D38E (p.Asp38Glu) variant of NRAS (GTPase NRas)
D38E (p.Asp38Glu) in NRAS (GTPase NRas) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.55 / 1. The record also includes population frequency data and structural context.
D38E (p.Asp38Glu) variant details
- p.Asp38Glu
- Ensembl rs2101742190
- Missense
- Variant Prioritization Score for Impact Estimate 0.553
- REVEL 0.69
- CADD 24.40
- PolyPhen-2 0.99
- SIFT 0.01
- Most common in the Finnish in Finland (FIN) population (allele frequency 2.3e-05)
- Structural context available