ClinVar Miner

List of variants in gene MEN1 reported as likely benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 136
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HGVS dbSNP
NM_000244.3(MEN1):c.60G>C (p.Val20=) rs776432516
NM_130799.2(MEN1):c.100C>T (p.Leu34=) rs771554497
NM_130799.2(MEN1):c.1020C>A (p.Ala340=) rs1060503796
NM_130799.2(MEN1):c.1026G>A (p.Ala342=) rs878855184
NM_130799.2(MEN1):c.1032G>A (p.Thr344=) rs760183888
NM_130799.2(MEN1):c.1049+9C>A rs200517349
NM_130799.2(MEN1):c.1049+9C>G rs200517349
NM_130799.2(MEN1):c.1071C>T (p.Asp357=) rs371964966
NM_130799.2(MEN1):c.1074G>A (p.Glu358=) rs776834299
NM_130799.2(MEN1):c.1080C>T (p.Ile360=) rs147331514
NM_130799.2(MEN1):c.1083C>T (p.Tyr361=) rs1168237114
NM_130799.2(MEN1):c.1131G>A (p.Lys377=) rs1555164674
NM_130799.2(MEN1):c.1149G>A (p.Leu383=) rs1555164667
NM_130799.2(MEN1):c.114C>G (p.Ser38=) rs1252317486
NM_130799.2(MEN1):c.1155G>A (p.Ala385=) rs201091135
NM_130799.2(MEN1):c.115T>C (p.Leu39=) rs863224438
NM_130799.2(MEN1):c.1167G>C (p.Arg389=) rs1194388602
NM_130799.2(MEN1):c.1170G>C (p.Pro390=) rs587780841
NM_130799.2(MEN1):c.1186-6G>A rs576193460
NM_130799.2(MEN1):c.1186-7C>T rs587780842
NM_130799.2(MEN1):c.1186-8delT rs1555164452
NM_130799.2(MEN1):c.1186-9C>T rs1555164455
NM_130799.2(MEN1):c.1191C>T (p.Thr397=) rs1166154585
NM_130799.2(MEN1):c.1203T>C (p.Gly401=) rs878855187
NM_130799.2(MEN1):c.1206C>A (p.Ser402=) rs770037856
NM_130799.2(MEN1):c.1206C>T (p.Ser402=) rs770037856
NM_130799.2(MEN1):c.1230C>T (p.Phe410=) rs878855188
NM_130799.2(MEN1):c.1251C>T (p.Tyr417=) rs751481164
NM_130799.2(MEN1):c.1287G>A (p.Thr429=) rs376598079
NM_130799.2(MEN1):c.1287G>T (p.Thr429=) rs376598079
NM_130799.2(MEN1):c.1314C>G (p.Thr438=) rs897481809
NM_130799.2(MEN1):c.132G>T (p.Val44=) rs1555166691
NM_130799.2(MEN1):c.1351-10A>G rs757569943
NM_130799.2(MEN1):c.1351-4C>T rs764408631
NM_130799.2(MEN1):c.1351-6G>A rs1555164004
NM_130799.2(MEN1):c.1378C>A (p.Arg460=) rs104894267
NM_130799.2(MEN1):c.1386C>A (p.Ala462=) rs771827808
NM_130799.2(MEN1):c.1386C>G (p.Ala462=) rs771827808
NM_130799.2(MEN1):c.1386C>T (p.Ala462=) rs771827808
NM_130799.2(MEN1):c.1392G>A (p.Ala464=) rs754445482
NM_130799.2(MEN1):c.1395C>T (p.Ala465=) rs748820252
NM_130799.2(MEN1):c.1401C>T (p.Ala467=) rs878855190
NM_130799.2(MEN1):c.1404G>A (p.Glu468=) rs755734265
