H38Q (p.His38Gln) variant of APOC3 (Apolipoprotein C-III)
H38Q (p.His38Gln) in APOC3 (Apolipoprotein C-III) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes variant effect predictions and structural context.
H38Q (p.His38Gln) variant details
- p.His38Gln
- ESP rs369731620
- ExAC rs369731620
- TOPMed rs369731620
- gnomAD rs369731620
- Likely benign
- Missense
- MetaLR 0.23
- MetaSVM -0.94
- SIFT 1.00
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available