S22S (p.Ser22Ser) variant of CPT2 (P23786)
S22S (p.Ser22Ser) in CPT2 (P23786) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data, published literature, and structural context.
S22S (p.Ser22Ser) variant details
- p.Ser22Ser
- rs2100254831
- gnomAD 1-53197009-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.208
- CADD 11.70
- Most common in the Non-Finnish European population (allele frequency 9.3e-07)
- Structural context available
- Literature evidence available