A31V (p.Ala31Val) variant of SLC22A1 (O15245)
A31V (p.Ala31Val) in SLC22A1 (O15245) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data and structural context.
A31V (p.Ala31Val) variant details
- p.Ala31Val
- TOPMed rs1228388059
- gnomAD rs1228388059
- Missense
- Variant Prioritization Score for Impact Estimate 0.135
- REVEL 0.10
- CADD 4.74
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available