"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "LAMA4"[ - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1598317	NM_001105206.3(LAMA4):c.5469C>T (p.Ala1823=)	LAMA4	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1JJ	GLikely benign
Select item 1154809	NM_001105206.3(LAMA4):c.5460T>C (p.Cys1820=)	LAMA4	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1JJ	GLikely benign
Select item 406142	NM_001105206.3(LAMA4):c.5458T>C (p.Cys1820Arg)	LAMA4 (C1813R +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ +1 more	GUncertain significance
Select item 178045	NM_001105206.3(LAMA4):c.5450T>C (p.Ile1817Thr)	LAMA4 (I1810T +1 more)	Single nucleotide variant (missense variant)	not provided +4 more	GBenign/Likely benign
Select item 2738897	NM_001105206.3(LAMA4):c.5443_5444dup (p.Val1815_Ser1816insTer)	LAMA4	Duplication (frameshift variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 213603	NM_001105206.3(LAMA4):c.5444dup (p.Ser1816fs)	LAMA4 (S1816fs +1 more)	Duplication (frameshift variant)	Dilated cardiomyopathy 1JJ +2 more	GConflicting classifications of pathogenicity
Select item 44408	NM_001105206.3(LAMA4):c.5443G>A (p.Val1815Ile)	LAMA4 (V1808I +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GBenign/Likely benign
Select item 178047	NM_001105206.3(LAMA4):c.5442C>T (p.Ala1814=)	LAMA4	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1JJ +2 more	GLikely benign
Select item 999603	NM_001105206.3(LAMA4):c.5440G>T (p.Ala1814Ser)	LAMA4 (A1807S +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 848167	NM_001105206.3(LAMA4):c.5440G>A (p.Ala1814Thr)	LAMA4 (A1807T +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1058525	NM_001105206.3(LAMA4):c.5439C>T (p.Gly1813=)	LAMA4	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 191678	NM_001105206.3(LAMA4):c.5437G>A (p.Gly1813Ser)	LAMA4 (G1806S +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ +2 more	GUncertain significance
Select item 2844181	NM_001105206.3(LAMA4):c.5419A>G (p.Lys1807Glu)	LAMA4 (K1800E +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 1562958	NM_001105206.3(LAMA4):c.5412C>T (p.Ser1804=)	LAMA4	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1JJ +1 more	GLikely benign
Select item 264038	NM_001105206.3(LAMA4):c.5405C>A (p.Pro1802Gln)	LAMA4 (P1795Q +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 387049	NM_001105206.3(LAMA4):c.5400A>G (p.Gly1800=)	LAMA4	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1JJ +2 more	GLikely benign
Select item 1506476	NM_001105206.3(LAMA4):c.5398G>A (p.Gly1800Arg)	LAMA4 (G1800R +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 1358760	NM_001105206.3(LAMA4):c.5393T>G (p.Ile1798Ser)	LAMA4 (I1798S +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 518608	NM_001105206.3(LAMA4):c.5393T>C (p.Ile1798Thr)	LAMA4 (I1791T +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 845361	NM_001105206.3(LAMA4):c.5384A>C (p.His1795Pro)	LAMA4 (H1795P +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 851295	NM_001105206.3(LAMA4):c.5383C>T (p.His1795Tyr)	LAMA4 (H1788Y +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1665193	NM_001105206.3(LAMA4):c.5382C>A (p.Arg1794=)	LAMA4	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1JJ	GLikely benign
Select item 505573	NM_001105206.3(LAMA4):c.5380C>T (p.Arg1794Cys)	LAMA4 (R1787C +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 541231	NM_001105206.3(LAMA4):c.5364C>A (p.Pro1788=)	LAMA4	Single nucleotide variant (synonymous variant)	not specified +2 more	GLikely benign
Select item 2787247	NM_001105206.3(LAMA4):c.5339_5359del (p.Thr1780_Ser1786del)	LAMA4	Deletion (inframe_deletion)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 2098557	NM_001105206.3(LAMA4):c.5327-8_5347del	LAMA4	Deletion (splice acceptor variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 453104	NM_001105206.3(LAMA4):c.5345G>A (p.Arg1782His)	LAMA4 (R1775H +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 178049	NM_001105206.3(LAMA4):c.5344C>T (p.Arg1782Cys)	LAMA4 (R1775C +1 more)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 213578	NM_001105206.3(LAMA4):c.5340A>G (p.Thr1780=)	LAMA4	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1JJ +2 more	GBenign/Likely benign
Select item 793083	NM_001105206.3(LAMA4):c.5335C>T (p.Leu1779=)	LAMA4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2845553	NM_001105206.3(LAMA4):c.5327-3C>T	LAMA4	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 1907609	NM_001105206.3(LAMA4):c.5327-9T>A	LAMA4	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1JJ	GLikely benign
