P14P (p.Pro14Pro) variant of CPT2 (P23786)
P14P (p.Pro14Pro) in CPT2 (P23786) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data, published literature, and structural context.
P14P (p.Pro14Pro) variant details
- p.Pro14Pro
- rs570576290
- gnomAD 1-53196985-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.119
- CADD 5.43
- Most common in the 1KG:BEB population (allele frequency 0.0051)
- Structural context available
- Literature evidence available