Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.35732756C>ACA405426045KMT2Bn.513C>A
c.6141C>A (p.Asp2047Glu)
c.3748C>A (n.3748C>A)
c.1425C>A (p.Asp475Glu)
n.1360C>A
c.1428C>A (p.Asp476Glu)
c.5749C>A
c.6207C>A (p.Asp2069Glu)
c.704+427C>A (n.704+427C>A)
c.3529C>A
c.5931C>A (p.Asp1977Glu)
c.5643C>A (p.Asp1881Glu)
c.3171C>A (p.Asp1057Glu)
19g.35732756C>GCA405426046KMT2Bn.513C>G
c.6141C>G (p.Asp2047Glu)
c.3748C>G (n.3748C>G)
c.1425C>G (p.Asp475Glu)
n.1360C>G
c.1428C>G (p.Asp476Glu)
c.5749C>G
c.6207C>G (p.Asp2069Glu)
c.704+427C>G (n.704+427C>G)
c.3529C>G
c.5931C>G (p.Asp1977Glu)
c.5643C>G (p.Asp1881Glu)
c.3171C>G (p.Asp1057Glu)
ClinVar dbSNP
19g.35732756C>TCA507308758KMT2Bn.513C>T
c.6141C>T (p.Asp2047=)
c.3748C>T (n.3748C>T)
c.1425C>T (p.Asp475=)
n.1360C>T
c.1428C>T (p.Asp476=)
c.5749C>T
c.6207C>T (p.Asp2069=)
c.704+427C>T (n.704+427C>T)
c.3529C>T
c.5931C>T (p.Asp1977=)
c.5643C>T (p.Asp1881=)
c.3171C>T (p.Asp1057=)
gnomAD v4
19g.35732757A>CCA405426049KMT2Bn.514A>C
c.6142A>C (p.Ser2048Arg)
c.3749A>C (n.3749A>C)
c.1426A>C (p.Ser476Arg)
n.1361A>C
c.1429A>C (p.Ser477Arg)
c.5750A>C
c.6208A>C (p.Ser2070Arg)
c.704+428A>C (n.704+428A>C)
c.3530A>C
c.5932A>C (p.Ser1978Arg)
c.5644A>C (p.Ser1882Arg)
c.3172A>C (p.Ser1058Arg)
19g.35732757A>GCA405426047KMT2Bn.514A>G
c.6142A>G (p.Ser2048Gly)
c.3749A>G (n.3749A>G)
c.1426A>G (p.Ser476Gly)
n.1361A>G
c.1429A>G (p.Ser477Gly)
c.5750A>G
c.6208A>G (p.Ser2070Gly)
c.704+428A>G (n.704+428A>G)
c.3530A>G
c.5932A>G (p.Ser1978Gly)
c.5644A>G (p.Ser1882Gly)
c.3172A>G (p.Ser1058Gly)
19g.35732757A>TCA405426048KMT2Bn.514A>T
c.6142A>T (p.Ser2048Cys)
c.3749A>T (n.3749A>T)
c.1426A>T (p.Ser476Cys)
n.1361A>T
c.1429A>T (p.Ser477Cys)
c.5750A>T
c.6208A>T (p.Ser2070Cys)
c.704+428A>T (n.704+428A>T)
c.3530A>T
c.5932A>T (p.Ser1978Cys)
c.5644A>T (p.Ser1882Cys)
c.3172A>T (p.Ser1058Cys)
19g.35732759_35732762delCA2573156247KMT2Bn.516_519del
c.6144_6147del (p.Ser2048ArgfsTer20)
c.3751_3754del (n.3751_3754del)
c.1428_1431del (p.Ser476ArgfsTer20)
n.1363_1366del
c.1431_1434del (p.Ser477ArgfsTer20)
c.5752_5755del
c.6210_6213del (p.Ser2070ArgfsTer20)
c.704+430_704+433del (n.704+430_704+433del)
c.3532_3535del
c.5934_5937del (p.Ser1978ArgfsTer20)
c.5646_5649del (p.Ser1882ArgfsTer20)
c.3174_3177del (p.Ser1058ArgfsTer20)
ClinVar dbSNP
19g.35732758G>ACA405426050KMT2Bn.515G>A
c.6143G>A (p.Ser2048Asn)
c.3750G>A (n.3750G>A)
c.1427G>A (p.Ser476Asn)
n.1362G>A
c.1430G>A (p.Ser477Asn)
c.5751G>A
c.6209G>A (p.Ser2070Asn)
c.704+429G>A (n.704+429G>A)
c.3531G>A
c.5933G>A (p.Ser1978Asn)
c.5645G>A (p.Ser1882Asn)
c.3173G>A (p.Ser1058Asn)
dbSNP gnomAD v2 gnomAD v4
19g.35732758G>CCA405426051KMT2Bn.515G>C
c.6143G>C (p.Ser2048Thr)
c.3750G>C (n.3750G>C)
c.1427G>C (p.Ser476Thr)
n.1362G>C
c.1430G>C (p.Ser477Thr)
c.5751G>C
c.6209G>C (p.Ser2070Thr)
c.704+429G>C (n.704+429G>C)
c.3531G>C
c.5933G>C (p.Ser1978Thr)
c.5645G>C (p.Ser1882Thr)
c.3173G>C (p.Ser1058Thr)
19g.35732758G=CA2333794492KMT2Bn.515G=
c.6143G= (p.Ser2048=)
c.3750G= (n.3750G=)
c.1427G= (p.Ser476=)
n.1362G=
c.1430G= (p.Ser477=)
c.5751G=
c.6209G= (p.Ser2070=)
c.704+429G= (n.704+429G=)
c.3531G=
c.5933G= (p.Ser1978=)
c.5645G= (p.Ser1882=)
c.3173G= (p.Ser1058=)
19g.35732758G>TCA405426052KMT2Bn.515G>T
c.6143G>T (p.Ser2048Ile)
c.3750G>T (n.3750G>T)
c.1427G>T (p.Ser476Ile)
n.1362G>T
c.1430G>T (p.Ser477Ile)
c.5751G>T
c.6209G>T (p.Ser2070Ile)
c.704+429G>T (n.704+429G>T)
c.3531G>T
c.5933G>T (p.Ser1978Ile)
c.5645G>T (p.Ser1882Ile)
c.3173G>T (p.Ser1058Ile)
19g.35732759T>ACA405426053KMT2Bn.516T>A
c.6144T>A (p.Ser2048Arg)
c.3751T>A (n.3751T>A)
c.1428T>A (p.Ser476Arg)
n.1363T>A
c.1431T>A (p.Ser477Arg)
c.5752T>A
c.6210T>A (p.Ser2070Arg)
c.704+430T>A (n.704+430T>A)
c.3532T>A
c.5934T>A (p.Ser1978Arg)
c.5646T>A (p.Ser1882Arg)
c.3174T>A (p.Ser1058Arg)
19g.35732759T>CCA507308768KMT2Bn.516T>C
c.6144T>C (p.Ser2048=)
c.3751T>C (n.3751T>C)
c.1428T>C (p.Ser476=)
n.1363T>C
c.1431T>C (p.Ser477=)
c.5752T>C
c.6210T>C (p.Ser2070=)
c.704+430T>C (n.704+430T>C)
c.3532T>C
c.5934T>C (p.Ser1978=)
c.5646T>C (p.Ser1882=)
c.3174T>C (p.Ser1058=)
gnomAD v4
19g.35732759T>GCA405426054KMT2Bn.516T>G
c.6144T>G (p.Ser2048Arg)
c.3751T>G (n.3751T>G)
c.1428T>G (p.Ser476Arg)
n.1363T>G
c.1431T>G (p.Ser477Arg)
c.5752T>G
c.6210T>G (p.Ser2070Arg)
c.704+430T>G (n.704+430T>G)
c.3532T>G
c.5934T>G (p.Ser1978Arg)
c.5646T>G (p.Ser1882Arg)
c.3174T>G (p.Ser1058Arg)
19g.35732760G>ACA405426055KMT2Bn.517G>A
c.6145G>A (p.Glu2049Lys)
c.3752G>A (n.3752G>A)
c.1429G>A (p.Glu477Lys)
n.1364G>A
c.1432G>A (p.Glu478Lys)
c.5753G>A
c.6211G>A (p.Glu2071Lys)
c.704+431G>A (n.704+431G>A)
c.3533G>A
c.5935G>A (p.Glu1979Lys)
c.5647G>A (p.Glu1883Lys)
c.3175G>A (p.Glu1059Lys)
19g.35732760G>CCA405426057KMT2Bn.517G>C
c.6145G>C (p.Glu2049Gln)
c.3752G>C (n.3752G>C)
c.1429G>C (p.Glu477Gln)
n.1364G>C
c.1432G>C (p.Glu478Gln)
c.5753G>C
c.6211G>C (p.Glu2071Gln)
c.704+431G>C (n.704+431G>C)
c.3533G>C
c.5935G>C (p.Glu1979Gln)
c.5647G>C (p.Glu1883Gln)
c.3175G>C (p.Glu1059Gln)
19g.35732760G>TCA405426056KMT2Bn.517G>T
c.6145G>T (p.Glu2049Ter)
c.3752G>T (n.3752G>T)
c.1429G>T (p.Glu477Ter)
n.1364G>T
c.1432G>T (p.Glu478Ter)
c.5753G>T
c.6211G>T (p.Glu2071Ter)
c.704+431G>T (n.704+431G>T)
c.3533G>T
c.5935G>T (p.Glu1979Ter)
c.5647G>T (p.Glu1883Ter)
c.3175G>T (p.Glu1059Ter)
19g.35732761A>CCA405426058KMT2Bn.518A>C
c.6146A>C (p.Glu2049Ala)
c.3753A>C (n.3753A>C)
c.1430A>C (p.Glu477Ala)
n.1365A>C
c.1433A>C (p.Glu478Ala)
c.5754A>C
c.6212A>C (p.Glu2071Ala)
c.704+432A>C (n.704+432A>C)
c.3534A>C
c.5936A>C (p.Glu1979Ala)
c.5648A>C (p.Glu1883Ala)
c.3176A>C (p.Glu1059Ala)
19g.35732761A>GCA405426059KMT2Bn.518A>G
c.6146A>G (p.Glu2049Gly)
c.3753A>G (n.3753A>G)
c.1430A>G (p.Glu477Gly)
n.1365A>G
c.1433A>G (p.Glu478Gly)
c.5754A>G
c.6212A>G (p.Glu2071Gly)
c.704+432A>G (n.704+432A>G)
c.3534A>G
c.5936A>G (p.Glu1979Gly)
c.5648A>G (p.Glu1883Gly)
c.3176A>G (p.Glu1059Gly)
gnomAD v4
19g.35732761A>TCA405426060KMT2Bn.518A>T
c.6146A>T (p.Glu2049Val)
c.3753A>T (n.3753A>T)
c.1430A>T (p.Glu477Val)
n.1365A>T
c.1433A>T (p.Glu478Val)
c.5754A>T
c.6212A>T (p.Glu2071Val)
c.704+432A>T (n.704+432A>T)
c.3534A>T
c.5936A>T (p.Glu1979Val)
c.5648A>T (p.Glu1883Val)
c.3176A>T (p.Glu1059Val)
19g.35732762G>ACA507308782KMT2Bn.519G>A
c.6147G>A (p.Glu2049=)
c.3754G>A (n.3754G>A)
c.1431G>A (p.Glu477=)
n.1366G>A
c.1434G>A (p.Glu478=)
c.5755G>A
c.6213G>A (p.Glu2071=)
c.704+433G>A (n.704+433G>A)
c.3535G>A
c.5937G>A (p.Glu1979=)
c.5649G>A (p.Glu1883=)
c.3177G>A (p.Glu1059=)
19g.35732762G>CCA405426061KMT2Bn.519G>C
c.6147G>C (p.Glu2049Asp)
c.3754G>C (n.3754G>C)
c.1431G>C (p.Glu477Asp)
n.1366G>C
c.1434G>C (p.Glu478Asp)
c.5755G>C
c.6213G>C (p.Glu2071Asp)
c.704+433G>C (n.704+433G>C)
c.3535G>C
c.5937G>C (p.Glu1979Asp)
c.5649G>C (p.Glu1883Asp)
c.3177G>C (p.Glu1059Asp)
19g.35732762G>TCA405426062KMT2Bn.519G>T
c.6147G>T (p.Glu2049Asp)
c.3754G>T (n.3754G>T)
c.1431G>T (p.Glu477Asp)
n.1366G>T
c.1434G>T (p.Glu478Asp)
c.5755G>T
c.6213G>T (p.Glu2071Asp)
c.704+433G>T (n.704+433G>T)
c.3535G>T
c.5937G>T (p.Glu1979Asp)
c.5649G>T (p.Glu1883Asp)
c.3177G>T (p.Glu1059Asp)
gnomAD v4
19g.35732763G>ACA405426063KMT2Bn.520G>A
c.6148G>A (p.Ala2050Thr)
c.3755G>A (n.3755G>A)
c.1432G>A (p.Ala478Thr)
n.1367G>A
c.1435G>A (p.Ala479Thr)
c.5756G>A
c.6214G>A (p.Ala2072Thr)
c.704+434G>A (n.704+434G>A)
c.3536G>A
c.5938G>A (p.Ala1980Thr)
c.5650G>A (p.Ala1884Thr)
c.3178G>A (p.Ala1060Thr)
19g.35732763G>CCA405426064KMT2Bn.520G>C
c.6148G>C (p.Ala2050Pro)
c.3755G>C (n.3755G>C)
c.1432G>C (p.Ala478Pro)
n.1367G>C
c.1435G>C (p.Ala479Pro)
c.5756G>C
c.6214G>C (p.Ala2072Pro)
c.704+434G>C (n.704+434G>C)
c.3536G>C
c.5938G>C (p.Ala1980Pro)
c.5650G>C (p.Ala1884Pro)
c.3178G>C (p.Ala1060Pro)
19g.35732763G>TCA405426065KMT2Bn.520G>T
c.6148G>T (p.Ala2050Ser)
c.3755G>T (n.3755G>T)
c.1432G>T (p.Ala478Ser)
n.1367G>T
c.1435G>T (p.Ala479Ser)
c.5756G>T
c.6214G>T (p.Ala2072Ser)
c.704+434G>T (n.704+434G>T)
c.3536G>T
c.5938G>T (p.Ala1980Ser)
c.5650G>T (p.Ala1884Ser)
c.3178G>T (p.Ala1060Ser)
gnomAD v4
19g.35732764C>ACA405426066KMT2Bn.521C>A
c.6149C>A (p.Ala2050Asp)
c.3756C>A (n.3756C>A)
c.1433C>A (p.Ala478Asp)
n.1368C>A
c.1436C>A (p.Ala479Asp)
c.5757C>A
c.6215C>A (p.Ala2072Asp)
c.704+435C>A (n.704+435C>A)
c.3537C>A
c.5939C>A (p.Ala1980Asp)
c.5651C>A (p.Ala1884Asp)
c.3179C>A (p.Ala1060Asp)
gnomAD v4
19g.35732764C>GCA405426067KMT2Bn.521C>G
c.6149C>G (p.Ala2050Gly)
c.3756C>G (n.3756C>G)
c.1433C>G (p.Ala478Gly)
n.1368C>G
c.1436C>G (p.Ala479Gly)
c.5757C>G
c.6215C>G (p.Ala2072Gly)
c.704+435C>G (n.704+435C>G)
c.3537C>G
c.5939C>G (p.Ala1980Gly)
c.5651C>G (p.Ala1884Gly)
c.3179C>G (p.Ala1060Gly)
19g.35732764C>TCA405426068KMT2Bn.521C>T
c.6149C>T (p.Ala2050Val)
c.3756C>T (n.3756C>T)
c.1433C>T (p.Ala478Val)
n.1368C>T
c.1436C>T (p.Ala479Val)
c.5757C>T
c.6215C>T (p.Ala2072Val)
c.704+435C>T (n.704+435C>T)
c.3537C>T
c.5939C>T (p.Ala1980Val)
c.5651C>T (p.Ala1884Val)
c.3179C>T (p.Ala1060Val)
gnomAD v4
19g.35732765T>ACA507308798KMT2Bn.522T>A
c.6150T>A (p.Ala2050=)
c.3757T>A (n.3757T>A)
c.1434T>A (p.Ala478=)
n.1369T>A
c.1437T>A (p.Ala479=)
c.5758T>A
c.6216T>A (p.Ala2072=)
c.704+436T>A (n.704+436T>A)
c.3538T>A
c.5940T>A (p.Ala1980=)
c.5652T>A (p.Ala1884=)
c.3180T>A (p.Ala1060=)
19g.35732765T>CCA507308796KMT2Bn.522T>C
c.6150T>C (p.Ala2050=)
c.3757T>C (n.3757T>C)
c.1434T>C (p.Ala478=)
n.1369T>C
c.1437T>C (p.Ala479=)
c.5758T>C
c.6216T>C (p.Ala2072=)
c.704+436T>C (n.704+436T>C)
c.3538T>C
c.5940T>C (p.Ala1980=)
c.5652T>C (p.Ala1884=)
c.3180T>C (p.Ala1060=)
gnomAD v4
19g.35732765T>GCA507308793KMT2Bn.522T>G
c.6150T>G (p.Ala2050=)
c.3757T>G (n.3757T>G)
c.1434T>G (p.Ala478=)
n.1369T>G
c.1437T>G (p.Ala479=)
c.5758T>G
c.6216T>G (p.Ala2072=)
c.704+436T>G (n.704+436T>G)
c.3538T>G
c.5940T>G (p.Ala1980=)
c.5652T>G (p.Ala1884=)
c.3180T>G (p.Ala1060=)
19g.35732766G>ACA405426070KMT2Bn.523G>A
c.6151G>A (p.Glu2051Lys)
c.3758G>A (n.3758G>A)
c.1435G>A (p.Glu479Lys)
n.1370G>A
c.1438G>A (p.Glu480Lys)
c.5759G>A
c.6217G>A (p.Glu2073Lys)
c.704+437G>A (n.704+437G>A)
c.3539G>A
c.5941G>A (p.Glu1981Lys)
c.5653G>A (p.Glu1885Lys)
c.3181G>A (p.Glu1061Lys)
19g.35732766G>CCA405426071KMT2Bn.523G>C
c.6151G>C (p.Glu2051Gln)
c.3758G>C (n.3758G>C)
c.1435G>C (p.Glu479Gln)
n.1370G>C
c.1438G>C (p.Glu480Gln)
c.5759G>C
c.6217G>C (p.Glu2073Gln)
c.704+437G>C (n.704+437G>C)
c.3539G>C
c.5941G>C (p.Glu1981Gln)
c.5653G>C (p.Glu1885Gln)
c.3181G>C (p.Glu1061Gln)
19g.35732766G>TCA405426069KMT2Bn.523G>T
c.6151G>T (p.Glu2051Ter)
c.3758G>T (n.3758G>T)
c.1435G>T (p.Glu479Ter)
n.1370G>T
c.1438G>T (p.Glu480Ter)
c.5759G>T
c.6217G>T (p.Glu2073Ter)
c.704+437G>T (n.704+437G>T)
c.3539G>T
c.5941G>T (p.Glu1981Ter)
c.5653G>T (p.Glu1885Ter)
c.3181G>T (p.Glu1061Ter)
19g.35732767A>CCA405426074KMT2Bn.524A>C
c.6152A>C (p.Glu2051Ala)
c.3759A>C (n.3759A>C)
c.1436A>C (p.Glu479Ala)
n.1371A>C
c.1439A>C (p.Glu480Ala)
c.5760A>C
c.6218A>C (p.Glu2073Ala)
c.704+438A>C (n.704+438A>C)
c.3540A>C
c.5942A>C (p.Glu1981Ala)
c.5654A>C (p.Glu1885Ala)
c.3182A>C (p.Glu1061Ala)
gnomAD v4
19g.35732767A>GCA405426072KMT2Bn.524A>G
c.6152A>G (p.Glu2051Gly)
c.3759A>G (n.3759A>G)
c.1436A>G (p.Glu479Gly)
n.1371A>G
c.1439A>G (p.Glu480Gly)
c.5760A>G
c.6218A>G (p.Glu2073Gly)
c.704+438A>G (n.704+438A>G)
c.3540A>G
c.5942A>G (p.Glu1981Gly)
c.5654A>G (p.Glu1885Gly)
c.3182A>G (p.Glu1061Gly)
gnomAD v4
19g.35732767A>TCA405426073KMT2Bn.524A>T
c.6152A>T (p.Glu2051Val)
c.3759A>T (n.3759A>T)
c.1436A>T (p.Glu479Val)
n.1371A>T
c.1439A>T (p.Glu480Val)
c.5760A>T
