V26G (p.Val26Gly) variant of H6PD (O95479)
V26G (p.Val26Gly) in H6PD (O95479) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.53 / 1. The record also includes population frequency data and structural context.
V26G (p.Val26Gly) variant details
- p.Val26Gly
- gnomAD rs1369751665
- Missense
- Variant Prioritization Score for Impact Estimate 0.527
- REVEL 0.51
- MetaLR 0.32
- MetaSVM -0.40
- CADD 26.40
- PolyPhen-2 0.71
- SIFT 0.00
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)
- Structural context available