NM_130799.2(MEN1):c.1410G>A (p.Pro470=) rs1060503795
NM_130799.2(MEN1):c.1428G>C (p.Arg476=) rs1555163730
NM_130799.2(MEN1):c.1443G>A (p.Arg481=) rs864622641
NM_130799.2(MEN1):c.1458G>A (p.Glu486=) rs1413990417
NM_130799.2(MEN1):c.1473G>A (p.Glu491=) rs1555163642
NM_130799.2(MEN1):c.1479G>A (p.Pro493=) rs546721780
NM_130799.2(MEN1):c.1482G>A (p.Pro494=) rs773363654
NM_130799.2(MEN1):c.1494A>T (p.Pro498=) rs1037335560
NM_130799.2(MEN1):c.1518C>T (p.Thr506=) rs749265222
NM_130799.2(MEN1):c.153C>T (p.Asn51=) rs1555166669
NM_130799.2(MEN1):c.1545C>A (p.Pro515=) rs1555163491
NM_130799.2(MEN1):c.1578C>A (p.Ala526=) rs767655504
NM_130799.2(MEN1):c.15C>A (p.Ala5=) rs757821521
NM_130799.2(MEN1):c.1608G>A (p.Gln536=) rs1055457298
NM_130799.2(MEN1):c.162C>T (p.Ile54=) rs1555166662
NM_130799.2(MEN1):c.1635G>A (p.Pro545=) rs1349729840
NM_130799.2(MEN1):c.1641G>A (p.Glu547=) rs1555163295
NM_130799.2(MEN1):c.1656T>C (p.Thr552=) rs143423552
NM_130799.2(MEN1):c.165T>A (p.Pro55=) rs1060503790
NM_130799.2(MEN1):c.1692G>T (p.Leu564=) rs367581776
NM_130799.2(MEN1):c.1695G>T (p.Leu565=) rs767677287
NM_130799.2(MEN1):c.1701C>T (p.Ala567=) rs757417271
NM_130799.2(MEN1):c.1740G>C (p.Thr580=) rs1114167530
NM_130799.2(MEN1):c.1749G>C (p.Ser583=) rs765105348
NM_130799.2(MEN1):c.1758G>A (p.Gln586=) rs759563305
NM_130799.2(MEN1):c.1764G>A (p.Lys588=) rs373669288
NM_130799.2(MEN1):c.1779C>T (p.Ser593=) rs1157546350
NM_130799.2(MEN1):c.1800G>T (p.Leu600=) rs148825200
NM_130799.2(MEN1):c.1806C>T (p.Phe602=) rs1060503794
NM_130799.2(MEN1):c.183C>A (p.Leu61=) rs1555166622
NM_130799.2(MEN1):c.18C>T (p.Ala6=) rs369348210
NM_130799.2(MEN1):c.195C>A (p.Pro65=) rs1438097332
NM_130799.2(MEN1):c.201C>T (p.Pro67=) rs1060503791
NM_130799.2(MEN1):c.240G>T (p.Val80=) rs1555166545
NM_130799.2(MEN1):c.282C>T (p.Thr94=) rs760442763
NM_130799.2(MEN1):c.300C>G (p.Ala100=) rs773136972
NM_130799.2(MEN1):c.303C>T (p.Val101=) rs1463347315
NM_130799.2(MEN1):c.307C>T (p.Leu103=) rs1313314117
NM_130799.2(MEN1):c.330G>C (p.Gly110=) rs1060503792
NM_130799.2(MEN1):c.333T>C (p.Gly111=) rs1555166432
NM_130799.2(MEN1):c.339C>T (p.Ser113=) rs559635859
NM_130799.2(MEN1):c.345T>C (p.Arg115=) rs748948131
NM_130799.2(MEN1):c.369T>C (p.Asp123=) rs1555166369
NM_130799.2(MEN1):c.375A>C (p.Ile125=) rs184896922
NM_130799.2(MEN1):c.375A>T (p.Ile125=) rs184896922
NM_130799.2(MEN1):c.426C>T (p.Ser142=) rs753252650
