R41T (p.Arg41Thr) variant of SLC30A8 (Q8IWU4)
R41T (p.Arg41Thr) in SLC30A8 (Q8IWU4) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data and structural context.
R41T (p.Arg41Thr) variant details
- p.Arg41Thr
- gnomAD rs927398701
- Missense
- Variant Prioritization Score for Impact Estimate 0.0955
- REVEL 0.04
- CADD 9.91
- PolyPhen-2 0.01
- SIFT 0.29
- Most common in the HGDP:BOUGAINVILLE population (allele frequency 0.045)
- Structural context available