A69T (p.Ala69Thr) variant of SRD5A2 (P31213)
A69T (p.Ala69Thr) in SRD5A2 (P31213) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data.
A69T (p.Ala69Thr) variant details
- p.Ala69Thr
- NCI-TCGA Cosmic COSV9925
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.468
- CADD 14.90
- PolyPhen-2 0.08
- SIFT 0.46
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available