question stringlengths 84 268 | answer stringlengths 6 879 | reference_sequence stringlengths 4.1k 4.1k | mutated_sequence stringlengths 4.1k 4.1k | cleaned_pathogenicity stringclasses 2
values | __index_level_0__ int64 67 343k |
|---|---|---|---|---|---|
Evaluate if the mutation on chromosome X at position 154837696 in F8 (coagulation factor VIII) is benign or pathogenic. Disease name(s) if pathogenic? | pathogenic; ['Hereditary_factor_VIII_deficiency_disease'] | TGAGTTCAATTTAATCTGGTTTTCTAACTCACTAATTTGGTTTTCTAGAGTGTCCATCTTGCTATTCAGTGCCCCTATTTGTTTTAAAAATCAGTGTTCACATTTTTATTTCCAGTGTAAAAACACAATTCTCAAAGGCATTTGTTTGTATGTGTCAATGTTTTATTTAACTCATTACTGAAGAAACCAGCAGGAAAATAAAAGAGCTAGTTCCATGAACATTTGAGAAATAGAGATGTATATAGTCAATGGGAAAAGAATGCCAAAATAAGATTATCAAGTTAAACATAACAGGAAATAAAACCATATCACCTTTGGGG... | TGAGTTCAATTTAATCTGGTTTTCTAACTCACTAATTTGGTTTTCTAGAGTGTCCATCTTGCTATTCAGTGCCCCTATTTGTTTTAAAAATCAGTGTTCACATTTTTATTTCCAGTGTAAAAACACAATTCTCAAAGGCATTTGTTTGTATGTGTCAATGTTTTATTTAACTCATTACTGAAGAAACCAGCAGGAAAATAAAAGAGCTAGTTCCATGAACATTTGAGAAATAGAGATGTATATAGTCAATGGGAAAAGAATGCCAAAATAAGATTATCAAGTTAAACATAACAGGAAATAAAACCATATCACCTTTGGGG... | pathogenic | 342,532 |
Benign or pathogenic: chromosome X, position 154903942, gene F8 (coagulation factor VIII) variant? Disease(s) if pathogenic? | pathogenic; ['Hereditary_factor_VIII_deficiency_disease', 'Thrombophilia,_X-linked,_due_to_factor_8_defect'] | GAACTCTGATGATTTCTACCAGCAATATTCATTTTAAATTTGATAATGATGTAAACTTGTATTTATTTCCTGACACAAGCAACCATTCCAGAAAGGAAGAAAGCTGTAAAGAAGTAGGCTGAGTAGGTAGGGAACCTCTGCCCACATTGCTACTCACTATTGCTGTACACCAGAAAAAGTGTGCTCATCCCAGCATGTAGATGCTCGCCAATAAGGCATTCCACCCGCCAAATTCCAGCTTTGGATGGTAACATTTCCACTGTCTCAAAAACACCTTATAAAAACCAACAGGAACAGAAATTATTTCTTTTCACTAAAAA... | GAACTCTGATGATTTCTACCAGCAATATTCATTTTAAATTTGATAATGATGTAAACTTGTATTTATTTCCTGACACAAGCAACCATTCCAGAAAGGAAGAAAGCTGTAAAGAAGTAGGCTGAGTAGGTAGGGAACCTCTGCCCACATTGCTACTCACTATTGCTGTACACCAGAAAAAGTGTGCTCATCCCAGCATGTAGATGCTCGCCAATAAGGCATTCCACCCGCCAAATTCCAGCTTTGGATGGTAACATTTCCACTGTCTCAAAAACACCTTATAAAAACCAACAGGAACAGAAATTATTTCTTTTCACTAAAAA... | pathogenic | 342,562 |
