N39S (p.Asn39Ser) variant of CDC42 (P60953)
N39S (p.Asn39Ser) in CDC42 (P60953) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data, published literature, and structural context.
N39S (p.Asn39Ser) variant details
- p.Asn39Ser
- rs1384009146
- gnomAD 1-22078811-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.41
- CADD 12.50
- Most common in the 1KG:MSL population (allele frequency 0.013)
- Structural context available
- Literature evidence available