P79S (p.Pro79Ser) variant of SRD5A2 (P31213)
P79S (p.Pro79Ser) in SRD5A2 (P31213) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.62 / 1. The record also includes population frequency data and structural context.
P79S (p.Pro79Ser) variant details
- p.Pro79Ser
- TOPMed rs1237144251
- gnomAD rs1237144251
- Missense
- Variant Prioritization Score for Impact Estimate 0.621
- CADD 21.10
- PolyPhen-2 0.23
- SIFT 0.76
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available