G66V (p.Gly66Val) variant of SRD5A2 (P31213)
G66V (p.Gly66Val) in SRD5A2 (P31213) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data.
G66V (p.Gly66Val) variant details
- p.Gly66Val
- gnomAD rs1250601374
- Missense
- Variant Prioritization Score for Impact Estimate 0.298
- CADD 12.00
- PolyPhen-2 0.28
- SIFT 0.50
- Most common in the African/African-American population (allele frequency 0.00031)