ClinVar Miner

List of variants in gene MEN1 reported as uncertain significance for adrenal gland disease

Included ClinVar conditions (122):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 235
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HGVS dbSNP
NM_000244.3(MEN1):c.108_122dup (p.Leu41_Gly42insLeuSerLeuValLeu) rs1555166695
NM_000244.3(MEN1):c.1406_1411dup (p.Ala470_Glu471insAlaAla) rs1555163821
NM_000244.3(MEN1):c.526C>T (p.Arg176Trp) rs143329068
NM_000244.3(MEN1):c.578C>T (p.Pro193Leu) rs199706698
NM_000244.3(MEN1):c.659_667delTGGCTGAGCinsGCCCCT (p.Val220_Arg223delinsGlyProTrp) rs386134257
NM_000244.3(MEN1):c.669+18C>T rs180737290
NM_000244.3(MEN1):c.791_796dup (p.Gln265_Gln266insLeuGln) rs1555165485
NM_130799.2(MEN1):c.-2C>T rs653534
NM_130799.2(MEN1):c.1003C>T (p.Arg335Trp) rs371364206
NM_130799.2(MEN1):c.1004G>A (p.Arg335Gln) rs764998893
NM_130799.2(MEN1):c.1009G>C (p.Ala337Pro) rs2071312
NM_130799.2(MEN1):c.100C>A (p.Leu34Met) rs771554497
NM_130799.2(MEN1):c.1012C>G (p.Leu338Val) rs759337318
NM_130799.2(MEN1):c.1024G>C (p.Ala342Pro) rs776561706
NM_130799.2(MEN1):c.1025C>T (p.Ala342Val) rs377715802
NM_130799.2(MEN1):c.1029C>G (p.Asp343Glu) rs878855185
NM_130799.2(MEN1):c.1031C>T (p.Thr344Met) rs1259681826
NM_130799.2(MEN1):c.1060T>C (p.Cys354Arg) rs371503251
NM_130799.2(MEN1):c.1061G>A (p.Cys354Tyr) rs904261642
NM_130799.2(MEN1):c.1063C>A (p.Arg355=) rs863224807
NM_130799.2(MEN1):c.1063C>T (p.Arg355Trp) rs863224807
NM_130799.2(MEN1):c.1075_1077delGAG (p.Glu359del) rs1060499971
NM_130799.2(MEN1):c.1092C>A (p.Phe364Leu) rs863224808
NM_130799.2(MEN1):c.1098A>T (p.Glu366Asp) rs149383809
NM_130799.2(MEN1):c.1099G>A (p.Val367Ile) rs758404089
NM_130799.2(MEN1):c.1123C>G (p.Leu375Val) rs1211957325
NM_130799.2(MEN1):c.1130A>G (p.Lys377Arg) rs766075737
NM_130799.2(MEN1):c.1139C>G (p.Ala380Gly)
NM_130799.2(MEN1):c.1154C>T (p.Ala385Val) rs1298484645
NM_130799.2(MEN1):c.1157G>A (p.Gly386Asp) rs761360623
NM_130799.2(MEN1):c.1158C>T (p.Gly386=) rs794728653
NM_130799.2(MEN1):c.1159G>A (p.Glu387Lys) rs773978650
NM_130799.2(MEN1):c.1165C>T (p.Arg389Trp) rs566593066
NM_130799.2(MEN1):c.1166G>A (p.Arg389Gln) rs775267651
NM_130799.2(MEN1):c.1169C>G (p.Pro390Arg) rs761102084
NM_130799.2(MEN1):c.1169C>T (p.Pro390Leu) rs761102084
NM_130799.2(MEN1):c.1177C>G (p.Gln393Glu) rs1060499984
NM_130799.2(MEN1):c.1181G>C (p.Ser394Thr) rs934222398
NM_130799.2(MEN1):c.1185+4A>G rs863224809
NM_130799.2(MEN1):c.1185+5A>G
NM_130799.2(MEN1):c.119_124delTGCTGG (p.Val40_Leu41del) rs386134248