NM_130799.2(MEN1):c.441C>T (p.Ile147=) rs878855193
NM_130799.2(MEN1):c.446-9C>A rs1371109251
NM_130799.2(MEN1):c.465C>T (p.Ser155=) rs936786553
NM_130799.2(MEN1):c.471G>A (p.Val157=) rs878855194
NM_130799.2(MEN1):c.474C>T (p.Ala158=) rs772526802
NM_130799.2(MEN1):c.48C>T (p.Ile16=) rs1060503797
NM_130799.2(MEN1):c.492C>T (p.Ala164=) rs146759807
NM_130799.2(MEN1):c.513G>C (p.Arg171=) rs560870111
NM_130799.2(MEN1):c.525C>T (p.Leu175=) rs200155578
NM_130799.2(MEN1):c.531G>A (p.Leu177=) rs146568011
NM_130799.2(MEN1):c.54C>T (p.Asp18=) rs1316973259
NM_130799.2(MEN1):c.570G>A (p.Gly190=) rs547249181
NM_130799.2(MEN1):c.585G>A (p.Glu195=) rs864622177
NM_130799.2(MEN1):c.609C>T (p.Asn203=) rs749844029
NM_130799.2(MEN1):c.621G>A (p.Arg207=) rs779966911
NM_130799.2(MEN1):c.639C>T (p.Ala213=) rs746067825
NM_130799.2(MEN1):c.654+10C>T rs921850475
NM_130799.2(MEN1):c.654+9C>A rs202134234
NM_130799.2(MEN1):c.654+9C>G rs202134234
NM_130799.2(MEN1):c.654+9C>T rs202134234
NM_130799.2(MEN1):c.655-4delT rs748005956
NM_130799.2(MEN1):c.655-6C>A rs77461664
NM_130799.2(MEN1):c.655-6C>G rs77461664
NM_130799.2(MEN1):c.685C>T (p.Arg229Cys) rs754378887
NM_130799.2(MEN1):c.711G>A (p.Ala237=) rs144677807
NM_130799.2(MEN1):c.720G>T (p.Val240=) rs1555165534
NM_130799.2(MEN1):c.726C>T (p.Ala242=) rs1198651608
NM_130799.2(MEN1):c.729C>T (p.Ile243=) rs1353237754
NM_130799.2(MEN1):c.753C>T (p.Thr251=) rs763326062
NM_130799.2(MEN1):c.759G>T (p.Ser253=) rs201829546
NM_130799.2(MEN1):c.762G>A (p.Leu254=) rs199909967
NM_130799.2(MEN1):c.783+7G>A rs1060503793
NM_130799.2(MEN1):c.784-10C>T rs71526470
NM_130799.2(MEN1):c.819G>T (p.Leu273=) rs748369241
NM_130799.2(MEN1):c.825-8T>C rs1555165330
NM_130799.2(MEN1):c.828C>T (p.Tyr276=) rs1060503789
NM_130799.2(MEN1):c.837C>T (p.Ala279=) rs762092675
NM_130799.2(MEN1):c.843G>C (p.Gly281=) rs562620826
NM_130799.2(MEN1):c.856C>T (p.Leu286=) rs542321016
NM_130799.2(MEN1):c.87A>C (p.Arg29=) rs1198070818
NM_130799.2(MEN1):c.909C>T (p.His303=) rs878855200
NM_130799.2(MEN1):c.921C>T (p.Ala307=) rs1060503788
NM_130799.2(MEN1):c.963C>T (p.Tyr321=) rs1555165094
NM_130799.2(MEN1):c.978C>T (p.Gly326=) rs1555165071
NM_130799.2(MEN1):c.993C>T (p.Asn331=) rs370176253
NM_130799.2(MEN1):c.999T>C (p.Asn333=) rs763133775
NM_130804.2(MEN1):c.928-4C>T rs770413697

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