ClinVar Miner

List of variants in gene MEN1 reported as uncertain significance for not provided

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Gene type:
ClinVar version:
Total variants: 76
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HGVS dbSNP gnomAD frequency
NM_001370259.2(MEN1):c.-6G>A rs768088337 0.00023
NM_001370259.2(MEN1):c.1351-4C>T rs764408631 0.00014
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.511C>T (p.Arg171Trp) rs143329068 0.00009
NM_001370259.2(MEN1):c.1185+12G>A rs373609932 0.00008
NM_001370259.2(MEN1):c.1391C>T (p.Ala464Val) rs778728934 0.00007
NM_001370259.2(MEN1):c.685C>T (p.Arg229Cys) rs754378887 0.00007
NM_001370259.2(MEN1):c.803A>G (p.Tyr268Cys) rs773500082 0.00006
NM_000244.4(MEN1):c.-24+3G>A rs892783738 0.00004
NM_001370259.2(MEN1):c.1098A>T (p.Glu366Asp) rs149383809 0.00004
NM_001370259.2(MEN1):c.774G>C (p.Gln258His) rs374659656 0.00004
NM_001370259.2(MEN1):c.941G>A (p.Arg314Gln) rs771645621 0.00004
NM_001370259.2(MEN1):c.1170G>A (p.Pro390=) rs587780841 0.00003
NM_001370259.2(MEN1):c.566A>G (p.Asn189Ser) rs587780844 0.00003
NM_001370259.2(MEN1):c.94C>T (p.Pro32Ser) rs773089218 0.00003
NM_001370259.2(MEN1):c.1012C>G (p.Leu338Val) rs759337318 0.00002
NM_001370259.2(MEN1):c.299C>T (p.Ala100Val) rs998337367 0.00002
NM_001370259.2(MEN1):c.989G>A (p.Arg330His) rs373135175 0.00002
NM_001370259.2(MEN1):c.1099G>A (p.Val367Ile) rs758404089 0.00001
NM_001370259.2(MEN1):c.1169C>T (p.Pro390Leu) rs761102084 0.00001
NM_001370259.2(MEN1):c.1379G>A (p.Arg460Gln) rs200035619 0.00001
NM_001370259.2(MEN1):c.1397A>T (p.Glu466Val) rs1352053477 0.00001
NM_001370259.2(MEN1):c.1516A>C (p.Thr506Pro) rs1060499994 0.00001
NM_001370259.2(MEN1):c.1580G>A (p.Arg527Gln) rs1085307502 0.00001
NM_001370259.2(MEN1):c.1589A>C (p.Glu530Ala) rs1565636654 0.00001
NM_001370259.2(MEN1):c.1701C>T (p.Ala567=) rs757417271 0.00001
NM_001370259.2(MEN1):c.189C>G (p.Phe63Leu) rs137880635 0.00001
NM_001370259.2(MEN1):c.344G>A (p.Arg115His) rs1114167507 0.00001
NM_001370259.2(MEN1):c.349C>T (p.Leu117=) rs1941984891 0.00001
NM_001370259.2(MEN1):c.526G>T (p.Ala176Ser) rs376872829 0.00001
NM_001370259.2(MEN1):c.539A>T (p.Asp180Val) rs1064794683 0.00001
NM_001370259.2(MEN1):c.635A>G (p.Asn212Ser) rs1438685841 0.00001
NM_001370259.2(MEN1):c.640G>A (p.Gly214Ser) rs781493730 0.00001
NM_001370259.2(MEN1):c.980A>G (p.Tyr327Cys) rs377403837 0.00001
NM_001370259.2(MEN1):c.-7_-1dup (p.Met1fs) rs758960344
NM_001370259.2(MEN1):c.1054_1056del (p.Asn352del) rs2136111453
NM_001370259.2(MEN1):c.1064G>A (p.Arg355Gln) rs1114167474
NM_001370259.2(MEN1):c.1231G>T (p.Ala411Ser) rs757179911
NM_001370259.2(MEN1):c.1241T>G (p.Leu414Arg) rs727504013
NM_001370259.2(MEN1):c.1255G>A (p.Gly419Ser)
NM_001370259.2(MEN1):c.1341T>G (p.Phe447Leu) rs1325598637
NM_001370259.2(MEN1):c.1364T>A (p.Val455Glu) rs878855189
NM_001370259.2(MEN1):c.1367G>A (p.Arg456His) rs372468697
NM_001370259.2(MEN1):c.1376G>A (p.Ser459Asn) rs1565638856
NM_001370259.2(MEN1):c.1398G>T (p.Glu466Asp) rs990566024
NM_001370259.2(MEN1):c.1435C>T (p.Arg479Trp) rs1941551498
NM_001370259.2(MEN1):c.1522C>G (p.Gln508Glu) rs386833403
NM_001370259.2(MEN1):c.1630C>T (p.Pro544Ser) rs1387157979
NM_001370259.2(MEN1):c.1648G>C (p.Val550Leu) rs562257963
NM_001370259.2(MEN1):c.1667AGA[1] (p.Lys557del) rs794728661
NM_001370259.2(MEN1):c.1710_1715del (p.Ile570_Ser572delinsMet) rs794728646
NM_001370259.2(MEN1):c.1747T>G (p.Ser583Ala) rs483352685
NM_001370259.2(MEN1):c.227C>A (p.Thr76Asn) rs886039752
NM_001370259.2(MEN1):c.281C>T (p.Thr94Ile) rs1565651820
NM_001370259.2(MEN1):c.320C>T (p.Pro107Leu)
NM_001370259.2(MEN1):c.341G>T (p.Ser114Ile) rs386833404
NM_001370259.2(MEN1):c.445+29C>T rs1421726469
NM_001370259.2(MEN1):c.524T>A (p.Leu175His) rs2136155339
NM_001370259.2(MEN1):c.526G>A (p.Ala176Thr) rs376872829
NM_001370259.2(MEN1):c.537G>C (p.Glu179Asp) rs1555165811
NM_001370259.2(MEN1):c.537G>T (p.Glu179Asp) rs1555165811
NM_001370259.2(MEN1):c.586G>T (p.Val196Phe)
NM_001370259.2(MEN1):c.617G>A (p.Arg206His) rs1565647825
NM_001370259.2(MEN1):c.61C>A (p.Arg21Ser) rs541476418
NM_001370259.2(MEN1):c.655-6C>A rs77461664
NM_001370259.2(MEN1):c.655-6C>T rs77461664
NM_001370259.2(MEN1):c.655A>G (p.Ser219Gly)
NM_001370259.2(MEN1):c.740T>C (p.Ile247Thr) rs1043531053
NM_001370259.2(MEN1):c.763G>A (p.Glu255Lys) rs104894268
NM_001370259.2(MEN1):c.763G>C (p.Glu255Gln) rs104894268
NM_001370259.2(MEN1):c.809T>C (p.Leu270Pro) rs1592647333
NM_001370259.2(MEN1):c.830C>T (p.Pro277Leu) rs1060499973
NM_001370259.2(MEN1):c.910A>G (p.Lys304Glu) rs1941774610
NM_001370259.2(MEN1):c.982C>G (p.His328Asp) rs794727882
NM_001370259.2(MEN1):c.9G>A (p.Leu3=)

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