D38G (p.Asp38Gly) variant of NRAS (GTPase NRas)
D38G (p.Asp38Gly) in NRAS (GTPase NRas) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.82 / 1. The record also includes population frequency data, published literature, and structural context.
D38G (p.Asp38Gly) variant details
- p.Asp38Gly
- gnomAD 1-114713977-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.821
- REVEL 0.94
- CADD 33.00
- PolyPhen-2 0.88
- SIFT 0.00
- Population evidence available
- Structural context available
- Literature evidence available