A137V (p.Ala137Val) variant of XRCC3 (DNA repair protein XRCC3)
A137V (p.Ala137Val) in XRCC3 (DNA repair protein XRCC3) 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 0.46 / 1. The record also includes population frequency data and structural context.
A137V (p.Ala137Val) variant details
- p.Ala137Val
- NCI-TCGA TCGA novel
- Ensembl rs2151931570
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.462
- REVEL 0.28
- CADD 22.40
- PolyPhen-2 0.08
- SIFT 0.08
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available