ClinVar Miner

List of variants in gene MEN1 studied for Hereditary cancer-predisposing syndrome

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Gene type:
ClinVar version:
Total variants: 230
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HGVS dbSNP
NM_000244.3(MEN1):c.1004G>A (p.Arg335His) rs373135175
NM_000244.3(MEN1):c.1008C>T (p.Asn336=) rs370176253
NM_000244.3(MEN1):c.100C>A (p.Leu34Met) rs771554497
NM_000244.3(MEN1):c.1014T>C (p.Asn338=) rs763133775
NM_000244.3(MEN1):c.1015G>A (p.Val339Met) rs1555165027
NM_000244.3(MEN1):c.1016_1020dup (p.Glu341fs) rs1114167483
NM_000244.3(MEN1):c.1018C>A (p.Arg340=) rs371364206
NM_000244.3(MEN1):c.1019delinsTT (p.Arg340fs) rs1114167506
NM_000244.3(MEN1):c.1022_1024dup (p.Glu341dup) rs1114167529
NM_000244.3(MEN1):c.1028T>C (p.Leu343Pro) rs1114167480
NM_000244.3(MEN1):c.1035C>A (p.Ala345=) rs1060503796
NM_000244.3(MEN1):c.1037G>A (p.Trp346Ter) rs1114167482
NM_000244.3(MEN1):c.1041G>A (p.Ala347=) rs878855184
NM_000244.3(MEN1):c.1047G>A (p.Thr349=) rs760183888
NM_000244.3(MEN1):c.1064+1G>C rs1114167489
NM_000244.3(MEN1):c.1068C>G (p.Tyr356Ter) rs767078097
NM_000244.3(MEN1):c.1075T>C (p.Cys359Arg) rs371503251
NM_000244.3(MEN1):c.1079G>A (p.Arg360Gln) rs1114167474
NM_000244.3(MEN1):c.1086C>T (p.Asp362=) rs371964966
NM_000244.3(MEN1):c.108_122del (p.Leu37_Leu41del) rs1555166695
NM_000244.3(MEN1):c.1093A>T (p.Ile365Phe) rs1114167475
NM_000244.3(MEN1):c.1095C>T (p.Ile365=) rs147331514
NM_000244.3(MEN1):c.1102_1104del (p.Glu368del) rs869025185
NM_000244.3(MEN1):c.1113A>T (p.Glu371Asp) rs149383809
NM_000244.3(MEN1):c.1114G>A (p.Val372Ile) rs758404089
NM_000244.3(MEN1):c.1117G>A (p.Ala373Thr) rs1114167473
NM_000244.3(MEN1):c.1117G>C (p.Ala373Pro) rs1114167473
NM_000244.3(MEN1):c.1138C>G (p.Leu380Val) rs1211957325
NM_000244.3(MEN1):c.113C>T (p.Ser38Phe) rs794728616
NM_000244.3(MEN1):c.1142T>C (p.Leu381Pro) rs1114167471
NM_000244.3(MEN1):c.1142T>G (p.Leu381Arg) rs1114167471
NM_000244.3(MEN1):c.1170G>A (p.Ala390=) rs201091135
NM_000244.3(MEN1):c.1172G>A (p.Gly391Asp) rs761360623
NM_000244.3(MEN1):c.1184C>T (p.Pro395Leu) rs761102084
NM_000244.3(MEN1):c.1185G>A (p.Pro395=) rs587780841
NM_000244.3(MEN1):c.1185G>C (p.Pro395=) rs587780841
NM_000244.3(MEN1):c.1192C>G (p.Gln398Glu) rs1060499984
NM_000244.3(MEN1):c.1192C>T (p.Gln398Ter) rs1060499984
NM_000244.3(MEN1):c.1200+12G>A rs373609932
NM_000244.3(MEN1):c.1203C>T (p.Gly401=) rs749418407
NM_000244.3(MEN1):c.1229dup (p.Asp411fs) rs1114167513