c.6218A>T (p.Glu2073Val)
c.704+438A>T (n.704+438A>T)
c.3540A>T
c.5942A>T (p.Glu1981Val)
c.5654A>T (p.Glu1885Val)
c.3182A>T (p.Glu1061Val)
19g.35732768G>ACA507308805KMT2Bn.525G>A
c.6153G>A (p.Glu2051=)
c.3760G>A (n.3760G>A)
c.1437G>A (p.Glu479=)
n.1372G>A
c.1440G>A (p.Glu480=)
c.5761G>A
c.6219G>A (p.Glu2073=)
c.704+439G>A (n.704+439G>A)
c.3541G>A
c.5943G>A (p.Glu1981=)
c.5655G>A (p.Glu1885=)
c.3183G>A (p.Glu1061=)
gnomAD v4
19g.35732768G>CCA405426075KMT2Bn.525G>C
c.6153G>C (p.Glu2051Asp)
c.3760G>C (n.3760G>C)
c.1437G>C (p.Glu479Asp)
n.1372G>C
c.1440G>C (p.Glu480Asp)
c.5761G>C
c.6219G>C (p.Glu2073Asp)
c.704+439G>C (n.704+439G>C)
c.3541G>C
c.5943G>C (p.Glu1981Asp)
c.5655G>C (p.Glu1885Asp)
c.3183G>C (p.Glu1061Asp)
19g.35732768G>TCA405426076KMT2Bn.525G>T
c.6153G>T (p.Glu2051Asp)
c.3760G>T (n.3760G>T)
c.1437G>T (p.Glu479Asp)
n.1372G>T
c.1440G>T (p.Glu480Asp)
c.5761G>T
c.6219G>T (p.Glu2073Asp)
c.704+439G>T (n.704+439G>T)
c.3541G>T
c.5943G>T (p.Glu1981Asp)
c.5655G>T (p.Glu1885Asp)
c.3183G>T (p.Glu1061Asp)
19g.35732769G>ACA405426077KMT2Bn.526G>A
c.6154G>A (p.Ala2052Thr)
c.3761G>A (n.3761G>A)
c.1438G>A (p.Ala480Thr)
n.1373G>A
c.1441G>A (p.Ala481Thr)
c.5762G>A
c.6220G>A (p.Ala2074Thr)
c.704+440G>A (n.704+440G>A)
c.3542G>A
c.5944G>A (p.Ala1982Thr)
c.5656G>A (p.Ala1886Thr)
c.3184G>A (p.Ala1062Thr)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.35732769G>CCA405426078KMT2Bn.526G>C
c.6154G>C (p.Ala2052Pro)
c.3761G>C (n.3761G>C)
c.1438G>C (p.Ala480Pro)
n.1373G>C
c.1441G>C (p.Ala481Pro)
c.5762G>C
c.6220G>C (p.Ala2074Pro)
c.704+440G>C (n.704+440G>C)
c.3542G>C
c.5944G>C (p.Ala1982Pro)
c.5656G>C (p.Ala1886Pro)
c.3184G>C (p.Ala1062Pro)
19g.35732769G=CA2333794493KMT2Bn.526G=
c.6154G= (p.Ala2052=)
c.3761G= (n.3761G=)
c.1438G= (p.Ala480=)
n.1373G=
c.1441G= (p.Ala481=)
c.5762G=
c.6220G= (p.Ala2074=)
c.704+440G= (n.704+440G=)
c.3542G=
c.5944G= (p.Ala1982=)
c.5656G= (p.Ala1886=)
c.3184G= (p.Ala1062=)
19g.35732769G>TCA405426079KMT2Bn.526G>T
c.6154G>T (p.Ala2052Ser)
c.3761G>T (n.3761G>T)
c.1438G>T (p.Ala480Ser)
n.1373G>T
c.1441G>T (p.Ala481Ser)
c.5762G>T
c.6220G>T (p.Ala2074Ser)
c.704+440G>T (n.704+440G>T)
c.3542G>T
c.5944G>T (p.Ala1982Ser)
c.5656G>T (p.Ala1886Ser)
c.3184G>T (p.Ala1062Ser)
19g.35732770C>ACA405426080KMT2Bn.527C>A
c.6155C>A (p.Ala2052Glu)
c.3762C>A (n.3762C>A)
c.1439C>A (p.Ala480Glu)
n.1374C>A
c.1442C>A (p.Ala481Glu)
c.5763C>A
c.6221C>A (p.Ala2074Glu)
c.704+441C>A (n.704+441C>A)
c.3543C>A
c.5945C>A (p.Ala1982Glu)
c.5657C>A (p.Ala1886Glu)
c.3185C>A (p.Ala1062Glu)
19g.35732770C=CA2333794494KMT2Bn.527C=
c.6155C= (p.Ala2052=)
c.3762C= (n.3762C=)
c.1439C= (p.Ala480=)
n.1374C=
c.1442C= (p.Ala481=)
c.5763C=
c.6221C= (p.Ala2074=)
c.704+441C= (n.704+441C=)
c.3543C=
c.5945C= (p.Ala1982=)
c.5657C= (p.Ala1886=)
c.3185C= (p.Ala1062=)
19g.35732770C>GCA405426081KMT2Bn.527C>G
c.6155C>G (p.Ala2052Gly)
c.3762C>G (n.3762C>G)
c.1439C>G (p.Ala480Gly)
n.1374C>G
c.1442C>G (p.Ala481Gly)
c.5763C>G
c.6221C>G (p.Ala2074Gly)
c.704+441C>G (n.704+441C>G)
c.3543C>G
c.5945C>G (p.Ala1982Gly)
c.5657C>G (p.Ala1886Gly)
c.3185C>G (p.Ala1062Gly)
19g.35732770C>TCA9385636KMT2Bn.527C>T
c.6155C>T (p.Ala2052Val)
c.3762C>T (n.3762C>T)
c.1439C>T (p.Ala480Val)
n.1374C>T
c.1442C>T (p.Ala481Val)
c.5763C>T
c.6221C>T (p.Ala2074Val)
c.704+441C>T (n.704+441C>T)
c.3543C>T
c.5945C>T (p.Ala1982Val)
c.5657C>T (p.Ala1886Val)
c.3185C>T (p.Ala1062Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732771G>ACA9385637KMT2Bn.528G>A
c.6156G>A (p.Ala2052=)
c.3763G>A (n.3763G>A)
c.1440G>A (p.Ala480=)
n.1375G>A
c.1443G>A (p.Ala481=)
c.5764G>A
c.6222G>A (p.Ala2074=)
c.704+442G>A (n.704+442G>A)
c.3544G>A
c.5946G>A (p.Ala1982=)
c.5658G>A (p.Ala1886=)
c.3186G>A (p.Ala1062=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.35732771G>CCA507308816KMT2Bn.528G>C
c.6156G>C (p.Ala2052=)
c.3763G>C (n.3763G>C)
c.1440G>C (p.Ala480=)
n.1375G>C
c.1443G>C (p.Ala481=)
c.5764G>C
c.6222G>C (p.Ala2074=)
c.704+442G>C (n.704+442G>C)
c.3544G>C
c.5946G>C (p.Ala1982=)
c.5658G>C (p.Ala1886=)
c.3186G>C (p.Ala1062=)
gnomAD v4
19g.35732771G=CA2333794495KMT2Bn.528G=
c.6156G= (p.Ala2052=)
c.3763G= (n.3763G=)
c.1440G= (p.Ala480=)
n.1375G=
c.1443G= (p.Ala481=)
c.5764G=
c.6222G= (p.Ala2074=)
c.704+442G= (n.704+442G=)
c.3544G=
c.5946G= (p.Ala1982=)
c.5658G= (p.Ala1886=)
c.3186G= (p.Ala1062=)
19g.35732771G>TCA507308817KMT2Bn.528G>T
c.6156G>T (p.Ala2052=)
c.3763G>T (n.3763G>T)
c.1440G>T (p.Ala480=)
n.1375G>T
c.1443G>T (p.Ala481=)
c.5764G>T
c.6222G>T (p.Ala2074=)
c.704+442G>T (n.704+442G>T)
c.3544G>T
c.5946G>T (p.Ala1982=)
c.5658G>T (p.Ala1886=)
c.3186G>T (p.Ala1062=)
19g.35732772G>ACA405426083KMT2Bn.529G>A
c.6157G>A (p.Val2053Met)
c.3764G>A (n.3764G>A)
c.1441G>A (p.Val481Met)
n.1376G>A
c.1444G>A (p.Val482Met)
c.5765G>A
c.6223G>A (p.Val2075Met)
c.704+443G>A (n.704+443G>A)
c.3545G>A
c.5947G>A (p.Val1983Met)
c.5659G>A (p.Val1887Met)
c.3187G>A (p.Val1063Met)
gnomAD v4
19g.35732772G>CCA405426082KMT2Bn.529G>C
c.6157G>C (p.Val2053Leu)
c.3764G>C (n.3764G>C)
c.1441G>C (p.Val481Leu)
n.1376G>C
c.1444G>C (p.Val482Leu)
c.5765G>C
c.6223G>C (p.Val2075Leu)
c.704+443G>C (n.704+443G>C)
c.3545G>C
c.5947G>C (p.Val1983Leu)
c.5659G>C (p.Val1887Leu)
c.3187G>C (p.Val1063Leu)
19g.35732772G=CA2333794496KMT2Bn.529G=
c.6157G= (p.Val2053=)
c.3764G= (n.3764G=)
c.1441G= (p.Val481=)
n.1376G=
c.1444G= (p.Val482=)
c.5765G=
c.6223G= (p.Val2075=)
c.704+443G= (n.704+443G=)
c.3545G=
c.5947G= (p.Val1983=)
c.5659G= (p.Val1887=)
c.3187G= (p.Val1063=)
19g.35732772G>TCA9385638KMT2Bn.529G>T
c.6157G>T (p.Val2053Leu)
c.3764G>T (n.3764G>T)
c.1441G>T (p.Val481Leu)
n.1376G>T
c.1444G>T (p.Val482Leu)
c.5765G>T
c.6223G>T (p.Val2075Leu)
c.704+443G>T (n.704+443G>T)
c.3545G>T
c.5947G>T (p.Val1983Leu)
c.5659G>T (p.Val1887Leu)
c.3187G>T (p.Val1063Leu)
dbSNP ExAC gnomAD v2
19g.35732773T>ACA405426084KMT2Bn.530T>A
c.6158T>A (p.Val2053Glu)
c.3765T>A (n.3765T>A)
c.1442T>A (p.Val481Glu)
n.1377T>A
c.1445T>A (p.Val482Glu)
c.5766T>A
c.6224T>A (p.Val2075Glu)
c.704+444T>A (n.704+444T>A)
c.3546T>A
c.5948T>A (p.Val1983Glu)
c.5660T>A (p.Val1887Glu)
c.3188T>A (p.Val1063Glu)
19g.35732773T>CCA405426085KMT2Bn.530T>C
c.6158T>C (p.Val2053Ala)
c.3765T>C (n.3765T>C)
c.1442T>C (p.Val481Ala)
n.1377T>C
c.1445T>C (p.Val482Ala)
c.5766T>C
c.6224T>C (p.Val2075Ala)
c.704+444T>C (n.704+444T>C)
c.3546T>C
c.5948T>C (p.Val1983Ala)
c.5660T>C (p.Val1887Ala)
c.3188T>C (p.Val1063Ala)
19g.35732773T>GCA405426086KMT2Bn.530T>G
c.6158T>G (p.Val2053Gly)
c.3765T>G (n.3765T>G)
c.1442T>G (p.Val481Gly)
n.1377T>G
c.1445T>G (p.Val482Gly)
c.5766T>G
c.6224T>G (p.Val2075Gly)
c.704+444T>G (n.704+444T>G)
c.3546T>G
c.5948T>G (p.Val1983Gly)
c.5660T>G (p.Val1887Gly)
c.3188T>G (p.Val1063Gly)
dbSNP
19g.35732773T=CA2333794497KMT2Bn.530T=
c.6158T= (p.Val2053=)
c.3765T= (n.3765T=)
c.1442T= (p.Val481=)
n.1377T=
c.1445T= (p.Val482=)
c.5766T=
c.6224T= (p.Val2075=)
c.704+444T= (n.704+444T=)
c.3546T=
c.5948T= (p.Val1983=)
c.5660T= (p.Val1887=)
c.3188T= (p.Val1063=)
19g.35732774G>ACA9385639KMT2Bn.531G>A
c.6159G>A (p.Val2053=)
c.3766G>A (n.3766G>A)
c.1443G>A (p.Val481=)
n.1378G>A
c.1446G>A (p.Val482=)
c.5767G>A
c.6225G>A (p.Val2075=)
c.704+445G>A (n.704+445G>A)
c.3547G>A
c.5949G>A (p.Val1983=)
c.5661G>A (p.Val1887=)
c.3189G>A (p.Val1063=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.35732774G>CCA507308837KMT2Bn.531G>C
c.6159G>C (p.Val2053=)
c.3766G>C (n.3766G>C)
c.1443G>C (p.Val481=)
n.1378G>C
c.1446G>C (p.Val482=)
c.5767G>C
c.6225G>C (p.Val2075=)
c.704+445G>C (n.704+445G>C)
c.3547G>C
c.5949G>C (p.Val1983=)
c.5661G>C (p.Val1887=)
c.3189G>C (p.Val1063=)
19g.35732774G=CA2333794498KMT2Bn.531G=
c.6159G= (p.Val2053=)
c.3766G= (n.3766G=)
c.1443G= (p.Val481=)
n.1378G=
c.1446G= (p.Val482=)
c.5767G=
c.6225G= (p.Val2075=)
c.704+445G= (n.704+445G=)
c.3547G=
c.5949G= (p.Val1983=)
c.5661G= (p.Val1887=)
c.3189G= (p.Val1063=)
19g.35732774G>TCA507308839KMT2Bn.531G>T
c.6159G>T (p.Val2053=)
c.3766G>T (n.3766G>T)
c.1443G>T (p.Val481=)
n.1378G>T
c.1446G>T (p.Val482=)
c.5767G>T
c.6225G>T (p.Val2075=)
c.704+445G>T (n.704+445G>T)
c.3547G>T
c.5949G>T (p.Val1983=)
c.5661G>T (p.Val1887=)
c.3189G>T (p.Val1063=)
19g.35732779_35732781delCA2576757217KMT2Bn.536_538del
c.6164_6166del (p.Gln2055del)
c.3771_3773del (n.3771_3773del)
c.1448_1450del (p.Gln483del)
n.1383_1385del
c.1451_1453del (p.Gln484del)
c.5772_5774del
c.6230_6232del (p.Gln2077del)
c.704+450_704+452del (n.704+450_704+452del)
c.3552_3554del
c.5954_5956del (p.Gln1985del)
c.5666_5668del (p.Gln1889del)
c.3194_3196del (p.Gln1065del)
19g.35732775C>ACA405426087KMT2Bn.532C>A
c.6160C>A (p.Gln2054Lys)
c.3767C>A (n.3767C>A)
c.1444C>A (p.Gln482Lys)
n.1379C>A
c.1447C>A (p.Gln483Lys)
c.5768C>A
c.6226C>A (p.Gln2076Lys)
c.704+446C>A (n.704+446C>A)
c.3548C>A
c.5950C>A (p.Gln1984Lys)
c.5662C>A (p.Gln1888Lys)
c.3190C>A (p.Gln1064Lys)
19g.35732775C>GCA405426088KMT2Bn.532C>G
c.6160C>G (p.Gln2054Glu)
c.3767C>G (n.3767C>G)
c.1444C>G (p.Gln482Glu)
n.1379C>G
c.1447C>G (p.Gln483Glu)
c.5768C>G
c.6226C>G (p.Gln2076Glu)
c.704+446C>G (n.704+446C>G)
c.3548C>G
c.5950C>G (p.Gln1984Glu)
c.5662C>G (p.Gln1888Glu)
c.3190C>G (p.Gln1064Glu)
19g.35732775C>TCA405426089KMT2Bn.532C>T
c.6160C>T (p.Gln2054Ter)
c.3767C>T (n.3767C>T)
c.1444C>T (p.Gln482Ter)
n.1379C>T
c.1447C>T (p.Gln483Ter)
c.5768C>T
c.6226C>T (p.Gln2076Ter)
c.704+446C>T (n.704+446C>T)
c.3548C>T
c.5950C>T (p.Gln1984Ter)
c.5662C>T (p.Gln1888Ter)
c.3190C>T (p.Gln1064Ter)
gnomAD v4 COSMIC
19g.35732776A=CA2333794499KMT2Bn.533A=
c.6161A= (p.Gln2054=)
c.3768A= (n.3768A=)
c.1445A= (p.Gln482=)
n.1380A=
c.1448A= (p.Gln483=)
c.5769A=
c.6227A= (p.Gln2076=)
c.704+447A= (n.704+447A=)
c.3549A=
c.5951A= (p.Gln1984=)
c.5663A= (p.Gln1888=)
c.3191A= (p.Gln1064=)
19g.35732776A>CCA405426090KMT2Bn.533A>C
c.6161A>C (p.Gln2054Pro)
c.3768A>C (n.3768A>C)
c.1445A>C (p.Gln482Pro)
n.1380A>C
c.1448A>C (p.Gln483Pro)
c.5769A>C
c.6227A>C (p.Gln2076Pro)
c.704+447A>C (n.704+447A>C)
c.3549A>C
c.5951A>C (p.Gln1984Pro)
c.5663A>C (p.Gln1888Pro)
c.3191A>C (p.Gln1064Pro)
19g.35732776A>GCA405426091KMT2Bn.533A>G
c.6161A>G (p.Gln2054Arg)
c.3768A>G (n.3768A>G)
c.1445A>G (p.Gln482Arg)
n.1380A>G
c.1448A>G (p.Gln483Arg)
c.5769A>G
c.6227A>G (p.Gln2076Arg)
c.704+447A>G (n.704+447A>G)
c.3549A>G
c.5951A>G (p.Gln1984Arg)
c.5663A>G (p.Gln1888Arg)
c.3191A>G (p.Gln1064Arg)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.35732776A>TCA405426092KMT2Bn.533A>T
c.6161A>T (p.Gln2054Leu)
c.3768A>T (n.3768A>T)
c.1445A>T (p.Gln482Leu)
n.1380A>T
c.1448A>T (p.Gln483Leu)
c.5769A>T
c.6227A>T (p.Gln2076Leu)
c.704+447A>T (n.704+447A>T)
c.3549A>T
c.5951A>T (p.Gln1984Leu)
c.5663A>T (p.Gln1888Leu)
c.3191A>T (p.Gln1064Leu)
19g.35732777G>ACA507308849KMT2Bn.534G>A
c.6162G>A (p.Gln2054=)
c.3769G>A (n.3769G>A)
c.1446G>A (p.Gln482=)
n.1381G>A
c.1449G>A (p.Gln483=)
c.5770G>A
c.6228G>A (p.Gln2076=)
c.704+448G>A (n.704+448G>A)
c.3550G>A
c.5952G>A (p.Gln1984=)
c.5664G>A (p.Gln1888=)
c.3192G>A (p.Gln1064=)
19g.35732777G>CCA405426093KMT2Bn.534G>C
c.6162G>C (p.Gln2054His)
c.3769G>C (n.3769G>C)
c.1446G>C (p.Gln482His)
n.1381G>C
c.1449G>C (p.Gln483His)
c.5770G>C
c.6228G>C (p.Gln2076His)
c.704+448G>C (n.704+448G>C)
c.3550G>C
c.5952G>C (p.Gln1984His)
c.5664G>C (p.Gln1888His)
c.3192G>C (p.Gln1064His)
19g.35732777G>TCA405426094KMT2Bn.534G>T
c.6162G>T (p.Gln2054His)
c.3769G>T (n.3769G>T)
c.1446G>T (p.Gln482His)
n.1381G>T
c.1449G>T (p.Gln483His)
c.5770G>T
c.6228G>T (p.Gln2076His)
