ClinVar Miner

List of variants in gene LAMB3 reported by Myriad Genetics, Inc.

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 56
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HGVS dbSNP gnomAD frequency
NM_000228.3(LAMB3):c.1903C>T (p.Arg635Ter) rs80356682 0.00049
NM_000228.3(LAMB3):c.124C>T (p.Arg42Ter) rs80356680 0.00006
NM_000228.3(LAMB3):c.727C>T (p.Gln243Ter) rs80356681 0.00005
NM_000228.3(LAMB3):c.565-2A>G rs370148688 0.00003
NM_000228.3(LAMB3):c.1143T>A (p.Cys381Ter) rs769748910
NM_000228.3(LAMB3):c.1204A>T (p.Lys402Ter)
NM_000228.3(LAMB3):c.121del (p.Leu41fs)
NM_000228.3(LAMB3):c.1266C>G (p.Tyr422Ter) rs766227083
NM_000228.3(LAMB3):c.1319_1325delinsAGG (p.Arg440fs)
NM_000228.3(LAMB3):c.1426C>T (p.Gln476Ter) rs1666507638
NM_000228.3(LAMB3):c.1435G>T (p.Glu479Ter)
NM_000228.3(LAMB3):c.1474C>T (p.Gln492Ter) rs1666505168
NM_000228.3(LAMB3):c.1479C>A (p.Cys493Ter) rs1447665931
NM_000228.3(LAMB3):c.1510G>T (p.Glu504Ter) rs1666482613
NM_000228.3(LAMB3):c.1665C>A (p.Cys555Ter) rs1666432128
NM_000228.3(LAMB3):c.1783C>T (p.Gln595Ter) rs1666422338
NM_000228.3(LAMB3):c.1876delinsAAATT (p.Asp626fs)
NM_000228.3(LAMB3):c.202A>T (p.Lys68Ter) rs2076427827
NM_000228.3(LAMB3):c.2089_2100delinsA (p.Gln697fs)
NM_000228.3(LAMB3):c.2166C>A (p.Tyr722Ter)
NM_000228.3(LAMB3):c.222_223del (p.His75fs)
NM_000228.3(LAMB3):c.2257_2258insGCCACAAGCT (p.Val753fs)
NM_000228.3(LAMB3):c.2327C>A (p.Ser776Ter)
NM_000228.3(LAMB3):c.239_240del (p.His80fs)
NM_000228.3(LAMB3):c.2421_2422del (p.Gln808fs)
NM_000228.3(LAMB3):c.2482del (p.Ala828fs)
NM_000228.3(LAMB3):c.2592dup (p.Ser865fs)
NM_000228.3(LAMB3):c.2677del (p.Gln893fs)
NM_000228.3(LAMB3):c.2706dup (p.Asp903fs)
NM_000228.3(LAMB3):c.2773_2774del (p.Ala926fs)
NM_000228.3(LAMB3):c.2800del (p.Glu934fs)
NM_000228.3(LAMB3):c.2992C>T (p.Gln998Ter) rs1666039804
NM_000228.3(LAMB3):c.3034del (p.Gln1012fs)
NM_000228.3(LAMB3):c.3055C>T (p.Gln1019Ter) rs1666017894
NM_000228.3(LAMB3):c.3130G>T (p.Glu1044Ter) rs1666014535
NM_000228.3(LAMB3):c.3226G>T (p.Glu1076Ter)
NM_000228.3(LAMB3):c.378del (p.Met127fs)
NM_000228.3(LAMB3):c.385del (p.Ala129fs)
NM_000228.3(LAMB3):c.421A>T (p.Lys141Ter)
NM_000228.3(LAMB3):c.444C>G (p.Tyr148Ter)
NM_000228.3(LAMB3):c.446_447delinsCAAAGGAAGA (p.Leu149fs)
NM_000228.3(LAMB3):c.459C>A (p.Cys153Ter) rs565416040
NM_000228.3(LAMB3):c.497_498delinsT (p.Gln166fs)
NM_000228.3(LAMB3):c.519C>A (p.Cys173Ter) rs1666819553
NM_000228.3(LAMB3):c.528_529delinsT (p.Pro177fs)
NM_000228.3(LAMB3):c.714C>A (p.Tyr238Ter) rs1666736220
NM_000228.3(LAMB3):c.758_759del (p.His253fs)
NM_000228.3(LAMB3):c.76del (p.Cys26fs)
NM_000228.3(LAMB3):c.784A>T (p.Lys262Ter) rs1666731883
NM_000228.3(LAMB3):c.81T>A (p.Tyr27Ter)
NM_000228.3(LAMB3):c.823-1G>A rs778372285
NM_000228.3(LAMB3):c.852_853insCCTAGTA (p.Thr285fs)
NM_000228.3(LAMB3):c.940C>T (p.Gln314Ter) rs1666646272
NM_000228.3(LAMB3):c.948C>A (p.Cys316Ter) rs779681550
NM_000228.3(LAMB3):c.975T>A (p.Cys325Ter) rs1666615300
NM_000228.3(LAMB3):c.981del (p.Phe327fs)

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