Gene F8 (coagulation factor VIII) variant at chromosome position 154928853 on chromosome X: benign or pathogenic? If pathogenic, what disease(s) is it associated with? | pathogenic; ['Hereditary_factor_VIII_deficiency_disease'] | GAGATCTGAGAATATCTCCAGATATTCAACTGGAATTATCTGCAGATAGATAGTACTTAAAATCATGAGGCTAAACAATGTCGTCACAGAGTGAGTATAAATAGAATAAAGAAGAAGTTGGAGAACTAATCCCTGGAGCACTCTAACCTTTAAAGATTAGGGGGATGAAGAAGGACTCGCAAAGTTGACAAAGATTGGCAGTAAGTTTAGTAGAAAAGTGAAGAAAAGTGGTGTTAGAGAAACCAAGTGAGAACCTGTATCAACGATGGAGTAATCACCTCTCAAATACTACTGAGAATTCAAATAAGATGAGGGCTAGT... | GAGATCTGAGAATATCTCCAGATATTCAACTGGAATTATCTGCAGATAGATAGTACTTAAAATCATGAGGCTAAACAATGTCGTCACAGAGTGAGTATAAATAGAATAAAGAAGAAGTTGGAGAACTAATCCCTGGAGCACTCTAACCTTTAAAGATTAGGGGGATGAAGAAGGACTCGCAAAGTTGACAAAGATTGGCAGTAAGTTTAGTAGAAAAGTGAAGAAAAGTGGTGTTAGAGAAACCAAGTGAGAACCTGTATCAACGATGGAGTAATCACCTCTCAAATACTACTGAGAATTCAAATAAGATGAGGGCTAGT... | pathogenic | 342,581 |
Assess the clinical significance (benign or pathogenic) of the variant at chromosome X, position 154929410, gene F8 (coagulation factor VIII). What disease(s) is it linked to if pathogenic? | pathogenic; ['Hereditary_factor_VIII_deficiency_disease', 'Thrombophilia,_X-linked,_due_to_factor_8_defect'] | AAAGGAGAAATTGCTGGAGCAACATTTTTTATGAAGGGAGAAGAGATGGGAATCAAGTACAAAACTGGAGAGGTTGGCCTTAGGAGCACAGACACTCTATTTATTGTAATAAGTGTGCAGGCAGAGTATATGGGTACAAATGCCAGTAAATGTGATGTTGGGAGTCTGTGGAGGTTCATTGCACAGCATCAGCTAAGAGTGAAAATGGGCATTGGAGAATGGAAAAAAGGTGCTCGAGATTTAAGGAAAACACAGAAAATCTAAGATAGAGGTCCAGGAGAATGAGAAAGTCAGTGGACTAGGGAAATAGTCTATGGTTG... | AAAGGAGAAATTGCTGGAGCAACATTTTTTATGAAGGGAGAAGAGATGGGAATCAAGTACAAAACTGGAGAGGTTGGCCTTAGGAGCACAGACACTCTATTTATTGTAATAAGTGTGCAGGCAGAGTATATGGGTACAAATGCCAGTAAATGTGATGTTGGGAGTCTGTGGAGGTTCATTGCACAGCATCAGCTAAGAGTGAAAATGGGCATTGGAGAATGGAAAAAAGGTGCTCGAGATTTAAGGAAAACACAGAAAATCTAAGATAGAGGTCCAGGAGAATGAGAAAGTCAGTGGACTAGGGAAATAGTCTATGGTTG... | pathogenic | 342,584 |
Evaluate if the mutation on chromosome X at position 154929410 in F8 (coagulation factor VIII) is benign or pathogenic. Disease name(s) if pathogenic? | pathogenic; ['Hereditary_factor_VIII_deficiency_disease'] | AAAGGAGAAATTGCTGGAGCAACATTTTTTATGAAGGGAGAAGAGATGGGAATCAAGTACAAAACTGGAGAGGTTGGCCTTAGGAGCACAGACACTCTATTTATTGTAATAAGTGTGCAGGCAGAGTATATGGGTACAAATGCCAGTAAATGTGATGTTGGGAGTCTGTGGAGGTTCATTGCACAGCATCAGCTAAGAGTGAAAATGGGCATTGGAGAATGGAAAAAAGGTGCTCGAGATTTAAGGAAAACACAGAAAATCTAAGATAGAGGTCCAGGAGAATGAGAAAGTCAGTGGACTAGGGAAATAGTCTATGGTTG... | AAAGGAGAAATTGCTGGAGCAACATTTTTTATGAAGGGAGAAGAGATGGGAATCAAGTACAAAACTGGAGAGGTTGGCCTTAGGAGCACAGACACTCTATTTATTGTAATAAGTGTGCAGGCAGAGTATATGGGTACAAATGCCAGTAAATGTGATGTTGGGAGTCTGTGGAGGTTCATTGCACAGCATCAGCTAAGAGTGAAAATGGGCATTGGAGAATGGAAAAAAGGTGCTCGAGATTTAAGGAAAACACAGAAAATCTAAGATAGAGGTCCAGGAGAATGAGAAAGTCAGTGGACTAGGGAAATAGTCTATGGTTG... | pathogenic | 342,585 |
