T37R (p.Thr37Arg) variant of SRD5A2 (P31213)
T37R (p.Thr37Arg) 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 0.07 / 1. The record also includes population frequency data and structural context.
T37R (p.Thr37Arg) variant details
- p.Thr37Arg
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.0686
- CADD 0.18
- PolyPhen-2 0.21
- SIFT 0.56
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available