V91G (p.Val91Gly) variant of ETFB (P38117)
V91G (p.Val91Gly) in ETFB (P38117) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.73 / 1. The record also includes population frequency data and structural context.
V91G (p.Val91Gly) variant details
- p.Val91Gly
- Ensembl rs1599842088
- Missense
- Variant Prioritization Score for Impact Estimate 0.729
- REVEL 0.80
- CADD 26.10
- PolyPhen-2 0.97
- SIFT 0.05
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available