Y26H (p.Tyr26His) variant of SRD5A2 (P31213)
Y26H (p.Tyr26His) in SRD5A2 (P31213) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
Y26H (p.Tyr26His) variant details
- p.Tyr26His
- gnomAD rs1305084717
- Missense
- Variant Prioritization Score for Impact Estimate 0.36
- CADD 15.70
- PolyPhen-2 0.85
- SIFT 0.79
- Most common in the 1KG:MSL population (allele frequency 0.013)
- Structural context available