V10G (p.Val10Gly) variant of SLC47A1 (Q96FL8)
V10G (p.Val10Gly) in SLC47A1 (Q96FL8) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.04 / 1. The record also includes population frequency data and structural context.
V10G (p.Val10Gly) variant details
- p.Val10Gly
- ExAC rs750264871
- TOPMed rs750264871
- gnomAD rs750264871
- Missense
- Variant Prioritization Score for Impact Estimate 0.0364
- REVEL 0.01
- CADD 1.33
- PolyPhen-2 0.00
- SIFT 0.60
- Most common in the Middle Eastern population (allele frequency 0.00023)
- Structural context available