V39G (p.Val39Gly) variant of XRCC2 (DNA repair protein XRCC2)
V39G (p.Val39Gly) in XRCC2 (DNA repair protein XRCC2) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data, published literature, and structural context.
V39G (p.Val39Gly) variant details
- p.Val39Gly
- gnomAD 7-152660706-A-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.258
- REVEL 0.10
- MetaLR 0.12
- MetaSVM -1.05
- CADD 22.40
- PolyPhen-2 0.01
- SIFT 0.40
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available