ClinVar Miner

List of variants in gene MEN1 reported as benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 92
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HGVS dbSNP gnomAD frequency
NM_001370259.2(MEN1):c.1299T>C (p.His433=) rs540012 0.97595
NM_001370259.2(MEN1):c.1621A>G (p.Thr541Ala) rs2959656 0.89377
NM_001370259.2(MEN1):c.912+283C>T rs504195 0.89058
NC_000011.10:g.64811334T>C rs149426934 0.44068
NC_000011.10:g.64811336T>C rs143462807 0.40104
NM_001370259.2(MEN1):c.1350+103G>C rs654440 0.32314
NM_001370259.2(MEN1):c.1254C>T (p.Asp418=) rs2071313 0.30843
NC_000011.10:g.64811338T>C rs199711128 0.28237
NM_001370259.2(MEN1):c.445+183G>A rs624975 0.12188
NM_001370259.2(MEN1):c.-23-16C>G rs509606 0.11597
NM_001370259.2(MEN1):c.1621= (p.Thr541=) rs2959656 0.10623
NM_130803.3(MEN1):c.-358T>C rs7949944 0.09264
NC_000011.10:g.64811551T>C rs10897528 0.09018
NM_130799.2(MEN1):c.-844C>T rs7934756 0.08485
NC_000011.10:g.64811340T>C rs1169663422 0.07751
NM_130803.3(MEN1):c.-43C>T rs11231874 0.07542
NC_000011.10:g.64811379T>G rs147112489 0.07528
NC_000011.10:g.64811375T>G rs145617061 0.06842
NC_000011.10:g.64811383T>G rs866352161 0.03087
NM_001370259.2(MEN1):c.435C>T (p.Ser145=) rs61736636 0.02784
NM_001370259.2(MEN1):c.1299= (p.His433=) rs540012 0.02405
NM_001370259.2(MEN1):c.-23-14G>C rs886048479 0.01869
NM_001370259.2(MEN1):c.*302C>T rs1804849 0.01607
NM_130803.3(MEN1):c.-33T>A rs650277 0.01572
NC_000011.10:g.64811367T>G rs2518905 0.01480
NM_001370259.2(MEN1):c.512G>A (p.Arg171Gln) rs607969 0.01309
NM_001370259.2(MEN1):c.*307T>G rs1804848 0.00855
NM_001370259.2(MEN1):c.654+82C>T rs114202287 0.00242
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.*185C>T rs111895237 0.00133
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.-6G>A rs768088337 0.00023
NM_001370259.2(MEN1):c.*794G>A rs117705251 0.00020
NM_001370259.2(MEN1):c.762G>A (p.Leu254=) rs199909967 0.00018
NM_001370259.2(MEN1):c.1508G>A (p.Gly503Asp) rs375804228 0.00015
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.913-42G>C rs529037188 0.00013
NM_001370259.2(MEN1):c.1409C>T (p.Pro470Leu) rs750112288 0.00012
NM_001370259.2(MEN1):c.1535C>T (p.Ser512Leu) rs141679530 0.00011
NM_001370259.2(MEN1):c.339C>T (p.Ser113=) rs559635859 0.00011
NM_001370259.2(MEN1):c.1638G>A (p.Pro546=) rs368783097 0.00010
NM_001370259.2(MEN1):c.492C>T (p.Ala164=) rs146759807 0.00010
NM_001370259.2(MEN1):c.511C>T (p.Arg171Trp) rs143329068 0.00009
NM_001370259.2(MEN1):c.655-4del rs748005956 0.00009
NM_001370259.2(MEN1):c.1391C>T (p.Ala464Val) rs778728934 0.00007
NM_001370259.2(MEN1):c.1003C>A (p.Arg335=) rs371364206 0.00006
NM_001370259.2(MEN1):c.803A>G (p.Tyr268Cys) rs773500082 0.00006
NM_001370259.2(MEN1):c.563C>T (p.Pro188Leu) rs199706698 0.00005
NM_001370259.2(MEN1):c.1098A>T (p.Glu366Asp) rs149383809 0.00004
NM_001370259.2(MEN1):c.1434C>T (p.Gly478=) rs200280309 0.00004
NM_001370259.2(MEN1):c.1518C>T (p.Thr506=) rs749265222 0.00004
NM_001370259.2(MEN1):c.784-10C>T rs71526470 0.00004
NM_001370259.2(MEN1):c.1170G>A (p.Pro390=) rs587780841 0.00003
NM_001370259.2(MEN1):c.759G>A (p.Ser253=) rs201829546 0.00003
NM_001370259.2(MEN1):c.1012C>G (p.Leu338Val) rs759337318 0.00002
NM_001370259.2(MEN1):c.1050-71G>A rs919026003 0.00001
NM_001370259.2(MEN1):c.1399G>A (p.Ala467Thr) rs779589005 0.00001
NM_001370259.2(MEN1):c.784-129T>A rs536461697 0.00001
NM_001370259.2(MEN1):c.843G>C (p.Gly281=) rs562620826 0.00001
NC_000011.10:g.64811306CA[12] rs1207317757
NC_000011.10:g.64811306CA[15] rs1207317757
NC_000011.10:g.64811306CA[16] rs1207317757
NC_000011.10:g.64811306CA[17] rs1207317757
NC_000011.10:g.64811371T>G rs139163950
NC_000011.10:g.64811382_64811388del rs869164525
NC_000011.10:g.64811384_64811388del rs869164525
NM_000244.4(MEN1):c.-35A>C rs679946
NM_000244.4(MEN1):c.-35A>T rs679946
NM_001370259.2(MEN1):c.*126C>T rs138595686
NM_001370259.2(MEN1):c.1049+115A>G rs669976
NM_001370259.2(MEN1):c.1050-65T>A rs537795635
NM_001370259.2(MEN1):c.1072GAG[1] (p.Glu359del) rs1060499971
NM_001370259.2(MEN1):c.1185+18C>T rs780329058
NM_001370259.2(MEN1):c.1212C>G (p.Leu404=) rs577268289
NM_001370259.2(MEN1):c.1648G>T (p.Val550Leu) rs562257963
NM_001370259.2(MEN1):c.591C>G (p.Thr197=) rs527294715
NM_001370259.2(MEN1):c.61C>A (p.Arg21Ser) rs541476418
NM_001370259.2(MEN1):c.654+18C>T rs180737290
NM_001370259.2(MEN1):c.654+18del rs112700230
NM_001370259.2(MEN1):c.654+18dup rs112700230
NM_001370259.2(MEN1):c.655-5del rs772016629
NM_001370259.2(MEN1):c.655-5dup rs772016629
NM_001370259.2(MEN1):c.655-6C>A rs77461664
NM_001370259.2(MEN1):c.655-6C>G rs77461664
NM_001370259.2(MEN1):c.655-6C>T rs77461664
NM_001370259.2(MEN1):c.784-19TC[2] rs764290037

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