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_38300 | This variant lies on Chromosome 7. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TGAACCAAGATTGTGGCATTGCACTCCAGCCTGGGCAACAAGAGCAAAACCCTGTCTCAAAAAAAAAAAAACCTCAACATTCAACCATTCCCCAGGCCAGCTGCATCAGAACTCCTGCGGGTGAACGCAAGCATCAGTATTATTAAAAGTCCCAAGGCTATTCTAAATTTGGAGAATATTAATGTAGAGCATGCTTTGTACACAAGTGCTTCCCAACCCTTACTGCACATCATTACCCAAGAAGCTCTTAGAAATGACTGTCCTCGGCCGGGCACGGTGGCTCACACCTGTAATCTCAGCACTTTAGGAGGCTGAGGCGG... | TGAACCAAGATTGTGGCATTGCACTCCAGCCTGGGCAACAAGAGCAAAACCCTGTCTCAAAAAAAAAAAAACCTCAACATTCAACCATTCCCCAGGCCAGCTGCATCAGAACTCCTGCGGGTGAACGCAAGCATCAGTATTATTAAAAGTCCCAAGGCTATTCTAAATTTGGAGAATATTAATGTAGAGCATGCTTTGTACACAAGTGCTTCCCAACCCTTACTGCACATCATTACCCAAGAAGCTCTTAGAAATGACTGTCCTCGGCCGGGCACGGTGGCTCACACCTGTAATCTCAGCACTTTAGGAGGCTGAGGCGG... |
Task1_train_38301 | Here is a mutation located on Chromosome 7. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TAAAAATACAAAAACTAGCCAGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGTGAGGCAGCAGTTGCAGTGAGCCAAAATCACGCCACCACACTCCAGCCTGGGCGACAGAGCAAGACTCCATCTCAAAATAATAATAATAATAGAACTTCTTGCCCCAAATCCTTACCATGCTCCAGAAGAACCCACCTGACCTGTCTTGCTCCCAGCCTCTCCCTGAGCACCCCACCCCAGCTCTGCAAGTCCTCTGGAAGTCCCTTCCACATCTCAACCATCACAGACTC... | TAAAAATACAAAAACTAGCCAGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGTGAGGCAGCAGTTGCAGTGAGCCAAAATCACGCCACCACACTCCAGCCTGGGCGACAGAGCAAGACTCCATCTCAAAATAATAATAATAATAGAACTTCTTGCCCCAAATCCTTACCATGCTCCAGAAGAACCCACCTGACCTGTCTTGCTCCCAGCCTCTCCCTGAGCACCCCACCCCAGCTCTGCAAGTCCTCTGGAAGTCCCTTCCACATCTCAACCATCACAGACTC... |
Task1_train_38302 | Here is a variant on Chromosome 7. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CGTATGTGCTAGACTTCCATGGGACTGGCAGTGCAGTGGGTTTGTTTACACCAGCATCACCACACTCACGAGGCACGCGTTGCCCTTGGACTGTTACAGTGACGGGAGTTTTCAGCTATGTTGTGATCTTATGGACCGCCATCATATGTGGTCTGTTGTTGACCGTATGTATGAGGTACATGACTGTACTTTGTAAAGGCCCTTCAAGGATTCTGAAATTATAGATAATAAAACCTGCCCCACAATTTAAAAAAAAAATCATGTCATGTTAGTGAAGAATGTGAATGTAACGTTGGTCAGGAGTGAGAGGAAGGGAATTT... | CGTATGTGCTAGACTTCCATGGGACTGGCAGTGCAGTGGGTTTGTTTACACCAGCATCACCACACTCACGAGGCACGCGTTGCCCTTGGACTGTTACAGTGACGGGAGTTTTCAGCTATGTTGTGATCTTATGGACCGCCATCATATGTGGTCTGTTGTTGACCGTATGTATGAGGTACATGACTGTACTTTGTAAAGGCCCTTCAAGGATTCTGAAATTATAGATAATAAAACCTGCCCCACAATTTAAAAAAAAAATCATGTCATGTTAGTGAAGAATGTGAATGTAACGTTGGTCAGGAGTGAGAGGAAGGGAATTT... |
Task1_train_38303 | This sequence variant lies on Chromosome 7. Is it clinically significant, and what condition might it cause if any? | Benign | TCCCAACCTAAGGATAGGCCAGCTTGGACACTCGCTCCCTCGGCCAGGGGACTCTGGCCTCACCTAGGCCAGGTAGCGTGAGGGTGAGGTAGGTGGCTGTGCAGACAAGCCCAGGCCACAGCAGCTTTCATTATTAACCCCGAGGATATATCGAAAGCTCTGCGGGAATCAAAGGACAAAGTTAATTTACTACAGAACGTTTTGCTAAAGCCTCTGATTCCTCATAATTTGTCAGTAATTGGAGGAGCTGCTGGCTGTGTTTGGAGGTGGCCCCTCTACCTTTGAGGGTCCAAGAGAAATCAGAGAAAGGGAGTCGAGAG... | TCCCAACCTAAGGATAGGCCAGCTTGGACACTCGCTCCCTCGGCCAGGGGACTCTGGCCTCACCTAGGCCAGGTAGCGTGAGGGTGAGGTAGGTGGCTGTGCAGACAAGCCCAGGCCACAGCAGCTTTCATTATTAACCCCGAGGATATATCGAAAGCTCTGCGGGAATCAAAGGACAAAGTTAATTTACTACAGAACGTTTTGCTAAAGCCTCTGATTCCTCATAATTTGTCAGTAATTGGAGGAGCTGCTGGCTGTGTTTGGAGGTGGCCCCTCTACCTTTGAGGGTCCAAGAGAAATCAGAGAAAGGGAGTCGAGAG... |
Task1_train_38304 | Given a variant located on Chromosome 7, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CTCAAAAAAAAAAAAAAAAAAAAAAGAGAGAAGTAAAAGGAGTGCTTGGCAAGAAAACAGTCTCTATTTTAAAACACTTAAAACTGTCTTCATCTCATTTTGCAATCACAGTGACACCAAAAGGGCATGGCTGTTCAGCAGGGTTTTAAATGCGCCACCAAGGCAGTGTCACTTAGATTAGATGGAGATGGATTGCCTTGTAAGGACTTTTTCTTTGGGACTCTGAGCACCAACCGAAAGGATCACAAGGCAGGACTTCATTGTTTCTTGGGAGCAGAGAGTTGAGTTCAGGTCTAGCCTTATATTGTTTTTCAAGCTCT... | CTCAAAAAAAAAAAAAAAAAAAAAAGAGAGAAGTAAAAGGAGTGCTTGGCAAGAAAACAGTCTCTATTTTAAAACACTTAAAACTGTCTTCATCTCATTTTGCAATCACAGTGACACCAAAAGGGCATGGCTGTTCAGCAGGGTTTTAAATGCGCCACCAAGGCAGTGTCACTTAGATTAGATGGAGATGGATTGCCTTGTAAGGACTTTTTCTTTGGGACTCTGAGCACCAACCGAAAGGATCACAAGGCAGGACTTCATTGTTTCTTGGGAGCAGAGAGTTGAGTTCAGGTCTAGCCTTATATTGTTTTTCAAGCTCT... |
Task1_train_38305 | Chromosome 7 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GGTGGCTCACGCCTGTAATCCTACCACTTTGGGAGGCCGAGGCAGGCGGATCACCTGAGGTCAAGAGTTCGAGACCAGCCTGACCAACATGGAGAAACCCCGTCTCTACTAAAAATACAAAATTAGCCGGGCGTGGAGGCGCATGCCTGTAATCCCAGTTACTCGGGAGGCTGAGGCAGGAGAATTACTTGAACCCCGGAGGTGGAGGTTGCAGTGAGCTGAGATCAGGCCATTCCACTCCAGCCTGGGCAACAAGAGTGAAACCCCGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAATTAGCTGTCCACAGTGGCATGC... | GGTGGCTCACGCCTGTAATCCTACCACTTTGGGAGGCCGAGGCAGGCGGATCACCTGAGGTCAAGAGTTCGAGACCAGCCTGACCAACATGGAGAAACCCCGTCTCTACTAAAAATACAAAATTAGCCGGGCGTGGAGGCGCATGCCTGTAATCCCAGTTACTCGGGAGGCTGAGGCAGGAGAATTACTTGAACCCCGGAGGTGGAGGTTGCAGTGAGCTGAGATCAGGCCATTCCACTCCAGCCTGGGCAACAAGAGTGAAACCCCGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAATTAGCTGTCCACAGTGGCATGC... |
Task1_train_38306 | Consider this mutation on Chromosome 7. Is this a benign change or a disease-causing variant? | Benign | GCTTGTAGCAGTTGGACGCTGCTACTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACAGTCTTGCTCTGTCGCCCAAGCTGGAACGCAGTGGCACGATCTCGGCTCACTGCAGCCTCTGCCTCCTGGGCTCAAGCCATTCTCCTGCCTCACCTCCCGAGTAGCTGGGATTACAGGTACCTGCCACCACGCCTGGCTATGTATTTATTTATTTATTTATTTATTTTTTTGAGGCGGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCATGATCTCAGCTCACCGCAACCTCCGCCTCCCAG... | GCTTGTAGCAGTTGGACGCTGCTACTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACAGTCTTGCTCTGTCGCCCAAGCTGGAACGCAGTGGCACGATCTCGGCTCACTGCAGCCTCTGCCTCCTGGGCTCAAGCCATTCTCCTGCCTCACCTCCCGAGTAGCTGGGATTACAGGTACCTGCCACCACGCCTGGCTATGTATTTATTTATTTATTTATTTATTTTTTTGAGGCGGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCATGATCTCAGCTCACCGCAACCTCCGCCTCCCAG... |
Task1_train_38307 | This mutation occurs on Chromosome 7. Does this change lead to a known medical condition, or is it benign? | Benign | GGAGGTGGCTCAGGGGTCTGGCTCTGTCATCAGGTCTCCTTGGAGAGCGGTGAGTTCACCAGGGCTGCCCTGGGCAGAGTGAGCTGGTGCTGAGAGAACTGCAACTGTGACAGCCTAGGGGCCAGACGCTGGACACGTGGCTGTGATGAATGGCATAGATGAGAGGTAACAGCCTGGGGCTGGGGCAGGGAGTGCGGACGGGGTGGCTGCCAAAGGGAGAGAACCCAAAGGGAGGGCAGGCAGGGGAATGAAGTCTTAGAACATGGCTGCAGGGCAGGGACACTGAGGATGGATTTGGGTTTGGCCACATGTGTGACCTG... | GGAGGTGGCTCAGGGGTCTGGCTCTGTCATCAGGTCTCCTTGGAGAGCGGTGAGTTCACCAGGGCTGCCCTGGGCAGAGTGAGCTGGTGCTGAGAGAACTGCAACTGTGACAGCCTAGGGGCCAGACGCTGGACACGTGGCTGTGATGAATGGCATAGATGAGAGGTAACAGCCTGGGGCTGGGGCAGGGAGTGCGGACGGGGTGGCTGCCAAAGGGAGAGAACCCAAAGGGAGGGCAGGCAGGGGAATGAAGTCTTAGAACATGGCTGCAGGGCAGGGACACTGAGGATGGATTTGGGTTTGGCCACATGTGTGACCTG... |
Task1_train_38308 | Here is a genetic alteration on Chromosome 7. Based on the data, is it a benign variant or a cause of disease? | Benign | AGGATCACTTTTTGTTCCATTCAAGTATTAGTGAAATAAAGGCCTTAGGACCCCATCTGAAAGCCCTGGAGGACAGGAGTGAAGGTGAATGGCATGGGAGGTTGCTGTACTGGGACCTAGTCAGTGGCCTGGGGTAGCTGTAACCATACTAGGCAGCTTCTTCTTTTATAACCATGTCACGTCCCAGGTTTCTTGGAATTGCCTGGATCTGTCCAGTAAATGGCAGGTTCCTGCAAATCAGGGGTTGCTTGGGATTCAGGCCTGAGACCGACTCTATCCTCCCTCTTTCCATCCCAGCCCTGGGTCTCTAAATGGTGCCT... | AGGATCACTTTTTGTTCCATTCAAGTATTAGTGAAATAAAGGCCTTAGGACCCCATCTGAAAGCCCTGGAGGACAGGAGTGAAGGTGAATGGCATGGGAGGTTGCTGTACTGGGACCTAGTCAGTGGCCTGGGGTAGCTGTAACCATACTAGGCAGCTTCTTCTTTTATAACCATGTCACGTCCCAGGTTTCTTGGAATTGCCTGGATCTGTCCAGTAAATGGCAGGTTCCTGCAAATCAGGGGTTGCTTGGGATTCAGGCCTGAGACCGACTCTATCCTCCCTCTTTCCATCCCAGCCCTGGGTCTCTAAATGGTGCCT... |
Task1_train_38309 | A variant was discovered on Chromosome 7. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CACCCTACTTCCTGCAGGTGACTCAGGCCTTGGGTTCTTCTTGTGGCTAGAGGTCTGATCCATTCCAGGCTCCTCATTCTTAATCTTCAGGACCACGCTAATATTCCACCTGCAGTCTATCACAGCCTGGTTTGTGCCAAAGTCAAGAGGAAATGCCTTTGGCAGATTGGTGAAGCCAAACTAGGGCCTCCTGCAGCCAACAAGCCAGCCAGGCCGCTGTGCAAGGGCAGGTCTAATCCTGGTTTTGTGGGGGCTTAGAACAGGCGGAATTCTTTTACATTTTTTTGGAGGTGGGGAATGGCGGGGAGGGGAATGGAGTC... | CACCCTACTTCCTGCAGGTGACTCAGGCCTTGGGTTCTTCTTGTGGCTAGAGGTCTGATCCATTCCAGGCTCCTCATTCTTAATCTTCAGGACCACGCTAATATTCCACCTGCAGTCTATCACAGCCTGGTTTGTGCCAAAGTCAAGAGGAAATGCCTTTGGCAGATTGGTGAAGCCAAACTAGGGCCTCCTGCAGCCAACAAGCCAGCCAGGCCGCTGTGCAAGGGCAGGTCTAATCCTGGTTTTGTGGGGGCTTAGAACAGGCGGAATTCTTTTACATTTTTTTGGAGGTGGGGAATGGCGGGGAGGGGAATGGAGTC... |
Task1_train_38310 | This variant is present on Chromosome 7. Is the change likely to result in a pathogenic outcome? | Benign | GGACAGGATGCCTGATTCTGGGTGCAGGGCTCCTGACTGCCTCTAGGAGATGCTTGTTCTCAAGGCATTGTCAGCAGATTCTTTGGGGACACATCTTGTATCTTTGTGAATATTTAAGGAAGTAAAAGAATGATTCATGCCTGGGGGCAAGGAAGGAGGATGCATGTTCTTTCTTGGTTTATTTTGGATTTGCAAGTTGGAGATGCTTCAAAGGCAGGCCACAGTCTTAGGGTGTTAGATTCAAAGTTTTTATCTTGGGCAGGTGCAGTGGCTCACGCCTGTACTCCCAGCACTTTGGGAGGCCGAGGCAGGTGGATCAC... | GGACAGGATGCCTGATTCTGGGTGCAGGGCTCCTGACTGCCTCTAGGAGATGCTTGTTCTCAAGGCATTGTCAGCAGATTCTTTGGGGACACATCTTGTATCTTTGTGAATATTTAAGGAAGTAAAAGAATGATTCATGCCTGGGGGCAAGGAAGGAGGATGCATGTTCTTTCTTGGTTTATTTTGGATTTGCAAGTTGGAGATGCTTCAAAGGCAGGCCACAGTCTTAGGGTGTTAGATTCAAAGTTTTTATCTTGGGCAGGTGCAGTGGCTCACGCCTGTACTCCCAGCACTTTGGGAGGCCGAGGCAGGTGGATCAC... |
Task1_train_38311 | This sequence change occurs on Chromosome 7. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GGGCCGGGCCCGGATGGCGCCTACTCCCTCTCCGAGTGCCATCGAATTGTGTGCTAATTAGCCACAATTTGCACCGCGGCAGGGGCGCCCCGAGGCCACGCCTGCCCTCTAGGGGGTGGCAGGGATCGGGTTGGGTACCCCCCACCCAGACACCCAGGCAGTGACAGTCGCCAACCCCGTGGCGCGAGGACACGCGCAGCAGGGATGCGGCACAGCGCGCGCTGCGCTCGGCACCGGCCAGCCCGGGACGCCCCAGGGGCCGCCGCATCGTGTCCCCCGGGCCGGGTGAGTGGCCGGGCCGGGAATGGTTAAGCCCACCG... | GGGCCGGGCCCGGATGGCGCCTACTCCCTCTCCGAGTGCCATCGAATTGTGTGCTAATTAGCCACAATTTGCACCGCGGCAGGGGCGCCCCGAGGCCACGCCTGCCCTCTAGGGGGTGGCAGGGATCGGGTTGGGTACCCCCCACCCAGACACCCAGGCAGTGACAGTCGCCAACCCCGTGGCGCGAGGACACGCGCAGCAGGGATGCGGCACAGCGCGCGCTGCGCTCGGCACCGGCCAGCCCGGGACGCCCCAGGGGCCGCCGCATCGTGTCCCCCGGGCCGGGTGAGTGGCCGGGCCGGGAATGGTTAAGCCCACCG... |
