V62G (p.Val62Gly) variant of SLC34A3 (Q8N130)
V62G (p.Val62Gly) in SLC34A3 (Q8N130) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data, published literature, and structural context.
V62G (p.Val62Gly) variant details
- p.Val62Gly
- gnomAD 9-137232584-T-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.11
- MetaLR 0.04
- MetaSVM -1.00
- CADD 0.61
- PolyPhen-2 0.01
- SIFT 0.16
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available