WormBase Tree Display for Variation: WBVar00395676
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| WBVar00395676 | Name | Public_name | gk172433 | ||
|---|---|---|---|---|---|
| Other_name | T08A11.1a.1:c.2587+533C>T | ||||
| T08A11.1c.1:c.2587+533C>T | |||||
| T08A11.1e.1:c.2587+533C>T | |||||
| T08A11.1d.1:c.2593+533C>T | |||||
| T08A11.1b.1:c.2593+533C>T | |||||
| T08A11.1f.1:c.2593+533C>T | |||||
| T08A11.1g.1:c.2587+533C>T | |||||
| T08A11.1h.1:c.2593+533C>T | |||||
| HGVSg | CHROMOSOME_III:g.4257178G>A | ||||
| Sequence_details | SMap | S_parent | Sequence | T08A11 | |
| Flanking_sequences | CCTAATGCCCCCTTAGAACGCGATGCCCCCTCTCTCGATGCCCCCTGGGA | CATAGGCCAGATTTTCCAGGTTTTCCAGATTTCGAAAATTTTATCGAATT | |||
| Mapping_target | T08A11 | ||||
| Type_of_mutation | Substitution | G | A | ||
| SeqStatus | Sequenced | ||||
| Variation_type | Allele | ||||
| Origin | Species | Caenorhabditis elegans | |||
| Strain | WBStrain00038824 | ||||
| Laboratory | VC | ||||
| Analysis | Million_Mutation_Project | ||||
| Status | Live | ||||
| Affects | Gene | WBGene00011604 | |||
| Transcript | T08A11.1e.1 | VEP_consequence | intron_variant | ||
| VEP_impact | MODIFIER | ||||
| HGVSc | T08A11.1e.1:c.2587+533C>T | ||||
| Intron_number | 9/17 | ||||
| T08A11.1g.1 | VEP_consequence | intron_variant | |||
| VEP_impact | MODIFIER | ||||
| HGVSc | T08A11.1g.1:c.2587+533C>T | ||||
| Intron_number | 10/18 | ||||
| T08A11.1h.1 | VEP_consequence | intron_variant | |||
| VEP_impact | MODIFIER | ||||
| HGVSc | T08A11.1h.1:c.2593+533C>T | ||||
| Intron_number | 10/18 | ||||
| T08A11.1d.1 | VEP_consequence | intron_variant | |||
| VEP_impact | MODIFIER | ||||
| HGVSc | T08A11.1d.1:c.2593+533C>T | ||||
| Intron_number | 10/18 | ||||
| T08A11.1f.1 | VEP_consequence | intron_variant | |||
| VEP_impact | MODIFIER | ||||
| HGVSc | T08A11.1f.1:c.2593+533C>T | ||||
| Intron_number | 9/17 | ||||
| T08A11.1c.1 | VEP_consequence | intron_variant | |||
| VEP_impact | MODIFIER | ||||
| HGVSc | T08A11.1c.1:c.2587+533C>T | ||||
| Intron_number | 9/17 | ||||
| T08A11.1b.1 | VEP_consequence | intron_variant | |||
| VEP_impact | MODIFIER | ||||
| HGVSc | T08A11.1b.1:c.2593+533C>T | ||||
| Intron_number | 10/18 | ||||
| T08A11.1a.1 | VEP_consequence | intron_variant | |||
| VEP_impact | MODIFIER | ||||
| HGVSc | T08A11.1a.1:c.2587+533C>T | ||||
| Intron_number | 10/18 | ||||
| Reference | WBPaper00042537 | ||||
| Method | Million_mutation |
