A15V (p.Ala15Val) variant of CETP (P11597)
A15V (p.Ala15Val) in CETP (P11597) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely benign in the context of not specified. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes structural context.
A15V (p.Ala15Val) variant details
- p.Ala15Val
- rs34065661
- ClinGen CA395995695
- ClinVar RCV004153753
- Likely benign
- not specified
- Missense
- Variant Prioritization Score for Impact Estimate 0.212
- AlphaMissense 0.08
- MetaLR 0.00
- MetaSVM -1.01
- PolyPhen-2 0.08
- SIFT 0.03
- ClinVar: Likely benign (not specified)
- EBI: Likely benign (in dbSNP:rs34065661)
- UniProt: Likely benign (in dbSNP:rs34065661)
- Structural context available