ClinVar Miner

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

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Total variants: 79
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HGVS dbSNP
NM_000244.3(MEN1):c.1229dup (p.Asp411Glyfs) rs1114167513
NM_000244.3(MEN1):c.1267G>A (p.Asp423Asn) rs104894264
NM_000244.3(MEN1):c.1397_1404dup (p.Ala469Argfs) rs1114167531
NM_000244.3(MEN1):c.1421_1428dup (p.Gly477Serfs) rs1114167536
NM_000244.3(MEN1):c.1653_1654dup (p.Glu552Glyfs) rs1114167496
NM_000244.3(MEN1):c.1A>G (p.Met1Val) rs386134250
NM_130799.2(MEN1):c.1001_1005dup (p.Glu336Cysfs) rs1114167483
NM_130799.2(MEN1):c.1004delGinsTT (p.Arg335Leufs) rs1114167506
NM_130799.2(MEN1):c.1022G>A (p.Trp341Ter) rs1114167482
NM_130799.2(MEN1):c.1053C>G (p.Tyr351Ter) rs767078097
NM_130799.2(MEN1):c.1087_1089delGAG (p.Glu363del) rs869025185
NM_130799.2(MEN1):c.1177C>T (p.Gln393Ter) rs1060499984
NM_130799.2(MEN1):c.1224_1225insGTCC (p.Cys409Valfs) rs1114167524
NM_130799.2(MEN1):c.1243C>T (p.Arg415Ter) rs1060499974
NM_130799.2(MEN1):c.1247_1254delTCTACGAC (p.Phe416Trpfs) rs1114167542
NM_130799.2(MEN1):c.1252G>T (p.Asp418Tyr) rs104894264
NM_130799.2(MEN1):c.1269G>A (p.Trp423Ter) rs1114167533
NM_130799.2(MEN1):c.1270G>T (p.Glu424Ter) rs1114167477
NM_130799.2(MEN1):c.1306T>C (p.Trp436Arg) rs104894259
NM_130799.2(MEN1):c.1308G>T (p.Trp436Cys) rs398124435
NM_130799.2(MEN1):c.1330delC (p.Leu444Terfs) rs1114167520
NM_130799.2(MEN1):c.1348C>T (p.Gln450Ter) rs1114167509
NM_130799.2(MEN1):c.1378C>T (p.Arg460Ter) rs104894267
NM_130799.2(MEN1):c.1390delGinsCCT (p.Ala464Profs) rs1114167500
NM_130799.2(MEN1):c.1391_1392ins13 (p.?)
NM_130799.2(MEN1):c.1429G>T (p.Glu477Ter) rs863224526
NM_130799.2(MEN1):c.1464delG (p.Lys488Asnfs) rs886039420
NM_130799.2(MEN1):c.1504_1507dup (p.Gly503Glufs) rs1114167476
NM_130799.2(MEN1):c.1529_1530delCA (p.Ala510Glyfs) rs1114167522
NM_130799.2(MEN1):c.1533_1534dupGT (p.Ser512Cysfs) rs794728659
NM_130799.2(MEN1):c.1546dupC (p.Arg516Profs) rs767319284
NM_130799.2(MEN1):c.1549A>T (p.Lys517Ter) rs794728630
NM_130799.2(MEN1):c.1574delC (p.Thr525Lysfs) rs1114167514
NM_130799.2(MEN1):c.1579C>T (p.Arg527Ter) rs104894261
NM_130799.2(MEN1):c.1643_1721del79insTG (p.Gly548Valfs) rs1555163136
NM_130799.2(MEN1):c.1660C>T (p.Gln554Ter) rs794728631
NM_130799.2(MEN1):c.1665_1668delTGAG (p.Ser555Argfs) rs1114167510
NM_130799.2(MEN1):c.1666G>T (p.Glu556Ter) rs1114167501
NM_130799.2(MEN1):c.16_17delGC (p.Ala6Profs) rs1114167523
NM_130799.2(MEN1):c.1A>T (p.Met1Leu) rs386134250
NM_130799.2(MEN1):c.223delC (p.Leu75Serfs) rs1114167485
NM_130799.2(MEN1):c.237delC (p.Val80Trpfs) rs1114167486
NM_130799.2(MEN1):c.249_252delGTCT (p.Ile85Serfs) rs587776841
NM_130799.2(MEN1):c.265delC (p.Leu89Serfs) rs1114167490
NM_130799.2(MEN1):c.270T>A (p.Tyr90Ter) rs1114167527
NM_130799.2(MEN1):c.273_276delCCGC (p.Arg92Serfs) rs1114167516
NM_130799.2(MEN1):c.307delC (p.Leu103Cysfs) rs794728639
NM_130799.2(MEN1):c.322C>T (p.Arg108Ter) rs794728647
NM_130799.2(MEN1):c.336delC (p.Ser113Profs) rs1114167478
NM_130799.2(MEN1):c.340dupA (p.Ser114Lysfs) rs886041213
NM_130799.2(MEN1):c.358_360delAAG (p.Lys120del) rs794728657
NM_130799.2(MEN1):c.378delG (p.Trp126Terfs) rs1114167492
NM_130799.2(MEN1):c.402delC (p.Phe134Leufs) rs397515385
NM_130799.2(MEN1):c.415C>G (p.His139Asp) rs104894263
NM_130799.2(MEN1):c.416A>G (p.His139Arg) rs1114167515
NM_130799.2(MEN1):c.417delC (p.His139Glnfs) rs1114167540
NM_130799.2(MEN1):c.429_432delCTTCinsATT (p.Phe144Leufs) rs1114167481
NM_130799.2(MEN1):c.431_432delTCinsAA (p.Phe144Ter) rs1114167511
NM_130799.2(MEN1):c.467G>A (p.Gly156Asp) rs794728648
NM_130799.2(MEN1):c.529_530delCT (p.Leu177Valfs) rs1114167470
NM_130799.2(MEN1):c.530delT (p.Leu177Argfs) rs1114167503
NM_130799.2(MEN1):c.625delC (p.Gln209Argfs) rs1114167538
NM_130799.2(MEN1):c.628_631delACAG (p.Thr210Serfs) rs794728640
NM_130799.2(MEN1):c.660G>A (p.Trp220Ter) rs886039414
NM_130799.2(MEN1):c.682_685dup (p.Arg229Hisfs) rs1114167519
NM_130799.2(MEN1):c.697A>T (p.Lys233Ter) rs1114167499
NM_130799.2(MEN1):c.706_709dup (p.Ala237Glyfs) rs1114167534
NM_130799.2(MEN1):c.727_734delATCAACCC (p.Ile243Phefs) rs1114167532
NM_130799.2(MEN1):c.778C>T (p.Gln260Ter) rs104894266
NM_130799.2(MEN1):c.783+1G>A rs794728652
NM_130799.2(MEN1):c.784-2A>G rs1114167472
NM_130799.2(MEN1):c.828C>A (p.Tyr276Ter) rs1060503789
NM_130799.2(MEN1):c.85C>T (p.Arg29Ter) rs794728615
NM_130799.2(MEN1):c.912+1G>A rs398124437
NM_130799.2(MEN1):c.912+1G>C rs398124437
NM_130799.2(MEN1):c.959C>T (p.Pro320Leu) rs1114167469
NM_130799.2(MEN1):c.967delT (p.Tyr323Thrfs) rs1114167541
NM_130799.2(MEN1):c.969C>A (p.Tyr323Ter) rs750904332
NM_130799.2(MEN1):c.970delC (p.Leu324Trpfs) rs1114167508

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