ClinVar Miner

List of variants in gene APOB reported as likely pathogenic

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
Download table as spreadsheet
HGVS dbSNP
NM_000384.3(APOB):c.10182G>T (p.Lys3394Asn) rs1382988295
NM_000384.3(APOB):c.10186G>A (p.Ala3396Thr) rs1553383017
NM_000384.3(APOB):c.10187C>A (p.Ala3396Asp) rs730880052
NM_000384.3(APOB):c.10580G>A (p.Arg3527Gln) rs5742904
NM_000384.3(APOB):c.11477C>T (p.Thr3826Met) rs61744153
NM_000384.3(APOB):c.11789-1G>C rs1558560212
NM_000384.3(APOB):c.11812_11813del (p.Asp3938fs) rs1553382678
NM_000384.3(APOB):c.13025del (p.Pro4342fs) rs797045253
NM_000384.3(APOB):c.13477_13479CAG[1] (p.Gln4494del) rs562574661
NM_000384.3(APOB):c.2096C>T (p.Pro699Leu) rs776107514
NM_000384.3(APOB):c.3491G>C (p.Arg1164Thr) rs759845943
NM_000384.3(APOB):c.4471A>T (p.Arg1491Ter) rs1558565733
NM_000384.3(APOB):c.631C>T (p.Gln211Ter) rs143301836
NM_000384.3(APOB):c.7851del (p.Phe2617fs) rs1220363895
NM_000384.3(APOB):c.9175C>T (p.Arg3059Cys) rs146377316

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.