NM_130799.2(MEN1):c.1202G>T (p.Gly401Val) rs878855186
NM_130799.2(MEN1):c.1207G>A (p.Ala403Thr) rs746135199
NM_130799.2(MEN1):c.1210C>T (p.Leu404Phe) rs1060499989
NM_130799.2(MEN1):c.1219C>G (p.Pro407Ala) rs1060499985
NM_130799.2(MEN1):c.1226G>A (p.Cys409Tyr) rs1060499988
NM_130799.2(MEN1):c.1231G>A (p.Ala411Thr) rs757179911
NM_130799.2(MEN1):c.1231G>T (p.Ala411Ser) rs757179911
NM_130799.2(MEN1):c.1244G>A (p.Arg415Gln) rs1446518998
NM_130799.2(MEN1):c.1244G>C (p.Arg415Pro) rs1446518998
NM_130799.2(MEN1):c.1267T>C (p.Trp423Arg) rs1555164270
NM_130799.2(MEN1):c.1279A>C (p.Ser427Arg) rs1555164245
NM_130799.2(MEN1):c.1294_1302del9 (p.Leu432_Val434del) rs1555164218
NM_130799.2(MEN1):c.1308G>T (p.Trp436Cys) rs398124435
NM_130799.2(MEN1):c.1333G>T (p.Gly445Cys) rs1555164153
NM_130799.2(MEN1):c.1337G>A (p.Arg446His) rs1555164143
NM_130799.2(MEN1):c.133G>A (p.Glu45Lys) rs1114167491
NM_130799.2(MEN1):c.1350+4_1350+6delAGG
NM_130799.2(MEN1):c.1350+5G>A
NM_130799.2(MEN1):c.1350+6G>A
NM_130799.2(MEN1):c.1351-8T>G rs751932519
NM_130799.2(MEN1):c.1354C>T (p.Arg452Trp) rs863224810
NM_130799.2(MEN1):c.1355G>A (p.Arg452Gln)
NM_130799.2(MEN1):c.135G>C (p.Glu45Asp) rs778670301
NM_130799.2(MEN1):c.1364T>A (p.Val455Glu) rs878855189
NM_130799.2(MEN1):c.1367G>A (p.Arg456His) rs372468697
NM_130799.2(MEN1):c.1379G>C (p.Arg460Pro) rs200035619
NM_130799.2(MEN1):c.1389G>C (p.Glu463Asp) rs1555163863
NM_130799.2(MEN1):c.1391C>T (p.Ala464Val) rs778728934
NM_130799.2(MEN1):c.1393_1407delGCCGAGGCCGAGGAG (p.Ala465_Glu469del) rs1064792907
NM_130799.2(MEN1):c.1397A>T (p.Glu466Val) rs1352053477
NM_130799.2(MEN1):c.1398G>T (p.Glu466Asp) rs990566024
NM_130799.2(MEN1):c.1399G>A (p.Ala467Thr) rs779589005
NM_130799.2(MEN1):c.1406A>C (p.Glu469Ala)
NM_130799.2(MEN1):c.1407_1421delGCCGTGGGGCGAGGA (p.Pro470_Glu474del) rs1033303123
NM_130799.2(MEN1):c.1416C>T (p.Gly472=) rs764509990
NM_130799.2(MEN1):c.1429G>C (p.Glu477Gln) rs863224526
NM_130799.2(MEN1):c.1431A>T (p.Glu477Asp) rs863224811
NM_130799.2(MEN1):c.1436G>C (p.Arg479Pro) rs1555163716
NM_130799.2(MEN1):c.1453C>T (p.Arg485Trp) rs1254459338
NM_130799.2(MEN1):c.1459T>C (p.Ser487Pro) rs1057427859
NM_130799.2(MEN1):c.1465C>T (p.Pro489Ser) rs587778440
NM_130799.2(MEN1):c.146C>T (p.Ala49Val) rs1555166674
NM_130799.2(MEN1):c.1478C>T (p.Pro493Leu) rs766604600
NM_130799.2(MEN1):c.1481C>T (p.Pro494Leu) rs1060499993
NM_130799.2(MEN1):c.1506G>C (p.Lys502Asn) rs774296730
NM_130799.2(MEN1):c.1516A>C (p.Thr506Pro) rs1060499994
