGTCAGAATCCACTGCAGCCACAGGCTGGCTGTGGTTGTGTATGAATAGCATGGATATCAGAGGAGAGCTGGAGTGAGCAGGGAAGGCTTCCATGGAGGAATGGGCCTCAATGGGGTGTGGGGGCATCATGAGACAGGTAAAGGGGAGCAAGGGAGGGCATGCCAGCTTGTGCACTCTGCAAGCAAAGGCATCAGTCAGGGGTATGGGCATGCGCAATACTAACAGCCCCTTTCCTGAGGTCTCCTCCCCTGCGGGC... | AGGGGACACGAAGGAAGTACAAAGCATAGTCCCTGCCCTCGGAGAGCTACTACATAGCCAAGGGGTCAGAATCCACTGCAGCCACAGGCTGGCTGTGGTTGTGTATGAATAGCATGGATATCAGAGGAGAGCTGGAGTGAGCAGGGAAGGCTTCCATGGAGGAATGGGCCTCAATGGGGTGTGGGGGCATCATGAGACAGGTAAAGGGGAGCAAGGGAGGGCATGCCAGCTTGTGCACTCTGCAAGCAAAGGCATCAGTCAGGGGTATGGGCATGCGCAATACTAACAGCCCCTTTCCTGAGGTCTCCTCCCCTGCGGGC... |
Task1_train_43215 | A genomic variant on Chromosome 14 is under review. What is the biological outcome — benign or pathogenic? | Benign | TTGAGACAGGGTCTCACTCTGAAGCCTAGACTGACATGCAGTGGTGGCATTATGGCTCACTGCAGCCTCAACTACCTGGGCTCAAGTGATCCTCCAACCTTAGCCTCCCAAGTACGTGGGACTATAGGCATGTGCCACTGTGCCTGGATAATTTTTTTTTTTTTAATTTTTGTAGAGATGGGGTCTTTCTGTGTTGCCCAGGCTGGTCTCGAACTCCTGGTCTCAAGTGATCCTCCTGCTTTGGCCTTCCAAAATGCTGGGATTACAGGTGTGGGCTACCATGCCCAGCCATAAGTCATTTTTAATGGCTACAGGGTTTT... | TTGAGACAGGGTCTCACTCTGAAGCCTAGACTGACATGCAGTGGTGGCATTATGGCTCACTGCAGCCTCAACTACCTGGGCTCAAGTGATCCTCCAACCTTAGCCTCCCAAGTACGTGGGACTATAGGCATGTGCCACTGTGCCTGGATAATTTTTTTTTTTTTAATTTTTGTAGAGATGGGGTCTTTCTGTGTTGCCCAGGCTGGTCTCGAACTCCTGGTCTCAAGTGATCCTCCTGCTTTGGCCTTCCAAAATGCTGGGATTACAGGTGTGGGCTACCATGCCCAGCCATAAGTCATTTTTAATGGCTACAGGGTTTT... |
Task1_train_43216 | A mutation located on Chromosome 14 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TGGGGCAACTGCTGCAGAAGGGGTGGGGACAACCACCTCTGCCCTCTCCTGGGGGGCCCTCTCACCAGTCCTGATCAGCCCCTTTCCCCCAAGCTTCTCTATTCCAGCCCAAGAGACACATAGGGAAGTTTGGCAAGGGTCGGTGCGGGAGCCATCAAGGGTGGATGTGGGCAGATTGTGCTGTCATCTCCAAATGAAGTAAGTTTTAAAAACAAAGGGGGCCAGCTGACAGGTCCCAAACGTCTGTACTGTTGTTGCCTCATTGGTCAGAAGCCTCGAGAGGCCACCGCGCTGCGCACCGAGCGGGGACTCCCACGATG... | TGGGGCAACTGCTGCAGAAGGGGTGGGGACAACCACCTCTGCCCTCTCCTGGGGGGCCCTCTCACCAGTCCTGATCAGCCCCTTTCCCCCAAGCTTCTCTATTCCAGCCCAAGAGACACATAGGGAAGTTTGGCAAGGGTCGGTGCGGGAGCCATCAAGGGTGGATGTGGGCAGATTGTGCTGTCATCTCCAAATGAAGTAAGTTTTAAAAACAAAGGGGGCCAGCTGACAGGTCCCAAACGTCTGTACTGTTGTTGCCTCATTGGTCAGAAGCCTCGAGAGGCCACCGCGCTGCGCACCGAGCGGGGACTCCCACGATG... |
Task1_train_43217 | This variant is located on Chromosome 14. Evaluate its biological effect and specify any disease association. | Benign | ATTTTGTATTATTAATAGTTTAGAAAAGAAAATTCAGCTTCACAGCTTGTTATTGGTAATGAGATAAATAATTAAATTTACTATTGTCAAATTTTAGAAAACCTCTATTAAGTCTTTTATGTATGCGATGTAATATTTCAGGGTGTTTGAGATTTTTCTTGTATAGTGACTAATTTTGATTACTCATAATTATATGACTTTCATAAAGTCCATTGCTGAGCCCCTTACAGGGTCTTTATAGAGGTCTGTACAGTGAGGATCCCTGAAGCATAAACTTTGTCTGGTTTTGATCATATTATATTATAATTATCTGTTTTTTG... | ATTTTGTATTATTAATAGTTTAGAAAAGAAAATTCAGCTTCACAGCTTGTTATTGGTAATGAGATAAATAATTAAATTTACTATTGTCAAATTTTAGAAAACCTCTATTAAGTCTTTTATGTATGCGATGTAATATTTCAGGGTGTTTGAGATTTTTCTTGTATAGTGACTAATTTTGATTACTCATAATTATATGACTTTCATAAAGTCCATTGCTGAGCCCCTTACAGGGTCTTTATAGAGGTCTGTACAGTGAGGATCCCTGAAGCATAAACTTTGTCTGGTTTTGATCATATTATATTATAATTATCTGTTTTTTG... |
Task1_train_43218 | Chromosome 14 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AAATAATTAAATTTACTATTGTCAAATTTTAGAAAACCTCTATTAAGTCTTTTATGTATGCGATGTAATATTTCAGGGTGTTTGAGATTTTTCTTGTATAGTGACTAATTTTGATTACTCATAATTATATGACTTTCATAAAGTCCATTGCTGAGCCCCTTACAGGGTCTTTATAGAGGTCTGTACAGTGAGGATCCCTGAAGCATAAACTTTGTCTGGTTTTGATCATATTATATTATAATTATCTGTTTTTTGTTTGTTTCTACACATGCTCAGTGCTTACTAGCCTCACTTTTGACAGTCATTTGAGACTATGATGA... | AAATAATTAAATTTACTATTGTCAAATTTTAGAAAACCTCTATTAAGTCTTTTATGTATGCGATGTAATATTTCAGGGTGTTTGAGATTTTTCTTGTATAGTGACTAATTTTGATTACTCATAATTATATGACTTTCATAAAGTCCATTGCTGAGCCCCTTACAGGGTCTTTATAGAGGTCTGTACAGTGAGGATCCCTGAAGCATAAACTTTGTCTGGTTTTGATCATATTATATTATAATTATCTGTTTTTTGTTTGTTTCTACACATGCTCAGTGCTTACTAGCCTCACTTTTGACAGTCATTTGAGACTATGATGA... |
Task1_train_43219 | A variant was discovered on Chromosome 14. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | ACTTTCATAAAGTCCATTGCTGAGCCCCTTACAGGGTCTTTATAGAGGTCTGTACAGTGAGGATCCCTGAAGCATAAACTTTGTCTGGTTTTGATCATATTATATTATAATTATCTGTTTTTTGTTTGTTTCTACACATGCTCAGTGCTTACTAGCCTCACTTTTGACAGTCATTTGAGACTATGATGAAATATATGGATACTCTCCTCAGCAAAAAAAGTCATGAAATACATAAAATATTGAATACAATATTACTGACCTCCTAAAGCTTATTCTTGCTCCTGCCACAGTTTCTGCACTAAATTGATAATTTATTTAAT... | ACTTTCATAAAGTCCATTGCTGAGCCCCTTACAGGGTCTTTATAGAGGTCTGTACAGTGAGGATCCCTGAAGCATAAACTTTGTCTGGTTTTGATCATATTATATTATAATTATCTGTTTTTTGTTTGTTTCTACACATGCTCAGTGCTTACTAGCCTCACTTTTGACAGTCATTTGAGACTATGATGAAATATATGGATACTCTCCTCAGCAAAAAAAGTCATGAAATACATAAAATATTGAATACAATATTACTGACCTCCTAAAGCTTATTCTTGCTCCTGCCACAGTTTCTGCACTAAATTGATAATTTATTTAAT... |
Task1_train_43220 | This alteration on Chromosome 14 may affect genome function. Does it lead to a disease or is it benign? | Benign | CCTCCTAAAGCTTATTCTTGCTCCTGCCACAGTTTCTGCACTAAATTGATAATTTATTTAATGCTCTGTATTTTGATTTTCTTTCTCTAATATCTAGCACAATGTCCTGCACTTTGTATGCTCCAAACACATAAAGACTTGTTTAATAAATAGAAAAAGAAATGGATAAGTGTTGCCAGCCAGACTGTATGACAGGTGCAGAAATTCCCCACTTTCAAAAACTGTTGGTAAATATATTTGAGCAAACACTCAGACTCTTCCCTGGCGATCCTAAAATACTAGACTCTACAATGGTTTTTGCCCTAATAAGAAAAGAGTTC... | CCTCCTAAAGCTTATTCTTGCTCCTGCCACAGTTTCTGCACTAAATTGATAATTTATTTAATGCTCTGTATTTTGATTTTCTTTCTCTAATATCTAGCACAATGTCCTGCACTTTGTATGCTCCAAACACATAAAGACTTGTTTAATAAATAGAAAAAGAAATGGATAAGTGTTGCCAGCCAGACTGTATGACAGGTGCAGAAATTCCCCACTTTCAAAAACTGTTGGTAAATATATTTGAGCAAACACTCAGACTCTTCCCTGGCGATCCTAAAATACTAGACTCTACAATGGTTTTTGCCCTAATAAGAAAAGAGTTC... |
Task1_train_43221 | This variant is present on Chromosome 14. Is the change likely to result in a pathogenic outcome? | Benign | CCTGTGATGCTGATGATATTGGCCCAAGGTCTACATTTTGAGTAGGAAGGTTTTAAAGCAGCATATCTGAACCAATATACTGGTTAACTGAGACCCACCCTCAGAGTTTCTGATTTCTTAAGTCTGGAGTAGGATCCTAGGATTTGCATTTCTAACTGTTTCCCAGGTGATGCTGACACTGCAGGTCTGGGGCCAGCACTCTGACAACCGGTGCTCTAGAATCTTTCTTTTTCTTAACATTAAGGAAGGGAGGGCACTAAAAAATATGTCAGGCTTCTCCATTGACTCCAAAATCAAATCCAAACTCTTCATCCAAAAGC... | CCTGTGATGCTGATGATATTGGCCCAAGGTCTACATTTTGAGTAGGAAGGTTTTAAAGCAGCATATCTGAACCAATATACTGGTTAACTGAGACCCACCCTCAGAGTTTCTGATTTCTTAAGTCTGGAGTAGGATCCTAGGATTTGCATTTCTAACTGTTTCCCAGGTGATGCTGACACTGCAGGTCTGGGGCCAGCACTCTGACAACCGGTGCTCTAGAATCTTTCTTTTTCTTAACATTAAGGAAGGGAGGGCACTAAAAAATATGTCAGGCTTCTCCATTGACTCCAAAATCAAATCCAAACTCTTCATCCAAAAGC... |
Task1_train_43222 | This variant is present on Chromosome 14. Is the change likely to result in a pathogenic outcome? | Benign | AAGGACACAGAACGAGGGTCACTAGGAAGTCACTGAAGTTAGCAAACTTTCTGGCTGCCTCTGGGCAGGGGAATCTCAAGAGAGAAAACAGTCCTAAGGCAGACTCATGGATGAGTAGATAACTTCGCTTCCCCGGCAGCCCCTTCCTGACGTCCCTCCCACACCCTGCTGGCTCTCAGAGCCAGTCTGTTCTGTGTCAGGACTTGGGGGGCCCCCAGGGCCCCAGGGCCACAACCACCAGGGCTCCTGCCTGTGGGCACGGCAGGTTGAAAGCAGCAAGCAAGCTGCTCAAACCCACCGACTGTGGTCCTGCAGCAAAG... | AAGGACACAGAACGAGGGTCACTAGGAAGTCACTGAAGTTAGCAAACTTTCTGGCTGCCTCTGGGCAGGGGAATCTCAAGAGAGAAAACAGTCCTAAGGCAGACTCATGGATGAGTAGATAACTTCGCTTCCCCGGCAGCCCCTTCCTGACGTCCCTCCCACACCCTGCTGGCTCTCAGAGCCAGTCTGTTCTGTGTCAGGACTTGGGGGGCCCCCAGGGCCCCAGGGCCACAACCACCAGGGCTCCTGCCTGTGGGCACGGCAGGTTGAAAGCAGCAAGCAAGCTGCTCAAACCCACCGACTGTGGTCCTGCAGCAAAG... |
Task1_train_43223 | A genomic change on Chromosome 14 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GCCCCACACCCCCATGTTTCCTGCCTTCAGGCCTGCCCCAGGAAGGCACATTCCCGAGTGACAAATGCCTCACACTCTATGTAAGAAAGGGCACTCAAGGAGAGTCACCGCTGGGTGTGTGCCACAGAACCCGGGGCTGGGGGGAGCCCTTGAAGGTCAGCCTCTGCCTTCTAAGAGCTATTGTTGTACCTAACCTGGTCTAGACAAAGGAGTAGTCATTCTTAGTGATTTTCAAAGACTGACACCATAACCCTCTTGGATTTTTTAAAAATCTGATTAAAAACTCCTTAGCCAAGTATAAATGTATCCTGCTGCAGGCT... | GCCCCACACCCCCATGTTTCCTGCCTTCAGGCCTGCCCCAGGAAGGCACATTCCCGAGTGACAAATGCCTCACACTCTATGTAAGAAAGGGCACTCAAGGAGAGTCACCGCTGGGTGTGTGCCACAGAACCCGGGGCTGGGGGGAGCCCTTGAAGGTCAGCCTCTGCCTTCTAAGAGCTATTGTTGTACCTAACCTGGTCTAGACAAAGGAGTAGTCATTCTTAGTGATTTTCAAAGACTGACACCATAACCCTCTTGGATTTTTTAAAAATCTGATTAAAAACTCCTTAGCCAAGTATAAATGTATCCTGCTGCAGGCT... |
Task1_train_43224 | Chromosome 14 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TTATATTAAAAGCATTATGTGGCCAGACATCGTGGCTCACTCCTATAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATCACTTGAGGCCACGAGTTTGAGACCAGCTGGCCAAGATGGAGAAACCCCGTCTCCACTAAAAAACACAAAAATTAGCCAGGTGTAGTGGTGCGCGCCTGTAATCCCAGCTACTCTGGAGGCTAAGGCACAAGAATCACTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCAAGATCCTGCTGCTGCACTCCAGCCTGGGCAACAGAGCAACACCCTGTCTCAAAAAATAATGATAATAA... | TTATATTAAAAGCATTATGTGGCCAGACATCGTGGCTCACTCCTATAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATCACTTGAGGCCACGAGTTTGAGACCAGCTGGCCAAGATGGAGAAACCCCGTCTCCACTAAAAAACACAAAAATTAGCCAGGTGTAGTGGTGCGCGCCTGTAATCCCAGCTACTCTGGAGGCTAAGGCACAAGAATCACTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCAAGATCCTGCTGCTGCACTCCAGCCTGGGCAACAGAGCAACACCCTGTCTCAAAAAATAATGATAATAA... |
