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_34500 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | AAGCAGGCACACATCATTTATTGCATGCACATCTGTGAAAAAGCTGACATATTTGATTAGATTGTTCTTCCTAACCAGCTCCAAAAATACTTTTTTTGTTTATTTCCCATAGACAGGGACAGCATAGCCTTCCCAAATGCTCATCACAGGGAAATGCAACCACAAACATGACTTTTCTCTTTAAAACAGGGCACAGTGGGATTTGAAAACCAGATCAACAAATGCCTGGAACTGGCTGAATACCTCTATGCCAAGATTAAAAACAGAGAAGAATTTGAGATGGTTTTCAATGGCGAGGTAGGTAATCATCATGGACCAGG... | AAGCAGGCACACATCATTTATTGCATGCACATCTGTGAAAAAGCTGACATATTTGATTAGATTGTTCTTCCTAACCAGCTCCAAAAATACTTTTTTTGTTTATTTCCCATAGACAGGGACAGCATAGCCTTCCCAAATGCTCATCACAGGGAAATGCAACCACAAACATGACTTTTCTCTTTAAAACAGGGCACAGTGGGATTTGAAAACCAGATCAACAAATGCCTGGAACTGGCTGAATACCTCTATGCCAAGATTAAAAACAGAGAAGAATTTGAGATGGTTTTCAATGGCGAGGTAGGTAATCATCATGGACCAGG... |
Task1_train_34501 | A sequence alteration has been identified on Chromosome 2. Is it disease-inducing or harmless? | Benign | AAGGATGGTATAAGGGATGATGTGCATAGATGCATAGATTATATGCAAATACTGCACCATTTTATATAAGGTACTTGAGCATCCATGGGTTTTGGTATTTGTGAGGGGTCCTGGAAGCAATCCCCTGTGGTTTCCAAGGAATTACTTTAAATCTAAATAATGGCCTTCAACATGTATATCAAGCATGCTTGTCACATACTCTCCTTCTATAATAACTGATTATAACATTTATTCCAATCTATATTTCAGCATACTCTTAAAGAGCTGCCAAATTCAGGGGAAGTTTTTAGTCCTTTTATCACAATTTTATCACTGTGACA... | AAGGATGGTATAAGGGATGATGTGCATAGATGCATAGATTATATGCAAATACTGCACCATTTTATATAAGGTACTTGAGCATCCATGGGTTTTGGTATTTGTGAGGGGTCCTGGAAGCAATCCCCTGTGGTTTCCAAGGAATTACTTTAAATCTAAATAATGGCCTTCAACATGTATATCAAGCATGCTTGTCACATACTCTCCTTCTATAATAACTGATTATAACATTTATTCCAATCTATATTTCAGCATACTCTTAAAGAGCTGCCAAATTCAGGGGAAGTTTTTAGTCCTTTTATCACAATTTTATCACTGTGACA... |
Task1_train_34502 | This variant lies on Chromosome 2. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ACAGGCACTTGGAAGGCAGAGGGGTTGGGGTAGGAGCTTTATGCTGAACAGTTTGGCCAAACATACATACGTAACAGGTTACAGGAGGAGCTATGAATATTAATGGAGGTGGTCCTTACACATGCATATTGAACAAACATGCATGTAACATGTTCTCTTTGGGGTGGAGACTTAACATTTAATTGTATTACTTCAAATACATTTAAATGTATTACTTCAAACCTACACTTCAAAAGGTCTTTTCAGGACGTGAATGCATACAAGTGCACAATCCCTGTACACTGGCCAGAACCGGTCCATGGTCGGTCTTCTTATCATGA... | ACAGGCACTTGGAAGGCAGAGGGGTTGGGGTAGGAGCTTTATGCTGAACAGTTTGGCCAAACATACATACGTAACAGGTTACAGGAGGAGCTATGAATATTAATGGAGGTGGTCCTTACACATGCATATTGAACAAACATGCATGTAACATGTTCTCTTTGGGGTGGAGACTTAACATTTAATTGTATTACTTCAAATACATTTAAATGTATTACTTCAAACCTACACTTCAAAAGGTCTTTTCAGGACGTGAATGCATACAAGTGCACAATCCCTGTACACTGGCCAGAACCGGTCCATGGTCGGTCTTCTTATCATGA... |
Task1_train_34503 | Here is a mutation located on Chromosome 2. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AGAGGTATCCCACTAGCGATTTCATTATCAAGGAAATGAAGACACCTTTTCTGCAGAATTCATTTCTTTCTCATAAAACAAAAATCAACTTCATTCCACATAGCTTTTTAGGTTGAACTGACTAAATTCTGTGTCCTAATGTACTCGGTTTTAGTGATTTAAAAAATCTTTTCCTTCCCTTCCTACTTAGCAACCTTAGGAGATTGGTAAAAACAAACAAGTAAGTACCAGAATGTTCACTATAGTCGGATTAAGGATAGCAAAAACCAAACAGAAACATCCATAGAGAACTGTATAAATAAATTGTTATAGCCTTAGGA... | AGAGGTATCCCACTAGCGATTTCATTATCAAGGAAATGAAGACACCTTTTCTGCAGAATTCATTTCTTTCTCATAAAACAAAAATCAACTTCATTCCACATAGCTTTTTAGGTTGAACTGACTAAATTCTGTGTCCTAATGTACTCGGTTTTAGTGATTTAAAAAATCTTTTCCTTCCCTTCCTACTTAGCAACCTTAGGAGATTGGTAAAAACAAACAAGTAAGTACCAGAATGTTCACTATAGTCGGATTAAGGATAGCAAAAACCAAACAGAAACATCCATAGAGAACTGTATAAATAAATTGTTATAGCCTTAGGA... |
Task1_train_34504 | A variant was discovered on Chromosome 2. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TAAGCCCTCATATCTTCTGTTATTGGGCATTTTAATACAAAATAACTAATATTTTAAGTAGTATATGACAGTAGTATTTATGAATAGTCTGGAGGTTTTTTTAAGAATTAAAGAAGGATTTTGTTACTATATCAGTTTTTTTTTAAAAAACTCATGATGTTTTTATATAGACTTTCTCTAAAATTCAGTTCCATGTGTGATTCCTATGAAATTGCTCTTTCTGGTTCTGATTTGTGTGCTTTAATATAAAATCATTCTATTTTCCTCTTCTTTAACCAAAGTGTGTGAGGTAACAGGAATGTTTCTTTTGAGAGACTTTG... | TAAGCCCTCATATCTTCTGTTATTGGGCATTTTAATACAAAATAACTAATATTTTAAGTAGTATATGACAGTAGTATTTATGAATAGTCTGGAGGTTTTTTTAAGAATTAAAGAAGGATTTTGTTACTATATCAGTTTTTTTTTAAAAAACTCATGATGTTTTTATATAGACTTTCTCTAAAATTCAGTTCCATGTGTGATTCCTATGAAATTGCTCTTTCTGGTTCTGATTTGTGTGCTTTAATATAAAATCATTCTATTTTCCTCTTCTTTAACCAAAGTGTGTGAGGTAACAGGAATGTTTCTTTTGAGAGACTTTG... |
Task1_train_34505 | A variant on Chromosome 2 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GCTCTGTGGCCAGATGGTTGTAAGAGCTGGACTCCATATTGCCCTCTAATCTGGTGGCTCATGTTTTTCAATTCACTTCACAATTTGAGAACTGCAACGGTAGTGGTGAAGCTTTTCATAAGTAAAACCCAATAAAGGGGGTGAGCTTATATTATTCTGCATCTGCCTCACCTTTCTATAGAAACATTTACTTAATTTGAATGGTTTTGATATGGGCACTTCTATTTGCTTTTCACCAGATCTGTTATTTGTAATCTGACATCCTACCTGATGCTTTATAATGGGTGTGTCCTAATGTTTTCTGCCCTCTGAACAAGTAT... | GCTCTGTGGCCAGATGGTTGTAAGAGCTGGACTCCATATTGCCCTCTAATCTGGTGGCTCATGTTTTTCAATTCACTTCACAATTTGAGAACTGCAACGGTAGTGGTGAAGCTTTTCATAAGTAAAACCCAATAAAGGGGGTGAGCTTATATTATTCTGCATCTGCCTCACCTTTCTATAGAAACATTTACTTAATTTGAATGGTTTTGATATGGGCACTTCTATTTGCTTTTCACCAGATCTGTTATTTGTAATCTGACATCCTACCTGATGCTTTATAATGGGTGTGTCCTAATGTTTTCTGCCCTCTGAACAAGTAT... |
Task1_train_34506 | This sequence variant lies on Chromosome 2. Is it clinically significant, and what condition might it cause if any? | Benign | GTCGATCCCTGGAGCCAGAATGCAGTCAACTCTCCCGATCACGTGGCTACATGGAGGGGGATGGAGACTGAGCAAAATCAGGGTTCTATTGGAAGGCAAAATTCCAGAGAAGTCAAGGCGAGGAAAGAAGGCATTGTGATTCTGTATGCTACTGCTCATGTGACGTATGTAAAGTAGTCAAAGTCACAGAAACAGGAAGTAGAAGACAGTTAACAAGTGGCGGTCAGGGGGCAGGGGAGAAGGGAGGGGAAATGGAGAAAGAGGAAGGTAGAGATTAGTGGGTATAGAGTTTCAGTGTTGCAAGATGAAACAGTTACAGA... | GTCGATCCCTGGAGCCAGAATGCAGTCAACTCTCCCGATCACGTGGCTACATGGAGGGGGATGGAGACTGAGCAAAATCAGGGTTCTATTGGAAGGCAAAATTCCAGAGAAGTCAAGGCGAGGAAAGAAGGCATTGTGATTCTGTATGCTACTGCTCATGTGACGTATGTAAAGTAGTCAAAGTCACAGAAACAGGAAGTAGAAGACAGTTAACAAGTGGCGGTCAGGGGGCAGGGGAGAAGGGAGGGGAAATGGAGAAAGAGGAAGGTAGAGATTAGTGGGTATAGAGTTTCAGTGTTGCAAGATGAAACAGTTACAGA... |
Task1_train_34507 | Consider a variant on Chromosome 2. Determine its clinical classification and disease relevance. | Benign | TCCACATACTTAAGTTAGAAAGTTTTAAGGCTTTAAAATACATCTTTAAAATATATAGTAAAAATAAATCCTGGCAATTTGTTTACCAACTTGGATTTGCTTTGACATTATTTTTAAAATCTATATAAAAGGACCTTGGTTAGAAGTCAATCAAACATTTTTTTACAAAGGGGAGAGGAGATAAAAGAAAAGTAAATCTCACATTCACACAAGGCATTTAACATTATGTTAACTGCCTCCATGTTTCTATCCATATTAAATCAAAATACATGTAACAATAAATTACAGTAGTCACTGAAAACAGGAATCAAAGCACCACT... | TCCACATACTTAAGTTAGAAAGTTTTAAGGCTTTAAAATACATCTTTAAAATATATAGTAAAAATAAATCCTGGCAATTTGTTTACCAACTTGGATTTGCTTTGACATTATTTTTAAAATCTATATAAAAGGACCTTGGTTAGAAGTCAATCAAACATTTTTTTACAAAGGGGAGAGGAGATAAAAGAAAAGTAAATCTCACATTCACACAAGGCATTTAACATTATGTTAACTGCCTCCATGTTTCTATCCATATTAAATCAAAATACATGTAACAATAAATTACAGTAGTCACTGAAAACAGGAATCAAAGCACCACT... |
Task1_train_34508 | A mutation on Chromosome 2 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GGAGTTGGTAAAATCTCTCAAGGCTTCACCTCCTCAGTGGGCTAGGTGCAATTCTAACCAGGGGGCAAGTTTCCTTAGCTTTCCCTACGACCCCAGTTAGGCAGCTCAGGTTACTATTGCAGCTTGATGGCCCTTGGGACTCCAGGTTTTTGAGTGGACGTGGCTGCTACTGCAGCAGGTGATCCACCAACCAAGTTCTCTATCAGGGTAATGTTAAGAATAAACCTTGGCCGGGCGCGGTAGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTG... | GGAGTTGGTAAAATCTCTCAAGGCTTCACCTCCTCAGTGGGCTAGGTGCAATTCTAACCAGGGGGCAAGTTTCCTTAGCTTTCCCTACGACCCCAGTTAGGCAGCTCAGGTTACTATTGCAGCTTGATGGCCCTTGGGACTCCAGGTTTTTGAGTGGACGTGGCTGCTACTGCAGCAGGTGATCCACCAACCAAGTTCTCTATCAGGGTAATGTTAAGAATAAACCTTGGCCGGGCGCGGTAGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTG... |
Task1_train_34509 | Given this context: Chromosome 2 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TTGGAATTTTTAACGGAATCTTCCTTCTCTTCTTTTCCTGTTTAAGACAATAGTAGTTAGTTGTCCACTAATCGTTAATACACGATTTTCTAACAAAGACTTGCATATCCTTTTGGCTAAAAAGTGGCCAAATATCAGAGAGCTAGAAGTTTGGGAGACAGCCTTTAGTCTTTTCCAAAGCATGTAAGCCCTTTTGAATCATTTTGGGTAAATGGCGAAGATTAAACAGAATTCATAAAGGGTTTCTGATACATAAGTGGAATGTGCCTGTGAGGACACTACACATGACAATAATCTAAGCATGCTCTCTTTTAGTCCCA... | TTGGAATTTTTAACGGAATCTTCCTTCTCTTCTTTTCCTGTTTAAGACAATAGTAGTTAGTTGTCCACTAATCGTTAATACACGATTTTCTAACAAAGACTTGCATATCCTTTTGGCTAAAAAGTGGCCAAATATCAGAGAGCTAGAAGTTTGGGAGACAGCCTTTAGTCTTTTCCAAAGCATGTAAGCCCTTTTGAATCATTTTGGGTAAATGGCGAAGATTAAACAGAATTCATAAAGGGTTTCTGATACATAAGTGGAATGTGCCTGTGAGGACACTACACATGACAATAATCTAAGCATGCTCTCTTTTAGTCCCA... |
Task1_train_34510 | This variant is present on Chromosome 2. Is the change likely to result in a pathogenic outcome? | Benign | AGTAGTTAGTTGTCCACTAATCGTTAATACACGATTTTCTAACAAAGACTTGCATATCCTTTTGGCTAAAAAGTGGCCAAATATCAGAGAGCTAGAAGTTTGGGAGACAGCCTTTAGTCTTTTCCAAAGCATGTAAGCCCTTTTGAATCATTTTGGGTAAATGGCGAAGATTAAACAGAATTCATAAAGGGTTTCTGATACATAAGTGGAATGTGCCTGTGAGGACACTACACATGACAATAATCTAAGCATGCTCTCTTTTAGTCCCAAAACGTGTAGAGTAATGTCACATGAAATTTACAGGAGGCCATTGACTTGGA... | AGTAGTTAGTTGTCCACTAATCGTTAATACACGATTTTCTAACAAAGACTTGCATATCCTTTTGGCTAAAAAGTGGCCAAATATCAGAGAGCTAGAAGTTTGGGAGACAGCCTTTAGTCTTTTCCAAAGCATGTAAGCCCTTTTGAATCATTTTGGGTAAATGGCGAAGATTAAACAGAATTCATAAAGGGTTTCTGATACATAAGTGGAATGTGCCTGTGAGGACACTACACATGACAATAATCTAAGCATGCTCTCTTTTAGTCCCAAAACGTGTAGAGTAATGTCACATGAAATTTACAGGAGGCCATTGACTTGGA... |
Task1_train_34511 | This mutation on Chromosome 2 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GTTTTTCTTAAATTTTCACCTCACTCCAAGACACATTAAAATAATGCAATAAAATAGATCTGGATTCAAAATATGGCTCAACCACATACTAGCTATGCAATCTTGAGCAGATTACTTAAACTCTGCACGCCTCAGTTATTGCATTTGCAAAATGGTAAAAATATCTACACTTCATAGAATTGTTGTATAAATTAAATGAAATTATGTATCATTTGGCACAGTGTCCGACACATAGTAGTAACTGCTTAATTGTAGCCATTATTATTACCAGAAAACACATGTATTTATATGAAACACATTTCTAACTTCTTATAAAGAAA... | GTTTTTCTTAAATTTTCACCTCACTCCAAGACACATTAAAATAATGCAATAAAATAGATCTGGATTCAAAATATGGCTCAACCACATACTAGCTATGCAATCTTGAGCAGATTACTTAAACTCTGCACGCCTCAGTTATTGCATTTGCAAAATGGTAAAAATATCTACACTTCATAGAATTGTTGTATAAATTAAATGAAATTATGTATCATTTGGCACAGTGTCCGACACATAGTAGTAACTGCTTAATTGTAGCCATTATTATTACCAGAAAACACATGTATTTATATGAAACACATTTCTAACTTCTTATAAAGAAA... |
Task1_train_34512 | A mutation on Chromosome 2 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TCGGGTCGTGCTGGGGTGGTGGGGGTGGGAAGTGGTGCGAGACCCTGGCGGGAGTGTGGGTGAACCGAGGCACTGCTTGGGTGGAAATCCGTGGATGCCTTTATTGCTGTCGTTTGGCGCCCCCATCTGTTTTCCTCGCGGTTTCGGCTGCTGTGAGTTGGTTTTCAAGTCGGAGACGCAGTCACTGGGGACTAAGGTGAGGACTGACGACCCCTTCCTCTATCACTCAGCCCGAGGCTCTCCCACATCTTCCCTTCCTCTGGGACCCGACGCCTCTGGTCCCAAAGGCTGCGCCAAACCGGACCTCAGTCTGTCGAAAG... | TCGGGTCGTGCTGGGGTGGTGGGGGTGGGAAGTGGTGCGAGACCCTGGCGGGAGTGTGGGTGAACCGAGGCACTGCTTGGGTGGAAATCCGTGGATGCCTTTATTGCTGTCGTTTGGCGCCCCCATCTGTTTTCCTCGCGGTTTCGGCTGCTGTGAGTTGGTTTTCAAGTCGGAGACGCAGTCACTGGGGACTAAGGTGAGGACTGACGACCCCTTCCTCTATCACTCAGCCCGAGGCTCTCCCACATCTTCCCTTCCTCTGGGACCCGACGCCTCTGGTCCCAAAGGCTGCGCCAAACCGGACCTCAGTCTGTCGAAAG... |
