F96L (p.Phe96Leu) variant of SRD5A2 (P31213)
F96L (p.Phe96Leu) in SRD5A2 (P31213) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data and structural context.
F96L (p.Phe96Leu) variant details
- p.Phe96Leu
- 1000Genomes rs562449429
- ExAC rs562449429
- TOPMed rs562449429
- gnomAD rs562449429
- Missense
- Variant Prioritization Score for Impact Estimate 0.261
- CADD 16.40
- PolyPhen-2 0.52
- SIFT 0.19
- Most common in the Non-Finnish European population (allele frequency 8.8e-05)
- Structural context available