D13G (p.Asp13Gly) variant of RAD51C (O43502)
D13G (p.Asp13Gly) in RAD51C (O43502) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
D13G (p.Asp13Gly) variant details
- p.Asp13Gly
- ExAC rs777004225
- Missense
- Variant Prioritization Score for Impact Estimate 0.295
- REVEL 0.13
- CADD 25.60
- PolyPhen-2 0.01
- SIFT 0.04
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available