c.704+448G>T (n.704+448G>T)
c.3550G>T
c.5952G>T (p.Gln1984His)
c.5664G>T (p.Gln1888His)
c.3192G>T (p.Gln1064His)
19g.35732778C>ACA405426096KMT2Bn.535C>A
c.6163C>A (p.Gln2055Lys)
c.3770C>A (n.3770C>A)
c.1447C>A (p.Gln483Lys)
n.1382C>A
c.1450C>A (p.Gln484Lys)
c.5771C>A
c.6229C>A (p.Gln2077Lys)
c.704+449C>A (n.704+449C>A)
c.3551C>A
c.5953C>A (p.Gln1985Lys)
c.5665C>A (p.Gln1889Lys)
c.3193C>A (p.Gln1065Lys)
19g.35732778C>GCA405426097KMT2Bn.535C>G
c.6163C>G (p.Gln2055Glu)
c.3770C>G (n.3770C>G)
c.1447C>G (p.Gln483Glu)
n.1382C>G
c.1450C>G (p.Gln484Glu)
c.5771C>G
c.6229C>G (p.Gln2077Glu)
c.704+449C>G (n.704+449C>G)
c.3551C>G
c.5953C>G (p.Gln1985Glu)
c.5665C>G (p.Gln1889Glu)
c.3193C>G (p.Gln1065Glu)
19g.35732778C>TCA405426095KMT2Bn.535C>T
c.6163C>T (p.Gln2055Ter)
c.3770C>T (n.3770C>T)
c.1447C>T (p.Gln483Ter)
n.1382C>T
c.1450C>T (p.Gln484Ter)
c.5771C>T
c.6229C>T (p.Gln2077Ter)
c.704+449C>T (n.704+449C>T)
c.3551C>T
c.5953C>T (p.Gln1985Ter)
c.5665C>T (p.Gln1889Ter)
c.3193C>T (p.Gln1065Ter)
19g.35732779A>CCA405426098KMT2Bn.536A>C
c.6164A>C (p.Gln2055Pro)
c.3771A>C (n.3771A>C)
c.1448A>C (p.Gln483Pro)
n.1383A>C
c.1451A>C (p.Gln484Pro)
c.5772A>C
c.6230A>C (p.Gln2077Pro)
c.704+450A>C (n.704+450A>C)
c.3552A>C
c.5954A>C (p.Gln1985Pro)
c.5666A>C (p.Gln1889Pro)
c.3194A>C (p.Gln1065Pro)
19g.35732779A>GCA405426099KMT2Bn.536A>G
c.6164A>G (p.Gln2055Arg)
c.3771A>G (n.3771A>G)
c.1448A>G (p.Gln483Arg)
n.1383A>G
c.1451A>G (p.Gln484Arg)
c.5772A>G
c.6230A>G (p.Gln2077Arg)
c.704+450A>G (n.704+450A>G)
c.3552A>G
c.5954A>G (p.Gln1985Arg)
c.5666A>G (p.Gln1889Arg)
c.3194A>G (p.Gln1065Arg)
19g.35732779A>TCA405426100KMT2Bn.536A>T
c.6164A>T (p.Gln2055Leu)
c.3771A>T (n.3771A>T)
c.1448A>T (p.Gln483Leu)
n.1383A>T
c.1451A>T (p.Gln484Leu)
c.5772A>T
c.6230A>T (p.Gln2077Leu)
c.704+450A>T (n.704+450A>T)
c.3552A>T
c.5954A>T (p.Gln1985Leu)
c.5666A>T (p.Gln1889Leu)
c.3194A>T (p.Gln1065Leu)
19g.35732780G>ACA9385640KMT2Bn.537G>A
c.6165G>A (p.Gln2055=)
c.3772G>A (n.3772G>A)
c.1449G>A (p.Gln483=)
n.1384G>A
c.1452G>A (p.Gln484=)
c.5773G>A
c.6231G>A (p.Gln2077=)
c.704+451G>A (n.704+451G>A)
c.3553G>A
c.5955G>A (p.Gln1985=)
c.5667G>A (p.Gln1889=)
c.3195G>A (p.Gln1065=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.35732780G>CCA405426101KMT2Bn.537G>C
c.6165G>C (p.Gln2055His)
c.3772G>C (n.3772G>C)
c.1449G>C (p.Gln483His)
n.1384G>C
c.1452G>C (p.Gln484His)
c.5773G>C
c.6231G>C (p.Gln2077His)
c.704+451G>C (n.704+451G>C)
c.3553G>C
c.5955G>C (p.Gln1985His)
c.5667G>C (p.Gln1889His)
c.3195G>C (p.Gln1065His)
19g.35732780G=CA2333794500KMT2Bn.537G=
c.6165G= (p.Gln2055=)
c.3772G= (n.3772G=)
c.1449G= (p.Gln483=)
n.1384G=
c.1452G= (p.Gln484=)
c.5773G=
c.6231G= (p.Gln2077=)
c.704+451G= (n.704+451G=)
c.3553G=
c.5955G= (p.Gln1985=)
c.5667G= (p.Gln1889=)
c.3195G= (p.Gln1065=)
19g.35732780G>TCA405426102KMT2Bn.537G>T
c.6165G>T (p.Gln2055His)
c.3772G>T (n.3772G>T)
c.1449G>T (p.Gln483His)
n.1384G>T
c.1452G>T (p.Gln484His)
c.5773G>T
c.6231G>T (p.Gln2077His)
c.704+451G>T (n.704+451G>T)
c.3553G>T
c.5955G>T (p.Gln1985His)
c.5667G>T (p.Gln1889His)
c.3195G>T (p.Gln1065His)
19g.35732781C>ACA405426105KMT2Bn.538C>A
c.6166C>A (p.Pro2056Thr)
c.3773C>A (n.3773C>A)
c.1450C>A (p.Pro484Thr)
n.1385C>A
c.1453C>A (p.Pro485Thr)
c.5774C>A
c.6232C>A (p.Pro2078Thr)
c.704+452C>A (n.704+452C>A)
c.3554C>A
c.5956C>A (p.Pro1986Thr)
c.5668C>A (p.Pro1890Thr)
c.3196C>A (p.Pro1066Thr)
19g.35732781C=CA2333794501KMT2Bn.538C=
c.6166C= (p.Pro2056=)
c.3773C= (n.3773C=)
c.1450C= (p.Pro484=)
n.1385C=
c.1453C= (p.Pro485=)
c.5774C=
c.6232C= (p.Pro2078=)
c.704+452C= (n.704+452C=)
c.3554C=
c.5956C= (p.Pro1986=)
c.5668C= (p.Pro1890=)
c.3196C= (p.Pro1066=)
19g.35732781C>GCA405426103KMT2Bn.538C>G
c.6166C>G (p.Pro2056Ala)
c.3773C>G (n.3773C>G)
c.1450C>G (p.Pro484Ala)
n.1385C>G
c.1453C>G (p.Pro485Ala)
c.5774C>G
c.6232C>G (p.Pro2078Ala)
c.704+452C>G (n.704+452C>G)
c.3554C>G
c.5956C>G (p.Pro1986Ala)
c.5668C>G (p.Pro1890Ala)
c.3196C>G (p.Pro1066Ala)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.35732781C>TCA405426104KMT2Bn.538C>T
c.6166C>T (p.Pro2056Ser)
c.3773C>T (n.3773C>T)
c.1450C>T (p.Pro484Ser)
n.1385C>T
c.1453C>T (p.Pro485Ser)
c.5774C>T
c.6232C>T (p.Pro2078Ser)
c.704+452C>T (n.704+452C>T)
c.3554C>T
c.5956C>T (p.Pro1986Ser)
c.5668C>T (p.Pro1890Ser)
c.3196C>T (p.Pro1066Ser)
gnomAD v4
19g.35732782_35732803delCA2584575160KMT2Bn.539_560del
c.6167_6188del (p.Pro2056LeufsTer6)
c.3774_3795del (n.3774_3795del)
c.1451_1472del (p.Pro484LeufsTer6)
n.1386_1407del
c.1454_1475del (p.Pro485LeufsTer6)
c.5775_5796del
c.6233_6254del (p.Pro2078LeufsTer6)
c.704+453_704+474del (n.704+453_704+474del)
c.3555_3576del
c.5957_5978del (p.Pro1986LeufsTer6)
c.5669_5690del (p.Pro1890LeufsTer6)
c.3197_3218del (p.Pro1066LeufsTer6)
gnomAD v4
19g.35732782C>ACA405426106KMT2Bn.539C>A
c.6167C>A (p.Pro2056His)
c.3774C>A (n.3774C>A)
c.1451C>A (p.Pro484His)
n.1386C>A
c.1454C>A (p.Pro485His)
c.5775C>A
c.6233C>A (p.Pro2078His)
c.704+453C>A (n.704+453C>A)
c.3555C>A
c.5957C>A (p.Pro1986His)
c.5669C>A (p.Pro1890His)
c.3197C>A (p.Pro1066His)
19g.35732782C=CA2333794502KMT2Bn.539C=
c.6167C= (p.Pro2056=)
c.3774C= (n.3774C=)
c.1451C= (p.Pro484=)
n.1386C=
c.1454C= (p.Pro485=)
c.5775C=
c.6233C= (p.Pro2078=)
c.704+453C= (n.704+453C=)
c.3555C=
c.5957C= (p.Pro1986=)
c.5669C= (p.Pro1890=)
c.3197C= (p.Pro1066=)
19g.35732782C>GCA405426107KMT2Bn.539C>G
c.6167C>G (p.Pro2056Arg)
c.3774C>G (n.3774C>G)
c.1451C>G (p.Pro484Arg)
n.1386C>G
c.1454C>G (p.Pro485Arg)
c.5775C>G
c.6233C>G (p.Pro2078Arg)
c.704+453C>G (n.704+453C>G)
c.3555C>G
c.5957C>G (p.Pro1986Arg)
c.5669C>G (p.Pro1890Arg)
c.3197C>G (p.Pro1066Arg)
dbSNP
19g.35732782C>TCA405426108KMT2Bn.539C>T
c.6167C>T (p.Pro2056Leu)
c.3774C>T (n.3774C>T)
c.1451C>T (p.Pro484Leu)
n.1386C>T
c.1454C>T (p.Pro485Leu)
c.5775C>T
c.6233C>T (p.Pro2078Leu)
c.704+453C>T (n.704+453C>T)
c.3555C>T
c.5957C>T (p.Pro1986Leu)
c.5669C>T (p.Pro1890Leu)
c.3197C>T (p.Pro1066Leu)
19g.35732783T>ACA507308876KMT2Bn.540T>A
c.6168T>A (p.Pro2056=)
c.3775T>A (n.3775T>A)
c.1452T>A (p.Pro484=)
n.1387T>A
c.1455T>A (p.Pro485=)
c.5776T>A
c.6234T>A (p.Pro2078=)
c.704+454T>A (n.704+454T>A)
c.3556T>A
c.5958T>A (p.Pro1986=)
c.5670T>A (p.Pro1890=)
c.3198T>A (p.Pro1066=)
19g.35732783T>CCA507308878KMT2Bn.540T>C
c.6168T>C (p.Pro2056=)
c.3775T>C (n.3775T>C)
c.1452T>C (p.Pro484=)
n.1387T>C
c.1455T>C (p.Pro485=)
c.5776T>C
c.6234T>C (p.Pro2078=)
c.704+454T>C (n.704+454T>C)
c.3556T>C
c.5958T>C (p.Pro1986=)
c.5670T>C (p.Pro1890=)
c.3198T>C (p.Pro1066=)
19g.35732783T>GCA507308879KMT2Bn.540T>G
c.6168T>G (p.Pro2056=)
c.3775T>G (n.3775T>G)
c.1452T>G (p.Pro484=)
n.1387T>G
c.1455T>G (p.Pro485=)
c.5776T>G
c.6234T>G (p.Pro2078=)
c.704+454T>G (n.704+454T>G)
c.3556T>G
c.5958T>G (p.Pro1986=)
c.5670T>G (p.Pro1890=)
c.3198T>G (p.Pro1066=)
19g.35732794_35732815dupCA658799186KMT2Bn.551_572dup
c.6179_6200dup (p.Val2068HisfsTer25)
c.3786_3807dup (n.3786_3807dup)
c.1463_1484dup (p.Val496HisfsTer25)
n.1398_1419dup
c.1466_1487dup (p.Val497HisfsTer25)
c.5787_5808dup
c.6245_6266dup (p.Val2090HisfsTer25)
c.704+465_704+486dup (n.704+465_704+486dup)
c.3567_3588dup
c.5969_5990dup (p.Val1998HisfsTer25)
c.5681_5702dup (p.Val1902HisfsTer25)
c.3209_3230dup (p.Val1078HisfsTer25)
ClinVar dbSNP
19g.35732794_35732815delCA2697556450KMT2Bn.551_572del
c.6179_6200del (p.Gly2060GlufsTer2)
c.3786_3807del (n.3786_3807del)
c.1463_1484del (p.Gly488GlufsTer2)
n.1398_1419del
c.1466_1487del (p.Gly489GlufsTer2)
c.5787_5808del
c.6245_6266del (p.Gly2082GlufsTer2)
c.704+465_704+486del (n.704+465_704+486del)
c.3567_3588del
c.5969_5990del (p.Gly1990GlufsTer2)
c.5681_5702del (p.Gly1894GlufsTer2)
c.3209_3230del (p.Gly1070GlufsTer2)
ClinVar
19g.35732784C>ACA507308880KMT2Bn.541C>A
c.6169C>A (p.Arg2057=)
c.3776C>A (n.3776C>A)
c.1453C>A (p.Arg485=)
n.1388C>A
c.1456C>A (p.Arg486=)
c.5777C>A
c.6235C>A (p.Arg2079=)
c.704+455C>A (n.704+455C>A)
c.3557C>A
c.5959C>A (p.Arg1987=)
c.5671C>A (p.Arg1891=)
c.3199C>A (p.Arg1067=)
19g.35732784C=CA2333794503KMT2Bn.541C=
c.6169C= (p.Arg2057=)
c.3776C= (n.3776C=)
c.1453C= (p.Arg485=)
n.1388C=
c.1456C= (p.Arg486=)
c.5777C=
c.6235C= (p.Arg2079=)
c.704+455C= (n.704+455C=)
c.3557C=
c.5959C= (p.Arg1987=)
c.5671C= (p.Arg1891=)
c.3199C= (p.Arg1067=)
19g.35732784C>GCA405426109KMT2Bn.541C>G
c.6169C>G (p.Arg2057Gly)
c.3776C>G (n.3776C>G)
c.1453C>G (p.Arg485Gly)
n.1388C>G
c.1456C>G (p.Arg486Gly)
c.5777C>G
c.6235C>G (p.Arg2079Gly)
c.704+455C>G (n.704+455C>G)
c.3557C>G
c.5959C>G (p.Arg1987Gly)
c.5671C>G (p.Arg1891Gly)
c.3199C>G (p.Arg1067Gly)
19g.35732784C>TCA405426110KMT2Bn.541C>T
c.6169C>T (p.Arg2057Trp)
c.3776C>T (n.3776C>T)
c.1453C>T (p.Arg485Trp)
n.1388C>T
c.1456C>T (p.Arg486Trp)
c.5777C>T
c.6235C>T (p.Arg2079Trp)
c.704+455C>T (n.704+455C>T)
c.3557C>T
c.5959C>T (p.Arg1987Trp)
c.5671C>T (p.Arg1891Trp)
c.3199C>T (p.Arg1067Trp)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.35732785G>ACA405427194KMT2Bn.542G>A
c.6170G>A (p.Arg2057Gln)
c.3777G>A (n.3777G>A)
c.1454G>A (p.Arg485Gln)
n.1389G>A
c.1457G>A (p.Arg486Gln)
c.5778G>A
c.6236G>A (p.Arg2079Gln)
c.704+456G>A (n.704+456G>A)
c.3558G>A
c.5960G>A (p.Arg1987Gln)
c.5672G>A (p.Arg1891Gln)
c.3200G>A (p.Arg1067Gln)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.35732785G>CCA405427199KMT2Bn.542G>C
c.6170G>C (p.Arg2057Pro)
c.3777G>C (n.3777G>C)
c.1454G>C (p.Arg485Pro)
n.1389G>C
c.1457G>C (p.Arg486Pro)
c.5778G>C
c.6236G>C (p.Arg2079Pro)
c.704+456G>C (n.704+456G>C)
c.3558G>C
c.5960G>C (p.Arg1987Pro)
c.5672G>C (p.Arg1891Pro)
c.3200G>C (p.Arg1067Pro)
gnomAD v4
19g.35732785G=CA2333794504KMT2Bn.542G=
c.6170G= (p.Arg2057=)
c.3777G= (n.3777G=)
c.1454G= (p.Arg485=)
n.1389G=
c.1457G= (p.Arg486=)
c.5778G=
c.6236G= (p.Arg2079=)
c.704+456G= (n.704+456G=)
c.3558G=
c.5960G= (p.Arg1987=)
c.5672G= (p.Arg1891=)
c.3200G= (p.Arg1067=)
19g.35732785G>TCA9385641KMT2Bn.542G>T
c.6170G>T (p.Arg2057Leu)
c.3777G>T (n.3777G>T)
c.1454G>T (p.Arg485Leu)
n.1389G>T
c.1457G>T (p.Arg486Leu)
c.5778G>T
c.6236G>T (p.Arg2079Leu)
c.704+456G>T (n.704+456G>T)
c.3558G>T
c.5960G>T (p.Arg1987Leu)
c.5672G>T (p.Arg1891Leu)
c.3200G>T (p.Arg1067Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.35732786G>ACA507308217KMT2Bn.543G>A
c.6171G>A (p.Arg2057=)
c.3778G>A (n.3778G>A)
c.1455G>A (p.Arg485=)
n.1390G>A
c.1458G>A (p.Arg486=)
c.5779G>A
c.6237G>A (p.Arg2079=)
c.704+457G>A (n.704+457G>A)
c.3559G>A
c.5961G>A (p.Arg1987=)
c.5673G>A (p.Arg1891=)
c.3201G>A (p.Arg1067=)
dbSNP gnomAD v2
19g.35732786G>CCA507308220KMT2Bn.543G>C
c.6171G>C (p.Arg2057=)
c.3778G>C (n.3778G>C)
c.1455G>C (p.Arg485=)
n.1390G>C
c.1458G>C (p.Arg486=)
c.5779G>C
c.6237G>C (p.Arg2079=)
c.704+457G>C (n.704+457G>C)
c.3559G>C
c.5961G>C (p.Arg1987=)
c.5673G>C (p.Arg1891=)
c.3201G>C (p.Arg1067=)
19g.35732786G=CA2333794505KMT2Bn.543G=
c.6171G= (p.Arg2057=)
c.3778G= (n.3778G=)
c.1455G= (p.Arg485=)
n.1390G=
c.1458G= (p.Arg486=)
c.5779G=
c.6237G= (p.Arg2079=)
c.704+457G= (n.704+457G=)
c.3559G=
c.5961G= (p.Arg1987=)
c.5673G= (p.Arg1891=)
c.3201G= (p.Arg1067=)
19g.35732786G>TCA507308219KMT2Bn.543G>T
c.6171G>T (p.Arg2057=)
c.3778G>T (n.3778G>T)
c.1455G>T (p.Arg485=)
n.1390G>T
c.1458G>T (p.Arg486=)
c.5779G>T
c.6237G>T (p.Arg2079=)
c.704+457G>T (n.704+457G>T)
c.3559G>T
c.5961G>T (p.Arg1987=)
c.5673G>T (p.Arg1891=)
c.3201G>T (p.Arg1067=)
19g.35732787G>ACA405427200KMT2Bn.544G>A
c.6172G>A (p.Gly2058Ser)
c.3779G>A (n.3779G>A)
c.1456G>A (p.Gly486Ser)
n.1391G>A
c.1459G>A (p.Gly487Ser)
c.5780G>A
