Q56K (p.Gln56Lys) variant of SRD5A2 (P31213)
Q56K (p.Gln56Lys) 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 0.76 / 1. The record also includes population frequency data and structural context.
Q56K (p.Gln56Lys) variant details
- p.Gln56Lys
- NCI-TCGA Cosmic COSV9925
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.757
- CADD 24.40
- PolyPhen-2 0.89
- SIFT 0.03
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available