ClinVar Miner

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

Included ClinVar conditions (122):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 100
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HGVS dbSNP
MEN1, 1-BP DEL, 7773C
MEN1, 1-BP INS, 1657C
MEN1, 12-BP DEL, NT1466
MEN1, 3-BP DEL, 2641GAA
MEN1, 4-BP DEL, 4480CAGT
MEN1, 6-BP INS, NT879
NC_000011.10:g.(?_64803514)_(64804816_?)del
NC_000011.10:g.(?_64803514)_(64810132_?)del
NC_000011.10:g.(?_64809659)_(64810115_?)del
NM_000244.3(MEN1):c.1077C>A (p.Cys359Ter) rs104894265
NM_000244.3(MEN1):c.1208dup (p.Ser404Glufs) rs1555164430
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.1669A>T (p.Thr557Ser) rs121913035
NM_000244.3(MEN1):c.211_212delCC (p.Pro71Alafs) rs386134251
NM_000244.3(MEN1):c.566T>A (p.Val189Glu) rs104894262
NM_000244.3(MEN1):c.608G>A (p.Trp203Ter) rs104894258
NM_000244.3(MEN1):c.778G>A (p.Glu260Lys) rs104894268
NM_130799.2(MEN1):c.1022G>A (p.Trp341Ter) rs1114167482
NM_130799.2(MEN1):c.1024delG (p.Ala342Argfs) rs1555164986
NM_130799.2(MEN1):c.1049+1G>A rs1114167489
NM_130799.2(MEN1):c.1050-2A>T
NM_130799.2(MEN1):c.1087_1089delGAG (p.Glu363del) rs869025185
NM_130799.2(MEN1):c.1103C>A (p.Ala368Asp) rs1555164707
NM_130799.2(MEN1):c.1174G>T (p.Glu392Ter) rs772588551
NM_130799.2(MEN1):c.1174delG (p.Glu392Serfs) rs386134247
NM_130799.2(MEN1):c.1213C>T (p.Gln405Ter) rs864622615
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.1306T>A (p.Trp436Arg) rs104894259
NM_130799.2(MEN1):c.1307G>A (p.Trp436Ter) rs104894260
NM_130799.2(MEN1):c.1334delG (p.Gly445Alafs)
NM_130799.2(MEN1):c.1350+1_1350+11delGTGAGGGACAG rs764570645
NM_130799.2(MEN1):c.1351-2_*132del
NM_130799.2(MEN1):c.1351_*820del
NM_130799.2(MEN1):c.1375_1382delAGCCGAGA (p.Ser459Glyfs) rs1555163883
NM_130799.2(MEN1):c.1378C>T (p.Arg460Ter) rs104894267
NM_130799.2(MEN1):c.1382_1404dup (p.Glu469Argfs) rs1555163780
NM_130799.2(MEN1):c.1412G>A (p.Trp471Ter) rs1060499991
NM_130799.2(MEN1):c.1429G>T (p.Glu477Ter) rs863224526
NM_130799.2(MEN1):c.142delC (p.Leu48Trpfs) rs1555166681
NM_130799.2(MEN1):c.1473delG (p.Glu491Aspfs) rs1555163646
NM_130799.2(MEN1):c.1535C>G (p.Ser512Ter) rs141679530
NM_130799.2(MEN1):c.1546delC (p.Arg516Glyfs) rs767319284
NM_130799.2(MEN1):c.1546dupC (p.Arg516Profs) rs767319284
NM_130799.2(MEN1):c.1579C>T (p.Arg527Ter) rs104894261
NM_130799.2(MEN1):c.1664G>A (p.Ser555Asn) rs863224527
NM_130799.2(MEN1):c.1674dup (p.Lys559Glufs)
NM_130799.2(MEN1):c.168delC (p.Asn57Thrfs) rs1060499990
NM_130799.2(MEN1):c.196_200dupAGCCC (p.Asp70Profs) rs1555166609
