ClinVar Miner

List of variants in gene MEN1 reported by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 137
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HGVS dbSNP
NM_000244.3(MEN1):c.-20G>A rs386134244
NM_000244.3(MEN1):c.-22C>A rs374749001
NM_000244.3(MEN1):c.-24+3G>A rs892783738
NM_000244.3(MEN1):c.-32G>C rs1021174779
NM_000244.3(MEN1):c.-35A>C rs679946
NM_000244.3(MEN1):c.-35A>T rs679946
NM_000244.3(MEN1):c.-40G>C rs552417059
NM_000244.3(MEN1):c.1018C>A (p.Arg340=) rs371364206
NM_000244.3(MEN1):c.1028T>C (p.Leu343Pro) rs1114167480
NM_000244.3(MEN1):c.105dup (p.Leu36fs) rs1555166711
NM_000244.3(MEN1):c.1064+1G>C rs1114167489
NM_000244.3(MEN1):c.1064+9C>T rs200517349
NM_000244.3(MEN1):c.1102_1104del (p.Glu368del) rs869025185
NM_000244.3(MEN1):c.1125del (p.Asp375fs) rs794728658
NM_000244.3(MEN1):c.1132C>G (p.Pro378Ala) rs794728627
NM_000244.3(MEN1):c.1189G>T (p.Glu397Ter) rs772588551
NM_000244.3(MEN1):c.1189del (p.Glu397fs) rs386134247
NM_000244.3(MEN1):c.1200+12G>A rs373609932
NM_000244.3(MEN1):c.1207C>T (p.Gln403Ter) rs886039418
NM_000244.3(MEN1):c.1213C>T (p.Gln405Ter) rs886039419
NM_000244.3(MEN1):c.1228C>T (p.Gln410Ter) rs864622615
NM_000244.3(MEN1):c.1258C>T (p.Arg420Ter) rs1060499974
NM_000244.3(MEN1):c.1262dup (p.Tyr422fs) rs1555164305
NM_000244.3(MEN1):c.1267G>C (p.Asp423His) rs104894264
NM_000244.3(MEN1):c.1277G>A (p.Cys426Tyr) rs386134249
NM_000244.3(MEN1):c.1311G>A (p.Leu437=) rs138770431
NM_000244.3(MEN1):c.1321T>A (p.Trp441Arg) rs104894259
NM_000244.3(MEN1):c.1322G>A (p.Trp441Ter) rs104894260
NM_000244.3(MEN1):c.1339C>T (p.Gln447Ter) rs794728654
NM_000244.3(MEN1):c.1351del (p.Arg451fs) rs886041746
NM_000244.3(MEN1):c.1356del (p.Phe452fs) rs794728643
NM_000244.3(MEN1):c.1365+1_1365+11del rs764570645
NM_000244.3(MEN1):c.1366-4C>T rs764408631
NM_000244.3(MEN1):c.1393C>T (p.Arg465Ter) rs104894267
NM_000244.3(MEN1):c.1393delinsACATAGT (p.Arg465delinsThrTer) rs1064796889
NM_000244.3(MEN1):c.1419G>A (p.Glu473=) rs755734265
NM_000244.3(MEN1):c.1424C>T (p.Pro475Leu) rs750112288
NM_000244.3(MEN1):c.1444G>T (p.Glu482Ter) rs863224526
NM_000244.3(MEN1):c.1444dup (p.Glu482fs) rs886041214
NM_000244.3(MEN1):c.1479del (p.Lys493fs) rs886039420
NM_000244.3(MEN1):c.147dup (p.Val50fs) rs794728638
NM_000244.3(MEN1):c.1494G>A (p.Pro498=) rs546721780
NM_000244.3(MEN1):c.1520dup (p.Leu509fs) rs1555163591
NM_000244.3(MEN1):c.1523G>A (p.Gly508Asp) rs375804228
