R69G (p.Arg69Gly) variant of SLC22A6 (Q4U2R8)
R69G (p.Arg69Gly) in SLC22A6 (Q4U2R8) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
R69G (p.Arg69Gly) variant details
- p.Arg69Gly
- 1000Genomes rs147795711
- ESP rs147795711
- ExAC rs147795711
- TOPMed rs147795711
- Missense
- Variant Prioritization Score for Impact Estimate 0.23
- REVEL 0.07
- MetaLR 0.14
- MetaSVM -0.86
- CADD 21.90
- PolyPhen-2 0.15
- SIFT 0.34
- Population evidence available
- Structural context available