S15G (p.Ser15Gly) variant of SLC18A2 (Q05940)
S15G (p.Ser15Gly) in SLC18A2 (Q05940) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data, published literature, and structural context.
S15G (p.Ser15Gly) variant details
- p.Ser15Gly
- gnomAD 10-117241736-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.315
- CADD 22.50
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- Literature evidence available