Evaluate the clinical significance of the mutation at chromosome X, position 154929665 in gene F8 (coagulation factor VIII): benign or pathogenic? What disease(s) does a pathogenic variant suggest? | pathogenic; ['Hereditary_factor_VIII_deficiency_disease', 'Thrombophilia,_X-linked,_due_to_factor_8_defect'] | AAAATCTAAGATAGAGGTCCAGGAGAATGAGAAAGTCAGTGGACTAGGGAAATAGTCTATGGTTGCAATGCAGCAATAAGGGCTTACTTGAGCTAGAAAGCAAGGTGGGAAAGTGACAAGTCATGCTTGTCCCTTCTTGTTCCTCAAACATGGTAAACTTTTTCCATTCTCAGGGCCTTTGCATTTTCTCTTCCCTCTGTCTGGAAACATCTTCTCTCAGAGCTCCATCAGCTGGCCTGTTATCATCATTTAGGTCTCAACTCCTCAAAGATGATTTCTATGACCACCACAGCTAATGTAACACTCTACCGTATTACTCT... | AAAATCTAAGATAGAGGTCCAGGAGAATGAGAAAGTCAGTGGACTAGGGAAATAGTCTATGGTTGCAATGCAGCAATAAGGGCTTACTTGAGCTAGAAAGCAAGGTGGGAAAGTGACAAGTCATGCTTGTCCCTTCTTGTTCCTCAAACATGGTAAACTTTTTCCATTCTCAGGGCCTTTGCATTTTCTCTTCCCTCTGTCTGGAAACATCTTCTCTCAGAGCTCCATCAGCTGGCCTGTTATCATCATTTAGGTCTCAACTCCTCAAAGATGATTTCTATGACCACCACAGCTAATGTAACACTCTACCGTATTACTCT... | pathogenic | 342,586 |
Does the genetic variant at chromosome X, position 154930152, impacting gene F8 (coagulation factor VIII), appear benign or pathogenic? If pathogenic, name the associated disease(s). | pathogenic; ['Hereditary_factor_VIII_deficiency_disease'] | TGTTCCATAAATATTTGTGACTGACTGACTCTCCTTATGTTTATATTCCACATTTCTCTGTACTACTTGACTGCTCAACCTCCCTCTACTCACCTAAAAATAAAATCATCCTACTTTGCCCTCTGGATCCCCAGTATCATGAAAACCAATCCTCCCCAAGTCCTTAACCTCTTTAACACGAACTTGCTTCTTCCTTCTGCCTTGCTTAAAGTTCTCTGATGAGACTAAGATTTCCCCTGCAGCTCATAAGGTTGATAGGTGAGGTTGACTTTCTTCCTGCTCCCCATTGCTCCTTCTTGTCCCTGATTCCTCTACCCTCT... | TGTTCCATAAATATTTGTGACTGACTGACTCTCCTTATGTTTATATTCCACATTTCTCTGTACTACTTGACTGCTCAACCTCCCTCTACTCACCTAAAAATAAAATCATCCTACTTTGCCCTCTGGATCCCCAGTATCATGAAAACCAATCCTCCCCAAGTCCTTAACCTCTTTAACACGAACTTGCTTCTTCCTTCTGCCTTGCTTAAAGTTCTCTGATGAGACTAAGATTTCCCCTGCAGCTCATAAGGTTGATAGGTGAGGTTGACTTTCTTCCTGCTCCCCATTGCTCCTTCTTGTCCCTGATTCCTCTACCCTCT... | pathogenic | 342,589 |
