List of variants in gene LAMC3 reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 43

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HGVS	dbSNP	gnomAD frequency
NM_006059.4(LAMC3):c.219T>G (p.His73Gln)	rs3739512	0.56936
NM_006059.4(LAMC3):c.1932C>T (p.Ser644=)	rs12349966	0.48282
NM_006059.4(LAMC3):c.963C>T (p.Ala321=)	rs2275131	0.40359
NM_006059.4(LAMC3):c.4378-4A>G	rs4740413	0.38051
NM_006059.4(LAMC3):c.3114C>G (p.Leu1038=)	rs10901345	0.33677
NM_006059.4(LAMC3):c.3108G>A (p.Gly1036=)	rs10901344	0.33663
NM_006059.4(LAMC3):c.521C>A (p.Pro174His)	rs2275137	0.29468
NM_006059.4(LAMC3):c.4298C>T (p.Thr1433Met)	rs7024108	0.28739
NM_006059.4(LAMC3):c.1564C>T (p.Pro522Ser)	rs869457	0.28273
NM_006059.4(LAMC3):c.4231-10C>T	rs4740411	0.20977
NM_006059.4(LAMC3):c.4376G>A (p.Arg1459Gln)	rs4740412	0.20674
NM_006059.4(LAMC3):c.1218G>A (p.Thr406=)	rs2293518	0.20549
NM_006059.4(LAMC3):c.3507C>T (p.Thr1169=)	rs3818800	0.14515
NM_006059.4(LAMC3):c.75C>T (p.Cys25=)	rs13286358	0.10217
NM_006059.4(LAMC3):c.1047C>T (p.Gly349=)	rs45603838	0.06722
NM_006059.4(LAMC3):c.3790C>T (p.Arg1264Trp)	rs11244275	0.04427
NM_006059.4(LAMC3):c.92G>T (p.Arg31Leu)	rs116259120	0.02047
NM_006059.4(LAMC3):c.2559C>T (p.Ser853=)	rs34652877	0.01902
NM_006059.4(LAMC3):c.4561T>G (p.Ser1521Ala)	rs117361076	0.01275
NM_006059.4(LAMC3):c.454C>T (p.Arg152Cys)	rs45628035	0.00975
NM_006059.4(LAMC3):c.3371C>T (p.Ser1124Phe)	rs113259170	0.00738
NM_006059.4(LAMC3):c.2352G>A (p.Arg784=)	rs35654564	0.00652
NM_006059.4(LAMC3):c.786G>A (p.Val262=)	rs2275133	0.00543
NM_006059.4(LAMC3):c.517C>T (p.Arg173Trp)	rs145775274	0.00378
NM_006059.4(LAMC3):c.4092C>T (p.Ser1364=)	rs141724499	0.00360
NM_006059.4(LAMC3):c.2891-8C>T	rs199535979	0.00339
NM_006059.4(LAMC3):c.3069+22C>T	rs117621658	0.00303
NM_006059.4(LAMC3):c.2517G>A (p.Thr839=)	rs140540789	0.00292
NM_006059.4(LAMC3):c.368G>T (p.Arg123Leu)	rs140461419	0.00284
NM_006059.4(LAMC3):c.558C>T (p.Arg186=)	rs2275135	0.00105
NM_006059.4(LAMC3):c.4338G>A (p.Ala1446=)	rs375730811	0.00041
NM_006059.4(LAMC3):c.944G>A (p.Arg315Gln)	rs45444592	0.00012
NM_006059.4(LAMC3):c.3765C>G (p.Ser1255=)	rs148370295	0.00011
NM_006059.4(LAMC3):c.1884C>T (p.Leu628=)	rs762552193	0.00009
NM_006059.4(LAMC3):c.4614G>A (p.Gln1538=)	rs754251028	0.00003
NM_006059.4(LAMC3):c.2308C>G (p.Arg770Gly)	rs3739510
NM_006059.4(LAMC3):c.3250G>C (p.Glu1084Gln)	rs146221263
NM_006059.4(LAMC3):c.3379G>A (p.Glu1127Lys)	rs140955110
NM_006059.4(LAMC3):c.4146G>C (p.Arg1382Ser)	rs147092908
NM_006059.4(LAMC3):c.4271G>A (p.Arg1424His)	rs34724991
NM_006059.4(LAMC3):c.521_522delinsAG (p.Pro174Gln)	rs386738954
NM_006059.4(LAMC3):c.522C>G (p.Pro174=)	rs2275136
NM_006059.4(LAMC3):c.855A>G (p.Ala285=)	rs2275132

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