ClinVar Miner

List of variants in gene MEN1 reported as uncertain significance for Hereditary cancer-predisposing syndrome

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Total variants: 61
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HGVS dbSNP
NM_000244.3(MEN1):c.1004G>A (p.Arg335His) rs373135175
NM_000244.3(MEN1):c.100C>A (p.Leu34Met) rs771554497
NM_000244.3(MEN1):c.1015G>A (p.Val339Met) rs1555165027
NM_000244.3(MEN1):c.1022_1024dup (p.Glu341dup) rs1114167529
NM_000244.3(MEN1):c.1075T>C (p.Cys359Arg) rs371503251
NM_000244.3(MEN1):c.108_122del (p.Leu37_Leu41del) rs1555166695
NM_000244.3(MEN1):c.1093A>T (p.Ile365Phe) rs1114167475
NM_000244.3(MEN1):c.1113A>T (p.Glu371Asp) rs149383809
NM_000244.3(MEN1):c.1114G>A (p.Val372Ile) rs758404089
NM_000244.3(MEN1):c.1138C>G (p.Leu380Val) rs1211957325
NM_000244.3(MEN1):c.1142T>G (p.Leu381Arg) rs1114167471
NM_000244.3(MEN1):c.1172G>A (p.Gly391Asp) rs761360623
NM_000244.3(MEN1):c.1184C>T (p.Pro395Leu) rs761102084
NM_000244.3(MEN1):c.1192C>G (p.Gln398Glu) rs1060499984
NM_000244.3(MEN1):c.1274T>G (p.Ile425Ser) rs1114167539
NM_000244.3(MEN1):c.1285G>A (p.Glu429Lys) rs1114167477
NM_000244.3(MEN1):c.1325C>T (p.Ala442Val) rs1555164188
NM_000244.3(MEN1):c.1366-4C>T rs764408631
NM_000244.3(MEN1):c.1369C>T (p.Arg457Trp) rs863224810
NM_000244.3(MEN1):c.1370G>C (p.Arg457Pro) rs775922507
NM_000244.3(MEN1):c.1411G>A (p.Glu471Lys) rs1114167497
NM_000244.3(MEN1):c.1449C>T (p.Gly483=) rs200280309
NM_000244.3(MEN1):c.1521G>C (p.Lys507Asn) rs774296730
NM_000244.3(MEN1):c.1537C>A (p.Gln513Lys) rs386833403
NM_000244.3(MEN1):c.154C>T (p.Arg52Cys) rs1555166664
NM_000244.3(MEN1):c.1550C>T (p.Ser517Leu) rs141679530
NM_000244.3(MEN1):c.1556C>G (p.Pro519Arg) rs753022747
NM_000244.3(MEN1):c.1561C>T (p.Arg521Trp)
NM_000244.3(MEN1):c.1609G>T (p.Gly537Cys) rs587780843
NM_000244.3(MEN1):c.1624G>A (p.Val542Met) rs1057521847
NM_000244.3(MEN1):c.1633C>T (p.Pro545Ser) rs745404679
NM_000244.3(MEN1):c.16G>T (p.Ala6Ser) rs966793401
NM_000244.3(MEN1):c.1714G>C (p.Ala572Pro) rs1555163185
NM_000244.3(MEN1):c.194C>A (p.Pro65His) rs1114167484
NM_000244.3(MEN1):c.210C>A (p.Asp70Glu) rs150308912
NM_000244.3(MEN1):c.311C>A (p.Ser104Tyr) rs1114167512
NM_000244.3(MEN1):c.317A>G (p.Tyr106Cys) rs1555166469
NM_000244.3(MEN1):c.326A>G (p.Glu109Gly) rs1555166447
NM_000244.3(MEN1):c.329G>C (p.Gly110Ala) rs1389398299
NM_000244.3(MEN1):c.32T>C (p.Phe11Ser) rs1114167535
NM_000244.3(MEN1):c.344G>A (p.Arg115His) rs1114167507
NM_000244.3(MEN1):c.433A>C (p.Ser145Arg) rs778932605
NM_000244.3(MEN1):c.442A>G (p.Thr148Ala) rs1114167537
NM_000244.3(MEN1):c.461-3C>A rs377461506
NM_000244.3(MEN1):c.491T>C (p.Phe164Ser) rs1555165861
NM_000244.3(MEN1):c.541G>T (p.Ala181Ser) rs376872829
NM_000244.3(MEN1):c.578C>T (p.Pro193Leu) rs199706698
NM_000244.3(MEN1):c.615C>T (p.Gly205=) rs1114167479
NM_000244.3(MEN1):c.61C>A (p.Arg21Ser) rs541476418
NM_000244.3(MEN1):c.653_654delinsAA (p.Ala218Glu) rs1114167518
NM_000244.3(MEN1):c.670-4del rs748005956
NM_000244.3(MEN1):c.773C>T (p.Ser258Leu) rs386134259
NM_000244.3(MEN1):c.789G>C (p.Gln263His) rs374659656
NM_000244.3(MEN1):c.800A>G (p.Lys267Arg) rs1555165373
NM_000244.3(MEN1):c.842A>G (p.Tyr281Cys) rs1555165327
NM_000244.3(MEN1):c.849G>A (p.Met283Ile) rs794728626
NM_000244.3(MEN1):c.898C>T (p.Arg300Trp) rs1046929915
NM_000244.3(MEN1):c.94C>T (p.Pro32Ser) rs773089218
NM_000244.3(MEN1):c.956G>A (p.Arg319Gln) rs771645621
NM_000244.3(MEN1):c.959A>T (p.Asp320Val) rs1114167487
NM_000244.3:c.563C>T

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