R16H (p.Arg16His) variant of SLC18A2 (Q05940)
R16H (p.Arg16His) in SLC18A2 (Q05940) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.56 / 1. The record also includes population frequency data and structural context.
R16H (p.Arg16His) variant details
- p.Arg16His
- TOPMed rs925216254
- gnomAD rs925216254
- Missense
- Variant Prioritization Score for Impact Estimate 0.564
- CADD 25.20
- PolyPhen-2 0.02
- SIFT 0.04
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available