Task1_train_38312 | Mutation context: Chromosome 7. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TTTGCACCGCGGCAGGGGCGCCCCGAGGCCACGCCTGCCCTCTAGGGGGTGGCAGGGATCGGGTTGGGTACCCCCCACCCAGACACCCAGGCAGTGACAGTCGCCAACCCCGTGGCGCGAGGACACGCGCAGCAGGGATGCGGCACAGCGCGCGCTGCGCTCGGCACCGGCCAGCCCGGGACGCCCCAGGGGCCGCCGCATCGTGTCCCCCGGGCCGGGTGAGTGGCCGGGCCGGGAATGGTTAAGCCCACCGAGCTGCGGCTGCCTAGAGCGGCGGCGGCGACGGCGGCGGCGGCGGCGGGGGCCGGGGCGCGGGGGCG... | TTTGCACCGCGGCAGGGGCGCCCCGAGGCCACGCCTGCCCTCTAGGGGGTGGCAGGGATCGGGTTGGGTACCCCCCACCCAGACACCCAGGCAGTGACAGTCGCCAACCCCGTGGCGCGAGGACACGCGCAGCAGGGATGCGGCACAGCGCGCGCTGCGCTCGGCACCGGCCAGCCCGGGACGCCCCAGGGGCCGCCGCATCGTGTCCCCCGGGCCGGGTGAGTGGCCGGGCCGGGAATGGTTAAGCCCACCGAGCTGCGGCTGCCTAGAGCGGCGGCGGCGACGGCGGCGGCGGCGGCGGGGGCCGGGGCGCGGGGGCG... |
Task1_train_38313 | This mutation on Chromosome 7 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GGTTTTATTAAATCAATATATTCTTGGAAAAATGGCCAGAAAGCAAACTTTTATAAATCAAAGCATTGTCTTCCATTACAAAATGGAAAACATATGATGTTATAGGGAGAAGAGATGTTGAAATCAGAGTTGGGAACGGAGAAAGCCTCCTCAAGTCACATGTAGAAAGAAGGATTGGGATTTTCCAGTAGCACAATAGTAATACTCAAAACGAGAATCTCATGGTGTACACGGTGCGGAAAGAGAAGCGTAGTAACGGAGTGGTGCTGTTTTTGCAGGGCCTCCCAGGTTTATGCCTCCCAAAGTGTTGCGATTACAAG... | GGTTTTATTAAATCAATATATTCTTGGAAAAATGGCCAGAAAGCAAACTTTTATAAATCAAAGCATTGTCTTCCATTACAAAATGGAAAACATATGATGTTATAGGGAGAAGAGATGTTGAAATCAGAGTTGGGAACGGAGAAAGCCTCCTCAAGTCACATGTAGAAAGAAGGATTGGGATTTTCCAGTAGCACAATAGTAATACTCAAAACGAGAATCTCATGGTGTACACGGTGCGGAAAGAGAAGCGTAGTAACGGAGTGGTGCTGTTTTTGCAGGGCCTCCCAGGTTTATGCCTCCCAAAGTGTTGCGATTACAAG... |
Task1_train_38314 | A mutation found on Chromosome 7 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CACATGAGGGTGATGCTGGCTCACAGCCCCCACTCTCCCATGTCCTGCAGGAAGAAGCCTGACCTGCCGGCTTCCTGGCACCTGTCTCTCCTCCTAGCCCCGTTGTGCCTTGCAAGTGCCTGCATCCTGTCTGTGCTGAGACCTCTTGGCGTTCCCTGCTGGCCTGGTTCATGTGTGTTGAGGACCAGGTAAGCGTCTCTTTGTCCTGTGTATCAGGTGGGCTTTTCCTTCTGGCTAAACATGGGCCACCCTCGGGCTGTGTGATGCTTCCTTGTGGATAAAGACTGGGATAAATGCCTGATTTACTCCAGGAAAGAGCA... | CACATGAGGGTGATGCTGGCTCACAGCCCCCACTCTCCCATGTCCTGCAGGAAGAAGCCTGACCTGCCGGCTTCCTGGCACCTGTCTCTCCTCCTAGCCCCGTTGTGCCTTGCAAGTGCCTGCATCCTGTCTGTGCTGAGACCTCTTGGCGTTCCCTGCTGGCCTGGTTCATGTGTGTTGAGGACCAGGTAAGCGTCTCTTTGTCCTGTGTATCAGGTGGGCTTTTCCTTCTGGCTAAACATGGGCCACCCTCGGGCTGTGTGATGCTTCCTTGTGGATAAAGACTGGGATAAATGCCTGATTTACTCCAGGAAAGAGCA... |
Task1_train_38315 | A variant on Chromosome 7 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CAGTAACCCGTTTTCTGACCCTTTTCTATGATGCCTGTTTTTTCACAGTGAAGCCGGGCCTGTGTGGGTCTGTGTTTTCCTGCGGCTCTAGGTCCCCATATGGAATGTATGTGGGACGAGGCAGTGCCAAGGGCATGCAGCCTGGCAGGGGCCAGCGTGCGACATGAGGGGCTACCCGAGGCCTACTGGGACCTCCTGGGCTCCGACTTTCCCTCTAGGGCAGCACTCAGTGGTCCAGGCTTATCCAGCTAGGTGACGGCTGAAATGGGCAGGGGACCCAGGTGGGGTGAGGAGGAGATTTCCACACCAGCTGTGGGAGC... | CAGTAACCCGTTTTCTGACCCTTTTCTATGATGCCTGTTTTTTCACAGTGAAGCCGGGCCTGTGTGGGTCTGTGTTTTCCTGCGGCTCTAGGTCCCCATATGGAATGTATGTGGGACGAGGCAGTGCCAAGGGCATGCAGCCTGGCAGGGGCCAGCGTGCGACATGAGGGGCTACCCGAGGCCTACTGGGACCTCCTGGGCTCCGACTTTCCCTCTAGGGCAGCACTCAGTGGTCCAGGCTTATCCAGCTAGGTGACGGCTGAAATGGGCAGGGGACCCAGGTGGGGTGAGGAGGAGATTTCCACACCAGCTGTGGGAGC... |
Task1_train_38316 | A mutation has occurred on Chromosome 7. What is the medical relevance of this mutation? | Benign | AGGAGCCCCACCGAGCCAGCTCCATCTACATGTTGTTCATTGCCTGCACAGGTGCCTCGCAAGGCTGAAGGGAGAGGGCAGGGGTGCAGCTTGGTGTGAGAGGGGCAGAATGGGGGAAGCTGAGCAAAGCTTAGAGCTGACAGGCCGGGCACGGTGGCTCACCCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGTAGACCACCTGAGGTCAGGAGTTTGAGACTAGCCTGACCAACACTGAGAAACCCCATCTCTACTAAAATCATCATCATCATCATCATCATCTGGGCGCACGCCTGTAACTCCAGTTACTCGG... | AGGAGCCCCACCGAGCCAGCTCCATCTACATGTTGTTCATTGCCTGCACAGGTGCCTCGCAAGGCTGAAGGGAGAGGGCAGGGGTGCAGCTTGGTGTGAGAGGGGCAGAATGGGGGAAGCTGAGCAAAGCTTAGAGCTGACAGGCCGGGCACGGTGGCTCACCCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGTAGACCACCTGAGGTCAGGAGTTTGAGACTAGCCTGACCAACACTGAGAAACCCCATCTCTACTAAAATCATCATCATCATCATCATCATCTGGGCGCACGCCTGTAACTCCAGTTACTCGG... |
Task1_train_38317 | This variant is present on Chromosome 7. Is the change likely to result in a pathogenic outcome? | Benign | AAGCGAAGCCTTTCCTGCCCGGCCGGGAGCCGGGTGCGAACCTGCTGTCGCCCTGGGCGTTCCCCGCCGCAGTGGCCCCGCCGGCCGGGAGGCCGGAGACCACGTGCGACGTGTGCGGCAAGGTCTTCCCGCACCGCTCGCGGCTGGCCAAGCACCAGCGCTACCACGCGGCCGTCAAGCCCTTCGGCTGCGAGGAGTGCGGCAAGGGCTTCGTGTACCGCTCGCACTTGGCCATCCACCAGCGCACGCACACCGGCGAGAAGCCCTTCCCGTGCCCGGACTGCGGCAAGCGCTTCGTCTACAAGTCGCACCTGGTTACG... | AAGCGAAGCCTTTCCTGCCCGGCCGGGAGCCGGGTGCGAACCTGCTGTCGCCCTGGGCGTTCCCCGCCGCAGTGGCCCCGCCGGCCGGGAGGCCGGAGACCACGTGCGACGTGTGCGGCAAGGTCTTCCCGCACCGCTCGCGGCTGGCCAAGCACCAGCGCTACCACGCGGCCGTCAAGCCCTTCGGCTGCGAGGAGTGCGGCAAGGGCTTCGTGTACCGCTCGCACTTGGCCATCCACCAGCGCACGCACACCGGCGAGAAGCCCTTCCCGTGCCCGGACTGCGGCAAGCGCTTCGTCTACAAGTCGCACCTGGTTACG... |
Task1_train_38318 | A mutation on Chromosome 7 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TTACTTGTCTATAGTCTAGTATTGTTATACCATGTGGTCTTGTTATAATCATGGTTTCCATTCTGTGAGTCTTCAGATTATGAGTCCAACACACAAGGGGATGTCCACACTAACCTGTGTGAACTCTCTGATGTACAAGGTGTTTGACTTCAGGCAGGAGTTTCTGATTCACTATACTGAAAGGGTTCTCTGATATAAAATGAGGTCTGACTTCAGAGAAGCCTTCCCACATCTATTACATTCATATTGCCTCTCCTATGAATTCTCTGATGGCTGTTGAATGCTGATTTGTGGTAGAATTTTTTTCCACATTCAGTACA... | TTACTTGTCTATAGTCTAGTATTGTTATACCATGTGGTCTTGTTATAATCATGGTTTCCATTCTGTGAGTCTTCAGATTATGAGTCCAACACACAAGGGGATGTCCACACTAACCTGTGTGAACTCTCTGATGTACAAGGTGTTTGACTTCAGGCAGGAGTTTCTGATTCACTATACTGAAAGGGTTCTCTGATATAAAATGAGGTCTGACTTCAGAGAAGCCTTCCCACATCTATTACATTCATATTGCCTCTCCTATGAATTCTCTGATGGCTGTTGAATGCTGATTTGTGGTAGAATTTTTTTCCACATTCAGTACA... |
Task1_train_38319 | Given this context: Chromosome 7 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AGGCCGAGGTGGGCGGATCCTTTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTAAAACCCCGTCTCTACAAAAATTAGCTGGGTGTTGTGGTACTCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCAGGGGTTGCAGCAAGCCAAGATCATGCCACTGCACTCCAGCCTGGGCAACAGAAAGCGACTCCATTTCAAAAACAAAAAAAAAAGTAGATGGGTTTCACCTGAAATTTGTGTTGTCTTCCTAGGAGATAAAGTTCATGTGGAAACCCACCAAGTTGTT... | AGGCCGAGGTGGGCGGATCCTTTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTAAAACCCCGTCTCTACAAAAATTAGCTGGGTGTTGTGGTACTCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCAGGGGTTGCAGCAAGCCAAGATCATGCCACTGCACTCCAGCCTGGGCAACAGAAAGCGACTCCATTTCAAAAACAAAAAAAAAAGTAGATGGGTTTCACCTGAAATTTGTGTTGTCTTCCTAGGAGATAAAGTTCATGTGGAAACCCACCAAGTTGTT... |
Task1_train_38320 | This sequence variant lies on Chromosome 7. Is it clinically significant, and what condition might it cause if any? | Benign | GTTGATATTTTATGTCTTTCCCCCCAGAGTTCAATAGGCCCTTTTCTTTATATAATGCTCCATGCACTAGAAGGGTTAAAAAGGCATATTGAGAGTCAGCGTAAATGTTGACATTCTTAGCTTCACTGAGTTCTAAGGCCCGAATTAAAGCAATGAGTTCAGCTTTCTGAGCTGAAGTGCCCTGGGGAAACGATCTGGCTTCAACAACAGTGTCCAGAGTTACCACCGCATATCTTGCACATCTCTCTCCTCGTGGGTTGATGAAGCTGCTCCCATCCACGTATAGTTCCCAGTCTACTGATGCCTAAGGCTGGTCCTGG... | GTTGATATTTTATGTCTTTCCCCCCAGAGTTCAATAGGCCCTTTTCTTTATATAATGCTCCATGCACTAGAAGGGTTAAAAAGGCATATTGAGAGTCAGCGTAAATGTTGACATTCTTAGCTTCACTGAGTTCTAAGGCCCGAATTAAAGCAATGAGTTCAGCTTTCTGAGCTGAAGTGCCCTGGGGAAACGATCTGGCTTCAACAACAGTGTCCAGAGTTACCACCGCATATCTTGCACATCTCTCTCCTCGTGGGTTGATGAAGCTGCTCCCATCCACGTATAGTTCCCAGTCTACTGATGCCTAAGGCTGGTCCTGG... |
Task1_train_38321 | This mutation on Chromosome 7 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TTCAATAGGCCCTTTTCTTTATATAATGCTCCATGCACTAGAAGGGTTAAAAAGGCATATTGAGAGTCAGCGTAAATGTTGACATTCTTAGCTTCACTGAGTTCTAAGGCCCGAATTAAAGCAATGAGTTCAGCTTTCTGAGCTGAAGTGCCCTGGGGAAACGATCTGGCTTCAACAACAGTGTCCAGAGTTACCACCGCATATCTTGCACATCTCTCTCCTCGTGGGTTGATGAAGCTGCTCCCATCCACGTATAGTTCCCAGTCTACTGATGCCTAAGGCTGGTCCTGGAGGTTAGGTCTGCTAGAGTAAACTGAGTC... | TTCAATAGGCCCTTTTCTTTATATAATGCTCCATGCACTAGAAGGGTTAAAAAGGCATATTGAGAGTCAGCGTAAATGTTGACATTCTTAGCTTCACTGAGTTCTAAGGCCCGAATTAAAGCAATGAGTTCAGCTTTCTGAGCTGAAGTGCCCTGGGGAAACGATCTGGCTTCAACAACAGTGTCCAGAGTTACCACCGCATATCTTGCACATCTCTCTCCTCGTGGGTTGATGAAGCTGCTCCCATCCACGTATAGTTCCCAGTCTACTGATGCCTAAGGCTGGTCCTGGAGGTTAGGTCTGCTAGAGTAAACTGAGTC... |
Task1_train_38322 | With a mutation on Chromosome 7, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | AGGAGGTTTTTATACATGGGTATAAAAAAGGATATGCACATATGTGTACATTTGTATATGTGGTTGTTTATTTTTCACTCTATTTGTAAAAGATCTGAGTTGATCAAGCCTCCAAATATTTAACAAAAATCTGTGGGCCATTTAAGAGAGATTGTAAACATGTTGCTGGAAACAGAAGTTCCCTCATAAACACATGAGGGAAAACATTCATTTTTATGAGAGAAATAGGAAGATCTAACATAACAAGAATTCAATGGATAAACACATCAAATTAAAGAACATTGAATAACTGCATAGACAGAGGTTAAATTTAAGTAGAA... | AGGAGGTTTTTATACATGGGTATAAAAAAGGATATGCACATATGTGTACATTTGTATATGTGGTTGTTTATTTTTCACTCTATTTGTAAAAGATCTGAGTTGATCAAGCCTCCAAATATTTAACAAAAATCTGTGGGCCATTTAAGAGAGATTGTAAACATGTTGCTGGAAACAGAAGTTCCCTCATAAACACATGAGGGAAAACATTCATTTTTATGAGAGAAATAGGAAGATCTAACATAACAAGAATTCAATGGATAAACACATCAAATTAAAGAACATTGAATAACTGCATAGACAGAGGTTAAATTTAAGTAGAA... |
Task1_train_38323 | A genomic change on Chromosome 7 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CATGGATAGGTAGAATCAATATTGTGACAATGACCATACTGCCAAAAGCCATACACAAATTCATTGAAATTCCCATCAGAATACCATCATCATTCTTCACAGAATTAGACAAAAACAATTCTGAAATTCATATGCAACCAAAAAAGAGCCCACATAGCCAAAGCAAGACTAAGCAAAAAGAACAAATCTGGAGGCATCAATTACCTGATTTCAAACTACACTATAAGGCCATAGTTACCAAAACAGCATGGTACTGGTATAAAATAGGCACATAGACCAGTGGAACAGAATAAAGAACCCAGAAATAAACCATCATACTT... | CATGGATAGGTAGAATCAATATTGTGACAATGACCATACTGCCAAAAGCCATACACAAATTCATTGAAATTCCCATCAGAATACCATCATCATTCTTCACAGAATTAGACAAAAACAATTCTGAAATTCATATGCAACCAAAAAAGAGCCCACATAGCCAAAGCAAGACTAAGCAAAAAGAACAAATCTGGAGGCATCAATTACCTGATTTCAAACTACACTATAAGGCCATAGTTACCAAAACAGCATGGTACTGGTATAAAATAGGCACATAGACCAGTGGAACAGAATAAAGAACCCAGAAATAAACCATCATACTT... |
Task1_train_38324 | This mutation is located on Chromosome 7. Is it associated with a disease or is it a benign polymorphism? | Benign | GCTTTTGGAAAAATGACTCCTTTTATGATTATGCTGTAAAAGTCAACCACAAAGTGCTATTATGTCAGAAAAATTATAACCAACCCCCCCAAAACATACTTGATGCATTATTAAAACTTAATGCACTGCTGAAATTAAAGGCCAAATTTTATTGAAATATGTTTTTAACCCTAAGTGATAACACTATTAGACATAAAGAGTTGAGCCAGGTATGGTGGCTCACACTTGTAGTCTCAACTCTTTGGGAGGCCAAGGCAGGAGGATTCCTTGAGGCCAGGCATTCCAGACTCAACTGGGCAACAAAGCGAGAGCCCATCTCT... | GCTTTTGGAAAAATGACTCCTTTTATGATTATGCTGTAAAAGTCAACCACAAAGTGCTATTATGTCAGAAAAATTATAACCAACCCCCCCAAAACATACTTGATGCATTATTAAAACTTAATGCACTGCTGAAATTAAAGGCCAAATTTTATTGAAATATGTTTTTAACCCTAAGTGATAACACTATTAGACATAAAGAGTTGAGCCAGGTATGGTGGCTCACACTTGTAGTCTCAACTCTTTGGGAGGCCAAGGCAGGAGGATTCCTTGAGGCCAGGCATTCCAGACTCAACTGGGCAACAAAGCGAGAGCCCATCTCT... |
