G13R (p.Gly13Arg) variant of SRD5A2 (P31213)
G13R (p.Gly13Arg) in SRD5A2 (P31213) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.66 / 1. The record also includes population frequency data and structural context.
G13R (p.Gly13Arg) variant details
- p.Gly13Arg
- Ensembl rs1667068129
- Missense
- Variant Prioritization Score for Impact Estimate 0.656
- CADD 23.20
- PolyPhen-2 1.00
- SIFT 0.34
- Most common in the 1KG:MXL population (allele frequency 0.0081)
- Structural context available