NM_000244.3(MEN1):c.1239_1240insGTCC (p.Cys414fs) rs1114167524
NM_000244.3(MEN1):c.1245C>T (p.Phe415=) rs878855188
NM_000244.3(MEN1):c.1258C>T (p.Arg420Ter) rs1060499974
NM_000244.3(MEN1):c.1262_1269del (p.Phe421fs) rs1114167542
NM_000244.3(MEN1):c.1267G>A (p.Asp423Asn) rs104894264
NM_000244.3(MEN1):c.1267G>T (p.Asp423Tyr) rs104894264
NM_000244.3(MEN1):c.1269C>T (p.Asp423=) rs2071313
NM_000244.3(MEN1):c.1273A>T (p.Ile425Phe) rs1114167526
NM_000244.3(MEN1):c.1274T>G (p.Ile425Ser) rs1114167539
NM_000244.3(MEN1):c.1277G>A (p.Cys426Tyr) rs386134249
NM_000244.3(MEN1):c.1284G>A (p.Trp428Ter) rs1114167533
NM_000244.3(MEN1):c.1285G>A (p.Glu429Lys) rs1114167477
NM_000244.3(MEN1):c.1285G>T (p.Glu429Ter) rs1114167477
NM_000244.3(MEN1):c.1296T>A (p.Ser432Arg) rs1114167528
NM_000244.3(MEN1):c.12G>A (p.Lys4=) rs1555166817
NM_000244.3(MEN1):c.1311G>A (p.Leu437=) rs138770431
NM_000244.3(MEN1):c.1321T>C (p.Trp441Arg) rs104894259
NM_000244.3(MEN1):c.1323G>T (p.Trp441Cys) rs398124435
NM_000244.3(MEN1):c.1325C>T (p.Ala442Val) rs1555164188
NM_000244.3(MEN1):c.133G>A (p.Glu45Lys) rs1114167491
NM_000244.3(MEN1):c.1345del (p.Ser448_Leu449insTer) rs1114167520
NM_000244.3(MEN1):c.1363C>T (p.Gln455Ter) rs1114167509
NM_000244.3(MEN1):c.1366-4C>T rs764408631
NM_000244.3(MEN1):c.1369C>T (p.Arg457Trp) rs863224810
NM_000244.3(MEN1):c.1370G>C (p.Arg457Pro) rs775922507
NM_000244.3(MEN1):c.1393C>T (p.Arg465Ter) rs104894267
NM_000244.3(MEN1):c.1397_1404dup (p.Ala469fs) rs1114167531
NM_000244.3(MEN1):c.1405delinsCCT (p.Ala469fs) rs1114167500
NM_000244.3(MEN1):c.1410C>G (p.Ala470=) rs748820252
NM_000244.3(MEN1):c.1410C>T (p.Ala470=) rs748820252
NM_000244.3(MEN1):c.1411G>A (p.Glu471Lys) rs1114167497
NM_000244.3(MEN1):c.1419G>A (p.Glu473=) rs755734265
NM_000244.3(MEN1):c.1421_1428dup (p.Gly477fs) rs1114167536
NM_000244.3(MEN1):c.1424C>T (p.Pro475Leu) rs750112288
NM_000244.3(MEN1):c.1431C>T (p.Gly477=) rs764509990
NM_000244.3(MEN1):c.1444G>T (p.Glu482Ter) rs863224526
NM_000244.3(MEN1):c.1449C>T (p.Gly483=) rs200280309
NM_000244.3(MEN1):c.1479del (p.Lys493fs) rs886039420
NM_000244.3(MEN1):c.1494G>A (p.Pro498=) rs546721780
NM_000244.3(MEN1):c.1497G>A (p.Pro499=) rs773363654
NM_000244.3(MEN1):c.1519_1522dup (p.Gly508fs) rs1114167476
NM_000244.3(MEN1):c.1521G>C (p.Lys507Asn) rs774296730
NM_000244.3(MEN1):c.1523G>A (p.Gly508Asp) rs375804228
NM_000244.3(MEN1):c.1533C>T (p.Thr511=) rs749265222
NM_000244.3(MEN1):c.1537C>A (p.Gln513Lys) rs386833403
NM_000244.3(MEN1):c.1544_1545del (p.Ala515fs) rs1114167522