Task1_train_38325 | This mutation on Chromosome 7 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | AATATGCAACATACTTATATCGATCTAATAGTGAGTTGTATCGTAACAGGATTCCATTATATCATATTTGAGTCCACATAAAGAAAAATATTAGGTTGGTGCAAAAGTAATTGTGGTTTTTGACACTAAAAGTAATGGAAAAACCCGTAATTACTTTTGAACCAACCTGATAATTATCTATCAGCTTGAGATTCTAATGTGATATGTCATCATTGAAAGCCTAGATGAAAACCATTCTAGAGAGGTAACAAAAGAACAAAAGTACAGTTTATTTGGTTGGTTTCTGAACATTTATTCTTAATATTACCATAACATCATTA... | AATATGCAACATACTTATATCGATCTAATAGTGAGTTGTATCGTAACAGGATTCCATTATATCATATTTGAGTCCACATAAAGAAAAATATTAGGTTGGTGCAAAAGTAATTGTGGTTTTTGACACTAAAAGTAATGGAAAAACCCGTAATTACTTTTGAACCAACCTGATAATTATCTATCAGCTTGAGATTCTAATGTGATATGTCATCATTGAAAGCCTAGATGAAAACCATTCTAGAGAGGTAACAAAAGAACAAAAGTACAGTTTATTTGGTTGGTTTCTGAACATTTATTCTTAATATTACCATAACATCATTA... |
Task1_train_38326 | A mutation is present on Chromosome 7. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | AGAAGTCACTTGTTTGTGAGTAATATTGGGTCCACACTCTTGAAATCCAAGAAGCTTAAAAATCCAAGTGTTTTGTAAGGTTCACACAAACTTACTTGATGGCAAAGCCTAACGGAACTGGTAGGAGTTTATTTGTAGTATTTATTTCTCATACTCTGTAAATAGGATTTATACTTTTCTCCGCAGAAATAATGTTTGATTATAGGATAATACCATGGACTTCACTGGGGGTATTAGTGTAATATATGGTGCATGTTCCATGTTACCCTTGAAAATCTGAGAAATTATGAATTCTGAAACACATCTGGTTCTTAAAGTTT... | AGAAGTCACTTGTTTGTGAGTAATATTGGGTCCACACTCTTGAAATCCAAGAAGCTTAAAAATCCAAGTGTTTTGTAAGGTTCACACAAACTTACTTGATGGCAAAGCCTAACGGAACTGGTAGGAGTTTATTTGTAGTATTTATTTCTCATACTCTGTAAATAGGATTTATACTTTTCTCCGCAGAAATAATGTTTGATTATAGGATAATACCATGGACTTCACTGGGGGTATTAGTGTAATATATGGTGCATGTTCCATGTTACCCTTGAAAATCTGAGAAATTATGAATTCTGAAACACATCTGGTTCTTAAAGTTT... |
Task1_train_38327 | A change on Chromosome 7 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TTACCTTTTTAAAATTCATTCCGTTTGTGATGTACACAAAGTAAAACCAGCTCATTTGTATTGTGAGTTATCAATTTGCTTTTTAGGTTATAACATACATTGCCAGTACAACTACACACATCTAAGTCATACCTCTGCTTGTTTTTTAGTGTTTTTTCACAAGACAAGCTAGGAGGTAATTACTTGTGTTGCAAAATAAGTTTCACTTAACAAAATGAAAATAAGCCACTGATATTTTTTAAATAGCTGGCTCCTTTAGTCTATATAAAATATATTCCATTAGCACAAATACCAGGAAGATCATTGTACTAAGTGGACTA... | TTACCTTTTTAAAATTCATTCCGTTTGTGATGTACACAAAGTAAAACCAGCTCATTTGTATTGTGAGTTATCAATTTGCTTTTTAGGTTATAACATACATTGCCAGTACAACTACACACATCTAAGTCATACCTCTGCTTGTTTTTTAGTGTTTTTTCACAAGACAAGCTAGGAGGTAATTACTTGTGTTGCAAAATAAGTTTCACTTAACAAAATGAAAATAAGCCACTGATATTTTTTAAATAGCTGGCTCCTTTAGTCTATATAAAATATATTCCATTAGCACAAATACCAGGAAGATCATTGTACTAAGTGGACTA... |
Task1_train_38328 | This sequence variant lies on Chromosome 7. Is it clinically significant, and what condition might it cause if any? | Benign | ATGGTGATCTCTTTTCATCTTTTAAATTAAATGGATTCTCACTACTCTGAGCAACAAATGTCTAACCTTTATTACTAAATTTTTATTTATTCTGTCTTATTTTTTCTTTGTCTTAATTCTCATAAGGATTTGTATTCTCAACCTGTATTACATCATTGATCCCTTAAATATTCTAATGAAACTGTGGACAGTACAGAAAAAGACATGTACCAGCATAATTTTGCATATACAAAGACTTCCAAGATTCTTCTAAATTTCAATCCTTGGTCTTATCAGAAGATCCATTGACCTCAAATTAACTATCTCTTTCCTATCATGTC... | ATGGTGATCTCTTTTCATCTTTTAAATTAAATGGATTCTCACTACTCTGAGCAACAAATGTCTAACCTTTATTACTAAATTTTTATTTATTCTGTCTTATTTTTTCTTTGTCTTAATTCTCATAAGGATTTGTATTCTCAACCTGTATTACATCATTGATCCCTTAAATATTCTAATGAAACTGTGGACAGTACAGAAAAAGACATGTACCAGCATAATTTTGCATATACAAAGACTTCCAAGATTCTTCTAAATTTCAATCCTTGGTCTTATCAGAAGATCCATTGACCTCAAATTAACTATCTCTTTCCTATCATGTC... |
Task1_train_38329 | A variant was discovered on Chromosome 7. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | ATAATAAATCTGTGTAATTTCAGTTTACAATACACTTGGCCACCAATTTTTAAATTATGTAATTATTAATCATTTGGAAATATTTTGAGGGATTTGCAGTTTTTCCCATTAAGTTAATCATTGTTAATATTTTAACATCTTTTTTCAAGTTTCCACAAAAAATTTCAAAATTGCATGAAATTTGATCTTCCTCTACATCTTAAGATTTCATCTATGTAGAAATTTATAACTAATACTGGATGGAGATATACTAAAACTCTAAAAAAGCAACCGAAATTAATTCTAGATGGTGAAATTTAGAGTGACTATTTTTTTTTTCT... | ATAATAAATCTGTGTAATTTCAGTTTACAATACACTTGGCCACCAATTTTTAAATTATGTAATTATTAATCATTTGGAAATATTTTGAGGGATTTGCAGTTTTTCCCATTAAGTTAATCATTGTTAATATTTTAACATCTTTTTTCAAGTTTCCACAAAAAATTTCAAAATTGCATGAAATTTGATCTTCCTCTACATCTTAAGATTTCATCTATGTAGAAATTTATAACTAATACTGGATGGAGATATACTAAAACTCTAAAAAAGCAACCGAAATTAATTCTAGATGGTGAAATTTAGAGTGACTATTTTTTTTTTCT... |
Task1_train_38330 | A change on Chromosome 7 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | ATAAATTTTCCGCTTAAGATTTAAACCAAAGCAATGCAATTATATGGCTACAGATGTATTTTTACAAATTCACTTTTTAGGTTTCTTCTTACTACTTTACATTTTCTAGTTATTTGGCATTTAACACTTTATTTGAACCATATTTGGTAGATCATTCAATAGCTGTCTTTGCTTGAAGCTAAAACATTTGTAGATATATAGTACCTTATAACTAAACCTCAAATCATTTCAGAGGGTAATTTTACCAATAACAAATAAGCTATTGCCCCTTGAATCTCTGATTTCAGAAATTTAATTCTTTAGAATCTTTGAATAAATTA... | ATAAATTTTCCGCTTAAGATTTAAACCAAAGCAATGCAATTATATGGCTACAGATGTATTTTTACAAATTCACTTTTTAGGTTTCTTCTTACTACTTTACATTTTCTAGTTATTTGGCATTTAACACTTTATTTGAACCATATTTGGTAGATCATTCAATAGCTGTCTTTGCTTGAAGCTAAAACATTTGTAGATATATAGTACCTTATAACTAAACCTCAAATCATTTCAGAGGGTAATTTTACCAATAACAAATAAGCTATTGCCCCTTGAATCTCTGATTTCAGAAATTTAATTCTTTAGAATCTTTGAATAAATTA... |
Task1_train_38331 | A variant affecting Chromosome 7 has been observed. Determine if it's benign or associated with disease. | Benign | ATTTGAACCATATTTGGTAGATCATTCAATAGCTGTCTTTGCTTGAAGCTAAAACATTTGTAGATATATAGTACCTTATAACTAAACCTCAAATCATTTCAGAGGGTAATTTTACCAATAACAAATAAGCTATTGCCCCTTGAATCTCTGATTTCAGAAATTTAATTCTTTAGAATCTTTGAATAAATTATATTTAATAAGTATTTTAAAATGTAGAGTCCTATACCAGCTTTGATAAGAATATTTTAATATATACACAGTAAAACTGAATTGTCTTGTAAAATGGTTTTTAAAGAAAATTATGCTATATTTTAGGCCTT... | ATTTGAACCATATTTGGTAGATCATTCAATAGCTGTCTTTGCTTGAAGCTAAAACATTTGTAGATATATAGTACCTTATAACTAAACCTCAAATCATTTCAGAGGGTAATTTTACCAATAACAAATAAGCTATTGCCCCTTGAATCTCTGATTTCAGAAATTTAATTCTTTAGAATCTTTGAATAAATTATATTTAATAAGTATTTTAAAATGTAGAGTCCTATACCAGCTTTGATAAGAATATTTTAATATATACACAGTAAAACTGAATTGTCTTGTAAAATGGTTTTTAAAGAAAATTATGCTATATTTTAGGCCTT... |
Task1_train_38332 | Assess the clinical impact of this variant found on Chromosome 7. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | AAAGTACTCCTACAAATCAATAAAAAAGGCAAGCAAAAGGATATCAATTAGCACAAAAACAAATCTAAATGATTATTTGAAAAAAGAAACCCAAATAAATAGATAACCTTTGGCAACTTCTATCTAGGAAAAATCAAAAACCATAACAGTGGAAAGATACAACTAAACAACTTTGGAGATGAGAAAAGTAAAATAGCTATACATAAGAAGACAATTTTAAATTATACAAGAATACTACATGTAATTGTATACAAGAATTTGAAATCTAAATGTGACAAATGATTTTCTGGCAAAATAAAAATGATGAAATTGACTCAAGA... | AAAGTACTCCTACAAATCAATAAAAAAGGCAAGCAAAAGGATATCAATTAGCACAAAAACAAATCTAAATGATTATTTGAAAAAAGAAACCCAAATAAATAGATAACCTTTGGCAACTTCTATCTAGGAAAAATCAAAAACCATAACAGTGGAAAGATACAACTAAACAACTTTGGAGATGAGAAAAGTAAAATAGCTATACATAAGAAGACAATTTTAAATTATACAAGAATACTACATGTAATTGTATACAAGAATTTGAAATCTAAATGTGACAAATGATTTTCTGGCAAAATAAAAATGATGAAATTGACTCAAGA... |
Task1_train_38333 | This variant is present on Chromosome 7. Is the change likely to result in a pathogenic outcome? | Benign | ATTGATTCTTATGTGCCCCACTAGTTAGCAATAACCTCAAGAATAACTGTGCTTTATTCATGTTGCTATCCATTGACTCTGGTACCTATCATAAAACTAAGAAAACACCACCAACAACCAAAAGTCCTTTTGTATTAATAAGCCCCTTCCTACAATACACAAATGACTCTGACAATGTTAAGAAACATATTTAGTCACTCATGTGTAAGGGGATTTGGTTCAACTTGTTTTTCTCTTAAATGCCACTGAATGAAGTTTTTATTGAAGAAATGGGTCTGTTTGGGAAAGAAAACGGCTAGATCACTTATTACAATGGAAGG... | ATTGATTCTTATGTGCCCCACTAGTTAGCAATAACCTCAAGAATAACTGTGCTTTATTCATGTTGCTATCCATTGACTCTGGTACCTATCATAAAACTAAGAAAACACCACCAACAACCAAAAGTCCTTTTGTATTAATAAGCCCCTTCCTACAATACACAAATGACTCTGACAATGTTAAGAAACATATTTAGTCACTCATGTGTAAGGGGATTTGGTTCAACTTGTTTTTCTCTTAAATGCCACTGAATGAAGTTTTTATTGAAGAAATGGGTCTGTTTGGGAAAGAAAACGGCTAGATCACTTATTACAATGGAAGG... |
Task1_train_38334 | This is a variant located on Chromosome 7. Is this mutation a likely cause of disease or not? | Benign | ATCATAAAACTAAGAAAACACCACCAACAACCAAAAGTCCTTTTGTATTAATAAGCCCCTTCCTACAATACACAAATGACTCTGACAATGTTAAGAAACATATTTAGTCACTCATGTGTAAGGGGATTTGGTTCAACTTGTTTTTCTCTTAAATGCCACTGAATGAAGTTTTTATTGAAGAAATGGGTCTGTTTGGGAAAGAAAACGGCTAGATCACTTATTACAATGGAAGGTGTGAATATTAGGGATGGGATATTCAGGAGTAAATGTGAGAAGCAGAAGTAGAGAATTCCCCTTACCATCCTATACTGTGTTGCTCA... | ATCATAAAACTAAGAAAACACCACCAACAACCAAAAGTCCTTTTGTATTAATAAGCCCCTTCCTACAATACACAAATGACTCTGACAATGTTAAGAAACATATTTAGTCACTCATGTGTAAGGGGATTTGGTTCAACTTGTTTTTCTCTTAAATGCCACTGAATGAAGTTTTTATTGAAGAAATGGGTCTGTTTGGGAAAGAAAACGGCTAGATCACTTATTACAATGGAAGGTGTGAATATTAGGGATGGGATATTCAGGAGTAAATGTGAGAAGCAGAAGTAGAGAATTCCCCTTACCATCCTATACTGTGTTGCTCA... |
Task1_train_38335 | This mutation on Chromosome 7 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GGAAGTTATATGGTACATGACTATAATTTGGGGTATTGTTTGAAACAAAGTATCTCAAAATTATCTGTACCCAATATTATACTCATGACATCACACAACAGTAGTACTGGAAGGCACTTTATAGATTACTGAGTCCAGATACCTTGTTTAACAAGTGCTGAATCCATGGCCTTTGAGCTTAAATGGTTAATAACTTCAGAAAACTGAACAGAGGTAAGGCTAAGCATAGGAAATTGTGTGTAGCTGAGTTAATAATTCTCATTTCTTCCATTAATAAATCACAAATCCTTTCCTAATCAAATATTAAAATAAATATCCTA... | GGAAGTTATATGGTACATGACTATAATTTGGGGTATTGTTTGAAACAAAGTATCTCAAAATTATCTGTACCCAATATTATACTCATGACATCACACAACAGTAGTACTGGAAGGCACTTTATAGATTACTGAGTCCAGATACCTTGTTTAACAAGTGCTGAATCCATGGCCTTTGAGCTTAAATGGTTAATAACTTCAGAAAACTGAACAGAGGTAAGGCTAAGCATAGGAAATTGTGTGTAGCTGAGTTAATAATTCTCATTTCTTCCATTAATAAATCACAAATCCTTTCCTAATCAAATATTAAAATAAATATCCTA... |
Task1_train_38336 | A genetic alteration is present on Chromosome 7. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TCAAAATTATCTGTACCCAATATTATACTCATGACATCACACAACAGTAGTACTGGAAGGCACTTTATAGATTACTGAGTCCAGATACCTTGTTTAACAAGTGCTGAATCCATGGCCTTTGAGCTTAAATGGTTAATAACTTCAGAAAACTGAACAGAGGTAAGGCTAAGCATAGGAAATTGTGTGTAGCTGAGTTAATAATTCTCATTTCTTCCATTAATAAATCACAAATCCTTTCCTAATCAAATATTAAAATAAATATCCTATACCCTCAACGTAAATTTTGCAGTTAGGAGAGATGCTAAATTAAACACAGAGGT... | TCAAAATTATCTGTACCCAATATTATACTCATGACATCACACAACAGTAGTACTGGAAGGCACTTTATAGATTACTGAGTCCAGATACCTTGTTTAACAAGTGCTGAATCCATGGCCTTTGAGCTTAAATGGTTAATAACTTCAGAAAACTGAACAGAGGTAAGGCTAAGCATAGGAAATTGTGTGTAGCTGAGTTAATAATTCTCATTTCTTCCATTAATAAATCACAAATCCTTTCCTAATCAAATATTAAAATAAATATCCTATACCCTCAACGTAAATTTTGCAGTTAGGAGAGATGCTAAATTAAACACAGAGGT... |
Task1_train_38337 | A variant affecting Chromosome 7 has been observed. Determine if it's benign or associated with disease. | Benign | TGTAGCTGAGTTAATAATTCTCATTTCTTCCATTAATAAATCACAAATCCTTTCCTAATCAAATATTAAAATAAATATCCTATACCCTCAACGTAAATTTTGCAGTTAGGAGAGATGCTAAATTAAACACAGAGGTCATTCATCTTAAACACATTTACGTAACTTCTGGCTGAAAACCACTTTTAAAATGTCTTGTATAGGAAATATTTGGATTAATAAAGAGTAACTTACTTTCTAAAAATGACCAAGTAAATCTTGAAATTTTGGGTCTACAAATCAAACAAGGGCTGGTTGGATTTTTGTCTCCTTCAACATAGCAG... | TGTAGCTGAGTTAATAATTCTCATTTCTTCCATTAATAAATCACAAATCCTTTCCTAATCAAATATTAAAATAAATATCCTATACCCTCAACGTAAATTTTGCAGTTAGGAGAGATGCTAAATTAAACACAGAGGTCATTCATCTTAAACACATTTACGTAACTTCTGGCTGAAAACCACTTTTAAAATGTCTTGTATAGGAAATATTTGGATTAATAAAGAGTAACTTACTTTCTAAAAATGACCAAGTAAATCTTGAAATTTTGGGTCTACAAATCAAACAAGGGCTGGTTGGATTTTTGTCTCCTTCAACATAGCAG... |