Task1_train_43225 | Given this variant on Chromosome 14, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | AGTTCAAGACCAGCCTGAGCAACATAGCAAGACTCCAATCTCTACAAAAAATAAATAATTAGCCATGTGTGGTGGCTCACACCTGTGATCCCAGCTACTTGGGAGGCTGAGATGGGAGGATTCCTTGAGCCTGGGAGGTTGAGGATGCATTGAGCCATGATCACGCCACTGCACTCCAGACTGGGCAAAAGAACAAGACCCTGTCTTAAAAAAAAAAAAAAAAAAAAAAAATATATATATATATATATATATATATATATAGTTTATTTATTTATTTATTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG... | AGTTCAAGACCAGCCTGAGCAACATAGCAAGACTCCAATCTCTACAAAAAATAAATAATTAGCCATGTGTGGTGGCTCACACCTGTGATCCCAGCTACTTGGGAGGCTGAGATGGGAGGATTCCTTGAGCCTGGGAGGTTGAGGATGCATTGAGCCATGATCACGCCACTGCACTCCAGACTGGGCAAAAGAACAAGACCCTGTCTTAAAAAAAAAAAAAAAAAAAAAAAATATATATATATATATATATATATATATATAGTTTATTTATTTATTTATTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG... |
Task1_train_43226 | A mutation on Chromosome 14 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | AACTTGATCCAAGTAAATTTCAGTTTAACTTTCATTCAGAGAAAACTTTGATATTTTGGCTCAGTGGTTTCGAAAGCTTAGAGATTTTTGTCCAAGTTAGACTTGAAGGAGTAGATATTTTACAAAGTGAAAGCTAAGACCTCTCATCTGGCAAGCCCTTCCTTCTTGGTTGTGTGTGGTTCGGCAGGCTTAGCGTGGTTTGTGCGTGGTTTGTTCTGCTTCAGTGTTCTGGGTTTTGTTATAAGACAAGGATAACTAGATGTTTGGCACCAGGGATGTTAGAGATGAGTAAACGTCCTTCCTCACCTGAGATTCAGCGA... | AACTTGATCCAAGTAAATTTCAGTTTAACTTTCATTCAGAGAAAACTTTGATATTTTGGCTCAGTGGTTTCGAAAGCTTAGAGATTTTTGTCCAAGTTAGACTTGAAGGAGTAGATATTTTACAAAGTGAAAGCTAAGACCTCTCATCTGGCAAGCCCTTCCTTCTTGGTTGTGTGTGGTTCGGCAGGCTTAGCGTGGTTTGTGCGTGGTTTGTTCTGCTTCAGTGTTCTGGGTTTTGTTATAAGACAAGGATAACTAGATGTTTGGCACCAGGGATGTTAGAGATGAGTAAACGTCCTTCCTCACCTGAGATTCAGCGA... |
Task1_train_43227 | This sequence variant lies on Chromosome 14. Is it clinically significant, and what condition might it cause if any? | Benign | CTACAAAAAATAAAAAAATTAGCTGGGTATGATGGCATGTGCCTATAGTCCCAACTATTCGAGAGACTGAGGCTGGAGGACCACTTGAGTCTCGGAGGTAGAGGCTGCTGTGAGCTTTGATCGTGCCTCTGCATTCCAGCCTGGGAGACAGAGTGAGATCCCATCTGAAAAACATTAAAACCAGAAAAAAGTTATCCTCATCCTGCCCCTTTCACAAGATCACTGTTAGCATTTCATTTTAGCCCCTTTCACATTATTCTCTCCATATATGCTTACATATTTGTAATTATTGCATAGTAATCACCATTTTGCATTCTGTG... | CTACAAAAAATAAAAAAATTAGCTGGGTATGATGGCATGTGCCTATAGTCCCAACTATTCGAGAGACTGAGGCTGGAGGACCACTTGAGTCTCGGAGGTAGAGGCTGCTGTGAGCTTTGATCGTGCCTCTGCATTCCAGCCTGGGAGACAGAGTGAGATCCCATCTGAAAAACATTAAAACCAGAAAAAAGTTATCCTCATCCTGCCCCTTTCACAAGATCACTGTTAGCATTTCATTTTAGCCCCTTTCACATTATTCTCTCCATATATGCTTACATATTTGTAATTATTGCATAGTAATCACCATTTTGCATTCTGTG... |
Task1_train_43228 | An alteration has been detected on Chromosome 14. Is it pathogenic, and if so, what disease is involved? | Benign | GCATTATTACCAGAAGGGGAGATGGGAGCTGAGCAGACAGAGAAGTGGATTGTCAGCCACAGGCCAGTCCCCTGGCTGGTGGCTGAATCACTCCCGACCACCCTATCCTGCCTGGGCTGCGTGGGTGCTGGGGTTAGGATGCGACGGGGCCCAAGGCCTGATGTGGCCATGATGCCGTCTCCCCTGCCTCCCGCATCTCTGCCCACAGGTTGTCGGCTGTGATCACGAGCTGGACTCGTCCAAGCAGGAGGACAAGTGTCTGCGGTGTGGGGGTGACGGCACGACCTGCTACCCCGTCGCAGGCACCTTTGACGCTAATG... | GCATTATTACCAGAAGGGGAGATGGGAGCTGAGCAGACAGAGAAGTGGATTGTCAGCCACAGGCCAGTCCCCTGGCTGGTGGCTGAATCACTCCCGACCACCCTATCCTGCCTGGGCTGCGTGGGTGCTGGGGTTAGGATGCGACGGGGCCCAAGGCCTGATGTGGCCATGATGCCGTCTCCCCTGCCTCCCGCATCTCTGCCCACAGGTTGTCGGCTGTGATCACGAGCTGGACTCGTCCAAGCAGGAGGACAAGTGTCTGCGGTGTGGGGGTGACGGCACGACCTGCTACCCCGTCGCAGGCACCTTTGACGCTAATG... |
Task1_train_43229 | Assess the clinical impact of this variant found on Chromosome 14. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GTCCAGCTCAGAGTTCTGGGTAAAGTGGCAGTCCTGAGTGGCCTTTGAGGTCAGGTGGCATGGGTAGGGCAGGATCTTCATAGTGGCTGACAATGACTTGTCCTTGTGCCCAGGGGAGCTGACAATCTCAGGACTGCCCCCTACTGTGACAGTGCCAGAGGGTGATACGGCCAGGCTATTGTGTGTGGTAGCAGGAGAAAGTGTGAACATCAGGTGGTCCAGGTAAAGGCTCTATTCCAAGTTGTCCCTGTCCCCAGACCTTCACAACCTCAGGTGTGGGTGTCCACCTTTCTGCCAGGGATGTCACTGTCACCACTGCT... | GTCCAGCTCAGAGTTCTGGGTAAAGTGGCAGTCCTGAGTGGCCTTTGAGGTCAGGTGGCATGGGTAGGGCAGGATCTTCATAGTGGCTGACAATGACTTGTCCTTGTGCCCAGGGGAGCTGACAATCTCAGGACTGCCCCCTACTGTGACAGTGCCAGAGGGTGATACGGCCAGGCTATTGTGTGTGGTAGCAGGAGAAAGTGTGAACATCAGGTGGTCCAGGTAAAGGCTCTATTCCAAGTTGTCCCTGTCCCCAGACCTTCACAACCTCAGGTGTGGGTGTCCACCTTTCTGCCAGGGATGTCACTGTCACCACTGCT... |
Task1_train_43230 | A change on Chromosome 14 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CAAAATCTAAAAGCCTTGGCAAGTGTTTGGATAGGCTTGCAACTGAGAAAGAGGGAGTGTTGAAAGCTCAAACAGAGAAAGGTCCTAGAGGCCATGTACTGTAGTCTAATATGCTTATCATTGCTTGAAACATTGTAAACCCTCTTGGAAGGCAGTTTGGTAAAACCTATTAATAATCACAAAAAGTATCTTACTTTTTGACCCAGCACTTTTATTTCTGGGAGTTTATCTTAAATGATTCAAATGAAGACAAGGAATCTTTATGTACAAAGCAATTAGTTGCATGACAGACAGTGACCACGTTCTCAAAAATTACACCC... | CAAAATCTAAAAGCCTTGGCAAGTGTTTGGATAGGCTTGCAACTGAGAAAGAGGGAGTGTTGAAAGCTCAAACAGAGAAAGGTCCTAGAGGCCATGTACTGTAGTCTAATATGCTTATCATTGCTTGAAACATTGTAAACCCTCTTGGAAGGCAGTTTGGTAAAACCTATTAATAATCACAAAAAGTATCTTACTTTTTGACCCAGCACTTTTATTTCTGGGAGTTTATCTTAAATGATTCAAATGAAGACAAGGAATCTTTATGTACAAAGCAATTAGTTGCATGACAGACAGTGACCACGTTCTCAAAAATTACACCC... |
Task1_train_43231 | A variant found on Chromosome 14 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | AGACTAGAAGGAAAAAACAGTCAAGTAGCCATTTCTCCTGGGGAGTCTCTAGTAACTTGATTTTGTGCTTCTTCTTGTTTTTTGAGACAAGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAATGGTACGATCTCGGCTCACTGCAACCTCCACCTCCCGAGTTCAAGCAATTCTCCTGTCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCAAGTCACCACACCTGGCTAATTTTTGTAATTTTTAAATTATTATTTATTTTTATTTTTTTGAGGCGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCCA... | AGACTAGAAGGAAAAAACAGTCAAGTAGCCATTTCTCCTGGGGAGTCTCTAGTAACTTGATTTTGTGCTTCTTCTTGTTTTTTGAGACAAGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAATGGTACGATCTCGGCTCACTGCAACCTCCACCTCCCGAGTTCAAGCAATTCTCCTGTCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCAAGTCACCACACCTGGCTAATTTTTGTAATTTTTAAATTATTATTTATTTTTATTTTTTTGAGGCGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCCA... |
Task1_train_43232 | A variant on Chromosome 14 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GCTACAAGAATCAACATCTATCAAGATATACAAAAGAAAAGAAAAAAAAAGAATCAACATGGATGAATCTCCAAACCACTGTTGAGTGAAACAGTCAAACCCTAGGAGAACACATTCAGTATCATTCCATTTAGATACAATTCAAAAACTAGGCAAAATAAAATATTAAGGTACATAATCTAAGTGGTAATACTATGAAGAAAACCAAGAGTGATACACAGAAAGTCCAGGATACTGGAAAGAGAGGAAAGGGCACAGGGGTCTGTGGGACGTTGATGGTTTGCGGGTATCAGCACTGAACTATGTCTTAAAAGTGTTGC... | GCTACAAGAATCAACATCTATCAAGATATACAAAAGAAAAGAAAAAAAAAGAATCAACATGGATGAATCTCCAAACCACTGTTGAGTGAAACAGTCAAACCCTAGGAGAACACATTCAGTATCATTCCATTTAGATACAATTCAAAAACTAGGCAAAATAAAATATTAAGGTACATAATCTAAGTGGTAATACTATGAAGAAAACCAAGAGTGATACACAGAAAGTCCAGGATACTGGAAAGAGAGGAAAGGGCACAGGGGTCTGTGGGACGTTGATGGTTTGCGGGTATCAGCACTGAACTATGTCTTAAAAGTGTTGC... |
Task1_train_43233 | A mutation found on Chromosome 14 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AGGAGCCTGGCTACTTTTGCCTCAGACGAGTCCGGAGCGCCGGGTTAACCGGTCTGAAGTCCCAGGGGCTTTCTGGGACTGCTCAGCCACCGGCAGCTTCCGGCACCAGGGGACGCCGGACGCCGTCCGGACATTCGGCGCGCTTGCCACGATCTTGGACGGGTCTCGGGCCTCGACCTTTGAATTCCCCGCTCCGGCTCCAAGATGTCAGCAACGCTGATCCTGGAGCCCCCAGGCCGCTGCTGCTGGAACGAGCCGGTGCGCATTGCCGTGCGCGGCCTGGCCCCGGAGCAGCGGGTTACGCTGCGCGCGTCCCTGCG... | AGGAGCCTGGCTACTTTTGCCTCAGACGAGTCCGGAGCGCCGGGTTAACCGGTCTGAAGTCCCAGGGGCTTTCTGGGACTGCTCAGCCACCGGCAGCTTCCGGCACCAGGGGACGCCGGACGCCGTCCGGACATTCGGCGCGCTTGCCACGATCTTGGACGGGTCTCGGGCCTCGACCTTTGAATTCCCCGCTCCGGCTCCAAGATGTCAGCAACGCTGATCCTGGAGCCCCCAGGCCGCTGCTGCTGGAACGAGCCGGTGCGCATTGCCGTGCGCGGCCTGGCCCCGGAGCAGCGGGTTACGCTGCGCGCGTCCCTGCG... |
Task1_train_43234 | This sequence variant lies on Chromosome 14. Is it clinically significant, and what condition might it cause if any? | Benign | AAAAAACAAGGCGGCCAGGCGCGGTGGCTCACGCCTCTAATCCCGGCACTTTGGGAGGCCAAGGTGGGTGGATCACGAGGTCAGGAGTTCAAGACCAGCCTGGCCAAGATGGTGAAACCCTGTCTCTACTAAAAATACAAAAAATTAGCCGGGCATGGTGGCGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCCGGCAGGTGGAGGTTGCAGTGAGCCAAAATCACACCACATCACTCCAGCCTGGGCAACAGAGAGAGACTCTGTCTGATAAAAAAAAAAAAAAAAAAACAAAAA... | AAAAAACAAGGCGGCCAGGCGCGGTGGCTCACGCCTCTAATCCCGGCACTTTGGGAGGCCAAGGTGGGTGGATCACGAGGTCAGGAGTTCAAGACCAGCCTGGCCAAGATGGTGAAACCCTGTCTCTACTAAAAATACAAAAAATTAGCCGGGCATGGTGGCGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCCGGCAGGTGGAGGTTGCAGTGAGCCAAAATCACACCACATCACTCCAGCCTGGGCAACAGAGAGAGACTCTGTCTGATAAAAAAAAAAAAAAAAAAACAAAAA... |
Task1_train_43235 | A mutation has occurred on Chromosome 14. What is the medical relevance of this mutation? | Benign | AATAAGATTAATGTAAATGTATATAGAGAAAATGACTATAAAGAGATATTTTTTGAGACAACTGGAGACATTTGAATGAGAATGGTGTATTTGATTATATGAAGTAATCATTAATTTTGTTGGGTATGATAATGGTATTATGGTTTTGTAAAGAAAGTCCTTATCTGATAACAGAAATAATTAATTAATTAAAACATTTTGGCCAGGTGCGGTGGCTCACGTCTGTAATCCCAGTACTTTGGGAGGCCAAGGCGGGCAGATCACCTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTACTAA... | AATAAGATTAATGTAAATGTATATAGAGAAAATGACTATAAAGAGATATTTTTTGAGACAACTGGAGACATTTGAATGAGAATGGTGTATTTGATTATATGAAGTAATCATTAATTTTGTTGGGTATGATAATGGTATTATGGTTTTGTAAAGAAAGTCCTTATCTGATAACAGAAATAATTAATTAATTAAAACATTTTGGCCAGGTGCGGTGGCTCACGTCTGTAATCCCAGTACTTTGGGAGGCCAAGGCGGGCAGATCACCTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTACTAA... |