Task1_train_34513 | A mutation found on Chromosome 2 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GAGAGGACGAGAGCGAGTGAGTCTCTATGCCTGGGCTCCTAAGGAAACTCTCTGGCAGAGCCAGAGGAGCCCCAGACATCCCCACCCCCCCGTCCTCACTCCCTCTCTCCCCCCCACCAGAGCAGGAGGAAGAGGCCGATTGCGTTCCCCAGAGCCACCCAATTGGTCGCCATAACTCACACAATAAAGTGGCAGCGCGGCGGTCAGTCTTGCCCTCCGGCGGCGCCTGTGTGGTCTCAGTGCAGGAGCCCGCGATCTAACCAATTCCAGCTTGGCTCGGAGACCGAGGGTCCTGCTGCAGGCTGAGACTGGCGCCGGTC... | GAGAGGACGAGAGCGAGTGAGTCTCTATGCCTGGGCTCCTAAGGAAACTCTCTGGCAGAGCCAGAGGAGCCCCAGACATCCCCACCCCCCCGTCCTCACTCCCTCTCTCCCCCCCACCAGAGCAGGAGGAAGAGGCCGATTGCGTTCCCCAGAGCCACCCAATTGGTCGCCATAACTCACACAATAAAGTGGCAGCGCGGCGGTCAGTCTTGCCCTCCGGCGGCGCCTGTGTGGTCTCAGTGCAGGAGCCCGCGATCTAACCAATTCCAGCTTGGCTCGGAGACCGAGGGTCCTGCTGCAGGCTGAGACTGGCGCCGGTC... |
Task1_train_34514 | This alteration on Chromosome 2 may affect genome function. Does it lead to a disease or is it benign? | Benign | TAAAACGAGAAAAAAACAGCTTCATCTGGCATTCAATCAGTTGGGAACTCAGAGGGCGGCGGGGAAGGGGGGACGCTTTTAAGGCCTGGGGGTTCTCCCCCAGGGAGGCGGGCTGAGGAGGCTTCCGGGATGCCGGCGGGTGGAAGAGAAATCTGGAACCGTTGTAAATATTCATGTGGGGGGATGCCCCTTCACCCTTCACCCGCCTCTCCCAGCTGCATTCCCCCCTCAGTGATAGTGGGGGAGGGCAAGGCGACTGCCCCACTGTCCTTAGACAAAGGTGATCTCCCCATATTTTTGTTCTCCAGTCGCTTGACTTA... | TAAAACGAGAAAAAAACAGCTTCATCTGGCATTCAATCAGTTGGGAACTCAGAGGGCGGCGGGGAAGGGGGGACGCTTTTAAGGCCTGGGGGTTCTCCCCCAGGGAGGCGGGCTGAGGAGGCTTCCGGGATGCCGGCGGGTGGAAGAGAAATCTGGAACCGTTGTAAATATTCATGTGGGGGGATGCCCCTTCACCCTTCACCCGCCTCTCCCAGCTGCATTCCCCCCTCAGTGATAGTGGGGGAGGGCAAGGCGACTGCCCCACTGTCCTTAGACAAAGGTGATCTCCCCATATTTTTGTTCTCCAGTCGCTTGACTTA... |
Task1_train_34515 | This sequence variant lies on Chromosome 2. Is it clinically significant, and what condition might it cause if any? | Benign | TCTGCCGCTGAGGGCATTTGTTCCTTTCTGGAAAATACCACTTGGTAAGGAGGAGGGTTATTTGGATCCTGGTGGGGGAGGGTGGTTAATAAAGCCGCCATCCTTGGGATGGATTATTTTTCTTTCTTTCTTTCTTTTTTTCTTTCTTAAGAAGAATATTCTGGTTGTTCGCCTGCTTGGTAACCCTGACCCTGGCAGAAGAATGAGGGAACTCATTGCTTCAAATTGTCGCCAAGCCCATTAGGCTACCTGAACTGTCTCAGAAAGTGCGGGTGGCTGCGTCGAACGGTGGTGGCTCAGAGGAAGAGATTGGGGCCGGC... | TCTGCCGCTGAGGGCATTTGTTCCTTTCTGGAAAATACCACTTGGTAAGGAGGAGGGTTATTTGGATCCTGGTGGGGGAGGGTGGTTAATAAAGCCGCCATCCTTGGGATGGATTATTTTTCTTTCTTTCTTTCTTTTTTTCTTTCTTAAGAAGAATATTCTGGTTGTTCGCCTGCTTGGTAACCCTGACCCTGGCAGAAGAATGAGGGAACTCATTGCTTCAAATTGTCGCCAAGCCCATTAGGCTACCTGAACTGTCTCAGAAAGTGCGGGTGGCTGCGTCGAACGGTGGTGGCTCAGAGGAAGAGATTGGGGCCGGC... |
Task1_train_34516 | A genomic variant on Chromosome 2 is under review. What is the biological outcome — benign or pathogenic? | Benign | CATTTCCAATCAAACTCAAGAACTCCAGCAGTGCAGGAACCACAGACCTCTTTAACTTTGTGCTGATTCCTAGGCATCCACCCTCTACTGGCTCCCCTCAACCTGGGGACATCCCTCCCCCATCCTGCAGCAACTTCGGGTCCATCAGTAGTCCACATTTTGGTAGGGCTTTGTTTATTCACAAGTCCACAACCCTGGAAGGAACTGGCTCCCTGGGCTGTGATGGCGCCTATTCTAAAGACTTCCTCAGAGTGGAAATTTAGGCAACAACAGCTCAATCGCTCTTTTATGACAAGTCAATCAGTAAAACAATGATAAAA... | CATTTCCAATCAAACTCAAGAACTCCAGCAGTGCAGGAACCACAGACCTCTTTAACTTTGTGCTGATTCCTAGGCATCCACCCTCTACTGGCTCCCCTCAACCTGGGGACATCCCTCCCCCATCCTGCAGCAACTTCGGGTCCATCAGTAGTCCACATTTTGGTAGGGCTTTGTTTATTCACAAGTCCACAACCCTGGAAGGAACTGGCTCCCTGGGCTGTGATGGCGCCTATTCTAAAGACTTCCTCAGAGTGGAAATTTAGGCAACAACAGCTCAATCGCTCTTTTATGACAAGTCAATCAGTAAAACAATGATAAAA... |
Task1_train_34517 | Chromosome 2 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GCAAAGTCACGTTAAAAGGAAGCCTAGTCAAAAAGTGAAAATTTTGTCCCGCCCTAGGCACACAGCACTCACAGCATAAGATGTAGTTCCATGAGTCCTAGGAAAGGGGGAAGAAAGGAAAAAACCAAACATCTGCTCTAGGTTTAGAAGAGGGATAACATCAGCGCCAAGCAAACCGAAAGCGCAGAGGACTCAGAAGAGGGGAAGAGGAATAACTTTATCTGTCCTGGAGGTGGGCGAAGAGCAGTCTCCACCGGCCGCGCGTCACGCTCCCATTTAACCTTTTCCATGCCGCGACGCCCACACTCCGCCCTCGAGGG... | GCAAAGTCACGTTAAAAGGAAGCCTAGTCAAAAAGTGAAAATTTTGTCCCGCCCTAGGCACACAGCACTCACAGCATAAGATGTAGTTCCATGAGTCCTAGGAAAGGGGGAAGAAAGGAAAAAACCAAACATCTGCTCTAGGTTTAGAAGAGGGATAACATCAGCGCCAAGCAAACCGAAAGCGCAGAGGACTCAGAAGAGGGGAAGAGGAATAACTTTATCTGTCCTGGAGGTGGGCGAAGAGCAGTCTCCACCGGCCGCGCGTCACGCTCCCATTTAACCTTTTCCATGCCGCGACGCCCACACTCCGCCCTCGAGGG... |
Task1_train_34518 | A sequence alteration has been identified on Chromosome 2. Is it disease-inducing or harmless? | Benign | TTTGGAAGGATTAAAAGCAAATCTCCTCTTCCCGAACAAAAACAAACATTAGTACAAAAACTGAAAGAGGAAGTTAAGAGAATTATACCATTTCTAAATACTTATAAAATTATTAATTTATGCGCAACCATAACAGAGACTGGGGACCACCCTATATATATTCATAGCTACGGCTGTAAGCAAAAATTCCAGGTAAAAAGGCAAAAATCCAAATTTCTTATTAATAATCAGTATAACATCCAACAATAACAATCACTTACCATAGGGGTTAACATTTACTGTAAGCCAAAATCCTAGAAAACATTAATATAAAATACAAT... | TTTGGAAGGATTAAAAGCAAATCTCCTCTTCCCGAACAAAAACAAACATTAGTACAAAAACTGAAAGAGGAAGTTAAGAGAATTATACCATTTCTAAATACTTATAAAATTATTAATTTATGCGCAACCATAACAGAGACTGGGGACCACCCTATATATATTCATAGCTACGGCTGTAAGCAAAAATTCCAGGTAAAAAGGCAAAAATCCAAATTTCTTATTAATAATCAGTATAACATCCAACAATAACAATCACTTACCATAGGGGTTAACATTTACTGTAAGCCAAAATCCTAGAAAACATTAATATAAAATACAAT... |
Task1_train_34519 | A genomic variant on Chromosome 2 is under review. What is the biological outcome — benign or pathogenic? | Benign | AAGGTATGGAACTCATACTTTTATTCTTCTCATTCTCAGTTCAGTGCTTATTTTTTCCTAAAAAATTAAAAAGTAAAAATTAAAAATTTCAGTTTTTAAAAAACCAAAAATATTAATAAGCTTCCACACTTAATATATGTCAGTATCCACAAGGAGGCAAAATCATTTCTGTAAAATCAAAAATAGAACATGAAGAAAAACGTTTATTATAAAACTTAAGAAGCAACCAATCAACCAAATTATGAAAAAAAATTTTGTCACTGACCAAACCTCATAACCTGAAAAGAACCAAGAAAAGAAATTCCCATTATACTTGTACT... | AAGGTATGGAACTCATACTTTTATTCTTCTCATTCTCAGTTCAGTGCTTATTTTTTCCTAAAAAATTAAAAAGTAAAAATTAAAAATTTCAGTTTTTAAAAAACCAAAAATATTAATAAGCTTCCACACTTAATATATGTCAGTATCCACAAGGAGGCAAAATCATTTCTGTAAAATCAAAAATAGAACATGAAGAAAAACGTTTATTATAAAACTTAAGAAGCAACCAATCAACCAAATTATGAAAAAAAATTTTGTCACTGACCAAACCTCATAACCTGAAAAGAACCAAGAAAAGAAATTCCCATTATACTTGTACT... |
Task1_train_34520 | A mutation located on Chromosome 2 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CTGCAAGCGTGCACCACCATGCCTGGCTGATTTTTGTATTTTTAGTAGAGACGGGGTTTCACTCTGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCGTGATCTGCCAACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTAAGCCACCATGCCTGGTCTAAGTTTTTTTTTTTTTTTTTTTTTTTTTTTTAGAGATGGGGTTTCACCATATTGGCCAAGCTGGTCTTGAACTCCTGACCTCAGGTGATCCACCTGCCTTGGCTTCCCAAAGTACAGGGATTACAGGCATAAGCCACCATGCCCAGCCATCAGCTAAT... | CTGCAAGCGTGCACCACCATGCCTGGCTGATTTTTGTATTTTTAGTAGAGACGGGGTTTCACTCTGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCGTGATCTGCCAACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTAAGCCACCATGCCTGGTCTAAGTTTTTTTTTTTTTTTTTTTTTTTTTTTTAGAGATGGGGTTTCACCATATTGGCCAAGCTGGTCTTGAACTCCTGACCTCAGGTGATCCACCTGCCTTGGCTTCCCAAAGTACAGGGATTACAGGCATAAGCCACCATGCCCAGCCATCAGCTAAT... |
Task1_train_34521 | Located on Chromosome 2, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | CATGTCTTTCCTGTTCCTCATTATATATCTAGCTCCTGGCATAGAGCCTGGCACACAGTTGGAGTACAATAAGTATTTATCTGGTTGACTTCATAGCAACCTAGGTCTTAGCATCCAGAACTTGTTCATTTGAAGAACTCCGCCCTCGGTCTACTTAGGGGTTTATTCCTTTCACTTCATTCCAATGCCACTGCTAAATCCAGGCCTTGTTTCTGGATTTCTACTGGGTTTCTGACCTCTCCTCTAAGGCTTGTTAACAAGAAGGCATTTCCCACTTTGCTTGCACTCTATGATTTCTCTTAGTTCCACAGCTGAGCAGT... | CATGTCTTTCCTGTTCCTCATTATATATCTAGCTCCTGGCATAGAGCCTGGCACACAGTTGGAGTACAATAAGTATTTATCTGGTTGACTTCATAGCAACCTAGGTCTTAGCATCCAGAACTTGTTCATTTGAAGAACTCCGCCCTCGGTCTACTTAGGGGTTTATTCCTTTCACTTCATTCCAATGCCACTGCTAAATCCAGGCCTTGTTTCTGGATTTCTACTGGGTTTCTGACCTCTCCTCTAAGGCTTGTTAACAAGAAGGCATTTCCCACTTTGCTTGCACTCTATGATTTCTCTTAGTTCCACAGCTGAGCAGT... |
Task1_train_34522 | This mutation occurs on Chromosome 2. Does this change lead to a known medical condition, or is it benign? | Benign | GGGTTCAAGTGATTCTCCCACCTGAGCCTCCCGAGTAGCTGGGATTACAGGTGCACGCCACCTTGTCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGTCAGGCTGGTCTCAAACGCCTGACCTCAGGTGATCTGCCCGACTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCACCTGGCCTCCAGCCTCTTTTCTTTTTTTTTTTTGAGACAAGTCTAACTCTGTCACCCAGGCTGGAGAGCAGCGGCATGATCATGGCTCACTGCTGCCTCAACCTCAGAGGCTCAAGTCAT... | GGGTTCAAGTGATTCTCCCACCTGAGCCTCCCGAGTAGCTGGGATTACAGGTGCACGCCACCTTGTCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGTCAGGCTGGTCTCAAACGCCTGACCTCAGGTGATCTGCCCGACTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCACCTGGCCTCCAGCCTCTTTTCTTTTTTTTTTTTGAGACAAGTCTAACTCTGTCACCCAGGCTGGAGAGCAGCGGCATGATCATGGCTCACTGCTGCCTCAACCTCAGAGGCTCAAGTCAT... |
Task1_train_34523 | The following genetic variant occurs on Chromosome 2. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GCAAATGATAAATTCCATCTTTTTCCTTTTAAGTTCAAACTCCCATACCCTCATGGAATAAGTTTCAAGTGTGGCCTTCAAGTGTGGCCCTCAAGTGTAAGAAGACACAGAAACCATATATTTATCTGCTAACACAGGTATTAGGGATATAGCATACAGGGTCCCTGCCCTCAAGAGCCAACAGAGTAGTGTGGGATTTTTGTCTGTTAATAGGCACCTGAAGTATGGAATGGGATATGTTACAACAAGCCTAAGTGCAGGCTGTAGCGGAGGTTGCAGTGAGCCAAGATCATGCCACTGCACTCTAGCCTGGGTGACAG... | GCAAATGATAAATTCCATCTTTTTCCTTTTAAGTTCAAACTCCCATACCCTCATGGAATAAGTTTCAAGTGTGGCCTTCAAGTGTGGCCCTCAAGTGTAAGAAGACACAGAAACCATATATTTATCTGCTAACACAGGTATTAGGGATATAGCATACAGGGTCCCTGCCCTCAAGAGCCAACAGAGTAGTGTGGGATTTTTGTCTGTTAATAGGCACCTGAAGTATGGAATGGGATATGTTACAACAAGCCTAAGTGCAGGCTGTAGCGGAGGTTGCAGTGAGCCAAGATCATGCCACTGCACTCTAGCCTGGGTGACAG... |
Task1_train_34524 | Chromosome 2 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | ATATATCCAACCTTGTCAGGGAATCAAGAGTCCCACCAACTGAATTTTCCAGAAAAATGGAAGCTTAATCAATTTTTGACCAACTTTTATTTTTATGAAAGAAATTTTTCTATCCTTTCTACCTCATAAAATAATAATTTTAAAATCTTATTTGTTTCCTGATGAATCAAGGTTGTCATTAAGTACAGTAAAGTTGGGCTGTTACAAAAATAGTAGCTGAGATGCTGTTAGGTGGTGGTGATTTGCTTCTCTGTTTAAATTTTTCAGACAGATTTTTAAAAGAGTTTTTCTAGGCCCCTTTTTGCCATCTTTATCTTCTC... | ATATATCCAACCTTGTCAGGGAATCAAGAGTCCCACCAACTGAATTTTCCAGAAAAATGGAAGCTTAATCAATTTTTGACCAACTTTTATTTTTATGAAAGAAATTTTTCTATCCTTTCTACCTCATAAAATAATAATTTTAAAATCTTATTTGTTTCCTGATGAATCAAGGTTGTCATTAAGTACAGTAAAGTTGGGCTGTTACAAAAATAGTAGCTGAGATGCTGTTAGGTGGTGGTGATTTGCTTCTCTGTTTAAATTTTTCAGACAGATTTTTAAAAGAGTTTTTCTAGGCCCCTTTTTGCCATCTTTATCTTCTC... |
