ClinVar Miner

List of variants in gene LAMA4 reported as benign by Invitae

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Gene type:
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Total variants: 83
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HGVS dbSNP gnomAD frequency
NM_001105206.3(LAMA4):c.849= (p.Asp283=) rs9387061 0.99999
NM_001105206.3(LAMA4):c.3283-15C>T rs2032568 0.77184
NM_001105206.3(LAMA4):c.3349G>A (p.Gly1117Ser) rs2032567 0.77036
NM_001105206.3(LAMA4):c.1492T>C (p.Tyr498His) rs1050348 0.66129
NM_001105206.3(LAMA4):c.1077+3450A>G rs6907109 0.45207
NM_001105206.3(LAMA4):c.5160T>A (p.Val1720=) rs1050353 0.29327
NM_001105206.3(LAMA4):c.651C>T (p.Thr217=) rs2072021 0.26664
NM_001105206.3(LAMA4):c.5326+6T>G rs3734289 0.24973
NM_001105206.3(LAMA4):c.5326+15A>C rs3734290 0.24942
NM_001105206.3(LAMA4):c.3356C>G (p.Pro1119Arg) rs1050349 0.21500
NM_001105206.3(LAMA4):c.1710T>C (p.Ser570=) rs3752577 0.08618
NM_001105206.3(LAMA4):c.1357+4G>T rs6917763 0.07821
NM_001105206.3(LAMA4):c.4716C>T (p.Leu1572=) rs35679345 0.06874
NM_001105206.3(LAMA4):c.460C>T (p.Arg154Trp) rs11757455 0.04245
NM_001105206.3(LAMA4):c.1190-8C>G rs73538515 0.03405
NM_001105206.3(LAMA4):c.423-4T>G rs79008328 0.01927
NM_001105206.3(LAMA4):c.4173T>C (p.Tyr1391=) rs35042032 0.01889
NM_001105206.3(LAMA4):c.280G>A (p.Gly94Ser) rs35349917 0.01717
NM_001105206.3(LAMA4):c.196-12T>C rs78871662 0.01634
NM_001105206.3(LAMA4):c.423-10C>T rs75058449 0.01596
NM_001105206.3(LAMA4):c.4646A>G (p.Asn1549Ser) rs12110554 0.01544
NM_001105206.3(LAMA4):c.531C>T (p.Pro177=) rs61742228 0.01462
NM_001105206.3(LAMA4):c.4065C>T (p.Phe1355=) rs34753919 0.01154
NM_001105206.3(LAMA4):c.4287+15C>T rs116361180 0.01137
NM_001105206.3(LAMA4):c.3239G>A (p.Arg1080Gln) rs41289902 0.01045
NM_001105206.3(LAMA4):c.888C>T (p.Ser296=) rs17073495 0.00461
NM_001105206.3(LAMA4):c.422+20G>T rs188820838 0.00271
NM_001105206.3(LAMA4):c.4314A>C (p.Ser1438=) rs77367833 0.00251
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.5016T>A (p.Ile1672=) rs148517180 0.00210
NM_001105206.3(LAMA4):c.924T>C (p.His308=) rs143580603 0.00205
NM_001105206.3(LAMA4):c.2250G>A (p.Gln750=) rs112305543 0.00180
NM_001105206.3(LAMA4):c.2493+15G>T rs77901141 0.00178
NM_001105206.3(LAMA4):c.196-9C>T rs144850734 0.00174
NM_001105206.3(LAMA4):c.5443G>A (p.Val1815Ile) rs3734292 0.00174
NM_001105206.3(LAMA4):c.4822-3C>T rs191447048 0.00151
NM_001105206.3(LAMA4):c.4665+8G>T rs184220860 0.00112
NM_001105206.3(LAMA4):c.1475T>A (p.Leu492His) rs3752579 0.00093
NM_001105206.3(LAMA4):c.3834+19C>G rs187178059 0.00084
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.297+8G>A rs200595773 0.00075
NM_001105206.3(LAMA4):c.3943G>A (p.Val1315Ile) rs70940811 0.00064
NM_001105206.3(LAMA4):c.1035G>A (p.Thr345=) rs147069572 0.00060
NM_001105206.3(LAMA4):c.196-15G>C rs371906362 0.00060
NM_001105206.3(LAMA4):c.2655C>T (p.Leu885=) rs35772073 0.00051
NM_001105206.3(LAMA4):c.5340A>G (p.Thr1780=) rs139241892 0.00050
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.921T>G (p.Ala307=) rs186498011 0.00045
NM_001105206.3(LAMA4):c.641G>A (p.Arg214His) rs139146419 0.00044
NM_001105206.3(LAMA4):c.967-15C>G rs375041786 0.00043
NM_001105206.3(LAMA4):c.2493+20A>T rs143397006 0.00040
NM_001105206.3(LAMA4):c.1158G>A (p.Glu386=) rs147894075 0.00027
NM_001105206.3(LAMA4):c.1614G>A (p.Ala538=) rs143587921 0.00027
NM_001105206.3(LAMA4):c.3175G>A (p.Val1059Met) rs373650093 0.00016
NM_001105206.3(LAMA4):c.1326C>T (p.Leu442=) rs3752580 0.00014
NM_001105206.3(LAMA4):c.1999G>T (p.Asp667Tyr) rs397516720 0.00011
NM_001105206.3(LAMA4):c.1020C>T (p.Asn340=) rs147822567 0.00006
NM_001105206.3(LAMA4):c.1551+8G>A rs782128294 0.00006
NM_001105206.3(LAMA4):c.2354-18A>T rs781939034 0.00005
NM_001105206.3(LAMA4):c.2226C>T (p.Asn742=) rs530906240 0.00004
NM_001105206.3(LAMA4):c.1988T>C (p.Ile663Thr) rs538726706 0.00002
NM_001105206.3(LAMA4):c.3375G>A (p.Thr1125=) rs143728627 0.00002
NM_001105206.3(LAMA4):c.1078-14C>T rs397516714 0.00001
NM_001105206.3(LAMA4):c.1668+12C>T rs752501051 0.00001
NM_001105206.3(LAMA4):c.3110+17A>G rs782353162 0.00001
NM_001105206.3(LAMA4):c.4665+14A>G rs782460821 0.00001
NM_001105206.3(LAMA4):c.4665+18A>G rs782722526 0.00001
NM_001105206.3(LAMA4):c.486T>C (p.Ala162=) rs397516734 0.00001
NM_001105206.3(LAMA4):c.1647A>C (p.Ser549=) rs149459643
NM_001105206.3(LAMA4):c.1647A>T (p.Ser549=) rs149459643
NM_001105206.3(LAMA4):c.1669-7del rs531072297
NM_001105206.3(LAMA4):c.2475C>T (p.Thr825=)
NM_001105206.3(LAMA4):c.264C>T (p.Ser88=) rs201152817
NM_001105206.3(LAMA4):c.2977-12del
NM_001105206.3(LAMA4):c.3111-18G>A rs80168443
NM_001105206.3(LAMA4):c.3111-18G>T rs80168443
NM_001105206.3(LAMA4):c.848= (p.Asp283=) rs879974322
NM_001105206.3(LAMA4):c.848_849= (p.Asp283=) rs71543223
NM_001105206.3(LAMA4):c.848_849delinsCA (p.Asp283Ala) rs71543223
NM_001105206.3(LAMA4):c.85G>C (p.Asp29His) rs150662822

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