Task1_train_43236 | Located on Chromosome 14, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | GTAGCACTTTGGGGCTAAGCTGCGAAGGCACTCGTATTGTACAAGTAATTTCGAAGAGAGCCTAAATTTGCTACCCCCCTGCTTCTACAGGGTATACCAGATTTTTGCTGTCTTGGGACACTGAGCTCATGGAAGCCTGTGGAGGAAACTAACCGGTAAGCTGGGGATCTAGGTAGTCATCCAAGAGTCTGGAGGGAGAAGAAATTTGTTACTTCCACAGCTGGGGTCCTGTAGAACCATACTAATGTACAAATGGATGCTGAAAAATACCTGCATAGTTTCAAAACAAAACTCCCTCTCCACTCCCAGTTACTGACATG... | GTAGCACTTTGGGGCTAAGCTGCGAAGGCACTCGTATTGTACAAGTAATTTCGAAGAGAGCCTAAATTTGCTACCCCCCTGCTTCTACAGGGTATACCAGATTTTTGCTGTCTTGGGACACTGAGCTCATGGAAGCCTGTGGAGGAAACTAACCGGTAAGCTGGGGATCTAGGTAGTCATCCAAGAGTCTGGAGGGAGAAGAAATTTGTTACTTCCACAGCTGGGGTCCTGTAGAACCATACTAATGTACAAATGGATGCTGAAAAATACCTGCATAGTTTCAAAACAAAACTCCCTCTCCACTCCCAGTTACTGACATG... |
Task1_train_43237 | This is a variant located on Chromosome 14. Is this mutation a likely cause of disease or not? | Benign | TAGGGAGGTGGTGAAGGGGATCGCTGTTTTATAGTTATCGTCTCACTTCCTCTTTGGATTTTCTGCCTCAGTTTCTCCCAAGCTAGTTTTTTTTTTGTTTTTGTTGTTGTTGTTGTTGCTTTTTGAGACAAAGTCTCACTCTGTCTCCGCCCAGGCTGGAGTGCAGTGGTGCGATCTCGGCTCAAGGAGTTGAACCTCCAAGTTCAAGCAATTCTCCTCCCTCAGCCTCCCAAGTAGCTGGAATTACAGGTGTGAGTCACCGTGCCCAGGCCCAAGTTGGTCTTCTTAAGGCCCCACATGATCAAAACACTCCTTTGCTT... | TAGGGAGGTGGTGAAGGGGATCGCTGTTTTATAGTTATCGTCTCACTTCCTCTTTGGATTTTCTGCCTCAGTTTCTCCCAAGCTAGTTTTTTTTTTGTTTTTGTTGTTGTTGTTGTTGCTTTTTGAGACAAAGTCTCACTCTGTCTCCGCCCAGGCTGGAGTGCAGTGGTGCGATCTCGGCTCAAGGAGTTGAACCTCCAAGTTCAAGCAATTCTCCTCCCTCAGCCTCCCAAGTAGCTGGAATTACAGGTGTGAGTCACCGTGCCCAGGCCCAAGTTGGTCTTCTTAAGGCCCCACATGATCAAAACACTCCTTTGCTT... |
Task1_train_43238 | A mutation on Chromosome 14 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TTGTTGTTGTTGCTTTTTGAGACAAAGTCTCACTCTGTCTCCGCCCAGGCTGGAGTGCAGTGGTGCGATCTCGGCTCAAGGAGTTGAACCTCCAAGTTCAAGCAATTCTCCTCCCTCAGCCTCCCAAGTAGCTGGAATTACAGGTGTGAGTCACCGTGCCCAGGCCCAAGTTGGTCTTCTTAAGGCCCCACATGATCAAAACACTCCTTTGCTTAAAAAAAAAAAAAAAAAAAAATCTTTGCTCTTTACTGACTCCCTCCTGCAATGTGAGATAAAACCTGCAACCCTCCCCTCAGGGTTCAAGGCGGTTCCGCTTCCAT... | TTGTTGTTGTTGCTTTTTGAGACAAAGTCTCACTCTGTCTCCGCCCAGGCTGGAGTGCAGTGGTGCGATCTCGGCTCAAGGAGTTGAACCTCCAAGTTCAAGCAATTCTCCTCCCTCAGCCTCCCAAGTAGCTGGAATTACAGGTGTGAGTCACCGTGCCCAGGCCCAAGTTGGTCTTCTTAAGGCCCCACATGATCAAAACACTCCTTTGCTTAAAAAAAAAAAAAAAAAAAAATCTTTGCTCTTTACTGACTCCCTCCTGCAATGTGAGATAAAACCTGCAACCCTCCCCTCAGGGTTCAAGGCGGTTCCGCTTCCAT... |
Task1_train_43239 | This is a variant located on Chromosome 14. Is this mutation a likely cause of disease or not? | Benign | GAGTTGAACCTCCAAGTTCAAGCAATTCTCCTCCCTCAGCCTCCCAAGTAGCTGGAATTACAGGTGTGAGTCACCGTGCCCAGGCCCAAGTTGGTCTTCTTAAGGCCCCACATGATCAAAACACTCCTTTGCTTAAAAAAAAAAAAAAAAAAAAATCTTTGCTCTTTACTGACTCCCTCCTGCAATGTGAGATAAAACCTGCAACCCTCCCCTCAGGGTTCAAGGCGGTTCCGCTTCCATTTGTACCTCCCACCACCCATGTGCCTGGACCTGCATCCTAGCTGACTGCTTACCTCCCAACCCCTCACTCTCCCTGCACG... | GAGTTGAACCTCCAAGTTCAAGCAATTCTCCTCCCTCAGCCTCCCAAGTAGCTGGAATTACAGGTGTGAGTCACCGTGCCCAGGCCCAAGTTGGTCTTCTTAAGGCCCCACATGATCAAAACACTCCTTTGCTTAAAAAAAAAAAAAAAAAAAAATCTTTGCTCTTTACTGACTCCCTCCTGCAATGTGAGATAAAACCTGCAACCCTCCCCTCAGGGTTCAAGGCGGTTCCGCTTCCATTTGTACCTCCCACCACCCATGTGCCTGGACCTGCATCCTAGCTGACTGCTTACCTCCCAACCCCTCACTCTCCCTGCACG... |
Task1_train_43240 | A change on Chromosome 14 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CAGTGGAATCTTAAGGTGAATTCAAAGAAACATAAAGTAGAATGGTGGTTACCAAGGGTTAGGGGATGGGGCGGGGACTGGGGAGATGCTGGTCAAACGAAATATAATTTCAGTTAGGAAAAAAGAATAAGTTCAGGAAATCTATTGTATAACATGATGACTATCATTAGTAACAGTGTATTATACACTTCAAAATAGCTAAAAGAGCAGATTTTAAATGTTCTCACCACAAAAAAATAAGATTTGAGGTAATGGGTATGTTAATTAGCTTGATTATATCAAAGCATCATGTTGTATGCCATAAATATGTATTCTTTTTA... | CAGTGGAATCTTAAGGTGAATTCAAAGAAACATAAAGTAGAATGGTGGTTACCAAGGGTTAGGGGATGGGGCGGGGACTGGGGAGATGCTGGTCAAACGAAATATAATTTCAGTTAGGAAAAAAGAATAAGTTCAGGAAATCTATTGTATAACATGATGACTATCATTAGTAACAGTGTATTATACACTTCAAAATAGCTAAAAGAGCAGATTTTAAATGTTCTCACCACAAAAAAATAAGATTTGAGGTAATGGGTATGTTAATTAGCTTGATTATATCAAAGCATCATGTTGTATGCCATAAATATGTATTCTTTTTA... |
Task1_train_43241 | This variant is found on Chromosome 14. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CTTGTTTCTCACAAAGTCTTCCTCCAGCCCAGCCTGCTTCAGGGTGTCTAGATACCACTGTTCTGCTTCTTTCTTGGCTAGATCCTGTGGGATGGAAATTAATCTGTTGTAGCTGTCTTATGAATTACCAGACAATTCTAAATTACTTAATCAGTATTGTTACAATACTGCCACAACCACCACCACCCTTATTGTGGGGCATAGATTTGCAAGAAAATTATTTAACCCTTGTTTTCCAGCCTTAATGTGTATATAAATCACCTGAGGTCTTGTTAAAATGCAGATTTCACATTTGGTAGGTGTCAGATGAGGACTGTAAT... | CTTGTTTCTCACAAAGTCTTCCTCCAGCCCAGCCTGCTTCAGGGTGTCTAGATACCACTGTTCTGCTTCTTTCTTGGCTAGATCCTGTGGGATGGAAATTAATCTGTTGTAGCTGTCTTATGAATTACCAGACAATTCTAAATTACTTAATCAGTATTGTTACAATACTGCCACAACCACCACCACCCTTATTGTGGGGCATAGATTTGCAAGAAAATTATTTAACCCTTGTTTTCCAGCCTTAATGTGTATATAAATCACCTGAGGTCTTGTTAAAATGCAGATTTCACATTTGGTAGGTGTCAGATGAGGACTGTAAT... |
Task1_train_43242 | This variant is located on Chromosome 14. Evaluate its biological effect and specify any disease association. | Benign | GCCCACATGCATGCAAGCCTTTCCTCTTCACTTTCTCTCAGCCTTTTTCTGGTTTCAAGGGAATCTGCCCAGGCTGTTTGTAAGTTCCCTTTTTGTCTTTTTATGCTTGAGAGTTTCCAAGTGCAGCAGAGTCTTAGCCGTTGGTATTGGTGTTCTTTTGACACAGCTCTCAGACACCTTGAGTTCCTTGGTTTGGTCCACGTCCCATGAACATGCAGCAGAGCTAGTTAGCATGGATGAGGAAAAATTTGTGGATGCCGTTAACTCTGCCTTTGTGAGTATCAATTTACCCAGCTGATGATGTGCTGCAGGGGGAGATA... | GCCCACATGCATGCAAGCCTTTCCTCTTCACTTTCTCTCAGCCTTTTTCTGGTTTCAAGGGAATCTGCCCAGGCTGTTTGTAAGTTCCCTTTTTGTCTTTTTATGCTTGAGAGTTTCCAAGTGCAGCAGAGTCTTAGCCGTTGGTATTGGTGTTCTTTTGACACAGCTCTCAGACACCTTGAGTTCCTTGGTTTGGTCCACGTCCCATGAACATGCAGCAGAGCTAGTTAGCATGGATGAGGAAAAATTTGTGGATGCCGTTAACTCTGCCTTTGTGAGTATCAATTTACCCAGCTGATGATGTGCTGCAGGGGGAGATA... |
Task1_train_43243 | The following genetic variant occurs on Chromosome 14. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TAAGTAGCTGGGACTACAGGCACGTGCCACCATGCCCAGCTAATTTTTCTATTTTTAGTAGAGATGAGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAAGTGATCTGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCACCCAGCCAGAAAGGTGGTTTTGAGTCAGGAAAAAGGAGTAACCAGTCAGCTGTCCCTTTCTACTTTGTAACTATAATGCTTGGTCTAGATTATGTGGAGGAGTGTACACACGGAAATGCAAAACAATAGAAATAATAAATAATAACCTTTT... | TAAGTAGCTGGGACTACAGGCACGTGCCACCATGCCCAGCTAATTTTTCTATTTTTAGTAGAGATGAGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAAGTGATCTGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCACCCAGCCAGAAAGGTGGTTTTGAGTCAGGAAAAAGGAGTAACCAGTCAGCTGTCCCTTTCTACTTTGTAACTATAATGCTTGGTCTAGATTATGTGGAGGAGTGTACACACGGAAATGCAAAACAATAGAAATAATAAATAATAACCTTTT... |
Task1_train_43244 | This mutation is located on Chromosome 14. Is it associated with a disease or is it a benign polymorphism? | Benign | TCCACTGCAAACCCATTACCTCTGTGGAAGAGGACTGAGAACCAGAGGTAGGAAAGTGGATGTGGAGGGTGGCAGTATAGAAAGGTCCACATGTACATATGTGTGAAAATATTTAGAATTCAAATACAGGTGAAATATTCTTAAATATGTACATATTTATATATCATGGTACCTACCATATATAAGGGGGAGTGTTTTGTTAATGCTTATACAATAAATATTTAGAAAAATCTCTTCCTTTACCACTTTAATCTTTGAATCCATCCTTTTTCCTCTCCACCTCTATATAAATGATTATGGTTTCTCAGGCATCCTTAAAG... | TCCACTGCAAACCCATTACCTCTGTGGAAGAGGACTGAGAACCAGAGGTAGGAAAGTGGATGTGGAGGGTGGCAGTATAGAAAGGTCCACATGTACATATGTGTGAAAATATTTAGAATTCAAATACAGGTGAAATATTCTTAAATATGTACATATTTATATATCATGGTACCTACCATATATAAGGGGGAGTGTTTTGTTAATGCTTATACAATAAATATTTAGAAAAATCTCTTCCTTTACCACTTTAATCTTTGAATCCATCCTTTTTCCTCTCCACCTCTATATAAATGATTATGGTTTCTCAGGCATCCTTAAAG... |
Task1_train_43245 | This sequence variant lies on Chromosome 14. Is it clinically significant, and what condition might it cause if any? | Benign | TCTCCACCAGTGCTTGGAGTTCTTTCAGGTCATGGGGACAGGAGTTTTTTATTTGACATTCTAAAATAAATATCTTTTGATGAGTAAAATTTGTTGTTAGGGGCATAATTATTTAAGCAGCCCATTTTCTTTTTTAGCACCGACTAGAACAAGAGGCTGAAAAGAAGATAATAATGCTAGCAGAGAGAGCCCACCATGAGGCTATTGTGTAAGAGACTGCTGCCTACTTTCTGACTCTGATTACCTCTCTTACCTCTTTGCTGGTCTCTTTTCTTCTTACTTTCTTGTCTTCCCCCTTCTGTTCTGGCTTACTTGCTTCA... | TCTCCACCAGTGCTTGGAGTTCTTTCAGGTCATGGGGACAGGAGTTTTTTATTTGACATTCTAAAATAAATATCTTTTGATGAGTAAAATTTGTTGTTAGGGGCATAATTATTTAAGCAGCCCATTTTCTTTTTTAGCACCGACTAGAACAAGAGGCTGAAAAGAAGATAATAATGCTAGCAGAGAGAGCCCACCATGAGGCTATTGTGTAAGAGACTGCTGCCTACTTTCTGACTCTGATTACCTCTCTTACCTCTTTGCTGGTCTCTTTTCTTCTTACTTTCTTGTCTTCCCCCTTCTGTTCTGGCTTACTTGCTTCA... |
