R16G (p.Arg16Gly) variant of SLC18A2 (Q05940)
R16G (p.Arg16Gly) in SLC18A2 (Q05940) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data, published literature, and structural context.
R16G (p.Arg16Gly) variant details
- p.Arg16Gly
- gnomAD 10-117241739-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.505
- CADD 27.00
- PolyPhen-2 0.51
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available