P2L (p.Pro2Leu) variant of SLC22A1 (O15245)
P2L (p.Pro2Leu) in SLC22A1 (O15245) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data and structural context.
P2L (p.Pro2Leu) variant details
- p.Pro2Leu
- Ensembl rs1583318072
- Missense
- Variant Prioritization Score for Impact Estimate 0.156
- REVEL 0.10
- CADD 10.60
- PolyPhen-2 0.02
- SIFT 0.10
- Most common in the Non-Finnish European population (allele frequency 8.1e-06)
- Structural context available