WormBase Tree Display for Variation: WBVar02134154
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| WBVar02134154 | Evidence | Paper_evidence | WBPaper00045317 | |||
|---|---|---|---|---|---|---|
| Name | Public_name | h13962 | ||||
| Other_name | B0496.3h.2:c.113-1097C>T | |||||
| B0496.3a.1:c.113-1097C>T | ||||||
| B0496.3a.2:c.113-1097C>T | ||||||
| B0496.3g.1:c.113-1097C>T | ||||||
| B0496.3b.1:c.113-1097C>T | ||||||
| B0496.3f.1:c.113-1097C>T | ||||||
| B0496.3h.1:c.113-1097C>T | ||||||
| B0496.3d.1:c.113-1097C>T | ||||||
| B0496.3e.1:c.830-1097C>T | ||||||
| HGVSg | CHROMOSOME_IV:g.7430768C>T | |||||
| Sequence_details | SMap | S_parent | Sequence | B0496 | ||
| Flanking_sequences | TGGAAAAGGCGGGCGGGAACCGGAAAACGGAGAGTTTCCT | CAAAAAGTTTATGAGTCGAAAAAAGAAAGACGGGTTAACG | ||||
| Mapping_target | CHROMOSOME_IV | |||||
| Source_location | 200 | CHROMOSOME_IV | 7430752 | 7430752 | ||
| Type_of_mutation | Substitution | C | T | |||
| SeqStatus | Sequenced | |||||
| Variation_type | Allele | |||||
| Origin | Species | Caenorhabditis elegans | ||||
| Strain | WBStrain00023886 | |||||
| Laboratory | KR | |||||
| Analysis | WGS_Rose | |||||
| Status | Live | |||||
| Affects | Gene | WBGene00006814 | ||||
| Transcript | B0496.3h.2 | VEP_consequence | intron_variant | |||
| VEP_impact | MODIFIER | |||||
| HGVSc | B0496.3h.2:c.113-1097C>T | |||||
| Intron_number | 1/27 | |||||
| B0496.3a.2 | VEP_consequence | intron_variant | ||||
| VEP_impact | MODIFIER | |||||
| HGVSc | B0496.3a.2:c.113-1097C>T | |||||
| Intron_number | 2/27 | |||||
| B0496.3b.1 | VEP_consequence | intron_variant | ||||
| VEP_impact | MODIFIER | |||||
| HGVSc | B0496.3b.1:c.113-1097C>T | |||||
| Intron_number | 1/30 | |||||
| B0496.3g.1 | VEP_consequence | intron_variant | ||||
| VEP_impact | MODIFIER | |||||
| HGVSc | B0496.3g.1:c.113-1097C>T | |||||
| Intron_number | 4/31 | |||||
| B0496.3a.1 | VEP_consequence | intron_variant | ||||
| VEP_impact | MODIFIER | |||||
| HGVSc | B0496.3a.1:c.113-1097C>T | |||||
| Intron_number | 7/32 | |||||
| B0496.3e.1 | VEP_consequence | intron_variant | ||||
| VEP_impact | MODIFIER | |||||
| HGVSc | B0496.3e.1:c.830-1097C>T | |||||
| Intron_number | 7/34 | |||||
| B0496.3f.1 | VEP_consequence | intron_variant | ||||
| VEP_impact | MODIFIER | |||||
| HGVSc | B0496.3f.1:c.113-1097C>T | |||||
| Intron_number | 1/28 | |||||
| B0496.3h.1 | VEP_consequence | intron_variant | ||||
| VEP_impact | MODIFIER | |||||
| HGVSc | B0496.3h.1:c.113-1097C>T | |||||
| Intron_number | 4/30 | |||||
| B0496.3d.1 | VEP_consequence | intron_variant | ||||
| VEP_impact | MODIFIER | |||||
| HGVSc | B0496.3d.1:c.113-1097C>T | |||||
| Intron_number | 4/32 | |||||
| Reference | WBPaper00040589 | |||||
| WBPaper00000975 | ||||||
| WBPaper00003985 | ||||||
| WBPaper00000699 | ||||||
| WBPaper00045317 | ||||||
| Method | WGS_Rose |