NM_000244.3(MEN1):c.1546_1547GT[3] (p.Ser517fs) rs794728659
NM_000244.3(MEN1):c.154C>T (p.Arg52Cys) rs1555166664
NM_000244.3(MEN1):c.1550C>T (p.Ser517Leu) rs141679530
NM_000244.3(MEN1):c.1556C>G (p.Pro519Arg) rs753022747
NM_000244.3(MEN1):c.1561C>T (p.Arg521Trp)
NM_000244.3(MEN1):c.1561dup (p.Arg521fs) rs767319284
NM_000244.3(MEN1):c.1564A>T (p.Lys522Ter) rs794728630
NM_000244.3(MEN1):c.1589del (p.Thr530fs) rs1114167514
NM_000244.3(MEN1):c.1594C>T (p.Arg532Ter) rs104894261
NM_000244.3(MEN1):c.1609G>T (p.Gly537Cys) rs587780843
NM_000244.3(MEN1):c.1623G>A (p.Gln541=) rs1055457298
NM_000244.3(MEN1):c.1624G>A (p.Val542Met) rs1057521847
NM_000244.3(MEN1):c.162C>T (p.Ile54=) rs1555166662
NM_000244.3(MEN1):c.1633C>T (p.Pro545Ser) rs745404679
NM_000244.3(MEN1):c.1653G>A (p.Pro551=) rs368783097
NM_000244.3(MEN1):c.1653_1654dup (p.Glu552fs) rs1114167496
NM_000244.3(MEN1):c.1658_1736delinsTG (p.Gly553fs) rs1555163136
NM_000244.3(MEN1):c.1671T>C (p.Thr557=) rs143423552
NM_000244.3(MEN1):c.1674C>T (p.Phe558=) rs1299138529
NM_000244.3(MEN1):c.1675C>T (p.Gln559Ter) rs794728631
NM_000244.3(MEN1):c.1679G>A (p.Ser560Asn) rs863224527
NM_000244.3(MEN1):c.1680_1683del (p.Ser560fs) rs1114167510
NM_000244.3(MEN1):c.1681G>T (p.Glu561Ter) rs1114167501
NM_000244.3(MEN1):c.1684A>G (p.Lys562Glu) rs1114167517
NM_000244.3(MEN1):c.16G>T (p.Ala6Ser) rs966793401
NM_000244.3(MEN1):c.16_17del (p.Ala6fs) rs1114167523
NM_000244.3(MEN1):c.1710G>T (p.Leu570=) rs767677287
NM_000244.3(MEN1):c.1714G>C (p.Ala572Pro) rs1555163185
NM_000244.3(MEN1):c.1716C>T (p.Ala572=) rs757417271
NM_000244.3(MEN1):c.1723_1743del (p.Ile575_Lys581del) rs1555163115
NM_000244.3(MEN1):c.1740del (p.Lys581fs) rs1555163124
NM_000244.3(MEN1):c.1745T>C (p.Leu582Pro) rs794728634
NM_000244.3(MEN1):c.1755G>C (p.Thr585=) rs1114167530
NM_000244.3(MEN1):c.1779G>A (p.Lys593=) rs373669288
NM_000244.3(MEN1):c.18C>T (p.Ala6=) rs369348210
NM_000244.3(MEN1):c.194C>A (p.Pro65His) rs1114167484
NM_000244.3(MEN1):c.1A>G (p.Met1Val) rs386134250
NM_000244.3(MEN1):c.1A>T (p.Met1Leu) rs386134250
NM_000244.3(MEN1):c.201C>T (p.Pro67=) rs1060503791
NM_000244.3(MEN1):c.210C>A (p.Asp70Glu) rs150308912
NM_000244.3(MEN1):c.223del (p.Leu75fs) rs1114167485
NM_000244.3(MEN1):c.237del (p.Val80fs) rs1114167486
NM_000244.3(MEN1):c.249_252del (p.Ile85fs) rs587776841
NM_000244.3(MEN1):c.265del (p.Leu89fs) rs1114167490
NM_000244.3(MEN1):c.270T>A (p.Tyr90Ter) rs1114167527
NM_000244.3(MEN1):c.273_276del (p.Arg92fs) rs1114167516
