WormBase Tree Display for Variation: WBVar00241360
expand all nodes | collapse all nodes | view schema
| WBVar00241360 | Evidence | Paper_evidence | WBPaper00001234 | ||||
|---|---|---|---|---|---|---|---|
| Name | Public_name | r441 | |||||
| Other_name | F11C3.3.1:c.1370G>A | ||||||
| CE09349:p.Gly457Asp | |||||||
| HGVSg | CHROMOSOME_I:g.14860910C>T | ||||||
| Sequence_details | SMap | S_parent | Sequence | F11C3 | |||
| Flanking_sequences | aaaagggtattgatcgtgattatttcatcg | tgtgctcgatatcgccggtttcgaaatctt | |||||
| Mapping_target | F11C3 | ||||||
| Type_of_mutation | Substitution | g | a | Paper_evidence | WBPaper00001234 | ||
| SeqStatus | Sequenced | ||||||
| Variation_type | Allele | ||||||
| Origin | Species | Caenorhabditis elegans | |||||
| Laboratory | TR | ||||||
| Status | Live | ||||||
| Affects | Gene | WBGene00006789 | |||||
| Transcript | F11C3.3.1 | VEP_consequence | missense_variant | ||||
| VEP_impact | MODERATE | ||||||
| SIFT | 0 | deleterious | |||||
| PolyPhen | 1 | probably_damaging | |||||
| HGVSc | F11C3.3.1:c.1370G>A | ||||||
| HGVSp | CE09349:p.Gly457Asp | ||||||
| cDNA_position | 1402 | ||||||
| CDS_position | 1370 | ||||||
| Protein_position | 457 | ||||||
| Exon_number | 6/11 | ||||||
| Codon_change | gGt/gAt | ||||||
| Amino_acid_change | G/D | ||||||
| Genetics | Interpolated_map_position | I | 27.9615 | ||||
| Reference | WBPaper00001234 | ||||||
| Method | Substitution_allele |
