P86L (p.Pro86Leu) variant of SLC22A2 (O15244)
P86L (p.Pro86Leu) in SLC22A2 (O15244) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data and structural context.
P86L (p.Pro86Leu) variant details
- p.Pro86Leu
- gnomAD rs1783315829
- Missense
- Variant Prioritization Score for Impact Estimate 0.123
- REVEL 0.06
- CADD 7.30
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available