V94M (p.Val94Met) variant of SLC22A2 (O15244)
V94M (p.Val94Met) in SLC22A2 (O15244) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data and structural context.
V94M (p.Val94Met) variant details
- p.Val94Met
- TOPMed rs1273586077
- gnomAD rs1273586077
- Missense
- Variant Prioritization Score for Impact Estimate 0.457
- REVEL 0.32
- CADD 24.10
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available