Select item 2843384	NM_001105206.3(LAMA4):c.5327-16T>C	LAMA4	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1JJ	GLikely benign
Select item 44405	NM_001105206.3(LAMA4):c.5326+15A>C	LAMA4	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 44406	NM_001105206.3(LAMA4):c.5326+6T>G	LAMA4	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1JJ +1 more	GBenign
Select item 793349	NM_001105206.3(LAMA4):c.5298G>A (p.Arg1766=)	LAMA4	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1JJ	GLikely benign
Select item 1014034	NM_001105206.3(LAMA4):c.5288T>C (p.Ile1763Thr)	LAMA4 (I1756T +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 44404	NM_001105206.3(LAMA4):c.5270C>T (p.Pro1757Leu)	LAMA4 (P1750L +1 more)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 691712	NM_001105206.3(LAMA4):c.5269C>T (p.Pro1757Ser)	LAMA4 (P1757S +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ +1 more	GUncertain significance
Select item 517367	NM_001105206.3(LAMA4):c.5267G>A (p.Gly1756Glu)	LAMA4 (G1749E +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 1977558	NM_001105206.3(LAMA4):c.5259T>C (p.His1753=)	LAMA4	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 643208	NM_001105206.3(LAMA4):c.5254A>G (p.Asn1752Asp)	LAMA4 (N1745D +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ +1 more	GUncertain significance
Select item 504530	NM_001105206.3(LAMA4):c.5241G>A (p.Val1747=)	LAMA4	Single nucleotide variant (synonymous variant)	not specified +2 more	GLikely benign
Select item 406146	NM_001105206.3(LAMA4):c.5237A>G (p.Asp1746Gly)	LAMA4 (D1739G +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 2996188	NM_001105206.3(LAMA4):c.5233T>C (p.Leu1745=)	LAMA4	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1JJ	GLikely benign
Select item 1717285	NM_001105206.3(LAMA4):c.5232G>T (p.Gln1744His)	LAMA4 (Q1737H +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 2866776	NM_001105206.3(LAMA4):c.5224G>A (p.Val1742Met)	LAMA4 (V1735M +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 2877301	NM_001105206.3(LAMA4):c.5214A>C (p.Arg1738Ser)	LAMA4 (R1738S +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 756215	NM_001105206.3(LAMA4):c.5211T>C (p.Ile1737=)	LAMA4	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1JJ	GLikely benign
Select item 2696723	NM_001105206.3(LAMA4):c.5207-8C>A	LAMA4	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1JJ	GLikely benign
Select item 1611147	NM_001105206.3(LAMA4):c.5207-13C>A	LAMA4	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1JJ	GLikely benign
Select item 213577	NM_001105206.3(LAMA4):c.5207-14G>C	LAMA4	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1JJ +1 more	GBenign/Likely benign
Select item 1641081	NM_001105206.3(LAMA4):c.5207-16_5207-15del	LAMA4	Deletion (intron variant)	Dilated cardiomyopathy 1JJ	GLikely benign
Select item 2129031	NM_001105206.3(LAMA4):c.5206+16G>T	LAMA4	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1JJ	GLikely benign
Select item 635222	NM_001105206.3(LAMA4):c.5206+1G>A	LAMA4	Single nucleotide variant (splice donor variant)	not provided +2 more	GUncertain significance
Select item 1410735	NM_001105206.3(LAMA4):c.5194C>T (p.His1732Tyr)	LAMA4 (H1732Y +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ +1 more	GUncertain significance
Select item 1063059	NM_001105206.3(LAMA4):c.5186G>A (p.Gly1729Asp)	LAMA4 (G1722D +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ +1 more	GUncertain significance
Select item 541228	NM_001105206.3(LAMA4):c.5184T>C (p.Asp1728=)	LAMA4	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1JJ	GLikely benign
Select item 1700735	NM_001105206.3(LAMA4):c.5172G>T (p.Gln1724His)	LAMA4 (Q1717H +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2893752	NM_001105206.3(LAMA4):c.5162C>T (p.Thr1721Ile)	LAMA4 (T1721I +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 44401	NM_001105206.3(LAMA4):c.5160T>A (p.Val1720=)	LAMA4	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1JJ +1 more	GBenign
Select item 2094517	NM_001105206.3(LAMA4):c.5155T>C (p.Ser1719Pro)	LAMA4 (S1712P +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 2188740	NM_001105206.3(LAMA4):c.5139C>T (p.Ile1713=)	LAMA4	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1JJ	GLikely benign
Select item 1101391	NM_001105206.3(LAMA4):c.5133T>C (p.Asn1711=)	LAMA4	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 581348	NM_001105206.3(LAMA4):c.5129A>G (p.Asn1710Ser)	LAMA4 (N1703S +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 1421699	NM_001105206.3(LAMA4):c.5126T>C (p.Val1709Ala)	LAMA4 (V1709A +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2061585	NM_001105206.3(LAMA4):c.5117T>C (p.Ile1706Thr)	LAMA4 (I1699T +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1997859	NM_001105206.3(LAMA4):c.5115C>T (p.Val1705=)	LAMA4	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1JJ	GLikely benign