Task1_train_34525 | A genomic variant on Chromosome 2 is under review. What is the biological outcome — benign or pathogenic? | Benign | TACTTTTCCAAGCTATTCAGGCACTCCTTATGTCAGAGACAGCGTAAAATGAGCGAACAAAGTGTTGGCCGTTACACTTTGCTCTGGTAATATTTGTCATGATAATTTTGTGTGACATCATCAGAGAAAATGTAAGACGTTAAAGTGTTGCTTACAGGAGGGTAAATGCAAACATCACCAATGCCTTACATTTCTGATTCAGTAGGTATTGGTGCACATATCAAGTGATATGCACAGCATCATTCTCTTTTAGGTGGACAGGACATCTTCAATGGGGATTTTCTCAACCCACTGAGGCATACTTAGACATCAACAGTATG... | TACTTTTCCAAGCTATTCAGGCACTCCTTATGTCAGAGACAGCGTAAAATGAGCGAACAAAGTGTTGGCCGTTACACTTTGCTCTGGTAATATTTGTCATGATAATTTTGTGTGACATCATCAGAGAAAATGTAAGACGTTAAAGTGTTGCTTACAGGAGGGTAAATGCAAACATCACCAATGCCTTACATTTCTGATTCAGTAGGTATTGGTGCACATATCAAGTGATATGCACAGCATCATTCTCTTTTAGGTGGACAGGACATCTTCAATGGGGATTTTCTCAACCCACTGAGGCATACTTAGACATCAACAGTATG... |
Task1_train_34526 | A genomic variant on Chromosome 2 is under review. What is the biological outcome — benign or pathogenic? | Benign | CTTTCTCTGTTGGTGTTGGTTTTGTCTCTGTGGGTGATACGGCTTTCGGGTGAGAAGGTTCTGGAGATTTCACTCGTTTTGGAGACTTAACTGCTTCTGGGGATTTCACCCGAGGCTCTGGGGATTTGACTCTTGGTGGTGATGTCACAGCCTTTTCAGTTACCCTGGCCTTTTGAATAGTCAGAGTGAACTCTGCTTCTTGTTTCCCTTCACTGTTTTCTACCACCACGCTGTAATTGCCCTCATCGGAAGCCTGGACTGAAGAGATCTCAAAGGTTGATTTGTACTTTGTGGTGGTCACTTGGTGGCGGGCAGAAGTA... | CTTTCTCTGTTGGTGTTGGTTTTGTCTCTGTGGGTGATACGGCTTTCGGGTGAGAAGGTTCTGGAGATTTCACTCGTTTTGGAGACTTAACTGCTTCTGGGGATTTCACCCGAGGCTCTGGGGATTTGACTCTTGGTGGTGATGTCACAGCCTTTTCAGTTACCCTGGCCTTTTGAATAGTCAGAGTGAACTCTGCTTCTTGTTTCCCTTCACTGTTTTCTACCACCACGCTGTAATTGCCCTCATCGGAAGCCTGGACTGAAGAGATCTCAAAGGTTGATTTGTACTTTGTGGTGGTCACTTGGTGGCGGGCAGAAGTA... |
Task1_train_34527 | With a mutation on Chromosome 2, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TAACATTGCCAGTCCTCCTTCCTTTCCTCTCTTCCTCCTTCCCTTCTCTCTTTTCTTCCTTCCATTCCTTTCTTCCTAACTCCCTCCTCTTCTCTTTCATAAGAGTGAAGATATTAAAAAAAAAATCAAGCCTAAGTGTGTTGAAAACCTCTGAGAAAAGGAGGTTTAGAAACCTGAGAAAAGGAGGTTTAGAAACCTTAGAAAGACCACAGGGTTAATTTTGTGACCTATTTTTATTTACATTAGGGCATATTAAAAACAAATTCTTTTTTGTTAACATTCAGAATCAGAGGTGGGGAGAGTGGTGGAAGGGCCTGTGG... | TAACATTGCCAGTCCTCCTTCCTTTCCTCTCTTCCTCCTTCCCTTCTCTCTTTTCTTCCTTCCATTCCTTTCTTCCTAACTCCCTCCTCTTCTCTTTCATAAGAGTGAAGATATTAAAAAAAAAATCAAGCCTAAGTGTGTTGAAAACCTCTGAGAAAAGGAGGTTTAGAAACCTGAGAAAAGGAGGTTTAGAAACCTTAGAAAGACCACAGGGTTAATTTTGTGACCTATTTTTATTTACATTAGGGCATATTAAAAACAAATTCTTTTTTGTTAACATTCAGAATCAGAGGTGGGGAGAGTGGTGGAAGGGCCTGTGG... |
Task1_train_34528 | A sequence alteration has been identified on Chromosome 2. Is it disease-inducing or harmless? | Benign | GGAATTGACAAGCTGCCAAGCTGTTGTACCCGATTCACGCTTTTCAACTATGTAATTAGTAATTTCAGTGCCTCCTCCATCTTTAGGTTCTCCCCATGACAGGACACACGATTCAGCTGAGACAGATGAGACCTCAATGGGGCCGGTTACTGGACCTGGCCTTCCAATGACCACAACTGTGACGCTAAATGTTTTAACACCAGCTGTATTTTCCAGGGTCAAGAAGTATCTTCCAGAGTCACCTCTCATGCTGTCCTTTACAGTCAGTGTGGTTCTGTCTTTTGTTGTTGTAATGCTCACTCGATCTGTCTCTTTAAGTC... | GGAATTGACAAGCTGCCAAGCTGTTGTACCCGATTCACGCTTTTCAACTATGTAATTAGTAATTTCAGTGCCTCCTCCATCTTTAGGTTCTCCCCATGACAGGACACACGATTCAGCTGAGACAGATGAGACCTCAATGGGGCCGGTTACTGGACCTGGCCTTCCAATGACCACAACTGTGACGCTAAATGTTTTAACACCAGCTGTATTTTCCAGGGTCAAGAAGTATCTTCCAGAGTCACCTCTCATGCTGTCCTTTACAGTCAGTGTGGTTCTGTCTTTTGTTGTTGTAATGCTCACTCGATCTGTCTCTTTAAGTC... |
Task1_train_34529 | This is a variant located on Chromosome 2. Is this mutation a likely cause of disease or not? | Benign | TTAATTCATAGCATCCACTATTAAGGCGATCGGCATCTTTGATGAGTATAGATGCGAGGTCCGTGGTATTTTCAACACACACCAGTGCATTGGTTTGTAATTCTTTATCATCTTTATACCACTCAATAGTAGGCGCAGGTTTGCCAGAAATGCCAGCTCTGAGCTTCACAGATGTACCTGCTCTGTATTTGACAACTTCTGTATATTCTAGAGGCAAATCAATTACAGGACCACCTGCAAGAAAAACAGATGAGAAATATTTAAAATATTATAAGGATGGAAAAAAAAATAGTTGCACCAACCTTAAAGTAAGGTCATTG... | TTAATTCATAGCATCCACTATTAAGGCGATCGGCATCTTTGATGAGTATAGATGCGAGGTCCGTGGTATTTTCAACACACACCAGTGCATTGGTTTGTAATTCTTTATCATCTTTATACCACTCAATAGTAGGCGCAGGTTTGCCAGAAATGCCAGCTCTGAGCTTCACAGATGTACCTGCTCTGTATTTGACAACTTCTGTATATTCTAGAGGCAAATCAATTACAGGACCACCTGCAAGAAAAACAGATGAGAAATATTTAAAATATTATAAGGATGGAAAAAAAAATAGTTGCACCAACCTTAAAGTAAGGTCATTG... |
Task1_train_34530 | A variant on Chromosome 2 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TGGTCCTGCTGGTGGACCAGGCTTATCAAGTACTTTGCAATTAACGGCCACAGACCGAGTGCCGGCAACATTCTTCAGTGTTAGTACATATTGCCCAGTGTCTCGTCTTATACAGTCTTTAACTGTTAACAAAGTATGATTGTCTGTTGAGATGATTTCTGTTCTTGCTCTTTCTTCAATTTCTATACCATCCTTGGCCCAGGAAATTACTGGCAGAGGTCGCCCTGCAATGTCTGCATTTATCTTAAGGACCTCTCCAGCTTTGACAACAATAACGTCTCGGAACTTGACATCCATCATAACTCTTGGAGGCTCAACAT... | TGGTCCTGCTGGTGGACCAGGCTTATCAAGTACTTTGCAATTAACGGCCACAGACCGAGTGCCGGCAACATTCTTCAGTGTTAGTACATATTGCCCAGTGTCTCGTCTTATACAGTCTTTAACTGTTAACAAAGTATGATTGTCTGTTGAGATGATTTCTGTTCTTGCTCTTTCTTCAATTTCTATACCATCCTTGGCCCAGGAAATTACTGGCAGAGGTCGCCCTGCAATGTCTGCATTTATCTTAAGGACCTCTCCAGCTTTGACAACAATAACGTCTCGGAACTTGACATCCATCATAACTCTTGGAGGCTCAACAT... |
Task1_train_34531 | A mutation on Chromosome 2 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TTGGTCGGCCTATAACTGGAATTTCTATTTTAAGATCTTCTCCAGCTTGGATACTATATGTGTTAAATGGTAACTTTAAACTAGGCTGTATAGTCAAGTCCTTGGCTATGACAGGAACACCCAACACTCTTGGATCGCTTTTTCCTTTCTCATTATAAGCCTTGACACGGAACTGATATTCTTGTCCAGAACTCAAACCAGTAACAACTGCATTACAGACTTTGGATTCAGCCACAATGCTCCATTTTTCAGTTCCTTTGGGCTGCATTTCAACAACGTACCCCAGGACTCTGCTACCGCCATCATGTTCAGGTTTCTCC... | TTGGTCGGCCTATAACTGGAATTTCTATTTTAAGATCTTCTCCAGCTTGGATACTATATGTGTTAAATGGTAACTTTAAACTAGGCTGTATAGTCAAGTCCTTGGCTATGACAGGAACACCCAACACTCTTGGATCGCTTTTTCCTTTCTCATTATAAGCCTTGACACGGAACTGATATTCTTGTCCAGAACTCAAACCAGTAACAACTGCATTACAGACTTTGGATTCAGCCACAATGCTCCATTTTTCAGTTCCTTTGGGCTGCATTTCAACAACGTACCCCAGGACTCTGCTACCGCCATCATGTTCAGGTTTCTCC... |
Task1_train_34532 | A genetic alteration is present on Chromosome 2. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | CCCATCCAACAAAGGAGGTTCCCATGTAATTGATACTGAGTCTTTGGTGATTTCTGTGACTTTCAGGTTAACAGGTGGACTTGGCGTGTCCAGAACTCTCACAGTAACAAAGGCAGACTTTGTTCCACTGCTGTTTTCTAATGTAAGCGTATATTTTCCACTATCATATCGGTTGACATTGTCAAGAACAAGAGAGGTGAAACTGCTAGTGACATCAATTATAGCTGCATCTCGGATTTCACCATCCACCTTTCCCCATTTAACTTCTGGTGTAGGACGACCTTTTATAGGAACAAATAACCTTAAGGAGCCACCTGCCC... | CCCATCCAACAAAGGAGGTTCCCATGTAATTGATACTGAGTCTTTGGTGATTTCTGTGACTTTCAGGTTAACAGGTGGACTTGGCGTGTCCAGAACTCTCACAGTAACAAAGGCAGACTTTGTTCCACTGCTGTTTTCTAATGTAAGCGTATATTTTCCACTATCATATCGGTTGACATTGTCAAGAACAAGAGAGGTGAAACTGCTAGTGACATCAATTATAGCTGCATCTCGGATTTCACCATCCACCTTTCCCCATTTAACTTCTGGTGTAGGACGACCTTTTATAGGAACAAATAACCTTAAGGAGCCACCTGCCC... |
Task1_train_34533 | Here’s a variant located on Chromosome 2. What is the predicted biological effect — harmless or disease-causing? | Benign | GAATTAATCCAGTGATAGTGGCTTCAGTGACCTTGACTGTGGCACACGTGGCCCATTTGTCACTGCCTTTGGTCTGCATCTCCACAATGTAGCCTAGAATTCGGCTGCCTCCATCATGCTCTGGTTTCTCCCAAGAGAGTGACACACTATTTCTTGTGACATCCATCAAAGTTATTTTTCCTGGAGGAAGAGGTCGTTCTGATGCTTTCACAGATTCTGCGGTTTCAGCAGGCAGCCCAATGCCATATTCATTTTCTGCGAGAACCCTGAAATAGTAGCTACAGCCTTCTTGAAGCTGGTCTACCTTCCAGGAAGTCTTG... | GAATTAATCCAGTGATAGTGGCTTCAGTGACCTTGACTGTGGCACACGTGGCCCATTTGTCACTGCCTTTGGTCTGCATCTCCACAATGTAGCCTAGAATTCGGCTGCCTCCATCATGCTCTGGTTTCTCCCAAGAGAGTGACACACTATTTCTTGTGACATCCATCAAAGTTATTTTTCCTGGAGGAAGAGGTCGTTCTGATGCTTTCACAGATTCTGCGGTTTCAGCAGGCAGCCCAATGCCATATTCATTTTCTGCGAGAACCCTGAAATAGTAGCTACAGCCTTCTTGAAGCTGGTCTACCTTCCAGGAAGTCTTG... |
Task1_train_34534 | This alteration occurs on Chromosome 2. Is it associated with a disease or is it a benign variant? | Benign | TCCTTGAACTCGAGATGATACCCTACAAAAGACCCAGGGATGTATCAAGTATAAATGCAGCTTGATTTTACAATATATATGTGTTGCCCAAATTATTTATACATATCCATATATATTGAACAAGTAGTCATTCTTGCTAGTATCTATACTTTTATTACCCAAGCATAGTGCCATTTTTTTTTTCCTCTTGGAATATGCATAGTTGTTGTCTTTTTTGGTGAACAATTTTAACTTACAAAAATAGATATTATAATTAAGAAATACTTTATTAACTATTACATTAGGATATTTTCAATAAAATTAAACATTAACCATATGTA... | TCCTTGAACTCGAGATGATACCCTACAAAAGACCCAGGGATGTATCAAGTATAAATGCAGCTTGATTTTACAATATATATGTGTTGCCCAAATTATTTATACATATCCATATATATTGAACAAGTAGTCATTCTTGCTAGTATCTATACTTTTATTACCCAAGCATAGTGCCATTTTTTTTTTCCTCTTGGAATATGCATAGTTGTTGTCTTTTTTGGTGAACAATTTTAACTTACAAAAATAGATATTATAATTAAGAAATACTTTATTAACTATTACATTAGGATATTTTCAATAAAATTAAACATTAACCATATGTA... |
Task1_train_34535 | With a mutation on Chromosome 2, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TTTTTCTCCTTCACAAAAACATACCAAATGGGAACTGCGCAACCATCTTTGGAGATGTGAGAGGCTCTGAAATGCCAAATCGGTTTTCAGCACGGACCCGGAAGATGTACTCCTGGCCTGGGATCAGCTTTCCAACCCTGCAGGAAGTTTTTGTGACTGAAGCTAGAGCCGTGACCCAGTCACCTCGGCTTACATCACACTTCTCCACTATATAATTGGTGATGTTACTGCCTCCGTCCTCCAGAGGGATGTGCCATGACAGGGAGCAAGCATCAGCGTCTATATCAGAAATGTCAAATGGAGGCTGAGGGGGGCCGGGG... | TTTTTCTCCTTCACAAAAACATACCAAATGGGAACTGCGCAACCATCTTTGGAGATGTGAGAGGCTCTGAAATGCCAAATCGGTTTTCAGCACGGACCCGGAAGATGTACTCCTGGCCTGGGATCAGCTTTCCAACCCTGCAGGAAGTTTTTGTGACTGAAGCTAGAGCCGTGACCCAGTCACCTCGGCTTACATCACACTTCTCCACTATATAATTGGTGATGTTACTGCCTCCGTCCTCCAGAGGGATGTGCCATGACAGGGAGCAAGCATCAGCGTCTATATCAGAAATGTCAAATGGAGGCTGAGGGGGGCCGGGG... |
Task1_train_34536 | This mutation occurs on Chromosome 2. Does this change lead to a known medical condition, or is it benign? | Benign | ATTAGCTGCCTTTATACGGAATCTGTACTCATTTCCTTCAATTAGTCCAGGTACCCTAAAGGCACATTGCCTAATGAGTTCATCTTTATTAATCCTGTTCCATTGTGCTGTGCCAGGTTTCTGACATTCCACTACATATCCTAGAATGGGGCTACCACCATCACTGAGAGGCTTTGTCCACACCAAATCAGCTGTTTCTCTGCTCTTGTCTTTCAGTTTAGGATTAATAGGTGGTCCAGGTGGTTTGATGGGCCGGCAAGCTTTTATTGGATCAGAACTTGGGGATGGTTTGCTTAGTCCTGCAAGATTTTCAGCAAAAA... | ATTAGCTGCCTTTATACGGAATCTGTACTCATTTCCTTCAATTAGTCCAGGTACCCTAAAGGCACATTGCCTAATGAGTTCATCTTTATTAATCCTGTTCCATTGTGCTGTGCCAGGTTTCTGACATTCCACTACATATCCTAGAATGGGGCTACCACCATCACTGAGAGGCTTTGTCCACACCAAATCAGCTGTTTCTCTGCTCTTGTCTTTCAGTTTAGGATTAATAGGTGGTCCAGGTGGTTTGATGGGCCGGCAAGCTTTTATTGGATCAGAACTTGGGGATGGTTTGCTTAGTCCTGCAAGATTTTCAGCAAAAA... |
