G28G (p.Gly28Gly) variant of CPT2 (P23786)
G28G (p.Gly28Gly) in CPT2 (P23786) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data, published literature, and structural context.
G28G (p.Gly28Gly) variant details
- p.Gly28Gly
- rs772541454
- gnomAD 1-53197027-C-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.272
- CADD 13.90
- Most common in the Finnish in Finland (FIN) population (allele frequency 2.7e-05)
- Structural context available
- Literature evidence available