ClinVar Miner

List of variants in gene APOB reported as likely benign by CeGaT Praxis fuer Humangenetik Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 36
Download table as spreadsheet
HGVS dbSNP
NM_000384.3(APOB):c.10131G>A (p.Leu3377=) rs1799812
NM_000384.3(APOB):c.10575C>T (p.Ser3525=) rs142573551
NM_000384.3(APOB):c.10740C>T (p.Asn3580=) rs150312765
NM_000384.3(APOB):c.10764C>A (p.Thr3588=) rs142252921
NM_000384.3(APOB):c.11354C>T (p.Thr3785Ile) rs143710616
NM_000384.3(APOB):c.11391A>G (p.Leu3797=) rs140002021
NM_000384.3(APOB):c.11442C>T (p.Thr3814=) rs72654408
NM_000384.3(APOB):c.12381C>T (p.Asp4127=) rs145704672
NM_000384.3(APOB):c.12382G>A (p.Val4128Met)
NM_000384.3(APOB):c.12794T>C (p.Val4265Ala) rs61743502
NM_000384.3(APOB):c.12940A>G (p.Ile4314Val)
NM_000384.3(APOB):c.13020T>C (p.Tyr4340=) rs141339310
NM_000384.3(APOB):c.13302C>T (p.Ser4434=) rs144040999
NM_000384.3(APOB):c.13368C>T (p.Thr4456=) rs1553382258
NM_000384.3(APOB):c.13452G>A (p.Thr4484=) rs200374122
NM_000384.3(APOB):c.2331C>G (p.Leu777=) rs759073099
NM_000384.3(APOB):c.2478T>C (p.Phe826=)
NM_000384.3(APOB):c.2853G>A (p.Glu951=) rs151193347
NM_000384.3(APOB):c.3178T>C (p.Leu1060=) rs72653073
NM_000384.3(APOB):c.3426G>A (p.Ser1142=) rs142448733
NM_000384.3(APOB):c.3471T>C (p.Tyr1157=) rs201128198
NM_000384.3(APOB):c.3774G>C (p.Leu1258=) rs752823240
NM_000384.3(APOB):c.4825T>C (p.Leu1609=) rs72653083
NM_000384.3(APOB):c.5028C>T (p.Gly1676=) rs201446451
NM_000384.3(APOB):c.6874A>C (p.Ile2292Leu) rs1553383634
NM_000384.3(APOB):c.6875T>C (p.Ile2292Thr) rs145977507
NM_000384.3(APOB):c.6927A>G (p.Arg2309=) rs201066460
NM_000384.3(APOB):c.741C>T (p.Tyr247=) rs753975855
NM_000384.3(APOB):c.751G>A (p.Ala251Thr) rs61741625
NM_000384.3(APOB):c.7696G>A (p.Glu2566Lys) rs1801696
NM_000384.3(APOB):c.7863A>C (p.Leu2621=) rs138497378
NM_000384.3(APOB):c.7998A>G (p.Val2666=) rs1042006
NM_000384.3(APOB):c.8148C>T (p.Ile2716=) rs6413458
NM_000384.3(APOB):c.8462C>T (p.Pro2821Leu) rs72653095
NM_000384.3(APOB):c.9105T>C (p.Asn3035=) rs147510760
NM_000384.3(APOB):c.9294C>T (p.Tyr3098=) rs145777339

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.