Task1_train_34537 | Mutation context: Chromosome 2. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CGGCTTATTCCAGACTAGGGAGACTTCAGTCTTGTCAACATCTACATGGTGCAGGTCCTTGGGTGGCCCTGGGGGATCTTTTCAAAGAAGAAGTTATGATGAAAAAGTAATATTCTTAAAGACAGTCAAACAATAGTTTTGTATTCAGAGAAAGCAACTTACGGAGAGGATCCAAAGCCTTGATTGGTTTTGGTGTTTCAACAAAAGGACCACGTCCATACTGGTTCTCCGCAGCTACTCGGAAGAGGTACTGGTTGCCTTCATTCAGATGCTTAGCGAAGTGACTCTTTTTCTTTGATGTAGCTGAGAGAGGTGACCAC... | CGGCTTATTCCAGACTAGGGAGACTTCAGTCTTGTCAACATCTACATGGTGCAGGTCCTTGGGTGGCCCTGGGGGATCTTTTCAAAGAAGAAGTTATGATGAAAAAGTAATATTCTTAAAGACAGTCAAACAATAGTTTTGTATTCAGAGAAAGCAACTTACGGAGAGGATCCAAAGCCTTGATTGGTTTTGGTGTTTCAACAAAAGGACCACGTCCATACTGGTTCTCCGCAGCTACTCGGAAGAGGTACTGGTTGCCTTCATTCAGATGCTTAGCGAAGTGACTCTTTTTCTTTGATGTAGCTGAGAGAGGTGACCAC... |
Task1_train_34538 | Given a variant located on Chromosome 2, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TCTTGAAGTTTTCCTGTAAAATATGGGTCTCCCTCTGCAAGTAAAGTATAAGTGAAAAGCTTTTATTAATCACCTTAGGGAAATGACAATCTCTTGGAAAGTTTAAGACACAACTCACAGAGTTCTGAGTATCTTTTAAAATTGTGTCAAGTGTTCAATCATTTAACCTGTTTATGTTCAAAAGTTCTCTAAATATTAGGAAGGGAATCAGTGTGTGGGATTTATCAAGATCTAATCCATTCATATTGAATTTTGAAACATTTTATTAACAGTAGCTAAAAAGACTGAAATTTAGCTTCAAATACAATTTTGTGTTCCTC... | TCTTGAAGTTTTCCTGTAAAATATGGGTCTCCCTCTGCAAGTAAAGTATAAGTGAAAAGCTTTTATTAATCACCTTAGGGAAATGACAATCTCTTGGAAAGTTTAAGACACAACTCACAGAGTTCTGAGTATCTTTTAAAATTGTGTCAAGTGTTCAATCATTTAACCTGTTTATGTTCAAAAGTTCTCTAAATATTAGGAAGGGAATCAGTGTGTGGGATTTATCAAGATCTAATCCATTCATATTGAATTTTGAAACATTTTATTAACAGTAGCTAAAAAGACTGAAATTTAGCTTCAAATACAATTTTGTGTTCCTC... |
Task1_train_34539 | A variant has been detected on Chromosome 2. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | AACATGGCACATGTATACATACGTAACAACCTGCACGTTGTGCACATGTACCCTAGAACTTAAAGTATAATAAAAATATATATATATATAAAAAGAAAAATATTTTCCAGAGCACAAGAGATAGATCATCTGAAGCCTAAAATCAGTGACAAATACCTTTAACAGGTGGGACTTCAGGCTTTTTAGGAGGAGCCGAGGGCACTTTCTTTTCAAGGACAACTTCTTTGGGAGCCTCTGGCACTTAAAAGATATTAGTAAAGTTACATGTGGAGCTATGGAGACTACTAGCAAAATATACAGCAGAGGAATTGGATCTTCTG... | AACATGGCACATGTATACATACGTAACAACCTGCACGTTGTGCACATGTACCCTAGAACTTAAAGTATAATAAAAATATATATATATATAAAAAGAAAAATATTTTCCAGAGCACAAGAGATAGATCATCTGAAGCCTAAAATCAGTGACAAATACCTTTAACAGGTGGGACTTCAGGCTTTTTAGGAGGAGCCGAGGGCACTTTCTTTTCAAGGACAACTTCTTTGGGAGCCTCTGGCACTTAAAAGATATTAGTAAAGTTACATGTGGAGCTATGGAGACTACTAGCAAAATATACAGCAGAGGAATTGGATCTTCTG... |
Task1_train_34540 | A mutation located on Chromosome 2 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TATGCAAAAGGAATGTATTTTACTTGAAGAACTTTCCACTAAAGAGGAGGAGCCAACCATTGAGCATAAGCATAATTTGATGGTAAAATTCAGAGATGAATACCGGGTAAACTGCTCCTGTGGCCAGTTGAGAGGCGCTTGTCATGGCATTAATGTTGTTAATATTGTCATGGGGAAAGATCTGCTATGGCTCACCAAGTTATGCTGCATGGGTGAATTATCATGCTATTCCACTGATGGATTATAAGGATGTACCTTTTGCTGGCGGAGGCTTCTCCTTTTTAGGAATAAGCACAGGAACTTTCTCCTCTGGCTTCTTA... | TATGCAAAAGGAATGTATTTTACTTGAAGAACTTTCCACTAAAGAGGAGGAGCCAACCATTGAGCATAAGCATAATTTGATGGTAAAATTCAGAGATGAATACCGGGTAAACTGCTCCTGTGGCCAGTTGAGAGGCGCTTGTCATGGCATTAATGTTGTTAATATTGTCATGGGGAAAGATCTGCTATGGCTCACCAAGTTATGCTGCATGGGTGAATTATCATGCTATTCCACTGATGGATTATAAGGATGTACCTTTTGCTGGCGGAGGCTTCTCCTTTTTAGGAATAAGCACAGGAACTTTCTCCTCTGGCTTCTTA... |
Task1_train_34541 | This sequence variant lies on Chromosome 2. Is it clinically significant, and what condition might it cause if any? | Benign | ACAAATATGGCATTGACTCCTGGAATGTAATGAGGTAATATATTTTCTTGCTCATTTTAAAACATTTTAAGACATTATAGTGACTTCTGCAATTGACTTAATGGATTATAACTTGTATTTTTTAAATGCCTAGAATAAAAAAATTAAAGGATTATAATATAAAATATATTTCTGTCTGTGGATTGTGGTACAAGCAATGTTTGAGAAACACCAATTAGGCATTAGGCTACTAAGGTAAAGCTTATGCCAGCCCACCATGCTGAAGCCAAGTCCTGTTTAATGAAAGGATATATGTATATGGAGATACCTGCCCTGATTAA... | ACAAATATGGCATTGACTCCTGGAATGTAATGAGGTAATATATTTTCTTGCTCATTTTAAAACATTTTAAGACATTATAGTGACTTCTGCAATTGACTTAATGGATTATAACTTGTATTTTTTAAATGCCTAGAATAAAAAAATTAAAGGATTATAATATAAAATATATTTCTGTCTGTGGATTGTGGTACAAGCAATGTTTGAGAAACACCAATTAGGCATTAGGCTACTAAGGTAAAGCTTATGCCAGCCCACCATGCTGAAGCCAAGTCCTGTTTAATGAAAGGATATATGTATATGGAGATACCTGCCCTGATTAA... |
Task1_train_34542 | Here’s a variant located on Chromosome 2. What is the predicted biological effect — harmless or disease-causing? | Benign | TTCTGCCAGACACTCTCCAGTTGTCATTGCCTGTCTCCACCTCTTCATAATGCATGAAACTGCTTTTATTAAGAAAAAGTTACATTTATGAAGGATGAAAGGTTTTTTCCTAGAAACATGTCAGTAGAAAACAAGTTTCACAAACATTTCCTCTTTCTCTAAAAGAGGGAAGATATTAAAAATGTAAGATAGCAGTTTGACATAGTTACTTCCTTTAACAATACTTTTTGGTGATGTCTTAGGAATATTCAGTATAATAAATAAAGTATGTCAAGAGCATGGCACGGAAGCTGACAAACAGTAAAAACACAAGAAGAATG... | TTCTGCCAGACACTCTCCAGTTGTCATTGCCTGTCTCCACCTCTTCATAATGCATGAAACTGCTTTTATTAAGAAAAAGTTACATTTATGAAGGATGAAAGGTTTTTTCCTAGAAACATGTCAGTAGAAAACAAGTTTCACAAACATTTCCTCTTTCTCTAAAAGAGGGAAGATATTAAAAATGTAAGATAGCAGTTTGACATAGTTACTTCCTTTAACAATACTTTTTGGTGATGTCTTAGGAATATTCAGTATAATAAATAAAGTATGTCAAGAGCATGGCACGGAAGCTGACAAACAGTAAAAACACAAGAAGAATG... |
Task1_train_34543 | Here is a genetic alteration on Chromosome 2. Based on the data, is it a benign variant or a cause of disease? | Benign | AAATATTGCAATCACCTTGAACGGTAAGGAAAGTTGATGCAGAAACTTCTCCCACGCTGTTTTCAGCTTTGCAGATATATTCTCCACTATCATTAATATCAACCTGGTTGAAAACCAGTGTAGCAACATTATTCCTAAAATGCATTTTGTAAGTCGTAGTGGGTCTCAATTTTGTATCTCCTTTATACCAGGATACCCCAATTTCAGGGGTTCCAGCAAGCTGGCATTGTAGAGAGGCAGAATCTCCAACAGACACCTTAACCGGCTCCAACTGCTTGACAAAATACGGTGGTTCTGCAGCCAAGAGAGATAATCAATCA... | AAATATTGCAATCACCTTGAACGGTAAGGAAAGTTGATGCAGAAACTTCTCCCACGCTGTTTTCAGCTTTGCAGATATATTCTCCACTATCATTAATATCAACCTGGTTGAAAACCAGTGTAGCAACATTATTCCTAAAATGCATTTTGTAAGTCGTAGTGGGTCTCAATTTTGTATCTCCTTTATACCAGGATACCCCAATTTCAGGGGTTCCAGCAAGCTGGCATTGTAGAGAGGCAGAATCTCCAACAGACACCTTAACCGGCTCCAACTGCTTGACAAAATACGGTGGTTCTGCAGCCAAGAGAGATAATCAATCA... |
Task1_train_34544 | An alteration has been detected on Chromosome 2. Is it pathogenic, and if so, what disease is involved? | Benign | GTATGAGTATTTGTGCTGAACAGGAATCTTTTCCAGAGGCATTTTCAATGTAGCAGTTGTATTGTCCTGCATCCTCTACTGTGCTACTTGGAATTTCCAGGATTGCCGATTTTTCAGTCGTAGTTATATTACACCTCTGAGAAGGAGTTACATTTATGCCATTTTTCTTCCAGGTAACCGAAATGGGAGGAGTTCCAGTGAATGTACCCTCTAGGATCAGGGGTTTTCCTTTCTCTATGCTGTAATCATTCAGCCTCTTCACAAATTTGGCTGGGGCTAAAGTGACCAAATTGAAAATATAAAATCAAACACATATACAT... | GTATGAGTATTTGTGCTGAACAGGAATCTTTTCCAGAGGCATTTTCAATGTAGCAGTTGTATTGTCCTGCATCCTCTACTGTGCTACTTGGAATTTCCAGGATTGCCGATTTTTCAGTCGTAGTTATATTACACCTCTGAGAAGGAGTTACATTTATGCCATTTTTCTTCCAGGTAACCGAAATGGGAGGAGTTCCAGTGAATGTACCCTCTAGGATCAGGGGTTTTCCTTTCTCTATGCTGTAATCATTCAGCCTCTTCACAAATTTGGCTGGGGCTAAAGTGACCAAATTGAAAATATAAAATCAAACACATATACAT... |
Task1_train_34545 | Chromosome 2 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GTGTAGTCTCCACTGTCTTCAACACTGAGATTGTGCATTTCCAGCACAGCCACCGAGTCAACGAATGACATTCTGAATTTACTGCTCTCTTGAATTTCAGTCTCGTCCTTATACCATAAAACTTTGATTTCTGGAGACCCACCGATTTTGCATTCATACCTTGTGAATTCATCCTGTTTCACAATTCTTGAAGGTTCTAGCTTCTTAATGAACCTGGGTGGTTCTATGGAACCAAGAGGAAAAACACAGGGTAAGGGATGGAACAGATGCATATAATTCAAGATGAGGTGGAAAAAATAATCTTTGCTAGAGAGGTCTTT... | GTGTAGTCTCCACTGTCTTCAACACTGAGATTGTGCATTTCCAGCACAGCCACCGAGTCAACGAATGACATTCTGAATTTACTGCTCTCTTGAATTTCAGTCTCGTCCTTATACCATAAAACTTTGATTTCTGGAGACCCACCGATTTTGCATTCATACCTTGTGAATTCATCCTGTTTCACAATTCTTGAAGGTTCTAGCTTCTTAATGAACCTGGGTGGTTCTATGGAACCAAGAGGAAAAACACAGGGTAAGGGATGGAACAGATGCATATAATTCAAGATGAGGTGGAAAAAATAATCTTTGCTAGAGAGGTCTTT... |
Task1_train_34546 | A variant on Chromosome 2 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | AGGGACAAAATCCATTCATTTACTAAGTACTGTGGGAAAAAAGTCATTTGCAATAACTTCGCTTTTGTCCTATGATACCGTCTTTCAAACTAGGATTTTCTTGCAATTTTGTAGAGTTTCGGTTATCTCTCTCTAGTCTCTATTTTTAGTCTCTTAAAATGGACTTTTGGTCCATGTTTTCCTAGTTTTAAATTTTTTTTTTAAAGTAATTAAAAAATACTTGTCTCCATTTGGAAGGTCCTTGATCCACTTGATCCATTTTCATCACTAGACCCTGGTCCTAAACATAGCTCTCTCTCAAGCACACCCACCCTCCTATA... | AGGGACAAAATCCATTCATTTACTAAGTACTGTGGGAAAAAAGTCATTTGCAATAACTTCGCTTTTGTCCTATGATACCGTCTTTCAAACTAGGATTTTCTTGCAATTTTGTAGAGTTTCGGTTATCTCTCTCTAGTCTCTATTTTTAGTCTCTTAAAATGGACTTTTGGTCCATGTTTTCCTAGTTTTAAATTTTTTTTTTAAAGTAATTAAAAAATACTTGTCTCCATTTGGAAGGTCCTTGATCCACTTGATCCATTTTCATCACTAGACCCTGGTCCTAAACATAGCTCTCTCTCAAGCACACCCACCCTCCTATA... |
Task1_train_34547 | A mutation located on Chromosome 2 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | ACTATTTGTACCAAGGTATAGTCATATAATTTTTAAAGGATAGGAAGTGATCCTTGAGAGAGAAGGAAAAAATATTATTGTCCTGTTTTAAACATAAGTTTAAAACCTGTATTGCTTTCACTTTGCATAGATATAGTAAAAGTGCTTGTTATTAATGATATAGATTATAGTGAGAATGATATATCTGTAAGTTGATTGAAAGCAAAAGACTAATTTTAAAATGCCTACTTCATTTTTTTGTGCAGTTTTGAAACATCACGTTTGATGTTTGGCAAATGTGTTGAGGTAATCAGAATTATGACACTGGAATAACAAAAATA... | ACTATTTGTACCAAGGTATAGTCATATAATTTTTAAAGGATAGGAAGTGATCCTTGAGAGAGAAGGAAAAAATATTATTGTCCTGTTTTAAACATAAGTTTAAAACCTGTATTGCTTTCACTTTGCATAGATATAGTAAAAGTGCTTGTTATTAATGATATAGATTATAGTGAGAATGATATATCTGTAAGTTGATTGAAAGCAAAAGACTAATTTTAAAATGCCTACTTCATTTTTTTGTGCAGTTTTGAAACATCACGTTTGATGTTTGGCAAATGTGTTGAGGTAATCAGAATTATGACACTGGAATAACAAAAATA... |
Task1_train_34548 | Chromosome 2 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CTGCCTCCTGGCTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGCGTGACACCACGCCTGGCTAATTTTTTATATTTTTAGTAGAGATCGGGTTTCACTGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTTGTGATCCGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAAGCGTGAGCCACCGTGCCCAGCCGTCTTATTTTTAAATTAGTAAAAATGCCTAGAGAGAATCCTAGTTTTCAGTCCTATACTAGCTCCCTGTCTTACATTAGGATTTAATTTTAGACTTAGACACTGA... | CTGCCTCCTGGCTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGCGTGACACCACGCCTGGCTAATTTTTTATATTTTTAGTAGAGATCGGGTTTCACTGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTTGTGATCCGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAAGCGTGAGCCACCGTGCCCAGCCGTCTTATTTTTAAATTAGTAAAAATGCCTAGAGAGAATCCTAGTTTTCAGTCCTATACTAGCTCCCTGTCTTACATTAGGATTTAATTTTAGACTTAGACACTGA... |
Task1_train_34549 | A genetic alteration is present on Chromosome 2. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | AGCTGTTAGGATGTCTATTTCCTCATATATAATAGCACACAAAGCATCCCTAAGTTCCATTTTCAGGTTAGCCATTTGAGGATCAACATCTTCAATAATGATGGTTACTTCTTCTGTTACAGACTTTGCCGAAGTAACAAGGTACATGCACATGATGTGTCTGGGCTCTTGGGTGATGTTTACAGCCTCGACCTCCACCTTTTCAATATTTCTTAGCCACTCAGAGAAAAGACCTGGCTGCTCGCTGGCCACGGCTGCTTGCAAAGCCCGGCAGATTTGAATTTTCAGGTTTAATCTCTGCTCTTCTGGAATACCAGAAA... | AGCTGTTAGGATGTCTATTTCCTCATATATAATAGCACACAAAGCATCCCTAAGTTCCATTTTCAGGTTAGCCATTTGAGGATCAACATCTTCAATAATGATGGTTACTTCTTCTGTTACAGACTTTGCCGAAGTAACAAGGTACATGCACATGATGTGTCTGGGCTCTTGGGTGATGTTTACAGCCTCGACCTCCACCTTTTCAATATTTCTTAGCCACTCAGAGAAAAGACCTGGCTGCTCGCTGGCCACGGCTGCTTGCAAAGCCCGGCAGATTTGAATTTTCAGGTTTAATCTCTGCTCTTCTGGAATACCAGAAA... |
