ClinVar Miner

List of variants in gene LAMA4 reported as uncertain significance by Ambry Genetics

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Total variants: 29
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HGVS dbSNP
NM_001105206.3(LAMA4):c.*1C>T rs148811960
NM_001105206.3(LAMA4):c.122C>T (p.Ala41Val) rs553474007
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.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.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.3594C>A (p.Phe1198Leu) rs530201164
NM_001105206.3(LAMA4):c.3704G>C (p.Arg1235Pro) rs559725422
NM_001105206.3(LAMA4):c.4134-1G>A rs886039116
NM_001105206.3(LAMA4):c.4235T>C (p.Leu1412Pro) rs376369192
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.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.5393T>C (p.Ile1798Thr) rs377204776
NM_001105206.3(LAMA4):c.5405C>A (p.Pro1802Gln) rs886039017
NM_001105206.3(LAMA4):c.547A>G (p.Thr183Ala) rs782667094
NM_001105206.3(LAMA4):c.82_84GAC[1] (p.Asp29del) rs781840950
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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