C62G (p.Cys62Gly) variant of SLC22A1 (O15245)
C62G (p.Cys62Gly) in SLC22A1 (O15245) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.60 / 1. The record also includes population frequency data and structural context.
C62G (p.Cys62Gly) variant details
- p.Cys62Gly
- ExAC rs765280158
- gnomAD rs765280158
- Missense
- Variant Prioritization Score for Impact Estimate 0.597
- REVEL 0.67
- CADD 26.30
- PolyPhen-2 1.00
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available