A19T (p.Ala19Thr) variant of SRD5A2 (P31213)
A19T (p.Ala19Thr) 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 0.34 / 1. The record also includes population frequency data and structural context.
A19T (p.Ala19Thr) variant details
- p.Ala19Thr
- NCI-TCGA Cosmic COSV5187
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.343
- CADD 8.24
- PolyPhen-2 0.01
- SIFT 0.36
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available