NM_000244.3(MEN1):c.282C>T (p.Thr94=) rs760442763
NM_000244.3(MEN1):c.307del (p.Leu103fs) rs794728639
NM_000244.3(MEN1):c.30G>T (p.Leu10=) rs371192390
NM_000244.3(MEN1):c.311C>A (p.Ser104Tyr) rs1114167512
NM_000244.3(MEN1):c.317A>G (p.Tyr106Cys) rs1555166469
NM_000244.3(MEN1):c.322C>T (p.Arg108Ter) rs794728647
NM_000244.3(MEN1):c.326A>G (p.Glu109Gly) rs1555166447
NM_000244.3(MEN1):c.329G>C (p.Gly110Ala) rs1389398299
NM_000244.3(MEN1):c.32T>C (p.Phe11Ser) rs1114167535
NM_000244.3(MEN1):c.336del (p.Ser113fs) rs1114167478
NM_000244.3(MEN1):c.339C>T (p.Ser113=) rs559635859
NM_000244.3(MEN1):c.340dup (p.Ser114fs) rs886041213
NM_000244.3(MEN1):c.344G>A (p.Arg115His) rs1114167507
NM_000244.3(MEN1):c.355_357AAG[1] (p.Lys120del) rs794728657
NM_000244.3(MEN1):c.378del (p.Ile125_Trp126insTer) rs1114167492
NM_000244.3(MEN1):c.402del (p.Phe134fs) rs397515385
NM_000244.3(MEN1):c.415C>G (p.His139Asp) rs104894263
NM_000244.3(MEN1):c.416A>G (p.His139Arg) rs1114167515
NM_000244.3(MEN1):c.417del (p.His139fs) rs1114167540
NM_000244.3(MEN1):c.429_432delinsATT (p.Phe144fs) rs1114167481
NM_000244.3(MEN1):c.430T>G (p.Phe144Val) rs1114167543
NM_000244.3(MEN1):c.431_432delinsAA (p.Phe144Ter) rs1114167511
NM_000244.3(MEN1):c.433A>C (p.Ser145Arg) rs778932605
NM_000244.3(MEN1):c.435C>T (p.Ser145=) rs61736636
NM_000244.3(MEN1):c.442A>G (p.Thr148Ala) rs1114167537
NM_000244.3(MEN1):c.461-2A>G rs886042035
NM_000244.3(MEN1):c.461-3C>A rs377461506
NM_000244.3(MEN1):c.482G>A (p.Gly161Asp) rs794728648
NM_000244.3(MEN1):c.486G>A (p.Val162=) rs878855194
NM_000244.3(MEN1):c.491T>C (p.Phe164Ser) rs1555165861
NM_000244.3(MEN1):c.526C>T (p.Arg176Trp) rs143329068
NM_000244.3(MEN1):c.527G>A (p.Arg176Gln) rs607969
NM_000244.3(MEN1):c.529G>T (p.Asp177Tyr) rs1114167494
NM_000244.3(MEN1):c.530A>T (p.Asp177Val) rs794728618
NM_000244.3(MEN1):c.531T>C (p.Asp177=) rs912509147
NM_000244.3(MEN1):c.540C>T (p.Leu180=) rs200155578
NM_000244.3(MEN1):c.541G>C (p.Ala181Pro) rs376872829
NM_000244.3(MEN1):c.541G>T (p.Ala181Ser) rs376872829
NM_000244.3(MEN1):c.544_545del (p.Leu182fs) rs1114167470
NM_000244.3(MEN1):c.545del (p.Leu182fs) rs1114167503
NM_000244.3(MEN1):c.546G>A (p.Leu182=) rs146568011
NM_000244.3(MEN1):c.578C>T (p.Pro193Leu) rs199706698
NM_000244.3(MEN1):c.585G>A (p.Gly195=) rs547249181
NM_000244.3(MEN1):c.612C>T (p.His204=) rs150512958
NM_000244.3(MEN1):c.615C>T (p.Gly205=) rs1114167479
NM_000244.3(MEN1):c.61C>A (p.Arg21Ser) rs541476418
NM_000244.3(MEN1):c.624C>T (p.Asn208=) rs749844029
NM_000244.3(MEN1):c.640del (p.Gln214fs) rs1114167538