c.6238G>A (p.Gly2080Ser)
c.704+458G>A (n.704+458G>A)
c.3560G>A
c.5962G>A (p.Gly1988Ser)
c.5674G>A (p.Gly1892Ser)
c.3202G>A (p.Gly1068Ser)
dbSNP gnomAD v2
19g.35732787G>CCA405427201KMT2Bn.544G>C
c.6172G>C (p.Gly2058Arg)
c.3779G>C (n.3779G>C)
c.1456G>C (p.Gly486Arg)
n.1391G>C
c.1459G>C (p.Gly487Arg)
c.5780G>C
c.6238G>C (p.Gly2080Arg)
c.704+458G>C (n.704+458G>C)
c.3560G>C
c.5962G>C (p.Gly1988Arg)
c.5674G>C (p.Gly1892Arg)
c.3202G>C (p.Gly1068Arg)
19g.35732787G=CA2333794506KMT2Bn.544G=
c.6172G= (p.Gly2058=)
c.3779G= (n.3779G=)
c.1456G= (p.Gly486=)
n.1391G=
c.1459G= (p.Gly487=)
c.5780G=
c.6238G= (p.Gly2080=)
c.704+458G= (n.704+458G=)
c.3560G=
c.5962G= (p.Gly1988=)
c.5674G= (p.Gly1892=)
c.3202G= (p.Gly1068=)
19g.35732787G>TCA405427202KMT2Bn.544G>T
c.6172G>T (p.Gly2058Cys)
c.3779G>T (n.3779G>T)
c.1456G>T (p.Gly486Cys)
n.1391G>T
c.1459G>T (p.Gly487Cys)
c.5780G>T
c.6238G>T (p.Gly2080Cys)
c.704+458G>T (n.704+458G>T)
c.3560G>T
c.5962G>T (p.Gly1988Cys)
c.5674G>T (p.Gly1892Cys)
c.3202G>T (p.Gly1068Cys)
COSMIC
19g.35732788G>ACA405427205KMT2Bn.545G>A
c.6173G>A (p.Gly2058Asp)
c.3780G>A (n.3780G>A)
c.1457G>A (p.Gly486Asp)
n.1392G>A
c.1460G>A (p.Gly487Asp)
c.5781G>A
c.6239G>A (p.Gly2080Asp)
c.704+459G>A (n.704+459G>A)
c.3561G>A
c.5963G>A (p.Gly1988Asp)
c.5675G>A (p.Gly1892Asp)
c.3203G>A (p.Gly1068Asp)
19g.35732788G>CCA405427208KMT2Bn.545G>C
c.6173G>C (p.Gly2058Ala)
c.3780G>C (n.3780G>C)
c.1457G>C (p.Gly486Ala)
n.1392G>C
c.1460G>C (p.Gly487Ala)
c.5781G>C
c.6239G>C (p.Gly2080Ala)
c.704+459G>C (n.704+459G>C)
c.3561G>C
c.5963G>C (p.Gly1988Ala)
c.5675G>C (p.Gly1892Ala)
c.3203G>C (p.Gly1068Ala)
19g.35732788G>TCA405427211KMT2Bn.545G>T
c.6173G>T (p.Gly2058Val)
c.3780G>T (n.3780G>T)
c.1457G>T (p.Gly486Val)
n.1392G>T
c.1460G>T (p.Gly487Val)
c.5781G>T
c.6239G>T (p.Gly2080Val)
c.704+459G>T (n.704+459G>T)
c.3561G>T
c.5963G>T (p.Gly1988Val)
c.5675G>T (p.Gly1892Val)
c.3203G>T (p.Gly1068Val)
19g.35732789C>ACA507308225KMT2Bn.546C>A
c.6174C>A (p.Gly2058=)
c.3781C>A (n.3781C>A)
c.1458C>A (p.Gly486=)
n.1393C>A
c.1461C>A (p.Gly487=)
c.5782C>A
c.6240C>A (p.Gly2080=)
c.704+460C>A (n.704+460C>A)
c.3562C>A
c.5964C>A (p.Gly1988=)
c.5676C>A (p.Gly1892=)
c.3204C>A (p.Gly1068=)
gnomAD v4
19g.35732789C=CA2333794507KMT2Bn.546C=
c.6174C= (p.Gly2058=)
c.3781C= (n.3781C=)
c.1458C= (p.Gly486=)
n.1393C=
c.1461C= (p.Gly487=)
c.5782C=
c.6240C= (p.Gly2080=)
c.704+460C= (n.704+460C=)
c.3562C=
c.5964C= (p.Gly1988=)
c.5676C= (p.Gly1892=)
c.3204C= (p.Gly1068=)
19g.35732789C>GCA507308227KMT2Bn.546C>G
c.6174C>G (p.Gly2058=)
c.3781C>G (n.3781C>G)
c.1458C>G (p.Gly486=)
n.1393C>G
c.1461C>G (p.Gly487=)
c.5782C>G
c.6240C>G (p.Gly2080=)
c.704+460C>G (n.704+460C>G)
c.3562C>G
c.5964C>G (p.Gly1988=)
c.5676C>G (p.Gly1892=)
c.3204C>G (p.Gly1068=)
19g.35732789C>TCA9385642KMT2Bn.546C>T
c.6174C>T (p.Gly2058=)
c.3781C>T (n.3781C>T)
c.1458C>T (p.Gly486=)
n.1393C>T
c.1461C>T (p.Gly487=)
c.5782C>T
c.6240C>T (p.Gly2080=)
c.704+460C>T (n.704+460C>T)
c.3562C>T
c.5964C>T (p.Gly1988=)
c.5676C>T (p.Gly1892=)
c.3204C>T (p.Gly1068=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.35732790C>ACA405427216KMT2Bn.547C>A
c.6175C>A (p.Gln2059Lys)
c.3782C>A (n.3782C>A)
c.1459C>A (p.Gln487Lys)
n.1394C>A
c.1462C>A (p.Gln488Lys)
c.5783C>A
c.6241C>A (p.Gln2081Lys)
c.704+461C>A (n.704+461C>A)
c.3563C>A
c.5965C>A (p.Gln1989Lys)
c.5677C>A (p.Gln1893Lys)
c.3205C>A (p.Gln1069Lys)
gnomAD v4
19g.35732790C=CA2333794508KMT2Bn.547C=
c.6175C= (p.Gln2059=)
c.3782C= (n.3782C=)
c.1459C= (p.Gln487=)
n.1394C=
c.1462C= (p.Gln488=)
c.5783C=
c.6241C= (p.Gln2081=)
c.704+461C= (n.704+461C=)
c.3563C=
c.5965C= (p.Gln1989=)
c.5677C= (p.Gln1893=)
c.3205C= (p.Gln1069=)
19g.35732790C>GCA405427218KMT2Bn.547C>G
c.6175C>G (p.Gln2059Glu)
c.3782C>G (n.3782C>G)
c.1459C>G (p.Gln487Glu)
n.1394C>G
c.1462C>G (p.Gln488Glu)
c.5783C>G
c.6241C>G (p.Gln2081Glu)
c.704+461C>G (n.704+461C>G)
c.3563C>G
c.5965C>G (p.Gln1989Glu)
c.5677C>G (p.Gln1893Glu)
c.3205C>G (p.Gln1069Glu)
dbSNP gnomAD v3 gnomAD v4
19g.35732790C>TCA405427227KMT2Bn.547C>T
c.6175C>T (p.Gln2059Ter)
c.3782C>T (n.3782C>T)
c.1459C>T (p.Gln487Ter)
n.1394C>T
c.1462C>T (p.Gln488Ter)
c.5783C>T
c.6241C>T (p.Gln2081Ter)
c.704+461C>T (n.704+461C>T)
c.3563C>T
c.5965C>T (p.Gln1989Ter)
c.5677C>T (p.Gln1893Ter)
c.3205C>T (p.Gln1069Ter)
19g.35732791A>CCA405427232KMT2Bn.548A>C
c.6176A>C (p.Gln2059Pro)
c.3783A>C (n.3783A>C)
c.1460A>C (p.Gln487Pro)
n.1395A>C
c.1463A>C (p.Gln488Pro)
c.5784A>C
c.6242A>C (p.Gln2081Pro)
c.704+462A>C (n.704+462A>C)
c.3564A>C
c.5966A>C (p.Gln1989Pro)
c.5678A>C (p.Gln1893Pro)
c.3206A>C (p.Gln1069Pro)
19g.35732791A>GCA405427235KMT2Bn.548A>G
c.6176A>G (p.Gln2059Arg)
c.3783A>G (n.3783A>G)
c.1460A>G (p.Gln487Arg)
n.1395A>G
c.1463A>G (p.Gln488Arg)
c.5784A>G
c.6242A>G (p.Gln2081Arg)
c.704+462A>G (n.704+462A>G)
c.3564A>G
c.5966A>G (p.Gln1989Arg)
c.5678A>G (p.Gln1893Arg)
c.3206A>G (p.Gln1069Arg)
19g.35732791A>TCA405427239KMT2Bn.548A>T
c.6176A>T (p.Gln2059Leu)
c.3783A>T (n.3783A>T)
c.1460A>T (p.Gln487Leu)
n.1395A>T
c.1463A>T (p.Gln488Leu)
c.5784A>T
c.6242A>T (p.Gln2081Leu)
c.704+462A>T (n.704+462A>T)
c.3564A>T
c.5966A>T (p.Gln1989Leu)
c.5678A>T (p.Gln1893Leu)
c.3206A>T (p.Gln1069Leu)
19g.35732792G>ACA507308230KMT2Bn.549G>A
c.6177G>A (p.Gln2059=)
c.3784G>A (n.3784G>A)
c.1461G>A (p.Gln487=)
n.1396G>A
c.1464G>A (p.Gln488=)
c.5785G>A
c.6243G>A (p.Gln2081=)
c.704+463G>A (n.704+463G>A)
c.3565G>A
c.5967G>A (p.Gln1989=)
c.5679G>A (p.Gln1893=)
c.3207G>A (p.Gln1069=)
gnomAD v4
19g.35732792G>CCA405427247KMT2Bn.549G>C
c.6177G>C (p.Gln2059His)
c.3784G>C (n.3784G>C)
c.1461G>C (p.Gln487His)
n.1396G>C
c.1464G>C (p.Gln488His)
c.5785G>C
c.6243G>C (p.Gln2081His)
c.704+463G>C (n.704+463G>C)
c.3565G>C
c.5967G>C (p.Gln1989His)
c.5679G>C (p.Gln1893His)
c.3207G>C (p.Gln1069His)
dbSNP gnomAD v2
19g.35732792G=CA2333794509KMT2Bn.549G=
c.6177G= (p.Gln2059=)
c.3784G= (n.3784G=)
c.1461G= (p.Gln487=)
n.1396G=
c.1464G= (p.Gln488=)
c.5785G=
c.6243G= (p.Gln2081=)
c.704+463G= (n.704+463G=)
c.3565G=
c.5967G= (p.Gln1989=)
c.5679G= (p.Gln1893=)
c.3207G= (p.Gln1069=)
19g.35732792G>TCA405427245KMT2Bn.549G>T
c.6177G>T (p.Gln2059His)
c.3784G>T (n.3784G>T)
c.1461G>T (p.Gln487His)
n.1396G>T
c.1464G>T (p.Gln488His)
c.5785G>T
c.6243G>T (p.Gln2081His)
c.704+463G>T (n.704+463G>T)
c.3565G>T
c.5967G>T (p.Gln1989His)
c.5679G>T (p.Gln1893His)
c.3207G>T (p.Gln1069His)
19g.35732794delCA2814254939KMT2Bn.551del
c.6179del (p.Gly2060AlafsTer9)
c.3786del (n.3786del)
c.1463del (p.Gly488AlafsTer9)
n.1398del
c.1466del (p.Gly489AlafsTer9)
c.5787del
c.6245del (p.Gly2082AlafsTer9)
c.704+465del (n.704+465del)
c.3567del
c.5969del (p.Gly1990AlafsTer9)
c.5681del (p.Gly1894AlafsTer9)
c.3209del (p.Gly1070AlafsTer9)
19g.35732793G>ACA405427252KMT2Bn.550G>A
c.6178G>A (p.Gly2060Ser)
c.3785G>A (n.3785G>A)
c.1462G>A (p.Gly488Ser)
n.1397G>A
c.1465G>A (p.Gly489Ser)
c.5786G>A
c.6244G>A (p.Gly2082Ser)
c.704+464G>A (n.704+464G>A)
c.3566G>A
c.5968G>A (p.Gly1990Ser)
c.5680G>A (p.Gly1894Ser)
c.3208G>A (p.Gly1070Ser)
19g.35732793G>CCA405427257KMT2Bn.550G>C
c.6178G>C (p.Gly2060Arg)
c.3785G>C (n.3785G>C)
c.1462G>C (p.Gly488Arg)
n.1397G>C
c.1465G>C (p.Gly489Arg)
c.5786G>C
c.6244G>C (p.Gly2082Arg)
c.704+464G>C (n.704+464G>C)
c.3566G>C
c.5968G>C (p.Gly1990Arg)
c.5680G>C (p.Gly1894Arg)
c.3208G>C (p.Gly1070Arg)
19g.35732793G>TCA405427256KMT2Bn.550G>T
c.6178G>T (p.Gly2060Cys)
c.3785G>T (n.3785G>T)
c.1462G>T (p.Gly488Cys)
n.1397G>T
c.1465G>T (p.Gly489Cys)
c.5786G>T
c.6244G>T (p.Gly2082Cys)
c.704+464G>T (n.704+464G>T)
c.3566G>T
c.5968G>T (p.Gly1990Cys)
c.5680G>T (p.Gly1894Cys)
c.3208G>T (p.Gly1070Cys)
19g.35732794G>ACA405427263KMT2Bn.551G>A
c.6179G>A (p.Gly2060Asp)
c.3786G>A (n.3786G>A)
c.1463G>A (p.Gly488Asp)
n.1398G>A
c.1466G>A (p.Gly489Asp)
c.5787G>A
c.6245G>A (p.Gly2082Asp)
c.704+465G>A (n.704+465G>A)
c.3567G>A
c.5969G>A (p.Gly1990Asp)
c.5681G>A (p.Gly1894Asp)
c.3209G>A (p.Gly1070Asp)
gnomAD v4
19g.35732794G>CCA405427272KMT2Bn.551G>C
c.6179G>C (p.Gly2060Ala)
c.3786G>C (n.3786G>C)
c.1463G>C (p.Gly488Ala)
n.1398G>C
c.1466G>C (p.Gly489Ala)
c.5787G>C
c.6245G>C (p.Gly2082Ala)
c.704+465G>C (n.704+465G>C)
c.3567G>C
c.5969G>C (p.Gly1990Ala)
c.5681G>C (p.Gly1894Ala)
c.3209G>C (p.Gly1070Ala)
19g.35732794G>TCA405427266KMT2Bn.551G>T
c.6179G>T (p.Gly2060Val)
c.3786G>T (n.3786G>T)
c.1463G>T (p.Gly488Val)
n.1398G>T
c.1466G>T (p.Gly489Val)
c.5787G>T
c.6245G>T (p.Gly2082Val)
c.704+465G>T (n.704+465G>T)
c.3567G>T
c.5969G>T (p.Gly1990Val)
c.5681G>T (p.Gly1894Val)
c.3209G>T (p.Gly1070Val)
gnomAD v4
19g.35732795C>ACA507308234KMT2Bn.552C>A
c.6180C>A (p.Gly2060=)
c.3787C>A (n.3787C>A)
c.1464C>A (p.Gly488=)
n.1399C>A
c.1467C>A (p.Gly489=)
c.5788C>A
c.6246C>A (p.Gly2082=)
c.704+466C>A (n.704+466C>A)
c.3568C>A
c.5970C>A (p.Gly1990=)
c.5682C>A (p.Gly1894=)
c.3210C>A (p.Gly1070=)
19g.35732795C>GCA507308236KMT2Bn.552C>G
c.6180C>G (p.Gly2060=)
c.3787C>G (n.3787C>G)
c.1464C>G (p.Gly488=)
n.1399C>G
c.1467C>G (p.Gly489=)
c.5788C>G
c.6246C>G (p.Gly2082=)
c.704+466C>G (n.704+466C>G)
c.3568C>G
c.5970C>G (p.Gly1990=)
c.5682C>G (p.Gly1894=)
c.3210C>G (p.Gly1070=)
19g.35732795C>TCA507308239KMT2Bn.552C>T
c.6180C>T (p.Gly2060=)
c.3787C>T (n.3787C>T)
c.1464C>T (p.Gly488=)
n.1399C>T
c.1467C>T (p.Gly489=)
c.5788C>T
c.6246C>T (p.Gly2082=)
c.704+466C>T (n.704+466C>T)
c.3568C>T
c.5970C>T (p.Gly1990=)
c.5682C>T (p.Gly1894=)
c.3210C>T (p.Gly1070=)
19g.35732796A>CCA405427277KMT2Bn.553A>C
c.6181A>C (p.Thr2061Pro)
c.3788A>C (n.3788A>C)
c.1465A>C (p.Thr489Pro)
n.1400A>C
c.1468A>C (p.Thr490Pro)
c.5789A>C
c.6247A>C (p.Thr2083Pro)
c.704+467A>C (n.704+467A>C)
c.3569A>C
c.5971A>C (p.Thr1991Pro)
c.5683A>C (p.Thr1895Pro)
c.3211A>C (p.Thr1071Pro)
19g.35732796A>GCA405427279KMT2Bn.553A>G
c.6181A>G (p.Thr2061Ala)
c.3788A>G (n.3788A>G)
c.1465A>G (p.Thr489Ala)
n.1400A>G
c.1468A>G (p.Thr490Ala)
c.5789A>G
c.6247A>G (p.Thr2083Ala)
c.704+467A>G (n.704+467A>G)
c.3569A>G
c.5971A>G (p.Thr1991Ala)
c.5683A>G (p.Thr1895Ala)
c.3211A>G (p.Thr1071Ala)
19g.35732796A>TCA405427283KMT2Bn.553A>T
c.6181A>T (p.Thr2061Ser)
c.3788A>T (n.3788A>T)
c.1465A>T (p.Thr489Ser)
n.1400A>T
c.1468A>T (p.Thr490Ser)
c.5789A>T
c.6247A>T (p.Thr2083Ser)
c.704+467A>T (n.704+467A>T)
c.3569A>T
c.5971A>T (p.Thr1991Ser)
c.5683A>T (p.Thr1895Ser)
c.3211A>T (p.Thr1071Ser)
gnomAD v4
19g.35732797C>ACA405427288KMT2Bn.554C>A
c.6182C>A (p.Thr2061Lys)
c.3789C>A (n.3789C>A)
c.1466C>A (p.Thr489Lys)
n.1401C>A
c.1469C>A (p.Thr490Lys)
c.5790C>A
c.6248C>A (p.Thr2083Lys)
c.704+468C>A (n.704+468C>A)
c.3570C>A
c.5972C>A (p.Thr1991Lys)
c.5684C>A (p.Thr1895Lys)
c.3212C>A (p.Thr1071Lys)
19g.35732797C=CA2333794510KMT2Bn.554C=
c.6182C= (p.Thr2061=)
c.3789C= (n.3789C=)
c.1466C= (p.Thr489=)
n.1401C=
c.1469C= (p.Thr490=)
c.5790C=
c.6248C= (p.Thr2083=)
c.704+468C= (n.704+468C=)
c.3570C=
c.5972C= (p.Thr1991=)
c.5684C= (p.Thr1895=)
c.3212C= (p.Thr1071=)
19g.35732797C>GCA405427291KMT2Bn.554C>G
c.6182C>G (p.Thr2061Arg)
c.3789C>G (n.3789C>G)
c.1466C>G (p.Thr489Arg)
n.1401C>G
c.1469C>G (p.Thr490Arg)
c.5790C>G
c.6248C>G (p.Thr2083Arg)
c.704+468C>G (n.704+468C>G)
c.3570C>G
c.5972C>G (p.Thr1991Arg)
c.5684C>G (p.Thr1895Arg)
c.3212C>G (p.Thr1071Arg)
19g.35732797C>TCA9385643KMT2Bn.554C>T
c.6182C>T (p.Thr2061Met)
c.3789C>T (n.3789C>T)
c.1466C>T (p.Thr489Met)
n.1401C>T
c.1469C>T (p.Thr490Met)
c.5790C>T
c.6248C>T (p.Thr2083Met)
c.704+468C>T (n.704+468C>T)
c.3570C>T
c.5972C>T (p.Thr1991Met)
c.5684C>T (p.Thr1895Met)