NM_130799.2(MEN1):c.1517C>T (p.Thr506Ile)
NM_130799.2(MEN1):c.1519G>T (p.Gly507Cys) rs1423874145
NM_130799.2(MEN1):c.1522C>A (p.Gln508Lys) rs386833403
NM_130799.2(MEN1):c.1526G>T (p.Gly509Val) rs769355346
NM_130799.2(MEN1):c.1535C>T (p.Ser512Leu) rs141679530
NM_130799.2(MEN1):c.1540C>A (p.Pro514Thr) rs150202288
NM_130799.2(MEN1):c.1540C>T (p.Pro514Ser)
NM_130799.2(MEN1):c.1541C>G (p.Pro514Arg) rs753022747
NM_130799.2(MEN1):c.1541C>T (p.Pro514Leu) rs753022747
NM_130799.2(MEN1):c.1543C>T (p.Pro515Ser)
NM_130799.2(MEN1):c.1546C>G (p.Arg516Gly)
NM_130799.2(MEN1):c.1561A>T (p.Thr521Ser)
NM_130799.2(MEN1):c.1562C>T (p.Thr521Ile)
NM_130799.2(MEN1):c.1564G>C (p.Val522Leu) rs1060499983
NM_130799.2(MEN1):c.1567G>A (p.Ala523Thr) rs760683615
NM_130799.2(MEN1):c.1567G>C (p.Ala523Pro) rs760683615
NM_130799.2(MEN1):c.1583G>A (p.Gly528Asp) rs1555163392
NM_130799.2(MEN1):c.1594G>T (p.Gly532Cys) rs587780843
NM_130799.2(MEN1):c.1618C>T (p.Pro540Ser) rs745404679
NM_130799.2(MEN1):c.1636_1638dupCCG (p.Pro546_Glu547insPro) rs774350463
NM_130799.2(MEN1):c.1637C>T (p.Pro546Leu) rs779413959
NM_130799.2(MEN1):c.1640A>G (p.Glu547Gly) rs914488914
NM_130799.2(MEN1):c.16G>T (p.Ala6Ser) rs966793401
NM_130799.2(MEN1):c.175C>G (p.Pro59Ala) rs1352823623
NM_130799.2(MEN1):c.1761G>A (p.Met587Ile) rs1555163058
NM_130799.2(MEN1):c.1765_1767delAAG (p.Lys589del)
NM_130799.2(MEN1):c.1777T>C (p.Ser593Pro)
NM_130799.2(MEN1):c.177C>T (p.Pro59=) rs749001511
NM_130799.2(MEN1):c.1798_1799delCT (p.Leu600Valfs) rs1555163017
NM_130799.2(MEN1):c.1826G>T (p.Gly609Val) rs1186858249
NM_130799.2(MEN1):c.184A>C (p.Thr62Pro) rs1555166619
NM_130799.2(MEN1):c.189C>G (p.Phe63Leu) rs137880635
NM_130799.2(MEN1):c.193C>A (p.Pro65Thr) rs1235900915
NM_130799.2(MEN1):c.202G>A (p.Ala68Thr)
NM_130799.2(MEN1):c.203C>T (p.Ala68Val)
NM_130799.2(MEN1):c.205C>T (p.Pro69Ser) rs1060499995
NM_130799.2(MEN1):c.215C>A (p.Pro72His)
NM_130799.2(MEN1):c.236C>G (p.Pro79Arg) rs1555166557
NM_130799.2(MEN1):c.244G>C (p.Asp82His) rs1419086083
NM_130799.2(MEN1):c.246C>G (p.Asp82Glu) rs1238113583
NM_130799.2(MEN1):c.266_286del21 (p.Leu89_Ala95del) rs1064792906
NM_130799.2(MEN1):c.267C>G (p.Leu89=) rs1060499972
NM_130799.2(MEN1):c.269A>G (p.Tyr90Cys)
NM_130799.2(MEN1):c.281C>T (p.Thr94Ile)
NM_130799.2(MEN1):c.299C>T (p.Ala100Val) rs998337367
NM_130799.2(MEN1):c.322C>G (p.Arg108Gly)
NM_130799.2(MEN1):c.326A>G (p.Glu109Gly) rs1555166447
NM_130799.2(MEN1):c.327A>C (p.Glu109Asp) rs773976527
NM_130799.2(MEN1):c.343C>G (p.Arg115Gly)
