N39H (p.Asn39His) variant of CDC42 (P60953)
N39H (p.Asn39His) in CDC42 (P60953) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data, published literature, and structural context.
N39H (p.Asn39His) variant details
- p.Asn39His
- gnomAD 1-22078753-A-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.342
- CADD 19.60
- Most common in the HGDP:YAKUT population (allele frequency 0.04)
- Structural context available
- Literature evidence available