"GeneDx"[submitter] AND "LAMC1"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 60076	GRCh38/hg38 1q25.2-32.1(chr1:179032905-199724897)x1	LOC129932021, LOC129932022 +478 more	Copy number loss	See cases	GPathogenic
Select item 1282385	NM_002293.4(LAMC1):c.-118A>G	LAMC1, LOC129932071	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 1179935	NM_002293.4(LAMC1):c.174C>T (p.Ala58=)	LAMC1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1268679	NM_002293.4(LAMC1):c.418+89G>T	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1225486	NM_002293.4(LAMC1):c.418+112C>G	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1259725	NM_002293.4(LAMC1):c.418+169T>C	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1229870	NM_002293.4(LAMC1):c.657C>T (p.Asn219=)	LAMC1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1276723	NM_002293.4(LAMC1):c.723+141T>C	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1266163	NM_002293.4(LAMC1):c.724-115_724-114insG	LAMC1	Insertion (intron variant)	not provided	GBenign
Select item 1252177	NM_002293.4(LAMC1):c.854+74C>T	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1294806	NM_002293.4(LAMC1):c.854+77C>T	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1178636	NM_002293.4(LAMC1):c.855-211C>T	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1250945	NM_002293.4(LAMC1):c.855-114C>T	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1259085	NM_002293.4(LAMC1):c.882G>A (p.Glu294=)	LAMC1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1290361	NM_002293.4(LAMC1):c.894C>T (p.Asn298=)	LAMC1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1294845	NM_002293.4(LAMC1):c.999G>A (p.Ala333=)	LAMC1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1263091	NM_002293.4(LAMC1):c.1021+64T>C	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1294847	NM_002293.4(LAMC1):c.1022-118T>C	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1294801	NM_002293.4(LAMC1):c.1211-48A>G	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1264795	NM_002293.4(LAMC1):c.1211-47C>A	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1291744	NM_002293.4(LAMC1):c.1211-12T>C	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1279625	NM_002293.4(LAMC1):c.1242C>A (p.Gly414=)	LAMC1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1237159	NM_002293.4(LAMC1):c.1329-144C>T	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1287150	NM_002293.4(LAMC1):c.1329-88dup	LAMC1	Duplication (intron variant)	not provided	GBenign
Select item 1244913	NM_002293.4(LAMC1):c.1329-89_1329-88dup	LAMC1	Duplication (intron variant)	not provided	GBenign
Select item 1228140	NM_002293.4(LAMC1):c.1329-16A>G	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1238059	NM_002293.4(LAMC1):c.1372A>G (p.Ile458Val)	LAMC1 (I458V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1241130	NM_002293.4(LAMC1):c.1564+152T>C	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1294803	NM_002293.4(LAMC1):c.1564+200G>A	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1242927	NM_002293.4(LAMC1):c.1776A>C (p.Ala592=)	LAMC1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1239319	NM_002293.4(LAMC1):c.1990+204A>T	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1178948	NM_002293.4(LAMC1):c.1990+234A>C	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1259633	NM_002293.4(LAMC1):c.1991-107A>G	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 781586	NM_002293.4(LAMC1):c.2191G>A (p.Glu731Lys)	LAMC1 (E731K)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1259023	NM_002293.4(LAMC1):c.2213-40T>C	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1180166	NM_002293.4(LAMC1):c.2213-17G>A	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276821	NM_002293.4(LAMC1):c.2401+13G>A	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1296709	NM_002293.4(LAMC1):c.2511T>C (p.Asn837=)	LAMC1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1250674	NM_002293.4(LAMC1):c.2647+180T>C	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1175537	NM_002293.4(LAMC1):c.2647+199T>C	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1230236	NM_002293.4(LAMC1):c.2648-218T>C	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1221045	NM_002293.4(LAMC1):c.2648-210C>T	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1290680	NM_002293.4(LAMC1):c.2663T>C (p.Leu888Pro)	LAMC1 (L888P)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1277005	NM_002293.4(LAMC1):c.2801+117G>A	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1253488	NM_002293.4(LAMC1):c.2802-231C>T	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1294800	NM_002293.4(LAMC1):c.2802-207G>A	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1266189	NM_002293.4(LAMC1):c.2802-57_2802-56del	LAMC1	Deletion (intron variant)	not provided	GBenign