NM_130799.2(MEN1):c.344G>A (p.Arg115His) rs1114167507
NM_130799.2(MEN1):c.352G>A (p.Val118Met) rs1060499975
NM_130799.2(MEN1):c.361G>A (p.Val121Ile) rs863224812
NM_130799.2(MEN1):c.361G>T (p.Val121Phe)
NM_130799.2(MEN1):c.38T>G (p.Leu13Arg)
NM_130799.2(MEN1):c.398A>G (p.Tyr133Cys) rs1555166357
NM_130799.2(MEN1):c.403A>C (p.Lys135Gln) rs121913034
NM_130799.2(MEN1):c.409C>T (p.Arg137Trp)
NM_130799.2(MEN1):c.418A>T (p.Ile140Phe) rs376510601
NM_130799.2(MEN1):c.446-3C>A rs377461506
NM_130799.2(MEN1):c.458A>T (p.Asp153Val)
NM_130799.2(MEN1):c.466G>A (p.Gly156Ser)
NM_130799.2(MEN1):c.467G>A (p.Gly156Asp) rs794728648
NM_130799.2(MEN1):c.469G>A (p.Val157Met) rs1555165872
NM_130799.2(MEN1):c.473C>A (p.Ala158Asp) rs794728617
NM_130799.2(MEN1):c.473C>T (p.Ala158Val)
NM_130799.2(MEN1):c.485T>C (p.Val162Ala) rs748648909
NM_130799.2(MEN1):c.491C>T (p.Ala164Val)
NM_130799.2(MEN1):c.494G>A (p.Cys165Tyr) rs1057521111
NM_130799.2(MEN1):c.49G>A (p.Asp17Asn) rs1399824473
NM_130799.2(MEN1):c.502C>G (p.Leu168Val) rs1555165846
NM_130799.2(MEN1):c.512G>A (p.Arg171Gln) rs607969
NM_130799.2(MEN1):c.526G>T (p.Ala176Ser) rs376872829
NM_130799.2(MEN1):c.537_538delGGinsTT (p.Glu179_Asp180delinsAspTyr) rs1555165809
NM_130799.2(MEN1):c.554T>C (p.Val185Ala) rs764847812
NM_130799.2(MEN1):c.566A>G (p.Asn189Ser) rs587780844
NM_130799.2(MEN1):c.568G>A (p.Gly190Arg) rs1555165742
NM_130799.2(MEN1):c.569G>A (p.Gly190Glu) rs878855195
NM_130799.2(MEN1):c.597C>A (p.His199Gln) rs150512958
NM_130799.2(MEN1):c.617G>A (p.Arg206His)
NM_130799.2(MEN1):c.618C>T (p.Arg206=) rs1555165717
NM_130799.2(MEN1):c.61C>G (p.Arg21Gly) rs541476418
NM_130799.2(MEN1):c.627G>C (p.Gln209His)
NM_130799.2(MEN1):c.629C>G (p.Thr210Arg) rs756287855
NM_130799.2(MEN1):c.632T>G (p.Val211Gly)
NM_130799.2(MEN1):c.634A>G (p.Asn212Asp) rs1060499980
NM_130799.2(MEN1):c.635A>G (p.Asn212Ser) rs1438685841
NM_130799.2(MEN1):c.640G>A (p.Gly214Ser) rs781493730
NM_130799.2(MEN1):c.643G>A (p.Val215Met) rs794728621
NM_130799.2(MEN1):c.652C>T (p.Arg218Trp) rs794728620
NM_130799.2(MEN1):c.655-5C>G rs752563214
NM_130799.2(MEN1):c.655-6C>G rs77461664
NM_130799.2(MEN1):c.655-6_655-4delCCT rs1555165623
NM_130799.2(MEN1):c.655-7C>A rs771297371
NM_130799.2(MEN1):c.660G>T (p.Trp220Cys)
NM_130799.2(MEN1):c.665A>C (p.Tyr222Ser) rs1555165601
NM_130799.2(MEN1):c.682A>G (p.Met228Val) rs1060499982
NM_130799.2(MEN1):c.686G>A (p.Arg229His) rs878855197
NM_130799.2(MEN1):c.694C>T (p.Arg232Cys) rs1225847249
NM_130799.2(MEN1):c.702G>A (p.Met234Ile) rs1448041546
