G13D (p.Gly13Asp) variant of SRD5A2 (P31213)
G13D (p.Gly13Asp) in SRD5A2 (P31213) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.75 / 1. The record also includes population frequency data and structural context.
G13D (p.Gly13Asp) variant details
- p.Gly13Asp
- ESP rs368219567
- ExAC rs368219567
- TOPMed rs368219567
- gnomAD rs368219567
- Missense
- Variant Prioritization Score for Impact Estimate 0.752
- CADD 23.10
- PolyPhen-2 1.00
- SIFT 0.20
- Most common in the Non-Finnish European population (allele frequency 8.8e-05)
- Structural context available