V37M (p.Val37Met) variant of SLC22A1 (O15245)
V37M (p.Val37Met) in SLC22A1 (O15245) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.45 / 1. The record also includes population frequency data and structural context.
V37M (p.Val37Met) variant details
- p.Val37Met
- ExAC rs761516344
- gnomAD rs761516344
- Missense
- Variant Prioritization Score for Impact Estimate 0.455
- REVEL 0.45
- CADD 18.80
- PolyPhen-2 0.31
- SIFT 0.01
- Most common in the South Asian population (allele frequency 3.5e-05)
- Structural context available