M67V (p.Met67Val) variant of CETP (P11597)
M67V (p.Met67Val) in CETP (P11597) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.03 / 1. The record also includes population frequency data and structural context.
M67V (p.Met67Val) variant details
- p.Met67Val
- gnomAD rs1243908679
- Missense
- Variant Prioritization Score for Impact Estimate 0.0289
- REVEL 0.00
- CADD 0.12
- PolyPhen-2 0.00
- SIFT 0.55
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available