ClinVar Miner

List of variants in gene LAMA4 reported by Ambry Genetics

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Total variants: 62
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HGVS dbSNP
NM_001105206.3(LAMA4):c.*1C>T rs148811960
NM_001105206.3(LAMA4):c.1035G>A (p.Thr345=) rs147069572
NM_001105206.3(LAMA4):c.1131C>T (p.Thr377=) rs1554344450
NM_001105206.3(LAMA4):c.1200C>T (p.Asn400=) rs375622742
NM_001105206.3(LAMA4):c.122C>T (p.Ala41Val) rs553474007
NM_001105206.3(LAMA4):c.1475T>A (p.Leu492His) rs3752579
NM_001105206.3(LAMA4):c.1633C>T (p.Arg545Cys) rs138153075
NM_001105206.3(LAMA4):c.1647A>C (p.Ser549=) rs149459643
NM_001105206.3(LAMA4):c.1959T>C (p.Asp653=) rs143269044
NM_001105206.3(LAMA4):c.1962G>A (p.Ala654=) rs140246538
NM_001105206.3(LAMA4):c.1999G>T (p.Asp667Tyr) rs397516720
NM_001105206.3(LAMA4):c.2090G>A (p.Arg697His) rs397516723
NM_001105206.3(LAMA4):c.2171G>A (p.Arg724Lys) rs146868519
NM_001105206.3(LAMA4):c.2250G>A (p.Gln750=) rs112305543
NM_001105206.3(LAMA4):c.2334G>A (p.Val778=) rs559504162
NM_001105206.3(LAMA4):c.2403G>A (p.Thr801=) rs142559688
NM_001105206.3(LAMA4):c.2417G>A (p.Arg806Gln) rs1554334150
NM_001105206.3(LAMA4):c.2527G>C (p.Ala843Pro) rs536755553
NM_001105206.3(LAMA4):c.254A>G (p.Asn85Ser) rs145301300
NM_001105206.3(LAMA4):c.2569G>A (p.Ala857Thr) rs144123257
NM_001105206.3(LAMA4):c.2619A>G (p.Glu873=) rs138949462
NM_001105206.3(LAMA4):c.264C>T (p.Ser88=) rs201152817
NM_001105206.3(LAMA4):c.2655C>T (p.Leu885=) rs35772073
NM_001105206.3(LAMA4):c.2810A>G (p.Glu937Gly) rs35605307
NM_001105206.3(LAMA4):c.3054G>T (p.Leu1018Phe) rs183262122
NM_001105206.3(LAMA4):c.3055T>C (p.Tyr1019His) rs73532636
NM_001105206.3(LAMA4):c.307C>T (p.Arg103Trp) rs138176093
NM_001105206.3(LAMA4):c.3175G>A (p.Val1059Met) rs373650093
NM_001105206.3(LAMA4):c.3372T>C (p.Asp1124=) rs782596488
NM_001105206.3(LAMA4):c.3594C>A (p.Phe1198Leu) rs530201164
NM_001105206.3(LAMA4):c.3704G>C (p.Arg1235Pro) rs559725422
NM_001105206.3(LAMA4):c.3819C>T (p.Phe1273=) rs138232283
NM_001105206.3(LAMA4):c.3834G>A (p.Gly1278=) rs141988342
NM_001105206.3(LAMA4):c.3943G>A (p.Val1315Ile) rs70940811
NM_001105206.3(LAMA4):c.4134-1G>A rs886039116
NM_001105206.3(LAMA4):c.4235T>C (p.Leu1412Pro) rs376369192
NM_001105206.3(LAMA4):c.4255T>C (p.Leu1419=) rs782225670
NM_001105206.3(LAMA4):c.449dup (p.Asn150fs) rs1249093492
NM_001105206.3(LAMA4):c.4583G>A (p.Arg1528His) rs782805733
NM_001105206.3(LAMA4):c.4645A>T (p.Asn1549Tyr) rs141261442
NM_001105206.3(LAMA4):c.4678C>A (p.Arg1560=) rs150069819
NM_001105206.3(LAMA4):c.4746T>G (p.Thr1582=) rs941191492
NM_001105206.3(LAMA4):c.4822-3C>T rs191447048
NM_001105206.3(LAMA4):c.486T>C (p.Ala162=) rs397516734
NM_001105206.3(LAMA4):c.5005A>G (p.Lys1669Glu) rs782716382
NM_001105206.3(LAMA4):c.5021T>G (p.Phe1674Cys) rs1209180229
NM_001105206.3(LAMA4):c.5035A>G (p.Arg1679Gly) rs781995760
NM_001105206.3(LAMA4):c.514G>A (p.Gly172Ser) rs147695488
NM_001105206.3(LAMA4):c.5340A>G (p.Thr1780=) rs139241892
NM_001105206.3(LAMA4):c.5393T>C (p.Ile1798Thr) rs377204776
NM_001105206.3(LAMA4):c.5405C>A (p.Pro1802Gln) rs886039017
NM_001105206.3(LAMA4):c.5450T>C (p.Ile1817Thr) rs144482486
NM_001105206.3(LAMA4):c.547A>G (p.Thr183Ala) rs782667094
NM_001105206.3(LAMA4):c.641G>A (p.Arg214His) rs139146419
NM_001105206.3(LAMA4):c.72C>T (p.Ala24=) rs782814489
NM_001105206.3(LAMA4):c.82_84GAC[1] (p.Asp29del) rs781840950
NM_001105206.3(LAMA4):c.848= (p.Asp283=) rs879974322
NM_001105206.3(LAMA4):c.849= (p.Asp283=) rs9387061
NM_001105206.3(LAMA4):c.85G>C (p.Asp29His) rs150662822
NM_001105206.3(LAMA4):c.874G>A (p.Glu292Lys) rs781838464
NM_001105206.3(LAMA4):c.892G>A (p.Val298Met) rs927160835
NM_001105206.3(LAMA4):c.952A>G (p.Ile318Val) rs141372605

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