NM_130799.2(MEN1):c.710C>T (p.Ala237Val) rs760289964
NM_130799.2(MEN1):c.71C>T (p.Ala24Val) rs1328062930
NM_130799.2(MEN1):c.722G>A (p.Cys241Tyr) rs794728624
NM_130799.2(MEN1):c.736T>G (p.Ser246Ala) rs1175283759
NM_130799.2(MEN1):c.739A>G (p.Ile247Val) rs1555165508
NM_130799.2(MEN1):c.74C>T (p.Ala25Val)
NM_130799.2(MEN1):c.754G>C (p.Asp252His)
NM_130799.2(MEN1):c.754G>T (p.Asp252Tyr) rs770368608
NM_130799.2(MEN1):c.758C>G (p.Ser253Trp) rs386134259
NM_130799.2(MEN1):c.758C>T (p.Ser253Leu) rs386134259
NM_130799.2(MEN1):c.763G>C (p.Glu255Gln) rs104894268
NM_130799.2(MEN1):c.766C>T (p.Leu256Phe) rs878855198
NM_130799.2(MEN1):c.772C>G (p.Gln258Glu)
NM_130799.2(MEN1):c.774G>C (p.Gln258His) rs374659656
NM_130799.2(MEN1):c.784-10C>A rs71526470
NM_130799.2(MEN1):c.784-15_784-14delTC rs764290037
NM_130799.2(MEN1):c.785A>G (p.Lys262Arg) rs1555165373
NM_130799.2(MEN1):c.801C>G (p.Leu267=)
NM_130799.2(MEN1):c.803A>G (p.Tyr268Cys) rs773500082
NM_130799.2(MEN1):c.805G>A (p.Asp269Asn) rs878855199
NM_130799.2(MEN1):c.811G>A (p.Gly271Arg)
NM_130799.2(MEN1):c.825-10C>G rs999121619
NM_130799.2(MEN1):c.827A>G (p.Tyr276Cys) rs1555165327
NM_130799.2(MEN1):c.830C>A (p.Pro277His) rs1060499973
NM_130799.2(MEN1):c.830C>T (p.Pro277Leu) rs1060499973
NM_130799.2(MEN1):c.869A>C (p.Glu290Ala) rs1213891703
NM_130799.2(MEN1):c.880G>A (p.Gly294Ser)
NM_130799.2(MEN1):c.883C>T (p.Arg295Trp) rs1046929915
NM_130799.2(MEN1):c.884G>A (p.Arg295Gln) rs1397110438
NM_130799.2(MEN1):c.892C>G (p.Pro298Ala) rs1555165268
NM_130799.2(MEN1):c.913G>A (p.Gly305Ser) rs1555165146
NM_130799.2(MEN1):c.92A>G (p.Glu31Gly) rs1060499977
NM_130799.2(MEN1):c.92A>T (p.Glu31Val) rs1060499977
NM_130799.2(MEN1):c.932C>T (p.Thr311Ile)
NM_130799.2(MEN1):c.941G>A (p.Arg314Gln) rs771645621
NM_130799.2(MEN1):c.94C>T (p.Pro32Ser) rs773089218
NM_130799.2(MEN1):c.952A>G (p.Ile318Val)
NM_130799.2(MEN1):c.955T>G (p.Tyr319Asp) rs1555165101
NM_130799.2(MEN1):c.964A>G (p.Met322Val) rs1555165089
NM_130799.2(MEN1):c.964A>T (p.Met322Leu) rs1555165089
NM_130799.2(MEN1):c.966G>A (p.Met322Ile)
NM_130799.2(MEN1):c.974C>A (p.Ala325Asp) rs370840265
NM_130799.2(MEN1):c.980A>G (p.Tyr327Cys)
NM_130799.2(MEN1):c.982C>A (p.His328Asn)
NM_130799.2(MEN1):c.982C>G (p.His328Asp) rs794727882
NM_130799.2(MEN1):c.988C>T (p.Arg330Cys)
NM_130799.2(MEN1):c.989G>A (p.Arg330His) rs373135175
NM_130799.2(MEN1):c.989G>C (p.Arg330Pro) rs373135175
NM_130799.2(MEN1):c.989G>T (p.Arg330Leu) rs373135175

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