A mutation at chromosome position 154930152 on chromosome X in gene F8 (coagulation factor VIII): benign or pathogenic? If pathogenic, which disease(s) is it linked to? | pathogenic; ['Hereditary_factor_IX_deficiency_disease', 'Hereditary_factor_VIII_deficiency_disease'] | TGTTCCATAAATATTTGTGACTGACTGACTCTCCTTATGTTTATATTCCACATTTCTCTGTACTACTTGACTGCTCAACCTCCCTCTACTCACCTAAAAATAAAATCATCCTACTTTGCCCTCTGGATCCCCAGTATCATGAAAACCAATCCTCCCCAAGTCCTTAACCTCTTTAACACGAACTTGCTTCTTCCTTCTGCCTTGCTTAAAGTTCTCTGATGAGACTAAGATTTCCCCTGCAGCTCATAAGGTTGATAGGTGAGGTTGACTTTCTTCCTGCTCCCCATTGCTCCTTCTTGTCCCTGATTCCTCTACCCTCT... | TGTTCCATAAATATTTGTGACTGACTGACTCTCCTTATGTTTATATTCCACATTTCTCTGTACTACTTGACTGCTCAACCTCCCTCTACTCACCTAAAAATAAAATCATCCTACTTTGCCCTCTGGATCCCCAGTATCATGAAAACCAATCCTCCCCAAGTCCTTAACCTCTTTAACACGAACTTGCTTCTTCCTTCTGCCTTGCTTAAAGTTCTCTGATGAGACTAAGATTTCCCCTGCAGCTCATAAGGTTGATAGGTGAGGTTGACTTTCTTCCTGCTCCCCATTGCTCCTTCTTGTCCCTGATTCCTCTACCCTCT... | pathogenic | 342,590 |
Clinical significance of chromosome X, position 154930695, gene F8 (coagulation factor VIII): benign or pathogenic? Name the disease(s) if pathogenic. | pathogenic; ['Hereditary_factor_VIII_deficiency_disease'] | GTGTTTTCTTTTGAAAGCTGCGGGGGCTCTGATTTTCATCCTCATCATAAATGTCAAAATCTTCCTTCTTCATTTCAACTGATATGGTATCATCATAGTCAATTTCCTCTTGATCTGACTGAAGAGTAGTACGAGTTATTTCCCGTTGATGGCGTTTCAAGACTGGTGGGTTTTGAGAGCACAGCCTTTCAGTCCTACCTTGCTTTGCCCAGGTGACTTCTATTTCGGGCTTATTTTGTCCCTCATTTATTGCTGCTATTGCATGATTGCTTTCACAAGCGTTCAGGGACAAAATGGTATCCTTTTTCTTAAAAGCTGTT... | GTGTTTTCTTTTGAAAGCTGCGGGGGCTCTGATTTTCATCCTCATCATAAATGTCAAAATCTTCCTTCTTCATTTCAACTGATATGGTATCATCATAGTCAATTTCCTCTTGATCTGACTGAAGAGTAGTACGAGTTATTTCCCGTTGATGGCGTTTCAAGACTGGTGGGTTTTGAGAGCACAGCCTTTCAGTCCTACCTTGCTTTGCCCAGGTGACTTCTATTTCGGGCTTATTTTGTCCCTCATTTATTGCTGCTATTGCATGATTGCTTTCACAAGCGTTCAGGGACAAAATGGTATCCTTTTTCTTAAAAGCTGTT... | pathogenic | 342,594 |
Does the genetic variant at chromosome X, position 154930844, impacting gene F8 (coagulation factor VIII), appear benign or pathogenic? If pathogenic, name the associated disease(s). | pathogenic; ['Hereditary_factor_VIII_deficiency_disease'] | TGGCGTTTCAAGACTGGTGGGTTTTGAGAGCACAGCCTTTCAGTCCTACCTTGCTTTGCCCAGGTGACTTCTATTTCGGGCTTATTTTGTCCCTCATTTATTGCTGCTATTGCATGATTGCTTTCACAAGCGTTCAGGGACAAAATGGTATCCTTTTTCTTAAAAGCTGTTTTTTCTGGTGACTTCTCTTGGGATTTCCACTCTTCTTTTGGTATCTGAGTACCATAGTGGTTATCCCAAGCAAGAGGATCCAATAGCTTGGAGGGAGTCTTTGCAGAGCTTTCTGTTGCTACTCTCAGAAAGGGAACTTTTCCAGGTCT... | TGGCGTTTCAAGACTGGTGGGTTTTGAGAGCACAGCCTTTCAGTCCTACCTTGCTTTGCCCAGGTGACTTCTATTTCGGGCTTATTTTGTCCCTCATTTATTGCTGCTATTGCATGATTGCTTTCACAAGCGTTCAGGGACAAAATGGTATCCTTTTTCTTAAAAGCTGTTTTTTCTGGTGACTTCTCTTGGGATTTCCACTCTTCTTTTGGTATCTGAGTACCATAGTGGTTATCCCAAGCAAGAGGATCCAATAGCTTGGAGGGAGTCTTTGCAGAGCTTTCTGTTGCTACTCTCAGAAAGGGAACTTTTCCAGGTCT... | pathogenic | 342,597 |
