WormBase Tree Display for Variation: WBVar00090750
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| WBVar00090750 | Evidence | Paper_evidence | WBPaper00029251 | ||||
|---|---|---|---|---|---|---|---|
| Name | Public_name | n3687 | |||||
| Other_name | R06C7.7b.1:c.1327C>T | ||||||
| CE31573:p.Gln443Ter | |||||||
| CE37542:p.Gln322Ter | |||||||
| R06C7.7a.1:c.964C>T | |||||||
| HGVSg | CHROMOSOME_I:g.7249629G>A | ||||||
| Sequence_details | SMap | S_parent | Sequence | R06C7 | |||
| Flanking_sequences | aagtttgagctcatcgaccccttggctcag | aattcaataacctccacgtcgcttcgattc | |||||
| Mapping_target | R06C7 | ||||||
| Type_of_mutation | Substitution | c | t | Paper_evidence | WBPaper00029251 | ||
| SeqStatus | Sequenced | ||||||
| Variation_type | Allele | ||||||
| Origin | Species | Caenorhabditis elegans | |||||
| Laboratory | MT | ||||||
| Status | Live | ||||||
| Affects | Gene | WBGene00003041 | |||||
| Transcript | R06C7.7b.1 | VEP_consequence | stop_gained | ||||
| VEP_impact | HIGH | ||||||
| HGVSc | R06C7.7b.1:c.1327C>T | ||||||
| HGVSp | CE31573:p.Gln443Ter | ||||||
| cDNA_position | 1327 | ||||||
| CDS_position | 1327 | ||||||
| Protein_position | 443 | ||||||
| Exon_number | 5/7 | ||||||
| Codon_change | Caa/Taa | ||||||
| Amino_acid_change | Q/* | ||||||
| R06C7.7a.1 | VEP_consequence | stop_gained | |||||
| VEP_impact | HIGH | ||||||
| HGVSc | R06C7.7a.1:c.964C>T | ||||||
| HGVSp | CE37542:p.Gln322Ter | ||||||
| cDNA_position | 964 | ||||||
| CDS_position | 964 | ||||||
| Protein_position | 322 | ||||||
| Exon_number | 4/7 | ||||||
| Codon_change | Caa/Taa | ||||||
| Amino_acid_change | Q/* | ||||||
| Genetics | Interpolated_map_position | I | 1.85866 | ||||
| Reference | WBPaper00029251 | ||||||
| Method | Substitution_allele |