NM_000244.3(MEN1):c.1546_1547GT[3] (p.Ser517fs) rs794728659
NM_000244.3(MEN1):c.1561del (p.Arg521fs) rs767319284
NM_000244.3(MEN1):c.1561dup (p.Arg521fs) rs767319284
NM_000244.3(MEN1):c.1563dup (p.Lys522fs) rs761695866
NM_000244.3(MEN1):c.1594C>T (p.Arg532Ter) rs104894261
NM_000244.3(MEN1):c.1595G>A (p.Arg532Gln) rs1085307502
NM_000244.3(MEN1):c.1605del (p.Gly536fs) rs886039421
NM_000244.3(MEN1):c.1617_1633del (p.Ala540fs) rs794728660
NM_000244.3(MEN1):c.1617_1633dup (p.Pro545fs) rs794728660
NM_000244.3(MEN1):c.1624G>A (p.Val542Met) rs1057521847
NM_000244.3(MEN1):c.164dup (p.Thr56fs) rs794728656
NM_000244.3(MEN1):c.1653G>A (p.Pro551=) rs368783097
NM_000244.3(MEN1):c.1666del (p.Leu556fs) rs794728645
NM_000244.3(MEN1):c.1675C>T (p.Gln559Ter) rs794728631
NM_000244.3(MEN1):c.1682_1684AGA[1] (p.Lys562del) rs794728661
NM_000244.3(MEN1):c.168del (p.Asn57fs) rs1060499990
NM_000244.3(MEN1):c.1702G>T (p.Glu568Ter) rs794728632
NM_000244.3(MEN1):c.1725_1730del (p.Ile575_Ser577delinsMet) rs794728646
NM_000244.3(MEN1):c.1745T>C (p.Leu582Pro) rs794728634
NM_000244.3(MEN1):c.1815G>T (p.Leu605=) rs148825200
NM_000244.3(MEN1):c.189C>G (p.Phe63Leu) rs137880635
NM_000244.3(MEN1):c.18C>T (p.Ala6=) rs369348210
NM_000244.3(MEN1):c.197_201GCCCC[3] (p.Asp70fs) rs730882136
NM_000244.3(MEN1):c.1A>G (p.Met1Val) rs386134250
NM_000244.3(MEN1):c.207del (p.Asp70fs) rs1057517902
NM_000244.3(MEN1):c.211_212del (p.Pro71fs) rs386134251
NM_000244.3(MEN1):c.225C>A (p.Leu75=) rs1333791405
NM_000244.3(MEN1):c.227C>A (p.Thr76Asn) rs886039752
NM_000244.3(MEN1):c.249_252del (p.Ile85fs) rs587776841
NM_000244.3(MEN1):c.266_286del (p.Leu89_Ala95del) rs1064792906
NM_000244.3(MEN1):c.292C>T (p.Arg98Ter) rs886039413
NM_000244.3(MEN1):c.300C>G (p.Ala100=) rs773136972
NM_000244.3(MEN1):c.307del (p.Leu103fs) rs794728639
NM_000244.3(MEN1):c.30G>T (p.Leu10=) rs371192390
NM_000244.3(MEN1):c.322C>T (p.Arg108Ter) rs794728647
NM_000244.3(MEN1):c.332dup (p.Val112fs) rs1555166435
NM_000244.3(MEN1):c.340dup (p.Ser114fs) rs886041213
NM_000244.3(MEN1):c.355_357AAG[1] (p.Lys120del) rs794728657
NM_000244.3(MEN1):c.402del (p.Phe134fs) rs397515385
NM_000244.3(MEN1):c.421C>T (p.Gln141Ter) rs886039553
NM_000244.3(MEN1):c.432del (p.Phe144fs) rs1064793613
NM_000244.3(MEN1):c.461-1G>A rs1064793672
NM_000244.3(MEN1):c.461-2A>C rs886042035
NM_000244.3(MEN1):c.481G>C (p.Gly161Arg) rs1085307471
NM_000244.3(MEN1):c.482G>A (p.Gly161Asp) rs794728648