Task1_train_34550 | This alteration occurs on Chromosome 2. Is it associated with a disease or is it a benign variant? | Benign | TGAGAATTAAAGCACTTATGAAGAGGAATATTAATAACGAAAACATTTTTAAAAGAGATGAAGTTAATATATTAAGATTGAAATGTCAAACAGATTATAGAGTTAGTTGCCAATTGGGAGAAGCTGGTTTTTGTTGTTTGTTTTGCCTATTCTAAGTCAAAGTAAATAAACATGAGTTTGGATGCAAAGGGGTTAAAATTCCAAAAATAACTTAGAATGGGAGCAGAGAGATTTGCCCTTACCAATTTGTCTGCGTGGTCATCTGATATGGTCTCCACTTTTACATTGTACTTTTGCATATATGGTTTATCTGCTAAAAG... | TGAGAATTAAAGCACTTATGAAGAGGAATATTAATAACGAAAACATTTTTAAAAGAGATGAAGTTAATATATTAAGATTGAAATGTCAAACAGATTATAGAGTTAGTTGCCAATTGGGAGAAGCTGGTTTTTGTTGTTTGTTTTGCCTATTCTAAGTCAAAGTAAATAAACATGAGTTTGGATGCAAAGGGGTTAAAATTCCAAAAATAACTTAGAATGGGAGCAGAGAGATTTGCCCTTACCAATTTGTCTGCGTGGTCATCTGATATGGTCTCCACTTTTACATTGTACTTTTGCATATATGGTTTATCTGCTAAAAG... |
Task1_train_34551 | A variant was discovered on Chromosome 2. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TGTCAGAAATTCTCTCAGAGTGAATATTTGGTAAATAGTCACTTTGGGCACATTCTTGTACATTTTCCTTTTCTGATCTACCAAGTTTTCCAAAATTATTTCTTATTTCTTTCTTAATAGTGACATCACTGAAATCATCAACAAATGGATAAACAGTACCCTCTGCTTGGTGCAGCTTTGATTTTTCACTTACATGTCTCTCTTTCCCTTCAGCCTGACATTGTATGAATTCAGCCCTGATGGGCTTGCTGATTTTTATGGTTCTTGAAGCACCATGCACAAATCTGGGAATTTTTTCTCTAGAAGGTATGCAACGCACC... | TGTCAGAAATTCTCTCAGAGTGAATATTTGGTAAATAGTCACTTTGGGCACATTCTTGTACATTTTCCTTTTCTGATCTACCAAGTTTTCCAAAATTATTTCTTATTTCTTTCTTAATAGTGACATCACTGAAATCATCAACAAATGGATAAACAGTACCCTCTGCTTGGTGCAGCTTTGATTTTTCACTTACATGTCTCTCTTTCCCTTCAGCCTGACATTGTATGAATTCAGCCCTGATGGGCTTGCTGATTTTTATGGTTCTTGAAGCACCATGCACAAATCTGGGAATTTTTTCTCTAGAAGGTATGCAACGCACC... |
Task1_train_34552 | A mutation on Chromosome 2 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TTATCAAATCAGTCCTCATTTATTAATATTTAGCATTTCTTGAACACTATCCCTCAAATATACAGTCTATGGTATTTGTCCATACTGGCCATACAATACTAAACATTGATGTTTATATAATTCCTCTCTATGGCTATAATAAAATGAATGTATTGAGCCCCAGTTACCTGGCAGCCATGCCTATAGGTGCTTTACATACATTATATCTTTTAATTATGCTCATAAAATCAAATAGGTCTATTAGATTTCTAGATCACCATCTCCATTCCTGAGGAGGAAATAATTGGGTCAGAAGACCAACTGAAGTACTAACCTGTTGA... | TTATCAAATCAGTCCTCATTTATTAATATTTAGCATTTCTTGAACACTATCCCTCAAATATACAGTCTATGGTATTTGTCCATACTGGCCATACAATACTAAACATTGATGTTTATATAATTCCTCTCTATGGCTATAATAAAATGAATGTATTGAGCCCCAGTTACCTGGCAGCCATGCCTATAGGTGCTTTACATACATTATATCTTTTAATTATGCTCATAAAATCAAATAGGTCTATTAGATTTCTAGATCACCATCTCCATTCCTGAGGAGGAAATAATTGGGTCAGAAGACCAACTGAAGTACTAACCTGTTGA... |
Task1_train_34553 | The following genetic variant occurs on Chromosome 2. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CTCTTGCATCTAGGTTAGACTCAAAACAAGGTCAGCTTGAGATTCAGCCTTAAGATTTCTAATGAGGAGAGCAGAGGTTTAACAGCACTTCCCTGGGGACTGCTCAGAGGCTCCTCAGGAGTGCTTGGTAGCATGTGGAATTCCCTGTCCAAAGTAAGAGCCCCTGTTCTTAGAGCTTGGGGTAGAGAGGATCGAGTTCCACATTGCCTGAGGCTCTCTAGGCCTTCCAGGGTCTCAAAGAGGACTTTTGAGTTCTCCCAGGCACTCCATATCAGAGGCTGGAAACACCCCTTTCACTTGGTAGTGCTGCTAGGACTTGA... | CTCTTGCATCTAGGTTAGACTCAAAACAAGGTCAGCTTGAGATTCAGCCTTAAGATTTCTAATGAGGAGAGCAGAGGTTTAACAGCACTTCCCTGGGGACTGCTCAGAGGCTCCTCAGGAGTGCTTGGTAGCATGTGGAATTCCCTGTCCAAAGTAAGAGCCCCTGTTCTTAGAGCTTGGGGTAGAGAGGATCGAGTTCCACATTGCCTGAGGCTCTCTAGGCCTTCCAGGGTCTCAAAGAGGACTTTTGAGTTCTCCCAGGCACTCCATATCAGAGGCTGGAAACACCCCTTTCACTTGGTAGTGCTGCTAGGACTTGA... |
Task1_train_34554 | Given this variant on Chromosome 2, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | AAATAGCATGTAGAAAAATTAACATTTTTAACAGCTTTATTGAGATATAATTCACATACTGTACAATCCACCAATTTAAAGTATACAATTCAATGAATTTCCATGTATTCATCATTGTGTAGCCATCACCATAATTTTAGAACATTCTCATTCCCCAAGAAGAAATCATGTAACCCTTAGCCATCACCCCAAGGACTTTTCTATTGTCTCCCCTGTAGACCTAAGCAACCACCAATCTACATCTCTATAGATTTGTGTATCTTGGACATTTCATATAAATGGAATCATACAATATGTGGTCTTTGTATGGTCTCTGGCTT... | AAATAGCATGTAGAAAAATTAACATTTTTAACAGCTTTATTGAGATATAATTCACATACTGTACAATCCACCAATTTAAAGTATACAATTCAATGAATTTCCATGTATTCATCATTGTGTAGCCATCACCATAATTTTAGAACATTCTCATTCCCCAAGAAGAAATCATGTAACCCTTAGCCATCACCCCAAGGACTTTTCTATTGTCTCCCCTGTAGACCTAAGCAACCACCAATCTACATCTCTATAGATTTGTGTATCTTGGACATTTCATATAAATGGAATCATACAATATGTGGTCTTTGTATGGTCTCTGGCTT... |
Task1_train_34555 | Consider a variant on Chromosome 2. Determine its clinical classification and disease relevance. | Benign | AGTTTCACCCCATTGCCTCCACTCTTATCATCCATTAGCAGAAATAATTACTGCTTTAACAAGCTAGTTGCTTATGTATCTGTCCTCTCTAAATTATGAATTTCTCAAGAAAAAAATCATTTCTTATTTAGTTTTGTGTCCTGAGTTTCTACAAGTGTCTGACCAATGGTAGGTACTTTAAAAACACTGGGTGAAATCACAGAGGAGTTCATAGTTTATTCCTGTTTCCACACATTTAAAACATGTAATTTATATTAAATGTATAAAAATGCTGAATCTGAAATTTTGTTTTACAAGTCTTTTCATGGTCCGATCTCTGA... | AGTTTCACCCCATTGCCTCCACTCTTATCATCCATTAGCAGAAATAATTACTGCTTTAACAAGCTAGTTGCTTATGTATCTGTCCTCTCTAAATTATGAATTTCTCAAGAAAAAAATCATTTCTTATTTAGTTTTGTGTCCTGAGTTTCTACAAGTGTCTGACCAATGGTAGGTACTTTAAAAACACTGGGTGAAATCACAGAGGAGTTCATAGTTTATTCCTGTTTCCACACATTTAAAACATGTAATTTATATTAAATGTATAAAAATGCTGAATCTGAAATTTTGTTTTACAAGTCTTTTCATGGTCCGATCTCTGA... |
Task1_train_34556 | A variant has been detected on Chromosome 2. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TCTTGCACGTATTAGAAGGCACCTCAAACTCATTCAGATCTAAAATAGAATATATTATTGTTGCCCCCACAACTATGTTTTTCCTATATTCTCAATTTTAGCTGGTAGTCATTCAGTATATCCAGGTACCCAGGCTCAAAAATCTTGGAATAATCCTCAATACTCTCTTTTCCTTACCACTTGGATTTAATCAGTCACTAGACTTTTTTGATTTAACTACTAAAACATCCTAATAAATGTTGGTTGGATAAGTAAACCAATGAATACATTTATGGAAAAATAAAAAATACACATTCTTTATCTCAGAGGAGGAAAACATA... | TCTTGCACGTATTAGAAGGCACCTCAAACTCATTCAGATCTAAAATAGAATATATTATTGTTGCCCCCACAACTATGTTTTTCCTATATTCTCAATTTTAGCTGGTAGTCATTCAGTATATCCAGGTACCCAGGCTCAAAAATCTTGGAATAATCCTCAATACTCTCTTTTCCTTACCACTTGGATTTAATCAGTCACTAGACTTTTTTGATTTAACTACTAAAACATCCTAATAAATGTTGGTTGGATAAGTAAACCAATGAATACATTTATGGAAAAATAAAAAATACACATTCTTTATCTCAGAGGAGGAAAACATA... |
Task1_train_34557 | A sequence alteration has been identified on Chromosome 2. Is it disease-inducing or harmless? | Benign | ATTTGAGAAACTGATCTTTGCAAACGTGTATTAAAATGATTTGAGGAGATATGAATAGGGTCCAGCATTATCAACTTCTTTACTCACCGAGACCAAAGTTGGTGGAGTAACAGGAATTTCAACAGGTGCTGGTACTCTTGCTGTTTCTGTTACCTAGATTTTTACAAATTATATTACAAAATGCTCATGAAATTAAGGGAAATCTCATAAACTCTTAGCTCATGCAACATTATATAATTATAAAAATATAAAAATAATTATAAAAATAATTTGAGAAAATGATCTCTGACCCATACTATGCTCCATAAAAATCAAGTCTT... | ATTTGAGAAACTGATCTTTGCAAACGTGTATTAAAATGATTTGAGGAGATATGAATAGGGTCCAGCATTATCAACTTCTTTACTCACCGAGACCAAAGTTGGTGGAGTAACAGGAATTTCAACAGGTGCTGGTACTCTTGCTGTTTCTGTTACCTAGATTTTTACAAATTATATTACAAAATGCTCATGAAATTAAGGGAAATCTCATAAACTCTTAGCTCATGCAACATTATATAATTATAAAAATATAAAAATAATTATAAAAATAATTTGAGAAAATGATCTCTGACCCATACTATGCTCCATAAAAATCAAGTCTT... |
Task1_train_34558 | A mutation located on Chromosome 2 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CATCCCCAGATCAATGTGATGAGACCCCTGTTTCTACTCCTGGTGTATGTTCACAGAGTTCTTTTTCATACTCACAAGGGGAGCATTCAGGGACACTACCAAACTTTGGTATCCAGTACCCAGAAATTTACACATACAACAAGGGGATCTTATTAGTATGCTAACAACCATGTGGCCCAAGGAACAACACTCTTCATGGTAAAGGTGATTATCTGTGTTGACCCCTGTAAGAACCTCAGTGAATTTAAAATACAAACCCATTTTCACCTGCTCATGAGTTACGTGCATCTGCTCTTGCTTTGTGGTAATTACTTCTTTGG... | CATCCCCAGATCAATGTGATGAGACCCCTGTTTCTACTCCTGGTGTATGTTCACAGAGTTCTTTTTCATACTCACAAGGGGAGCATTCAGGGACACTACCAAACTTTGGTATCCAGTACCCAGAAATTTACACATACAACAAGGGGATCTTATTAGTATGCTAACAACCATGTGGCCCAAGGAACAACACTCTTCATGGTAAAGGTGATTATCTGTGTTGACCCCTGTAAGAACCTCAGTGAATTTAAAATACAAACCCATTTTCACCTGCTCATGAGTTACGTGCATCTGCTCTTGCTTTGTGGTAATTACTTCTTTGG... |
Task1_train_34559 | This sequence variant lies on Chromosome 2. Is it clinically significant, and what condition might it cause if any? | Benign | TCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATCACGAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCATCTCTACTAAAAGTACAAAAAAGTAGCCGGGCGTGGTGGTGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGTGTGAACCCGGGAGGCAGAGCTTGCAGTGAGTCGAGATCACGTCACTGCACTCCAGCCTGGGAAACAGAGCGACACTCCATCTCAAAAATAAATAAATAAATAAATAACTGTGATGGAAGGAATGTCTGACTCAGGCCTGAAGCACTTATG... | TCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATCACGAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCATCTCTACTAAAAGTACAAAAAAGTAGCCGGGCGTGGTGGTGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGTGTGAACCCGGGAGGCAGAGCTTGCAGTGAGTCGAGATCACGTCACTGCACTCCAGCCTGGGAAACAGAGCGACACTCCATCTCAAAAATAAATAAATAAATAAATAACTGTGATGGAAGGAATGTCTGACTCAGGCCTGAAGCACTTATG... |
Task1_train_34560 | Consider this mutation on Chromosome 2. Is this a benign change or a disease-causing variant? | Benign | TTATTTCAGAAAGAAGCCAGTCACCCAACATTATGGAAAAGACATTTCCCAGCTCAAATCTCTAGTGTTGAAGATTCGCTCATCACACCCAACTCCTCAGAGACGCCATTCATTATAGGGTATAATTTTTACTTCAAAAGGCATAAAATATGCATTAGAAACATTTGATTTCTGCACTATAATTTTCCTGTCAACTTGAGCCTAACCTCAGGTTCATTATGCAAGTGCTCCAATCTCAGCTCAGCACAGTGGGGCTGCCAGGGCCAAGGCCAGAAGAGGATTGGAGAACAATTTACATTATTTGCACAAAGTGAGACTTC... | TTATTTCAGAAAGAAGCCAGTCACCCAACATTATGGAAAAGACATTTCCCAGCTCAAATCTCTAGTGTTGAAGATTCGCTCATCACACCCAACTCCTCAGAGACGCCATTCATTATAGGGTATAATTTTTACTTCAAAAGGCATAAAATATGCATTAGAAACATTTGATTTCTGCACTATAATTTTCCTGTCAACTTGAGCCTAACCTCAGGTTCATTATGCAAGTGCTCCAATCTCAGCTCAGCACAGTGGGGCTGCCAGGGCCAAGGCCAGAAGAGGATTGGAGAACAATTTACATTATTTGCACAAAGTGAGACTTC... |
Task1_train_34561 | A mutation has occurred on Chromosome 2. What is the medical relevance of this mutation? | Benign | ATATACACCATGGAATACTATGCAGTCATAAAAATTATGAGTTCATGTCCTTTGTAGGGACATGGATGAAATTGGAAATCATCATTCTCAGTAAACTATCGCAAGAACAAAAAACCAAACACCGCATATTCTCACTCATAGTTGGGAACTGAACAATGAGAACACATGGACACAGGAAGGGGAACATCACACTCTGGGGACTGTTGTGGGGTGGGGGGAGGGGGGAGGGATAGCTTTAGGAGATATATGTAATGCTAAATGACGAGTTAATGGGTGCAGCACACCAGAATGCCACATGCATACATATGTAACTAACCTGC... | ATATACACCATGGAATACTATGCAGTCATAAAAATTATGAGTTCATGTCCTTTGTAGGGACATGGATGAAATTGGAAATCATCATTCTCAGTAAACTATCGCAAGAACAAAAAACCAAACACCGCATATTCTCACTCATAGTTGGGAACTGAACAATGAGAACACATGGACACAGGAAGGGGAACATCACACTCTGGGGACTGTTGTGGGGTGGGGGGAGGGGGGAGGGATAGCTTTAGGAGATATATGTAATGCTAAATGACGAGTTAATGGGTGCAGCACACCAGAATGCCACATGCATACATATGTAACTAACCTGC... |