Clinically, how would you classify the variant at chromosome X, position 154947224, gene F8 (coagulation factor VIII): benign or pathogenic? If pathogenic, specify the associated illness(es). | pathogenic; ['Mild_hemophilia_A', 'Thrombophilia,_X-linked,_due_to_factor_8_defect'] | AAAAAAGAACTAATACCAGCTCTTCACAAACTATCCCAAAAATCAAGGGGGAAAAATACTTCCAAACTGATTCCACAAGGCCAGTATTACCCTGAAACCAAACCAGACAAAGACACACACATACACAAAAAGAAACTACAGGCCAATATCTCTGATGAACATTGATGCAAAAATCCTCAACGAACTACTAGCAAACCAAATTCAACAACACAGTAAAAGATCATTCATCATGATCAAGGGGGATTCATCCCAGGGATGCAAGGATGGTTCAACATATGGAAATGAATCAATGTGATACATCATATCAACAGAATGAAGGA... | AAAAAAGAACTAATACCAGCTCTTCACAAACTATCCCAAAAATCAAGGGGGAAAAATACTTCCAAACTGATTCCACAAGGCCAGTATTACCCTGAAACCAAACCAGACAAAGACACACACATACACAAAAAGAAACTACAGGCCAATATCTCTGATGAACATTGATGCAAAAATCCTCAACGAACTACTAGCAAACCAAATTCAACAACACAGTAAAAGATCATTCATCATGATCAAGGGGGATTCATCCCAGGGATGCAAGGATGGTTCAACATATGGAAATGAATCAATGTGATACATCATATCAACAGAATGAAGGA... | pathogenic | 342,606 |
Variant chromosome X, position 154957007, gene F8 (coagulation factor VIII): benign or pathogenic? Disease(s)? | pathogenic; ['Hereditary_factor_VIII_deficiency_disease'] | TAATCAAATGGACATGTAGTCAAGCCTCAGCAATATGGCACTGAGTTATTCTGGGGCCGAGCAATGAGTTTTTGTGAAGAACTAAGCTTTTCTTGTTCAGAGAATTTAGCTTTATTTTTTAAAGCAGTAGAAATGGTCCAAATTCTAGCCATATTTTGAAATATTTTATATCTTTCCCTATGTTTTGCCCAAAAGTATTTATTAAGCTTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACAGGGTGTCGCTTTGTCATCCAGGCTCACTGCAGCCTCGACCTCCTGGGCTCAAGCTATCTTCCCACCTCAGCCTCCTGAG... | TAATCAAATGGACATGTAGTCAAGCCTCAGCAATATGGCACTGAGTTATTCTGGGGCCGAGCAATGAGTTTTTGTGAAGAACTAAGCTTTTCTTGTTCAGAGAATTTAGCTTTATTTTTTAAAGCAGTAGAAATGGTCCAAATTCTAGCCATATTTTGAAATATTTTATATCTTTCCCTATGTTTTGCCCAAAAGTATTTATTAAGCTTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACAGGGTGTCGCTTTGTCATCCAGGCTCACTGCAGCCTCGACCTCCTGGGCTCAAGCTATCTTCCCACCTCAGCCTCCTGAG... | pathogenic | 342,615 |
Is the chromosome X, position 154984717 variant in F8 (coagulation factor VIII) clinically benign or pathogenic? If pathogenic, what condition(s) is