NM_130799.2(MEN1):c.206_207insGCCCC (p.Asp70Profs) rs730882136
NM_130799.2(MEN1):c.231C>G (p.Tyr77Ter) rs1555166567
NM_130799.2(MEN1):c.237delC (p.Val80Trpfs) rs1114167486
NM_130799.2(MEN1):c.249_252delGTCT (p.Ile85Serfs) rs587776841
NM_130799.2(MEN1):c.252_253insTT (p.Ile85Leufs) rs386134253
NM_130799.2(MEN1):c.280_284dupACCGC (p.Gln96Profs) rs1555166494
NM_130799.2(MEN1):c.307delC (p.Leu103Cysfs) rs794728639
NM_130799.2(MEN1):c.317_318delAT (p.Tyr106Serfs) rs1555166466
NM_130799.2(MEN1):c.318T>A (p.Tyr106Ter) rs1060499987
NM_130799.2(MEN1):c.322C>T (p.Arg108Ter) rs794728647
NM_130799.2(MEN1):c.322_323insT (p.Arg108Leufs)
NM_130799.2(MEN1):c.323delG (p.Arg108Glnfs) rs878855191
NM_130799.2(MEN1):c.346G>T (p.Glu116Ter) rs1060499992
NM_130799.2(MEN1):c.358A>T (p.Lys120Ter) rs878855192
NM_130799.2(MEN1):c.358_360delAAG (p.Lys120del) rs794728657
NM_130799.2(MEN1):c.378G>A (p.Trp126Ter) rs1555166365
NM_130799.2(MEN1):c.386delT (p.Leu129Profs)
NM_130799.2(MEN1):c.3G>A (p.Met1Ile) rs786204242
NM_130799.2(MEN1):c.402delC (p.Phe134Leufs) rs397515385
NM_130799.2(MEN1):c.415C>G (p.His139Asp) rs104894263
NM_130799.2(MEN1):c.421C>T (p.Gln141Ter) rs886039553
NM_130799.2(MEN1):c.478G>C (p.Ala160Pro)
NM_130799.2(MEN1):c.503T>C (p.Leu168Pro) rs386134256
NM_130799.2(MEN1):c.548G>A (p.Trp183Ter) rs794728650
NM_130799.2(MEN1):c.563_564delCC (p.Pro188Glnfs) rs1555165756
NM_130799.2(MEN1):c.594G>A (p.Trp198Ter) rs104894257
NM_130799.2(MEN1):c.625C>T (p.Gln209Ter)
NM_130799.2(MEN1):c.628_631delACAG (p.Thr210Serfs) rs794728640
NM_130799.2(MEN1):c.633delC (p.Asn212Metfs) rs878855196
NM_130799.2(MEN1):c.654+1G>A
NM_130799.2(MEN1):c.654+1G>T rs794728622
NM_130799.2(MEN1):c.659G>A (p.Trp220Ter)
NM_130799.2(MEN1):c.65T>G (p.Leu22Arg) rs104894256
NM_130799.2(MEN1):c.681C>A (p.Tyr227Ter) rs778921501
NM_130799.2(MEN1):c.739_745delATTGACC (p.Ile247Cysfs) rs1555165503
NM_130799.2(MEN1):c.772C>T (p.Gln258Ter) rs886039416
NM_130799.2(MEN1):c.778C>T (p.Gln260Ter) rs104894266
NM_130799.2(MEN1):c.781C>T (p.Gln261Ter) rs1057520733
NM_130799.2(MEN1):c.783+1G>A rs794728652
NM_130799.2(MEN1):c.784-9G>A rs794728625
NM_130799.2(MEN1):c.823delA (p.Arg275Glyfs) rs1555165360
NM_130799.2(MEN1):c.824+1G>A
NM_130799.2(MEN1):c.824+1G>T rs1060499976
NM_130799.2(MEN1):c.85C>T (p.Arg29Ter) rs794728615
NM_130799.2(MEN1):c.913-2A>G rs1114167498
NM_130799.2(MEN1):c.940_1050-227del rs1555164870
NM_130799.2(MEN1):c.969C>A (p.Tyr323Ter) rs750904332
NM_130799.2(MEN1):c.969C>G (p.Tyr323Ter) rs750904332
NM_130804.2:c.749delC

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