Task1_train_38338 | This alteration occurs on Chromosome 7. Is it associated with a disease or is it a benign variant? | Benign | AATAATATTTTAAAGTATACCTAAAATGCTGCTTACAACACTAATTAAGCCATTAAATGTTAAGAGTAATCTGGTATTAGAAGAGGTATCTACCATCAAACCAATAATAATATTACAAACACTACCAGTCCTAAAATCACAGGTTTCACTAATGTTTAATAATATTTTATATCAATTAAGGACAAATATTAAGAAATTACCACTACAATAAAGTACATTTTGGTTTTGCCATTTTGGCTTGTGCCATATAGCTGGGTTATAGAAAAAAATATTTCTGTAATAAAATATAGTAGTTAGTAATGCAATGTATTAAAATTTCA... | AATAATATTTTAAAGTATACCTAAAATGCTGCTTACAACACTAATTAAGCCATTAAATGTTAAGAGTAATCTGGTATTAGAAGAGGTATCTACCATCAAACCAATAATAATATTACAAACACTACCAGTCCTAAAATCACAGGTTTCACTAATGTTTAATAATATTTTATATCAATTAAGGACAAATATTAAGAAATTACCACTACAATAAAGTACATTTTGGTTTTGCCATTTTGGCTTGTGCCATATAGCTGGGTTATAGAAAAAAATATTTCTGTAATAAAATATAGTAGTTAGTAATGCAATGTATTAAAATTTCA... |
Task1_train_38339 | Consider this mutation on Chromosome 7. Is this a benign change or a disease-causing variant? | Benign | AGTAATCTGGTATTAGAAGAGGTATCTACCATCAAACCAATAATAATATTACAAACACTACCAGTCCTAAAATCACAGGTTTCACTAATGTTTAATAATATTTTATATCAATTAAGGACAAATATTAAGAAATTACCACTACAATAAAGTACATTTTGGTTTTGCCATTTTGGCTTGTGCCATATAGCTGGGTTATAGAAAAAAATATTTCTGTAATAAAATATAGTAGTTAGTAATGCAATGTATTAAAATTTCAAAATGTCATCTGTATCAGTAACATCTGGTTGTCAAAATGGGTATATGCAGTGTGTAAAAATTAT... | AGTAATCTGGTATTAGAAGAGGTATCTACCATCAAACCAATAATAATATTACAAACACTACCAGTCCTAAAATCACAGGTTTCACTAATGTTTAATAATATTTTATATCAATTAAGGACAAATATTAAGAAATTACCACTACAATAAAGTACATTTTGGTTTTGCCATTTTGGCTTGTGCCATATAGCTGGGTTATAGAAAAAAATATTTCTGTAATAAAATATAGTAGTTAGTAATGCAATGTATTAAAATTTCAAAATGTCATCTGTATCAGTAACATCTGGTTGTCAAAATGGGTATATGCAGTGTGTAAAAATTAT... |
Task1_train_38340 | This genomic variant is located on Chromosome 7. Can you determine its pathogenicity and name any linked disease? | Benign | TAGAAAAAAATATTTCTGTAATAAAATATAGTAGTTAGTAATGCAATGTATTAAAATTTCAAAATGTCATCTGTATCAGTAACATCTGGTTGTCAAAATGGGTATATGCAGTGTGTAAAAATTATTAAACCCCTTGCCTAACTACTGGGAAAACCTAAGTGAATACAACTCTACTAGCAGTAGGGTAGAAAATCACGTGTATTCAGAACCTTAAAAATCTTGATGAAAATTTTTTTTAAAGCCTGGGTTACTTCAGTCCATACTTTCACAAATTCAACAAATGTTTAGTAATTTTTATTTATCTGTTGCTATTCTAGGTA... | TAGAAAAAAATATTTCTGTAATAAAATATAGTAGTTAGTAATGCAATGTATTAAAATTTCAAAATGTCATCTGTATCAGTAACATCTGGTTGTCAAAATGGGTATATGCAGTGTGTAAAAATTATTAAACCCCTTGCCTAACTACTGGGAAAACCTAAGTGAATACAACTCTACTAGCAGTAGGGTAGAAAATCACGTGTATTCAGAACCTTAAAAATCTTGATGAAAATTTTTTTTAAAGCCTGGGTTACTTCAGTCCATACTTTCACAAATTCAACAAATGTTTAGTAATTTTTATTTATCTGTTGCTATTCTAGGTA... |
Task1_train_38341 | This variant is found on Chromosome 7. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GTATGTATTTCAAAACACTGAAATAAAATTATATGTTGAGAACATTGTCTTAGTTTCTATAATCATGTAAAGTAGACAATAATGCATTATTTGCTTTGAGATTATGGCCAATAATGATATATTACATCAACTTTAGATGTCATTTGGAAATAAAACAGTAGTTAAAAACAGAATGTGAAATTGGAGTGTGTGTCATTGTTTTTATGAAAAAAGATTGCATTACAGACTCAGCAAAAAATTAACCATAGGAGAAAACTTATTGTAATTATTATTTTTGCTGACATTAAGAGAGATTTCTGAGAATGCTAGAAATTTAAAGG... | GTATGTATTTCAAAACACTGAAATAAAATTATATGTTGAGAACATTGTCTTAGTTTCTATAATCATGTAAAGTAGACAATAATGCATTATTTGCTTTGAGATTATGGCCAATAATGATATATTACATCAACTTTAGATGTCATTTGGAAATAAAACAGTAGTTAAAAACAGAATGTGAAATTGGAGTGTGTGTCATTGTTTTTATGAAAAAAGATTGCATTACAGACTCAGCAAAAAATTAACCATAGGAGAAAACTTATTGTAATTATTATTTTTGCTGACATTAAGAGAGATTTCTGAGAATGCTAGAAATTTAAAGG... |
Task1_train_38342 | This variant is found on Chromosome 7. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | AATGAGACTTAGCCACAATGCCACACATTAAAATTAAACACTGTTAAAATTTCAATGTCTTTCCAGAGATCTTTTTACATTAGTGCTTAAAAAGGAAAATGATTCCTGTGTCTGCAGTATTTATAAAATGTGAATAACAATAAGGAAAACAAGCCTTTTGCTAAGACATAATCTTATATGATGTGATCTCTCTCCAGGGGCCAATGGTAGTTGCATGACCTCTAGGTTAAAAGAAAATCGACTTTAAGAATGAACTCACACCCAAAAAGTGTATAATTATATAGGGTAAAATTGTGAGTGATGATGAACACGTTAGTAAT... | AATGAGACTTAGCCACAATGCCACACATTAAAATTAAACACTGTTAAAATTTCAATGTCTTTCCAGAGATCTTTTTACATTAGTGCTTAAAAAGGAAAATGATTCCTGTGTCTGCAGTATTTATAAAATGTGAATAACAATAAGGAAAACAAGCCTTTTGCTAAGACATAATCTTATATGATGTGATCTCTCTCCAGGGGCCAATGGTAGTTGCATGACCTCTAGGTTAAAAGAAAATCGACTTTAAGAATGAACTCACACCCAAAAAGTGTATAATTATATAGGGTAAAATTGTGAGTGATGATGAACACGTTAGTAAT... |
Task1_train_38343 | An alteration has been detected on Chromosome 7. Is it pathogenic, and if so, what disease is involved? | Benign | TGTGAATGCACCTGGGATTCAAAACTAATTTTGACGAAAGCCCCATGGCCTGTTAGATCTGCTTCATATACAGTGAGTTTGACTTTCTCTATAGCTGTTGGAAAATGTCTCCAGCACTGTTGTCGACAATTGCTTTAGTGCAGGAGTTTTTTATTTGTTGTAGTGTAAAATATATTTCTGTCTTTAAAAATAAAGCATATAGCCGCTGCTTTTTTTGTGAAATACAAATAGTGGATTATCTAGAACTTTGGATTTTCTTTTCTTTTATTTCTAGATCTTGATAAAAGAATAAGTGTATTCCAGTGGGAAAATATAGAATA... | TGTGAATGCACCTGGGATTCAAAACTAATTTTGACGAAAGCCCCATGGCCTGTTAGATCTGCTTCATATACAGTGAGTTTGACTTTCTCTATAGCTGTTGGAAAATGTCTCCAGCACTGTTGTCGACAATTGCTTTAGTGCAGGAGTTTTTTATTTGTTGTAGTGTAAAATATATTTCTGTCTTTAAAAATAAAGCATATAGCCGCTGCTTTTTTTGTGAAATACAAATAGTGGATTATCTAGAACTTTGGATTTTCTTTTCTTTTATTTCTAGATCTTGATAAAAGAATAAGTGTATTCCAGTGGGAAAATATAGAATA... |
Task1_train_38344 | The following genetic variant occurs on Chromosome 7. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CCTCTGTACCTCATTGGGATATTGGCCAATCACTCTGTGATTCTCCCCCATGCCCGCTGATAAATTTGTATGCCATTTGTCCTGTTAATCTGCCTTTTGTGACTTGATTTTTCAGTGAAACTTCAGAGGGTAGAGGGGAAGTTTTCCCTTGGCCCCTACACTATGAACTGAGATAGACAAAATAAATTAGTATGTTTATAAAGTGGAATACCATATGGTCAGTAAAAACCGGTAGCTCTATGAGTACTGTGTGTTGATACACAGACACACACACACACACACACACACACACACACACACACACACACACGGGGGGGGAT... | CCTCTGTACCTCATTGGGATATTGGCCAATCACTCTGTGATTCTCCCCCATGCCCGCTGATAAATTTGTATGCCATTTGTCCTGTTAATCTGCCTTTTGTGACTTGATTTTTCAGTGAAACTTCAGAGGGTAGAGGGGAAGTTTTCCCTTGGCCCCTACACTATGAACTGAGATAGACAAAATAAATTAGTATGTTTATAAAGTGGAATACCATATGGTCAGTAAAAACCGGTAGCTCTATGAGTACTGTGTGTTGATACACAGACACACACACACACACACACACACACACACACACACACACACACACGGGGGGGGAT... |
Task1_train_38345 | This variant lies on Chromosome 7. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TATTGACCTTCCAGGGATTCATGTAATTTGAGAAATTGAATGAAAACAATTTTACATGCATGAAATTCAGCTTTCTTACTCTATACATCCTGAGTGATTTGCCTTTTTCAGTAACAGAATCCTTTGCTATACCAGCTTGTTAAATGAATGCCAAATCAAGAGTAAAATTTCCATCTGTATTCCATAGTGTTTTAGCCATGCTGCAAAAGCAAAACCTGTAGGTAAAACAAAGAAAATTATCACCTTGAAGCTAGGTAACAGGTAACCCAGAAGTCCGGCCAAGCATAAAATTACAGCCACAAACAGCCCTGCAGAGAACA... | TATTGACCTTCCAGGGATTCATGTAATTTGAGAAATTGAATGAAAACAATTTTACATGCATGAAATTCAGCTTTCTTACTCTATACATCCTGAGTGATTTGCCTTTTTCAGTAACAGAATCCTTTGCTATACCAGCTTGTTAAATGAATGCCAAATCAAGAGTAAAATTTCCATCTGTATTCCATAGTGTTTTAGCCATGCTGCAAAAGCAAAACCTGTAGGTAAAACAAAGAAAATTATCACCTTGAAGCTAGGTAACAGGTAACCCAGAAGTCCGGCCAAGCATAAAATTACAGCCACAAACAGCCCTGCAGAGAACA... |
Task1_train_38346 | A mutation is present on Chromosome 7. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TTTATTCTGTTGCTCCATCAATGCAACGGAATTATATCCAGCTGCAAAAATCTTTTACAAGGAGTAAAGGAATATATGCTGCACAAGGCAGCTCTTGCTTCAAAGCAAAGTCAACAGTGTTCATATAATGAATTGCATGTTTGGTTCCACCTATGTTCTTTACCAGTATTTCTGAAGAAAAACCCACTTCTTTTGTGAAATGGTTCACCTAACTCATTCTCATGAATGAAGAAACAAATGATACTATTCCCCCATGAAATGCTGTACTCAATAATATTTTCTGTATAGCGATGGAAGTACCAGAATTTATTGCATATGCC... | TTTATTCTGTTGCTCCATCAATGCAACGGAATTATATCCAGCTGCAAAAATCTTTTACAAGGAGTAAAGGAATATATGCTGCACAAGGCAGCTCTTGCTTCAAAGCAAAGTCAACAGTGTTCATATAATGAATTGCATGTTTGGTTCCACCTATGTTCTTTACCAGTATTTCTGAAGAAAAACCCACTTCTTTTGTGAAATGGTTCACCTAACTCATTCTCATGAATGAAGAAACAAATGATACTATTCCCCCATGAAATGCTGTACTCAATAATATTTTCTGTATAGCGATGGAAGTACCAGAATTTATTGCATATGCC... |
Task1_train_38347 | An alteration has been detected on Chromosome 7. Is it pathogenic, and if so, what disease is involved? | Benign | AACATCAGAGCAAACTGTACAACTGTATATATCTTTAATAGCTGAGATGAAGATGATGAGAAGGGAACTTCTTTGCCGGTGACCTAGGGAGACAAGAACCATTTCCTTTATATTGCTCCAGACTCATTTTTCTTACTGAAATTCACACTAAGAGATATTTGAAAAAAGTATCTGCTATTTTTTTTAAAAAAAGACAAACATAATTTTTAAAAATAGAAACATGTCTAAGTTAGGAGACTTTCTCATTTTGAAAGCATTACAATTATGACGTAGTCTGCCTTAAAGAGCAGCATAAGAACTAATTCAACAATATGTGCAAA... | AACATCAGAGCAAACTGTACAACTGTATATATCTTTAATAGCTGAGATGAAGATGATGAGAAGGGAACTTCTTTGCCGGTGACCTAGGGAGACAAGAACCATTTCCTTTATATTGCTCCAGACTCATTTTTCTTACTGAAATTCACACTAAGAGATATTTGAAAAAAGTATCTGCTATTTTTTTTAAAAAAAGACAAACATAATTTTTAAAAATAGAAACATGTCTAAGTTAGGAGACTTTCTCATTTTGAAAGCATTACAATTATGACGTAGTCTGCCTTAAAGAGCAGCATAAGAACTAATTCAACAATATGTGCAAA... |
Task1_train_38348 | Given this variant on Chromosome 7, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TTTCCAAACTCCAATATTCAGAAAGTAAAATAGTCATATGAGAACCTGAAACTGCCTTTGTGAAAATTATAACTGAGGAAATTAGGACAGTGAAAGATCAGTCCTAACTAACTCCATCTTGCTTCTAACCATTAAGCTCATTCCTTGGCATAGGCCGAACTAACCTTGGGAAGGAATTTAGTTTATGGTTTGACTCTGGAACAAAATTGATAATAGCCCTTTCCCAAAAAGACCCCTTTCTTGCCTGGGGACCAGTCTGCCTTCACAGGACTAACAAATTAGCTACAAGATTAGAAATTACAGTTTAGGGGTCATGCATC... | TTTCCAAACTCCAATATTCAGAAAGTAAAATAGTCATATGAGAACCTGAAACTGCCTTTGTGAAAATTATAACTGAGGAAATTAGGACAGTGAAAGATCAGTCCTAACTAACTCCATCTTGCTTCTAACCATTAAGCTCATTCCTTGGCATAGGCCGAACTAACCTTGGGAAGGAATTTAGTTTATGGTTTGACTCTGGAACAAAATTGATAATAGCCCTTTCCCAAAAAGACCCCTTTCTTGCCTGGGGACCAGTCTGCCTTCACAGGACTAACAAATTAGCTACAAGATTAGAAATTACAGTTTAGGGGTCATGCATC... |
Task1_train_38349 | A variant has been detected on Chromosome 7. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | AGACAGAAGGGCTTGGAGATTTTTTTTCTTTACAATTCAGTCTTCAGCAACTTGAGAGCTTTCTTCATGTTGTCAAGCACTAATGGGGGATAAAAGCAGGAGAGTCAAGACACCATCGTGCGTTATATCGATATAATAAACCCCAAACTTGGATGCTCAATTCATTATTTAATGGGATGCTTTTTTTTTTGAGACAAGGTCTCACTCCCACTCAGGCTGGCATGCAGTGGTGCAATCTCCACTCAGTGCAACCTCTGCCTCCTGGGTTCAAGTGATTCTTCAGCCTTAGCCTCCTGAGTAGCTGGGATTAGAGGTGTGCT... | AGACAGAAGGGCTTGGAGATTTTTTTTCTTTACAATTCAGTCTTCAGCAACTTGAGAGCTTTCTTCATGTTGTCAAGCACTAATGGGGGATAAAAGCAGGAGAGTCAAGACACCATCGTGCGTTATATCGATATAATAAACCCCAAACTTGGATGCTCAATTCATTATTTAATGGGATGCTTTTTTTTTTGAGACAAGGTCTCACTCCCACTCAGGCTGGCATGCAGTGGTGCAATCTCCACTCAGTGCAACCTCTGCCTCCTGGGTTCAAGTGATTCTTCAGCCTTAGCCTCCTGAGTAGCTGGGATTAGAGGTGTGCT... |