Task1_train_43246 | With a mutation on Chromosome 14, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | ATGGATAGTTTGCTTTGTAGTTTTCTTTTTTTCTTTCTTTTTTTTTTTGAGACGGAGTTTCACTCTTTTCTCCCAGGCTGGAGCACAGTGGCGCGATCTCAGCTTACTGCAGCCTCCGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGACAGCTGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGAGCTTTCATCACATTGTCCAGGCTGGTCTCGAACTCCTGACCTCAGATGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCAC... | ATGGATAGTTTGCTTTGTAGTTTTCTTTTTTTCTTTCTTTTTTTTTTTGAGACGGAGTTTCACTCTTTTCTCCCAGGCTGGAGCACAGTGGCGCGATCTCAGCTTACTGCAGCCTCCGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGACAGCTGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGAGCTTTCATCACATTGTCCAGGCTGGTCTCGAACTCCTGACCTCAGATGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCAC... |
Task1_train_43247 | Located on Chromosome 14, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TTTTAATAACCCAAACATAAATAAAATAAAAAAGCCCCACATCCCTCGCCCTGTGGCAGCACATAGCTGGCACAGAAAAAAAAAATCAACCTATAAAAGGGGAGACTTGTATAACAAAACATGTAATTTATTAATGAAGGTTTCAAAATGGCTCTAGTCCTATGACTAGAAAGAACTTCCCCTAGCCTATTTGTTCAACAAATGTTTGGGCAGCCTGCTCTGTTCCAGGTACTGCAGATAAGTAGATAACAACTACAGTCTGATGAGGGCTTCTTTAAATGGCTTAAAGAGCCCTACATGACTCAACCCCTGCCTGCCTC... | TTTTAATAACCCAAACATAAATAAAATAAAAAAGCCCCACATCCCTCGCCCTGTGGCAGCACATAGCTGGCACAGAAAAAAAAAATCAACCTATAAAAGGGGAGACTTGTATAACAAAACATGTAATTTATTAATGAAGGTTTCAAAATGGCTCTAGTCCTATGACTAGAAAGAACTTCCCCTAGCCTATTTGTTCAACAAATGTTTGGGCAGCCTGCTCTGTTCCAGGTACTGCAGATAAGTAGATAACAACTACAGTCTGATGAGGGCTTCTTTAAATGGCTTAAAGAGCCCTACATGACTCAACCCCTGCCTGCCTC... |
Task1_train_43248 | Chromosome 14 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AATCATTTGTAGGTAATCAGCACTTCAAGCATATGGAGGCTCTGGCTGAGGCAGCAGAGTCCTGGGAGACTGAACACTGGGAGATTCAGTGTCCCCCACAGAAACCTAGACCTGGGCTCAGCCCACCACTGCTAGGGGTCCTGCACAGGACCCATGTGGCTCCTGCACGGGATCTATGTGGCGAACCTGAGCTCGATCTTCGCTGTCAGTCCTCCTGGTCTCTCCTGAGGGCCGCCGACCCGCCACAGTGTGGCTCTCCTTCCAAAAGCCAGAGCTTCATTCCACTTTGATTCTCATCAGCTCCCATCTTCCTCCTCCAC... | AATCATTTGTAGGTAATCAGCACTTCAAGCATATGGAGGCTCTGGCTGAGGCAGCAGAGTCCTGGGAGACTGAACACTGGGAGATTCAGTGTCCCCCACAGAAACCTAGACCTGGGCTCAGCCCACCACTGCTAGGGGTCCTGCACAGGACCCATGTGGCTCCTGCACGGGATCTATGTGGCGAACCTGAGCTCGATCTTCGCTGTCAGTCCTCCTGGTCTCTCCTGAGGGCCGCCGACCCGCCACAGTGTGGCTCTCCTTCCAAAAGCCAGAGCTTCATTCCACTTTGATTCTCATCAGCTCCCATCTTCCTCCTCCAC... |
Task1_train_43249 | A mutation found on Chromosome 14 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AGGCTGGGTCAGAGGCAGGGAGGGCCTGGCTCTCACCCCGTGTACTCGTCCAGAGGCCACCCAGAACCCGGAGCAAGGAGGTCTTGCCAGTGCCCGTGTTGCCTGTGATGAGCAGGCTCTGTCCCTCGGAGATCTTTAGGCTCAGATCCTTGATTAGGGGTTTGTCAGAGGAGGGGGCAGAGATGGAGACCCGCTCAAGGAGAAATGCTGTGTCTGCTGGCTCTGCCGCTGGCCACCCTGGGGGTCTGTGTCAGAGAAGAGAGGGGGCGTGAGGAAGATGGGCAGGGTCAGTATTGCTGTGGGGGAGGCACTGCTCCCGG... | AGGCTGGGTCAGAGGCAGGGAGGGCCTGGCTCTCACCCCGTGTACTCGTCCAGAGGCCACCCAGAACCCGGAGCAAGGAGGTCTTGCCAGTGCCCGTGTTGCCTGTGATGAGCAGGCTCTGTCCCTCGGAGATCTTTAGGCTCAGATCCTTGATTAGGGGTTTGTCAGAGGAGGGGGCAGAGATGGAGACCCGCTCAAGGAGAAATGCTGTGTCTGCTGGCTCTGCCGCTGGCCACCCTGGGGGTCTGTGTCAGAGAAGAGAGGGGGCGTGAGGAAGATGGGCAGGGTCAGTATTGCTGTGGGGGAGGCACTGCTCCCGG... |
Task1_train_43250 | A mutation on Chromosome 14 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CCAGGCTTGAGTGCAGTGGAGCTATCTCAGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCGATTTTCCTGTCCCAGCCTCCTGAGTAGCTGGATTACAGGTGCCCACCACCGTGCCCATATTTTTAGTAGAGACAGGGTTTCACTATGTTGGCCAGTCTGGTCTCGAACTTGTGACCTCAGGTGATCTGCCCACCTCAGCCTCCCAAAGTGGTGGGATTATAGACGTGAGCTTCCGTGCCCAGCTGGAGGCAGGGTCTTTAAAGAGATGATGTTAACATGAAGTTGTTGGGGTGGGACCCTAATCCAATATGACTGGT... | CCAGGCTTGAGTGCAGTGGAGCTATCTCAGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCGATTTTCCTGTCCCAGCCTCCTGAGTAGCTGGATTACAGGTGCCCACCACCGTGCCCATATTTTTAGTAGAGACAGGGTTTCACTATGTTGGCCAGTCTGGTCTCGAACTTGTGACCTCAGGTGATCTGCCCACCTCAGCCTCCCAAAGTGGTGGGATTATAGACGTGAGCTTCCGTGCCCAGCTGGAGGCAGGGTCTTTAAAGAGATGATGTTAACATGAAGTTGTTGGGGTGGGACCCTAATCCAATATGACTGGT... |
Task1_train_43251 | Here’s a variant located on Chromosome 14. What is the predicted biological effect — harmless or disease-causing? | Benign | CCACGGTCCCCAGGATGAAATACCCGAAGATGCTCACAGGCCCGAGCCAGCCTGTGCTGAAATAGAGAGAGAGGGAGAGAAGGGAGAGGGTGTGGGGTGCCACCTATCCCCACATGCCTCAGCCCTGACTCCTGTTCCCTCTCAGGTAGCCCCTGTCCAATCTGAGTGGCCCAATGGGCCCTCTGCTCCTATGTGGGGGCATCTGGTATGAGCTCTCAGAGCCAGGATATCTGTGACACTGCAACACAGGGCCAAAGGAAGGGCAGGGGCCTGAGCACGTGGGATGGGTGAGCACGTGGTAAGGTACGGTGGGAGAGAGG... | CCACGGTCCCCAGGATGAAATACCCGAAGATGCTCACAGGCCCGAGCCAGCCTGTGCTGAAATAGAGAGAGAGGGAGAGAAGGGAGAGGGTGTGGGGTGCCACCTATCCCCACATGCCTCAGCCCTGACTCCTGTTCCCTCTCAGGTAGCCCCTGTCCAATCTGAGTGGCCCAATGGGCCCTCTGCTCCTATGTGGGGGCATCTGGTATGAGCTCTCAGAGCCAGGATATCTGTGACACTGCAACACAGGGCCAAAGGAAGGGCAGGGGCCTGAGCACGTGGGATGGGTGAGCACGTGGTAAGGTACGGTGGGAGAGAGG... |
Task1_train_43252 | Located on Chromosome 14, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | CAGGCTAGAGTACAGTGGCTATTCCCAAGTGTGCTCACGGTGCACTACTCCTGGGCTCAAGTGATCCTCCTGCCTCAGCCTCCTGAGTTGTTGGGACTACAGGTGCATGCCACTGCACCTGGCAGGCTTCTTCTTTTTAGCTGCCTATTCACAGCCCTGCAGCTTCTCCAGGAGTCCTCTGCAGGGCACCCTCCCCCATGACTCTGGGCAGCAGCATTTGAAAACGACTGCAGATGATCTCCTTGGTGTCTGCCACCAGCAGTCTCCAGGGCTAGGCCAGAAGGAAAGGACCACACAGAGTGTAGAAAGGACTGAGTTGG... | CAGGCTAGAGTACAGTGGCTATTCCCAAGTGTGCTCACGGTGCACTACTCCTGGGCTCAAGTGATCCTCCTGCCTCAGCCTCCTGAGTTGTTGGGACTACAGGTGCATGCCACTGCACCTGGCAGGCTTCTTCTTTTTAGCTGCCTATTCACAGCCCTGCAGCTTCTCCAGGAGTCCTCTGCAGGGCACCCTCCCCCATGACTCTGGGCAGCAGCATTTGAAAACGACTGCAGATGATCTCCTTGGTGTCTGCCACCAGCAGTCTCCAGGGCTAGGCCAGAAGGAAAGGACCACACAGAGTGTAGAAAGGACTGAGTTGG... |
Task1_train_43253 | A mutation found on Chromosome 14 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AGTACAGTGGCTATTCCCAAGTGTGCTCACGGTGCACTACTCCTGGGCTCAAGTGATCCTCCTGCCTCAGCCTCCTGAGTTGTTGGGACTACAGGTGCATGCCACTGCACCTGGCAGGCTTCTTCTTTTTAGCTGCCTATTCACAGCCCTGCAGCTTCTCCAGGAGTCCTCTGCAGGGCACCCTCCCCCATGACTCTGGGCAGCAGCATTTGAAAACGACTGCAGATGATCTCCTTGGTGTCTGCCACCAGCAGTCTCCAGGGCTAGGCCAGAAGGAAAGGACCACACAGAGTGTAGAAAGGACTGAGTTGGGGCGCCTA... | AGTACAGTGGCTATTCCCAAGTGTGCTCACGGTGCACTACTCCTGGGCTCAAGTGATCCTCCTGCCTCAGCCTCCTGAGTTGTTGGGACTACAGGTGCATGCCACTGCACCTGGCAGGCTTCTTCTTTTTAGCTGCCTATTCACAGCCCTGCAGCTTCTCCAGGAGTCCTCTGCAGGGCACCCTCCCCCATGACTCTGGGCAGCAGCATTTGAAAACGACTGCAGATGATCTCCTTGGTGTCTGCCACCAGCAGTCTCCAGGGCTAGGCCAGAAGGAAAGGACCACACAGAGTGTAGAAAGGACTGAGTTGGGGCGCCTA... |
Task1_train_43254 | A variant affecting Chromosome 14 has been observed. Determine if it's benign or associated with disease. | Benign | CACGGCGATGGCGAGTGTGGCTAGGAAGAGGGCCCGGCGGGAGGTGGTGCTGGCCAGGCGGAAGTCCCCTTTGGAGATGGCCTTGCTGGTCTAGGGAGAGAGACATGCTGATGAACAGGAGTGTCCCCACACCCAGCCAAACAGCCCAGCCTGCCAGGCCCCTGACCCCATCCTGCAGACGGGATGCCAAGCCCTCCAGTAGAGTGACGGGCCAGAGAAGGGACCTGGGCCCCAGGTGCTCTTACCCCCTGGGAGAAGTAGAAGGCAGCAATGCCCAGTGGCCAGAAGCAGCAGAGCATGGAGAAGAGAGTAAGTCCCAG... | CACGGCGATGGCGAGTGTGGCTAGGAAGAGGGCCCGGCGGGAGGTGGTGCTGGCCAGGCGGAAGTCCCCTTTGGAGATGGCCTTGCTGGTCTAGGGAGAGAGACATGCTGATGAACAGGAGTGTCCCCACACCCAGCCAAACAGCCCAGCCTGCCAGGCCCCTGACCCCATCCTGCAGACGGGATGCCAAGCCCTCCAGTAGAGTGACGGGCCAGAGAAGGGACCTGGGCCCCAGGTGCTCTTACCCCCTGGGAGAAGTAGAAGGCAGCAATGCCCAGTGGCCAGAAGCAGCAGAGCATGGAGAAGAGAGTAAGTCCCAG... |
Task1_train_43255 | Consider this mutation on Chromosome 14. Is this a benign change or a disease-causing variant? | Benign | TTGCTTCAGCCAGAGCAATCAGGAGGGAGAGGCAGGCTGAACTGAAGACAGACAGCAGCCAGGAGGGGAGGAGGAGCCATTTCTGCCTGAGCCCAGGGCCAGGGAGCCTTCAGGCTGGAGACAAGCTGGTGTCAATGAATCTTACAGACAGATGACAGCTGGCTTCTAGAAGATGTGAGCCCTGGCCCTGCTCTGGAGCTGCCCACTCAGGATGAGGCAATGCCGTGCCCTTCTTCAGGAGAATGAAACCTAGCCCACTGTTACTCTTTTCTTCCCTTTGGAGACAAGGCTGCTATAGGGTTAAATGGTCTGATCCAAGA... | TTGCTTCAGCCAGAGCAATCAGGAGGGAGAGGCAGGCTGAACTGAAGACAGACAGCAGCCAGGAGGGGAGGAGGAGCCATTTCTGCCTGAGCCCAGGGCCAGGGAGCCTTCAGGCTGGAGACAAGCTGGTGTCAATGAATCTTACAGACAGATGACAGCTGGCTTCTAGAAGATGTGAGCCCTGGCCCTGCTCTGGAGCTGCCCACTCAGGATGAGGCAATGCCGTGCCCTTCTTCAGGAGAATGAAACCTAGCCCACTGTTACTCTTTTCTTCCCTTTGGAGACAAGGCTGCTATAGGGTTAAATGGTCTGATCCAAGA... |
Task1_train_43256 | This mutation occurs on Chromosome 14. Does this change lead to a known medical condition, or is it benign? | Benign | GTGGCTGGAAAGGGGTGTCTGCAGTGTGAGGCCATGGGGCCTTGCATGCTCGCACAGCTTGGGAGGGTGGATGAGGGCCATCCTTTGGTAAGCATCCCATAGCAAGGCCAGGAAAGGTGGTGGACAGGGCCTCATGCGGTGGCTGAAGCATTAAAGCGATTGGTGGTGCTTGAGCCAAGCAAGGGCATGGAGGCAATGACCGAAGCTTACAGCCAGAGGCTAAGCTGGGAGAGATGAAAGCAGGCAAGGCTGATTGGAAACCTCTGGCCTGATGTCACGGTGTCTTCCCAGCTAGGAAATCATCCTCAAGGCCCCTGCCT... | GTGGCTGGAAAGGGGTGTCTGCAGTGTGAGGCCATGGGGCCTTGCATGCTCGCACAGCTTGGGAGGGTGGATGAGGGCCATCCTTTGGTAAGCATCCCATAGCAAGGCCAGGAAAGGTGGTGGACAGGGCCTCATGCGGTGGCTGAAGCATTAAAGCGATTGGTGGTGCTTGAGCCAAGCAAGGGCATGGAGGCAATGACCGAAGCTTACAGCCAGAGGCTAAGCTGGGAGAGATGAAAGCAGGCAAGGCTGATTGGAAACCTCTGGCCTGATGTCACGGTGTCTTCCCAGCTAGGAAATCATCCTCAAGGCCCCTGCCT... |
