S22R (p.Ser22Arg) variant of CPT2 (P23786)
S22R (p.Ser22Arg) in CPT2 (P23786) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
S22R (p.Ser22Arg) variant details
- p.Ser22Arg
- Ensembl rs1645327051
- Missense
- Variant Prioritization Score for Impact Estimate 0.176
- REVEL 0.17
- AlphaMissense 0.10
- MetaLR 0.27
- MetaSVM -0.80
- CADD 0.70
- PolyPhen-2 0.00
- Most common in the East Asian population (allele frequency 0.00019)
- Structural context available