Task1_train_34562 | Chromosome 2 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AGCTCTTAAAGAGGTTCAGTTTCTGTTTTCTAAGTAAGTTGCCCTATAGCAGGAACTAAGCAGTTCATTCTAAAACTTCTGTCTATGAGGGCTATTTAAATTTGAAACCTTTCATGACATTAGACTCTATGCCCTCCTTGCCCACAATGGCTGCCCAACCCAGCAAGGCTGCCCCACAAAACAGGTGAGCAGGTGAGGTAAACTTACTGCTAGAATACTCGGGCTCCGCTGGAGTTTGTTGTAAGGGCTGTATTTTGGCTTCAGTGGTTTCCCTGCAACTCGATCTTTATGCCTTCGGCTAGAAATGTGCTGAAAAAGTT... | AGCTCTTAAAGAGGTTCAGTTTCTGTTTTCTAAGTAAGTTGCCCTATAGCAGGAACTAAGCAGTTCATTCTAAAACTTCTGTCTATGAGGGCTATTTAAATTTGAAACCTTTCATGACATTAGACTCTATGCCCTCCTTGCCCACAATGGCTGCCCAACCCAGCAAGGCTGCCCCACAAAACAGGTGAGCAGGTGAGGTAAACTTACTGCTAGAATACTCGGGCTCCGCTGGAGTTTGTTGTAAGGGCTGTATTTTGGCTTCAGTGGTTTCCCTGCAACTCGATCTTTATGCCTTCGGCTAGAAATGTGCTGAAAAAGTT... |
Task1_train_34563 | Consider this mutation on Chromosome 2. Is this a benign change or a disease-causing variant? | Benign | AGTCTCGCCTTTCTCTGCTTTACTTTTCTTCATAGCACTTACCACTACTGGATATATCATATATTTATTTATTTACTGTCTTTGTTTACCATTTCCCTCCCCTGAACTATAAGTCTCAACGAGTAGAGACTCTGTTCACTGTTTTATCTCTAGTACCTAAAACAAACCTGAGCAAACAGTAGAAGATTAATACATATTAATAACATTTTAAAAATAATCTAATAACTCTAAGGTCTTAAGCACTTAATAAAATGAATGGGTTCCCATTTTTACATGTAAAAGTCATGAACTAAGGTTAAAGTGTAGAAAATAAACTAAAA... | AGTCTCGCCTTTCTCTGCTTTACTTTTCTTCATAGCACTTACCACTACTGGATATATCATATATTTATTTATTTACTGTCTTTGTTTACCATTTCCCTCCCCTGAACTATAAGTCTCAACGAGTAGAGACTCTGTTCACTGTTTTATCTCTAGTACCTAAAACAAACCTGAGCAAACAGTAGAAGATTAATACATATTAATAACATTTTAAAAATAATCTAATAACTCTAAGGTCTTAAGCACTTAATAAAATGAATGGGTTCCCATTTTTACATGTAAAAGTCATGAACTAAGGTTAAAGTGTAGAAAATAAACTAAAA... |
Task1_train_34564 | A variant found on Chromosome 2 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | ATTTATTTATTTACTGTCTTTGTTTACCATTTCCCTCCCCTGAACTATAAGTCTCAACGAGTAGAGACTCTGTTCACTGTTTTATCTCTAGTACCTAAAACAAACCTGAGCAAACAGTAGAAGATTAATACATATTAATAACATTTTAAAAATAATCTAATAACTCTAAGGTCTTAAGCACTTAATAAAATGAATGGGTTCCCATTTTTACATGTAAAAGTCATGAACTAAGGTTAAAGTGTAGAAAATAAACTAAAATTTCTAGTCTACTGTTTTTTCCTTTTTACCAACCCTGAAGATGAGGGTTCAGGTAAAAAAAA... | ATTTATTTATTTACTGTCTTTGTTTACCATTTCCCTCCCCTGAACTATAAGTCTCAACGAGTAGAGACTCTGTTCACTGTTTTATCTCTAGTACCTAAAACAAACCTGAGCAAACAGTAGAAGATTAATACATATTAATAACATTTTAAAAATAATCTAATAACTCTAAGGTCTTAAGCACTTAATAAAATGAATGGGTTCCCATTTTTACATGTAAAAGTCATGAACTAAGGTTAAAGTGTAGAAAATAAACTAAAATTTCTAGTCTACTGTTTTTTCCTTTTTACCAACCCTGAAGATGAGGGTTCAGGTAAAAAAAA... |
Task1_train_34565 | Here is a variant on Chromosome 2. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CTAAAACAAACCTGAGCAAACAGTAGAAGATTAATACATATTAATAACATTTTAAAAATAATCTAATAACTCTAAGGTCTTAAGCACTTAATAAAATGAATGGGTTCCCATTTTTACATGTAAAAGTCATGAACTAAGGTTAAAGTGTAGAAAATAAACTAAAATTTCTAGTCTACTGTTTTTTCCTTTTTACCAACCCTGAAGATGAGGGTTCAGGTAAAAAAAAAAAAAAAAACTATTTCCCTTAGGGCTCATGGCCTACATGTTTGTTAAATCCAATTTGCTCAGCTTGTAAGTTCTGTGGAATGCACTGTCCATGA... | CTAAAACAAACCTGAGCAAACAGTAGAAGATTAATACATATTAATAACATTTTAAAAATAATCTAATAACTCTAAGGTCTTAAGCACTTAATAAAATGAATGGGTTCCCATTTTTACATGTAAAAGTCATGAACTAAGGTTAAAGTGTAGAAAATAAACTAAAATTTCTAGTCTACTGTTTTTTCCTTTTTACCAACCCTGAAGATGAGGGTTCAGGTAAAAAAAAAAAAAAAAACTATTTCCCTTAGGGCTCATGGCCTACATGTTTGTTAAATCCAATTTGCTCAGCTTGTAAGTTCTGTGGAATGCACTGTCCATGA... |
Task1_train_34566 | A mutation has occurred on Chromosome 2. What is the medical relevance of this mutation? | Benign | AACAAGATTCCTGGTGAATTGTATATATAAGTAGGTTTGAAAAGTGCTGGTACTGGAGCAAGACTGTCTGGTTTCAGATCCATGCTCTGTCACTAACTTGCTATGTTATTACCTTAGATACATTTTGGAATATTTCGGTTCTTCTCCTCAGTTGTAAAGTGGGGATTAAAATGATACCCCCCTTTATAATAGGGTTATTGTGAGGATTAAATGACTTAATGTGTTTAAGTTTTGTAGCAGTGTAAATCGAGTCAGTAAAGTGGCCACAGCAAGATAAAAATGGGAGAGACAGTGTAGCCTGTAGTGATGTGCTCTCACTG... | AACAAGATTCCTGGTGAATTGTATATATAAGTAGGTTTGAAAAGTGCTGGTACTGGAGCAAGACTGTCTGGTTTCAGATCCATGCTCTGTCACTAACTTGCTATGTTATTACCTTAGATACATTTTGGAATATTTCGGTTCTTCTCCTCAGTTGTAAAGTGGGGATTAAAATGATACCCCCCTTTATAATAGGGTTATTGTGAGGATTAAATGACTTAATGTGTTTAAGTTTTGTAGCAGTGTAAATCGAGTCAGTAAAGTGGCCACAGCAAGATAAAAATGGGAGAGACAGTGTAGCCTGTAGTGATGTGCTCTCACTG... |
Task1_train_34567 | The following genetic variant occurs on Chromosome 2. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TTAATGGCATCCAGAAGACCTTGTCTGTAGTATTGGGCACTGCTAGGTATCTGTTGCTGACATTTCCTGCTGCAACTGCCCTGTGCTTTTATGGATTAGCAATTACCACCTGTTCCCAATTTGGAGACACTTTCTTCATCTATGTCACATGCATTCATAAAATGACTGCAGGTCTGCAAGTCATCTTTTTTAATCGAGGTATTGGGATGCATCTCTTTCTGACTTACTGTATTGGTTTTACAGTTAAGCTGCCAGTTCAGTAGGCTATATTTTGGCCCCATTTCCCTTTTCAGGAATCTTCAATCCCCAAATTTATCATC... | TTAATGGCATCCAGAAGACCTTGTCTGTAGTATTGGGCACTGCTAGGTATCTGTTGCTGACATTTCCTGCTGCAACTGCCCTGTGCTTTTATGGATTAGCAATTACCACCTGTTCCCAATTTGGAGACACTTTCTTCATCTATGTCACATGCATTCATAAAATGACTGCAGGTCTGCAAGTCATCTTTTTTAATCGAGGTATTGGGATGCATCTCTTTCTGACTTACTGTATTGGTTTTACAGTTAAGCTGCCAGTTCAGTAGGCTATATTTTGGCCCCATTTCCCTTTTCAGGAATCTTCAATCCCCAAATTTATCATC... |
Task1_train_34568 | A mutation is present on Chromosome 2. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TGTACTAATTGACTACTATAGATATAAATCCCAACATTAACAACCTGATTAGATTTAGGCTCAGATTTATTACATGAATATATGACAAACCACCATTTTTGTGACTATGTATAAAATCATGCATTTATATTTTCTGGAAACATCAATAGCTTCAGATTCTCTGTAAAATCATGGAATGCAAAGGAGTAAAAGACTAAAAAGTAACAGTGCAAATTGTATGTGATAGTCAAGCAGCTTTTGATTTAAAGAAGGGTATGTTGGCATTTATTTATAATATGTATATACAAGCTTGTGCAAGTAATGTGTTGAATTGATATGTT... | TGTACTAATTGACTACTATAGATATAAATCCCAACATTAACAACCTGATTAGATTTAGGCTCAGATTTATTACATGAATATATGACAAACCACCATTTTTGTGACTATGTATAAAATCATGCATTTATATTTTCTGGAAACATCAATAGCTTCAGATTCTCTGTAAAATCATGGAATGCAAAGGAGTAAAAGACTAAAAAGTAACAGTGCAAATTGTATGTGATAGTCAAGCAGCTTTTGATTTAAAGAAGGGTATGTTGGCATTTATTTATAATATGTATATACAAGCTTGTGCAAGTAATGTGTTGAATTGATATGTT... |
Task1_train_34569 | A variant affecting Chromosome 2 has been observed. Determine if it's benign or associated with disease. | Benign | CCTCCAAGGATAAAACATTGATTGGATTTACCAAAATAGATTATAATTAGAGCTTAATTAATGAGCGAATACCGAGAGATTCTAATAGAAGATCTGATACAGTTTTTGTTTGAATTTGAGTTACCTCCTGTACTTTGAAGACATAATTTTGCATAAGTAATGCATATTTTTCTAAGAAGCAGTCAAATATTGTGTATCTTATATCTGCTGGGAATCATATCTCTGTAGTAATATTGCTCTCAGTAATTTCTTATAGCCACTTTTTTTATTTATAGATCATCTGTTTCTTATAGCCACATTTTTTTATTCATAGATCATCT... | CCTCCAAGGATAAAACATTGATTGGATTTACCAAAATAGATTATAATTAGAGCTTAATTAATGAGCGAATACCGAGAGATTCTAATAGAAGATCTGATACAGTTTTTGTTTGAATTTGAGTTACCTCCTGTACTTTGAAGACATAATTTTGCATAAGTAATGCATATTTTTCTAAGAAGCAGTCAAATATTGTGTATCTTATATCTGCTGGGAATCATATCTCTGTAGTAATATTGCTCTCAGTAATTTCTTATAGCCACTTTTTTTATTTATAGATCATCTGTTTCTTATAGCCACATTTTTTTATTCATAGATCATCT... |
Task1_train_34570 | This mutation on Chromosome 2 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | AGCCGAGATTGCGCCCCTACACTCCACTCTGGATGACACAGCAAGACTCTGTCACAAAAATAAATAAATAAGAAATATATTTTATGAAACAGTATTCATTTTGTGTCCATTGAGATTATATCATGCTTGATGGTAGGGATTCTTTTATACTTTATTCCAATAATGCCTGTACTCCCAAAAAAGATTGGCACACATTCCTGGTTTGTCAAGAATACATTTTGGCGACTGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGGATCACAAGGTCAGGAGATCGAGACCATCTTGGCTAACA... | AGCCGAGATTGCGCCCCTACACTCCACTCTGGATGACACAGCAAGACTCTGTCACAAAAATAAATAAATAAGAAATATATTTTATGAAACAGTATTCATTTTGTGTCCATTGAGATTATATCATGCTTGATGGTAGGGATTCTTTTATACTTTATTCCAATAATGCCTGTACTCCCAAAAAAGATTGGCACACATTCCTGGTTTGTCAAGAATACATTTTGGCGACTGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGGATCACAAGGTCAGGAGATCGAGACCATCTTGGCTAACA... |
Task1_train_34571 | A variant on Chromosome 2 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | ATTTTAGGGAAACCATCAGGCTTTTGCTTTGTTGAATTGATTAATCTTTTGATCAGAACTAAATTGTTCTGAAAAATTGGGAGTATTTTAGAAGCAGAATGAGAAGAGAGATAGATAGAGACCTGGAATCAAGAGGAACGGAAGCCTATAGGTTTTGGAGAGAGAGGAGATGAGTGGTAACAAAAGAAGGGATTTCTGTTCTTCAAGGTGTAAGGTTAAGACAACAGAGCTTCCAATAATTTGGAAGTATTTTCAGCACTTGGAGCGGGGCTAATTATTGGGGGTATATAACAAAGTCTTGAGTCTGTCCTTGGTGTGAG... | ATTTTAGGGAAACCATCAGGCTTTTGCTTTGTTGAATTGATTAATCTTTTGATCAGAACTAAATTGTTCTGAAAAATTGGGAGTATTTTAGAAGCAGAATGAGAAGAGAGATAGATAGAGACCTGGAATCAAGAGGAACGGAAGCCTATAGGTTTTGGAGAGAGAGGAGATGAGTGGTAACAAAAGAAGGGATTTCTGTTCTTCAAGGTGTAAGGTTAAGACAACAGAGCTTCCAATAATTTGGAAGTATTTTCAGCACTTGGAGCGGGGCTAATTATTGGGGGTATATAACAAAGTCTTGAGTCTGTCCTTGGTGTGAG... |
Task1_train_34572 | This is a variant located on Chromosome 2. Is this mutation a likely cause of disease or not? | Benign | CCCTTGAAGTAATGTAGACAGAAGTTCTCAAATTTGCATATTACATCAACTGGAACCAGCAGTGAATCTTAATGTTCACTTAAATCAGAACTTGCATAAGAAAGAGAATGGGAGTCTGGTTAAATAAAGATGACTATATCAGAGACTTGAAAAGGATCATTCTCTGTTTTCTGATAGTGTATATGGCCATTTTAGTGGGCACAGATCAGGATTTTTACAGTTTACTTGGAGTGTCCAAAACTGCAAGCAGTAGAGAAATAAGACAAGCTTTCAAGAAATTGGCATTGAAGTTACATCCTGATAAAAACCCGGTAGGTAAA... | CCCTTGAAGTAATGTAGACAGAAGTTCTCAAATTTGCATATTACATCAACTGGAACCAGCAGTGAATCTTAATGTTCACTTAAATCAGAACTTGCATAAGAAAGAGAATGGGAGTCTGGTTAAATAAAGATGACTATATCAGAGACTTGAAAAGGATCATTCTCTGTTTTCTGATAGTGTATATGGCCATTTTAGTGGGCACAGATCAGGATTTTTACAGTTTACTTGGAGTGTCCAAAACTGCAAGCAGTAGAGAAATAAGACAAGCTTTCAAGAAATTGGCATTGAAGTTACATCCTGATAAAAACCCGGTAGGTAAA... |
Task1_train_34573 | Given a variant located on Chromosome 2, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CCAGTCATTCTTGGTTCTAGAACAGAACTTTATGGCCTCTGTAGACATCCAGGCAGCCCTTGAAACTCTTTTATTATCCATGCAGAAACTTAAAGTTGCCTCTTTGCCTGTTATGATTTTAGTGATACATAGAGATAAAGGATAAATAGACCTTGATTTTTTACAAAACTAATGAGCAAAATCCAAACTTAAAAATCTAAGTTAGGTTTATTTTCATATTTTAAGATAATTCACATTGGATTTCTTTTAGCTATCCTTAAGCATCTTTTGGTTTCTCAAAAATGGGAACTTTCTAAAGGACATACACAGATTGAGCACCC... | CCAGTCATTCTTGGTTCTAGAACAGAACTTTATGGCCTCTGTAGACATCCAGGCAGCCCTTGAAACTCTTTTATTATCCATGCAGAAACTTAAAGTTGCCTCTTTGCCTGTTATGATTTTAGTGATACATAGAGATAAAGGATAAATAGACCTTGATTTTTTACAAAACTAATGAGCAAAATCCAAACTTAAAAATCTAAGTTAGGTTTATTTTCATATTTTAAGATAATTCACATTGGATTTCTTTTAGCTATCCTTAAGCATCTTTTGGTTTCTCAAAAATGGGAACTTTCTAAAGGACATACACAGATTGAGCACCC... |
Task1_train_34574 | A variant on Chromosome 2 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GCCATGTGTCCTGTCAACAACACAATGATATTGTTTTGGTACCAAAAGAGGAGCAGTAAGCCTTGTTACATGCTTCGCAGCAGGGATATTGAAAGCTTTTCCAACTGGTACAGGAATTTAGGACAAATTCCAGTTCTGCATTAGCAAGCAGAAAACCAAATTAAAGACAGTAAGAGATTCCAACATACTGAACAAGAGCCACTTTTTTCTTTAATAAACACCAAACTAATTGAAGAGAGATGCAGAGAGAATGCCCGCAAGTCTGAACTTGAAATGCATCTCCCTTTTGACAAATCTACTAAAGGGGAGAAGAACTTACT... | GCCATGTGTCCTGTCAACAACACAATGATATTGTTTTGGTACCAAAAGAGGAGCAGTAAGCCTTGTTACATGCTTCGCAGCAGGGATATTGAAAGCTTTTCCAACTGGTACAGGAATTTAGGACAAATTCCAGTTCTGCATTAGCAAGCAGAAAACCAAATTAAAGACAGTAAGAGATTCCAACATACTGAACAAGAGCCACTTTTTTCTTTAATAAACACCAAACTAATTGAAGAGAGATGCAGAGAGAATGCCCGCAAGTCTGAACTTGAAATGCATCTCCCTTTTGACAAATCTACTAAAGGGGAGAAGAACTTACT... |
