P26T (p.Pro26Thr) variant of APOC2 (Apolipoprotein C-II)
P26T (p.Pro26Thr) in APOC2 (Apolipoprotein C-II) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data and structural context.
P26T (p.Pro26Thr) variant details
- p.Pro26Thr
- cosmic curated COSV52990
- TOPMed rs1475130497
- gnomAD rs1475130497
- Missense
- Variant Prioritization Score for Impact Estimate 0.0954
- REVEL 0.12
- CADD 0.20
- PolyPhen-2 0.05
- SIFT 0.45
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available