c.3212C>T (p.Thr1071Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.35732798G>ACA9385645KMT2Bn.555G>A
c.6183G>A (p.Thr2061=)
c.3790G>A (n.3790G>A)
c.1467G>A (p.Thr489=)
n.1402G>A
c.1470G>A (p.Thr490=)
c.5791G>A
c.6249G>A (p.Thr2083=)
c.704+469G>A (n.704+469G>A)
c.3571G>A
c.5973G>A (p.Thr1991=)
c.5685G>A (p.Thr1895=)
c.3213G>A (p.Thr1071=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.35732798G>CCA507308247KMT2Bn.555G>C
c.6183G>C (p.Thr2061=)
c.3790G>C (n.3790G>C)
c.1467G>C (p.Thr489=)
n.1402G>C
c.1470G>C (p.Thr490=)
c.5791G>C
c.6249G>C (p.Thr2083=)
c.704+469G>C (n.704+469G>C)
c.3571G>C
c.5973G>C (p.Thr1991=)
c.5685G>C (p.Thr1895=)
c.3213G>C (p.Thr1071=)
19g.35732798G=CA2333794511KMT2Bn.555G=
c.6183G= (p.Thr2061=)
c.3790G= (n.3790G=)
c.1467G= (p.Thr489=)
n.1402G=
c.1470G= (p.Thr490=)
c.5791G=
c.6249G= (p.Thr2083=)
c.704+469G= (n.704+469G=)
c.3571G=
c.5973G= (p.Thr1991=)
c.5685G= (p.Thr1895=)
c.3213G= (p.Thr1071=)
19g.35732798G>TCA9385644KMT2Bn.555G>T
c.6183G>T (p.Thr2061=)
c.3790G>T (n.3790G>T)
c.1467G>T (p.Thr489=)
n.1402G>T
c.1470G>T (p.Thr490=)
c.5791G>T
c.6249G>T (p.Thr2083=)
c.704+469G>T (n.704+469G>T)
c.3571G>T
c.5973G>T (p.Thr1991=)
c.5685G>T (p.Thr1895=)
c.3213G>T (p.Thr1071=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732799C>ACA405427294KMT2Bn.556C>A
c.6184C>A (p.Pro2062Thr)
c.3791C>A (n.3791C>A)
c.1468C>A (p.Pro490Thr)
n.1403C>A
c.1471C>A (p.Pro491Thr)
c.5792C>A
c.6250C>A (p.Pro2084Thr)
c.704+470C>A (n.704+470C>A)
c.3572C>A
c.5974C>A (p.Pro1992Thr)
c.5686C>A (p.Pro1896Thr)
c.3214C>A (p.Pro1072Thr)
19g.35732799C>GCA405427295KMT2Bn.556C>G
c.6184C>G (p.Pro2062Ala)
c.3791C>G (n.3791C>G)
c.1468C>G (p.Pro490Ala)
n.1403C>G
c.1471C>G (p.Pro491Ala)
c.5792C>G
c.6250C>G (p.Pro2084Ala)
c.704+470C>G (n.704+470C>G)
c.3572C>G
c.5974C>G (p.Pro1992Ala)
c.5686C>G (p.Pro1896Ala)
c.3214C>G (p.Pro1072Ala)
19g.35732799C>TCA405427300KMT2Bn.556C>T
c.6184C>T (p.Pro2062Ser)
c.3791C>T (n.3791C>T)
c.1468C>T (p.Pro490Ser)
n.1403C>T
c.1471C>T (p.Pro491Ser)
c.5792C>T
c.6250C>T (p.Pro2084Ser)
c.704+470C>T (n.704+470C>T)
c.3572C>T
c.5974C>T (p.Pro1992Ser)
c.5686C>T (p.Pro1896Ser)
c.3214C>T (p.Pro1072Ser)
19g.35732800C>ACA405427319KMT2Bn.557C>A
c.6185C>A (p.Pro2062His)
c.3792C>A (n.3792C>A)
c.1469C>A (p.Pro490His)
n.1404C>A
c.1472C>A (p.Pro491His)
c.5793C>A
c.6251C>A (p.Pro2084His)
c.704+471C>A (n.704+471C>A)
c.3573C>A
c.5975C>A (p.Pro1992His)
c.5687C>A (p.Pro1896His)
c.3215C>A (p.Pro1072His)
19g.35732800C=CA2333794512KMT2Bn.557C=
c.6185C= (p.Pro2062=)
c.3792C= (n.3792C=)
c.1469C= (p.Pro490=)
n.1404C=
c.1472C= (p.Pro491=)
c.5793C=
c.6251C= (p.Pro2084=)
c.704+471C= (n.704+471C=)
c.3573C=
c.5975C= (p.Pro1992=)
c.5687C= (p.Pro1896=)
c.3215C= (p.Pro1072=)
19g.35732800C>GCA405427310KMT2Bn.557C>G
c.6185C>G (p.Pro2062Arg)
c.3792C>G (n.3792C>G)
c.1469C>G (p.Pro490Arg)
n.1404C>G
c.1472C>G (p.Pro491Arg)
c.5793C>G
c.6251C>G (p.Pro2084Arg)
c.704+471C>G (n.704+471C>G)
c.3573C>G
c.5975C>G (p.Pro1992Arg)
c.5687C>G (p.Pro1896Arg)
c.3215C>G (p.Pro1072Arg)
19g.35732800C>TCA405427305KMT2Bn.557C>T
c.6185C>T (p.Pro2062Leu)
c.3792C>T (n.3792C>T)
c.1469C>T (p.Pro490Leu)
n.1404C>T
c.1472C>T (p.Pro491Leu)
c.5793C>T
c.6251C>T (p.Pro2084Leu)
c.704+471C>T (n.704+471C>T)
c.3573C>T
c.5975C>T (p.Pro1992Leu)
c.5687C>T (p.Pro1896Leu)
c.3215C>T (p.Pro1072Leu)
dbSNP gnomAD v2 gnomAD v4
19g.35732801T>ACA507308253KMT2Bn.558T>A
c.6186T>A (p.Pro2062=)
c.3793T>A (n.3793T>A)
c.1470T>A (p.Pro490=)
n.1405T>A
c.1473T>A (p.Pro491=)
c.5794T>A
c.6252T>A (p.Pro2084=)
c.704+472T>A (n.704+472T>A)
c.3574T>A
c.5976T>A (p.Pro1992=)
c.5688T>A (p.Pro1896=)
c.3216T>A (p.Pro1072=)
gnomAD v4
19g.35732801T>CCA507308254KMT2Bn.558T>C
c.6186T>C (p.Pro2062=)
c.3793T>C (n.3793T>C)
c.1470T>C (p.Pro490=)
n.1405T>C
c.1473T>C (p.Pro491=)
c.5794T>C
c.6252T>C (p.Pro2084=)
c.704+472T>C (n.704+472T>C)
c.3574T>C
c.5976T>C (p.Pro1992=)
c.5688T>C (p.Pro1896=)
c.3216T>C (p.Pro1072=)
19g.35732801T>GCA507308256KMT2Bn.558T>G
c.6186T>G (p.Pro2062=)
c.3793T>G (n.3793T>G)
c.1470T>G (p.Pro490=)
n.1405T>G
c.1473T>G (p.Pro491=)
c.5794T>G
c.6252T>G (p.Pro2084=)
c.704+472T>G (n.704+472T>G)
c.3574T>G
c.5976T>G (p.Pro1992=)
c.5688T>G (p.Pro1896=)
c.3216T>G (p.Pro1072=)
gnomAD v4
19g.35732802C>ACA405427326KMT2Bn.559C>A
c.6187C>A (p.Pro2063Thr)
c.3794C>A (n.3794C>A)
c.1471C>A (p.Pro491Thr)
n.1406C>A
c.1474C>A (p.Pro492Thr)
c.5795C>A
c.6253C>A (p.Pro2085Thr)
c.704+473C>A (n.704+473C>A)
c.3575C>A
c.5977C>A (p.Pro1993Thr)
c.5689C>A (p.Pro1897Thr)
c.3217C>A (p.Pro1073Thr)
19g.35732802C>GCA405427330KMT2Bn.559C>G
c.6187C>G (p.Pro2063Ala)
c.3794C>G (n.3794C>G)
c.1471C>G (p.Pro491Ala)
n.1406C>G
c.1474C>G (p.Pro492Ala)
c.5795C>G
c.6253C>G (p.Pro2085Ala)
c.704+473C>G (n.704+473C>G)
c.3575C>G
c.5977C>G (p.Pro1993Ala)
c.5689C>G (p.Pro1897Ala)
c.3217C>G (p.Pro1073Ala)
19g.35732802C>TCA405427332KMT2Bn.559C>T
c.6187C>T (p.Pro2063Ser)
c.3794C>T (n.3794C>T)
c.1471C>T (p.Pro491Ser)
n.1406C>T
c.1474C>T (p.Pro492Ser)
c.5795C>T
c.6253C>T (p.Pro2085Ser)
c.704+473C>T (n.704+473C>T)
c.3575C>T
c.5977C>T (p.Pro1993Ser)
c.5689C>T (p.Pro1897Ser)
c.3217C>T (p.Pro1073Ser)
19g.35732803C>ACA405427337KMT2Bn.560C>A
c.6188C>A (p.Pro2063His)
c.3795C>A (n.3795C>A)
c.1472C>A (p.Pro491His)
n.1407C>A
c.1475C>A (p.Pro492His)
c.5796C>A
c.6254C>A (p.Pro2085His)
c.704+474C>A (n.704+474C>A)
c.3576C>A
c.5978C>A (p.Pro1993His)
c.5690C>A (p.Pro1897His)
c.3218C>A (p.Pro1073His)
gnomAD v4
19g.35732803C>GCA405427340KMT2Bn.560C>G
c.6188C>G (p.Pro2063Arg)
c.3795C>G (n.3795C>G)
c.1472C>G (p.Pro491Arg)
n.1407C>G
c.1475C>G (p.Pro492Arg)
c.5796C>G
c.6254C>G (p.Pro2085Arg)
c.704+474C>G (n.704+474C>G)
c.3576C>G
c.5978C>G (p.Pro1993Arg)
c.5690C>G (p.Pro1897Arg)
c.3218C>G (p.Pro1073Arg)
19g.35732803C>TCA405427345KMT2Bn.560C>T
c.6188C>T (p.Pro2063Leu)
c.3795C>T (n.3795C>T)
c.1472C>T (p.Pro491Leu)
n.1407C>T
c.1475C>T (p.Pro492Leu)
c.5796C>T
c.6254C>T (p.Pro2085Leu)
c.704+474C>T (n.704+474C>T)
c.3576C>T
c.5978C>T (p.Pro1993Leu)
c.5690C>T (p.Pro1897Leu)
c.3218C>T (p.Pro1073Leu)
19g.35732804_35732806delCA2584575161KMT2Bn.561_563del
c.6189_6191del (p.Ser2064del)
c.3796_3798del (n.3796_3798del)
c.1473_1475del (p.Ser492del)
n.1408_1410del
c.1476_1478del (p.Ser493del)
c.5797_5799del
c.6255_6257del (p.Ser2086del)
c.704+475_704+477del (n.704+475_704+477del)
c.3577_3579del
c.5979_5981del (p.Ser1994del)
c.5691_5693del (p.Ser1898del)
c.3219_3221del (p.Ser1074del)
gnomAD v4
19g.35732804T>ACA507308261KMT2Bn.561T>A
c.6189T>A (p.Pro2063=)
c.3796T>A (n.3796T>A)
c.1473T>A (p.Pro491=)
n.1408T>A
c.1476T>A (p.Pro492=)
c.5797T>A
c.6255T>A (p.Pro2085=)
c.704+475T>A (n.704+475T>A)
c.3577T>A
c.5979T>A (p.Pro1993=)
c.5691T>A (p.Pro1897=)
c.3219T>A (p.Pro1073=)
19g.35732804T>CCA507308268KMT2Bn.561T>C
c.6189T>C (p.Pro2063=)
c.3796T>C (n.3796T>C)
c.1473T>C (p.Pro491=)
n.1408T>C
c.1476T>C (p.Pro492=)
c.5797T>C
c.6255T>C (p.Pro2085=)
c.704+475T>C (n.704+475T>C)
c.3577T>C
c.5979T>C (p.Pro1993=)
c.5691T>C (p.Pro1897=)
c.3219T>C (p.Pro1073=)
19g.35732804T>GCA507308269KMT2Bn.561T>G
c.6189T>G (p.Pro2063=)
c.3796T>G (n.3796T>G)
c.1473T>G (p.Pro491=)
n.1408T>G
c.1476T>G (p.Pro492=)
c.5797T>G
c.6255T>G (p.Pro2085=)
c.704+475T>G (n.704+475T>G)
c.3577T>G
c.5979T>G (p.Pro1993=)
c.5691T>G (p.Pro1897=)
c.3219T>G (p.Pro1073=)
19g.35732805T>ACA405427349KMT2Bn.562T>A
c.6190T>A (p.Ser2064Thr)
c.3797T>A (n.3797T>A)
c.1474T>A (p.Ser492Thr)
n.1409T>A
c.1477T>A (p.Ser493Thr)
c.5798T>A
c.6256T>A (p.Ser2086Thr)
c.704+476T>A (n.704+476T>A)
c.3578T>A
c.5980T>A (p.Ser1994Thr)
c.5692T>A (p.Ser1898Thr)
c.3220T>A (p.Ser1074Thr)
19g.35732805T>CCA405427351KMT2Bn.562T>C
c.6190T>C (p.Ser2064Pro)
c.3797T>C (n.3797T>C)
c.1474T>C (p.Ser492Pro)
n.1409T>C
c.1477T>C (p.Ser493Pro)
c.5798T>C
c.6256T>C (p.Ser2086Pro)
c.704+476T>C (n.704+476T>C)
c.3578T>C
c.5980T>C (p.Ser1994Pro)
c.5692T>C (p.Ser1898Pro)
c.3220T>C (p.Ser1074Pro)
19g.35732805T>GCA405427354KMT2Bn.562T>G
c.6190T>G (p.Ser2064Ala)
c.3797T>G (n.3797T>G)
c.1474T>G (p.Ser492Ala)
n.1409T>G
c.1477T>G (p.Ser493Ala)
c.5798T>G
c.6256T>G (p.Ser2086Ala)
c.704+476T>G (n.704+476T>G)
c.3578T>G
c.5980T>G (p.Ser1994Ala)
c.5692T>G (p.Ser1898Ala)
c.3220T>G (p.Ser1074Ala)
19g.35732806C>ACA405427360KMT2Bn.563C>A
c.6191C>A (p.Ser2064Ter)
c.3798C>A (n.3798C>A)
c.1475C>A (p.Ser492Ter)
n.1410C>A
c.1478C>A (p.Ser493Ter)
c.5799C>A
c.6257C>A (p.Ser2086Ter)
c.704+477C>A (n.704+477C>A)
c.3579C>A
c.5981C>A (p.Ser1994Ter)
c.5693C>A (p.Ser1898Ter)
c.3221C>A (p.Ser1074Ter)
gnomAD v4
19g.35732806C=CA2333794513KMT2Bn.563C=
c.6191C= (p.Ser2064=)
c.3798C= (n.3798C=)
c.1475C= (p.Ser492=)
n.1410C=
c.1478C= (p.Ser493=)
c.5799C=
c.6257C= (p.Ser2086=)
c.704+477C= (n.704+477C=)
c.3579C=
c.5981C= (p.Ser1994=)
c.5693C= (p.Ser1898=)
c.3221C= (p.Ser1074=)
19g.35732806C>GCA405427362KMT2Bn.563C>G
c.6191C>G (p.Ser2064Trp)
c.3798C>G (n.3798C>G)
c.1475C>G (p.Ser492Trp)
n.1410C>G
c.1478C>G (p.Ser493Trp)
c.5799C>G
c.6257C>G (p.Ser2086Trp)
c.704+477C>G (n.704+477C>G)
c.3579C>G
c.5981C>G (p.Ser1994Trp)
c.5693C>G (p.Ser1898Trp)
c.3221C>G (p.Ser1074Trp)
19g.35732806C>TCA405427365KMT2Bn.563C>T
c.6191C>T (p.Ser2064Leu)
c.3798C>T (n.3798C>T)
c.1475C>T (p.Ser492Leu)
n.1410C>T
c.1478C>T (p.Ser493Leu)
c.5799C>T
c.6257C>T (p.Ser2086Leu)
c.704+477C>T (n.704+477C>T)
c.3579C>T
c.5981C>T (p.Ser1994Leu)
c.5693C>T (p.Ser1898Leu)
c.3221C>T (p.Ser1074Leu)
dbSNP gnomAD v2 gnomAD v4 COSMIC
19g.35732807G>ACA9385646KMT2Bn.564G>A
c.6192G>A (p.Ser2064=)
c.3799G>A (n.3799G>A)
c.1476G>A (p.Ser492=)
n.1411G>A
c.1479G>A (p.Ser493=)
c.5800G>A
c.6258G>A (p.Ser2086=)
c.704+478G>A (n.704+478G>A)
c.3580G>A
c.5982G>A (p.Ser1994=)
c.5694G>A (p.Ser1898=)
c.3222G>A (p.Ser1074=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732807G>CCA507308274KMT2Bn.564G>C
c.6192G>C (p.Ser2064=)
c.3799G>C (n.3799G>C)
c.1476G>C (p.Ser492=)
n.1411G>C
c.1479G>C (p.Ser493=)
c.5800G>C
c.6258G>C (p.Ser2086=)
c.704+478G>C (n.704+478G>C)
c.3580G>C
c.5982G>C (p.Ser1994=)
c.5694G>C (p.Ser1898=)
c.3222G>C (p.Ser1074=)
19g.35732807G=CA2333794514KMT2Bn.564G=
c.6192G= (p.Ser2064=)
c.3799G= (n.3799G=)
c.1476G= (p.Ser492=)
n.1411G=
c.1479G= (p.Ser493=)
c.5800G=
c.6258G= (p.Ser2086=)
c.704+478G= (n.704+478G=)
c.3580G=
c.5982G= (p.Ser1994=)
c.5694G= (p.Ser1898=)
c.3222G= (p.Ser1074=)
19g.35732807G>TCA507308277KMT2Bn.564G>T
c.6192G>T (p.Ser2064=)
c.3799G>T (n.3799G>T)
c.1476G>T (p.Ser492=)
n.1411G>T
c.1479G>T (p.Ser493=)
c.5800G>T
c.6258G>T (p.Ser2086=)
c.704+478G>T (n.704+478G>T)
c.3580G>T
c.5982G>T (p.Ser1994=)
c.5694G>T (p.Ser1898=)
c.3222G>T (p.Ser1074=)
19g.35732808G>ACA405427381KMT2Bn.565G>A
c.6193G>A (p.Gly2065Arg)
c.3800G>A (n.3800G>A)
c.1477G>A (p.Gly493Arg)
n.1412G>A
c.1480G>A (p.Gly494Arg)
c.5801G>A
c.6259G>A (p.Gly2087Arg)
c.704+479G>A (n.704+479G>A)
c.3581G>A
c.5983G>A (p.Gly1995Arg)
c.5695G>A (p.Gly1899Arg)
c.3223G>A (p.Gly1075Arg)
19g.35732808G>CCA405427373KMT2Bn.565G>C
c.6193G>C (p.Gly2065Arg)
c.3800G>C (n.3800G>C)
c.1477G>C (p.Gly493Arg)
n.1412G>C
c.1480G>C (p.Gly494Arg)
c.5801G>C
c.6259G>C (p.Gly2087Arg)
c.704+479G>C (n.704+479G>C)
c.3581G>C
c.5983G>C (p.Gly1995Arg)
c.5695G>C (p.Gly1899Arg)
c.3223G>C (p.Gly1075Arg)
19g.35732808G>TCA405427379KMT2Bn.565G>T
c.6193G>T (p.Gly2065Trp)
c.3800G>T (n.3800G>T)
c.1477G>T (p.Gly493Trp)
n.1412G>T
c.1480G>T (p.Gly494Trp)
c.5801G>T
c.6259G>T (p.Gly2087Trp)
c.704+479G>T (n.704+479G>T)
c.3581G>T
c.5983G>T (p.Gly1995Trp)
c.5695G>T (p.Gly1899Trp)
c.3223G>T (p.Gly1075Trp)
