P18P (p.Pro18Pro) variant of CPT2 (P23786)
P18P (p.Pro18Pro) in CPT2 (P23786) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data, published literature, and structural context.
P18P (p.Pro18Pro) variant details
- p.Pro18Pro
- gnomAD 1-53196997-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.133
- CADD 7.34
- Most common in the South Asian population (allele frequency 2.5e-05)
- Structural context available
- Literature evidence available