V16V (p.Val16Val) variant of CPT2 (P23786)
V16V (p.Val16Val) in CPT2 (P23786) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data, published literature, and structural context.
V16V (p.Val16Val) variant details
- p.Val16Val
- gnomAD 1-53196991-T-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0988
- CADD 2.57
- Most common in the East Asian population (allele frequency 8.7e-05)
- Structural context available
- Literature evidence available