Select item 1004787	NM_001105206.3(LAMA4):c.5113-2A>G	LAMA4	Single nucleotide variant (splice acceptor variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 1642477	NM_001105206.3(LAMA4):c.5113-15T>C	LAMA4	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1JJ	GLikely benign
Select item 1528730	NM_001105206.3(LAMA4):c.5112+15A>G	LAMA4	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1JJ	GLikely benign
Select item 1586941	NM_001105206.3(LAMA4):c.5112+11A>C	LAMA4	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1JJ	GLikely benign
Select item 1035567	NM_001105206.3(LAMA4):c.5093T>C (p.Val1698Ala)	LAMA4 (V1691A +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 2042513	NM_001105206.3(LAMA4):c.5075A>G (p.Asn1692Ser)	LAMA4 (N1685S +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 2184809	NM_001105206.3(LAMA4):c.5066A>T (p.His1689Leu)	LAMA4 (H1682L +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ +1 more	GUncertain significance
Select item 1429627	NM_001105206.3(LAMA4):c.5062G>A (p.Gly1688Ser)	LAMA4 (G1681S +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 2072622	NM_001105206.3(LAMA4):c.5061C>T (p.His1687=)	LAMA4	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +1 more	GLikely benign
Select item 1535858	NM_001105206.3(LAMA4):c.5058C>T (p.Val1686=)	LAMA4	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1JJ	GLikely benign
Select item 1016500	NM_001105206.3(LAMA4):c.5047G>A (p.Gly1683Arg)	LAMA4 (G1676R +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 509053	NM_001105206.3(LAMA4):c.5046C>T (p.Ser1682=)	LAMA4	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GLikely benign
Select item 1969806	NM_001105206.3(LAMA4):c.5038A>G (p.Ser1680Gly)	LAMA4 (S1673G +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 518848	NM_001105206.3(LAMA4):c.5035A>G (p.Arg1679Gly)	LAMA4 (R1672G +1 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 213609	NM_001105206.3(LAMA4):c.5030G>A (p.Arg1677His)	LAMA4 (R1670H +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 706858	NM_001105206.3(LAMA4):c.5029C>T (p.Arg1677Cys)	LAMA4 (R1677C +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ	GLikely benign
Select item 2421923	NM_001105206.3(LAMA4):c.5027T>G (p.Val1676Gly)	LAMA4 (V1669G +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 518525	NM_001105206.3(LAMA4):c.5021T>G (p.Phe1674Cys)	LAMA4 (F1667C +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ +1 more	GUncertain significance
Select item 44400	NM_001105206.3(LAMA4):c.5016T>A (p.Ile1672=)	LAMA4	Single nucleotide variant (synonymous variant)	Cardiomyopathy +2 more	GBenign/Likely benign
Select item 1417800	NM_001105206.3(LAMA4):c.5015T>C (p.Ile1672Thr)	LAMA4 (I1672T +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 213608	NM_001105206.3(LAMA4):c.5005A>G (p.Lys1669Glu)	LAMA4 (K1662E +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1329452	NM_001105206.3(LAMA4):c.5004G>A (p.Leu1668=)	LAMA4	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1JJ +2 more	GLikely benign
Select item 1744537	NM_001105206.3(LAMA4):c.5002T>G (p.Leu1668Val)	LAMA4 (L1661V +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ +1 more	GUncertain significance
Select item 227481	NM_001105206.3(LAMA4):c.5002T>C (p.Leu1668=)	LAMA4	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GLikely benign
Select item 1020761	NM_001105206.3(LAMA4):c.4992C>G (p.Phe1664Leu)	LAMA4 (F1657L +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 1910924	NM_001105206.3(LAMA4):c.4988C>T (p.Ser1663Phe)	LAMA4 (S1663F +1 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 180112	NM_001105206.3(LAMA4):c.4982-3del	LAMA4	Deletion (intron variant)	Dilated cardiomyopathy 1JJ +2 more	GUncertain significance
Select item 935968	NM_001105206.3(LAMA4):c.4982-6C>G	LAMA4	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1JJ	GUncertain significance
Select item 1594062	NM_001105206.3(LAMA4):c.4982-8C>T	LAMA4	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1JJ	GLikely benign
Select item 1087372	NM_001105206.3(LAMA4):c.4982-9T>C	LAMA4	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1JJ	GLikely benign
Select item 1595882	NM_001105206.3(LAMA4):c.4982-15T>C	LAMA4	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1JJ	GLikely benign
Select item 2719105	NM_001105206.3(LAMA4):c.4981+19A>G	LAMA4	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1JJ	GLikely benign

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