Task1_train_43257 | A variant has been detected on Chromosome 14. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TTCTGGAGTTGAGCACGTCCCAGCCGCAGGAAGTCCCCAGCTGTGCTCGGTAGAGCGTCTTGGCTGCAGCCCTGGGGTTCAGGGTGAGTGTGGTGGGGGTGCTGTGGGAAGCGGGAAGTGGGAGTGAGCAGGGCCTCGAGGACTGGCAGGGTGCCCTGGGCATAGCTCCTCGCTCCTCCTGCAGTTTCTGTCCCAACTCTCCCAAGGAGCAGGTTTTCTGGATCTGAGCTGCAGGGCTGTGGAAAGGGCCTGTCTGCCTCTTCTTTTTATATTTTATTTTATTTTATTTTATATTTTATTTTATTTGAGATGGGGTCTTG... | TTCTGGAGTTGAGCACGTCCCAGCCGCAGGAAGTCCCCAGCTGTGCTCGGTAGAGCGTCTTGGCTGCAGCCCTGGGGTTCAGGGTGAGTGTGGTGGGGGTGCTGTGGGAAGCGGGAAGTGGGAGTGAGCAGGGCCTCGAGGACTGGCAGGGTGCCCTGGGCATAGCTCCTCGCTCCTCCTGCAGTTTCTGTCCCAACTCTCCCAAGGAGCAGGTTTTCTGGATCTGAGCTGCAGGGCTGTGGAAAGGGCCTGTCTGCCTCTTCTTTTTATATTTTATTTTATTTTATTTTATATTTTATTTTATTTGAGATGGGGTCTTG... |
Task1_train_43258 | Consider this mutation on Chromosome 14. Is this a benign change or a disease-causing variant? | Benign | TATGTGTGTGTGCACACAAGGGTGTCGGGGTCTGCTCCAAATTGCATGCCGGTTCACAAGAGACAGAATCAGGAGGCTCTGAGTGTGGACACACATAAGCGTGTAAATTGAACGGTGTGCAAGGCTGGCAGATGTCTATGTGCACACATGGCAAGTGCTCTGTGAGGGAGGCAGACGACTGGAGATGACTCAGTGAGTTGTTTGAAAATGAATGAACCATGAGGCGTGGGAGAGAGAGGAAGCCAGGAGGAAAAGAAGATGGGCCGCCCTGGCACACTCCAGCCCAAATAATGACTTCCACTGCCGGCCTCTGCCCTGCA... | TATGTGTGTGTGCACACAAGGGTGTCGGGGTCTGCTCCAAATTGCATGCCGGTTCACAAGAGACAGAATCAGGAGGCTCTGAGTGTGGACACACATAAGCGTGTAAATTGAACGGTGTGCAAGGCTGGCAGATGTCTATGTGCACACATGGCAAGTGCTCTGTGAGGGAGGCAGACGACTGGAGATGACTCAGTGAGTTGTTTGAAAATGAATGAACCATGAGGCGTGGGAGAGAGAGGAAGCCAGGAGGAAAAGAAGATGGGCCGCCCTGGCACACTCCAGCCCAAATAATGACTTCCACTGCCGGCCTCTGCCCTGCA... |
Task1_train_43259 | A variant was discovered on Chromosome 14. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CCCACCACTTTGGGAGGCCGAGGCAGGTGGATCACCTGAGGTCAGGAGATCGAGACAAGCCTGGCCAACACGGTAAAACCCTGTCTCTACAAAAACACAAAAAATTAGCCGGGTGTGGTAGCGGGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGGATCCCTTGAACCTGGGAGGCGGAGGTTATAGTGAGCCGAGATCACGCCACTACACTCCAGCCTGGGCAACAAGAGTGAAACTCTGTCTCAAATAAATAAATGCCATATTATTGTCTTCCTGAATAACAGCTACTTGTACCATAAACACATCAAGG... | CCCACCACTTTGGGAGGCCGAGGCAGGTGGATCACCTGAGGTCAGGAGATCGAGACAAGCCTGGCCAACACGGTAAAACCCTGTCTCTACAAAAACACAAAAAATTAGCCGGGTGTGGTAGCGGGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGGATCCCTTGAACCTGGGAGGCGGAGGTTATAGTGAGCCGAGATCACGCCACTACACTCCAGCCTGGGCAACAAGAGTGAAACTCTGTCTCAAATAAATAAATGCCATATTATTGTCTTCCTGAATAACAGCTACTTGTACCATAAACACATCAAGG... |
Task1_train_43260 | This alteration occurs on Chromosome 14. Is it associated with a disease or is it a benign variant? | Benign | TGGAACTACACACACACACACACACACACACACACACACACACACACACACATATATATGAAATAAGAGGGCTTCAGAAAACACTTAAATTTAGGGAGTAGATGGGGAAAAGATAAATGCCAGACTTGGAAGAAGATGGAGCAAGAACATGAAAGAAGAAACCAAGAGGGCACAGGAGAACTGAGAAGAGCATTCTAAGTGGGTGGATAATCAGTAATGTCACATGAGTAGGCTGAAAAAATGAAGCTTTTGTCTTTGGAAAGTCACTGGTAGCTTTGTAGTTAAATAAAGTGGAGAAAGTAGAAGACAGGCCACAATGA... | TGGAACTACACACACACACACACACACACACACACACACACACACACACACATATATATGAAATAAGAGGGCTTCAGAAAACACTTAAATTTAGGGAGTAGATGGGGAAAAGATAAATGCCAGACTTGGAAGAAGATGGAGCAAGAACATGAAAGAAGAAACCAAGAGGGCACAGGAGAACTGAGAAGAGCATTCTAAGTGGGTGGATAATCAGTAATGTCACATGAGTAGGCTGAAAAAATGAAGCTTTTGTCTTTGGAAAGTCACTGGTAGCTTTGTAGTTAAATAAAGTGGAGAAAGTAGAAGACAGGCCACAATGA... |
Task1_train_43261 | A variant was discovered on Chromosome 14. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CTGCAGAGTTGGCCGGACACTGACTGGGTCAAGTGACCTTGGGCTGACCGCACCCCCACCCCCGGTCGCCCCGGGTCGCTGGTGCACTGCGCCTGCGCGCGTCTCCCCGAGGAGTTCGCGGCGAGGGGCGGAGCTTGGCGCGCCAGTGCCTCGGTTTCCAGGCACCGGGAATAACAGAAGCCAGCTGAGAGCGCCTGCGCGGCTGTCGGTTGATGGGGAGGTCAGGTCTGGGAAACTAGGCCCTGGGGTTTTCCCTGAGCAGGAGCGGTGCCCGAGGGCCTCAGGTACGCAGAAGGGCGGGGAGACATGGGATCAGCACC... | CTGCAGAGTTGGCCGGACACTGACTGGGTCAAGTGACCTTGGGCTGACCGCACCCCCACCCCCGGTCGCCCCGGGTCGCTGGTGCACTGCGCCTGCGCGCGTCTCCCCGAGGAGTTCGCGGCGAGGGGCGGAGCTTGGCGCGCCAGTGCCTCGGTTTCCAGGCACCGGGAATAACAGAAGCCAGCTGAGAGCGCCTGCGCGGCTGTCGGTTGATGGGGAGGTCAGGTCTGGGAAACTAGGCCCTGGGGTTTTCCCTGAGCAGGAGCGGTGCCCGAGGGCCTCAGGTACGCAGAAGGGCGGGGAGACATGGGATCAGCACC... |
Task1_train_43262 | A variant on Chromosome 14 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | CAAAACACTGCTAACAATAAATGGTATAGCTGATTTAGCCAACCCTCCAATGGGTAAGCCTGTGCCCTAGGGTAGGTGGGAGAGATGTGACTGTGCTTTTCCCCCAGCTGGTATCAGCCTCTGTGAGCCTCTCACAGGGCCAGCTCTGGCAAGGCTGAGAGTAATTAGATAATATGTTTCATGCAACATGACCGCTAAACAAAAACAACTATTAATATTTCATCTGGTGGTCAACTGTAGAAACAGGAGAGGAAAATGGCTGTGTTGGGTTAAGAGACAGTATACTGCTTTACAGTATCTTCTCGAGTTTTCCAGGGTAT... | CAAAACACTGCTAACAATAAATGGTATAGCTGATTTAGCCAACCCTCCAATGGGTAAGCCTGTGCCCTAGGGTAGGTGGGAGAGATGTGACTGTGCTTTTCCCCCAGCTGGTATCAGCCTCTGTGAGCCTCTCACAGGGCCAGCTCTGGCAAGGCTGAGAGTAATTAGATAATATGTTTCATGCAACATGACCGCTAAACAAAAACAACTATTAATATTTCATCTGGTGGTCAACTGTAGAAACAGGAGAGGAAAATGGCTGTGTTGGGTTAAGAGACAGTATACTGCTTTACAGTATCTTCTCGAGTTTTCCAGGGTAT... |
Task1_train_43263 | Here is a genetic alteration on Chromosome 14. Based on the data, is it a benign variant or a cause of disease? | Benign | TTTGACAGTTTCCTTAATATTCCCACACATGGCCGAGAAAAATAAATAAATAAATGCGCTGTCTTCTTTAAAAAAATAAATAAATAAAGTACCCAGTATCGTAAAGTAGGTTATCGTATTCTCTTATTTTGGATCCTCCACTTTCTGCTTCCAAACGCAGGAACAGTGCTAGTATTGCTCGAGCCCGAGGGCTGGAGGTTAGGGGATGAAGGTCTGCTTCCACGCTTTGCACTGAATTAGGGCTAGAATTGGGGATGGGGGTAGGGGCGCATTCCTTCGGGAGCCGAGGCTTAAGTCCTCGGGGTCCTGTACTCGATGCC... | TTTGACAGTTTCCTTAATATTCCCACACATGGCCGAGAAAAATAAATAAATAAATGCGCTGTCTTCTTTAAAAAAATAAATAAATAAAGTACCCAGTATCGTAAAGTAGGTTATCGTATTCTCTTATTTTGGATCCTCCACTTTCTGCTTCCAAACGCAGGAACAGTGCTAGTATTGCTCGAGCCCGAGGGCTGGAGGTTAGGGGATGAAGGTCTGCTTCCACGCTTTGCACTGAATTAGGGCTAGAATTGGGGATGGGGGTAGGGGCGCATTCCTTCGGGAGCCGAGGCTTAAGTCCTCGGGGTCCTGTACTCGATGCC... |
Task1_train_43264 | This variant lies on Chromosome 14. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CCCCCACCCCCAGAAATGTTTAGGATGACTTCTGGCTGGTGAATATCAGCTGTTGTGGTTGTCTCCTAGGAATGGCATGGCTGAGGGCTTTGTGGTTTATATCTGAGCAGTTAGGGGCTCTTTTGCAGGGGGAGGAAAGACAGGGGGACTTTTGCTTCTACAAAGGAAAGACTAGTGCCTTGTCTCCTGGGTGAGGCTTGTCATTGGGATGGATTCACAGGCGAGCAGAAATGGCAAAATTTATGGGGCCCGTGCTCCCAGGGGGTGGCCGCTCCTTCAGGGGGTTCCACAGTAGCAGAAAATGCATTATATTTTGGGAT... | CCCCCACCCCCAGAAATGTTTAGGATGACTTCTGGCTGGTGAATATCAGCTGTTGTGGTTGTCTCCTAGGAATGGCATGGCTGAGGGCTTTGTGGTTTATATCTGAGCAGTTAGGGGCTCTTTTGCAGGGGGAGGAAAGACAGGGGGACTTTTGCTTCTACAAAGGAAAGACTAGTGCCTTGTCTCCTGGGTGAGGCTTGTCATTGGGATGGATTCACAGGCGAGCAGAAATGGCAAAATTTATGGGGCCCGTGCTCCCAGGGGGTGGCCGCTCCTTCAGGGGGTTCCACAGTAGCAGAAAATGCATTATATTTTGGGAT... |
Task1_train_43265 | This mutation is located on Chromosome 14. Is it associated with a disease or is it a benign polymorphism? | Benign | CTATGGGCAGAGGCTTTATGACAGATGCAGCAGGCATGCTGAGGATGAAATGGCGGGTCCACTTCCCATTCCCAGGCACCTCGCTTTAGACACCTTGCTTTAGACAAAGTGATGGCCAGTGGAAACCTTTGTGCTTGAGGGTGCAAGTTACTCACATGCTTTTTCTCTTAGAGAAATAGAACTTATTGGGAAATAGACTCTGGACTTGGACAGGGAACCAAATTTCACCTTCAAAAGTGAAATGTAGATGGAGAATATGGCTTGCACTCTTGGCCAAAACAGGTTCACAAATGCCCCTCTCTGGAATGATCTAGACCTGG... | CTATGGGCAGAGGCTTTATGACAGATGCAGCAGGCATGCTGAGGATGAAATGGCGGGTCCACTTCCCATTCCCAGGCACCTCGCTTTAGACACCTTGCTTTAGACAAAGTGATGGCCAGTGGAAACCTTTGTGCTTGAGGGTGCAAGTTACTCACATGCTTTTTCTCTTAGAGAAATAGAACTTATTGGGAAATAGACTCTGGACTTGGACAGGGAACCAAATTTCACCTTCAAAAGTGAAATGTAGATGGAGAATATGGCTTGCACTCTTGGCCAAAACAGGTTCACAAATGCCCCTCTCTGGAATGATCTAGACCTGG... |
Task1_train_43266 | A mutation is present on Chromosome 14. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CTCCAGGGTCCCTGGAGAACATTGAGAGGGTTTTCCCGTTTTGGATGAAGTGTGAATAGGAATCCATGGACCAGAGAGCGGCCTTGGAAGCCATGTTCACTCAGCCCCAGGTGGTCTTCCCAGACTTTGTTCATAACAGAGACCAAGACGTGCATCCATGTTTAGCCTGAGCAGAAAAAGTTGCCCCAAACCAGCTGATGTGCTGGGTAAATGTTGGCCTAAGCATGCTTGTGTTTTTAGTGATTTGAAACGTAAAGGCAGCCCACTGACATTTTTTAGCAAGCTTTGCATAATTGGTTTTTAATTGTGGCTCTTTGGAA... | CTCCAGGGTCCCTGGAGAACATTGAGAGGGTTTTCCCGTTTTGGATGAAGTGTGAATAGGAATCCATGGACCAGAGAGCGGCCTTGGAAGCCATGTTCACTCAGCCCCAGGTGGTCTTCCCAGACTTTGTTCATAACAGAGACCAAGACGTGCATCCATGTTTAGCCTGAGCAGAAAAAGTTGCCCCAAACCAGCTGATGTGCTGGGTAAATGTTGGCCTAAGCATGCTTGTGTTTTTAGTGATTTGAAACGTAAAGGCAGCCCACTGACATTTTTTAGCAAGCTTTGCATAATTGGTTTTTAATTGTGGCTCTTTGGAA... |
Task1_train_43267 | This is a variant located on Chromosome 14. Is this mutation a likely cause of disease or not? | Benign | ATTAAGAGTTTCTTCATATGATTCTAATGTGCAGACAAAATGGAGAGCCACTTCCCAGAGCTTCAAGTTATTCATTTTCTGGTCTGAAGTTTAACAAAGAAAAAAAAAATAAAGAAGCAGTGATGCCCAGTAGCTCTCAAAATTTAATGTGTAAACAAATGAATCTCCTGGGCATCTTGTTAAAATGCAGCTTTCAATTCAGTGGGTCTAGGTTGGGCCTGACAACCTTCTTGGTTGTTTTGTGGTTGCCGTTTTGTTTTTTAAGGCCTTAACACTGGAGGGGATTCTGGCCTTCTAAAAAGCTCCCACAGGTGCCCACG... | ATTAAGAGTTTCTTCATATGATTCTAATGTGCAGACAAAATGGAGAGCCACTTCCCAGAGCTTCAAGTTATTCATTTTCTGGTCTGAAGTTTAACAAAGAAAAAAAAAATAAAGAAGCAGTGATGCCCAGTAGCTCTCAAAATTTAATGTGTAAACAAATGAATCTCCTGGGCATCTTGTTAAAATGCAGCTTTCAATTCAGTGGGTCTAGGTTGGGCCTGACAACCTTCTTGGTTGTTTTGTGGTTGCCGTTTTGTTTTTTAAGGCCTTAACACTGGAGGGGATTCTGGCCTTCTAAAAAGCTCCCACAGGTGCCCACG... |
