ClinVar Miner

List of variants in gene MEN1 reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 28
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HGVS dbSNP
NM_000244.3(MEN1):c.1018C>A (p.Arg340=) rs371364206
NM_000244.3(MEN1):c.60G>C (p.Val20=) rs776432516
NM_000244.3(MEN1):c.669+18C>T rs180737290
NM_130799.2(MEN1):c.-20G>A rs386134244
NM_130799.2(MEN1):c.-22C>A rs374749001
NM_130799.2(MEN1):c.-32G>C rs1021174779
NM_130799.2(MEN1):c.-40G>C rs552417059
NM_130799.2(MEN1):c.1049+9C>T rs200517349
NM_130799.2(MEN1):c.1080C>T (p.Ile360=) rs147331514
NM_130799.2(MEN1):c.1170G>A (p.Pro390=) rs587780841
NM_130799.2(MEN1):c.1185+12G>A rs373609932
NM_130799.2(MEN1):c.1186-6G>A rs576193460
NM_130799.2(MEN1):c.1296G>A (p.Leu432=) rs138770431
NM_130799.2(MEN1):c.1351-4C>T rs764408631
NM_130799.2(MEN1):c.1409C>T (p.Pro470Leu) rs750112288
NM_130799.2(MEN1):c.1479G>A (p.Pro493=) rs546721780
NM_130799.2(MEN1):c.1508G>A (p.Gly503Asp) rs375804228
NM_130799.2(MEN1):c.1609G>A (p.Val537Met) rs1057521847
NM_130799.2(MEN1):c.1800G>T (p.Leu600=) rs148825200
NM_130799.2(MEN1):c.18C>T (p.Ala6=) rs369348210
NM_130799.2(MEN1):c.225C>A (p.Leu75=) rs1333791405
NM_130799.2(MEN1):c.300C>G (p.Ala100=) rs773136972
NM_130799.2(MEN1):c.30G>T (p.Leu10=) rs371192390
NM_130799.2(MEN1):c.492C>T (p.Ala164=) rs146759807
NM_130799.2(MEN1):c.531G>A (p.Leu177=) rs146568011
NM_130799.2(MEN1):c.655-6C>G rs77461664
NM_130799.2(MEN1):c.825-10C>G rs999121619
NM_130804.2(MEN1):c.928-4C>T rs770413697

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