L119V (p.Leu119Val) variant of SLC22A2 (O15244)
L119V (p.Leu119Val) in SLC22A2 (O15244) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data and structural context.
L119V (p.Leu119Val) variant details
- p.Leu119Val
- gnomAD rs1783312038
- Missense
- Variant Prioritization Score for Impact Estimate 0.279
- REVEL 0.20
- CADD 15.30
- PolyPhen-2 0.39
- SIFT 0.06
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available