ClinVar Miner

List of variants in gene MEN1 reported as pathogenic for Hereditary cancer-predisposing syndrome

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Total variants: 94
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HGVS dbSNP
NM_000244.3(MEN1):c.1016_1020dup (p.Glu341fs) rs1114167483
NM_000244.3(MEN1):c.1019delinsTT (p.Arg340fs) rs1114167506
NM_000244.3(MEN1):c.1037G>A (p.Trp346Ter) rs1114167482
NM_000244.3(MEN1):c.1068C>G (p.Tyr356Ter) rs767078097
NM_000244.3(MEN1):c.1102_1104del (p.Glu368del) rs869025185
NM_000244.3(MEN1):c.1125del (p.Asp375fs) rs794728658
NM_000244.3(MEN1):c.1192C>T (p.Gln398Ter) rs1060499984
NM_000244.3(MEN1):c.1229dup (p.Asp411fs) rs1114167513
NM_000244.3(MEN1):c.1239_1240insGTCC (p.Cys414fs) rs1114167524
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>T (p.Asp423Tyr) rs104894264
NM_000244.3(MEN1):c.1284G>A (p.Trp428Ter) rs1114167533
NM_000244.3(MEN1):c.1285G>T (p.Glu429Ter) rs1114167477
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.1345del (p.Ser448_Leu449insTer) rs1114167520
NM_000244.3(MEN1):c.1363C>T (p.Gln455Ter) rs1114167509
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.1421_1428dup (p.Gly477fs) rs1114167536
NM_000244.3(MEN1):c.1444G>T (p.Glu482Ter) rs863224526
NM_000244.3(MEN1):c.1479del (p.Lys493fs) rs886039420
NM_000244.3(MEN1):c.1519_1522dup (p.Gly508fs) rs1114167476
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.1561del (p.Arg521fs) rs767319284
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.1653_1654dup (p.Glu552fs) rs1114167496
NM_000244.3(MEN1):c.1658_1736delinsTG (p.Gly553fs) rs1555163136
NM_000244.3(MEN1):c.1675C>T (p.Gln559Ter) rs794728631
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.16_17del (p.Ala6fs) rs1114167523
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.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.307del (p.Leu103fs) rs794728639
NM_000244.3(MEN1):c.322C>T (p.Arg108Ter) rs794728647
NM_000244.3(MEN1):c.336del (p.Ser113fs) rs1114167478
NM_000244.3(MEN1):c.340dup (p.Ser114fs) rs886041213
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.431_432delinsAA (p.Phe144Ter) rs1114167511
NM_000244.3(MEN1):c.461-1G>A rs1064793672
NM_000244.3(MEN1):c.461-2A>G rs886042035
NM_000244.3(MEN1):c.482G>A (p.Gly161Asp) rs794728648
NM_000244.3(MEN1):c.544_545del (p.Leu182fs) rs1114167470
NM_000244.3(MEN1):c.545del (p.Leu182fs) rs1114167503
NM_000244.3(MEN1):c.640del (p.Gln214fs) rs1114167538
NM_000244.3(MEN1):c.643_646del (p.Thr215fs) rs794728640
NM_000244.3(MEN1):c.675G>A (p.Trp225Ter) rs886039414
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.721_724dup (p.Ala242fs) rs1114167534
NM_000244.3(MEN1):c.742_749del (p.Ile248fs) rs1114167532
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.843C>A (p.Tyr281Ter) rs1060503789
NM_000244.3(MEN1):c.85C>T (p.Arg29Ter) rs794728615
NM_000244.3(MEN1):c.927+1G>A rs398124437
NM_000244.3(MEN1):c.927+1G>C rs398124437
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_001370259.2(MEN1):c.1015C>T (p.Gln339Ter) rs1592643178
NM_001370259.2(MEN1):c.1100_1131del (p.Val367fs) rs1592640213
NM_001370259.2(MEN1):c.1154_1155dup (p.Gly386fs) rs1592640081
NM_001370259.2(MEN1):c.1252G>A (p.Asp418Asn) rs104894264
NM_001370259.2(MEN1):c.32del (p.Phe11fs) rs1592661082
NM_001370259.2(MEN1):c.355_357AAG[1] (p.Lys120del) rs794728657
NM_001370259.2(MEN1):c.39_40GC[3] (p.Ser15fs) rs1592660983
NM_001370259.2(MEN1):c.577del (p.Thr193fs) rs1592650986
NM_001370259.2(MEN1):c.655-1G>C rs1592649615
NM_001370259.2(MEN1):c.666C>A (p.Tyr222Ter) rs1555165597
NM_001370259.2(MEN1):c.719_720TG[2] (p.Ala242fs) rs1592649069
NM_001370259.2(MEN1):c.825-1_828delinsTACCTAGAGGTT rs1592646831
NM_001370259.2(MEN1):c.911del (p.Lys304fs) rs1592646226
NM_130799.2(MEN1):c.1391_1392ins13 (p.?)

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