WormBase Tree Display for Variation: WBVar02147736
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| WBVar02147736 | Evidence | Paper_evidence | WBPaper00051175 | ||||
|---|---|---|---|---|---|---|---|
| Name | Public_name | ju831 | |||||
| Other_name | CE35833:p.Pro127Ser | ||||||
| C34C6.5a.1:c.529C>T | |||||||
| C34C6.5d.1:c.124C>T | |||||||
| C34C6.5b.1:c.379C>T | |||||||
| CE47276:p.Pro42Ser | |||||||
| C34C6.5c.1:c.292C>T | |||||||
| CE03053:p.Pro177Ser | |||||||
| CE44377:p.Pro98Ser | |||||||
| HGVSg | CHROMOSOME_II:g.8700419G>A | ||||||
| Sequence_details | SMap | S_parent | Sequence | C34C6 | |||
| Flanking_sequences | GAAGATGCATTCCGGATATTCCCAACTCTC | CAATCGGAATTGTTCCCAGCGGATCCGGAA | |||||
| Mapping_target | C34C6 | ||||||
| Type_of_mutation | Substitution | C | T | Paper_evidence | WBPaper00051175 | ||
| SeqStatus | Sequenced | ||||||
| Origin | Species | Caenorhabditis elegans | |||||
| Strain | WBStrain00005423 | ||||||
| WBStrain00005455 | |||||||
| Laboratory | CZ | ||||||
| Status | Live | ||||||
| Affects | Gene | WBGene00007918 | |||||
| Transcript | C34C6.5d.1 | VEP_consequence | missense_variant | ||||
| VEP_impact | MODERATE | ||||||
| HGVSc | C34C6.5d.1:c.124C>T | ||||||
| HGVSp | CE47276:p.Pro42Ser | ||||||
| cDNA_position | 124 | ||||||
| CDS_position | 124 | ||||||
| Protein_position | 42 | ||||||
| Exon_number | 2/5 | ||||||
| Codon_change | Cca/Tca | ||||||
| Amino_acid_change | P/S | ||||||
| C34C6.5c.1 | VEP_consequence | missense_variant | |||||
| VEP_impact | MODERATE | ||||||
| HGVSc | C34C6.5c.1:c.292C>T | ||||||
| HGVSp | CE44377:p.Pro98Ser | ||||||
| cDNA_position | 569 | ||||||
| CDS_position | 292 | ||||||
| Protein_position | 98 | ||||||
| Exon_number | 5/9 | ||||||
| Codon_change | Cca/Tca | ||||||
| Amino_acid_change | P/S | ||||||
| C34C6.5a.1 | VEP_consequence | missense_variant | |||||
| VEP_impact | MODERATE | ||||||
| HGVSc | C34C6.5a.1:c.529C>T | ||||||
| HGVSp | CE03053:p.Pro177Ser | ||||||
| cDNA_position | 530 | ||||||
| CDS_position | 529 | ||||||
| Protein_position | 177 | ||||||
| Exon_number | 5/9 | ||||||
| Codon_change | Cca/Tca | ||||||
| Amino_acid_change | P/S | ||||||
| C34C6.5b.1 | VEP_consequence | missense_variant | |||||
| VEP_impact | MODERATE | ||||||
| HGVSc | C34C6.5b.1:c.379C>T | ||||||
| HGVSp | CE35833:p.Pro127Ser | ||||||
| cDNA_position | 379 | ||||||
| CDS_position | 379 | ||||||
| Protein_position | 127 | ||||||
| Exon_number | 4/7 | ||||||
| Codon_change | Cca/Tca | ||||||
| Amino_acid_change | P/S | ||||||
| Genetics | Interpolated_map_position | II | 0.842425 | ||||
| Reference | WBPaper00051175 | ||||||
| Method | Substitution_allele |
