WormBase Tree Display for Variation: WBVar00145035
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WBVar00145035 | Name | Public_name | e2888 | |||
---|---|---|---|---|---|---|
Other_name | F23H12.4b.1:c.674G>A | |||||
CE05707:p.Gly291Glu | ||||||
F23H12.4a.1:c.872G>A | ||||||
CE46560:p.Gly225Glu | ||||||
HGVSg | CHROMOSOME_V:g.12354046G>A | |||||
Sequence_details (5) | ||||||
Variation_type | Allele | |||||
Origin | Species | Caenorhabditis elegans | ||||
Laboratory | CB | |||||
Status | Live | |||||
Affects | Gene | WBGene00005018 | ||||
Transcript | F23H12.4a.1 | VEP_consequence | missense_variant | |||
VEP_impact | MODERATE | |||||
SIFT | 0 | deleterious | ||||
PolyPhen | 0 | unknown | ||||
HGVSc | F23H12.4a.1:c.872G>A | |||||
HGVSp | CE05707:p.Gly291Glu | |||||
cDNA_position | 1148 | |||||
CDS_position | 872 | |||||
Protein_position | 291 | |||||
Exon_number | 4/5 | |||||
Codon_change | gGa/gAa | |||||
Amino_acid_change | G/E | |||||
F23H12.4b.1 (12) | ||||||
Isolation | Mutagen | EMS | Paper_evidence | WBPaper00024637 | ||
Genetics | Interpolated_map_position | V | 4.00901 | |||
Remark | This allele has the same nucleotide mutation (and hence the same amino acid change) at the same position as sc8, and was mutated by the same mutagen. | Paper_evidence | WBPaper00024637 | |||
Method | Substitution_allele |