S46R (p.Ser46Arg) variant of SLC18A2 (Q05940)
S46R (p.Ser46Arg) in SLC18A2 (Q05940) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data and structural context.
S46R (p.Ser46Arg) variant details
- p.Ser46Arg
- TOPMed rs1002490601
- Missense
- Variant Prioritization Score for Impact Estimate 0.252
- CADD 23.60
- PolyPhen-2 0.82
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available