Task1_train_38350 | A genomic variant on Chromosome 7 is under review. What is the biological outcome — benign or pathogenic? | Benign | ATTTATTACTGAAGGGGGGCATCTTTTTACATCTTTCTGTTTTTTTTTTTTTTTTGAGATGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGGGATCTCGGCTCACTGCAAGCTCCGCCACCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCCCGCCACTACGCCCGGCTAATTTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTTTTAGCCAGGATGGTCTCAATCTCCTGACCTCGTGATCCGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTG... | ATTTATTACTGAAGGGGGGCATCTTTTTACATCTTTCTGTTTTTTTTTTTTTTTTGAGATGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGGGATCTCGGCTCACTGCAAGCTCCGCCACCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCCCGCCACTACGCCCGGCTAATTTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTTTTAGCCAGGATGGTCTCAATCTCCTGACCTCGTGATCCGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTG... |
Task1_train_38351 | A mutation on Chromosome 7 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TTTTAAGAAAATTCATACTTTGTTTAGTAGTTACTTTAATGAATTATTAATCTATGTATGGATGCGTTAAACAAATCATTAAATACTGTGTGCAGACACAGTTTTAAGCACTAAGAAAACAACCTTCAGTGTCCTCATGGAGCTTATAGGATGGGGAGCAGGAAGTGAATTATTGAAATAAACAGTAATACAGGCCGGGTGCAATGGCTCATGCCTGTAATCCCAGCACTCTGGGAGGCCGATGTGGGTGGATAAGCTGAGGTGGGGAGTTCGAGACCAGCCTGACCAACATGGAGAAACCCCGTCTCTACTAAAAATAC... | TTTTAAGAAAATTCATACTTTGTTTAGTAGTTACTTTAATGAATTATTAATCTATGTATGGATGCGTTAAACAAATCATTAAATACTGTGTGCAGACACAGTTTTAAGCACTAAGAAAACAACCTTCAGTGTCCTCATGGAGCTTATAGGATGGGGAGCAGGAAGTGAATTATTGAAATAAACAGTAATACAGGCCGGGTGCAATGGCTCATGCCTGTAATCCCAGCACTCTGGGAGGCCGATGTGGGTGGATAAGCTGAGGTGGGGAGTTCGAGACCAGCCTGACCAACATGGAGAAACCCCGTCTCTACTAAAAATAC... |
Task1_train_38352 | A sequence alteration has been identified on Chromosome 7. Is it disease-inducing or harmless? | Benign | TAATTTGGTTGTTTCCCAACCTTGACAAGTAGTTTCATGTGACAGAATGAAAAAATTAGGTCTTGCTAAGGAATTTTTAATATAGTTAAGTGATTTGTAGACATGAAAACTGCCAGTGGGTAGCAGTCTCTTTTTTTTTTTTTTGCATATTTTGGTAGCTTGCAAGTTCCTGGTTTTAGTTCTTTTTTCCTGTATCTTTCAGCTCTTCCTCTAACTACTTATGAAATCTGAGGAACTACAGTGACCCTGAAATGTCATCTGGTCTAGAGTATTCCTCTTCCTGCAGGCAGAATTGCATCCAGAGCTATTCTCTCATATCT... | TAATTTGGTTGTTTCCCAACCTTGACAAGTAGTTTCATGTGACAGAATGAAAAAATTAGGTCTTGCTAAGGAATTTTTAATATAGTTAAGTGATTTGTAGACATGAAAACTGCCAGTGGGTAGCAGTCTCTTTTTTTTTTTTTTGCATATTTTGGTAGCTTGCAAGTTCCTGGTTTTAGTTCTTTTTTCCTGTATCTTTCAGCTCTTCCTCTAACTACTTATGAAATCTGAGGAACTACAGTGACCCTGAAATGTCATCTGGTCTAGAGTATTCCTCTTCCTGCAGGCAGAATTGCATCCAGAGCTATTCTCTCATATCT... |
Task1_train_38353 | A genomic variant on Chromosome 7 is under review. What is the biological outcome — benign or pathogenic? | Benign | CCCTAAAAAGATTCTGCTTTTACTTTTTAGCCAAATGGACATCTTTTATTCAGGTTCCCAAAACAAAATCCTTCTTTGGCTTACCCACATTTCTTTGAGGCTGTGTGTTTTCTTTCTAAATTCTAGCAGCCTTAATGGCCCTAATGTGGCTTCTTCTTGCTCCATCCTCATCTCAACCTTGAATCTTTTATCCTTTCACTCCTTCACCCCTGCTATCTGCACCTATTCAGCTCCCACCCATCTAAGAGCTTCAGTGCTTTGTGGGATCACCGCTTACACCCCACCACACCAGGACAATGCCTACTCTTCCTTGAGGTTCA... | CCCTAAAAAGATTCTGCTTTTACTTTTTAGCCAAATGGACATCTTTTATTCAGGTTCCCAAAACAAAATCCTTCTTTGGCTTACCCACATTTCTTTGAGGCTGTGTGTTTTCTTTCTAAATTCTAGCAGCCTTAATGGCCCTAATGTGGCTTCTTCTTGCTCCATCCTCATCTCAACCTTGAATCTTTTATCCTTTCACTCCTTCACCCCTGCTATCTGCACCTATTCAGCTCCCACCCATCTAAGAGCTTCAGTGCTTTGTGGGATCACCGCTTACACCCCACCACACCAGGACAATGCCTACTCTTCCTTGAGGTTCA... |
Task1_train_38354 | This alteration occurs on Chromosome 7. Is it associated with a disease or is it a benign variant? | Benign | TGACCTCCGCAAGTTGTGTCTGGGCCCATCCAGGGCTCTGACTAATTGTATTCAAATCAAGGCAGGAGCGGGCCAGCTGGCGTTGACTTAACCAAGCCATTTTATAAGCCTCCCGATCATTTTTAAGCCACTCTAAGTCGTGTAGTAGGATCTGGTCAGAGTTATGTATACTCTGATGGGCATGTGCTGTGTCGTCTAAAATGTCCAGAAGTTCTGAAACACTTTTAGATCTTCCAGAATTTCTTGAGGAAGTCTGCCTAAGTAACTGATGCACATCAAGTTCATCACCGGAGGAATCAAAAGAATTTCCATTTTCTATT... | TGACCTCCGCAAGTTGTGTCTGGGCCCATCCAGGGCTCTGACTAATTGTATTCAAATCAAGGCAGGAGCGGGCCAGCTGGCGTTGACTTAACCAAGCCATTTTATAAGCCTCCCGATCATTTTTAAGCCACTCTAAGTCGTGTAGTAGGATCTGGTCAGAGTTATGTATACTCTGATGGGCATGTGCTGTGTCGTCTAAAATGTCCAGAAGTTCTGAAACACTTTTAGATCTTCCAGAATTTCTTGAGGAAGTCTGCCTAAGTAACTGATGCACATCAAGTTCATCACCGGAGGAATCAAAAGAATTTCCATTTTCTATT... |
Task1_train_38355 | Given this variant on Chromosome 7, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GTTTGTAAATAACTGGCAGGGGTCACAGTGTCACATCTAGGAGATTTCATTTTATTTTATTTCGACAACCAGAGTTACAGCCTCTTTACAACTGAGAAGTGGTAATAAATGGTATTGTGCTTATTCTTCAACAACTCCATAGCACTGGCACCTGACATATATTTGCATGAATTTCATGTAACAAAATGTAGAAATCTTTCTTTCTAAAGGGCTTCAAAATTTCCCGAAACAGACTTCTGAACTTCATTTTATTCCTCTTGCTACATGGTTGTTCTGGATTAGTATATATATCAACACCTAAAAACAGAGTTACAAAAATT... | GTTTGTAAATAACTGGCAGGGGTCACAGTGTCACATCTAGGAGATTTCATTTTATTTTATTTCGACAACCAGAGTTACAGCCTCTTTACAACTGAGAAGTGGTAATAAATGGTATTGTGCTTATTCTTCAACAACTCCATAGCACTGGCACCTGACATATATTTGCATGAATTTCATGTAACAAAATGTAGAAATCTTTCTTTCTAAAGGGCTTCAAAATTTCCCGAAACAGACTTCTGAACTTCATTTTATTCCTCTTGCTACATGGTTGTTCTGGATTAGTATATATATCAACACCTAAAAACAGAGTTACAAAAATT... |
Task1_train_38356 | Mutation context: Chromosome 7. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CTACTAAGTTGTGTTCTGTTTTTGTAAGGTATACACAGAATCTCAAAGATGCAAAGGATTTTGGCATAAAAAGGACTATAGCTTCAAAAGTGTCTCTTGGTGCTGTGTACTTCTTTATGAATGGAACCTATGGACTTGCTTTTTGGTATGGAACCTCCTTGATTCTTAATGGAGAACCTGGATATACCATCGGGACTGTTCTTGCTGTAAGTCTTGTTTGAGAACAAGGTGTCAGGCCTGGATAATCTTTCCTTACCTAGTTTAGCCAAAATTCCTCTTTGAAGATAAATATTCAAAGATGGATGTTTTTATTAAACAAA... | CTACTAAGTTGTGTTCTGTTTTTGTAAGGTATACACAGAATCTCAAAGATGCAAAGGATTTTGGCATAAAAAGGACTATAGCTTCAAAAGTGTCTCTTGGTGCTGTGTACTTCTTTATGAATGGAACCTATGGACTTGCTTTTTGGTATGGAACCTCCTTGATTCTTAATGGAGAACCTGGATATACCATCGGGACTGTTCTTGCTGTAAGTCTTGTTTGAGAACAAGGTGTCAGGCCTGGATAATCTTTCCTTACCTAGTTTAGCCAAAATTCCTCTTTGAAGATAAATATTCAAAGATGGATGTTTTTATTAAACAAA... |
Task1_train_38357 | Chromosome 7 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | ATAGGTGAGAATTTCTCAACAGGATCACTGTTGTCATTTCGAGAGGGTAATTATTGTGAGGCTTCAATCACATTGCAGGTCCCTGGCACACTAAATGCTGTAGCAACCCCAGTCATTGAGAAAATGTTTAAAGTGTTCCCTCATGGGTCACCATGAGCCCACCAAGGTTTCTAATGATAAACTCTCATCTATCGGGAGCCACTAAGAAACTTTGCCAGCTGTTTTCCTTTAGAATATGCTTTGCAATTATGTTAGTATGTCCTAAGGAGGAGCTTCATTAAATAGCTTGTGAAAATATCTGGCAAGATCTCATTTACTTG... | ATAGGTGAGAATTTCTCAACAGGATCACTGTTGTCATTTCGAGAGGGTAATTATTGTGAGGCTTCAATCACATTGCAGGTCCCTGGCACACTAAATGCTGTAGCAACCCCAGTCATTGAGAAAATGTTTAAAGTGTTCCCTCATGGGTCACCATGAGCCCACCAAGGTTTCTAATGATAAACTCTCATCTATCGGGAGCCACTAAGAAACTTTGCCAGCTGTTTTCCTTTAGAATATGCTTTGCAATTATGTTAGTATGTCCTAAGGAGGAGCTTCATTAAATAGCTTGTGAAAATATCTGGCAAGATCTCATTTACTTG... |
Task1_train_38358 | Given a variant located on Chromosome 7, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CTGAGTCCTTTTAAGTTGCTATTTTTAATTCTTTGCTAGAATAAAATAATTATGTGATTACTTTATCTCTGCTATCTTTTTTTTTTTTTTTTTTTTTTTTGAGACAGAGAAGTCTCACTCTGTTGCCCAAGCTGGAGTGCAGTGGATGATCTCAGCTCACTGCAACCTCCACCTCCCAGGTTCAAGTGATTCTCGTGCCTTAGCTTCCTGAGTAGCTGGGATTACAGACATGTGCCACCATACCTGGTTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTACCATGTTGGCCAGGCTGGTTTCGAACTCCTGGCCTCAA... | CTGAGTCCTTTTAAGTTGCTATTTTTAATTCTTTGCTAGAATAAAATAATTATGTGATTACTTTATCTCTGCTATCTTTTTTTTTTTTTTTTTTTTTTTTGAGACAGAGAAGTCTCACTCTGTTGCCCAAGCTGGAGTGCAGTGGATGATCTCAGCTCACTGCAACCTCCACCTCCCAGGTTCAAGTGATTCTCGTGCCTTAGCTTCCTGAGTAGCTGGGATTACAGACATGTGCCACCATACCTGGTTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTACCATGTTGGCCAGGCTGGTTTCGAACTCCTGGCCTCAA... |
Task1_train_38359 | An alteration has been detected on Chromosome 7. Is it pathogenic, and if so, what disease is involved? | Benign | GTCAGCAGTTCGAGACCAGCCTGGTCAACACAAAAATTAGCTAGGCATGGTGGTGCATGCCTGTAATCCCAGCTTCAGGAGGTGGAGGCAGGAGAATTGCTTGAACCCAGGAGATGGAGGTTGCAGTGAGCTGACATCATGCCACTGCACTCCAGCCTGAATGACAAAGCAAGACTCTGTCTTAAAAAAAAAAAAAGATGAAGAAGATTAGTGTCCCTCACTCAACCCCAGATAGTCCAACACCTCAAAGTCCACACTTCCCCTCCAGGGTCTTCAACATAACCCTCATCGGCATCAGCCCCCATCCCACTTACGTTTCT... | GTCAGCAGTTCGAGACCAGCCTGGTCAACACAAAAATTAGCTAGGCATGGTGGTGCATGCCTGTAATCCCAGCTTCAGGAGGTGGAGGCAGGAGAATTGCTTGAACCCAGGAGATGGAGGTTGCAGTGAGCTGACATCATGCCACTGCACTCCAGCCTGAATGACAAAGCAAGACTCTGTCTTAAAAAAAAAAAAAGATGAAGAAGATTAGTGTCCCTCACTCAACCCCAGATAGTCCAACACCTCAAAGTCCACACTTCCCCTCCAGGGTCTTCAACATAACCCTCATCGGCATCAGCCCCCATCCCACTTACGTTTCT... |
Task1_train_38360 | This alteration occurs on Chromosome 7. Is it associated with a disease or is it a benign variant? | Benign | TGGGAACAAGGTAAAGCCATGTTCATTCACTGTCACATTGAAACACTGCTTCACCGGCCAATGAAAGGATTATTAATTATTTAGGGAAAAGTATCTTTTTTGGACTCATTAACTACTACTGATCGAAGTCTCAAACTCTGAAGTTACGTTTTTATTTACAGATTTTTGTTCAATACAGATGTAATTTATTTTGGAAAAACAAATTATTTTTTAAAAAACAAAGGATTATTTTGCCCTGTATGACATTAGTGAGTGTTGTTTTGAACCTAGCAAGCTGACTCATCCTGTCTTCCTCCAATGCTGCTAAATTTCTTTCTCGA... | TGGGAACAAGGTAAAGCCATGTTCATTCACTGTCACATTGAAACACTGCTTCACCGGCCAATGAAAGGATTATTAATTATTTAGGGAAAAGTATCTTTTTTGGACTCATTAACTACTACTGATCGAAGTCTCAAACTCTGAAGTTACGTTTTTATTTACAGATTTTTGTTCAATACAGATGTAATTTATTTTGGAAAAACAAATTATTTTTTAAAAAACAAAGGATTATTTTGCCCTGTATGACATTAGTGAGTGTTGTTTTGAACCTAGCAAGCTGACTCATCCTGTCTTCCTCCAATGCTGCTAAATTTCTTTCTCGA... |
Task1_train_38361 | With a mutation on Chromosome 7, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GAATGTAGTTTATGGAAATATTTGCAAATTTTTATTATGAAGCTGTTTTTTAAGTGAAACAAGTTTTAGGGAATACCTGTTATTTCCTTAAGAAAAAGAACAAAGCCCCCTCCTTTGCCATATTGCTAAACAAGGCGTGACCTTGGATACAGTTTATCTACCACTGTAAATATACTTAGTTATTTTGAGATGTCTTCTTTCAGAGAAAATACCTATATGACAGGCTTAATAACTAACATATTATAAAGCCCACACAGAATGATCAGATAACAAAATGACATAACTTTCAATGGCGTATTAGCTGATGAGAAGCTACACAC... | GAATGTAGTTTATGGAAATATTTGCAAATTTTTATTATGAAGCTGTTTTTTAAGTGAAACAAGTTTTAGGGAATACCTGTTATTTCCTTAAGAAAAAGAACAAAGCCCCCTCCTTTGCCATATTGCTAAACAAGGCGTGACCTTGGATACAGTTTATCTACCACTGTAAATATACTTAGTTATTTTGAGATGTCTTCTTTCAGAGAAAATACCTATATGACAGGCTTAATAACTAACATATTATAAAGCCCACACAGAATGATCAGATAACAAAATGACATAACTTTCAATGGCGTATTAGCTGATGAGAAGCTACACAC... |