Task1_train_34575 | A genomic variant on Chromosome 2 is under review. What is the biological outcome — benign or pathogenic? | Benign | CCCATTTCCTGAACTGGATATTGAGCTTTATCCTGTAGATGAAAATTTTAGAATTTCATTAGACGTATTTTGATAGAAAAATATTGCAAAAAACCTCCTAAATTACATTATTATAAATTAAAAAAAAATAACCTACATCATCTGGTCCTTTCACACATGGTGCTTCTTCTACTTCCCTACAAGCTTCCTTGGTATAGCTTATTAATACTAACAATGTTATCTCCTTTCTAATAACTAACTTTGGAAAGTTTACAAACCTTCCAAAGACATACTAGAAATCATACAGGTTATTAGTTCTTTCCAAAGTTGACGTGTCCAGA... | CCCATTTCCTGAACTGGATATTGAGCTTTATCCTGTAGATGAAAATTTTAGAATTTCATTAGACGTATTTTGATAGAAAAATATTGCAAAAAACCTCCTAAATTACATTATTATAAATTAAAAAAAAATAACCTACATCATCTGGTCCTTTCACACATGGTGCTTCTTCTACTTCCCTACAAGCTTCCTTGGTATAGCTTATTAATACTAACAATGTTATCTCCTTTCTAATAACTAACTTTGGAAAGTTTACAAACCTTCCAAAGACATACTAGAAATCATACAGGTTATTAGTTCTTTCCAAAGTTGACGTGTCCAGA... |
Task1_train_34576 | A variant found on Chromosome 2 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | TATTTTGATAGAAAAATATTGCAAAAAACCTCCTAAATTACATTATTATAAATTAAAAAAAAATAACCTACATCATCTGGTCCTTTCACACATGGTGCTTCTTCTACTTCCCTACAAGCTTCCTTGGTATAGCTTATTAATACTAACAATGTTATCTCCTTTCTAATAACTAACTTTGGAAAGTTTACAAACCTTCCAAAGACATACTAGAAATCATACAGGTTATTAGTTCTTTCCAAAGTTGACGTGTCCAGAGAATGCCTGCATTTTCAAAATGTAAACATAAAACAATATTTTTACGATAGCTGGAAATGGATTTA... | TATTTTGATAGAAAAATATTGCAAAAAACCTCCTAAATTACATTATTATAAATTAAAAAAAAATAACCTACATCATCTGGTCCTTTCACACATGGTGCTTCTTCTACTTCCCTACAAGCTTCCTTGGTATAGCTTATTAATACTAACAATGTTATCTCCTTTCTAATAACTAACTTTGGAAAGTTTACAAACCTTCCAAAGACATACTAGAAATCATACAGGTTATTAGTTCTTTCCAAAGTTGACGTGTCCAGAGAATGCCTGCATTTTCAAAATGTAAACATAAAACAATATTTTTACGATAGCTGGAAATGGATTTA... |
Task1_train_34577 | A variant affecting Chromosome 2 has been observed. Determine if it's benign or associated with disease. | Benign | TACATGTTTTTCCTCTGATAGAACTGTGTTCATACTGAATTCTAACAAATTATTGGGTGATCTGTTCCACAGAGTACAGAAGTTTTGCAAATTCTCGCTTTCTCCCGAGACTTGCAGACTCCCCCAAGTGGATATCTGAAAAATTTAGCCAAGTGCCTCTAAACAACTCTGACCCTTCATAATGAGCTTTGATCAAACCATACCAACTTTTTTTTCCCCTTTGTTTGAACTGAAGCATAATACAGGAAGAATGACTATGTAAATGTGGTAACTTCCCCTTTCTACCATCTATGAGTTATAATTTACTCACACTACTATTG... | TACATGTTTTTCCTCTGATAGAACTGTGTTCATACTGAATTCTAACAAATTATTGGGTGATCTGTTCCACAGAGTACAGAAGTTTTGCAAATTCTCGCTTTCTCCCGAGACTTGCAGACTCCCCCAAGTGGATATCTGAAAAATTTAGCCAAGTGCCTCTAAACAACTCTGACCCTTCATAATGAGCTTTGATCAAACCATACCAACTTTTTTTTCCCCTTTGTTTGAACTGAAGCATAATACAGGAAGAATGACTATGTAAATGTGGTAACTTCCCCTTTCTACCATCTATGAGTTATAATTTACTCACACTACTATTG... |
Task1_train_34578 | Given a variant located on Chromosome 2, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TCTATTTAAAATTATGTTTAAGATTCTTTTTCTAAAAAAGGATAAGAATTTTGCTTGAGAAGCAGACCAACATTAAGTGCGCTGTGAATAAATTCTAACTGGGCTGTTAGAGGTTCACAACTTTTAAACTTTGATCTGCTTCTAACAGTGAGCAGCTATTAGGTGTGAACAGTGTTGTAATTCAGACTTTACAATTCAAGCCAGGGCAAAGTTATTAAAAGAAGACTTTTTAAAAGTAGTCTTTGTTTCTCCAATCAATAAAGCCTCTCTTATTATTGTCTATATCAAAATTATTTCATTCCAAATCTACTTTTTGCTGA... | TCTATTTAAAATTATGTTTAAGATTCTTTTTCTAAAAAAGGATAAGAATTTTGCTTGAGAAGCAGACCAACATTAAGTGCGCTGTGAATAAATTCTAACTGGGCTGTTAGAGGTTCACAACTTTTAAACTTTGATCTGCTTCTAACAGTGAGCAGCTATTAGGTGTGAACAGTGTTGTAATTCAGACTTTACAATTCAAGCCAGGGCAAAGTTATTAAAAGAAGACTTTTTAAAAGTAGTCTTTGTTTCTCCAATCAATAAAGCCTCTCTTATTATTGTCTATATCAAAATTATTTCATTCCAAATCTACTTTTTGCTGA... |
Task1_train_34579 | Here is a mutation located on Chromosome 2. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | ATAAAGCACATATTTTACATTATATGTACACACAGCCACACATACATGATTTTCCCATTAATTTTATGCTTCAAAAGATGGGAAAAGAAGTCATTCTGTTACTTAGCAGATAAAGCTAAATGAAGCAATACATTGTGTTAGTGGTTAGATAAAGGAAATATCCAACTAAAATTTTCTTGTCTACTTATAATATTTAAAACACTGAATTTTTAGAATAGCAGGAATTTTCTTCACACAGAGTTCTGCTAAGGATAAGGTTTAGGGTTTCTTATATTTATGTGTTTGTCAGTATAGTTCTTTTCATCAGAACTCACTACAGT... | ATAAAGCACATATTTTACATTATATGTACACACAGCCACACATACATGATTTTCCCATTAATTTTATGCTTCAAAAGATGGGAAAAGAAGTCATTCTGTTACTTAGCAGATAAAGCTAAATGAAGCAATACATTGTGTTAGTGGTTAGATAAAGGAAATATCCAACTAAAATTTTCTTGTCTACTTATAATATTTAAAACACTGAATTTTTAGAATAGCAGGAATTTTCTTCACACAGAGTTCTGCTAAGGATAAGGTTTAGGGTTTCTTATATTTATGTGTTTGTCAGTATAGTTCTTTTCATCAGAACTCACTACAGT... |
Task1_train_34580 | This sequence change occurs on Chromosome 2. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CACATACATGATTTTCCCATTAATTTTATGCTTCAAAAGATGGGAAAAGAAGTCATTCTGTTACTTAGCAGATAAAGCTAAATGAAGCAATACATTGTGTTAGTGGTTAGATAAAGGAAATATCCAACTAAAATTTTCTTGTCTACTTATAATATTTAAAACACTGAATTTTTAGAATAGCAGGAATTTTCTTCACACAGAGTTCTGCTAAGGATAAGGTTTAGGGTTTCTTATATTTATGTGTTTGTCAGTATAGTTCTTTTCATCAGAACTCACTACAGTGTAATGTAATTCCAAATAAGTTATATTTTAAGTGAATT... | CACATACATGATTTTCCCATTAATTTTATGCTTCAAAAGATGGGAAAAGAAGTCATTCTGTTACTTAGCAGATAAAGCTAAATGAAGCAATACATTGTGTTAGTGGTTAGATAAAGGAAATATCCAACTAAAATTTTCTTGTCTACTTATAATATTTAAAACACTGAATTTTTAGAATAGCAGGAATTTTCTTCACACAGAGTTCTGCTAAGGATAAGGTTTAGGGTTTCTTATATTTATGTGTTTGTCAGTATAGTTCTTTTCATCAGAACTCACTACAGTGTAATGTAATTCCAAATAAGTTATATTTTAAGTGAATT... |
Task1_train_34581 | This alteration on Chromosome 2 may affect genome function. Does it lead to a disease or is it benign? | Benign | AATATTTAAAACACTGAATTTTTAGAATAGCAGGAATTTTCTTCACACAGAGTTCTGCTAAGGATAAGGTTTAGGGTTTCTTATATTTATGTGTTTGTCAGTATAGTTCTTTTCATCAGAACTCACTACAGTGTAATGTAATTCCAAATAAGTTATATTTTAAGTGAATTGTCTTTTATCTTGCATTTACTGCATGTTATGATATAATGTATAACTTCAGGATAATTTTAAATATTGAGACTAACAATTTCAAAAGAGTCAAAGCTCTCATAAAGCTAGTACTATCTCTTAGTTACCTTTGCCCATACCAATTGGGCTAT... | AATATTTAAAACACTGAATTTTTAGAATAGCAGGAATTTTCTTCACACAGAGTTCTGCTAAGGATAAGGTTTAGGGTTTCTTATATTTATGTGTTTGTCAGTATAGTTCTTTTCATCAGAACTCACTACAGTGTAATGTAATTCCAAATAAGTTATATTTTAAGTGAATTGTCTTTTATCTTGCATTTACTGCATGTTATGATATAATGTATAACTTCAGGATAATTTTAAATATTGAGACTAACAATTTCAAAAGAGTCAAAGCTCTCATAAAGCTAGTACTATCTCTTAGTTACCTTTGCCCATACCAATTGGGCTAT... |
Task1_train_34582 | This mutation on Chromosome 2 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | AATATCACAGAAGAGGCCATGAAGGTAGACAATTTTGGTCAGATAGAACTGGTTAAGAGCATATCCTCAACATTGCTCATAACAGCTATAAAAGCAACTTCAGGACAATATTTCCAAGTTATTCCAAACAGTAACCAACAAGTAAATGATATTGTGGCACCATGGAAAGTACTTACACCATATGAAGGCAATTCTGTCACAAAGATTTTAAAATTTGAAAAAATATTATAATGACTTTTTAAAGATGAAAATATTTGACTATTTTTTTTTCTCAAAAGTGTGCTATTTAACACATGCTTCTGTTTCTCTCTCTAGTGCTC... | AATATCACAGAAGAGGCCATGAAGGTAGACAATTTTGGTCAGATAGAACTGGTTAAGAGCATATCCTCAACATTGCTCATAACAGCTATAAAAGCAACTTCAGGACAATATTTCCAAGTTATTCCAAACAGTAACCAACAAGTAAATGATATTGTGGCACCATGGAAAGTACTTACACCATATGAAGGCAATTCTGTCACAAAGATTTTAAAATTTGAAAAAATATTATAATGACTTTTTAAAGATGAAAATATTTGACTATTTTTTTTTCTCAAAAGTGTGCTATTTAACACATGCTTCTGTTTCTCTCTCTAGTGCTC... |
Task1_train_34583 | Here’s a variant located on Chromosome 2. What is the predicted biological effect — harmless or disease-causing? | Benign | ATTCCAAACAGTAACCAACAAGTAAATGATATTGTGGCACCATGGAAAGTACTTACACCATATGAAGGCAATTCTGTCACAAAGATTTTAAAATTTGAAAAAATATTATAATGACTTTTTAAAGATGAAAATATTTGACTATTTTTTTTTCTCAAAAGTGTGCTATTTAACACATGCTTCTGTTTCTCTCTCTAGTGCTCCTGGAAGTGGCCCCATGTTCAAATCAACAACTGTTACTGTGAGAGAAAACTGTAATGAAATTTCCCAACGAGTTGTTGTGGATTCAGTTAATAACCAGCAAGATTTCAAATATACTTTGA... | ATTCCAAACAGTAACCAACAAGTAAATGATATTGTGGCACCATGGAAAGTACTTACACCATATGAAGGCAATTCTGTCACAAAGATTTTAAAATTTGAAAAAATATTATAATGACTTTTTAAAGATGAAAATATTTGACTATTTTTTTTTCTCAAAAGTGTGCTATTTAACACATGCTTCTGTTTCTCTCTCTAGTGCTCCTGGAAGTGGCCCCATGTTCAAATCAACAACTGTTACTGTGAGAGAAAACTGTAATGAAATTTCCCAACGAGTTGTTGTGGATTCAGTTAATAACCAGCAAGATTTCAAATATACTTTGA... |
Task1_train_34584 | A variant on Chromosome 2 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CATTGGCCCCTTCAAATACTGAAGAGGTTAACATAACTATACATAAGAAAACAAATTTCTGCAAAAGACAATGTGAGCCATTTGTACCTGTCCTTAACAAACACAGATCTACAGTTCTTCAGTGGCCATCAGAAATGCTGGTTTATACAACTACGAAACCATCAATTTCCTATAGCTGTAATCCTCTATGTTTTGACTTCAAGTCTACTAAAGTAAATAATAATCTAGATAAAAATAAGCCAGACTTAAAAGATCTTTGTTCTCAGCAGAAGCAGGAAGACATTTGCATGGGACCACTTTCAGATTACAAGGATGTATCT... | CATTGGCCCCTTCAAATACTGAAGAGGTTAACATAACTATACATAAGAAAACAAATTTCTGCAAAAGACAATGTGAGCCATTTGTACCTGTCCTTAACAAACACAGATCTACAGTTCTTCAGTGGCCATCAGAAATGCTGGTTTATACAACTACGAAACCATCAATTTCCTATAGCTGTAATCCTCTATGTTTTGACTTCAAGTCTACTAAAGTAAATAATAATCTAGATAAAAATAAGCCAGACTTAAAAGATCTTTGTTCTCAGCAGAAGCAGGAAGACATTTGCATGGGACCACTTTCAGATTACAAGGATGTATCT... |
Task1_train_34585 | This alteration occurs on Chromosome 2. Is it associated with a disease or is it a benign variant? | Benign | TATGAACTCTCTCCTTCAGCAGCATAGTACTGATTGTTTAGGGATACTGAGTTTTATTCATGAAACATGATCCATTTTCCTGGCAGAAAAAGTGTTAAGTTAGCTTTGTGCTAAACACACTACGGATTTTAGCAGAAAATAACCCAAACAAACATTTGGCAGTAATAATAATAATGACAGCTTGCATTTATTGAGCATATACTATTGACTAGGTGTTGTACTAAGCTAGAATGAAGGAAAACAATAATTGGGTAATATAAGATAAATTAAATATAAGAAATTGGGTAATATAAGATAAAAAGAATAAGACATAATTGCTC... | TATGAACTCTCTCCTTCAGCAGCATAGTACTGATTGTTTAGGGATACTGAGTTTTATTCATGAAACATGATCCATTTTCCTGGCAGAAAAAGTGTTAAGTTAGCTTTGTGCTAAACACACTACGGATTTTAGCAGAAAATAACCCAAACAAACATTTGGCAGTAATAATAATAATGACAGCTTGCATTTATTGAGCATATACTATTGACTAGGTGTTGTACTAAGCTAGAATGAAGGAAAACAATAATTGGGTAATATAAGATAAATTAAATATAAGAAATTGGGTAATATAAGATAAAAAGAATAAGACATAATTGCTC... |
Task1_train_34586 | Consider a variant on Chromosome 2. Determine its clinical classification and disease relevance. | Benign | TCCCTACTCTTTGATTCCCAAATCTAGCTTGGCTTTTATTTTCTATCTAAATTTTAATTTGTTACCTTACTTTAGTATCTGTTCTCAGCTTTCCTATCTAGGACAATTTGTATTTATTTGTATTATTTTATTTTATTTTTATTTTATTTGTATTATTTGTATTTATTTGTATTATCGCTTTTATTGGATACAAAGCCCGTCAATCTATATAAAGCATTAGCTTTTATTTTTGCCTATCAAATAATTCTTAACAATTAACTTTAGTCATTCCTATATATATAGACCACAGGCTCACCCTTTCAGCAGGGACTGGGAGAGAA... | TCCCTACTCTTTGATTCCCAAATCTAGCTTGGCTTTTATTTTCTATCTAAATTTTAATTTGTTACCTTACTTTAGTATCTGTTCTCAGCTTTCCTATCTAGGACAATTTGTATTTATTTGTATTATTTTATTTTATTTTTATTTTATTTGTATTATTTGTATTTATTTGTATTATCGCTTTTATTGGATACAAAGCCCGTCAATCTATATAAAGCATTAGCTTTTATTTTTGCCTATCAAATAATTCTTAACAATTAACTTTAGTCATTCCTATATATATAGACCACAGGCTCACCCTTTCAGCAGGGACTGGGAGAGAA... |
