WormBase Tree Display for Variation: WBVar00820781
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| WBVar00820781 | Name | Public_name | gk937289 | ||
|---|---|---|---|---|---|
| Other_name (16) | |||||
| HGVSg | CHROMOSOME_III:g.4258419G>A | ||||
| Sequence_details | SMap | S_parent | Sequence | T08A11 | |
| Flanking_sequences | TGGCTCCAATTTCTTCTTCTCAACTGATGGTGGTGGTGGTGGAAGTGGTG | AGGTGGAGGTGGATTACTAGCAATTGGTGCAGCTTTTTGAGTATTATTAT | |||
| Mapping_target | T08A11 | ||||
| Type_of_mutation | Substitution | G | A | ||
| SeqStatus | Sequenced | ||||
| Variation_type | Allele | ||||
| Origin | Species | Caenorhabditis elegans | |||
| Strain | WBStrain00039993 | ||||
| Laboratory | VC | ||||
| Analysis | Million_Mutation_Project | ||||
| Status | Live | ||||
| Affects | Gene | WBGene00011604 | |||
| Transcript | T08A11.1e.1 | VEP_consequence | missense_variant | ||
| VEP_impact | MODERATE | ||||
| HGVSc | T08A11.1e.1:c.1981C>T | ||||
| HGVSp | CE54607:p.Pro661Ser | ||||
| cDNA_position | 1981 | ||||
| CDS_position | 1981 | ||||
| Protein_position | 661 | ||||
| Exon_number | 7/18 | ||||
| Codon_change | Cca/Tca | ||||
| Amino_acid_change | P/S | ||||
| T08A11.1g.1 | VEP_consequence | missense_variant | |||
| VEP_impact | MODERATE | ||||
| HGVSc | T08A11.1g.1:c.1981C>T | ||||
| HGVSp | CE54616:p.Pro661Ser | ||||
| cDNA_position | 2077 | ||||
| CDS_position | 1981 | ||||
| Protein_position | 661 | ||||
| Exon_number | 8/19 | ||||
| Codon_change | Cca/Tca | ||||
| Amino_acid_change | P/S | ||||
| T08A11.1h.1 | VEP_consequence | missense_variant | |||
| VEP_impact | MODERATE | ||||
| HGVSc | T08A11.1h.1:c.1981C>T | ||||
| HGVSp | CE54610:p.Pro661Ser | ||||
| cDNA_position | 2077 | ||||
| CDS_position | 1981 | ||||
| Protein_position | 661 | ||||
| Exon_number | 8/19 | ||||
| Codon_change | Cca/Tca | ||||
| Amino_acid_change | P/S | ||||
| T08A11.1d.1 | VEP_consequence | missense_variant | |||
| VEP_impact | MODERATE | ||||
| HGVSc | T08A11.1d.1:c.1981C>T | ||||
| HGVSp | CE54612:p.Pro661Ser | ||||
| cDNA_position | 2077 | ||||
| CDS_position | 1981 | ||||
| Protein_position | 661 | ||||
| Exon_number | 8/19 | ||||
| Codon_change | Cca/Tca | ||||
| Amino_acid_change | P/S | ||||
| T08A11.1f.1 | VEP_consequence | missense_variant | |||
| VEP_impact | MODERATE | ||||
| HGVSc | T08A11.1f.1:c.1981C>T | ||||
| HGVSp | CE54622:p.Pro661Ser | ||||
| cDNA_position | 1981 | ||||
| CDS_position | 1981 | ||||
| Protein_position | 661 | ||||
| Exon_number | 7/18 | ||||
| Codon_change | Cca/Tca | ||||
| Amino_acid_change | P/S | ||||
| T08A11.1c.1 | VEP_consequence | missense_variant | |||
| VEP_impact | MODERATE | ||||
| HGVSc | T08A11.1c.1:c.1981C>T | ||||
| HGVSp | CE54609:p.Pro661Ser | ||||
| cDNA_position | 1981 | ||||
| CDS_position | 1981 | ||||
| Protein_position | 661 | ||||
| Exon_number | 7/18 | ||||
| Codon_change | Cca/Tca | ||||
| Amino_acid_change | P/S | ||||
| T08A11.1b.1 | VEP_consequence | missense_variant | |||
| VEP_impact | MODERATE | ||||
| HGVSc | T08A11.1b.1:c.1981C>T | ||||
| HGVSp | CE54613:p.Pro661Ser | ||||
| cDNA_position | 2077 | ||||
| CDS_position | 1981 | ||||
| Protein_position | 661 | ||||
| Exon_number | 8/19 | ||||
| Codon_change | Cca/Tca | ||||
| Amino_acid_change | P/S | ||||
| T08A11.1a.1 | VEP_consequence | missense_variant | |||
| VEP_impact | MODERATE | ||||
| HGVSc | T08A11.1a.1:c.1981C>T | ||||
| HGVSp | CE54207:p.Pro661Ser | ||||
| cDNA_position | 2081 | ||||
| CDS_position | 1981 | ||||
| Protein_position | 661 | ||||
| Exon_number | 8/19 | ||||
| Codon_change | Cca/Tca | ||||
| Amino_acid_change | P/S | ||||
| Reference | WBPaper00042537 | ||||
| Method | Million_mutation |