Task1_train_43268 | A sequence alteration has been identified on Chromosome 14. Is it disease-inducing or harmless? | Benign | CCTCAGCCTCCAGGAAGGGAAGAGGGGCTGAAAGTTAAATTAGTCACCAGTGTCCAATCAATTATGCCTGTGTAATGAAGCTTCCATAAAAACCCAAAAGGACTGGGTTTGGAGAGCTTCTGGGTAACAGAATACATGGAGATTCTTGGCCAGTAGTGTGCCTGGAGATCGCATAGAGGTTCTGTGCCTCCTTTCTCATACCTCGCCCTGTGCATGTCTTCCTCTATATCCTTTGTAATATCCTTTTTAATAAACCAGTAAACATAAATGTTTCTCTGAGTTCTGTGAGCTGCTCTAACAAATTAATTGATCCCAAGGAG... | CCTCAGCCTCCAGGAAGGGAAGAGGGGCTGAAAGTTAAATTAGTCACCAGTGTCCAATCAATTATGCCTGTGTAATGAAGCTTCCATAAAAACCCAAAAGGACTGGGTTTGGAGAGCTTCTGGGTAACAGAATACATGGAGATTCTTGGCCAGTAGTGTGCCTGGAGATCGCATAGAGGTTCTGTGCCTCCTTTCTCATACCTCGCCCTGTGCATGTCTTCCTCTATATCCTTTGTAATATCCTTTTTAATAAACCAGTAAACATAAATGTTTCTCTGAGTTCTGTGAGCTGCTCTAACAAATTAATTGATCCCAAGGAG... |
Task1_train_43269 | Consider this mutation on Chromosome 14. Is this a benign change or a disease-causing variant? | Benign | TCCCATAAGGGGCTGAAATAAAATGCGTGAGGATTTCCGATGTGGCTGTCCAAGGCCGAGGCTGATGGGAAAAGGGAGAAGCTCTCTGCCCCTTTCTCTCCTGCCTCTGTGGCTCCCTTGTCCTCAAAATGAAAGTGGAAAGGAGAGGGTAGGCCCCAAATTGCTTGCCAGAGGGGAGGGGCTATGAGACAGTCTGATCCTTGCGCCAATGCTGGGCTAGAATCTTCTCAAGCGGCATGTCTCTTTCAGGGTTGTAGGGACTGTGTGGGCACCTCAGACACCACCTGACTCTCCAGGTGCACCTCATACCACTTTGCTCT... | TCCCATAAGGGGCTGAAATAAAATGCGTGAGGATTTCCGATGTGGCTGTCCAAGGCCGAGGCTGATGGGAAAAGGGAGAAGCTCTCTGCCCCTTTCTCTCCTGCCTCTGTGGCTCCCTTGTCCTCAAAATGAAAGTGGAAAGGAGAGGGTAGGCCCCAAATTGCTTGCCAGAGGGGAGGGGCTATGAGACAGTCTGATCCTTGCGCCAATGCTGGGCTAGAATCTTCTCAAGCGGCATGTCTCTTTCAGGGTTGTAGGGACTGTGTGGGCACCTCAGACACCACCTGACTCTCCAGGTGCACCTCATACCACTTTGCTCT... |
Task1_train_43270 | A mutation is present on Chromosome 14. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CTGATTCTTGTATAACCTTCAGTGGACCTGGGTGGGATGACAGGAACATTGCTGTCTAGGGGATGACATTCGTGGCTCCTTCAGAAACATGCTAACATCCCTCTGTGGGTAACATAATGAGGTCCAGCATTCATACACCATAGTGTCTCCAGAGCCAAGTCGACGTGCTTGTAAACCCCCTTCTTTGCTGAAGATCCAGCCAGATCACAACTGTGCTGAGGCCTGACTGACCTCAGAAACCAAACTCAGTCCAAACCCCCCTCCCCAACCCATTGTCAGCCAAGAGAGCTGTCACAGCTTAGGGGGCTGTGAGGAGCAGT... | CTGATTCTTGTATAACCTTCAGTGGACCTGGGTGGGATGACAGGAACATTGCTGTCTAGGGGATGACATTCGTGGCTCCTTCAGAAACATGCTAACATCCCTCTGTGGGTAACATAATGAGGTCCAGCATTCATACACCATAGTGTCTCCAGAGCCAAGTCGACGTGCTTGTAAACCCCCTTCTTTGCTGAAGATCCAGCCAGATCACAACTGTGCTGAGGCCTGACTGACCTCAGAAACCAAACTCAGTCCAAACCCCCCTCCCCAACCCATTGTCAGCCAAGAGAGCTGTCACAGCTTAGGGGGCTGTGAGGAGCAGT... |
Task1_train_43271 | A variant has been detected on Chromosome 14. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GACTTCAAAGGGAATTACCACCACTCCGTTCAGACTGAAGTCCTGTCTCCCTTTGATGTTGTCACCTGTGTTAATTTATTATTAAATCAGCATGCTGCTTAGACTTGTTCCCAGGATTTATGCAAGGTATGAAAAAGGAAGCGTTTTCCCTACTTTACACATTGATAATTAGCTATTTAGAATTAACTATTTGAGCTTTCAGAATTAATTATTCATGAGGTATTTGACTTAATTTTCTGTACAGGACAGAGTGATCAATAAAAGGTGCTTTGGATGGAATTTTCCAAACCACTGGCTTTGTATTATAAATCTCAGCCTGT... | GACTTCAAAGGGAATTACCACCACTCCGTTCAGACTGAAGTCCTGTCTCCCTTTGATGTTGTCACCTGTGTTAATTTATTATTAAATCAGCATGCTGCTTAGACTTGTTCCCAGGATTTATGCAAGGTATGAAAAAGGAAGCGTTTTCCCTACTTTACACATTGATAATTAGCTATTTAGAATTAACTATTTGAGCTTTCAGAATTAATTATTCATGAGGTATTTGACTTAATTTTCTGTACAGGACAGAGTGATCAATAAAAGGTGCTTTGGATGGAATTTTCCAAACCACTGGCTTTGTATTATAAATCTCAGCCTGT... |
Task1_train_43272 | This alteration on Chromosome 14 may affect genome function. Does it lead to a disease or is it benign? | Benign | TCTCTGCCAACACTCTCCCCTGTCACTGTGATGAATTCAGCTTCTTTCTTAAACATGCAGCCACAAATCTTTTCCCTTTTTCCCCTCCCCCAGTGGTAGAAAGTTTTGAGTTGCAATTGACTGAATTTAAAGATATTAATAAGGCTAGAGAGGTGAAGAGCAGGAAGAAACAGCATGTCTTCCTTGCCTTTTTGTACTAATAGTAACAAAAGGCCAAGGAAAAAGACTGTAAATGACCATAGGTTGTTAAATAGACCCATCTTGAAAGTGTAGCACCTTTATTTTCTTTGTATCTTCATTCTCCCTCCTTTACGGCTTTC... | TCTCTGCCAACACTCTCCCCTGTCACTGTGATGAATTCAGCTTCTTTCTTAAACATGCAGCCACAAATCTTTTCCCTTTTTCCCCTCCCCCAGTGGTAGAAAGTTTTGAGTTGCAATTGACTGAATTTAAAGATATTAATAAGGCTAGAGAGGTGAAGAGCAGGAAGAAACAGCATGTCTTCCTTGCCTTTTTGTACTAATAGTAACAAAAGGCCAAGGAAAAAGACTGTAAATGACCATAGGTTGTTAAATAGACCCATCTTGAAAGTGTAGCACCTTTATTTTCTTTGTATCTTCATTCTCCCTCCTTTACGGCTTTC... |
Task1_train_43273 | A mutation on Chromosome 14 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GTCAACCCTCCCAGGAAGAGCGCTGGAAGGTCAGTTCAACCTAAATAAGACCTCTGTGTTCACACTGCATAGAAACACTTGGAAAACTCATCTGTAAAATGGGAATAGTATTAGTACTTATTTTCTCTTTCATGGAATTGCTATTGGGAGGGGAGGGACTCTGTAGATCAGTCATTCACTGCATTCTACCTGCCTGTCTCTATATTGCGGGGGCTGTGCTAAGTGCTGCTGGACACTGGGGAGCAGCCCAAGGTCTTGGCTTCGTGGGGCCTACAGCTTAAAAGAGCATGGGTTGGGTTTATGGTAGCCATTCTTTTGTT... | GTCAACCCTCCCAGGAAGAGCGCTGGAAGGTCAGTTCAACCTAAATAAGACCTCTGTGTTCACACTGCATAGAAACACTTGGAAAACTCATCTGTAAAATGGGAATAGTATTAGTACTTATTTTCTCTTTCATGGAATTGCTATTGGGAGGGGAGGGACTCTGTAGATCAGTCATTCACTGCATTCTACCTGCCTGTCTCTATATTGCGGGGGCTGTGCTAAGTGCTGCTGGACACTGGGGAGCAGCCCAAGGTCTTGGCTTCGTGGGGCCTACAGCTTAAAAGAGCATGGGTTGGGTTTATGGTAGCCATTCTTTTGTT... |
Task1_train_43274 | A genomic variant on Chromosome 14 is under review. What is the biological outcome — benign or pathogenic? | Benign | TAAGACCTCTGTGTTCACACTGCATAGAAACACTTGGAAAACTCATCTGTAAAATGGGAATAGTATTAGTACTTATTTTCTCTTTCATGGAATTGCTATTGGGAGGGGAGGGACTCTGTAGATCAGTCATTCACTGCATTCTACCTGCCTGTCTCTATATTGCGGGGGCTGTGCTAAGTGCTGCTGGACACTGGGGAGCAGCCCAAGGTCTTGGCTTCGTGGGGCCTACAGCTTAAAAGAGCATGGGTTGGGTTTATGGTAGCCATTCTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTGAGA... | TAAGACCTCTGTGTTCACACTGCATAGAAACACTTGGAAAACTCATCTGTAAAATGGGAATAGTATTAGTACTTATTTTCTCTTTCATGGAATTGCTATTGGGAGGGGAGGGACTCTGTAGATCAGTCATTCACTGCATTCTACCTGCCTGTCTCTATATTGCGGGGGCTGTGCTAAGTGCTGCTGGACACTGGGGAGCAGCCCAAGGTCTTGGCTTCGTGGGGCCTACAGCTTAAAAGAGCATGGGTTGGGTTTATGGTAGCCATTCTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTTGTTTGAGA... |
Task1_train_43275 | This mutation on Chromosome 14 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GATGTGGCAGAAAGAGCCAGTGATTCCTGACATGAGAGAGGATCATGTAAAGGGCTCAAGGAGGGAAGAGTAAATTGTTTTCAGCTGGGGAGGTAGACTCTGAGTGGGGTCTTAAAGCAAGAGACGGTTCGGTAGGATGGGAAGAGGGAGTGTAAACTTCTGTAGTGGGGCCATCAGCTCCAGGCAGGAAATGGGGAAAGAACAGGCCAGTTTCAGGGAGAGGCTAGAAAAGCAGGCTGGGGTCAGACCAGAAGCTCAAGGGCTGTGAAGGGATTGGATTGTGATGGGGTCAGTACAGGGAGGCAGGAAGGGTTGTGCGG... | GATGTGGCAGAAAGAGCCAGTGATTCCTGACATGAGAGAGGATCATGTAAAGGGCTCAAGGAGGGAAGAGTAAATTGTTTTCAGCTGGGGAGGTAGACTCTGAGTGGGGTCTTAAAGCAAGAGACGGTTCGGTAGGATGGGAAGAGGGAGTGTAAACTTCTGTAGTGGGGCCATCAGCTCCAGGCAGGAAATGGGGAAAGAACAGGCCAGTTTCAGGGAGAGGCTAGAAAAGCAGGCTGGGGTCAGACCAGAAGCTCAAGGGCTGTGAAGGGATTGGATTGTGATGGGGTCAGTACAGGGAGGCAGGAAGGGTTGTGCGG... |
Task1_train_43276 | Assess the clinical impact of this variant found on Chromosome 14. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TGCTGCCCCATTTACCAGGAGCTGGCATTTGGACCACTACCGTGGAGGTAGTGACAGGAAGCAGTCATACCAAGAACCAAGCAGAATGGCCCAGAAGCAGGCTGCCTGTAACCCTTAGTGTCTGCCAGCAAGGTGAGGGGACCAGCTGTTGAGGCCTGGCAGAAGATGAGGAGAGGCCACGTCAGGTCAGCTGGCAGGTCACCTCTCTGAGCCCCGTCCAAATGACAATGTGCACACAGATATACAAACTTTTTCCAACCCTGAGCCTGAAAGGACTTGGTTGTTGGAAGCACAAAACCTCCAAGAATTTTAAGTGTAGG... | TGCTGCCCCATTTACCAGGAGCTGGCATTTGGACCACTACCGTGGAGGTAGTGACAGGAAGCAGTCATACCAAGAACCAAGCAGAATGGCCCAGAAGCAGGCTGCCTGTAACCCTTAGTGTCTGCCAGCAAGGTGAGGGGACCAGCTGTTGAGGCCTGGCAGAAGATGAGGAGAGGCCACGTCAGGTCAGCTGGCAGGTCACCTCTCTGAGCCCCGTCCAAATGACAATGTGCACACAGATATACAAACTTTTTCCAACCCTGAGCCTGAAAGGACTTGGTTGTTGGAAGCACAAAACCTCCAAGAATTTTAAGTGTAGG... |
Task1_train_43277 | Consider a variant on Chromosome 14. Determine its clinical classification and disease relevance. | Benign | CCAGGGTGCCTGGCTCCTGTATCATTTTTTACTGAGACACATGTCTTCTCGATCTGAAAATTCACATCTTTTCGTTTTGGGAAAATCTTTCTTGGATAATTATCTTTAAATATTTCTTCTGTGTTATTATATTATAGGCTTTCTTCTTTGGGAACTCCAATTATGTATAAGTTAAATCTCCTTTATCTTTCACTACTGTCATTTTCTCTCTAATCCTTTCTAACCTTTAACTTCTCACTGTTTTTTTTATTTGTTTTGTTTGGATTTCCTTACCTTGTTTTCCACAGTTATCTATTCCTACTTGTGCTGCATACAATTTT... | CCAGGGTGCCTGGCTCCTGTATCATTTTTTACTGAGACACATGTCTTCTCGATCTGAAAATTCACATCTTTTCGTTTTGGGAAAATCTTTCTTGGATAATTATCTTTAAATATTTCTTCTGTGTTATTATATTATAGGCTTTCTTCTTTGGGAACTCCAATTATGTATAAGTTAAATCTCCTTTATCTTTCACTACTGTCATTTTCTCTCTAATCCTTTCTAACCTTTAACTTCTCACTGTTTTTTTTATTTGTTTTGTTTGGATTTCCTTACCTTGTTTTCCACAGTTATCTATTCCTACTTGTGCTGCATACAATTTT... |
