WormBase Tree Display for Variation: WBVar01453725
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| WBVar01453725 | Evidence | Paper_evidence | WBPaper00040707 | ||
|---|---|---|---|---|---|
| Name | Public_name | WBVar01453725 | |||
| Other_name | F27C8.1.1:c.1155+37G>T | ||||
| HGVSg | CHROMOSOME_IV:g.9599965C>A | ||||
| Sequence_details | SMap | S_parent | Sequence | F27C8 | |
| Flanking_sequences | TCTAAAATTGATGCTTCAAGAAACTCAGTA | CGGGAAATATTAAAAAAAAAAAGCTATCAC | |||
| Mapping_target | F27C8 | ||||
| Type_of_mutation | Substitution | c | a | ||
| SeqStatus | Sequenced | ||||
| Variation_type | SNP | ||||
| Natural_variant | |||||
| Origin (7) | |||||
| Affects | Gene | WBGene00000002 | |||
| Transcript | F27C8.1.1 | VEP_consequence | intron_variant | ||
| VEP_impact | MODIFIER | ||||
| HGVSc | F27C8.1.1:c.1155+37G>T | ||||
| Intron_number | 6/9 | ||||
| Reference | WBPaper00040707 | ||||
| Method | WGS_Andersen |
