V41G (p.Val41Gly) variant of GABRA1 (P14867)
V41G (p.Val41Gly) in GABRA1 (P14867) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.62 / 1. The record also includes population frequency data, published literature, and structural context.
V41G (p.Val41Gly) variant details
- p.Val41Gly
- rs1411116374
- gnomAD 5-161850642-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.622
- CADD 20.60
- SIFT 0.05
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00017)
- Structural context available
- Literature evidence available