ClinVar Miner

List of variants in gene LMX1B reported as uncertain significance for not provided

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Total variants: 101
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HGVS dbSNP gnomAD frequency
NM_001174147.2(LMX1B):c.972G>C (p.Gln324His) rs886063418 0.00009
NM_001174147.2(LMX1B):c.130G>A (p.Val44Met) rs1017526258 0.00007
NM_001174147.2(LMX1B):c.899G>A (p.Ser300Asn) rs866053996 0.00006
NM_001174147.2(LMX1B):c.742-7G>C rs534963836 0.00005
NM_001174147.2(LMX1B):c.349G>A (p.Gly117Ser) rs773332016 0.00004
NM_001174147.2(LMX1B):c.463G>A (p.Glu155Lys) rs776839118 0.00004
NM_001174147.2(LMX1B):c.874C>T (p.Arg292Trp) rs560914000 0.00004
NM_001174147.2(LMX1B):c.1120G>A (p.Gly374Ser) rs769220332 0.00003
NM_001174147.2(LMX1B):c.1171C>T (p.Arg391Trp) rs141496559 0.00003
NM_001174147.2(LMX1B):c.608G>A (p.Gly203Asp) rs750404792 0.00003
NM_001174147.2(LMX1B):c.958G>A (p.Val320Met) rs778847250 0.00003
NM_001174147.2(LMX1B):c.508G>A (p.Glu170Lys) rs199738980 0.00002
NM_001174147.2(LMX1B):c.991G>A (p.Asp331Asn) rs777089988 0.00002
NM_001174147.2(LMX1B):c.1035C>T (p.Asp345=) rs755830984 0.00001
NM_001174147.2(LMX1B):c.1052G>A (p.Gly351Glu) rs2030330651 0.00001
NM_001174147.2(LMX1B):c.1084G>A (p.Asp362Asn) rs1420619429 0.00001
NM_001174147.2(LMX1B):c.1153G>A (p.Val385Met) rs750526845 0.00001
NM_001174147.2(LMX1B):c.1201G>A (p.Ala401Thr) rs761796969 0.00001
NM_001174147.2(LMX1B):c.22G>A (p.Glu8Lys) rs756001518 0.00001
NM_001174147.2(LMX1B):c.376G>A (p.Glu126Lys) rs761336753 0.00001
NM_001174147.2(LMX1B):c.559G>A (p.Val187Met) rs765969991 0.00001
NM_001174147.2(LMX1B):c.637G>A (p.Gly213Arg) rs1472509996 0.00001
NM_001174147.2(LMX1B):c.902G>A (p.Arg301His) rs773510108 0.00001
NM_001174147.2(LMX1B):c.1002G>T (p.Gln334His) rs1469503021
NM_001174147.2(LMX1B):c.1007G>A (p.Gly336Asp)
NM_001174147.2(LMX1B):c.1057G>A (p.Asp353Asn) rs1310715839
NM_001174147.2(LMX1B):c.1061C>T (p.Ser354Phe)
NM_001174147.2(LMX1B):c.109C>T (p.Pro37Ser)
NM_001174147.2(LMX1B):c.1108G>A (p.Asp370Asn)
NM_001174147.2(LMX1B):c.1124C>T (p.Ser375Phe)
NM_001174147.2(LMX1B):c.1132G>A (p.Val378Met)
NM_001174147.2(LMX1B):c.1139C>T (p.Ser380Phe)
NM_001174147.2(LMX1B):c.139+5G>C rs1114167421
NM_001174147.2(LMX1B):c.140-3C>G
NM_001174147.2(LMX1B):c.157C>G (p.Pro53Ala) rs1228632022
NM_001174147.2(LMX1B):c.182G>C (p.Arg61Pro) rs2118823251
NM_001174147.2(LMX1B):c.193G>T (p.Asp65Tyr)
NM_001174147.2(LMX1B):c.209G>A (p.Arg70Gln)
NM_001174147.2(LMX1B):c.217G>C (p.Glu73Gln)
NM_001174147.2(LMX1B):c.221C>T (p.Ser74Leu) rs1835285052
NM_001174147.2(LMX1B):c.224C>G (p.Ser75Cys)
NM_001174147.2(LMX1B):c.226T>G (p.Trp76Gly) rs1057520783
NM_001174147.2(LMX1B):c.232G>A (p.Glu78Lys) rs1835285480
NM_001174147.2(LMX1B):c.237G>T (p.Glu79Asp) rs2118823518
NM_001174147.2(LMX1B):c.238T>C (p.Cys80Arg) rs2118823527
