WormBase Tree Display for Variation: WBVar00216744
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| WBVar00216744 | Name | Public_name | WBVar00216744 | ||
|---|---|---|---|---|---|
| Other_name | pas28520 | ||||
| cewivar00115770 | |||||
| R12H7.1b.1:c.328-11T>C | |||||
| R12H7.1a.2:c.520-11T>C | |||||
| R12H7.1a.1:c.520-11T>C | |||||
| HGVSg | CHROMOSOME_X:g.13214406T>C | ||||
| Sequence_details | SMap | S_parent | Sequence | R12H7 | |
| Flanking_sequences | ttacttttctgatttgcattactaacagttcaattttaaccaattcaagctacattccgcaaaacattccgcaaaaaaaaaaatagagttaccagttatcaatgatcggggtacacctattctagagataatctgattcaaagcattgaagctccgtaaacctaagttttgagatctgaatttttgatgctccacacccctctcggagaactccttcaaaactgaaaaaaaaacaacgatttctgaaaatttttgtttatcatcagattttttcggtttttcttctaatcttattatttt | aattttacagatgtccggaaatcgtctgaaactgctcaacttgattatttgcacacgatcttccggtgctgctgtcacgttcctctatatctctgtcaaaattctgtacaccgtgaacatcgtcggccaaatctttctactgaacacgtttctcggtaaccgtagcaaatggtacggactgcaagttctcaacgacttgatgaacggacgagaatgggaggagtctggtcattttccacgtgtaacgttatgtgactttgaagtaaaagtactgggaaacgtgcaccgacatacagtaca | |||
| Mapping_target | R12H7 | ||||
| Type_of_mutation | Substitution | T | C | ||
| SeqStatus | Sequenced | ||||
| Variation_type | SNP | ||||
| Predicted_SNP | |||||
| Natural_variant | |||||
| Origin | Species | Caenorhabditis elegans | |||
| Strain | WBStrain00000034 | From_analysis | Million_mutation_project_reanalysis | ||
| WBStrain00004604 | From_analysis | WGS_Pasadena_Quinlan | |||
| WBStrain00006625 | From_analysis | Million_mutation_project_reanalysis | |||
| WBStrain00022850 | From_analysis | Million_mutation_project_reanalysis | |||
| WBStrain00027647 | From_analysis | Million_mutation_project_reanalysis | |||
| Person | WBPerson6900 | ||||
| Analysis | WGS_Pasadena_Quinlan | ||||
| Million_mutation_project_reanalysis | |||||
| Status | Live | ||||
| Affects | Gene | WBGene00006749 | |||
| Transcript | R12H7.1a.2 | VEP_consequence | intron_variant | ||
| VEP_impact | MODIFIER | ||||
| HGVSc | R12H7.1a.2:c.520-11T>C | ||||
| Intron_number | 7/10 | ||||
| R12H7.1a.1 | VEP_consequence | intron_variant | |||
| VEP_impact | MODIFIER | ||||
| HGVSc | R12H7.1a.1:c.520-11T>C | ||||
| Intron_number | 6/9 | ||||
| R12H7.1b.1 | VEP_consequence | intron_variant | |||
| VEP_impact | MODIFIER | ||||
| HGVSc | R12H7.1b.1:c.328-11T>C | ||||
| Intron_number | 3/5 | ||||
| Method | WGS_Pasadena_Quinlan |
