D68N (p.Asp68Asn) variant of APOC2 (Apolipoprotein C-II)
D68N (p.Asp68Asn) in APOC2 (Apolipoprotein C-II) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data, published literature, and structural context.
D68N (p.Asp68Asn) variant details
- p.Asp68Asn
- gnomAD 19-44948847-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.443
- REVEL 0.35
- CADD 21.90
- PolyPhen-2 0.34
- SIFT 0.20
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available