Task1_train_38362 | Chromosome 7 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CCTAGTACCCACTGGTTATTTTTCCTGATCCTCTCCCTCCTTCCAATCCTTACCCTCCTTTAGATCCCAGTGTGTGTTGTGCCCCTCTATGTGTCCATGTGTTCTCATCATTTATTTCCCACTTAAAAGTGAGAAAATGCAGTATTTGGTTTTCTGCTCCTGCATTAGTTTGCTGAGGATAATGGCCTCCAGCTCCATCCATGTTCCTGCAAAGGACATGATCTCGTTGTTTTTTATGGCTGCATAGTATTCCATGTATACACGTACCACATTTTCTTTATCCAGTGTATCATTGATAGGCACTTAGGTTGATTCCATGT... | CCTAGTACCCACTGGTTATTTTTCCTGATCCTCTCCCTCCTTCCAATCCTTACCCTCCTTTAGATCCCAGTGTGTGTTGTGCCCCTCTATGTGTCCATGTGTTCTCATCATTTATTTCCCACTTAAAAGTGAGAAAATGCAGTATTTGGTTTTCTGCTCCTGCATTAGTTTGCTGAGGATAATGGCCTCCAGCTCCATCCATGTTCCTGCAAAGGACATGATCTCGTTGTTTTTTATGGCTGCATAGTATTCCATGTATACACGTACCACATTTTCTTTATCCAGTGTATCATTGATAGGCACTTAGGTTGATTCCATGT... |
Task1_train_38363 | This mutation is located on Chromosome 7. Is it associated with a disease or is it a benign polymorphism? | Benign | AATCCTTACCCTCCTTTAGATCCCAGTGTGTGTTGTGCCCCTCTATGTGTCCATGTGTTCTCATCATTTATTTCCCACTTAAAAGTGAGAAAATGCAGTATTTGGTTTTCTGCTCCTGCATTAGTTTGCTGAGGATAATGGCCTCCAGCTCCATCCATGTTCCTGCAAAGGACATGATCTCGTTGTTTTTTATGGCTGCATAGTATTCCATGTATACACGTACCACATTTTCTTTATCCAGTGTATCATTGATAGGCACTTAGGTTGATTCCATGTCTTTGCTATTGTGAATAGTGCTATAATGAACATACATGTGTGTG... | AATCCTTACCCTCCTTTAGATCCCAGTGTGTGTTGTGCCCCTCTATGTGTCCATGTGTTCTCATCATTTATTTCCCACTTAAAAGTGAGAAAATGCAGTATTTGGTTTTCTGCTCCTGCATTAGTTTGCTGAGGATAATGGCCTCCAGCTCCATCCATGTTCCTGCAAAGGACATGATCTCGTTGTTTTTTATGGCTGCATAGTATTCCATGTATACACGTACCACATTTTCTTTATCCAGTGTATCATTGATAGGCACTTAGGTTGATTCCATGTCTTTGCTATTGTGAATAGTGCTATAATGAACATACATGTGTGTG... |
Task1_train_38364 | This alteration on Chromosome 7 may affect genome function. Does it lead to a disease or is it benign? | Benign | ATTGGAGAGATTTCTAGCAAAGGAGAGTGACTATTTCTCATAAAAATTGAGATTAAAAGGTTTTTTCTTTCTACCTGAAGTAGAAGTCACAGATAAATTTTAAGTCATTTAACTTTTGAGGAAGAAAAAATAGATTGTTTATATCTCTCTCATTTTTATATGTAGGTATGCTTTTTAAGATTCTGGGCGCTCTCTCATTCTCTGTCTCTCTCTTTCTCTCTCTCCCTTCCTCTCTTTCTCCCTTTCTCTCTCCTTCTCCTCCCCCTCTGCCCCCACCTCCTCCTACTTGTCTCCCTTTCTCTTCTTTTTCCTCTTCCCAT... | ATTGGAGAGATTTCTAGCAAAGGAGAGTGACTATTTCTCATAAAAATTGAGATTAAAAGGTTTTTTCTTTCTACCTGAAGTAGAAGTCACAGATAAATTTTAAGTCATTTAACTTTTGAGGAAGAAAAAATAGATTGTTTATATCTCTCTCATTTTTATATGTAGGTATGCTTTTTAAGATTCTGGGCGCTCTCTCATTCTCTGTCTCTCTCTTTCTCTCTCTCCCTTCCTCTCTTTCTCCCTTTCTCTCTCCTTCTCCTCCCCCTCTGCCCCCACCTCCTCCTACTTGTCTCCCTTTCTCTTCTTTTTCCTCTTCCCAT... |
Task1_train_38365 | This is a variant located on Chromosome 7. Is this mutation a likely cause of disease or not? | Benign | AACCCAGGAGGCACACGTCGCAGTGAGCCAAGATCATACCACTGTACTCCAGCCTGGGCGACAGAGCAAGACTTCCTCTAAAAAAAAAAAAAAAAAAGTACTTAACCACCATTTCCCACACTTTTCTTGGTTTTTATTAGTTGGTATTGACAAAGCACCAAAATGATTTTAAAATTGAGCTCAAGTATCTGGAAGACGATCTCCTTTTGCGCCTTTCTGCGGCAGAGGGAAGCTTTCTGGATGACACCAAACTGGTAGAGAGATTGGAGGCAACAAAGACCACCGTGGCAGAGATAGAGCACAAGGTAGGAAGGGCAGAG... | AACCCAGGAGGCACACGTCGCAGTGAGCCAAGATCATACCACTGTACTCCAGCCTGGGCGACAGAGCAAGACTTCCTCTAAAAAAAAAAAAAAAAAAGTACTTAACCACCATTTCCCACACTTTTCTTGGTTTTTATTAGTTGGTATTGACAAAGCACCAAAATGATTTTAAAATTGAGCTCAAGTATCTGGAAGACGATCTCCTTTTGCGCCTTTCTGCGGCAGAGGGAAGCTTTCTGGATGACACCAAACTGGTAGAGAGATTGGAGGCAACAAAGACCACCGTGGCAGAGATAGAGCACAAGGTAGGAAGGGCAGAG... |
Task1_train_38366 | Located on Chromosome 7, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | ACAACAACAACAACAACGACAACAAAACACAGCAAATAACCAGATTTTAAAATAAGGACATAAGTGGACATTTCTCCAAAGATGTTATAAAAATGATCAACAAGCCTGGGCAACACAGAGAAACCCTGTCTCTACAAAAAAATTCAAAAATTAGCCAAGTGTGATGACACATGCCTGTGGTCTCAGCTACCCAAGAGGCTGAGGTGGGAGGGTTGCTTAGGACCGGGAGGTTGAGGCTGCAGTGAGCCACGGTCACTCCACCGCACTCCAGGCTGGATGACAGAATGAAAGTTTGTCTCAAACAAAAAAGGCAACAAACA... | ACAACAACAACAACAACGACAACAAAACACAGCAAATAACCAGATTTTAAAATAAGGACATAAGTGGACATTTCTCCAAAGATGTTATAAAAATGATCAACAAGCCTGGGCAACACAGAGAAACCCTGTCTCTACAAAAAAATTCAAAAATTAGCCAAGTGTGATGACACATGCCTGTGGTCTCAGCTACCCAAGAGGCTGAGGTGGGAGGGTTGCTTAGGACCGGGAGGTTGAGGCTGCAGTGAGCCACGGTCACTCCACCGCACTCCAGGCTGGATGACAGAATGAAAGTTTGTCTCAAACAAAAAAGGCAACAAACA... |
Task1_train_38367 | A variant on Chromosome 7 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TCAGTCATTTTCTGCACATCACAAGGCGACTTATCAGGATTTGGGAATTAAATTCCTATGAGCACATGTTTGGTTGTACAAAATGGCCTTTTCAAGAAAGTATATGTAAAAAACAAAGACCAGGATTGAGGGAAAGAGAATCAATTATTGAAAAGAACAGATCTGAGGCCAGGCGTGATGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCAAGTCGGGCGGATCGCTTGAGTCCAGAAGTTCGACACCAGCCTGGGTAACATGGGGAAACCCAGTCTCCATAAAAAATACAAAAGATTAGCTGGGCATGGTGATGC... | TCAGTCATTTTCTGCACATCACAAGGCGACTTATCAGGATTTGGGAATTAAATTCCTATGAGCACATGTTTGGTTGTACAAAATGGCCTTTTCAAGAAAGTATATGTAAAAAACAAAGACCAGGATTGAGGGAAAGAGAATCAATTATTGAAAAGAACAGATCTGAGGCCAGGCGTGATGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCAAGTCGGGCGGATCGCTTGAGTCCAGAAGTTCGACACCAGCCTGGGTAACATGGGGAAACCCAGTCTCCATAAAAAATACAAAAGATTAGCTGGGCATGGTGATGC... |
Task1_train_38368 | This mutation is located on Chromosome 7. Is it associated with a disease or is it a benign polymorphism? | Benign | TAGCTGCATTAACTCATAAGGTAAATTCTAGGAGGTAAGGCTATGAAGAAACTAAGGCCCCAAGGACGTCTATGGCTAACCCATGCTCACAGCTATATGTGTCAGAGCCAGGATTCAAACAAAGGGAGGCTGGCTCCCCCTCACCACTGCGCCTCTCCAGGCACCTCAAGTGGAAAGGACTTGGCTTTTCTTGCTATCAGGTGCAGTCAACCTGCTCAATTTATAACACATGAGCTGCCCCTGCAACACTGAAAGTGCTTCCCTCCTCACTCCCTTCAGGCAGTCCCTCCTGCCGGCAATCTCTCCTCTTCCTAGGTAGT... | TAGCTGCATTAACTCATAAGGTAAATTCTAGGAGGTAAGGCTATGAAGAAACTAAGGCCCCAAGGACGTCTATGGCTAACCCATGCTCACAGCTATATGTGTCAGAGCCAGGATTCAAACAAAGGGAGGCTGGCTCCCCCTCACCACTGCGCCTCTCCAGGCACCTCAAGTGGAAAGGACTTGGCTTTTCTTGCTATCAGGTGCAGTCAACCTGCTCAATTTATAACACATGAGCTGCCCCTGCAACACTGAAAGTGCTTCCCTCCTCACTCCCTTCAGGCAGTCCCTCCTGCCGGCAATCTCTCCTCTTCCTAGGTAGT... |
Task1_train_38369 | A mutation on Chromosome 7 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CTGGATGATTTTGTATATGCACAACACCTAGGAGTGTTTATCCACAATACTTGGAAGCGTCTTACATATTTGGTAAGGTTGTAATGATGGGTGGGCTCATTTCACTTAGACTACATGCCAATAGTCTACCTGAGAGTGTTCCCGTTCTTTCATGAAGAAAGTAGTGTGTATTTCCTTTTGGCAGAGGCATCCTTGCCAGCAAGATACTAGGAGTACACATTTCTACCAGGAAAGCAAAATACAGACTGGAAGCCAAAAGTCAAGGAATTCTGGCCAAAGATGTAAAGAGCCAAATTCTCTCAGAAATGGTTTCCTAGAAG... | CTGGATGATTTTGTATATGCACAACACCTAGGAGTGTTTATCCACAATACTTGGAAGCGTCTTACATATTTGGTAAGGTTGTAATGATGGGTGGGCTCATTTCACTTAGACTACATGCCAATAGTCTACCTGAGAGTGTTCCCGTTCTTTCATGAAGAAAGTAGTGTGTATTTCCTTTTGGCAGAGGCATCCTTGCCAGCAAGATACTAGGAGTACACATTTCTACCAGGAAAGCAAAATACAGACTGGAAGCCAAAAGTCAAGGAATTCTGGCCAAAGATGTAAAGAGCCAAATTCTCTCAGAAATGGTTTCCTAGAAG... |
Task1_train_38370 | Assess the clinical impact of this variant found on Chromosome 7. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GGTTGTAATGATGGGTGGGCTCATTTCACTTAGACTACATGCCAATAGTCTACCTGAGAGTGTTCCCGTTCTTTCATGAAGAAAGTAGTGTGTATTTCCTTTTGGCAGAGGCATCCTTGCCAGCAAGATACTAGGAGTACACATTTCTACCAGGAAAGCAAAATACAGACTGGAAGCCAAAAGTCAAGGAATTCTGGCCAAAGATGTAAAGAGCCAAATTCTCTCAGAAATGGTTTCCTAGAAGTAATTTGTGCTGACTATGCTTCAGTTCAAACAAACTCCTTTAAGAGCAAAATAGCAGTACGTGATATATCTAACCA... | GGTTGTAATGATGGGTGGGCTCATTTCACTTAGACTACATGCCAATAGTCTACCTGAGAGTGTTCCCGTTCTTTCATGAAGAAAGTAGTGTGTATTTCCTTTTGGCAGAGGCATCCTTGCCAGCAAGATACTAGGAGTACACATTTCTACCAGGAAAGCAAAATACAGACTGGAAGCCAAAAGTCAAGGAATTCTGGCCAAAGATGTAAAGAGCCAAATTCTCTCAGAAATGGTTTCCTAGAAGTAATTTGTGCTGACTATGCTTCAGTTCAAACAAACTCCTTTAAGAGCAAAATAGCAGTACGTGATATATCTAACCA... |
Task1_train_38371 | This variant lies on Chromosome 7. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GAAAAGAAATATAAGCCATTGTCCTTGCCTTTAAGAAGTTTGCAGTATGGATGGCTAGATAATATGTGTTACTTATTGAAATATGAATTCATAATAGAATAAAGCAGTTCATCATTATTTAAGAATGATACAACAAAAATATCATGAGAGCGAAAGGGAGAGAAAGGAGTTCCTTCAGGCTGGGATGACTATAGAAATCTATATGGAAGTAAACTCTGTCTTGCATTTGAAGAATGGGTAGACTTTGAAGAGGAAAGAAGAGAGAAAAAAGGTATTCTTGGTGAATAAAGAATGTGAACAATGTGAACAAGGCCATGGAG... | GAAAAGAAATATAAGCCATTGTCCTTGCCTTTAAGAAGTTTGCAGTATGGATGGCTAGATAATATGTGTTACTTATTGAAATATGAATTCATAATAGAATAAAGCAGTTCATCATTATTTAAGAATGATACAACAAAAATATCATGAGAGCGAAAGGGAGAGAAAGGAGTTCCTTCAGGCTGGGATGACTATAGAAATCTATATGGAAGTAAACTCTGTCTTGCATTTGAAGAATGGGTAGACTTTGAAGAGGAAAGAAGAGAGAAAAAAGGTATTCTTGGTGAATAAAGAATGTGAACAATGTGAACAAGGCCATGGAG... |
Task1_train_38372 | A variant was discovered on Chromosome 7. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CAAAAATATCATGAGAGCGAAAGGGAGAGAAAGGAGTTCCTTCAGGCTGGGATGACTATAGAAATCTATATGGAAGTAAACTCTGTCTTGCATTTGAAGAATGGGTAGACTTTGAAGAGGAAAGAAGAGAGAAAAAAGGTATTCTTGGTGAATAAAGAATGTGAACAATGTGAACAAGGCCATGGAGTCAAAGTCATTTTAGGAAGAAAGTGAGTAAATTGACTTTTTTGGGGAGGTATAAAATTGTTGATTAGACCAGAAGAATCTGGGTTGAGATTATAGAAAAGTGTGAATGCCAGGTAAGGACTAAGGACTTACCT... | CAAAAATATCATGAGAGCGAAAGGGAGAGAAAGGAGTTCCTTCAGGCTGGGATGACTATAGAAATCTATATGGAAGTAAACTCTGTCTTGCATTTGAAGAATGGGTAGACTTTGAAGAGGAAAGAAGAGAGAAAAAAGGTATTCTTGGTGAATAAAGAATGTGAACAATGTGAACAAGGCCATGGAGTCAAAGTCATTTTAGGAAGAAAGTGAGTAAATTGACTTTTTTGGGGAGGTATAAAATTGTTGATTAGACCAGAAGAATCTGGGTTGAGATTATAGAAAAGTGTGAATGCCAGGTAAGGACTAAGGACTTACCT... |
Task1_train_38373 | A variant has been detected on Chromosome 7. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | ATCTATATGGAAGTAAACTCTGTCTTGCATTTGAAGAATGGGTAGACTTTGAAGAGGAAAGAAGAGAGAAAAAAGGTATTCTTGGTGAATAAAGAATGTGAACAATGTGAACAAGGCCATGGAGTCAAAGTCATTTTAGGAAGAAAGTGAGTAAATTGACTTTTTTGGGGAGGTATAAAATTGTTGATTAGACCAGAAGAATCTGGGTTGAGATTATAGAAAAGTGTGAATGCCAGGTAAGGACTAAGGACTTACCTTTTAAGTGTGAGGACCCATTTAGGGAAGATTTTGAGAAAAGAAAACATATGATCCAAGTTGAG... | ATCTATATGGAAGTAAACTCTGTCTTGCATTTGAAGAATGGGTAGACTTTGAAGAGGAAAGAAGAGAGAAAAAAGGTATTCTTGGTGAATAAAGAATGTGAACAATGTGAACAAGGCCATGGAGTCAAAGTCATTTTAGGAAGAAAGTGAGTAAATTGACTTTTTTGGGGAGGTATAAAATTGTTGATTAGACCAGAAGAATCTGGGTTGAGATTATAGAAAAGTGTGAATGCCAGGTAAGGACTAAGGACTTACCTTTTAAGTGTGAGGACCCATTTAGGGAAGATTTTGAGAAAAGAAAACATATGATCCAAGTTGAG... |
Task1_train_38374 | With a mutation on Chromosome 7, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GAGGAAAGAAGAGAGAAAAAAGGTATTCTTGGTGAATAAAGAATGTGAACAATGTGAACAAGGCCATGGAGTCAAAGTCATTTTAGGAAGAAAGTGAGTAAATTGACTTTTTTGGGGAGGTATAAAATTGTTGATTAGACCAGAAGAATCTGGGTTGAGATTATAGAAAAGTGTGAATGCCAGGTAAGGACTAAGGACTTACCTTTTAAGTGTGAGGACCCATTTAGGGAAGATTTTGAGAAAAGAAAACATATGATCCAAGTTGAGTTTTACTGAAGTTAATTTGTCAGCTATGTTCTGTTTGAAAAGGAAGATAGAGA... | GAGGAAAGAAGAGAGAAAAAAGGTATTCTTGGTGAATAAAGAATGTGAACAATGTGAACAAGGCCATGGAGTCAAAGTCATTTTAGGAAGAAAGTGAGTAAATTGACTTTTTTGGGGAGGTATAAAATTGTTGATTAGACCAGAAGAATCTGGGTTGAGATTATAGAAAAGTGTGAATGCCAGGTAAGGACTAAGGACTTACCTTTTAAGTGTGAGGACCCATTTAGGGAAGATTTTGAGAAAAGAAAACATATGATCCAAGTTGAGTTTTACTGAAGTTAATTTGTCAGCTATGTTCTGTTTGAAAAGGAAGATAGAGA... |
