WormBase Tree Display for Variation: WBVar00275476
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| WBVar00275476 | Evidence | Paper_evidence | WBPaper00005425 | ||||
|---|---|---|---|---|---|---|---|
| Name | Public_name | zh32 | |||||
| Other_name | CE49310:p.Pro310Leu | ||||||
| CE31151:p.Pro310Leu | |||||||
| C05B10.1a.1:c.929C>T | |||||||
| C05B10.1b.1:c.929C>T | |||||||
| HGVSg | CHROMOSOME_IV:g.6844645C>T | ||||||
| Sequence_details | SMap | S_parent | Sequence | C05B10 | |||
| Flanking_sequences | gggttcaaaagagaaatgcaagcattgctc | aaattttcattttatgggacaactcacaga | |||||
| Mapping_target | C05B10 | ||||||
| Type_of_mutation | Substitution | c | t | Paper_evidence | WBPaper00005425 | ||
| SeqStatus | Sequenced | ||||||
| Variation_type | Allele | ||||||
| Origin | Species | Caenorhabditis elegans | |||||
| Laboratory | AH | ||||||
| Status | Live | ||||||
| Affects | Gene | WBGene00003043 | |||||
| Transcript | C05B10.1b.1 | VEP_consequence | missense_variant | ||||
| VEP_impact | MODERATE | ||||||
| SIFT | 0 | deleterious | |||||
| PolyPhen | 1 | probably_damaging | |||||
| HGVSc | C05B10.1b.1:c.929C>T | ||||||
| HGVSp | CE49310:p.Pro310Leu | ||||||
| cDNA_position | 935 | ||||||
| CDS_position | 929 | ||||||
| Protein_position | 310 | ||||||
| Exon_number | 9/11 | ||||||
| Codon_change | cCa/cTa | ||||||
| Amino_acid_change | P/L | ||||||
| C05B10.1a.1 | VEP_consequence | missense_variant | |||||
| VEP_impact | MODERATE | ||||||
| SIFT | 0 | deleterious | |||||
| PolyPhen | 1 | probably_damaging | |||||
| HGVSc | C05B10.1a.1:c.929C>T | ||||||
| HGVSp | CE31151:p.Pro310Leu | ||||||
| cDNA_position | 929 | ||||||
| CDS_position | 929 | ||||||
| Protein_position | 310 | ||||||
| Exon_number | 8/9 | ||||||
| Codon_change | cCa/cTa | ||||||
| Amino_acid_change | P/L | ||||||
| Genetics | Interpolated_map_position | IV | 3.24358 | ||||
| Reference | WBPaper00005425 | ||||||
| Method | Substitution_allele |