19g.35732809G>ACA405427386KMT2Bn.566G>A
c.6194G>A (p.Gly2065Glu)
c.3801G>A (n.3801G>A)
c.1478G>A (p.Gly493Glu)
n.1413G>A
c.1481G>A (p.Gly494Glu)
c.5802G>A
c.6260G>A (p.Gly2087Glu)
c.704+480G>A (n.704+480G>A)
c.3582G>A
c.5984G>A (p.Gly1995Glu)
c.5696G>A (p.Gly1899Glu)
c.3224G>A (p.Gly1075Glu)
19g.35732809G>CCA405427387KMT2Bn.566G>C
c.6194G>C (p.Gly2065Ala)
c.3801G>C (n.3801G>C)
c.1478G>C (p.Gly493Ala)
n.1413G>C
c.1481G>C (p.Gly494Ala)
c.5802G>C
c.6260G>C (p.Gly2087Ala)
c.704+480G>C (n.704+480G>C)
c.3582G>C
c.5984G>C (p.Gly1995Ala)
c.5696G>C (p.Gly1899Ala)
c.3224G>C (p.Gly1075Ala)
19g.35732809G>TCA405427388KMT2Bn.566G>T
c.6194G>T (p.Gly2065Val)
c.3801G>T (n.3801G>T)
c.1478G>T (p.Gly493Val)
n.1413G>T
c.1481G>T (p.Gly494Val)
c.5802G>T
c.6260G>T (p.Gly2087Val)
c.704+480G>T (n.704+480G>T)
c.3582G>T
c.5984G>T (p.Gly1995Val)
c.5696G>T (p.Gly1899Val)
c.3224G>T (p.Gly1075Val)
19g.35732810G>ACA507308282KMT2Bn.567G>A
c.6195G>A (p.Gly2065=)
c.3802G>A (n.3802G>A)
c.1479G>A (p.Gly493=)
n.1414G>A
c.1482G>A (p.Gly494=)
c.5803G>A
c.6261G>A (p.Gly2087=)
c.704+481G>A (n.704+481G>A)
c.3583G>A
c.5985G>A (p.Gly1995=)
c.5697G>A (p.Gly1899=)
c.3225G>A (p.Gly1075=)
19g.35732810G>CCA507308284KMT2Bn.567G>C
c.6195G>C (p.Gly2065=)
c.3802G>C (n.3802G>C)
c.1479G>C (p.Gly493=)
n.1414G>C
c.1482G>C (p.Gly494=)
c.5803G>C
c.6261G>C (p.Gly2087=)
c.704+481G>C (n.704+481G>C)
c.3583G>C
c.5985G>C (p.Gly1995=)
c.5697G>C (p.Gly1899=)
c.3225G>C (p.Gly1075=)
19g.35732810G>TCA507308286KMT2Bn.567G>T
c.6195G>T (p.Gly2065=)
c.3802G>T (n.3802G>T)
c.1479G>T (p.Gly493=)
n.1414G>T
c.1482G>T (p.Gly494=)
c.5803G>T
c.6261G>T (p.Gly2087=)
c.704+481G>T (n.704+481G>T)
c.3583G>T
c.5985G>T (p.Gly1995=)
c.5697G>T (p.Gly1899=)
c.3225G>T (p.Gly1075=)
gnomAD v4
19g.35732811C>ACA405427391KMT2Bn.568C>A
c.6196C>A (p.Pro2066Thr)
c.3803C>A (n.3803C>A)
c.1480C>A (p.Pro494Thr)
n.1415C>A
c.1483C>A (p.Pro495Thr)
c.5804C>A
c.6262C>A (p.Pro2088Thr)
c.704+482C>A (n.704+482C>A)
c.3584C>A
c.5986C>A (p.Pro1996Thr)
c.5698C>A (p.Pro1900Thr)
c.3226C>A (p.Pro1076Thr)
gnomAD v4
19g.35732811C=CA2333794515KMT2Bn.568C=
c.6196C= (p.Pro2066=)
c.3803C= (n.3803C=)
c.1480C= (p.Pro494=)
n.1415C=
c.1483C= (p.Pro495=)
c.5804C=
c.6262C= (p.Pro2088=)
c.704+482C= (n.704+482C=)
c.3584C=
c.5986C= (p.Pro1996=)
c.5698C= (p.Pro1900=)
c.3226C= (p.Pro1076=)
19g.35732811C>GCA405427394KMT2Bn.568C>G
c.6196C>G (p.Pro2066Ala)
c.3803C>G (n.3803C>G)
c.1480C>G (p.Pro494Ala)
n.1415C>G
c.1483C>G (p.Pro495Ala)
c.5804C>G
c.6262C>G (p.Pro2088Ala)
c.704+482C>G (n.704+482C>G)
c.3584C>G
c.5986C>G (p.Pro1996Ala)
c.5698C>G (p.Pro1900Ala)
c.3226C>G (p.Pro1076Ala)
19g.35732811C>TCA9385647KMT2Bn.568C>T
c.6196C>T (p.Pro2066Ser)
c.3803C>T (n.3803C>T)
c.1480C>T (p.Pro494Ser)
n.1415C>T
c.1483C>T (p.Pro495Ser)
c.5804C>T
c.6262C>T (p.Pro2088Ser)
c.704+482C>T (n.704+482C>T)
c.3584C>T
c.5986C>T (p.Pro1996Ser)
c.5698C>T (p.Pro1900Ser)
c.3226C>T (p.Pro1076Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732812C>ACA405427402KMT2Bn.569C>A
c.6197C>A (p.Pro2066Gln)
c.3804C>A (n.3804C>A)
c.1481C>A (p.Pro494Gln)
n.1416C>A
c.1484C>A (p.Pro495Gln)
c.5805C>A
c.6263C>A (p.Pro2088Gln)
c.704+483C>A (n.704+483C>A)
c.3585C>A
c.5987C>A (p.Pro1996Gln)
c.5699C>A (p.Pro1900Gln)
c.3227C>A (p.Pro1076Gln)
19g.35732812C>GCA405427405KMT2Bn.569C>G
c.6197C>G (p.Pro2066Arg)
c.3804C>G (n.3804C>G)
c.1481C>G (p.Pro494Arg)
n.1416C>G
c.1484C>G (p.Pro495Arg)
c.5805C>G
c.6263C>G (p.Pro2088Arg)
c.704+483C>G (n.704+483C>G)
c.3585C>G
c.5987C>G (p.Pro1996Arg)
c.5699C>G (p.Pro1900Arg)
c.3227C>G (p.Pro1076Arg)
19g.35732812C>TCA405427406KMT2Bn.569C>T
c.6197C>T (p.Pro2066Leu)
c.3804C>T (n.3804C>T)
c.1481C>T (p.Pro494Leu)
n.1416C>T
c.1484C>T (p.Pro495Leu)
c.5805C>T
c.6263C>T (p.Pro2088Leu)
c.704+483C>T (n.704+483C>T)
c.3585C>T
c.5987C>T (p.Pro1996Leu)
c.5699C>T (p.Pro1900Leu)
c.3227C>T (p.Pro1076Leu)
19g.35732812_35732815delinsCAGGCA2333794516KMT2Bn.569_572delinsCAGG
c.6197_6200delinsCAGG (p.Pro2066=)
c.3804_3807delinsCAGG (n.3804_3807delinsCAGG)
c.1481_1484delinsCAGG (p.Pro494=)
n.1416_1419delinsCAGG
c.1484_1487delinsCAGG (p.Pro495=)
c.5805_5808delinsCAGG
c.6263_6266delinsCAGG (p.Pro2088=)
c.704+483_704+486delinsCAGG (n.704+483_704+486delinsCAGG)
c.3585_3588delinsCAGG
c.5987_5990delinsCAGG (p.Pro1996=)
c.5699_5702delinsCAGG (p.Pro1900=)
c.3227_3230delinsCAGG (p.Pro1076=)
19g.35732813A>CCA507308293KMT2Bn.570A>C
c.6198A>C (p.Pro2066=)
c.3805A>C (n.3805A>C)
c.1482A>C (p.Pro494=)
n.1417A>C
c.1485A>C (p.Pro495=)
c.5806A>C
c.6264A>C (p.Pro2088=)
c.704+484A>C (n.704+484A>C)
c.3586A>C
c.5988A>C (p.Pro1996=)
c.5700A>C (p.Pro1900=)
c.3228A>C (p.Pro1076=)
19g.35732813A>GCA507308291KMT2Bn.570A>G
c.6198A>G (p.Pro2066=)
c.3805A>G (n.3805A>G)
c.1482A>G (p.Pro494=)
n.1417A>G
c.1485A>G (p.Pro495=)
c.5806A>G
c.6264A>G (p.Pro2088=)
c.704+484A>G (n.704+484A>G)
c.3586A>G
c.5988A>G (p.Pro1996=)
c.5700A>G (p.Pro1900=)
c.3228A>G (p.Pro1076=)
19g.35732813A>TCA507308289KMT2Bn.570A>T
c.6198A>T (p.Pro2066=)
c.3805A>T (n.3805A>T)
c.1482A>T (p.Pro494=)
n.1417A>T
c.1485A>T (p.Pro495=)
c.5806A>T
c.6264A>T (p.Pro2088=)
c.704+484A>T (n.704+484A>T)
c.3586A>T
c.5988A>T (p.Pro1996=)
c.5700A>T (p.Pro1900=)
c.3228A>T (p.Pro1076=)
19g.35732815_35732817delCA9385648KMT2Bn.572_574del
c.6200_6202del (p.Gly2067del)
c.3807_3809del (n.3807_3809del)
c.1484_1486del (p.Gly495del)
n.1419_1421del
c.1487_1489del (p.Gly496del)
c.5808_5810del
c.6266_6268del (p.Gly2089del)
c.704+486_704+488del (n.704+486_704+488del)
c.3588_3590del
c.5990_5992del (p.Gly1997del)
c.5702_5704del (p.Gly1901del)
c.3230_3232del (p.Gly1077del)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.35732814G>ACA405427412KMT2Bn.571G>A
c.6199G>A (p.Gly2067Arg)
c.3806G>A (n.3806G>A)
c.1483G>A (p.Gly495Arg)
n.1418G>A
c.1486G>A (p.Gly496Arg)
c.5807G>A
c.6265G>A (p.Gly2089Arg)
c.704+485G>A (n.704+485G>A)
c.3587G>A
c.5989G>A (p.Gly1997Arg)
c.5701G>A (p.Gly1901Arg)
c.3229G>A (p.Gly1077Arg)
gnomAD v4
19g.35732814G>CCA405427411KMT2Bn.571G>C
c.6199G>C (p.Gly2067Arg)
c.3806G>C (n.3806G>C)
c.1483G>C (p.Gly495Arg)
n.1418G>C
c.1486G>C (p.Gly496Arg)
c.5807G>C
c.6265G>C (p.Gly2089Arg)
c.704+485G>C (n.704+485G>C)
c.3587G>C
c.5989G>C (p.Gly1997Arg)
c.5701G>C (p.Gly1901Arg)
c.3229G>C (p.Gly1077Arg)
COSMIC
19g.35732814G>TCA405427408KMT2Bn.571G>T
c.6199G>T (p.Gly2067Ter)
c.3806G>T (n.3806G>T)
c.1483G>T (p.Gly495Ter)
n.1418G>T
c.1486G>T (p.Gly496Ter)
c.5807G>T
c.6265G>T (p.Gly2089Ter)
c.704+485G>T (n.704+485G>T)
c.3587G>T
c.5989G>T (p.Gly1997Ter)
c.5701G>T (p.Gly1901Ter)
c.3229G>T (p.Gly1077Ter)
gnomAD v4
19g.35732815G>ACA405427413KMT2Bn.572G>A
c.6200G>A (p.Gly2067Glu)
c.3807G>A (n.3807G>A)
c.1484G>A (p.Gly495Glu)
n.1419G>A
c.1487G>A (p.Gly496Glu)
c.5808G>A
c.6266G>A (p.Gly2089Glu)
c.704+486G>A (n.704+486G>A)
c.3588G>A
c.5990G>A (p.Gly1997Glu)
c.5702G>A (p.Gly1901Glu)
c.3230G>A (p.Gly1077Glu)
gnomAD v4
19g.35732815G>CCA9385649KMT2Bn.572G>C
c.6200G>C (p.Gly2067Ala)
c.3807G>C (n.3807G>C)
c.1484G>C (p.Gly495Ala)
n.1419G>C
c.1487G>C (p.Gly496Ala)
c.5808G>C
c.6266G>C (p.Gly2089Ala)
c.704+486G>C (n.704+486G>C)
c.3588G>C
c.5990G>C (p.Gly1997Ala)
c.5702G>C (p.Gly1901Ala)
c.3230G>C (p.Gly1077Ala)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732815G=CA2333794517KMT2Bn.572G=
c.6200G= (p.Gly2067=)
c.3807G= (n.3807G=)
c.1484G= (p.Gly495=)
n.1419G=
c.1487G= (p.Gly496=)
c.5808G=
c.6266G= (p.Gly2089=)
c.704+486G= (n.704+486G=)
c.3588G=
c.5990G= (p.Gly1997=)
c.5702G= (p.Gly1901=)
c.3230G= (p.Gly1077=)
19g.35732815G>TCA405427414KMT2Bn.572G>T
c.6200G>T (p.Gly2067Val)
c.3807G>T (n.3807G>T)
c.1484G>T (p.Gly495Val)
n.1419G>T
c.1487G>T (p.Gly496Val)
c.5808G>T
c.6266G>T (p.Gly2089Val)
c.704+486G>T (n.704+486G>T)
c.3588G>T
c.5990G>T (p.Gly1997Val)
c.5702G>T (p.Gly1901Val)
c.3230G>T (p.Gly1077Val)
19g.35732816A>CCA507308295KMT2Bn.573A>C
c.6201A>C (p.Gly2067=)
c.3808A>C (n.3808A>C)
c.1485A>C (p.Gly495=)
n.1420A>C
c.1488A>C (p.Gly496=)
c.5809A>C
c.6267A>C (p.Gly2089=)
c.704+487A>C (n.704+487A>C)
c.3589A>C
c.5991A>C (p.Gly1997=)
c.5703A>C (p.Gly1901=)
c.3231A>C (p.Gly1077=)
gnomAD v4
19g.35732816A>GCA507308297KMT2Bn.573A>G
c.6201A>G (p.Gly2067=)
c.3808A>G (n.3808A>G)
c.1485A>G (p.Gly495=)
n.1420A>G
c.1488A>G (p.Gly496=)
c.5809A>G
c.6267A>G (p.Gly2089=)
c.704+487A>G (n.704+487A>G)
c.3589A>G
c.5991A>G (p.Gly1997=)
c.5703A>G (p.Gly1901=)
c.3231A>G (p.Gly1077=)
19g.35732816A>TCA507308299KMT2Bn.573A>T
c.6201A>T (p.Gly2067=)
c.3808A>T (n.3808A>T)
c.1485A>T (p.Gly495=)
n.1420A>T
c.1488A>T (p.Gly496=)
c.5809A>T
c.6267A>T (p.Gly2089=)
c.704+487A>T (n.704+487A>T)
c.3589A>T
c.5991A>T (p.Gly1997=)
c.5703A>T (p.Gly1901=)
c.3231A>T (p.Gly1077=)
gnomAD v4
19g.35732817G>ACA405427419KMT2Bn.574G>A
c.6202G>A (p.Val2068Ile)
c.3809G>A (n.3809G>A)
c.1486G>A (p.Val496Ile)
n.1421G>A
c.1489G>A (p.Val497Ile)
c.5810G>A
c.6268G>A (p.Val2090Ile)
c.704+488G>A (n.704+488G>A)
c.3590G>A
c.5992G>A (p.Val1998Ile)
c.5704G>A (p.Val1902Ile)
c.3232G>A (p.Val1078Ile)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.35732817G>CCA405427423KMT2Bn.574G>C
c.6202G>C (p.Val2068Leu)
c.3809G>C (n.3809G>C)
c.1486G>C (p.Val496Leu)
n.1421G>C
c.1489G>C (p.Val497Leu)
c.5810G>C
c.6268G>C (p.Val2090Leu)
c.704+488G>C (n.704+488G>C)
c.3590G>C
c.5992G>C (p.Val1998Leu)
c.5704G>C (p.Val1902Leu)
c.3232G>C (p.Val1078Leu)
dbSNP gnomAD v2 gnomAD v4
19g.35732817G=CA2333794518KMT2Bn.574G=
c.6202G= (p.Val2068=)
c.3809G= (n.3809G=)
c.1486G= (p.Val496=)
n.1421G=
c.1489G= (p.Val497=)
c.5810G=
c.6268G= (p.Val2090=)
c.704+488G= (n.704+488G=)
c.3590G=
c.5992G= (p.Val1998=)
c.5704G= (p.Val1902=)
c.3232G= (p.Val1078=)
19g.35732817G>TCA405427426KMT2Bn.574G>T
c.6202G>T (p.Val2068Leu)
c.3809G>T (n.3809G>T)
c.1486G>T (p.Val496Leu)
n.1421G>T
c.1489G>T (p.Val497Leu)
c.5810G>T
c.6268G>T (p.Val2090Leu)
c.704+488G>T (n.704+488G>T)
c.3590G>T
c.5992G>T (p.Val1998Leu)
c.5704G>T (p.Val1902Leu)
c.3232G>T (p.Val1078Leu)
gnomAD v4
19g.35732818T>ACA405427430KMT2Bn.575T>A
c.6203T>A (p.Val2068Glu)
c.3810T>A (n.3810T>A)
c.1487T>A (p.Val496Glu)
n.1422T>A
c.1490T>A (p.Val497Glu)
c.5811T>A
c.6269T>A (p.Val2090Glu)
c.704+489T>A (n.704+489T>A)
c.3591T>A
c.5993T>A (p.Val1998Glu)
c.5705T>A (p.Val1902Glu)
c.3233T>A (p.Val1078Glu)
19g.35732818T>CCA405427432KMT2Bn.575T>C
c.6203T>C (p.Val2068Ala)
c.3810T>C (n.3810T>C)
c.1487T>C (p.Val496Ala)
n.1422T>C
c.1490T>C (p.Val497Ala)
c.5811T>C
c.6269T>C (p.Val2090Ala)
c.704+489T>C (n.704+489T>C)
c.3591T>C
c.5993T>C (p.Val1998Ala)
c.5705T>C (p.Val1902Ala)
c.3233T>C (p.Val1078Ala)
19g.35732818T>GCA405427436KMT2Bn.575T>G
c.6203T>G (p.Val2068Gly)
c.3810T>G (n.3810T>G)
c.1487T>G (p.Val496Gly)
n.1422T>G
c.1490T>G (p.Val497Gly)
c.5811T>G
c.6269T>G (p.Val2090Gly)
c.704+489T>G (n.704+489T>G)
c.3591T>G
c.5993T>G (p.Val1998Gly)
c.5705T>G (p.Val1902Gly)
c.3233T>G (p.Val1078Gly)
19g.35732819A>CCA507308306KMT2Bn.576A>C
c.6204A>C (p.Val2068=)
c.3811A>C (n.3811A>C)
c.1488A>C (p.Val496=)
n.1423A>C
c.1491A>C (p.Val497=)
c.5812A>C
c.6270A>C (p.Val2090=)
c.704+490A>C (n.704+490A>C)
c.3592A>C
c.5994A>C (p.Val1998=)
c.5706A>C (p.Val1902=)
c.3234A>C (p.Val1078=)
19g.35732819A>GCA507308309KMT2Bn.576A>G
c.6204A>G (p.Val2068=)
c.3811A>G (n.3811A>G)
c.1488A>G (p.Val496=)
n.1423A>G
c.1491A>G (p.Val497=)
c.5812A>G
c.6270A>G (p.Val2090=)
c.704+490A>G (n.704+490A>G)
c.3592A>G
c.5994A>G (p.Val1998=)
c.5706A>G (p.Val1902=)
c.3234A>G (p.Val1078=)
19g.35732819A>TCA507308307KMT2Bn.576A>T
c.6204A>T (p.Val2068=)
c.3811A>T (n.3811A>T)
