C36W (p.Cys36Trp) variant of SLC22A1 (O15245)
C36W (p.Cys36Trp) in SLC22A1 (O15245) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
C36W (p.Cys36Trp) variant details
- p.Cys36Trp
- TOPMed rs1415661322
- gnomAD rs1415661322
- Missense
- Variant Prioritization Score for Impact Estimate 0.227
- REVEL 0.28
- CADD 10.50
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available