R69W (p.Arg69Trp) variant of SLC22A6 (Q4U2R8)
R69W (p.Arg69Trp) in SLC22A6 (Q4U2R8) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data and structural context.
R69W (p.Arg69Trp) variant details
- p.Arg69Trp
- cosmic curated COSV64561
- 1000Genomes rs147795711
- ESP rs147795711
- ExAC rs147795711
- Missense
- Variant Prioritization Score for Impact Estimate 0.224
- REVEL 0.06
- MetaLR 0.14
- MetaSVM -0.81
- CADD 22.80
- PolyPhen-2 0.00
- SIFT 0.21
- Population evidence available
- Structural context available