V36F (p.Val36Phe) variant of CDC42 (P60953)
V36F (p.Val36Phe) in CDC42 (P60953) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.84 / 1. The record also includes population frequency data and structural context.
V36F (p.Val36Phe) variant details
- p.Val36Phe
- gnomAD rs1216194784
- Missense
- Variant Prioritization Score for Impact Estimate 0.838
- CADD 33.00
- PolyPhen-2 0.98
- SIFT 0.00
- Most common in the African/African-American population (allele frequency 0.00012)
- Structural context available