D38H (p.Asp38His) variant of HRAS (GTPase HRas)
D38H (p.Asp38His) in HRAS (GTPase HRas) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.75 / 1. The record also includes population frequency data and structural context.
D38H (p.Asp38His) variant details
- p.Asp38His
- ExAC rs750680771
- gnomAD rs750680771
- Missense
- Variant Prioritization Score for Impact Estimate 0.753
- REVEL 0.85
- AlphaMissense 1.00
- MetaLR 0.74
- MetaSVM 0.75
- CADD 32.00
- PolyPhen-2 1.00
- Most common in the Finnish in Finland (FIN) population (allele frequency 9.4e-05)
- Structural context available