ClinVar Miner

List of variants in gene MEN1 reported by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 76
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HGVS dbSNP gnomAD frequency
NM_001370259.2(MEN1):c.1254C>T (p.Asp418=) rs2071313 0.30843
NM_001370259.2(MEN1):c.435C>T (p.Ser145=) rs61736636 0.02784
NM_001370259.2(MEN1):c.-23-14G>C rs886048479 0.01869
NM_001370259.2(MEN1):c.512G>A (p.Arg171Gln) rs607969 0.01309
NM_001370259.2(MEN1):c.597C>T (p.His199=) rs150512958 0.00181
NM_001370259.2(MEN1):c.-20G>A rs386134244 0.00158
NM_001370259.2(MEN1):c.1296G>A (p.Leu432=) rs138770431 0.00119
NM_001370259.2(MEN1):c.30G>T (p.Leu10=) rs371192390 0.00111
NM_001370259.2(MEN1):c.-22C>A rs374749001 0.00073
NM_001370259.2(MEN1):c.1049+9C>T rs200517349 0.00048
NM_001370259.2(MEN1):c.18C>T (p.Ala6=) rs369348210 0.00039
NM_001370259.2(MEN1):c.*16G>A rs140924477 0.00029
NM_001370259.2(MEN1):c.-6G>A rs768088337 0.00023
NM_001370259.2(MEN1):c.1080C>T (p.Ile360=) rs147331514 0.00016
NM_001370259.2(MEN1):c.1351-4C>T rs764408631 0.00014
NM_001370259.2(MEN1):c.1506G>C (p.Lys502Asn) rs774296730 0.00014
NM_001370259.2(MEN1):c.1409C>T (p.Pro470Leu) rs750112288 0.00012
NM_001370259.2(MEN1):c.1618C>T (p.Pro540Ser) rs745404679 0.00012
NM_001370259.2(MEN1):c.1535C>T (p.Ser512Leu) rs141679530 0.00011
NM_001370259.2(MEN1):c.1638G>A (p.Pro546=) rs368783097 0.00010
NM_001370259.2(MEN1):c.1692G>T (p.Leu564=) rs367581776 0.00007
NM_001370259.2(MEN1):c.685C>T (p.Arg229Cys) rs754378887 0.00007
NM_001370259.2(MEN1):c.1003C>A (p.Arg335=) rs371364206 0.00006
NM_001370259.2(MEN1):c.1764G>A (p.Lys588=) rs373669288 0.00006
NM_001370259.2(MEN1):c.563C>T (p.Pro188Leu) rs199706698 0.00005
NM_001370259.2(MEN1):c.1401C>T (p.Ala467=) rs878855190 0.00004
NM_001370259.2(MEN1):c.1518C>T (p.Thr506=) rs749265222 0.00004
NM_001370259.2(MEN1):c.531G>A (p.Leu177=) rs146568011 0.00004
NM_001370259.2(MEN1):c.1071C>T (p.Asp357=) rs371964966 0.00003
NM_001370259.2(MEN1):c.1479G>A (p.Pro493=) rs546721780 0.00003
NM_001370259.2(MEN1):c.754G>T (p.Asp252Tyr) rs770368608 0.00003
NM_001370259.2(MEN1):c.808C>T (p.Leu270=) rs371556177 0.00003
NM_001370259.2(MEN1):c.115T>C (p.Leu39=) rs863224438 0.00002
NM_001370259.2(MEN1):c.1185+4A>G rs863224809 0.00002
NM_001370259.2(MEN1):c.299C>T (p.Ala100Val) rs998337367 0.00002
NM_001370259.2(MEN1):c.352G>A (p.Val118Met) rs1060499975 0.00002
NM_001370259.2(MEN1):c.654+9C>T rs202134234 0.00002
NM_001370259.2(MEN1):c.883C>T (p.Arg295Trp) rs1046929915 0.00002
NM_001370259.2(MEN1):c.1287G>A (p.Thr429=) rs376598079 0.00001
NM_001370259.2(MEN1):c.1589A>C (p.Glu530Ala) rs1565636654 0.00001
NM_001370259.2(MEN1):c.1608G>A (p.Gln536=) rs1055457298 0.00001
NM_001370259.2(MEN1):c.1656T>C (p.Thr552=) rs143423552 0.00001
NM_001370259.2(MEN1):c.177C>G (p.Pro59=) rs749001511 0.00001
NM_001370259.2(MEN1):c.189C>G (p.Phe63Leu) rs137880635 0.00001
NM_001370259.2(MEN1):c.300C>G (p.Ala100=) rs773136972 0.00001
NM_001370259.2(MEN1):c.345T>C (p.Arg115=) rs748948131 0.00001
NM_001370259.2(MEN1):c.839T>C (p.Leu280Ser) rs368619946 0.00001
NM_001370259.2(MEN1):c.843G>C (p.Gly281=) rs562620826 0.00001
NM_001370259.2(MEN1):c.*407C>T
NM_001370259.2(MEN1):c.-10G>A
NM_001370259.2(MEN1):c.-13_-7dup rs1217276136
NM_001370259.2(MEN1):c.-18C>T
NM_001370259.2(MEN1):c.-23-11T>G
NM_001370259.2(MEN1):c.-23-24T>A
NM_001370259.2(MEN1):c.-23-29G>C
NM_001370259.2(MEN1):c.1050-3C>G
NM_001370259.2(MEN1):c.1119C>A (p.Pro373=) rs535417698
NM_001370259.2(MEN1):c.1170G>C (p.Pro390=) rs587780841
NM_001370259.2(MEN1):c.1190C>T (p.Thr397Ile) rs1941628720
NM_001370259.2(MEN1):c.1251C>T (p.Tyr417=) rs751481164
NM_001370259.2(MEN1):c.1376G>A (p.Ser459Asn) rs1565638856
NM_001370259.2(MEN1):c.1494A>T (p.Pro498=) rs1037335560
NM_001370259.2(MEN1):c.1533G>C (p.Val511=)
NM_001370259.2(MEN1):c.1667AGA[1] (p.Lys557del) rs794728661
NM_001370259.2(MEN1):c.202_206dup (p.Asp70fs) rs730882136
NM_001370259.2(MEN1):c.205C>T (p.Pro69Ser) rs1060499995
NM_001370259.2(MEN1):c.237C>T (p.Pro79=) rs1592659200
NM_001370259.2(MEN1):c.406G>C (p.Asp136His) rs1941979334
NM_001370259.2(MEN1):c.446-7T>C rs2136160148
NM_001370259.2(MEN1):c.60G>C (p.Val20=) rs776432516
NM_001370259.2(MEN1):c.654+18C>T rs180737290
NM_001370259.2(MEN1):c.655-5del rs772016629
NM_001370259.2(MEN1):c.655-6C>G rs77461664
NM_001370259.2(MEN1):c.655-6C>T rs77461664
NM_001370259.2(MEN1):c.682A>G (p.Met228Val) rs1060499982
NM_001370259.2(MEN1):c.909C>T (p.His303=) rs878855200

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