R36W (p.Arg36Trp) variant of SLC47A1 (Q96FL8)
R36W (p.Arg36Trp) in SLC47A1 (Q96FL8) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data and structural context.
R36W (p.Arg36Trp) variant details
- p.Arg36Trp
- 1000Genomes rs557911875
- ExAC rs557911875
- gnomAD rs557911875
- Missense
- Variant Prioritization Score for Impact Estimate 0.119
- REVEL 0.07
- CADD 16.20
- PolyPhen-2 0.00
- SIFT 0.24
- Most common in the 1KG:PJL population (allele frequency 0.0052)
- Structural context available