WormBase Tree Display for Variation: WBVar00241368
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WBVar00241368 | Evidence | Paper_evidence | WBPaper00001234 | |||
---|---|---|---|---|---|---|
Name | Public_name | r554 | ||||
Other_name | CE09349:p.Gly229Asp | |||||
F11C3.3.1:c.686G>A | ||||||
HGVSg | CHROMOSOME_I:g.14861674C>T | |||||
Sequence_details (5) | ||||||
Variation_type | Allele | |||||
Origin | Species | Caenorhabditis elegans | ||||
Laboratory | TR | |||||
Status | Live | |||||
Affects | Gene | WBGene00006789 | ||||
Transcript | F11C3.3.1 | VEP_consequence | missense_variant | |||
VEP_impact | MODERATE | |||||
SIFT | 0 | deleterious | ||||
PolyPhen | 1 | probably_damaging | ||||
HGVSc | F11C3.3.1:c.686G>A | |||||
HGVSp | CE09349:p.Gly229Asp | |||||
cDNA_position | 718 | |||||
CDS_position | 686 | |||||
Protein_position | 229 | |||||
Exon_number | 5/11 | |||||
Codon_change | gGt/gAt | |||||
Amino_acid_change | G/D | |||||
Genetics | Interpolated_map_position | I | 27.9621 | |||
Reference | WBPaper00001234 | |||||
Method | Substitution_allele |