Task1_train_43278 | A variant affecting Chromosome 14 has been observed. Determine if it's benign or associated with disease. | Benign | GGGTCAAATTCATGCACATCCAATTCCCATCAAAGCCTACTCTTCCCAGGGCTTGCTGGGAGGGAAGGATAACTGCAGGCTCCCCTGGGATGCCCCCAGGTGAGGGAAGTTCACAGAGTTTGAGACAGAGGTGAATGGACAGGTGTGCTTCTTAGGGAAGCAGTCGAGAGGTGGCAAGAAGTTGGCAGCTGCCCTCAAGAGGGTCCTGGCACCATGGACAATGACAAGCCTCTTCAGCCTGAGACAGAAGGTGAAAGGGCATCCCATCTCTCACCACTCAGGCCCGTCCCTGCTGCCTCAGTACAACACCTAGTGATCAC... | GGGTCAAATTCATGCACATCCAATTCCCATCAAAGCCTACTCTTCCCAGGGCTTGCTGGGAGGGAAGGATAACTGCAGGCTCCCCTGGGATGCCCCCAGGTGAGGGAAGTTCACAGAGTTTGAGACAGAGGTGAATGGACAGGTGTGCTTCTTAGGGAAGCAGTCGAGAGGTGGCAAGAAGTTGGCAGCTGCCCTCAAGAGGGTCCTGGCACCATGGACAATGACAAGCCTCTTCAGCCTGAGACAGAAGGTGAAAGGGCATCCCATCTCTCACCACTCAGGCCCGTCCCTGCTGCCTCAGTACAACACCTAGTGATCAC... |
Task1_train_43279 | This alteration on Chromosome 14 may affect genome function. Does it lead to a disease or is it benign? | Benign | GCTGGGAGGGAAGGATAACTGCAGGCTCCCCTGGGATGCCCCCAGGTGAGGGAAGTTCACAGAGTTTGAGACAGAGGTGAATGGACAGGTGTGCTTCTTAGGGAAGCAGTCGAGAGGTGGCAAGAAGTTGGCAGCTGCCCTCAAGAGGGTCCTGGCACCATGGACAATGACAAGCCTCTTCAGCCTGAGACAGAAGGTGAAAGGGCATCCCATCTCTCACCACTCAGGCCCGTCCCTGCTGCCTCAGTACAACACCTAGTGATCACAGGACCCTGAAGCCCACTTCTTTCCTCACCTGGGACCCTCTAGAAGTAGGATGA... | GCTGGGAGGGAAGGATAACTGCAGGCTCCCCTGGGATGCCCCCAGGTGAGGGAAGTTCACAGAGTTTGAGACAGAGGTGAATGGACAGGTGTGCTTCTTAGGGAAGCAGTCGAGAGGTGGCAAGAAGTTGGCAGCTGCCCTCAAGAGGGTCCTGGCACCATGGACAATGACAAGCCTCTTCAGCCTGAGACAGAAGGTGAAAGGGCATCCCATCTCTCACCACTCAGGCCCGTCCCTGCTGCCTCAGTACAACACCTAGTGATCACAGGACCCTGAAGCCCACTTCTTTCCTCACCTGGGACCCTCTAGAAGTAGGATGA... |
Task1_train_43280 | A change on Chromosome 14 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | ACTTGGGGAATGTCGCTTTCAGCTTTCCAGGCTCTGCATGGATGAGAAGCCTGCTGTGAAGAAACAGCAGTGGGTGCCGAGGGCTCACCCATGGCATCTGCCATAGCGCTCAGCAGCAGTGTGCTGCTTCAGAGCACGAGGTGCACTTTGGATGTGTTGATTGAAGTGCCGGTGGGGTGTCCAGCAGCTGTGGAGGATGGAGAACTGGAAATGTAGCTTTGGGAGGCACTCCGGAAGGGTGGGAGGCCGTGCACTCCAGAAAGGGAAGTGTGGGGAACAAAGAGCAAGGGCCCCAGGGCTGAACCCTGAGGAAATGCTTC... | ACTTGGGGAATGTCGCTTTCAGCTTTCCAGGCTCTGCATGGATGAGAAGCCTGCTGTGAAGAAACAGCAGTGGGTGCCGAGGGCTCACCCATGGCATCTGCCATAGCGCTCAGCAGCAGTGTGCTGCTTCAGAGCACGAGGTGCACTTTGGATGTGTTGATTGAAGTGCCGGTGGGGTGTCCAGCAGCTGTGGAGGATGGAGAACTGGAAATGTAGCTTTGGGAGGCACTCCGGAAGGGTGGGAGGCCGTGCACTCCAGAAAGGGAAGTGTGGGGAACAAAGAGCAAGGGCCCCAGGGCTGAACCCTGAGGAAATGCTTC... |
Task1_train_43281 | A genetic alteration is present on Chromosome 14. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TCCAGGTAGGGCTGGGGCAGCATGTCGGCGCCGGGCACGCCCTCCTTGAAGAAGCGCACGGCTTCGGGGAGCAGGTCTCCAAGCAGGCGCCAGTCCCCGGAGCCGTGCTTCTTTTCGTACTCCAGGTACTTGAAACCCGAGGATAGGCCCCGGCCGAAGTCCTTCATGCAGTCCTGATACATCTGCTTGGCCACACCAGATGCACTGGAGTACACGTTGCCCGAGCCCGTGGGGTACTCAATGAACAGCTTCAATTCGTAGTCCATGCCGGGCTTGGAGACGGCGTCGAAGGCGAAAACGCGGCCCAGCAGCGAGTGGTC... | TCCAGGTAGGGCTGGGGCAGCATGTCGGCGCCGGGCACGCCCTCCTTGAAGAAGCGCACGGCTTCGGGGAGCAGGTCTCCAAGCAGGCGCCAGTCCCCGGAGCCGTGCTTCTTTTCGTACTCCAGGTACTTGAAACCCGAGGATAGGCCCCGGCCGAAGTCCTTCATGCAGTCCTGATACATCTGCTTGGCCACACCAGATGCACTGGAGTACACGTTGCCCGAGCCCGTGGGGTACTCAATGAACAGCTTCAATTCGTAGTCCATGCCGGGCTTGGAGACGGCGTCGAAGGCGAAAACGCGGCCCAGCAGCGAGTGGTC... |
Task1_train_43282 | This variant is located on Chromosome 14. Evaluate its biological effect and specify any disease association. | Benign | GCCCAGGGCGTGGGGAGGGGGTGGGGGGAGTACCGCAGCGCTGGCCGGGCCGTTAAGCAGCGTCTGCGGTAGCAGGTTGGGGGGCACGGTGAGCTGGGGGCCTCCGCCACCCCCCGGGTTGGGCAGCCCCGTAACCAGCCCACCGTGCGTTCCACGCCGAGACGCCACCGACGCCGCCGCTGAAGAAGAATTGGGGCTCTGACGGTTCAGCTCTGGGGGTCCCTCCTCTGGTGTTGGTTTGGGGAAGCCGTTTGGGCCCCCCAGGCCGTTGGGCAGTCGCGCGGTGTGGCTGCTGCTTCCCAGGCTCACCGGCGGTGGCG... | GCCCAGGGCGTGGGGAGGGGGTGGGGGGAGTACCGCAGCGCTGGCCGGGCCGTTAAGCAGCGTCTGCGGTAGCAGGTTGGGGGGCACGGTGAGCTGGGGGCCTCCGCCACCCCCCGGGTTGGGCAGCCCCGTAACCAGCCCACCGTGCGTTCCACGCCGAGACGCCACCGACGCCGCCGCTGAAGAAGAATTGGGGCTCTGACGGTTCAGCTCTGGGGGTCCCTCCTCTGGTGTTGGTTTGGGGAAGCCGTTTGGGCCCCCCAGGCCGTTGGGCAGTCGCGCGGTGTGGCTGCTGCTTCCCAGGCTCACCGGCGGTGGCG... |
Task1_train_43283 | Here’s a variant located on Chromosome 14. What is the predicted biological effect — harmless or disease-causing? | Benign | TTCTAGGGGTCTTGTCATGGGCTATTTGGCCAGGGGTGTTTGTCAACATGTGAATGTAACCCTCTTAGGCAGGCATGTGCTCACAGGCCACAGGCCCAGCACCAAGGCCAGGGACTGGGGAAGCGGGGAGCCTTCCAAACAACTCTCCCTTTCAGCCACTCAGCCACACACTTCCCATTCCCACCCTTCCCACCCCACCCGTCGAGAGCTCTTCCGGCAGGGGGCCACAGTGACTAAAGAGGGGTGCCCTGTCCCCCATTGCCCCCCGGTTCCCCCCTCCCTCACCCGGAGAGCTGTTCTGACAGGGGGCCATGGTGACT... | TTCTAGGGGTCTTGTCATGGGCTATTTGGCCAGGGGTGTTTGTCAACATGTGAATGTAACCCTCTTAGGCAGGCATGTGCTCACAGGCCACAGGCCCAGCACCAAGGCCAGGGACTGGGGAAGCGGGGAGCCTTCCAAACAACTCTCCCTTTCAGCCACTCAGCCACACACTTCCCATTCCCACCCTTCCCACCCCACCCGTCGAGAGCTCTTCCGGCAGGGGGCCACAGTGACTAAAGAGGGGTGCCCTGTCCCCCATTGCCCCCCGGTTCCCCCCTCCCTCACCCGGAGAGCTGTTCTGACAGGGGGCCATGGTGACT... |
Task1_train_43284 | Here is a mutation located on Chromosome 14. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GCTGGAGCCCACCCAGCATGGGTTAACACGCGCCTTCATCCTCTCTCTCCTCAGCCCATCCTCTATTCCTATTTCCGAAGCTCCTGCTCATGGAGAGTTCGAATTGGTAAGAGATGTGCCTCCTCCAGGATGAGTGCTGGAGTGGGGTGGACTGGGGCGGATAAGCCCGGGTGCAAAGCTGGCCTGGGATGGAAGGGTTGCTCTGTCAGAGAGGACCTCACCCCCAGCAACCAGCATCCCCCGGCTCCTAGAACCCCCATCCCTGCATGGCATCTCCACCCCGGAAACACAGGGTGAGGGTGGGAGGAAGGGGGTTGTTT... | GCTGGAGCCCACCCAGCATGGGTTAACACGCGCCTTCATCCTCTCTCTCCTCAGCCCATCCTCTATTCCTATTTCCGAAGCTCCTGCTCATGGAGAGTTCGAATTGGTAAGAGATGTGCCTCCTCCAGGATGAGTGCTGGAGTGGGGTGGACTGGGGCGGATAAGCCCGGGTGCAAAGCTGGCCTGGGATGGAAGGGTTGCTCTGTCAGAGAGGACCTCACCCCCAGCAACCAGCATCCCCCGGCTCCTAGAACCCCCATCCCTGCATGGCATCTCCACCCCGGAAACACAGGGTGAGGGTGGGAGGAAGGGGGTTGTTT... |
Task1_train_43285 | A variant has been detected on Chromosome 14. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CGCCTTCATCCTCTCTCTCCTCAGCCCATCCTCTATTCCTATTTCCGAAGCTCCTGCTCATGGAGAGTTCGAATTGGTAAGAGATGTGCCTCCTCCAGGATGAGTGCTGGAGTGGGGTGGACTGGGGCGGATAAGCCCGGGTGCAAAGCTGGCCTGGGATGGAAGGGTTGCTCTGTCAGAGAGGACCTCACCCCCAGCAACCAGCATCCCCCGGCTCCTAGAACCCCCATCCCTGCATGGCATCTCCACCCCGGAAACACAGGGTGAGGGTGGGAGGAAGGGGGTTGTTTTTTCCCTTGGGACTGACACTTCTCCCAACA... | CGCCTTCATCCTCTCTCTCCTCAGCCCATCCTCTATTCCTATTTCCGAAGCTCCTGCTCATGGAGAGTTCGAATTGGTAAGAGATGTGCCTCCTCCAGGATGAGTGCTGGAGTGGGGTGGACTGGGGCGGATAAGCCCGGGTGCAAAGCTGGCCTGGGATGGAAGGGTTGCTCTGTCAGAGAGGACCTCACCCCCAGCAACCAGCATCCCCCGGCTCCTAGAACCCCCATCCCTGCATGGCATCTCCACCCCGGAAACACAGGGTGAGGGTGGGAGGAAGGGGGTTGTTTTTTCCCTTGGGACTGACACTTCTCCCAACA... |
Task1_train_43286 | Mutation context: Chromosome 14. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TGGGTGCCAGGAGAAACTTTCCTCCAAGAAGATGAACCCATCCCTGGGCGCCAGTACCTCTGCCCTGGCTGAGCCAGAAGCCGGAGCAATATAGGTGCTGTCTGTACGGCCTGTGTGCTTTGGCCTTCCCTCCTCCAGGTGTCTCCTCCAGCCCCAAACACTGTCACTCCCCAGACTGGAGCTGACCAACACTAGGAGGAGCCTGGTATTGCCCAGGCTCTCCACACCATGACATGTCTGGTCCTCCTCCCCTCATTCCTTTGCCCTTCCCTGAGATTGGCCATCACCATACTTGAATGCCCAAGTGTGTGTAATACACA... | TGGGTGCCAGGAGAAACTTTCCTCCAAGAAGATGAACCCATCCCTGGGCGCCAGTACCTCTGCCCTGGCTGAGCCAGAAGCCGGAGCAATATAGGTGCTGTCTGTACGGCCTGTGTGCTTTGGCCTTCCCTCCTCCAGGTGTCTCCTCCAGCCCCAAACACTGTCACTCCCCAGACTGGAGCTGACCAACACTAGGAGGAGCCTGGTATTGCCCAGGCTCTCCACACCATGACATGTCTGGTCCTCCTCCCCTCATTCCTTTGCCCTTCCCTGAGATTGGCCATCACCATACTTGAATGCCCAAGTGTGTGTAATACACA... |
Task1_train_43287 | Given this context: Chromosome 14 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TAGGTGCTGTCTGTACGGCCTGTGTGCTTTGGCCTTCCCTCCTCCAGGTGTCTCCTCCAGCCCCAAACACTGTCACTCCCCAGACTGGAGCTGACCAACACTAGGAGGAGCCTGGTATTGCCCAGGCTCTCCACACCATGACATGTCTGGTCCTCCTCCCCTCATTCCTTTGCCCTTCCCTGAGATTGGCCATCACCATACTTGAATGCCCAAGTGTGTGTAATACACACATGCATGCACACGCACGCAGTCTTCTCCACTAGTGTTGACCCACCCAAGTTTTTTTTACCCTCAGCTTGCCAGGGGAAATTATCAAAAGG... | TAGGTGCTGTCTGTACGGCCTGTGTGCTTTGGCCTTCCCTCCTCCAGGTGTCTCCTCCAGCCCCAAACACTGTCACTCCCCAGACTGGAGCTGACCAACACTAGGAGGAGCCTGGTATTGCCCAGGCTCTCCACACCATGACATGTCTGGTCCTCCTCCCCTCATTCCTTTGCCCTTCCCTGAGATTGGCCATCACCATACTTGAATGCCCAAGTGTGTGTAATACACACATGCATGCACACGCACGCAGTCTTCTCCACTAGTGTTGACCCACCCAAGTTTTTTTTACCCTCAGCTTGCCAGGGGAAATTATCAAAAGG... |
Task1_train_43288 | This is a variant located on Chromosome 14. Is this mutation a likely cause of disease or not? | Benign | GACAATTTCATCCAGACAGTAAAAACTTGCGCTAACTTGAACAGGTAAGTTAACCTTTCTCAGCTGTAGTTTGTTCCTCTGTAAAATGGGAAGAAAATGATTGTTGACATGACTAAATCAGAAAATATAAATTTTTTTCCACCTCTGGCACAGAATAAGCATTCAATATCTGTAGGTTATCATTACTATTATTTTATTAGCAACAAATCCTACCTCAAGAGGAAGAGCTTGCTCTGGGCTACTATAATAAACCCCTACATGACATTAAAAAAAAAAATTATCACCCTGCATTCTGAGGGTAAGAGGAAGGAAAGTAAGCA... | GACAATTTCATCCAGACAGTAAAAACTTGCGCTAACTTGAACAGGTAAGTTAACCTTTCTCAGCTGTAGTTTGTTCCTCTGTAAAATGGGAAGAAAATGATTGTTGACATGACTAAATCAGAAAATATAAATTTTTTTCCACCTCTGGCACAGAATAAGCATTCAATATCTGTAGGTTATCATTACTATTATTTTATTAGCAACAAATCCTACCTCAAGAGGAAGAGCTTGCTCTGGGCTACTATAATAAACCCCTACATGACATTAAAAAAAAAAATTATCACCCTGCATTCTGAGGGTAAGAGGAAGGAAAGTAAGCA... |
