V97L (p.Val97Leu) variant of SRD5A2 (P31213)
V97L (p.Val97Leu) in SRD5A2 (P31213) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data and structural context.
V97L (p.Val97Leu) variant details
- p.Val97Leu
- ExAC rs774936492
- gnomAD rs774936492
- Missense
- Variant Prioritization Score for Impact Estimate 0.255
- CADD 16.50
- PolyPhen-2 0.13
- SIFT 0.02
- Most common in the 1KG:CLM population (allele frequency 0.0053)
- Structural context available