R41G (p.Arg41Gly) variant of SLC30A8 (Q8IWU4)
R41G (p.Arg41Gly) in SLC30A8 (Q8IWU4) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data, published literature, and structural context.
R41G (p.Arg41Gly) variant details
- p.Arg41Gly
- gnomAD 8-117147003-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.161
- REVEL 0.04
- CADD 13.40
- PolyPhen-2 0.00
- SIFT 0.17
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available