c.1488A>T (p.Val496=)
n.1423A>T
c.1491A>T (p.Val497=)
c.5812A>T
c.6270A>T (p.Val2090=)
c.704+490A>T (n.704+490A>T)
c.3592A>T
c.5994A>T (p.Val1998=)
c.5706A>T (p.Val1902=)
c.3234A>T (p.Val1078=)
19g.35732820G>ACA405427440KMT2Bn.577G>A
c.6205G>A (p.Val2069Ile)
c.3812G>A (n.3812G>A)
c.1489G>A (p.Val497Ile)
n.1424G>A
c.1492G>A (p.Val498Ile)
c.5813G>A
c.6271G>A (p.Val2091Ile)
c.704+491G>A (n.704+491G>A)
c.3593G>A
c.5995G>A (p.Val1999Ile)
c.5707G>A (p.Val1903Ile)
c.3235G>A (p.Val1079Ile)
19g.35732820G>CCA405427442KMT2Bn.577G>C
c.6205G>C (p.Val2069Leu)
c.3812G>C (n.3812G>C)
c.1489G>C (p.Val497Leu)
n.1424G>C
c.1492G>C (p.Val498Leu)
c.5813G>C
c.6271G>C (p.Val2091Leu)
c.704+491G>C (n.704+491G>C)
c.3593G>C
c.5995G>C (p.Val1999Leu)
c.5707G>C (p.Val1903Leu)
c.3235G>C (p.Val1079Leu)
19g.35732820G>TCA405427445KMT2Bn.577G>T
c.6205G>T (p.Val2069Phe)
c.3812G>T (n.3812G>T)
c.1489G>T (p.Val497Phe)
n.1424G>T
c.1492G>T (p.Val498Phe)
c.5813G>T
c.6271G>T (p.Val2091Phe)
c.704+491G>T (n.704+491G>T)
c.3593G>T
c.5995G>T (p.Val1999Phe)
c.5707G>T (p.Val1903Phe)
c.3235G>T (p.Val1079Phe)
gnomAD v4
19g.35732821T>ACA405427453KMT2Bn.578T>A
c.6206T>A (p.Val2069Asp)
c.3813T>A (n.3813T>A)
c.1490T>A (p.Val497Asp)
n.1425T>A
c.1493T>A (p.Val498Asp)
c.5814T>A
c.6272T>A (p.Val2091Asp)
c.704+492T>A (n.704+492T>A)
c.3594T>A
c.5996T>A (p.Val1999Asp)
c.5708T>A (p.Val1903Asp)
c.3236T>A (p.Val1079Asp)
19g.35732821T>CCA405427451KMT2Bn.578T>C
c.6206T>C (p.Val2069Ala)
c.3813T>C (n.3813T>C)
c.1490T>C (p.Val497Ala)
n.1425T>C
c.1493T>C (p.Val498Ala)
c.5814T>C
c.6272T>C (p.Val2091Ala)
c.704+492T>C (n.704+492T>C)
c.3594T>C
c.5996T>C (p.Val1999Ala)
c.5708T>C (p.Val1903Ala)
c.3236T>C (p.Val1079Ala)
gnomAD v4
19g.35732821T>GCA405427449KMT2Bn.578T>G
c.6206T>G (p.Val2069Gly)
c.3813T>G (n.3813T>G)
c.1490T>G (p.Val497Gly)
n.1425T>G
c.1493T>G (p.Val498Gly)
c.5814T>G
c.6272T>G (p.Val2091Gly)
c.704+492T>G (n.704+492T>G)
c.3594T>G
c.5996T>G (p.Val1999Gly)
c.5708T>G (p.Val1903Gly)
c.3236T>G (p.Val1079Gly)
gnomAD v4
19g.35732822C>ACA507308319KMT2Bn.579C>A
c.6207C>A (p.Val2069=)
c.3814C>A (n.3814C>A)
c.1491C>A (p.Val497=)
n.1426C>A
c.1494C>A (p.Val498=)
c.5815C>A
c.6273C>A (p.Val2091=)
c.704+493C>A (n.704+493C>A)
c.3595C>A
c.5997C>A (p.Val1999=)
c.5709C>A (p.Val1903=)
c.3237C>A (p.Val1079=)
19g.35732822C>GCA507308321KMT2Bn.579C>G
c.6207C>G (p.Val2069=)
c.3814C>G (n.3814C>G)
c.1491C>G (p.Val497=)
n.1426C>G
c.1494C>G (p.Val498=)
c.5815C>G
c.6273C>G (p.Val2091=)
c.704+493C>G (n.704+493C>G)
c.3595C>G
c.5997C>G (p.Val1999=)
c.5709C>G (p.Val1903=)
c.3237C>G (p.Val1079=)
19g.35732822C>TCA507308324KMT2Bn.579C>T
c.6207C>T (p.Val2069=)
c.3814C>T (n.3814C>T)
c.1491C>T (p.Val497=)
n.1426C>T
c.1494C>T (p.Val498=)
c.5815C>T
c.6273C>T (p.Val2091=)
c.704+493C>T (n.704+493C>T)
c.3595C>T
c.5997C>T (p.Val1999=)
c.5709C>T (p.Val1903=)
c.3237C>T (p.Val1079=)
19g.35732823C>ACA9385650KMT2Bn.580C>A
c.6208C>A (p.Arg2070=)
c.3815C>A (n.3815C>A)
c.1492C>A (p.Arg498=)
n.1427C>A
c.1495C>A (p.Arg499=)
c.5816C>A
c.6274C>A (p.Arg2092=)
c.704+494C>A (n.704+494C>A)
c.3596C>A
c.5998C>A (p.Arg2000=)
c.5710C>A (p.Arg1904=)
c.3238C>A (p.Arg1080=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732823C=CA2333794519KMT2Bn.580C=
c.6208C= (p.Arg2070=)
c.3815C= (n.3815C=)
c.1492C= (p.Arg498=)
n.1427C=
c.1495C= (p.Arg499=)
c.5816C=
c.6274C= (p.Arg2092=)
c.704+494C= (n.704+494C=)
c.3596C=
c.5998C= (p.Arg2000=)
c.5710C= (p.Arg1904=)
c.3238C= (p.Arg1080=)
19g.35732823C>GCA405427462KMT2Bn.580C>G
c.6208C>G (p.Arg2070Gly)
c.3815C>G (n.3815C>G)
c.1492C>G (p.Arg498Gly)
n.1427C>G
c.1495C>G (p.Arg499Gly)
c.5816C>G
c.6274C>G (p.Arg2092Gly)
c.704+494C>G (n.704+494C>G)
c.3596C>G
c.5998C>G (p.Arg2000Gly)
c.5710C>G (p.Arg1904Gly)
c.3238C>G (p.Arg1080Gly)
gnomAD v4
19g.35732823C>TCA405427459KMT2Bn.580C>T
c.6208C>T (p.Arg2070Trp)
c.3815C>T (n.3815C>T)
c.1492C>T (p.Arg498Trp)
n.1427C>T
c.1495C>T (p.Arg499Trp)
c.5816C>T
c.6274C>T (p.Arg2092Trp)
c.704+494C>T (n.704+494C>T)
c.3596C>T
c.5998C>T (p.Arg2000Trp)
c.5710C>T (p.Arg1904Trp)
c.3238C>T (p.Arg1080Trp)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.35732824G>ACA307796553KMT2Bn.581G>A
c.6209G>A (p.Arg2070Gln)
c.3816G>A (n.3816G>A)
c.1493G>A (p.Arg498Gln)
n.1428G>A
c.1496G>A (p.Arg499Gln)
c.5817G>A
c.6275G>A (p.Arg2092Gln)
c.704+495G>A (n.704+495G>A)
c.3597G>A
c.5999G>A (p.Arg2000Gln)
c.5711G>A (p.Arg1904Gln)
c.3239G>A (p.Arg1080Gln)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.35732824G>CCA405427467KMT2Bn.581G>C
c.6209G>C (p.Arg2070Pro)
c.3816G>C (n.3816G>C)
c.1493G>C (p.Arg498Pro)
n.1428G>C
c.1496G>C (p.Arg499Pro)
c.5817G>C
c.6275G>C (p.Arg2092Pro)
c.704+495G>C (n.704+495G>C)
c.3597G>C
c.5999G>C (p.Arg2000Pro)
c.5711G>C (p.Arg1904Pro)
c.3239G>C (p.Arg1080Pro)
19g.35732824G=CA2333794520KMT2Bn.581G=
c.6209G= (p.Arg2070=)
c.3816G= (n.3816G=)
c.1493G= (p.Arg498=)
n.1428G=
c.1496G= (p.Arg499=)
c.5817G=
c.6275G= (p.Arg2092=)
c.704+495G= (n.704+495G=)
c.3597G=
c.5999G= (p.Arg2000=)
c.5711G= (p.Arg1904=)
c.3239G= (p.Arg1080=)
19g.35732824G>TCA405427470KMT2Bn.581G>T
c.6209G>T (p.Arg2070Leu)
c.3816G>T (n.3816G>T)
c.1493G>T (p.Arg498Leu)
n.1428G>T
c.1496G>T (p.Arg499Leu)
c.5817G>T
c.6275G>T (p.Arg2092Leu)
c.704+495G>T (n.704+495G>T)
c.3597G>T
c.5999G>T (p.Arg2000Leu)
c.5711G>T (p.Arg1904Leu)
c.3239G>T (p.Arg1080Leu)
gnomAD v4
19g.35732825G>ACA9385652KMT2Bn.582G>A
c.6210G>A (p.Arg2070=)
c.3817G>A (n.3817G>A)
c.1494G>A (p.Arg498=)
n.1429G>A
c.1497G>A (p.Arg499=)
c.5818G>A
c.6276G>A (p.Arg2092=)
c.704+496G>A (n.704+496G>A)
c.3598G>A
c.6000G>A (p.Arg2000=)
c.5712G>A (p.Arg1904=)
c.3240G>A (p.Arg1080=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.35732825G>CCA507308334KMT2Bn.582G>C
c.6210G>C (p.Arg2070=)
c.3817G>C (n.3817G>C)
c.1494G>C (p.Arg498=)
n.1429G>C
c.1497G>C (p.Arg499=)
c.5818G>C
c.6276G>C (p.Arg2092=)
c.704+496G>C (n.704+496G>C)
c.3598G>C
c.6000G>C (p.Arg2000=)
c.5712G>C (p.Arg1904=)
c.3240G>C (p.Arg1080=)
19g.35732825G=CA2333794521KMT2Bn.582G=
c.6210G= (p.Arg2070=)
c.3817G= (n.3817G=)
c.1494G= (p.Arg498=)
n.1429G=
c.1497G= (p.Arg499=)
c.5818G=
c.6276G= (p.Arg2092=)
c.704+496G= (n.704+496G=)
c.3598G=
c.6000G= (p.Arg2000=)
c.5712G= (p.Arg1904=)
c.3240G= (p.Arg1080=)
19g.35732825G>TCA9385651KMT2Bn.582G>T
c.6210G>T (p.Arg2070=)
c.3817G>T (n.3817G>T)
c.1494G>T (p.Arg498=)
n.1429G>T
c.1497G>T (p.Arg499=)
c.5818G>T
c.6276G>T (p.Arg2092=)
c.704+496G>T (n.704+496G>T)
c.3598G>T
c.6000G>T (p.Arg2000=)
c.5712G>T (p.Arg1904=)
c.3240G>T (p.Arg1080=)
dbSNP ExAC gnomAD v2
19g.35732826G>ACA405427478KMT2Bn.583G>A
c.6211G>A (p.Ala2071Thr)
c.3818G>A (n.3818G>A)
c.1495G>A (p.Ala499Thr)
n.1430G>A
c.1498G>A (p.Ala500Thr)
c.5819G>A
c.6277G>A (p.Ala2093Thr)
c.704+497G>A (n.704+497G>A)
c.3599G>A
c.6001G>A (p.Ala2001Thr)
c.5713G>A (p.Ala1905Thr)
c.3241G>A (p.Ala1081Thr)
19g.35732826G>CCA405427482KMT2Bn.583G>C
c.6211G>C (p.Ala2071Pro)
c.3818G>C (n.3818G>C)
c.1495G>C (p.Ala499Pro)
n.1430G>C
c.1498G>C (p.Ala500Pro)
c.5819G>C
c.6277G>C (p.Ala2093Pro)
c.704+497G>C (n.704+497G>C)
c.3599G>C
c.6001G>C (p.Ala2001Pro)
c.5713G>C (p.Ala1905Pro)
c.3241G>C (p.Ala1081Pro)
19g.35732826G>TCA405427485KMT2Bn.583G>T
c.6211G>T (p.Ala2071Ser)
c.3818G>T (n.3818G>T)
c.1495G>T (p.Ala499Ser)
n.1430G>T
c.1498G>T (p.Ala500Ser)
c.5819G>T
c.6277G>T (p.Ala2093Ser)
c.704+497G>T (n.704+497G>T)
c.3599G>T
c.6001G>T (p.Ala2001Ser)
c.5713G>T (p.Ala1905Ser)
c.3241G>T (p.Ala1081Ser)
gnomAD v4
19g.35732827C>ACA405427488KMT2Bn.584C>A
c.6212C>A (p.Ala2071Glu)
c.3819C>A (n.3819C>A)
c.1496C>A (p.Ala499Glu)
n.1431C>A
c.1499C>A (p.Ala500Glu)
c.5820C>A
c.6278C>A (p.Ala2093Glu)
c.704+498C>A (n.704+498C>A)
c.3600C>A
c.6002C>A (p.Ala2001Glu)
c.5714C>A (p.Ala1905Glu)
c.3242C>A (p.Ala1081Glu)
gnomAD v4
19g.35732827C>GCA405427490KMT2Bn.584C>G
c.6212C>G (p.Ala2071Gly)
c.3819C>G (n.3819C>G)
c.1496C>G (p.Ala499Gly)
n.1431C>G
c.1499C>G (p.Ala500Gly)
c.5820C>G
c.6278C>G (p.Ala2093Gly)
c.704+498C>G (n.704+498C>G)
c.3600C>G
c.6002C>G (p.Ala2001Gly)
c.5714C>G (p.Ala1905Gly)
c.3242C>G (p.Ala1081Gly)
19g.35732827C>TCA405427493KMT2Bn.584C>T
c.6212C>T (p.Ala2071Val)
c.3819C>T (n.3819C>T)
c.1496C>T (p.Ala499Val)
n.1431C>T
c.1499C>T (p.Ala500Val)
c.5820C>T
c.6278C>T (p.Ala2093Val)
c.704+498C>T (n.704+498C>T)
c.3600C>T
c.6002C>T (p.Ala2001Val)
c.5714C>T (p.Ala1905Val)
c.3242C>T (p.Ala1081Val)
gnomAD v4
19g.35732828A=CA2333794522KMT2Bn.585A=
c.6213A= (p.Ala2071=)
c.3820A= (n.3820A=)
c.1497A= (p.Ala499=)
n.1432A=
c.1500A= (p.Ala500=)
c.5821A=
c.6279A= (p.Ala2093=)
c.704+499A= (n.704+499A=)
c.3601A=
c.6003A= (p.Ala2001=)
c.5715A= (p.Ala1905=)
c.3243A= (p.Ala1081=)
19g.35732828A>CCA507308344KMT2Bn.585A>C
c.6213A>C (p.Ala2071=)
c.3820A>C (n.3820A>C)
c.1497A>C (p.Ala499=)
n.1432A>C
c.1500A>C (p.Ala500=)
c.5821A>C
c.6279A>C (p.Ala2093=)
c.704+499A>C (n.704+499A>C)
c.3601A>C
c.6003A>C (p.Ala2001=)
c.5715A>C (p.Ala1905=)
c.3243A>C (p.Ala1081=)
19g.35732828A>GCA307796578KMT2Bn.585A>G
c.6213A>G (p.Ala2071=)
c.3820A>G (n.3820A>G)
c.1497A>G (p.Ala499=)
n.1432A>G
c.1500A>G (p.Ala500=)
c.5821A>G
c.6279A>G (p.Ala2093=)
c.704+499A>G (n.704+499A>G)
c.3601A>G
c.6003A>G (p.Ala2001=)
c.5715A>G (p.Ala1905=)
c.3243A>G (p.Ala1081=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.35732828A>TCA507308340KMT2Bn.585A>T
c.6213A>T (p.Ala2071=)
c.3820A>T (n.3820A>T)
c.1497A>T (p.Ala499=)
n.1432A>T
c.1500A>T (p.Ala500=)
c.5821A>T
c.6279A>T (p.Ala2093=)
c.704+499A>T (n.704+499A>T)
c.3601A>T
c.6003A>T (p.Ala2001=)
c.5715A>T (p.Ala1905=)
c.3243A>T (p.Ala1081=)
19g.35732829G>ACA405427503KMT2Bn.586G>A
c.6214G>A (p.Gly2072Arg)
c.3821G>A (n.3821G>A)
c.1498G>A (p.Gly500Arg)
n.1433G>A
c.1501G>A (p.Gly501Arg)
c.5822G>A
c.6280G>A (p.Gly2094Arg)
c.704+500G>A (n.704+500G>A)
c.3602G>A
c.6004G>A (p.Gly2002Arg)
c.5716G>A (p.Gly1906Arg)
c.3244G>A (p.Gly1082Arg)
gnomAD v4
19g.35732829G>CCA405427500KMT2Bn.586G>C
c.6214G>C (p.Gly2072Arg)
c.3821G>C (n.3821G>C)
c.1498G>C (p.Gly500Arg)
n.1433G>C
c.1501G>C (p.Gly501Arg)
c.5822G>C
c.6280G>C (p.Gly2094Arg)
c.704+500G>C (n.704+500G>C)
c.3602G>C
c.6004G>C (p.Gly2002Arg)
c.5716G>C (p.Gly1906Arg)
c.3244G>C (p.Gly1082Arg)
19g.35732829G>TCA405427497KMT2Bn.586G>T
c.6214G>T (p.Gly2072Trp)
c.3821G>T (n.3821G>T)
c.1498G>T (p.Gly500Trp)
n.1433G>T
c.1501G>T (p.Gly501Trp)
c.5822G>T
c.6280G>T (p.Gly2094Trp)
c.704+500G>T (n.704+500G>T)
c.3602G>T
c.6004G>T (p.Gly2002Trp)
c.5716G>T (p.Gly1906Trp)
c.3244G>T (p.Gly1082Trp)
19g.35732830G>ACA405427506KMT2Bn.587G>A
c.6215G>A (p.Gly2072Glu)
c.3822G>A (n.3822G>A)
c.1499G>A (p.Gly500Glu)
n.1434G>A
c.1502G>A (p.Gly501Glu)
c.5823G>A
c.6281G>A (p.Gly2094Glu)
c.704+501G>A (n.704+501G>A)
c.3603G>A
c.6005G>A (p.Gly2002Glu)
c.5717G>A (p.Gly1906Glu)
c.3245G>A (p.Gly1082Glu)
19g.35732830G>CCA405427507KMT2Bn.587G>C
c.6215G>C (p.Gly2072Ala)
c.3822G>C (n.3822G>C)
c.1499G>C (p.Gly500Ala)
n.1434G>C
c.1502G>C (p.Gly501Ala)
c.5823G>C
c.6281G>C (p.Gly2094Ala)
c.704+501G>C (n.704+501G>C)
c.3603G>C
c.6005G>C (p.Gly2002Ala)
c.5717G>C (p.Gly1906Ala)
c.3245G>C (p.Gly1082Ala)
19g.35732830G>TCA405427512KMT2Bn.587G>T
c.6215G>T (p.Gly2072Val)
c.3822G>T (n.3822G>T)
c.1499G>T (p.Gly500Val)
n.1434G>T
c.1502G>T (p.Gly501Val)
c.5823G>T
c.6281G>T (p.Gly2094Val)
c.704+501G>T (n.704+501G>T)
c.3603G>T
c.6005G>T (p.Gly2002Val)
c.5717G>T (p.Gly1906Val)
c.3245G>T (p.Gly1082Val)
19g.35732831G>ACA507308350KMT2Bn.588G>A
c.6216G>A (p.Gly2072=)
c.3823G>A (n.3823G>A)
c.1500G>A (p.Gly500=)