NM_000244.3(MEN1):c.643_646del (p.Thr215fs) rs794728640
NM_000244.3(MEN1):c.653_654delinsAA (p.Ala218Glu) rs1114167518
NM_000244.3(MEN1):c.654C>T (p.Ala218=) rs746067825
NM_000244.3(MEN1):c.670-4del rs748005956
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.697_700dup (p.Arg234fs) rs1114167519
NM_000244.3(MEN1):c.712A>T (p.Lys238Ter) rs1114167499
NM_000244.3(MEN1):c.718G>A (p.Glu240Lys) rs1114167488
NM_000244.3(MEN1):c.721_724dup (p.Ala242fs) rs1114167534
NM_000244.3(MEN1):c.726G>A (p.Ala242=) rs144677807
NM_000244.3(MEN1):c.737G>A (p.Cys246Tyr) rs794728624
NM_000244.3(MEN1):c.742_749del (p.Ile248fs) rs1114167532
NM_000244.3(MEN1):c.768C>T (p.Thr256=) rs763326062
NM_000244.3(MEN1):c.773C>T (p.Ser258Leu) rs386134259
NM_000244.3(MEN1):c.774G>T (p.Ser258=) rs201829546
NM_000244.3(MEN1):c.777G>A (p.Leu259=) rs199909967
NM_000244.3(MEN1):c.789G>C (p.Gln263His) rs374659656
NM_000244.3(MEN1):c.793C>T (p.Gln265Ter) rs104894266
NM_000244.3(MEN1):c.798+1G>A rs794728652
NM_000244.3(MEN1):c.799-2A>G rs1114167472
NM_000244.3(MEN1):c.800A>G (p.Lys267Arg) rs1555165373
NM_000244.3(MEN1):c.803T>C (p.Leu268Pro) rs1114167502
NM_000244.3(MEN1):c.839+1G>C rs1060499976
NM_000244.3(MEN1):c.840-1G>A rs1114167505
NM_000244.3(MEN1):c.842A>G (p.Tyr281Cys) rs1555165327
NM_000244.3(MEN1):c.843C>A (p.Tyr281Ter) rs1060503789
NM_000244.3(MEN1):c.843C>T (p.Tyr281=) rs1060503789
NM_000244.3(MEN1):c.845C>A (p.Pro282His) rs1060499973
NM_000244.3(MEN1):c.849G>A (p.Met283Ile) rs794728626
NM_000244.3(MEN1):c.856G>A (p.Gly286Arg) rs1114167493
NM_000244.3(MEN1):c.858G>C (p.Gly286=) rs562620826
NM_000244.3(MEN1):c.85C>T (p.Arg29Ter) rs794728615
NM_000244.3(MEN1):c.871C>T (p.Leu291=) rs542321016
NM_000244.3(MEN1):c.898C>T (p.Arg300Trp) rs1046929915
NM_000244.3(MEN1):c.927+1G>A rs398124437
NM_000244.3(MEN1):c.927+1G>C rs398124437
NM_000244.3(MEN1):c.928-2A>G rs1114167498
NM_000244.3(MEN1):c.937T>C (p.Ser313Pro) rs1064793169
NM_000244.3(MEN1):c.94C>T (p.Pro32Ser) rs773089218
NM_000244.3(MEN1):c.956G>A (p.Arg319Gln) rs771645621
NM_000244.3(MEN1):c.959A>T (p.Asp320Val) rs1114167487
NM_000244.3(MEN1):c.965A>G (p.His322Arg) rs1114167495
NM_000244.3(MEN1):c.974C>T (p.Pro325Leu) rs1114167469
NM_000244.3(MEN1):c.982del (p.Tyr328fs) rs1114167541
NM_000244.3(MEN1):c.984C>A (p.Tyr328Ter) rs750904332
NM_000244.3(MEN1):c.985del (p.Leu329fs) rs1114167508
NM_000244.3:c.563C>T
NM_130799.2(MEN1):c.1391_1392ins13 (p.?)

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