Task1_train_38375 | This sequence change occurs on Chromosome 7. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GGAGGTATAAAATTGTTGATTAGACCAGAAGAATCTGGGTTGAGATTATAGAAAAGTGTGAATGCCAGGTAAGGACTAAGGACTTACCTTTTAAGTGTGAGGACCCATTTAGGGAAGATTTTGAGAAAAGAAAACATATGATCCAAGTTGAGTTTTACTGAAGTTAATTTGTCAGCTATGTTCTGTTTGAAAAGGAAGATAGAGACAGTAATATGAGGATGTTTAGAAGACCAAGAAAGCAGCTGAAGTGTGAAGTAGAATAGAGGATATATGTAGTATTTCTGTTCAGCATCCCCTCTTTTCTGATTCAGTGATTCAGG... | GGAGGTATAAAATTGTTGATTAGACCAGAAGAATCTGGGTTGAGATTATAGAAAAGTGTGAATGCCAGGTAAGGACTAAGGACTTACCTTTTAAGTGTGAGGACCCATTTAGGGAAGATTTTGAGAAAAGAAAACATATGATCCAAGTTGAGTTTTACTGAAGTTAATTTGTCAGCTATGTTCTGTTTGAAAAGGAAGATAGAGACAGTAATATGAGGATGTTTAGAAGACCAAGAAAGCAGCTGAAGTGTGAAGTAGAATAGAGGATATATGTAGTATTTCTGTTCAGCATCCCCTCTTTTCTGATTCAGTGATTCAGG... |
Task1_train_38376 | A genomic variant on Chromosome 7 is under review. What is the biological outcome — benign or pathogenic? | Benign | ATAGAAAAGTGTGAATGCCAGGTAAGGACTAAGGACTTACCTTTTAAGTGTGAGGACCCATTTAGGGAAGATTTTGAGAAAAGAAAACATATGATCCAAGTTGAGTTTTACTGAAGTTAATTTGTCAGCTATGTTCTGTTTGAAAAGGAAGATAGAGACAGTAATATGAGGATGTTTAGAAGACCAAGAAAGCAGCTGAAGTGTGAAGTAGAATAGAGGATATATGTAGTATTTCTGTTCAGCATCCCCTCTTTTCTGATTCAGTGATTCAGGTGGAGATGACACCATTTGCCCTCAAAAGCCATAGGTAGGCCGGGCGC... | ATAGAAAAGTGTGAATGCCAGGTAAGGACTAAGGACTTACCTTTTAAGTGTGAGGACCCATTTAGGGAAGATTTTGAGAAAAGAAAACATATGATCCAAGTTGAGTTTTACTGAAGTTAATTTGTCAGCTATGTTCTGTTTGAAAAGGAAGATAGAGACAGTAATATGAGGATGTTTAGAAGACCAAGAAAGCAGCTGAAGTGTGAAGTAGAATAGAGGATATATGTAGTATTTCTGTTCAGCATCCCCTCTTTTCTGATTCAGTGATTCAGGTGGAGATGACACCATTTGCCCTCAAAAGCCATAGGTAGGCCGGGCGC... |
Task1_train_38377 | This is a variant located on Chromosome 7. Is this mutation a likely cause of disease or not? | Benign | ATCTCCTTCTACACTCTTCCCTGTGTGTACTATGAAGCCCTGATAACAGGTCTCCACAAATTTATGACTTTTTCTTTTTTTTTTGCATTCCTCTAAGACAAATGACATAGGAGCTATCACTTTTTTTCTTGAATGCAACATTTCCATAATCTATTAATTTTCTAATAATTATTTGATGGTTTACTTGGATAGAACTGTAATGTGCATGCATATGTGGTAAACAAGGAGAAGAACAACAATATTAAAAAGTAATCTTGTGAGGGTGGTAGAAGTTTGAAATATGGCCTTGTCCATGAACAAAATGTTTCTTATGTTGCTAA... | ATCTCCTTCTACACTCTTCCCTGTGTGTACTATGAAGCCCTGATAACAGGTCTCCACAAATTTATGACTTTTTCTTTTTTTTTTGCATTCCTCTAAGACAAATGACATAGGAGCTATCACTTTTTTTCTTGAATGCAACATTTCCATAATCTATTAATTTTCTAATAATTATTTGATGGTTTACTTGGATAGAACTGTAATGTGCATGCATATGTGGTAAACAAGGAGAAGAACAACAATATTAAAAAGTAATCTTGTGAGGGTGGTAGAAGTTTGAAATATGGCCTTGTCCATGAACAAAATGTTTCTTATGTTGCTAA... |
Task1_train_38378 | A mutation on Chromosome 7 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CCCTCCCAGAAAACTTGTACCATTTTAATTCCCTTAACGGTAATTTAGGAAATGATACATTTCACCACATTTGGAACAACAGTAAATACCAGCTTTTAAAATTTCTGCCAGTCTGATAAGTAAAGCATTTTATCTCTATTTTAAGTTGCATTTAACTTTATTTCATTTATTTACTATTTGATTTTTTTTGTGTGTGAATTGCCTGTTCATTATCTTTGCCCAAATTCATTTACTTTTCTCATTTATTTGTAAGAGCTATTTGTACATTAGGGCATTAGTTCTTCTCTTGTCATATATGTTAAAATTGCAATTTTCCTAGT... | CCCTCCCAGAAAACTTGTACCATTTTAATTCCCTTAACGGTAATTTAGGAAATGATACATTTCACCACATTTGGAACAACAGTAAATACCAGCTTTTAAAATTTCTGCCAGTCTGATAAGTAAAGCATTTTATCTCTATTTTAAGTTGCATTTAACTTTATTTCATTTATTTACTATTTGATTTTTTTTGTGTGTGAATTGCCTGTTCATTATCTTTGCCCAAATTCATTTACTTTTCTCATTTATTTGTAAGAGCTATTTGTACATTAGGGCATTAGTTCTTCTCTTGTCATATATGTTAAAATTGCAATTTTCCTAGT... |
Task1_train_38379 | Chromosome 7 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | ATACAAAGTTCCTTGAAAGTAGGATTAAGATTTCAGTAAGCAGAGATGAAAGACATTTCTAGAGCACAGAACAGCAAGAACATAAAGTACTTTCAGGGAATGGGAAATGTTTAATGGATTTTTAGTCATAAGCTTTTAATTATATAATAGTGGATCTACTTCGAGTATTAGACTGGGTATTCTATAAAGGTCCTTTTTACCTAATATCTAGATTTCTTGATAAATGCAGATCTACCCTTATAGACACTGAAAAAAATTTAAAAATATTTTTCTGATTATAATATCTGCTCATTGTAGAAATTTAGAAAGTATAAAAAAGC... | ATACAAAGTTCCTTGAAAGTAGGATTAAGATTTCAGTAAGCAGAGATGAAAGACATTTCTAGAGCACAGAACAGCAAGAACATAAAGTACTTTCAGGGAATGGGAAATGTTTAATGGATTTTTAGTCATAAGCTTTTAATTATATAATAGTGGATCTACTTCGAGTATTAGACTGGGTATTCTATAAAGGTCCTTTTTACCTAATATCTAGATTTCTTGATAAATGCAGATCTACCCTTATAGACACTGAAAAAAATTTAAAAATATTTTTCTGATTATAATATCTGCTCATTGTAGAAATTTAGAAAGTATAAAAAAGC... |
Task1_train_38380 | Given a variant located on Chromosome 7, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GTGAGGGAGCCTTGGGGGTGTGCCAGGTGGAAGGGCAGGTTAGAAGGGGAAACTCTATTCTGTTCTTCCTTTCGCTTTAACCAATTCTGCATTTGTTTTATGTATTCTGGTTCTATAAAAGATTTTATTTGACAAAAGGGTTTCACTGCTAAAATGTTTGAAAACTGTTGTCTAGTAATTTACTTACTGGTTCTCTTATGTCGTGTGGGTGTGTGTATAATGTAGCTGATGTAAGTACTATTGCTAATATTATTGGTATGCATAAAGCTTTTTCTATATATGGAATTATTTTCTTAGGGTATATTTTCCAAAAATGAAAT... | GTGAGGGAGCCTTGGGGGTGTGCCAGGTGGAAGGGCAGGTTAGAAGGGGAAACTCTATTCTGTTCTTCCTTTCGCTTTAACCAATTCTGCATTTGTTTTATGTATTCTGGTTCTATAAAAGATTTTATTTGACAAAAGGGTTTCACTGCTAAAATGTTTGAAAACTGTTGTCTAGTAATTTACTTACTGGTTCTCTTATGTCGTGTGGGTGTGTGTATAATGTAGCTGATGTAAGTACTATTGCTAATATTATTGGTATGCATAAAGCTTTTTCTATATATGGAATTATTTTCTTAGGGTATATTTTCCAAAAATGAAAT... |
Task1_train_38381 | Assess the clinical impact of this variant found on Chromosome 7. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GGGTGTGCCAGGTGGAAGGGCAGGTTAGAAGGGGAAACTCTATTCTGTTCTTCCTTTCGCTTTAACCAATTCTGCATTTGTTTTATGTATTCTGGTTCTATAAAAGATTTTATTTGACAAAAGGGTTTCACTGCTAAAATGTTTGAAAACTGTTGTCTAGTAATTTACTTACTGGTTCTCTTATGTCGTGTGGGTGTGTGTATAATGTAGCTGATGTAAGTACTATTGCTAATATTATTGGTATGCATAAAGCTTTTTCTATATATGGAATTATTTTCTTAGGGTATATTTTCCAAAAATGAAATTTCTGGTTCAAAGAA... | GGGTGTGCCAGGTGGAAGGGCAGGTTAGAAGGGGAAACTCTATTCTGTTCTTCCTTTCGCTTTAACCAATTCTGCATTTGTTTTATGTATTCTGGTTCTATAAAAGATTTTATTTGACAAAAGGGTTTCACTGCTAAAATGTTTGAAAACTGTTGTCTAGTAATTTACTTACTGGTTCTCTTATGTCGTGTGGGTGTGTGTATAATGTAGCTGATGTAAGTACTATTGCTAATATTATTGGTATGCATAAAGCTTTTTCTATATATGGAATTATTTTCTTAGGGTATATTTTCCAAAAATGAAATTTCTGGTTCAAAGAA... |
Task1_train_38382 | This sequence change occurs on Chromosome 7. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TTTTTCTAAATATAGAAAAGGTACAGTAAAAATATGGCATAAAAAATAAAATGGGCCGTGTGCAGTGGCTTATGCCTGTAATCCCAGCATTTGGGAGGCTGAGGCAGGCAGATCGCTTGAGCCCAGGAGTTTGAGACCAGCCTAGGCAACATGGCGAAACCCTGTCTCTACAAAAATACAAAAAATTAGCTGGGCCTGGTATTGTGTGTGTGCCTGTAATCCCAGCTACTTGGTGAGGGCTGAGGTGAGAGGATCACCTGAGCTTTGGATGCAGAGGTTGCAATGAGCTGTGATGGCACCATTGCCCTCCAGCCTGGGTG... | TTTTTCTAAATATAGAAAAGGTACAGTAAAAATATGGCATAAAAAATAAAATGGGCCGTGTGCAGTGGCTTATGCCTGTAATCCCAGCATTTGGGAGGCTGAGGCAGGCAGATCGCTTGAGCCCAGGAGTTTGAGACCAGCCTAGGCAACATGGCGAAACCCTGTCTCTACAAAAATACAAAAAATTAGCTGGGCCTGGTATTGTGTGTGTGCCTGTAATCCCAGCTACTTGGTGAGGGCTGAGGTGAGAGGATCACCTGAGCTTTGGATGCAGAGGTTGCAATGAGCTGTGATGGCACCATTGCCCTCCAGCCTGGGTG... |
Task1_train_38383 | Here is a variant on Chromosome 7. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TGTGTTCCCAGCTATGTGGGAGGCTGAGGGTGGGAAGATTGCCTGGGCCCAGGAGATTGAGACTGCAGTGAGCTGAGATTGCACCAAACAAACAAACAAACAAAGAGCTCCTATTTGTTTTAGTCTGTATAGTGAAAAAATATAGTTATATGGAATATTTTGATTCCAGGGGTTTGTTCACAAAGGCTGCTTCTCTTGTTTCTCAGGGTCAGTTTAAATTCAGTTCCTGTTCTATGCTGAGACTTTGATATTCATCATGATGTTCTTTGAACTGCTCTTTCAGAGTTTTTTTTCAGTCATCACGGATAATCATGTTCTTT... | TGTGTTCCCAGCTATGTGGGAGGCTGAGGGTGGGAAGATTGCCTGGGCCCAGGAGATTGAGACTGCAGTGAGCTGAGATTGCACCAAACAAACAAACAAACAAAGAGCTCCTATTTGTTTTAGTCTGTATAGTGAAAAAATATAGTTATATGGAATATTTTGATTCCAGGGGTTTGTTCACAAAGGCTGCTTCTCTTGTTTCTCAGGGTCAGTTTAAATTCAGTTCCTGTTCTATGCTGAGACTTTGATATTCATCATGATGTTCTTTGAACTGCTCTTTCAGAGTTTTTTTTCAGTCATCACGGATAATCATGTTCTTT... |
Task1_train_38384 | A change on Chromosome 7 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CGACAAAGCCAGACTCCATTCAAAAAATAAAAAAATAAAAAAAAAATGTGTCCCAATGAAATAATTTTTTTTGTAATCCTATGTATTTCATACATTTAAAAACATTCTGAGAAAAAGTCCAAAGATTTCACCTGACTGATAAAGGAGCCCCATGGCCACAAAAAGGTTAAGAATTCCTACATCGGTCTCAATTTTACCCTCTATACTACTGTGTAGTTGAAGAGAAAATAGTTCTTAAAAATGTTATTTAGTTTCTTGGACCTTGACTTCCCCACACCCCCTATTTCTTTTAAAAATGTGACCGGTTTGTATTTTGTGGT... | CGACAAAGCCAGACTCCATTCAAAAAATAAAAAAATAAAAAAAAAATGTGTCCCAATGAAATAATTTTTTTTGTAATCCTATGTATTTCATACATTTAAAAACATTCTGAGAAAAAGTCCAAAGATTTCACCTGACTGATAAAGGAGCCCCATGGCCACAAAAAGGTTAAGAATTCCTACATCGGTCTCAATTTTACCCTCTATACTACTGTGTAGTTGAAGAGAAAATAGTTCTTAAAAATGTTATTTAGTTTCTTGGACCTTGACTTCCCCACACCCCCTATTTCTTTTAAAAATGTGACCGGTTTGTATTTTGTGGT... |
Task1_train_38385 | Consider a variant on Chromosome 7. Determine its clinical classification and disease relevance. | Benign | TTTTTTGAGACAGAGTCTGGCTTTGTTGCCCAGGCTGGAGTGCTGTGGCACAATCTCGCCTCGCTGCAACCTCTGCCTCCCTAACTCAAGCCATCCTCTCACCTTAGCCTCCTAAGTAGCTAAGCTACAGGCATGCACCACCACACCCATGTATTTTTTCGTAGAGACGGGGTTTTGCCACATTGTCCAGGCTGGTCTCAAACTTCTGAGCTCAAACCATCTGTCCTCCTTGGCCTCCCAAAGTGTTGGAATTACAGGCATGAGCCACTGTGCCCAGCCAAAAATTATTTAAATTATAGCAGAAATACAGTTTCCTATTT... | TTTTTTGAGACAGAGTCTGGCTTTGTTGCCCAGGCTGGAGTGCTGTGGCACAATCTCGCCTCGCTGCAACCTCTGCCTCCCTAACTCAAGCCATCCTCTCACCTTAGCCTCCTAAGTAGCTAAGCTACAGGCATGCACCACCACACCCATGTATTTTTTCGTAGAGACGGGGTTTTGCCACATTGTCCAGGCTGGTCTCAAACTTCTGAGCTCAAACCATCTGTCCTCCTTGGCCTCCCAAAGTGTTGGAATTACAGGCATGAGCCACTGTGCCCAGCCAAAAATTATTTAAATTATAGCAGAAATACAGTTTCCTATTT... |
Task1_train_38386 | An alteration has been detected on Chromosome 7. Is it pathogenic, and if so, what disease is involved? | Benign | AGAGCTCTGAAAGTTGACACACAAGATGGAGTGGTCATCCTCTTTCTTTCTCCATTGTGTATATTCTTTGTTACAGTGTCAAGGTAAAAATTAGTGTAGCTACTCCAAAGGGTGTTTTGTAATTTTAATTATTGCTCATTGGGACTCTTCCCAGTTATTCAGGCTGCTTTCCAATGTTTCAGTGGTTAGGCTTCTCATTTTACTTGTTTTTTCTTTTTTTTACTTTTTATAATTTTACTCATATTGGCATTAAAAATACATTAAGAAGTTTTATATTGTTAAATAGTCCTGATGTAGATAGTTTTGTCAGACTTGATTTT... | AGAGCTCTGAAAGTTGACACACAAGATGGAGTGGTCATCCTCTTTCTTTCTCCATTGTGTATATTCTTTGTTACAGTGTCAAGGTAAAAATTAGTGTAGCTACTCCAAAGGGTGTTTTGTAATTTTAATTATTGCTCATTGGGACTCTTCCCAGTTATTCAGGCTGCTTTCCAATGTTTCAGTGGTTAGGCTTCTCATTTTACTTGTTTTTTCTTTTTTTTACTTTTTATAATTTTACTCATATTGGCATTAAAAATACATTAAGAAGTTTTATATTGTTAAATAGTCCTGATGTAGATAGTTTTGTCAGACTTGATTTT... |
Task1_train_38387 | A mutation found on Chromosome 7 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TCTGAAAGTTGACACACAAGATGGAGTGGTCATCCTCTTTCTTTCTCCATTGTGTATATTCTTTGTTACAGTGTCAAGGTAAAAATTAGTGTAGCTACTCCAAAGGGTGTTTTGTAATTTTAATTATTGCTCATTGGGACTCTTCCCAGTTATTCAGGCTGCTTTCCAATGTTTCAGTGGTTAGGCTTCTCATTTTACTTGTTTTTTCTTTTTTTTACTTTTTATAATTTTACTCATATTGGCATTAAAAATACATTAAGAAGTTTTATATTGTTAAATAGTCCTGATGTAGATAGTTTTGTCAGACTTGATTTTAGTAG... | TCTGAAAGTTGACACACAAGATGGAGTGGTCATCCTCTTTCTTTCTCCATTGTGTATATTCTTTGTTACAGTGTCAAGGTAAAAATTAGTGTAGCTACTCCAAAGGGTGTTTTGTAATTTTAATTATTGCTCATTGGGACTCTTCCCAGTTATTCAGGCTGCTTTCCAATGTTTCAGTGGTTAGGCTTCTCATTTTACTTGTTTTTTCTTTTTTTTACTTTTTATAATTTTACTCATATTGGCATTAAAAATACATTAAGAAGTTTTATATTGTTAAATAGTCCTGATGTAGATAGTTTTGTCAGACTTGATTTTAGTAG... |
