ClinVar Miner

List of variants in gene MEN1 studied for not specified

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Gene type:
ClinVar version:
Total variants: 59
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HGVS dbSNP
NM_000244.3(MEN1):c.-20G>A rs386134244
NM_000244.3(MEN1):c.-23-135G>A rs587777949
NM_000244.3(MEN1):c.-32G>C rs1021174779
NM_000244.3(MEN1):c.-35A>C rs679946
NM_000244.3(MEN1):c.-35A>T rs679946
NM_000244.3(MEN1):c.-40G>C rs552417059
NM_000244.3(MEN1):c.1018C>A (p.Arg340=) rs371364206
NM_000244.3(MEN1):c.1064+9C>T rs200517349
NM_000244.3(MEN1):c.1095C>T (p.Ile365=) rs147331514
NM_000244.3(MEN1):c.1185G>A (p.Pro395=) rs587780841
NM_000244.3(MEN1):c.119_124del (p.Val40_Leu41del) rs386134248
NM_000244.3(MEN1):c.1200+12G>A rs373609932
NM_000244.3(MEN1):c.1201-6G>A rs576193460
NM_000244.3(MEN1):c.1228C>T (p.Gln410Ter) rs864622615
NM_000244.3(MEN1):c.1311G>A (p.Leu437=) rs138770431
NM_000244.3(MEN1):c.1366-4C>T rs764408631
NM_000244.3(MEN1):c.1406del (p.Ala469fs) rs1555163858
NM_000244.3(MEN1):c.1424C>T (p.Pro475Leu) rs750112288
NM_000244.3(MEN1):c.1480C>T (p.Pro494Ser) rs587778440
NM_000244.3(MEN1):c.1494G>A (p.Pro498=) rs546721780
NM_000244.3(MEN1):c.1523G>A (p.Gly508Asp) rs375804228
NM_000244.3(MEN1):c.1624G>A (p.Val542Met) rs1057521847
NM_000244.3(MEN1):c.1636G>A (p.Ala546Thr) rs2959656
NM_000244.3(MEN1):c.1653G>A (p.Pro551=) rs368783097
NM_000244.3(MEN1):c.1815G>T (p.Leu605=) rs148825200
NM_000244.3(MEN1):c.18C>T (p.Ala6=) rs369348210
NM_000244.3(MEN1):c.1A>G (p.Met1Val) rs386134250
NM_000244.3(MEN1):c.225C>A (p.Leu75=) rs1333791405
NM_000244.3(MEN1):c.300C>G (p.Ala100=) rs773136972
NM_000244.3(MEN1):c.30G>T (p.Leu10=) rs371192390
NM_000244.3(MEN1):c.350del (p.Leu117fs) rs1555166387
NM_000244.3(MEN1):c.435C>T (p.Ser145=) rs61736636
NM_000244.3(MEN1):c.507C>T (p.Ala169=) rs146759807
NM_000244.3(MEN1):c.529G>T (p.Asp177Tyr) rs1114167494
NM_000244.3(MEN1):c.546G>A (p.Leu182=) rs146568011
NM_000244.3(MEN1):c.60G>C (p.Val20=) rs776432516
NM_000244.3(MEN1):c.612C>T (p.His204=) rs150512958
NM_000244.3(MEN1):c.659_667delinsGCCCCT (p.Val220_Arg223delinsGlyProTrp) rs386134257
NM_000244.3(MEN1):c.669+18C>T rs180737290
NM_000244.3(MEN1):c.670-4del rs748005956
NM_000244.3(MEN1):c.798+1G>A rs794728652
NM_000244.3(MEN1):c.799-19TC[2] rs764290037
NM_000244.3(MEN1):c.840-10C>G rs999121619
NM_000244.3(MEN1):c.928-4C>T rs770413697
NM_000244.3(MEN1):c.928-65_928-14del rs1555165154
NM_000244.3(MEN1):c.954T>G (p.Tyr318Ter) rs1555165128
NM_001370259.2(MEN1):c.-22C>A rs374749001
NM_001370259.2(MEN1):c.1254C>T (p.Asp418=) rs2071313
NM_001370259.2(MEN1):c.1299T>C (p.His433=) rs540012
NM_001370259.2(MEN1):c.1522C>A (p.Gln508Lys) rs386833403
NM_001370259.2(MEN1):c.1548G>A (p.Arg516=)
NM_001370259.2(MEN1):c.1621A>G (p.Thr541Ala) rs2959656
NM_001370259.2(MEN1):c.1664G>A (p.Ser555Asn) rs863224527
NM_001370259.2(MEN1):c.511C>T (p.Arg171Trp) rs143329068
NM_001370259.2(MEN1):c.512G>A (p.Arg171Gln) rs607969
NM_001370259.2(MEN1):c.563C>T (p.Pro188Leu) rs199706698
NM_001370259.2(MEN1):c.655-6C>A rs77461664
NM_001370259.2(MEN1):c.655-6C>G rs77461664
NM_001370259.2(MEN1):c.784-9G>A rs794728625

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