L13F (p.Leu13Phe) variant of APOC2 (Apolipoprotein C-II)
L13F (p.Leu13Phe) in APOC2 (Apolipoprotein C-II) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
L13F (p.Leu13Phe) variant details
- p.Leu13Phe
- TOPMed rs1039763443
- gnomAD rs1039763443
- Missense
- Variant Prioritization Score for Impact Estimate 0.303
- REVEL 0.28
- CADD 23.20
- PolyPhen-2 0.81
- SIFT 0.12
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available