S29S (p.Ser29Ser) variant of CPT2 (P23786)
S29S (p.Ser29Ser) in CPT2 (P23786) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data, published literature, and structural context.
S29S (p.Ser29Ser) variant details
- p.Ser29Ser
- gnomAD 1-53197030-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.173
- CADD 13.10
- Most common in the Non-Finnish European population (allele frequency 1.9e-06)
- Structural context available
- Literature evidence available