Task1_train_38388 | Mutation context: Chromosome 7. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TATAGCTAATAGTACTGCAGTGTTTACTTGAGACTTGCTGAGAGGGTGGACAGTAAGTGTCCTCACCACACACATGCAGAGGGTAACCATGCTGGGTGATGGATGTGTTCATTAGCTTGACTCAGTAGTTATCCCGTCACAATGTCTATGTCTATTGAATCATCACTTGTACATCTTGAACATACAGTTTCTGTGTGTCAATCATACCTCAGTAAGCTGCGGGGGAGTGACACATTCACCACTGGCCATCAGTAAGACTGGACAGGACCACCAAGGCAGACATAGGGGGGCTAGAAACCCAAAAGTGCAGATGGTGACCC... | TATAGCTAATAGTACTGCAGTGTTTACTTGAGACTTGCTGAGAGGGTGGACAGTAAGTGTCCTCACCACACACATGCAGAGGGTAACCATGCTGGGTGATGGATGTGTTCATTAGCTTGACTCAGTAGTTATCCCGTCACAATGTCTATGTCTATTGAATCATCACTTGTACATCTTGAACATACAGTTTCTGTGTGTCAATCATACCTCAGTAAGCTGCGGGGGAGTGACACATTCACCACTGGCCATCAGTAAGACTGGACAGGACCACCAAGGCAGACATAGGGGGGCTAGAAACCCAAAAGTGCAGATGGTGACCC... |
Task1_train_38389 | A variant has been detected on Chromosome 7. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | ACCTTAGGAAATGCTGAAGCAAATGTAAAATCAGTATGTTCAGCTCAGTTTTTATTTTATTTATTAATTTATTTTGAGATGGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCACAACCTTTGCTCACAGCAACCTCTGCTTCCCAGATTCAAGCGATTCTCCCACCTTAGCCTCCTGAGTAGCTAGGACTACAGGCATGTGCCACCATGCCCGGTTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCCAACTCCTGACCTCAGGTGGTCCACCCGCCTCAGTCTCCCAAA... | ACCTTAGGAAATGCTGAAGCAAATGTAAAATCAGTATGTTCAGCTCAGTTTTTATTTTATTTATTAATTTATTTTGAGATGGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCACAACCTTTGCTCACAGCAACCTCTGCTTCCCAGATTCAAGCGATTCTCCCACCTTAGCCTCCTGAGTAGCTAGGACTACAGGCATGTGCCACCATGCCCGGTTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCCAACTCCTGACCTCAGGTGGTCCACCCGCCTCAGTCTCCCAAA... |
Task1_train_38390 | This variant is found on Chromosome 7. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CCACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGTCTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGCGATCCACCCGCCTCAGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCGAGCCTGACCCAGCTCAGTTTTTAAAGTGTTCAAACTGAAATAATCTTACAGATGTTTTTCCTTGTGTTTTTCACAATTTATATACCTTTAAAATGTTAATTTTGTTTTCAAAATTTGTAGTCGTCGAGAATAAAATTTAGGCCTCAAATAAAACAACACATATGCAAACTATTAGGTCAT... | CCACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGTCTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGCGATCCACCCGCCTCAGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCGAGCCTGACCCAGCTCAGTTTTTAAAGTGTTCAAACTGAAATAATCTTACAGATGTTTTTCCTTGTGTTTTTCACAATTTATATACCTTTAAAATGTTAATTTTGTTTTCAAAATTTGTAGTCGTCGAGAATAAAATTTAGGCCTCAAATAAAACAACACATATGCAAACTATTAGGTCAT... |
Task1_train_38391 | Chromosome 7 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCACACCTGGCCCATGCTTCTTAGTTCTAATAAAGAAGAATTAAAATAAGTGGAAGAGTAGAAACCTAATGCTGTACTAGTTCCTGGAAAGATTTTTTTATAAGGGTTGTTAGAGGATGCTCATCTTTTAAAAATTCCCTAATAGTGACTGAATGGTTGGAGAGAGGTAGAGGCTTGGAAGAGCAGGAAATTAAGATGACAACTTGTTTTTTCAGTCCCTTATGTTACTGCACTGAAAAGTGTTTTTATGGGCTGGCCATGGTGGCTCATGCCTGTAATCCCAGCA... | CCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCACACCTGGCCCATGCTTCTTAGTTCTAATAAAGAAGAATTAAAATAAGTGGAAGAGTAGAAACCTAATGCTGTACTAGTTCCTGGAAAGATTTTTTTATAAGGGTTGTTAGAGGATGCTCATCTTTTAAAAATTCCCTAATAGTGACTGAATGGTTGGAGAGAGGTAGAGGCTTGGAAGAGCAGGAAATTAAGATGACAACTTGTTTTTTCAGTCCCTTATGTTACTGCACTGAAAAGTGTTTTTATGGGCTGGCCATGGTGGCTCATGCCTGTAATCCCAGCA... |
Task1_train_38392 | A mutation located on Chromosome 7 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | AGAGTAGAAACCTAATGCTGTACTAGTTCCTGGAAAGATTTTTTTATAAGGGTTGTTAGAGGATGCTCATCTTTTAAAAATTCCCTAATAGTGACTGAATGGTTGGAGAGAGGTAGAGGCTTGGAAGAGCAGGAAATTAAGATGACAACTTGTTTTTTCAGTCCCTTATGTTACTGCACTGAAAAGTGTTTTTATGGGCTGGCCATGGTGGCTCATGCCTGTAATCCCAGCACTTTGTGAGGCTGAGGCGGGCAGATCACTTGACGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAA... | AGAGTAGAAACCTAATGCTGTACTAGTTCCTGGAAAGATTTTTTTATAAGGGTTGTTAGAGGATGCTCATCTTTTAAAAATTCCCTAATAGTGACTGAATGGTTGGAGAGAGGTAGAGGCTTGGAAGAGCAGGAAATTAAGATGACAACTTGTTTTTTCAGTCCCTTATGTTACTGCACTGAAAAGTGTTTTTATGGGCTGGCCATGGTGGCTCATGCCTGTAATCCCAGCACTTTGTGAGGCTGAGGCGGGCAGATCACTTGACGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAA... |
Task1_train_38393 | A change on Chromosome 7 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GCCGGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGAAGGCCCAGGTGGGCGGATCATGAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATACAAAAGATTAGCTGGGCGTGGTGGCGGACGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCATGAACCTGGGAGGCAGAGCTTGCAGTGAGCTGAGATCGTGCCACTGCACTCGAGCCTGGGCAACACAGCAAGACTCTGTCTCAAAAATAAAAACAGGATTGGCCAGGCGCGGTGGCTCATGT... | GCCGGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGAAGGCCCAGGTGGGCGGATCATGAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATACAAAAGATTAGCTGGGCGTGGTGGCGGACGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCATGAACCTGGGAGGCAGAGCTTGCAGTGAGCTGAGATCGTGCCACTGCACTCGAGCCTGGGCAACACAGCAAGACTCTGTCTCAAAAATAAAAACAGGATTGGCCAGGCGCGGTGGCTCATGT... |
Task1_train_38394 | This variant is found on Chromosome 7. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CCTTTGCACCTGAACAACTCTCTCCCATGAGACTTTTTATGTGGGAGAGGTCCAGCGTTTAGACAATATACTGTCATTGCATGGACTTAGTGAGCAGCTATAGGATAAGGAGATTGATGCTTATATGTGGCTTAGGGGAAGCCATCCTATGATTTTATACCTTGAGCCATGCTTATTATACCTGGCCTTCTATAGTTCCCAATTTACAGGTATTTAGTTCCTTGTGTCTTTGCCTCTCTCTCCTGCTAGGAAACTTACTGTCTTAGAAACTTATGTTGAAAAGATGTAGTCATTTTTAAAGTTTCTAGACCACCTCTATA... | CCTTTGCACCTGAACAACTCTCTCCCATGAGACTTTTTATGTGGGAGAGGTCCAGCGTTTAGACAATATACTGTCATTGCATGGACTTAGTGAGCAGCTATAGGATAAGGAGATTGATGCTTATATGTGGCTTAGGGGAAGCCATCCTATGATTTTATACCTTGAGCCATGCTTATTATACCTGGCCTTCTATAGTTCCCAATTTACAGGTATTTAGTTCCTTGTGTCTTTGCCTCTCTCTCCTGCTAGGAAACTTACTGTCTTAGAAACTTATGTTGAAAAGATGTAGTCATTTTTAAAGTTTCTAGACCACCTCTATA... |
Task1_train_38395 | Consider this mutation on Chromosome 7. Is this a benign change or a disease-causing variant? | Benign | TGGTGTGACCAAAAACAAGCAGCCAGGGAATATTCTTCCCTACTTGAGGATAACTGATGCTACAGCAGATGCCATTTCCTTAGGGTAAACCAGAAAGGAAGGGGTTAATAAACATGTAGCTCCACTAAACAACTGAAATACACAGATCACTATTCCCCATAAAATTATACTTTTATACTAATCTTCTGGGGTAGTAAAATACAATATGTAGATGCATACATAGTTTTTATACCTTAAATTTATAATATTGTTAAAATTATTACTTTTTACTTGGTTAGAAAACCATTACTGTACCACCACATAAGCACTTGCAAGAATTC... | TGGTGTGACCAAAAACAAGCAGCCAGGGAATATTCTTCCCTACTTGAGGATAACTGATGCTACAGCAGATGCCATTTCCTTAGGGTAAACCAGAAAGGAAGGGGTTAATAAACATGTAGCTCCACTAAACAACTGAAATACACAGATCACTATTCCCCATAAAATTATACTTTTATACTAATCTTCTGGGGTAGTAAAATACAATATGTAGATGCATACATAGTTTTTATACCTTAAATTTATAATATTGTTAAAATTATTACTTTTTACTTGGTTAGAAAACCATTACTGTACCACCACATAAGCACTTGCAAGAATTC... |
Task1_train_38396 | A mutation found on Chromosome 7 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CAAATTTTAAACAGAGGGTGGCCCGAGAAGAAAGGGGTAGAGATTGGGAAAGACTTAGCACAGGAAGCCGGGTTTCTGAAGTTTGTGCTCTGCAGGGCTTCTTAACTGTAAGAACAAATCAAGGCTACCCTCTGAGGCATCTGATTGGGTTTAAATGAGGGAATTTTTTCTTTCACCTATAAAATTGTACCAGTTTAGAGAGTTTGCCCACCCTGTTTTAGTAACCTAAACATTTCTAGAAAATCTGTATAAAGATAAATCTCTTAGGACAAAGTATTTACAACCAGCAAACTCACACACATGAAAATGACTTAAATTAA... | CAAATTTTAAACAGAGGGTGGCCCGAGAAGAAAGGGGTAGAGATTGGGAAAGACTTAGCACAGGAAGCCGGGTTTCTGAAGTTTGTGCTCTGCAGGGCTTCTTAACTGTAAGAACAAATCAAGGCTACCCTCTGAGGCATCTGATTGGGTTTAAATGAGGGAATTTTTTCTTTCACCTATAAAATTGTACCAGTTTAGAGAGTTTGCCCACCCTGTTTTAGTAACCTAAACATTTCTAGAAAATCTGTATAAAGATAAATCTCTTAGGACAAAGTATTTACAACCAGCAAACTCACACACATGAAAATGACTTAAATTAA... |
Task1_train_38397 | With a mutation on Chromosome 7, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | AGGAGCCCTCTCAGAGCTCAAGAGCCTTCCTACTCTTTGGAACTTTTCCACAGTAGGCCAAGCTTGACAAGAGTTCAGCTCAAGTTGAACATACATACACACACTCTCACACACAAATTATGTGAGCCGTCAGAATCCAAGTGAATCCAGCTCAAGCTATCTACAAGGTTTTTACATGCAAGGTCAAGTATCTCAATCCAGAGGACTTTTGTTTTCTTAATGAAAAGCTTAGAAAACACATGAATCTTAGATTTTTAATGTTTTTTAAATGGAGTTTATTCTTAGCACATGGCTTTCTATGTAGCCACATCACAATTTGT... | AGGAGCCCTCTCAGAGCTCAAGAGCCTTCCTACTCTTTGGAACTTTTCCACAGTAGGCCAAGCTTGACAAGAGTTCAGCTCAAGTTGAACATACATACACACACTCTCACACACAAATTATGTGAGCCGTCAGAATCCAAGTGAATCCAGCTCAAGCTATCTACAAGGTTTTTACATGCAAGGTCAAGTATCTCAATCCAGAGGACTTTTGTTTTCTTAATGAAAAGCTTAGAAAACACATGAATCTTAGATTTTTAATGTTTTTTAAATGGAGTTTATTCTTAGCACATGGCTTTCTATGTAGCCACATCACAATTTGT... |
Task1_train_38398 | Here is a mutation located on Chromosome 7. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AGCTTAGAAAACACATGAATCTTAGATTTTTAATGTTTTTTAAATGGAGTTTATTCTTAGCACATGGCTTTCTATGTAGCCACATCACAATTTGTACAGTTCCACATAAGTCTAAATGCACTCCCCTCTCCCCAAAGACCGTGCCCCAGAAGGGGACAACAGTATCTCTGTAACAGTGTCTTAAATAAATGCAAGTAAGAAAAACTAACATGTCACACCTACCATCAAGGTCTACACATCTTAAGAATTAAATAATCTTGTGAGGTCCACAATGTCTACTCATTTATTCAGTTAAATACAAGCTTGGATGAGCTGCCTTA... | AGCTTAGAAAACACATGAATCTTAGATTTTTAATGTTTTTTAAATGGAGTTTATTCTTAGCACATGGCTTTCTATGTAGCCACATCACAATTTGTACAGTTCCACATAAGTCTAAATGCACTCCCCTCTCCCCAAAGACCGTGCCCCAGAAGGGGACAACAGTATCTCTGTAACAGTGTCTTAAATAAATGCAAGTAAGAAAAACTAACATGTCACACCTACCATCAAGGTCTACACATCTTAAGAATTAAATAATCTTGTGAGGTCCACAATGTCTACTCATTTATTCAGTTAAATACAAGCTTGGATGAGCTGCCTTA... |
Task1_train_38399 | The following genetic variant occurs on Chromosome 7. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | AGTAGGTAGTAGTGAGATTCACTTTCTTGCGGGTCTGGGAGGGTGGTGCTGGGTGTCTGCCAGTGTTGGGATACATAGGGACTTCCTGGGAATGGAGGCCCTCTGGGGCTGGATACATAGGTAGTTTGGGGGTGCCTCGAGCAGAGGCCTGTGCTAGGTAGTATTTTGGACGCGCCAGAGCAGGGCCGGCTGGCCTGGGGTTGGGGGTGTCTTTTGGGGTCCTCGGAGGCAGAGGGAATCCAAGGCGACCCAGTCTCTGCGGCCGCTCAGTCCACAAAAGTTGGGAGCTGGAGTAGGTGATGGGGGTGGGTAGAGTGCAG... | AGTAGGTAGTAGTGAGATTCACTTTCTTGCGGGTCTGGGAGGGTGGTGCTGGGTGTCTGCCAGTGTTGGGATACATAGGGACTTCCTGGGAATGGAGGCCCTCTGGGGCTGGATACATAGGTAGTTTGGGGGTGCCTCGAGCAGAGGCCTGTGCTAGGTAGTATTTTGGACGCGCCAGAGCAGGGCCGGCTGGCCTGGGGTTGGGGGTGTCTTTTGGGGTCCTCGGAGGCAGAGGGAATCCAAGGCGACCCAGTCTCTGCGGCCGCTCAGTCCACAAAAGTTGGGAGCTGGAGTAGGTGATGGGGGTGGGTAGAGTGCAG... |
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