ClinVar Miner

List of variants in gene MEN1 reported as pathogenic for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 76
Download table as spreadsheet
HGVS dbSNP
NM_000244.3(MEN1):c.105dup (p.Leu36fs) rs1555166711
NM_000244.3(MEN1):c.1064+1G>C rs1114167489
NM_000244.3(MEN1):c.1102_1104del (p.Glu368del) rs869025185
NM_000244.3(MEN1):c.1125del (p.Asp375fs) rs794728658
NM_000244.3(MEN1):c.1189G>T (p.Glu397Ter) rs772588551
NM_000244.3(MEN1):c.1207C>T (p.Gln403Ter) rs886039418
NM_000244.3(MEN1):c.1213C>T (p.Gln405Ter) rs886039419
NM_000244.3(MEN1):c.1228C>T (p.Gln410Ter) rs864622615
NM_000244.3(MEN1):c.1258C>T (p.Arg420Ter) rs1060499974
NM_000244.3(MEN1):c.1262dup (p.Tyr422fs) rs1555164305
NM_000244.3(MEN1):c.1267G>C (p.Asp423His) rs104894264
NM_000244.3(MEN1):c.1284G>A (p.Trp428Ter) rs1114167533
NM_000244.3(MEN1):c.1321T>A (p.Trp441Arg) rs104894259
NM_000244.3(MEN1):c.1322G>A (p.Trp441Ter) rs104894260
NM_000244.3(MEN1):c.1323G>T (p.Trp441Cys) rs398124435
NM_000244.3(MEN1):c.1339C>T (p.Gln447Ter) rs794728654
NM_000244.3(MEN1):c.1351del (p.Arg451fs) rs886041746
NM_000244.3(MEN1):c.1356del (p.Phe452fs) rs794728643
NM_000244.3(MEN1):c.1365+1_1365+11del rs764570645
NM_000244.3(MEN1):c.1393C>T (p.Arg465Ter) rs104894267
NM_000244.3(MEN1):c.1393delinsACATAGT (p.Arg465delinsThrTer) rs1064796889
NM_000244.3(MEN1):c.1444G>T (p.Glu482Ter) rs863224526
NM_000244.3(MEN1):c.1444dup (p.Glu482fs) rs886041214
NM_000244.3(MEN1):c.1479del (p.Lys493fs) rs886039420
NM_000244.3(MEN1):c.147dup (p.Val50fs) rs794728638
NM_000244.3(MEN1):c.1502del (p.Lys501fs) rs1565637724
NM_000244.3(MEN1):c.1520dup (p.Leu509fs) rs1555163591
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.1563dup (p.Lys522fs) rs761695866
NM_000244.3(MEN1):c.1594C>T (p.Arg532Ter) rs104894261
NM_000244.3(MEN1):c.1605del (p.Gly536fs) rs886039421
NM_000244.3(MEN1):c.1617_1633dup (p.Pro545fs) rs794728660
NM_000244.3(MEN1):c.164dup (p.Thr56fs) rs794728656
NM_000244.3(MEN1):c.1666del (p.Leu556fs) rs794728645
NM_000244.3(MEN1):c.1675C>T (p.Gln559Ter) rs794728631
NM_000244.3(MEN1):c.1700dup (p.Glu568fs) rs398124436
NM_000244.3(MEN1):c.1702G>T (p.Glu568Ter) rs794728632
NM_000244.3(MEN1):c.197_201GCCCC[3] (p.Asp70fs) rs730882136
NM_000244.3(MEN1):c.207del (p.Asp70fs) rs1057517902
NM_000244.3(MEN1):c.211_212del (p.Pro71fs) rs386134251
NM_000244.3(MEN1):c.249_252del (p.Ile85fs) rs587776841
NM_000244.3(MEN1):c.292C>T (p.Arg98Ter) rs886039413
NM_000244.3(MEN1):c.307del (p.Leu103fs) rs794728639
NM_000244.3(MEN1):c.322C>T (p.Arg108Ter) rs794728647
NM_000244.3(MEN1):c.332dup (p.Val112fs) rs1555166435
NM_000244.3(MEN1):c.340dup (p.Ser114fs) rs886041213
NM_000244.3(MEN1):c.355_357AAG[1] (p.Lys120del) rs794728657
NM_000244.3(MEN1):c.402del (p.Phe134fs) rs397515385
NM_000244.3(MEN1):c.421C>T (p.Gln141Ter) rs886039553
NM_000244.3(MEN1):c.432del (p.Phe144fs) rs1064793613
NM_000244.3(MEN1):c.461-1G>A rs1064793672
NM_000244.3(MEN1):c.461-2A>C rs886042035
NM_000244.3(MEN1):c.505_506delinsT (p.Ala169fs) rs886041634
NM_000244.3(MEN1):c.511C>T (p.Gln171Ter) rs1565648511
NM_000244.3(MEN1):c.55del (p.Val19fs) rs794728655
NM_000244.3(MEN1):c.57_58insT (p.Val20fs) rs794728636
NM_000244.3(MEN1):c.643_646del (p.Thr215fs) rs794728640
NM_000244.3(MEN1):c.669+1G>T rs794728622
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.787C>T (p.Gln263Ter) rs886039416
NM_000244.3(MEN1):c.796C>T (p.Gln266Ter) rs1057520733
NM_000244.3(MEN1):c.799-1G>C rs1555165377
NM_000244.3(MEN1):c.799-9G>A rs794728625
NM_000244.3(MEN1):c.79_88del (p.Leu27fs) rs794728637
NM_000244.3(MEN1):c.843C>A (p.Tyr281Ter) rs1060503789
NM_000244.3(MEN1):c.927+1G>A rs398124437
NM_000244.3(MEN1):c.927+2T>C rs1555165256
NM_000244.3(MEN1):c.928-1G>A rs1057518572
NM_000244.3(MEN1):c.938C>A (p.Ser313Ter) rs1565644366
NM_000244.3(MEN1):c.951C>G (p.Tyr317Ter) rs386134260
NM_000244.3(MEN1):c.958G>T (p.Asp320Tyr) rs747851909
NM_000244.3(MEN1):c.965_972del (p.His322fs) rs794728641
NM_000244.3(MEN1):c.984C>G (p.Tyr328Ter) rs750904332

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.