Q13R (p.Gln13Arg) variant of SLC18A2 (Q05940)
Q13R (p.Gln13Arg) in SLC18A2 (Q05940) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
Q13R (p.Gln13Arg) variant details
- p.Gln13Arg
- ExAC rs769689830
- gnomAD rs769689830
- Missense
- Variant Prioritization Score for Impact Estimate 0.183
- CADD 14.10
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available