A68G (p.Ala68Gly) variant of SLC30A8 (Q8IWU4)
A68G (p.Ala68Gly) in SLC30A8 (Q8IWU4) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data, published literature, and structural context.
A68G (p.Ala68Gly) variant details
- p.Ala68Gly
- gnomAD 8-117147085-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.0812
- REVEL 0.04
- MetaLR 0.09
- MetaSVM -1.06
- CADD 0.01
- PolyPhen-2 0.00
- SIFT 0.43
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available