NM_000244.3(MEN1):c.505_506delinsT (p.Ala169fs) rs886041634
NM_000244.3(MEN1):c.507C>T (p.Ala169=) rs146759807
NM_000244.3(MEN1):c.509G>A (p.Cys170Tyr) rs1057521111
NM_000244.3(MEN1):c.526C>T (p.Arg176Trp) rs143329068
NM_000244.3(MEN1):c.530A>T (p.Asp177Val) rs794728618
NM_000244.3(MEN1):c.541G>C (p.Ala181Pro) rs376872829
NM_000244.3(MEN1):c.550G>A (p.Glu184Lys) rs1064793167
NM_000244.3(MEN1):c.552G>C (p.Glu184Asp) rs1555165811
NM_000244.3(MEN1):c.552G>T (p.Glu184Asp) rs1555165811
NM_000244.3(MEN1):c.554A>T (p.Asp185Val) rs1064794683
NM_000244.3(MEN1):c.55del (p.Val19fs) rs794728655
NM_000244.3(MEN1):c.57_58insT (p.Val20fs) rs794728636
NM_000244.3(MEN1):c.643_646del (p.Thr215fs) rs794728640
NM_000244.3(MEN1):c.65T>G (p.Leu22Arg) rs104894256
NM_000244.3(MEN1):c.669+18C>T rs180737290
NM_000244.3(MEN1):c.669+1G>T rs794728622
NM_000244.3(MEN1):c.669+3A>T rs1064793168
NM_000244.3(MEN1):c.670-6C>A rs77461664
NM_000244.3(MEN1):c.670-6C>G rs77461664
NM_000244.3(MEN1):c.673T>C (p.Trp225Arg) rs1085307971
NM_000244.3(MEN1):c.675G>A (p.Trp225Ter) rs886039414
NM_000244.3(MEN1):c.683T>C (p.Leu228Pro) rs886039415
NM_000244.3(MEN1):c.688G>A (p.Gly230Arg) rs1057521110
NM_000244.3(MEN1):c.699del (p.Met233fs) rs1064795635
NM_000244.3(MEN1):c.703T>C (p.Cys235Arg) rs1555165570
NM_000244.3(MEN1):c.768C>T (p.Thr256=) rs763326062
NM_000244.3(MEN1):c.76G>A (p.Glu26Lys) rs28931612
NM_000244.3(MEN1):c.787C>T (p.Gln263Ter) rs886039416
NM_000244.3(MEN1):c.788_790dup (p.Gln263dup) rs1057517760
NM_000244.3(MEN1):c.789G>C (p.Gln263His) rs374659656
NM_000244.3(MEN1):c.796C>T (p.Gln266Ter) rs1057520733
NM_000244.3(MEN1):c.798+2T>G rs1057524571
NM_000244.3(MEN1):c.799-19TC[2] rs764290037
NM_000244.3(MEN1):c.799-1G>C rs1555165377
NM_000244.3(MEN1):c.799-9G>A rs794728625
NM_000244.3(MEN1):c.79_88del (p.Leu27fs) rs794728637
NM_000244.3(MEN1):c.839+5G>A rs1064793398
NM_000244.3(MEN1):c.840-10C>G rs999121619
NM_000244.3(MEN1):c.843C>A (p.Tyr281Ter) rs1060503789
NM_000244.3(MEN1):c.927+1G>A rs398124437
NM_000244.3(MEN1):c.927+2T>C rs1555165256
NM_000244.3(MEN1):c.928-1G>A rs1057518572
NM_000244.3(MEN1):c.937T>C (p.Ser313Pro) rs1064793169
NM_000244.3(MEN1):c.958G>T (p.Asp320Tyr) rs747851909
NM_000244.3(MEN1):c.965_972del (p.His322fs) rs794728641
NM_000244.3(MEN1):c.984C>G (p.Tyr328Ter) rs750904332
NM_130799.2(MEN1):c.-217T>A
NM_130799.2(MEN1):c.-844C>T

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