P58S (p.Pro58Ser) variant of CETP (P11597)
P58S (p.Pro58Ser) in CETP (P11597) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data, published literature, and structural context.
P58S (p.Pro58Ser) variant details
- p.Pro58Ser
- gnomAD 16-56963063-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.325
- REVEL 0.33
- CADD 19.80
- PolyPhen-2 1.00
- SIFT 0.06
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available
- Literature evidence available