S15N (p.Ser15Asn) variant of SLC18A2 (Q05940)
S15N (p.Ser15Asn) in SLC18A2 (Q05940) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.50 / 1. The record also includes population frequency data and structural context.
S15N (p.Ser15Asn) variant details
- p.Ser15Asn
- TOPMed rs1393107121
- gnomAD rs1393107121
- Missense
- Variant Prioritization Score for Impact Estimate 0.497
- CADD 22.50
- PolyPhen-2 0.04
- SIFT 0.18
- Most common in the African/African-American population (allele frequency 4.8e-05)
- Structural context available