NM_001174147.2(LMX1B):c.247T>C (p.Cys83Arg)
NM_001174147.2(LMX1B):c.253G>T (p.Ala85Ser)
NM_001174147.2(LMX1B):c.257G>C (p.Cys86Ser)
NM_001174147.2(LMX1B):c.311A>G (p.Lys104Arg)
NM_001174147.2(LMX1B):c.319T>G (p.Tyr107Asp)
NM_001174147.2(LMX1B):c.335C>T (p.Ala112Val)
NM_001174147.2(LMX1B):c.353G>A (p.Cys118Tyr) rs121909488
NM_001174147.2(LMX1B):c.36G>T (p.Arg12Ser)
NM_001174147.2(LMX1B):c.403G>A (p.Val135Met)
NM_001174147.2(LMX1B):c.406T>A (p.Tyr136Asn) rs2030102298
NM_001174147.2(LMX1B):c.409C>T (p.His137Tyr) rs2030102410
NM_001174147.2(LMX1B):c.436T>C (p.Cys146Arg)
NM_001174147.2(LMX1B):c.442C>T (p.Arg148Trp)
NM_001174147.2(LMX1B):c.443G>A (p.Arg148Gln) rs748017457
NM_001174147.2(LMX1B):c.448C>G (p.Leu150Val) rs2118987049
NM_001174147.2(LMX1B):c.451C>A (p.Arg151Ser)
NM_001174147.2(LMX1B):c.451C>T (p.Arg151Cys) rs149434820
NM_001174147.2(LMX1B):c.465A>C (p.Glu155Asp)
NM_001174147.2(LMX1B):c.469G>A (p.Val157Met) rs767072869
NM_001174147.2(LMX1B):c.544G>A (p.Asp182Asn)
NM_001174147.2(LMX1B):c.553G>A (p.Asp185Asn)
NM_001174147.2(LMX1B):c.558C>T (p.Ser186=)
NM_001174147.2(LMX1B):c.587T>G (p.Met196Arg) rs1167579696
NM_001174147.2(LMX1B):c.58G>A (p.Asp20Asn)
NM_001174147.2(LMX1B):c.627C>G (p.Ser209Arg)
NM_001174147.2(LMX1B):c.647C>T (p.Pro216Leu) rs779417752
NM_001174147.2(LMX1B):c.64G>A (p.Ala22Thr)
NM_001174147.2(LMX1B):c.674T>G (p.Ile225Ser)
NM_001174147.2(LMX1B):c.676C>T (p.Leu226Phe)
NM_001174147.2(LMX1B):c.705G>C (p.Lys235Asn)
NM_001174147.2(LMX1B):c.722C>T (p.Ser241Leu)
NM_001174147.2(LMX1B):c.725C>T (p.Ser242Leu) rs1002033502
NM_001174147.2(LMX1B):c.731C>G (p.Pro244Arg) rs2118992203
NM_001174147.2(LMX1B):c.742-7_742-6delinsCT
NM_001174147.2(LMX1B):c.745C>A (p.Arg249=) rs121909492
NM_001174147.2(LMX1B):c.746G>T (p.Arg249Leu)
NM_001174147.2(LMX1B):c.770G>T (p.Gly257Val) rs2118992774
NM_001174147.2(LMX1B):c.781C>G (p.Arg261Gly) rs886039576
NM_001174147.2(LMX1B):c.781C>T (p.Arg261Cys) rs886039576
NM_001174147.2(LMX1B):c.783C>T (p.Arg261=)
NM_001174147.2(LMX1B):c.788T>C (p.Val263Ala)
NM_001174147.2(LMX1B):c.796T>G (p.Trp266Gly) rs1588307482
NM_001174147.2(LMX1B):c.803A>C (p.Gln268Pro) rs2118992851
NM_001174147.2(LMX1B):c.82A>G (p.Ile28Val)
NM_001174147.2(LMX1B):c.856G>A (p.Glu286Lys)
NM_001174147.2(LMX1B):c.875G>A (p.Arg292Gln) rs775625232
NM_001174147.2(LMX1B):c.878T>G (p.Leu293Arg)
NM_001174147.2(LMX1B):c.883C>A (p.Gln295Lys) rs2118993442
NM_001174147.2(LMX1B):c.886+7_886+39dup
NM_001174147.2(LMX1B):c.888G>T (p.Glu296Asp)
NM_001174147.2(LMX1B):c.901C>T (p.Arg301Cys) rs376497496
NM_001174147.2(LMX1B):c.904A>C (p.Met302Leu) rs1782032990
NM_001174147.2(LMX1B):c.914T>C (p.Met305Thr)
NM_001174147.2(LMX1B):c.915G>A (p.Met305Ile) rs2118997138
NM_001174147.2(LMX1B):c.948G>T (p.Gln316His)
NM_001174147.2(LMX1B):c.976C>G (p.Pro326Ala)

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