Y25H (p.Tyr25His) variant of SLC37A4 (O43826)
Y25H (p.Tyr25His) in SLC37A4 (O43826) 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 and structural context.
Y25H (p.Tyr25His) variant details
- p.Tyr25His
- ExAC rs782031415
- gnomAD rs782031415
- Missense
- Variant Prioritization Score for Impact Estimate 0.62
- CADD 23.20
- PolyPhen-2 1.00
- SIFT 0.22
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available