WormBase Tree Display for Variation: WBVar00248997
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| WBVar00248997 | Name | Public_name | sy455 | ||||
|---|---|---|---|---|---|---|---|
| Other_name | C09E10.2d.1:c.2177C>T | ||||||
| CE08038:p.Ser880Leu | |||||||
| C09E10.2a.1:c.2639C>T | |||||||
| CE38268:p.Ser724Leu | |||||||
| CE38269:p.Ser726Leu | |||||||
| C09E10.2b.1:c.2645C>T | |||||||
| C09E10.2e.1:c.2546C>T | |||||||
| C09E10.2c.1:c.2171C>T | |||||||
| CE08039:p.Ser882Leu | |||||||
| CE38270:p.Ser849Leu | |||||||
| HGVSg | CHROMOSOME_X:g.985202G>A | ||||||
| Sequence_details | SMap | S_parent | Sequence | C09E10 | |||
| Flanking_sequences | agccaccgggaactatcacaatattgaaat | agctttgaaagtacgtttaaacagttttcc | |||||
| Mapping_target | C09E10 | ||||||
| Type_of_mutation | Substitution | c | t | Paper_evidence | WBPaper00024616 | ||
| SeqStatus | Sequenced | ||||||
| Variation_type | Allele | ||||||
| Origin | Species | Caenorhabditis elegans | |||||
| Laboratory | PS | ||||||
| Status | Live | ||||||
| Affects | Gene | WBGene00000958 | |||||
| Transcript | C09E10.2d.1 | VEP_consequence | missense_variant | ||||
| VEP_impact | MODERATE | ||||||
| HGVSc | C09E10.2d.1:c.2177C>T | ||||||
| HGVSp | CE38269:p.Ser726Leu | ||||||
| cDNA_position | 2177 | ||||||
| CDS_position | 2177 | ||||||
| Protein_position | 726 | ||||||
| Exon_number | 13/14 | ||||||
| Codon_change | tCa/tTa | ||||||
| Amino_acid_change | S/L | ||||||
| C09E10.2c.1 | VEP_consequence | missense_variant | |||||
| VEP_impact | MODERATE | ||||||
| HGVSc | C09E10.2c.1:c.2171C>T | ||||||
| HGVSp | CE38268:p.Ser724Leu | ||||||
| cDNA_position | 2171 | ||||||
| CDS_position | 2171 | ||||||
| Protein_position | 724 | ||||||
| Exon_number | 13/14 | ||||||
| Codon_change | tCa/tTa | ||||||
| Amino_acid_change | S/L | ||||||
| C09E10.2a.1 | VEP_consequence | missense_variant | |||||
| VEP_impact | MODERATE | ||||||
| HGVSc | C09E10.2a.1:c.2639C>T | ||||||
| HGVSp | CE08038:p.Ser880Leu | ||||||
| cDNA_position | 2782 | ||||||
| CDS_position | 2639 | ||||||
| Protein_position | 880 | ||||||
| Exon_number | 16/18 | ||||||
| Codon_change | tCa/tTa | ||||||
| Amino_acid_change | S/L | ||||||
| C09E10.2e.1 | VEP_consequence | missense_variant | |||||
| VEP_impact | MODERATE | ||||||
| HGVSc | C09E10.2e.1:c.2546C>T | ||||||
| HGVSp | CE38270:p.Ser849Leu | ||||||
| cDNA_position | 2546 | ||||||
| CDS_position | 2546 | ||||||
| Protein_position | 849 | ||||||
| Exon_number | 14/15 | ||||||
| Codon_change | tCa/tTa | ||||||
| Amino_acid_change | S/L | ||||||
| C09E10.2b.1 | VEP_consequence | missense_variant | |||||
| VEP_impact | MODERATE | ||||||
| HGVSc | C09E10.2b.1:c.2645C>T | ||||||
| HGVSp | CE08039:p.Ser882Leu | ||||||
| cDNA_position | 2788 | ||||||
| CDS_position | 2645 | ||||||
| Protein_position | 882 | ||||||
| Exon_number | 16/18 | ||||||
| Codon_change | tCa/tTa | ||||||
| Amino_acid_change | S/L | ||||||
| Genetics | Interpolated_map_position | X | -18.8719 | ||||
| Method | Substitution_allele |
