ClinVar Miner

List of variants in gene LAMA4 reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Gene type:
ClinVar version:
Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_001105206.3(LAMA4):c.5450T>C (p.Ile1817Thr) rs144482486 0.00228
NM_001105206.3(LAMA4):c.5207-14G>C rs112265545 0.00214
NM_001105206.3(LAMA4):c.196-9C>T rs144850734 0.00174
NM_001105206.3(LAMA4):c.4822-3C>T rs191447048 0.00151
NM_001105206.3(LAMA4):c.1633C>T (p.Arg545Cys) rs138153075 0.00135
NM_001105206.3(LAMA4):c.514G>A (p.Gly172Ser) rs147695488 0.00091
NM_001105206.3(LAMA4):c.2403G>A (p.Thr801=) rs142559688 0.00078
NM_001105206.3(LAMA4):c.4678C>A (p.Arg1560=) rs150069819 0.00078
NM_001105206.3(LAMA4):c.2950G>A (p.Val984Ile) rs145648026 0.00072
NM_001105206.3(LAMA4):c.674C>T (p.Ala225Val) rs149615862 0.00052
NM_001105206.3(LAMA4):c.2655C>T (p.Leu885=) rs35772073 0.00051
NM_001105206.3(LAMA4):c.1668+9G>A rs201457182 0.00049
NM_001105206.3(LAMA4):c.4665+15G>A rs377415750 0.00049
NM_001105206.3(LAMA4):c.641G>A (p.Arg214His) rs139146419 0.00044
NM_001105206.3(LAMA4):c.141G>A (p.Pro47=) rs141926228 0.00035
NM_001105206.3(LAMA4):c.4626T>C (p.Ile1542=) rs150791451 0.00031
NM_001105206.3(LAMA4):c.1614G>A (p.Ala538=) rs143587921 0.00027
NM_001105206.3(LAMA4):c.456T>A (p.Ala152=) rs149106800 0.00022
NM_001105206.3(LAMA4):c.4691G>T (p.Ser1564Ile) rs369887291 0.00018
NM_001105206.3(LAMA4):c.3087C>T (p.Pro1029=) rs146880158 0.00015
NM_001105206.3(LAMA4):c.1674G>A (p.Ala558=) rs150809897 0.00014
NM_001105206.3(LAMA4):c.1999G>T (p.Asp667Tyr) rs397516720 0.00011
NM_001105206.3(LAMA4):c.3819C>T (p.Phe1273=) rs138232283 0.00010
NM_001105206.3(LAMA4):c.5442C>T (p.Ala1814=) rs200300118 0.00009
NM_001105206.3(LAMA4):c.4305T>C (p.Asp1435=) rs147800037 0.00008
NM_001105206.3(LAMA4):c.1077+8dup rs397516713 0.00007
NM_001105206.3(LAMA4):c.2090G>A (p.Arg697His) rs397516723 0.00007
NM_001105206.3(LAMA4):c.1189+8T>C rs377133875 0.00006
NM_001105206.3(LAMA4):c.1353C>T (p.Tyr451=) rs782546070 0.00006
NM_001105206.3(LAMA4):c.228G>A (p.Ser76=) rs200589775 0.00006
NM_001105206.3(LAMA4):c.2569G>A (p.Ala857Thr) rs144123257 0.00006
NM_001105206.3(LAMA4):c.279C>T (p.Asp93=) rs397516726 0.00006
NM_001105206.3(LAMA4):c.2940A>C (p.Thr980=) rs397516727 0.00006
NM_001105206.3(LAMA4):c.3897A>G (p.Lys1299=) rs876657482 0.00006
NM_001105206.3(LAMA4):c.967-13C>T rs782148493 0.00006
NM_001105206.3(LAMA4):c.2056+12C>T rs397516722 0.00004
NM_001105206.3(LAMA4):c.412C>T (p.His138Tyr) rs727503113 0.00004
NM_001105206.3(LAMA4):c.1444A>G (p.Asn482Asp) rs782319667 0.00003
NM_001105206.3(LAMA4):c.997G>A (p.Ala333Thr) rs576711704 0.00003
NM_001105206.3(LAMA4):c.1988T>C (p.Ile663Thr) rs538726706 0.00002
NM_001105206.3(LAMA4):c.3357T>G (p.Pro1119=) rs782316528 0.00002
NM_001105206.3(LAMA4):c.3375G>A (p.Thr1125=) rs143728627 0.00002
NM_001105206.3(LAMA4):c.392C>T (p.Pro131Leu) rs374273620 0.00002
NM_001105206.3(LAMA4):c.465C>T (p.Cys155=) rs150354594 0.00002
NM_001105206.3(LAMA4):c.1209C>T (p.Leu403=) rs397516715 0.00001
NM_001105206.3(LAMA4):c.2577G>A (p.Thr859=) rs397516724 0.00001
NM_001105206.3(LAMA4):c.267C>T (p.Asn89=) rs727503114 0.00001
NM_001105206.3(LAMA4):c.3003C>T (p.Gly1001=) rs397516728 0.00001
NM_001105206.3(LAMA4):c.343G>A (p.Asp115Asn) rs781919095 0.00001
NM_001105206.3(LAMA4):c.486T>C (p.Ala162=) rs397516734 0.00001
NM_001105206.3(LAMA4):c.5241G>A (p.Val1747=) rs375447272 0.00001
NM_001105206.3(LAMA4):c.90C>T (p.Asn30=) rs542554847 0.00001
NM_001105206.3(LAMA4):c.106A>G (p.Ile36Val) rs727503116
NM_001105206.3(LAMA4):c.1374G>A (p.Glu458=) rs397516717
NM_001105206.3(LAMA4):c.140C>T (p.Pro47Leu) rs727503115
NM_001105206.3(LAMA4):c.264C>T (p.Ser88=) rs201152817
NM_001105206.3(LAMA4):c.2977-5C>T rs1554332652
NM_001105206.3(LAMA4):c.4386C>T (p.Ser1462=) rs397516729
NM_001105206.3(LAMA4):c.5002T>C (p.Leu1668=) rs369799390

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