G11W (p.Gly11Trp) variant of ACADVL (P49748)
G11W (p.Gly11Trp) in ACADVL (P49748) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.65 / 1. The record also includes population frequency data, published literature, and structural context.
G11W (p.Gly11Trp) variant details
- p.Gly11Trp
- gnomAD 17-7217152-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.65
- CADD 23.90
- Population evidence available
- Structural context available
- Literature evidence available