Annotation Detail
Information
- Associated Genes
- APOB
- Associated Variants
-
APOB p.Ser1203Gly (p.S1203G)
(
ENST00000233242.5 )
APOB p.Ser1203Gly (p.S1203G) ( ENST00000233242.5 ) - Source Database
- ClinVar
- Description
- NM_000384.3(APOB):c.3607A>G (p.Ser1203Gly) AND Cardiovascular phenotype
- ClinVar Allele ID
- 616432
- ClinVar RefSeq Alternation Syntax
- NM_000384.3:c.3607A>G
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2023-11-03
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV004027236
- Observed Origin Sample
- germline
Drugs