associated? | pathogenic; ['Hereditary_factor_VIII_deficiency_disease'] | TGCATAAAATTAACGGTAGTAGCCATCTCCTATTGTTATTGTGCTGAGCTCGAGTGCTGCAGGCATCCACTGAAAACTCTGCATGATGCTAATCATCTCTGCATAAGCATTTCATCTCTCCATAAACTTTGAAGGATACTTGGGACCCGTATAAAGTGCCACTAGTGATGCTGGAAGTACTCCCAAGAAGCAGAGAAAAGTATAAATAACATTTTCCTTTCTCTAGCTTACTTTATTGAAAATATACAGCATATAATACATACACAAAATATTTGTTGTTTATGTTATTGATAAGGCTTCTGATCAACAATAGGTCATTA... | TGCATAAAATTAACGGTAGTAGCCATCTCCTATTGTTATTGTGCTGAGCTCGAGTGCTGCAGGCATCCACTGAAAACTCTGCATGATGCTAATCATCTCTGCATAAGCATTTCATCTCTCCATAAACTTTGAAGGATACTTGGGACCCGTATAAAGTGCCACTAGTGATGCTGGAAGTACTCCCAAGAAGCAGAGAAAAGTATAAATAACATTTTCCTTTCTCTAGCTTACTTTATTGAAAATATACAGCATATAATACATACACAAAATATTTGTTGTTTATGTTATTGATAAGGCTTCTGATCAACAATAGGTCATTA... | pathogenic | 342,651 |
Determine whether the variant at chromosome X, position 154999531, in gene F8 (coagulation factor VIII) is benign or pathogenic. If pathogenic, identify the relevant disease(s). | pathogenic; ['Hereditary_factor_VIII_deficiency_disease'] | GAGGTAGAGGATACTTTCAGTGTAGTAGTCAGGAAGGGCCTCTCTGAGGAGGTGACATTTGAGTAGAGATCTGACTAATGAAAAAGAAGCAAGATTTTCAAAGATCTAGTGGAAGAGCATTGAAAACAGATAAAACAAATGCAAACGTCCAGAGGCAGAAATAAGTTTGGTATAGTCAAGTAAAGTGTGGCTGAAGCACAGTGAATCAGCAGAGGAGTAACAGAAAATATGGTCAAAAAGGAAACATAACATGTAGGACCTTGCAGGCCACAGGAATTTGGATGAATTTGGATTTTACAAGAAGTAAAATAAGAAGACTT... | GAGGTAGAGGATACTTTCAGTGTAGTAGTCAGGAAGGGCCTCTCTGAGGAGGTGACATTTGAGTAGAGATCTGACTAATGAAAAAGAAGCAAGATTTTCAAAGATCTAGTGGAAGAGCATTGAAAACAGATAAAACAAATGCAAACGTCCAGAGGCAGAAATAAGTTTGGTATAGTCAAGTAAAGTGTGGCTGAAGCACAGTGAATCAGCAGAGGAGTAACAGAAAATATGGTCAAAAAGGAAACATAACATGTAGGACCTTGCAGGCCACAGGAATTTGGATGAATTTGGATTTTACAAGAAGTAAAATAAGAAGACTT... | pathogenic | 342,665 |
Clinical classification of chromosome X, position 155506930, gene TMLHE (trimethyllysine hydroxylase, epsilon): benign or pathogenic? Disease(s) if pathogenic? | pathogenic; ['Epsilon-trimethyllysine_hydroxylase_deficiency'] | TGTGCAGAAGTATGAGAGTACTTCCTGTAGTGATAGTAATATTTTATATCTTGATAAGGGTTTGGGTTAAATAGGTATATGCATTGGTCAAAACTCAGTGAGTGTATATTTAATATTTTAAACATCATTGCATATACATTGTAACTTTAAAAAGCTGTAAGCAAATATTGAACTCTACTTAATGATATAAATGTTGAAGTATTAGGGAGATATGTACTGATATCTGCAATGTATTATACTTTAAAATTCACTGAAAATAAGATTAACTGATGAATGAATAGATGGGAAGATAGGTGATAAAGCAAGTATAGAAATATCTT... | TGTGCAGAAGTATGAGAGTACTTCCTGTAGTGATAGTAATATTTTATATCTTGATAAGGGTTTGGGTTAAATAGGTATATGCATTGGTCAAAACTCAGTGAGTGTATATTTAATATTTTAAACATCATTGCATATACATTGTAACTTTAAAAAGCTGTAAGCAAATATTGAACTCTACTTAATGATATAAATGTTGAAGTATTAGGGAGATATGTACTGATATCTGCAATGTATTATACTTTAAAATTCACTGAAAATAAGATTAACTGATGAATGAATAGATGGGAAGATAGGTGATAAAGCAAGTATAGAAATATCTT... | pathogenic | 342,675 |
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