Task1_train_34587 | A variant has been detected on Chromosome 2. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TATATAGACCACAGGCTCACCCTTTCAGCAGGGACTGGGAGAGAAAATGCTTTATGTTCCTTCCCCACATCTCAGCTAGGCAGATGTTTCTGAAAGCATCCAAATATTTTGACTGGATCTGTCTTGAGAAATGTTTTGTTAGAAATATTTAATGTATCTTTAAAAATTAGCTGGATCATAAACATCACATATTTTCTTTCCAAAATATTTGCATGTTGTGTGCCTAGACAGCAATTTAGTGATATTTTTAACAAAAAAAAAATCATTTATACTGATAATAAATGCCAGGGGAAAAAGAAACTTCTGAGAGACTGTGAATA... | TATATAGACCACAGGCTCACCCTTTCAGCAGGGACTGGGAGAGAAAATGCTTTATGTTCCTTCCCCACATCTCAGCTAGGCAGATGTTTCTGAAAGCATCCAAATATTTTGACTGGATCTGTCTTGAGAAATGTTTTGTTAGAAATATTTAATGTATCTTTAAAAATTAGCTGGATCATAAACATCACATATTTTCTTTCCAAAATATTTGCATGTTGTGTGCCTAGACAGCAATTTAGTGATATTTTTAACAAAAAAAAAATCATTTATACTGATAATAAATGCCAGGGGAAAAAGAAACTTCTGAGAGACTGTGAATA... |
Task1_train_34588 | A change on Chromosome 2 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GCTTGATTCAACTTTCAAAGATGAAAAAGTAAAATCACAAGAACAGATTCCTAATCATTGGTTTACAAAGGGAAACACTTGTTTTGAATGCAAAAGAAATATCAAACCACCTACAAAGCCTGGTTCTAGAAGCAAAGCTGCATTTCATGATTGGGAATTAAAGACTGAGCCACCATCTACTAATCATGAAGATATTTTAAAGAAAAAACTTTCTTCGAATAAAGACATTTCAACTTTCAGCCAAGATCAAAAGCATCAAATAGAAAAGGCTTCAGAAAACATAGTCACAAGTATTTTAAAGGAAATGCTCAAGGACATAT... | GCTTGATTCAACTTTCAAAGATGAAAAAGTAAAATCACAAGAACAGATTCCTAATCATTGGTTTACAAAGGGAAACACTTGTTTTGAATGCAAAAGAAATATCAAACCACCTACAAAGCCTGGTTCTAGAAGCAAAGCTGCATTTCATGATTGGGAATTAAAGACTGAGCCACCATCTACTAATCATGAAGATATTTTAAAGAAAAAACTTTCTTCGAATAAAGACATTTCAACTTTCAGCCAAGATCAAAAGCATCAAATAGAAAAGGCTTCAGAAAACATAGTCACAAGTATTTTAAAGGAAATGCTCAAGGACATAT... |
Task1_train_34589 | Chromosome 2 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AAAAGCTATCTCAGAGTCTCTTGACATTGACAACCCATCATTTGCTTCAATTATTGAGAAAATGGCCAAATCCACCAAAATAATCTCCAGCATAGTTTCCAGAAGGGTTCAGGAGGACAATAAAGAAGAGACTAAAAGCAAGGCAAAACCTGTTGCTCCTGTGTCTTCCAAAACACCAAGCACAAAAGAAATGCATCCAAATAAACTAAAAGCTGTAGCTTCAGATATTCTTAATATGGTTTTTGCTAAACTGGAAGGGTTTGCCAACGGACATTTAGAAATTTTGGGTGCTATTAATGATGGAAATAAGAAAAGCAATA... | AAAAGCTATCTCAGAGTCTCTTGACATTGACAACCCATCATTTGCTTCAATTATTGAGAAAATGGCCAAATCCACCAAAATAATCTCCAGCATAGTTTCCAGAAGGGTTCAGGAGGACAATAAAGAAGAGACTAAAAGCAAGGCAAAACCTGTTGCTCCTGTGTCTTCCAAAACACCAAGCACAAAAGAAATGCATCCAAATAAACTAAAAGCTGTAGCTTCAGATATTCTTAATATGGTTTTTGCTAAACTGGAAGGGTTTGCCAACGGACATTTAGAAATTTTGGGTGCTATTAATGATGGAAATAAGAAAAGCAATA... |
Task1_train_34590 | Chromosome 2 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GAGACTAAAAGCAAGGCAAAACCTGTTGCTCCTGTGTCTTCCAAAACACCAAGCACAAAAGAAATGCATCCAAATAAACTAAAAGCTGTAGCTTCAGATATTCTTAATATGGTTTTTGCTAAACTGGAAGGGTTTGCCAACGGACATTTAGAAATTTTGGGTGCTATTAATGATGGAAATAAGAAAAGCAATAAGATAGGCTGGGAATATGAAAGCACCAATATTTCCAGAGACACACATGAAGCATCATTTCTGTCTGCTTTATATATGCATGCAAAGAAGGTATCAAGTGCTATTTTGAAGGTTATTCAAACAGAATT... | GAGACTAAAAGCAAGGCAAAACCTGTTGCTCCTGTGTCTTCCAAAACACCAAGCACAAAAGAAATGCATCCAAATAAACTAAAAGCTGTAGCTTCAGATATTCTTAATATGGTTTTTGCTAAACTGGAAGGGTTTGCCAACGGACATTTAGAAATTTTGGGTGCTATTAATGATGGAAATAAGAAAAGCAATAAGATAGGCTGGGAATATGAAAGCACCAATATTTCCAGAGACACACATGAAGCATCATTTCTGTCTGCTTTATATATGCATGCAAAGAAGGTATCAAGTGCTATTTTGAAGGTTATTCAAACAGAATT... |
Task1_train_34591 | This is a variant located on Chromosome 2. Is this mutation a likely cause of disease or not? | Benign | TCGAAAAAACCTTAAACAAAATTGAAGTAAAACTCAAAGAACCACATATATCTCCAATTGCTCCCATTATAAGAAATATTTTGAATGAAATTTTTCAAAGTACTTTAATCAATCAATTAAATGTCCTTTCTCTCTCCCACTCTAATTTTAATGGCATGCCTCACAATGTTGATGAGCCAACTCCCCAAACATCTGTTCAATTTATGGATAAAATGATGGATCCTTTACTTTCGGAAGCAGATATAACCATAGTAACAGATAATATTGTTAGGACTGTATTTCACAAACTTTATTCAGCTGCCATGACAGAAAGAAATGTA... | TCGAAAAAACCTTAAACAAAATTGAAGTAAAACTCAAAGAACCACATATATCTCCAATTGCTCCCATTATAAGAAATATTTTGAATGAAATTTTTCAAAGTACTTTAATCAATCAATTAAATGTCCTTTCTCTCTCCCACTCTAATTTTAATGGCATGCCTCACAATGTTGATGAGCCAACTCCCCAAACATCTGTTCAATTTATGGATAAAATGATGGATCCTTTACTTTCGGAAGCAGATATAACCATAGTAACAGATAATATTGTTAGGACTGTATTTCACAAACTTTATTCAGCTGCCATGACAGAAAGAAATGTA... |
Task1_train_34592 | This mutation occurs on Chromosome 2. Does this change lead to a known medical condition, or is it benign? | Benign | GGTAGTTGTGACATCATTATATGAAAATAATAAAAGTAGGACAGAAGTTGAAATATCTGACCACAATGATTCCTTACTAATGAAACCATTAAGGTTTAGAGAAACTAAACAAGCAGGAAAAATAAGTAATTCCCCTAGATATGCGATATCACAGGCTTATTCTTATGTCGACAGTCAAAATATCTCTGTGATGGAAAACACTCTTTTGCCATATTTACCATTGCAAGTGAAGAAAGACTTAATTCAAATGGTTCTCAATAAGATCACAAATTTTGTCTCACTTCCTTTAAAGGTGAGCCCTAAGGACAACCCTAAGCCAT... | GGTAGTTGTGACATCATTATATGAAAATAATAAAAGTAGGACAGAAGTTGAAATATCTGACCACAATGATTCCTTACTAATGAAACCATTAAGGTTTAGAGAAACTAAACAAGCAGGAAAAATAAGTAATTCCCCTAGATATGCGATATCACAGGCTTATTCTTATGTCGACAGTCAAAATATCTCTGTGATGGAAAACACTCTTTTGCCATATTTACCATTGCAAGTGAAGAAAGACTTAATTCAAATGGTTCTCAATAAGATCACAAATTTTGTCTCACTTCCTTTAAAGGTGAGCCCTAAGGACAACCCTAAGCCAT... |
Task1_train_34593 | Mutation context: Chromosome 2. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TCCCAAGATGGACGGTAATGTAGCTACAACTACAAACTCTTAAATAGACTTACTCCAGGCATGACTTAATTGATTTCAGAAAAATAAACAAAAGCAAAACAAGCAAGAGAAGATCCATGATTTCATCACATTGACACTTGGCTCTAACAATTCTATATTCCTATTCTCAGACATCTCCAAGGTCTTCCAGTGACTTCGCTCATGTTCCTTCTTCCACTAGGAATACCTTTTCCTCATTCCCTGTATCTTGACATGGCCAAAACCTGTGTAGCAGTCAAAGCTCAGCTTAAAGTCTTCTATCTGTGTAGAGTCTTGCCTGA... | TCCCAAGATGGACGGTAATGTAGCTACAACTACAAACTCTTAAATAGACTTACTCCAGGCATGACTTAATTGATTTCAGAAAAATAAACAAAAGCAAAACAAGCAAGAGAAGATCCATGATTTCATCACATTGACACTTGGCTCTAACAATTCTATATTCCTATTCTCAGACATCTCCAAGGTCTTCCAGTGACTTCGCTCATGTTCCTTCTTCCACTAGGAATACCTTTTCCTCATTCCCTGTATCTTGACATGGCCAAAACCTGTGTAGCAGTCAAAGCTCAGCTTAAAGTCTTCTATCTGTGTAGAGTCTTGCCTGA... |
Task1_train_34594 | A variant was discovered on Chromosome 2. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CAGCAGTTGGCCATTGCAAATAGGTAATGATTTGTAACAAATAGAATTTTGGACAAAACAAATATAGAGTTCTTCACCTGGCTGGGCCAACCTTCCTTCTTTGTGACAAACTATAATCTAGGGACTAAAGTACTACTGCTATTGCAATCTATTACTAGCTTTTCTGGAGTTGCCACACTTTTATTTTAGTCAACTTGATATTGCAACACAACTCCTTAATGTCCTAAAAGTAAAACATAGCATAACATTAAATGTTTTGTCTAAAGCTATTTTAAAATAATTATATGGCACCTCTAGGTATCACTGGAGACATGGTAGGA... | CAGCAGTTGGCCATTGCAAATAGGTAATGATTTGTAACAAATAGAATTTTGGACAAAACAAATATAGAGTTCTTCACCTGGCTGGGCCAACCTTCCTTCTTTGTGACAAACTATAATCTAGGGACTAAAGTACTACTGCTATTGCAATCTATTACTAGCTTTTCTGGAGTTGCCACACTTTTATTTTAGTCAACTTGATATTGCAACACAACTCCTTAATGTCCTAAAAGTAAAACATAGCATAACATTAAATGTTTTGTCTAAAGCTATTTTAAAATAATTATATGGCACCTCTAGGTATCACTGGAGACATGGTAGGA... |
Task1_train_34595 | Chromosome 2 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TTATCAGAATACTTTTGGAAGAATGCACAAGCACTGCTTTTCCTGATAAAGGGTCTGTTTCAGAGGAAACATCAGCAGAAGAATGTCAACTTTTAAAAATGCTTCAAAGTGTAGAAGATGGAAAATCTGATTATCGTAAGGGAGGAATGGACTGTGAATGCCTTCAAGTAGATTACATGTCAGACCTTTTGGAGAATGTGGCAGAAATTGATCAAGACTTATTGACATCAGACTCTATGCTTACTATTATTTCCCACAGCTTGGTTAAATCATTGATGGACAAATTATCTCACAGCATACAACAAGCTCCGGAAAGTCTA... | TTATCAGAATACTTTTGGAAGAATGCACAAGCACTGCTTTTCCTGATAAAGGGTCTGTTTCAGAGGAAACATCAGCAGAAGAATGTCAACTTTTAAAAATGCTTCAAAGTGTAGAAGATGGAAAATCTGATTATCGTAAGGGAGGAATGGACTGTGAATGCCTTCAAGTAGATTACATGTCAGACCTTTTGGAGAATGTGGCAGAAATTGATCAAGACTTATTGACATCAGACTCTATGCTTACTATTATTTCCCACAGCTTGGTTAAATCATTGATGGACAAATTATCTCACAGCATACAACAAGCTCCGGAAAGTCTA... |
Task1_train_34596 | This variant is located on Chromosome 2. Evaluate its biological effect and specify any disease association. | Benign | AAAGATGGTGGATTCTGTATATTGTAATATTTTGCAAATGTCTGACTCTCTTGTTTCAATACAAAAAAGTATAGTAAGCCGAAGCCCAATTATGATTGACCAAATAGCCAGCTTTATCATCCAAGAGATTATCGAAAATCATCTTCAACCATTTTTGAGTGGAGAGGTTTTATGTCATCCAAGGACTCCACTGGATCCAGTGTCTACTATTGTTACACAGGTTCTGAGTGAAGTGATAGAGTCACACAGACCTCAGAAGCAATCACCTTTAGATATTCACCTTGATTCATTTGTAAGGGAGATTGTTGCCAGACTTTTGT... | AAAGATGGTGGATTCTGTATATTGTAATATTTTGCAAATGTCTGACTCTCTTGTTTCAATACAAAAAAGTATAGTAAGCCGAAGCCCAATTATGATTGACCAAATAGCCAGCTTTATCATCCAAGAGATTATCGAAAATCATCTTCAACCATTTTTGAGTGGAGAGGTTTTATGTCATCCAAGGACTCCACTGGATCCAGTGTCTACTATTGTTACACAGGTTCTGAGTGAAGTGATAGAGTCACACAGACCTCAGAAGCAATCACCTTTAGATATTCACCTTGATTCATTTGTAAGGGAGATTGTTGCCAGACTTTTGT... |
Task1_train_34597 | This mutation occurs on Chromosome 2. Does this change lead to a known medical condition, or is it benign? | Benign | TAAAAGAAATCTTTAACCATCATATTCAATCATTTTTATCTGAAGATAAAACTCTCCTTTTGGCAGCAGTTGATCAAACTTATAAATTGAAAGCAATAGATCCTAAACAAAGAGAATTATCTTTTATTGTGAACTCATCTGTCTTTTTGGAGGAAGTAATTTCTGAGCTCTTATGCAAAATTCTTTATGCATTTTCACATAACATGTTGGTTACTGAAAATCCAGATAGAGTGAAACTGAAACTTACCAGGATTGTTACAACATTGGTAAATTCAATTGTTCTGGAGTTCACCACATCAGAGATTTTAGTTGCAGATAAC... | TAAAAGAAATCTTTAACCATCATATTCAATCATTTTTATCTGAAGATAAAACTCTCCTTTTGGCAGCAGTTGATCAAACTTATAAATTGAAAGCAATAGATCCTAAACAAAGAGAATTATCTTTTATTGTGAACTCATCTGTCTTTTTGGAGGAAGTAATTTCTGAGCTCTTATGCAAAATTCTTTATGCATTTTCACATAACATGTTGGTTACTGAAAATCCAGATAGAGTGAAACTGAAACTTACCAGGATTGTTACAACATTGGTAAATTCAATTGTTCTGGAGTTCACCACATCAGAGATTTTAGTTGCAGATAAC... |
Task1_train_34598 | A mutation is present on Chromosome 2. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TAACATGTTGGTTACTGAAAATCCAGATAGAGTGAAACTGAAACTTACCAGGATTGTTACAACATTGGTAAATTCAATTGTTCTGGAGTTCACCACATCAGAGATTTTAGTTGCAGATAACTTTGATAAAAATTTGTGTTTCTCAGAAAGATACAAAGAAATGGTTCAAAAAATAGTCAACTCAGTATATGGAAAAGTATTAGATCAATATAAATCTCTGATTCAAATACATAGGGTTATACAAAGTGACACAATATGTTTTGGTAGGAAAATATATTATTTGCTATTGGAAGAAATATATGATTATCAAGTGCAGTCAT... | TAACATGTTGGTTACTGAAAATCCAGATAGAGTGAAACTGAAACTTACCAGGATTGTTACAACATTGGTAAATTCAATTGTTCTGGAGTTCACCACATCAGAGATTTTAGTTGCAGATAACTTTGATAAAAATTTGTGTTTCTCAGAAAGATACAAAGAAATGGTTCAAAAAATAGTCAACTCAGTATATGGAAAAGTATTAGATCAATATAAATCTCTGATTCAAATACATAGGGTTATACAAAGTGACACAATATGTTTTGGTAGGAAAATATATTATTTGCTATTGGAAGAAATATATGATTATCAAGTGCAGTCAT... |
Task1_train_34599 | A mutation on Chromosome 2 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CAGAAATGTGCTTAACATAATCACAAAGGATAGCCATGCCTTGCCACCATATATTACTGTGTTGCCTCATTCTCTTTTAGAAGATATGGTTTACAGGCTTCTAGGGCATGTCTTCCCTTCAACTCACACTGAAAATGAACTAAAAGAGAAAAAGTTTCCACCGGATGATGAATTTGTGGAGGCAGCTTCAAAATTGACTGATGAAATTATAAAAGAAATTTCTGAACATGAGATTCGACTTTCCATGGCAGAGGATAATGCAGAAAGTATGCAGTTAGAACCTATTGAAAATTTGGTCGACTCCATATGTAATAATATTT... | CAGAAATGTGCTTAACATAATCACAAAGGATAGCCATGCCTTGCCACCATATATTACTGTGTTGCCTCATTCTCTTTTAGAAGATATGGTTTACAGGCTTCTAGGGCATGTCTTCCCTTCAACTCACACTGAAAATGAACTAAAAGAGAAAAAGTTTCCACCGGATGATGAATTTGTGGAGGCAGCTTCAAAATTGACTGATGAAATTATAAAAGAAATTTCTGAACATGAGATTCGACTTTCCATGGCAGAGGATAATGCAGAAAGTATGCAGTTAGAACCTATTGAAAATTTGGTCGACTCCATATGTAATAATATTT... |
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