V9G (p.Val9Gly) variant of RAC1 (P63000)
V9G (p.Val9Gly) in RAC1 (P63000) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.72 / 1. The record also includes population frequency data and structural context.
V9G (p.Val9Gly) variant details
- p.Val9Gly
- Ensembl rs2115177190
- Missense
- Variant Prioritization Score for Impact Estimate 0.723
- REVEL 0.80
- CADD 32.00
- PolyPhen-2 0.97
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 2.3e-06)
- Structural context available