S46G (p.Ser46Gly) variant of SLC18A2 (Q05940)
S46G (p.Ser46Gly) in SLC18A2 (Q05940) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.64 / 1. The record also includes population frequency data and structural context.
S46G (p.Ser46Gly) variant details
- p.Ser46Gly
- ExAC rs776837489
- gnomAD rs776837489
- Missense
- Variant Prioritization Score for Impact Estimate 0.636
- CADD 25.90
- PolyPhen-2 0.40
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available