V26A (p.Val26Ala) variant of SLC18A2 (Q05940)
V26A (p.Val26Ala) in SLC18A2 (Q05940) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.67 / 1. The record also includes population frequency data and structural context.
V26A (p.Val26Ala) variant details
- p.Val26Ala
- TOPMed rs1177069927
- gnomAD rs1177069927
- Missense
- Variant Prioritization Score for Impact Estimate 0.672
- CADD 31.00
- PolyPhen-2 0.99
- SIFT 0.00
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available