WormBase Tree Display for Variation: WBVar00144305
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| WBVar00144305 | Evidence | Paper_evidence | WBPaper00001872 | ||||
|---|---|---|---|---|---|---|---|
| Name | Public_name | e1789 | |||||
| Other_name | T01C8.7.1:c.2177C>T | ||||||
| CE39109:p.Ser726Phe | |||||||
| HGVSg | CHROMOSOME_X:g.16803522G>A | ||||||
| Sequence_details | SMap | S_parent | Sequence | T01C8 | |||
| Flanking_sequences | gtggacaactcggtctttggtgcggaatat | cttccttacctgttgcgaatttgtgttcct | |||||
| Mapping_target | T01C8 | ||||||
| Type_of_mutation | Substitution | c | t | Paper_evidence | WBPaper00001872 | ||
| SeqStatus | Sequenced | ||||||
| Variation_type | Allele | ||||||
| Origin | Species | Caenorhabditis elegans | |||||
| Laboratory | CB | ||||||
| Status | Live | ||||||
| Affects | Gene | WBGene00003168 | |||||
| Transcript | T01C8.7.1 | VEP_consequence | missense_variant | ||||
| VEP_impact | MODERATE | ||||||
| HGVSc | T01C8.7.1:c.2177C>T | ||||||
| HGVSp | CE39109:p.Ser726Phe | ||||||
| cDNA_position | 2178 | ||||||
| CDS_position | 2177 | ||||||
| Protein_position | 726 | ||||||
| Exon_number | 16/17 | ||||||
| Codon_change | tCc/tTc | ||||||
| Amino_acid_change | S/F | ||||||
| Isolation | Mutagen | EMS | Paper_evidence | WBPaper00001872 | |||
| Genetics | Interpolated_map_position | X | 24.0624 | ||||
| Reference | WBPaper00001872 | ||||||
| Method | Substitution_allele |