Task1_train_43289 | Given this variant on Chromosome 14, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TCCAGACAGTAAAAACTTGCGCTAACTTGAACAGGTAAGTTAACCTTTCTCAGCTGTAGTTTGTTCCTCTGTAAAATGGGAAGAAAATGATTGTTGACATGACTAAATCAGAAAATATAAATTTTTTTCCACCTCTGGCACAGAATAAGCATTCAATATCTGTAGGTTATCATTACTATTATTTTATTAGCAACAAATCCTACCTCAAGAGGAAGAGCTTGCTCTGGGCTACTATAATAAACCCCTACATGACATTAAAAAAAAAAATTATCACCCTGCATTCTGAGGGTAAGAGGAAGGAAAGTAAGCATCTCTACCAA... | TCCAGACAGTAAAAACTTGCGCTAACTTGAACAGGTAAGTTAACCTTTCTCAGCTGTAGTTTGTTCCTCTGTAAAATGGGAAGAAAATGATTGTTGACATGACTAAATCAGAAAATATAAATTTTTTTCCACCTCTGGCACAGAATAAGCATTCAATATCTGTAGGTTATCATTACTATTATTTTATTAGCAACAAATCCTACCTCAAGAGGAAGAGCTTGCTCTGGGCTACTATAATAAACCCCTACATGACATTAAAAAAAAAAATTATCACCCTGCATTCTGAGGGTAAGAGGAAGGAAAGTAAGCATCTCTACCAA... |
Task1_train_43290 | This variant lies on Chromosome 14. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TTAATTTGTAAATACTGGCGCATGCAAGGGACAAGTGTTATAAGACTTACCTTTCTGTGTTTACTTGCTTAGTCTTTTAGACATTATGCTTAGAATTTCTACTGCTATGTTAAATATATGCCAACGATTTTTAATTTAATACAAAGCAGAGTTCGTAAGAAAAAAAGGCAAAATTTGTCAGGTGTTTTAAAGTAAAAGAATATAAAATCATGGGAAAGAGCTGGGTGAGTTGTGTGTGTGTTTGAATAAGGCAGCATTATGAGAGGGAAGATACTTGGGATCAGAGTAGAAGACAGAAAAAGGCACCATGTTGGAAGCCA... | TTAATTTGTAAATACTGGCGCATGCAAGGGACAAGTGTTATAAGACTTACCTTTCTGTGTTTACTTGCTTAGTCTTTTAGACATTATGCTTAGAATTTCTACTGCTATGTTAAATATATGCCAACGATTTTTAATTTAATACAAAGCAGAGTTCGTAAGAAAAAAAGGCAAAATTTGTCAGGTGTTTTAAAGTAAAAGAATATAAAATCATGGGAAAGAGCTGGGTGAGTTGTGTGTGTGTTTGAATAAGGCAGCATTATGAGAGGGAAGATACTTGGGATCAGAGTAGAAGACAGAAAAAGGCACCATGTTGGAAGCCA... |
Task1_train_43291 | This sequence change occurs on Chromosome 14. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | AGTAATCCTCACAATAATCCTATGAGGCAGATATTTTTAGTAATCACATTTTACAGATGAGGAAACTGACGTTTCAGACTCCAATCCAGGCACCCTGGCTCCACAGTAGTGCCTCAACCATTATACTTTATGGTGTCTATTTTAATTTCAGACCTAGAAAATTAATTTATATTTGCTACTTAAATAAGACAAGTTCTCTCCCCTCTACCCTTTCGTATTTCAAAAGAGCATCCTTTCAGTTGCATCGTGTGTGGTGTTCAGGAGGCTGAAAGAAGAAAGTGTGATGGATGGACTCTTTTGTCTTTGGACACTGAAATAAT... | AGTAATCCTCACAATAATCCTATGAGGCAGATATTTTTAGTAATCACATTTTACAGATGAGGAAACTGACGTTTCAGACTCCAATCCAGGCACCCTGGCTCCACAGTAGTGCCTCAACCATTATACTTTATGGTGTCTATTTTAATTTCAGACCTAGAAAATTAATTTATATTTGCTACTTAAATAAGACAAGTTCTCTCCCCTCTACCCTTTCGTATTTCAAAAGAGCATCCTTTCAGTTGCATCGTGTGTGGTGTTCAGGAGGCTGAAAGAAGAAAGTGTGATGGATGGACTCTTTTGTCTTTGGACACTGAAATAAT... |
Task1_train_43292 | A variant has been detected on Chromosome 14. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TGGGGGCCGAGAGGCGCGTGGTAAGGCTGGGGCAGGGGACTGAGATGGGGATAGGGTGGGGAGCCAGAAGCAGGGGGCGGCGAGGCCAGTAGGGTTCGGGTCGGCAGTCTAGATGTGATTAGCAGACGGAGGTGGGACCCGAACCCCGGCTGAAGCTGAAACTGAAGCTGAAGAGGCGCCAGGGGCAGAGCCACCCTGTCACTACCATTTGGGCAGATCTCAGAAAGGAAGCGGGGCAGGAATCAAGGCATTTCGAAACAGGAGTGAGTAGAAAATAACCTCGAGCCCAGGGCCCGGGTGGTGGCAGCGGCGGGGAAGGG... | TGGGGGCCGAGAGGCGCGTGGTAAGGCTGGGGCAGGGGACTGAGATGGGGATAGGGTGGGGAGCCAGAAGCAGGGGGCGGCGAGGCCAGTAGGGTTCGGGTCGGCAGTCTAGATGTGATTAGCAGACGGAGGTGGGACCCGAACCCCGGCTGAAGCTGAAACTGAAGCTGAAGAGGCGCCAGGGGCAGAGCCACCCTGTCACTACCATTTGGGCAGATCTCAGAAAGGAAGCGGGGCAGGAATCAAGGCATTTCGAAACAGGAGTGAGTAGAAAATAACCTCGAGCCCAGGGCCCGGGTGGTGGCAGCGGCGGGGAAGGG... |
Task1_train_43293 | Given a variant located on Chromosome 14, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TCGAAACAGGAGTGAGTAGAAAATAACCTCGAGCCCAGGGCCCGGGTGGTGGCAGCGGCGGGGAAGGGGCCCCGCGCGCGAAGGGGCTGCCGAGGTGGGTCCGCTCCGCGGGGAAGCCCAGGACAGAGCGCGGCGGAGGCTCGCGCCGTGGTGCGGGGCCCTGAGGCCGGGCGGCACCCACCCGCCAGCGCCCCGGCCTTGCGTACCTGAGGCGGCCGCCTGGCTCCCCTCCACTCCCTGGCAGTCCCCGACGCCGCCAGCCGACCCTGGGCGGGCTGTGGGGCTCCAGGAGCCCGGCCCCTCAGCCGCCTGCAGGTCAG... | TCGAAACAGGAGTGAGTAGAAAATAACCTCGAGCCCAGGGCCCGGGTGGTGGCAGCGGCGGGGAAGGGGCCCCGCGCGCGAAGGGGCTGCCGAGGTGGGTCCGCTCCGCGGGGAAGCCCAGGACAGAGCGCGGCGGAGGCTCGCGCCGTGGTGCGGGGCCCTGAGGCCGGGCGGCACCCACCCGCCAGCGCCCCGGCCTTGCGTACCTGAGGCGGCCGCCTGGCTCCCCTCCACTCCCTGGCAGTCCCCGACGCCGCCAGCCGACCCTGGGCGGGCTGTGGGGCTCCAGGAGCCCGGCCCCTCAGCCGCCTGCAGGTCAG... |
Task1_train_43294 | A mutation has occurred on Chromosome 14. What is the medical relevance of this mutation? | Benign | GCAAGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCCAGGGGGTGGAGCCTGCAGTGAGCCGAGATTGCGCCACTGCACTCCAGCCTGGGCGATAGCGAGACTCCATCTCAAACAAACAAACAAACAAAACAACAACAAAAAAAGAATGGTGCGGTGGTAGGCCAGGCGCAGTGGTTCATGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCGGGGGGGATCACCAGAGGTCAGGAGTTTGAGACCAGCCTGACCAACATGGAGAAACCCCATCTCTACTAAAAATACA... | GCAAGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCCAGGGGGTGGAGCCTGCAGTGAGCCGAGATTGCGCCACTGCACTCCAGCCTGGGCGATAGCGAGACTCCATCTCAAACAAACAAACAAACAAAACAACAACAAAAAAAGAATGGTGCGGTGGTAGGCCAGGCGCAGTGGTTCATGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCGGGGGGGATCACCAGAGGTCAGGAGTTTGAGACCAGCCTGACCAACATGGAGAAACCCCATCTCTACTAAAAATACA... |
Task1_train_43295 | Given this variant on Chromosome 14, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GTGGGAACTGAACAATGAGAACACATGGACACAGGGAGGGGAACAACACACCTGGGGCCTGTTGGGCGACGGTTGGGGGGTGGGGGAGAGCATTAGGAAAAAGAGCTAATGCATGCCAGGCTTAATACCTAGGTGATGGGTTGATAGGTGCAGTAAACCACCATGACACACGTTTACCTATGAAACAAGCCTGCACATCCTACACACATATCCCAGAACTTAAAAAATAAAATAAAATAAAAAATAAGTGCTTAGTTAGTGCTGGGCACGAGGGGAACCCTCAGCAAGTGGTAGTCATGGTTACCGATGCTGGCTGTTGG... | GTGGGAACTGAACAATGAGAACACATGGACACAGGGAGGGGAACAACACACCTGGGGCCTGTTGGGCGACGGTTGGGGGGTGGGGGAGAGCATTAGGAAAAAGAGCTAATGCATGCCAGGCTTAATACCTAGGTGATGGGTTGATAGGTGCAGTAAACCACCATGACACACGTTTACCTATGAAACAAGCCTGCACATCCTACACACATATCCCAGAACTTAAAAAATAAAATAAAATAAAAAATAAGTGCTTAGTTAGTGCTGGGCACGAGGGGAACCCTCAGCAAGTGGTAGTCATGGTTACCGATGCTGGCTGTTGG... |
Task1_train_43296 | Given a variant located on Chromosome 14, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TTGGCCCAGATTTTCAAATGGCAGAAACCGCAGTCAAGCAGCAAACCAAAATAACACCTTGCTTTCTGGTGGAAACTTTGTTCCAACTAGAGCATTTCACTTGTATGTACAGCCCCCATTTATCCTCAGAGGTCCTTACTGAGATAGGGCAGAAACAATTCTGCTTTCCAGTGAGGAAGACTGGGATGTAAAGAAGTTAAGTGGCTAGTCTAAGACACAACAGTATTAGCAGAATTAGGAACAGGAAATAGGTCTGTTGACTTGAGGGCCACTATGTTATTGCTAGATGAATTTGGGTGGTCAGGGTAAAGGAAAATCTT... | TTGGCCCAGATTTTCAAATGGCAGAAACCGCAGTCAAGCAGCAAACCAAAATAACACCTTGCTTTCTGGTGGAAACTTTGTTCCAACTAGAGCATTTCACTTGTATGTACAGCCCCCATTTATCCTCAGAGGTCCTTACTGAGATAGGGCAGAAACAATTCTGCTTTCCAGTGAGGAAGACTGGGATGTAAAGAAGTTAAGTGGCTAGTCTAAGACACAACAGTATTAGCAGAATTAGGAACAGGAAATAGGTCTGTTGACTTGAGGGCCACTATGTTATTGCTAGATGAATTTGGGTGGTCAGGGTAAAGGAAAATCTT... |
Task1_train_43297 | This mutation is located on Chromosome 14. Is it associated with a disease or is it a benign polymorphism? | Benign | TATACTATAGGGACTTTAGATTACTAAACCTCAGCTAATGGGACCAAGGGAAGATCCAAGTCCAAATTCAAATGTCAATGGAAATTCCATGATATACCGGGGGTTGCCTTATAACAAAGCCTCCAAAATGATTGATCAGAATTATCTCTAACTTCCTCTTCTTCTATTTTGCAATGGAAGTAAGCTTGTTTGTTTGCACCTATTCTTCACTATAGCTCACCTACTTTGGGAGGAAATCAAGGCTGTGCTGAATGGCCATGGTACCTACCTCCCGCAGCAGCTGAGAATATATATACATATATTTGTATGTATGTATGTAT... | TATACTATAGGGACTTTAGATTACTAAACCTCAGCTAATGGGACCAAGGGAAGATCCAAGTCCAAATTCAAATGTCAATGGAAATTCCATGATATACCGGGGGTTGCCTTATAACAAAGCCTCCAAAATGATTGATCAGAATTATCTCTAACTTCCTCTTCTTCTATTTTGCAATGGAAGTAAGCTTGTTTGTTTGCACCTATTCTTCACTATAGCTCACCTACTTTGGGAGGAAATCAAGGCTGTGCTGAATGGCCATGGTACCTACCTCCCGCAGCAGCTGAGAATATATATACATATATTTGTATGTATGTATGTAT... |
Task1_train_43298 | A mutation found on Chromosome 14 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AAAATGAAGTATTCAGGGTAATCCTAATGTTTCTCACTGCTAATGTGCCCCATTATTAAAAACAGAAAACTTAAGGCTTATCAGAAAAGCAAATAAGAATGTTTTCTAGAAATAATTATAATTCAATTACTTGAAAGTAATTAATGATAAGGTAGCTAGGATTAAATTTTTTAAAGTATTTTTGAAAATATGGGGATAGGTCTGGGAAGAAAATCATAAAACAAACTTGTACACAAGAAAAATAGTAAAACAAGACTATGGATTAATCAGTTAATTAATTTACTAATTAATTAAACTAATGAAGAGTTTTACTTTTTAGG... | AAAATGAAGTATTCAGGGTAATCCTAATGTTTCTCACTGCTAATGTGCCCCATTATTAAAAACAGAAAACTTAAGGCTTATCAGAAAAGCAAATAAGAATGTTTTCTAGAAATAATTATAATTCAATTACTTGAAAGTAATTAATGATAAGGTAGCTAGGATTAAATTTTTTAAAGTATTTTTGAAAATATGGGGATAGGTCTGGGAAGAAAATCATAAAACAAACTTGTACACAAGAAAAATAGTAAAACAAGACTATGGATTAATCAGTTAATTAATTTACTAATTAATTAAACTAATGAAGAGTTTTACTTTTTAGG... |
Task1_train_43299 | This variant lies on Chromosome 14. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TTATGCTTTTCTTTCTGCTTGAAATTCCCATCTGTTCCCTGCCTATCAAAATCCTACAAATCCTTCAAGTCTCAGATCAAATGCCTTATTCTTCCCAAAGCCTTCCCAAATCCTTAAGTCCTGGGTTCCCACAGCGTGTGGATTGCATTTTAGTCTCACTTCTATTCGACTAAATTTATAAAATCATCGGATTTTAGTTGTGGAAGACACTTTAGAGGTTTGGATTTTAGTTGTGGAAGACACTTTAGAGGTTACCTAAGACAACCCTGTATTTTACAGCTAAGGGAACTGAGACCCAGAAAGAGTAAATGTCTTGCTCA... | TTATGCTTTTCTTTCTGCTTGAAATTCCCATCTGTTCCCTGCCTATCAAAATCCTACAAATCCTTCAAGTCTCAGATCAAATGCCTTATTCTTCCCAAAGCCTTCCCAAATCCTTAAGTCCTGGGTTCCCACAGCGTGTGGATTGCATTTTAGTCTCACTTCTATTCGACTAAATTTATAAAATCATCGGATTTTAGTTGTGGAAGACACTTTAGAGGTTTGGATTTTAGTTGTGGAAGACACTTTAGAGGTTACCTAAGACAACCCTGTATTTTACAGCTAAGGGAACTGAGACCCAGAAAGAGTAAATGTCTTGCTCA... |
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