Select item 1255244	NM_002293.4(LAMC1):c.2802-21A>G	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1248917	NM_002293.4(LAMC1):c.2944+80G>A	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1264386	NM_002293.4(LAMC1):c.2944+199T>C	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 432283	NM_002293.4(LAMC1):c.2984G>A (p.Cys995Tyr)	LAMC1 (C995Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1259613	NM_002293.4(LAMC1):c.3123+43T>C	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1238270	NM_002293.4(LAMC1):c.3123+95G>A	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1224912	NM_002293.4(LAMC1):c.3123+129C>T	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1288142	NM_002293.4(LAMC1):c.3123+155T>C	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276213	NM_002293.4(LAMC1):c.3124-109del	LAMC1	Deletion (intron variant)	not provided	GBenign
Select item 1238331	NM_002293.4(LAMC1):c.3124-111_3124-109del	LAMC1	Deletion (intron variant)	not provided	GBenign
Select item 1232275	NM_002293.4(LAMC1):c.3124-113_3124-109del	LAMC1	Deletion (intron variant)	not provided	GBenign
Select item 1294804	NM_002293.4(LAMC1):c.3124-120A>T	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1294841	NM_002293.4(LAMC1):c.3124-119_3124-118insTT	LAMC1	Insertion (intron variant)	not provided	GBenign
Select item 1226516	NM_002293.4(LAMC1):c.3280+116A>G	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1264130	NM_002293.4(LAMC1):c.3281-99T>C	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1258483	NM_002293.4(LAMC1):c.3362G>A (p.Arg1121Gln)	LAMC1 (R1121Q)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1232501	NM_002293.4(LAMC1):c.3486+17G>A	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1264046	NM_002293.4(LAMC1):c.3486+137G>A	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1280012	NM_002293.4(LAMC1):c.3487-113_3487-109dup	LAMC1	Duplication (intron variant)	not provided	GBenign
Select item 1274180	NM_002293.4(LAMC1):c.3487-110_3487-109dup	LAMC1	Duplication (intron variant)	not provided	GBenign
Select item 1257680	NM_002293.4(LAMC1):c.3487-111_3487-109dup	LAMC1	Duplication (intron variant)	not provided	GBenign
Select item 1236871	NM_002293.4(LAMC1):c.3487-112_3487-109dup	LAMC1	Duplication (intron variant)	not provided	GBenign
Select item 1274402	NM_002293.4(LAMC1):c.3566+42T>C	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1294844	NM_002293.4(LAMC1):c.3566+50_3566+51insTGTGTGTGTGT	LAMC1	Insertion (intron variant)	not provided	GBenign
Select item 1266601	NM_002293.4(LAMC1):c.3566+50_3566+51insTGTGTGT	LAMC1	Insertion (intron variant)	not provided	GBenign
Select item 1258146	NM_002293.4(LAMC1):c.3566+50_3566+51insTGTGT	LAMC1	Insertion (intron variant)	not provided	GBenign
Select item 1247997	NM_002293.4(LAMC1):c.3566+50_3566+51insTGTGTGTGT	LAMC1	Insertion (intron variant)	not provided	GBenign
Select item 1228591	NM_002293.4(LAMC1):c.3566+51GT[17]	LAMC1	Microsatellite (intron variant)	not provided	GBenign
Select item 1267165	NM_002293.4(LAMC1):c.3566+83A>G	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1262055	NM_002293.4(LAMC1):c.3566+85T>G	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1294805	NM_002293.4(LAMC1):c.3567-233C>T	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1290084	NM_002293.4(LAMC1):c.3567-107AAT[8]	LAMC1	Microsatellite (intron variant)	not provided	GBenign
Select item 1294799	NM_002293.4(LAMC1):c.3567-91A>C	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1264225	NM_002293.4(LAMC1):c.3567-84T>G	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1174305	NM_002293.4(LAMC1):c.3567-64G>A	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1265468	NM_002293.4(LAMC1):c.3614A>G (p.Asn1205Ser)	LAMC1 (N1205S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1294852	NM_002293.4(LAMC1):c.3657G>A (p.Leu1219=)	LAMC1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1233530	NM_002293.4(LAMC1):c.3704+14G>A	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1294836	NM_002293.4(LAMC1):c.3849+34C>T	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276530	NM_002293.4(LAMC1):c.3849+170T>C	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1225373	NM_002293.4(LAMC1):c.3850-191A>G	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1243926	NM_002293.4(LAMC1):c.3850-142T>A	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1271083	NM_002293.4(LAMC1):c.3999+69G>A	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1181624	NM_002293.4(LAMC1):c.4000-98C>G	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1272967	NM_002293.4(LAMC1):c.4114+60del	LAMC1	Deletion (intron variant)	not provided	GBenign
Select item 1257008	NM_002293.4(LAMC1):c.4114+236T>C	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1260310	NM_002293.4(LAMC1):c.4115-197C>T	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1245525	NM_002293.4(LAMC1):c.4115-122C>G	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1294819	NM_002293.4(LAMC1):c.4115-19G>A	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1259999	NM_002293.4(LAMC1):c.4299G>A (p.Ala1433=)	LAMC1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1277536	NM_002293.4(LAMC1):c.4314+50C>T	LAMC1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1235617	NM_002293.4(LAMC1):c.4314+146del	LAMC1	Deletion (intron variant)	not provided	GBenign
Select item 1250443	NM_002293.4(LAMC1):c.4315-181_4315-180insG	LAMC1	Insertion (intron variant)	not provided	GBenign

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