List of variants in gene APOB reported by Mendelics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000384.3(APOB):c.3383G>A (p.Arg1128His)	rs12713843	0.00356
NM_000384.3(APOB):c.10579C>T (p.Arg3527Trp)	rs144467873	0.00006
NM_000384.3(APOB):c.10679A>G (p.Tyr3560Cys)	rs745721296	0.00001
NM_000384.3(APOB):c.11683A>C (p.Asn3895His)	rs2103350346
NM_000384.3(APOB):c.13392_13393del (p.Lys4465fs)	rs2103346437
NM_000384.3(APOB):c.13477CAG[1] (p.Gln4494del)	rs562574661
NM_000384.3(APOB):c.1468C>T (p.Arg490Trp)	rs771541567
NM_000384.3(APOB):c.1853C>T (p.Ala618Val)
NM_000384.3(APOB):c.2245G>T (p.Asp749Tyr)	rs1663700975
NM_000384.3(APOB):c.3491G>C (p.Arg1164Thr)
NM_000384.3(APOB):c.4651C>T (p.Gln1551Ter)
NM_000384.3(APOB):c.509_515del (p.Thr170fs)	rs1572802096
NM_000384.3(APOB):c.6640G>A (p.Glu2214Lys)	rs1239957664
NM_000384.3(APOB):c.8216C>T (p.Pro2739Leu)
NM_000384.3(APOB):c.9152_9155del (p.Asn3051fs)	rs1558562316
NM_000384.3(APOB):c.9835A>G (p.Ser3279Gly)

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