List of variants in gene APOB reported as uncertain significance by Cardiovascular Research Group, Instituto Nacional de Saude Doutor Ricardo Jorge

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_000384.3(APOB):c.2706C>T (p.Asn902=)	rs1801700	0.03627
NM_000384.3(APOB):c.10701G>A (p.Thr3567=)	rs12713558	0.02176
NM_000384.3(APOB):c.1353-12C>T	rs76202659	0.01423
NM_000384.3(APOB):c.1352+60C>A	rs12714224	0.00793
NM_000384.3(APOB):c.10131G>A (p.Leu3377=)	rs1799812	0.00564
NM_000384.3(APOB):c.905-15C>G	rs72653061	0.00554
NM_000384.3(APOB):c.7696G>A (p.Glu2566Lys)	rs1801696	0.00305
NM_000384.3(APOB):c.905-16A>C	rs12720810	0.00172
NM_000384.3(APOB):c.1470+15T>C	rs185550846	0.00078
NM_000384.3(APOB):c.5599C>T (p.Arg1867Trp)	rs200583769	0.00024
NM_000384.3(APOB):c.1829A>G (p.Asp610Gly)	rs199646491	0.00003
NM_000384.3(APOB):c.7853T>C (p.Ile2618Thr)	rs531273434	0.00003
NM_000384.3(APOB):c.10519C>T (p.Arg3507Trp)	rs754264874	0.00002
NM_000384.3(APOB):c.5690G>A (p.Arg1897His)	rs199510126	0.00002
NM_000384.3(APOB):c.10679A>G (p.Tyr3560Cys)	rs745721296	0.00001
NM_000384.3(APOB):c.1280G>A (p.Arg427Gln)	rs755407886	0.00001
NM_000384.3(APOB):c.3425C>T (p.Ser1142Leu)	rs199859104	0.00001
NM_000384.3(APOB):c.403A>G (p.Ile135Val)	rs769296548	0.00001
NM_000384.3(APOB):c.10193C>T (p.Ala3398Val)	rs1367798781
NM_000384.3(APOB):c.10602C>A (p.Gly3534=)	rs886039828
NM_000384.3(APOB):c.10629C>G (p.Asn3543Lys)	rs1553382944
NM_000384.3(APOB):c.11401T>A (p.Ser3801Thr)
NM_000384.3(APOB):c.11477C>T (p.Thr3826Met)
NM_000384.3(APOB):c.12460G>A (p.Glu4154Lys)	rs767587977
NM_000384.3(APOB):c.13441G>A (p.Ala4481Thr)
NM_000384.3(APOB):c.13451C>T (p.Thr4484Met)
NM_000384.3(APOB):c.1580C>T (p.Ala527Val)	rs886039827
NM_000384.3(APOB):c.2188G>A (p.Val730Ile)
NM_000384.3(APOB):c.2981C>T (p.Pro994Leu)
NM_000384.3(APOB):c.3491G>C (p.Arg1164Thr)
NM_000384.3(APOB):c.538-8C>T	rs886039826
NM_000384.3(APOB):c.6636TGA[1] (p.Asp2213del)	rs541497967
NM_000384.3(APOB):c.9835A>G (p.Ser3279Gly)

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