n.1435G>A
c.1503G>A (p.Gly501=)
c.5824G>A
c.6282G>A (p.Gly2094=)
c.704+502G>A (n.704+502G>A)
c.3604G>A
c.6006G>A (p.Gly2002=)
c.5718G>A (p.Gly1906=)
c.3246G>A (p.Gly1082=)
19g.35732831G>CCA507308351KMT2Bn.588G>C
c.6216G>C (p.Gly2072=)
c.3823G>C (n.3823G>C)
c.1500G>C (p.Gly500=)
n.1435G>C
c.1503G>C (p.Gly501=)
c.5824G>C
c.6282G>C (p.Gly2094=)
c.704+502G>C (n.704+502G>C)
c.3604G>C
c.6006G>C (p.Gly2002=)
c.5718G>C (p.Gly1906=)
c.3246G>C (p.Gly1082=)
19g.35732831G>TCA507308352KMT2Bn.588G>T
c.6216G>T (p.Gly2072=)
c.3823G>T (n.3823G>T)
c.1500G>T (p.Gly500=)
n.1435G>T
c.1503G>T (p.Gly501=)
c.5824G>T
c.6282G>T (p.Gly2094=)
c.704+502G>T (n.704+502G>T)
c.3604G>T
c.6006G>T (p.Gly2002=)
c.5718G>T (p.Gly1906=)
c.3246G>T (p.Gly1082=)
gnomAD v4
19g.35732832G>ACA405427515KMT2Bn.589G>A
c.6217G>A (p.Val2073Ile)
c.3824G>A (n.3824G>A)
c.1501G>A (p.Val501Ile)
n.1436G>A
c.1504G>A (p.Val502Ile)
c.5825G>A
c.6283G>A (p.Val2095Ile)
c.704+503G>A (n.704+503G>A)
c.3605G>A
c.6007G>A (p.Val2003Ile)
c.5719G>A (p.Val1907Ile)
c.3247G>A (p.Val1083Ile)
19g.35732832G>CCA405427517KMT2Bn.589G>C
c.6217G>C (p.Val2073Leu)
c.3824G>C (n.3824G>C)
c.1501G>C (p.Val501Leu)
n.1436G>C
c.1504G>C (p.Val502Leu)
c.5825G>C
c.6283G>C (p.Val2095Leu)
c.704+503G>C (n.704+503G>C)
c.3605G>C
c.6007G>C (p.Val2003Leu)
c.5719G>C (p.Val1907Leu)
c.3247G>C (p.Val1083Leu)
gnomAD v4
19g.35732832G>TCA405427519KMT2Bn.589G>T
c.6217G>T (p.Val2073Phe)
c.3824G>T (n.3824G>T)
c.1501G>T (p.Val501Phe)
n.1436G>T
c.1504G>T (p.Val502Phe)
c.5825G>T
c.6283G>T (p.Val2095Phe)
c.704+503G>T (n.704+503G>T)
c.3605G>T
c.6007G>T (p.Val2003Phe)
c.5719G>T (p.Val1907Phe)
c.3247G>T (p.Val1083Phe)
gnomAD v4
19g.35732833T>ACA405427522KMT2Bn.590T>A
c.6218T>A (p.Val2073Asp)
c.3825T>A (n.3825T>A)
c.1502T>A (p.Val501Asp)
n.1437T>A
c.1505T>A (p.Val502Asp)
c.5826T>A
c.6284T>A (p.Val2095Asp)
c.704+504T>A (n.704+504T>A)
c.3606T>A
c.6008T>A (p.Val2003Asp)
c.5720T>A (p.Val1907Asp)
c.3248T>A (p.Val1083Asp)
19g.35732833T>CCA9385653KMT2Bn.590T>C
c.6218T>C (p.Val2073Ala)
c.3825T>C (n.3825T>C)
c.1502T>C (p.Val501Ala)
n.1437T>C
c.1505T>C (p.Val502Ala)
c.5826T>C
c.6284T>C (p.Val2095Ala)
c.704+504T>C (n.704+504T>C)
c.3606T>C
c.6008T>C (p.Val2003Ala)
c.5720T>C (p.Val1907Ala)
c.3248T>C (p.Val1083Ala)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.35732833T>GCA405427528KMT2Bn.590T>G
c.6218T>G (p.Val2073Gly)
c.3825T>G (n.3825T>G)
c.1502T>G (p.Val501Gly)
n.1437T>G
c.1505T>G (p.Val502Gly)
c.5826T>G
c.6284T>G (p.Val2095Gly)
c.704+504T>G (n.704+504T>G)
c.3606T>G
c.6008T>G (p.Val2003Gly)
c.5720T>G (p.Val1907Gly)
c.3248T>G (p.Val1083Gly)
dbSNP
19g.35732833T=CA2333794523KMT2Bn.590T=
c.6218T= (p.Val2073=)
c.3825T= (n.3825T=)
c.1502T= (p.Val501=)
n.1437T=
c.1505T= (p.Val502=)
c.5826T=
c.6284T= (p.Val2095=)
c.704+504T= (n.704+504T=)
c.3606T=
c.6008T= (p.Val2003=)
c.5720T= (p.Val1907=)
c.3248T= (p.Val1083=)
19g.35732834C>ACA507308359KMT2Bn.591C>A
c.6219C>A (p.Val2073=)
c.3826C>A (n.3826C>A)
c.1503C>A (p.Val501=)
n.1438C>A
c.1506C>A (p.Val502=)
c.5827C>A
c.6285C>A (p.Val2095=)
c.704+505C>A (n.704+505C>A)
c.3607C>A
c.6009C>A (p.Val2003=)
c.5721C>A (p.Val1907=)
c.3249C>A (p.Val1083=)
19g.35732834C>GCA507308360KMT2Bn.591C>G
c.6219C>G (p.Val2073=)
c.3826C>G (n.3826C>G)
c.1503C>G (p.Val501=)
n.1438C>G
c.1506C>G (p.Val502=)
c.5827C>G
c.6285C>G (p.Val2095=)
c.704+505C>G (n.704+505C>G)
c.3607C>G
c.6009C>G (p.Val2003=)
c.5721C>G (p.Val1907=)
c.3249C>G (p.Val1083=)
gnomAD v4
19g.35732834C>TCA507308361KMT2Bn.591C>T
c.6219C>T (p.Val2073=)
c.3826C>T (n.3826C>T)
c.1503C>T (p.Val501=)
n.1438C>T
c.1506C>T (p.Val502=)
c.5827C>T
c.6285C>T (p.Val2095=)
c.704+505C>T (n.704+505C>T)
c.3607C>T
c.6009C>T (p.Val2003=)
c.5721C>T (p.Val1907=)
c.3249C>T (p.Val1083=)
gnomAD v4
19g.35732835C>ACA405427532KMT2Bn.592C>A
c.6220C>A (p.Leu2074Ile)
c.3827C>A (n.3827C>A)
c.1504C>A (p.Leu502Ile)
n.1439C>A
c.1507C>A (p.Leu503Ile)
c.5828C>A
c.6286C>A (p.Leu2096Ile)
c.704+506C>A (n.704+506C>A)
c.3608C>A
c.6010C>A (p.Leu2004Ile)
c.5722C>A (p.Leu1908Ile)
c.3250C>A (p.Leu1084Ile)
19g.35732835C=CA2333794524KMT2Bn.592C=
c.6220C= (p.Leu2074=)
c.3827C= (n.3827C=)
c.1504C= (p.Leu502=)
n.1439C=
c.1507C= (p.Leu503=)
c.5828C=
c.6286C= (p.Leu2096=)
c.704+506C= (n.704+506C=)
c.3608C=
c.6010C= (p.Leu2004=)
c.5722C= (p.Leu1908=)
c.3250C= (p.Leu1084=)
19g.35732835C>GCA405427534KMT2Bn.592C>G
c.6220C>G (p.Leu2074Val)
c.3827C>G (n.3827C>G)
c.1504C>G (p.Leu502Val)
n.1439C>G
c.1507C>G (p.Leu503Val)
c.5828C>G
c.6286C>G (p.Leu2096Val)
c.704+506C>G (n.704+506C>G)
c.3608C>G
c.6010C>G (p.Leu2004Val)
c.5722C>G (p.Leu1908Val)
c.3250C>G (p.Leu1084Val)
gnomAD v4
19g.35732835C>TCA405427537KMT2Bn.592C>T
c.6220C>T (p.Leu2074Phe)
c.3827C>T (n.3827C>T)
c.1504C>T (p.Leu502Phe)
n.1439C>T
c.1507C>T (p.Leu503Phe)
c.5828C>T
c.6286C>T (p.Leu2096Phe)
c.704+506C>T (n.704+506C>T)
c.3608C>T
c.6010C>T (p.Leu2004Phe)
c.5722C>T (p.Leu1908Phe)
c.3250C>T (p.Leu1084Phe)
dbSNP gnomAD v2 gnomAD v4
19g.35732836T>ACA405427547KMT2Bn.593T>A
c.6221T>A (p.Leu2074His)
c.3828T>A (n.3828T>A)
c.1505T>A (p.Leu502His)
n.1440T>A
c.1508T>A (p.Leu503His)
c.5829T>A
c.6287T>A (p.Leu2096His)
c.704+507T>A (n.704+507T>A)
c.3609T>A
c.6011T>A (p.Leu2004His)
c.5723T>A (p.Leu1908His)
c.3251T>A (p.Leu1084His)
19g.35732836T>CCA405427545KMT2Bn.593T>C
c.6221T>C (p.Leu2074Pro)
c.3828T>C (n.3828T>C)
c.1505T>C (p.Leu502Pro)
n.1440T>C
c.1508T>C (p.Leu503Pro)
c.5829T>C
c.6287T>C (p.Leu2096Pro)
c.704+507T>C (n.704+507T>C)
c.3609T>C
c.6011T>C (p.Leu2004Pro)
c.5723T>C (p.Leu1908Pro)
c.3251T>C (p.Leu1084Pro)
ClinVar gnomAD v4
19g.35732836T>GCA405427541KMT2Bn.593T>G
c.6221T>G (p.Leu2074Arg)
c.3828T>G (n.3828T>G)
c.1505T>G (p.Leu502Arg)
n.1440T>G
c.1508T>G (p.Leu503Arg)
c.5829T>G
c.6287T>G (p.Leu2096Arg)
c.704+507T>G (n.704+507T>G)
c.3609T>G
c.6011T>G (p.Leu2004Arg)
c.5723T>G (p.Leu1908Arg)
c.3251T>G (p.Leu1084Arg)
19g.35732837T>ACA507308366KMT2Bn.594T>A
c.6222T>A (p.Leu2074=)
c.3829T>A (n.3829T>A)
c.1506T>A (p.Leu502=)
n.1441T>A
c.1509T>A (p.Leu503=)
c.5830T>A
c.6288T>A (p.Leu2096=)
c.704+508T>A (n.704+508T>A)
c.3610T>A
c.6012T>A (p.Leu2004=)
c.5724T>A (p.Leu1908=)
c.3252T>A (p.Leu1084=)
19g.35732837T>CCA507308368KMT2Bn.594T>C
c.6222T>C (p.Leu2074=)
c.3829T>C (n.3829T>C)
c.1506T>C (p.Leu502=)
n.1441T>C
c.1509T>C (p.Leu503=)
c.5830T>C
c.6288T>C (p.Leu2096=)
c.704+508T>C (n.704+508T>C)
c.3610T>C
c.6012T>C (p.Leu2004=)
c.5724T>C (p.Leu1908=)
c.3252T>C (p.Leu1084=)
19g.35732837T>GCA507308370KMT2Bn.594T>G
c.6222T>G (p.Leu2074=)
c.3829T>G (n.3829T>G)
c.1506T>G (p.Leu502=)
n.1441T>G
c.1509T>G (p.Leu503=)
c.5830T>G
c.6288T>G (p.Leu2096=)
c.704+508T>G (n.704+508T>G)
c.3610T>G
c.6012T>G (p.Leu2004=)
c.5724T>G (p.Leu1908=)
c.3252T>G (p.Leu1084=)
19g.35732838G>ACA405427551KMT2Bn.595G>A
c.6223G>A (p.Gly2075Arg)
c.3830G>A (n.3830G>A)
c.1507G>A (p.Gly503Arg)
n.1442G>A
c.1510G>A (p.Gly504Arg)
c.5831G>A
c.6289G>A (p.Gly2097Arg)
c.704+509G>A (n.704+509G>A)
c.3611G>A
c.6013G>A (p.Gly2005Arg)
c.5725G>A (p.Gly1909Arg)
c.3253G>A (p.Gly1085Arg)
19g.35732838G>CCA405427553KMT2Bn.595G>C
c.6223G>C (p.Gly2075Arg)
c.3830G>C (n.3830G>C)
c.1507G>C (p.Gly503Arg)
n.1442G>C
c.1510G>C (p.Gly504Arg)
c.5831G>C
c.6289G>C (p.Gly2097Arg)
c.704+509G>C (n.704+509G>C)
c.3611G>C
c.6013G>C (p.Gly2005Arg)
c.5725G>C (p.Gly1909Arg)
c.3253G>C (p.Gly1085Arg)
19g.35732838G>TCA405427556KMT2Bn.595G>T
c.6223G>T (p.Gly2075Trp)
c.3830G>T (n.3830G>T)
c.1507G>T (p.Gly503Trp)
n.1442G>T
c.1510G>T (p.Gly504Trp)
c.5831G>T
c.6289G>T (p.Gly2097Trp)
c.704+509G>T (n.704+509G>T)
c.3611G>T
c.6013G>T (p.Gly2005Trp)
c.5725G>T (p.Gly1909Trp)
c.3253G>T (p.Gly1085Trp)
19g.35732839G>ACA405427565KMT2Bn.596G>A
c.6224G>A (p.Gly2075Glu)
c.3831G>A (n.3831G>A)
c.1508G>A (p.Gly503Glu)
n.1443G>A
c.1511G>A (p.Gly504Glu)
c.5832G>A
c.6290G>A (p.Gly2097Glu)
c.704+510G>A (n.704+510G>A)
c.3612G>A
c.6014G>A (p.Gly2005Glu)
c.5726G>A (p.Gly1909Glu)
c.3254G>A (p.Gly1085Glu)
dbSNP gnomAD v2
19g.35732839G>CCA405427567KMT2Bn.596G>C
c.6224G>C (p.Gly2075Ala)
c.3831G>C (n.3831G>C)
c.1508G>C (p.Gly503Ala)
n.1443G>C
c.1511G>C (p.Gly504Ala)
c.5832G>C
c.6290G>C (p.Gly2097Ala)
c.704+510G>C (n.704+510G>C)
c.3612G>C
c.6014G>C (p.Gly2005Ala)
c.5726G>C (p.Gly1909Ala)
c.3254G>C (p.Gly1085Ala)
19g.35732839G=CA2333794525KMT2Bn.596G=
c.6224G= (p.Gly2075=)
c.3831G= (n.3831G=)
c.1508G= (p.Gly503=)
n.1443G=
c.1511G= (p.Gly504=)
c.5832G=
c.6290G= (p.Gly2097=)
c.704+510G= (n.704+510G=)
c.3612G=
c.6014G= (p.Gly2005=)
c.5726G= (p.Gly1909=)
c.3254G= (p.Gly1085=)
19g.35732839G>TCA405427570KMT2Bn.596G>T
c.6224G>T (p.Gly2075Val)
c.3831G>T (n.3831G>T)
c.1508G>T (p.Gly503Val)
n.1443G>T
c.1511G>T (p.Gly504Val)
c.5832G>T
c.6290G>T (p.Gly2097Val)
c.704+510G>T (n.704+510G>T)
c.3612G>T
c.6014G>T (p.Gly2005Val)
c.5726G>T (p.Gly1909Val)
c.3254G>T (p.Gly1085Val)
19g.35732840G>ACA507308377KMT2Bn.597G>A
c.6225G>A (p.Gly2075=)
c.3832G>A (n.3832G>A)
c.1509G>A (p.Gly503=)
n.1444G>A
c.1512G>A (p.Gly504=)
c.5833G>A
c.6291G>A (p.Gly2097=)
c.704+511G>A (n.704+511G>A)
c.3613G>A
c.6015G>A (p.Gly2005=)
c.5727G>A (p.Gly1909=)
c.3255G>A (p.Gly1085=)
19g.35732840G>CCA507308384KMT2Bn.597G>C
c.6225G>C (p.Gly2075=)
c.3832G>C (n.3832G>C)
c.1509G>C (p.Gly503=)
n.1444G>C
c.1512G>C (p.Gly504=)
c.5833G>C
c.6291G>C (p.Gly2097=)
c.704+511G>C (n.704+511G>C)
c.3613G>C
c.6015G>C (p.Gly2005=)
c.5727G>C (p.Gly1909=)
c.3255G>C (p.Gly1085=)
19g.35732840G>TCA507308381KMT2Bn.597G>T
c.6225G>T (p.Gly2075=)
c.3832G>T (n.3832G>T)
c.1509G>T (p.Gly503=)
n.1444G>T
c.1512G>T (p.Gly504=)
c.5833G>T
c.6291G>T (p.Gly2097=)
c.704+511G>T (n.704+511G>T)
c.3613G>T
c.6015G>T (p.Gly2005=)
c.5727G>T (p.Gly1909=)
c.3255G>T (p.Gly1085=)
19g.35732841G>ACA9385654KMT2Bn.598G>A
c.6226G>A (p.Ala2076Thr)
c.3833G>A (n.3833G>A)
c.1510G>A (p.Ala504Thr)
n.1445G>A
c.1513G>A (p.Ala505Thr)
c.5834G>A
c.6292G>A (p.Ala2098Thr)
c.704+512G>A (n.704+512G>A)
c.3614G>A
c.6016G>A (p.Ala2006Thr)
c.5728G>A (p.Ala1910Thr)
c.3256G>A (p.Ala1086Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732841G>CCA405427575KMT2Bn.598G>C
c.6226G>C (p.Ala2076Pro)
c.3833G>C (n.3833G>C)
c.1510G>C (p.Ala504Pro)
n.1445G>C
c.1513G>C (p.Ala505Pro)
c.5834G>C
c.6292G>C (p.Ala2098Pro)
c.704+512G>C (n.704+512G>C)
c.3614G>C
c.6016G>C (p.Ala2006Pro)
c.5728G>C (p.Ala1910Pro)
c.3256G>C (p.Ala1086Pro)
dbSNP gnomAD v2 gnomAD v4
19g.35732841G=CA2333794526KMT2Bn.598G=
c.6226G= (p.Ala2076=)
c.3833G= (n.3833G=)
c.1510G= (p.Ala504=)
n.1445G=
c.1513G= (p.Ala505=)
c.5834G=
c.6292G= (p.Ala2098=)
c.704+512G= (n.704+512G=)
c.3614G=
c.6016G= (p.Ala2006=)
c.5728G= (p.Ala1910=)
c.3256G= (p.Ala1086=)
19g.35732841G>TCA405427577KMT2Bn.598G>T
c.6226G>T (p.Ala2076Ser)
c.3833G>T (n.3833G>T)
c.1510G>T (p.Ala504Ser)
n.1445G>T
c.1513G>T (p.Ala505Ser)
c.5834G>T
c.6292G>T (p.Ala2098Ser)
c.704+512G>T (n.704+512G>T)
c.3614G>T
c.6016G>T (p.Ala2006Ser)
c.5728G>T (p.Ala1910Ser)
c.3256G>T (p.Ala1086Ser)
dbSNP gnomAD v4
19g.35732842C>ACA9385655KMT2Bn.599C>A
c.6227C>A (p.Ala2076Asp)
c.3834C>A (n.3834C>A)
c.1511C>A (p.Ala504Asp)
n.1446C>A
c.1514C>A (p.Ala505Asp)
c.5835C>A
c.6293C>A (p.Ala2098Asp)
c.704+513C>A (n.704+513C>A)
c.3615C>A
c.6017C>A (p.Ala2006Asp)
c.5729C>A (p.Ala1910Asp)
c.3257C>A (p.Ala1086Asp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732842C=CA2333794527KMT2Bn.599C=
c.6227C= (p.Ala2076=)
c.3834C= (n.3834C=)
c.1511C= (p.Ala504=)
n.1446C=
c.1514C= (p.Ala505=)
c.5835C=
c.6293C= (p.Ala2098=)
c.704+513C= (n.704+513C=)
c.3615C=
c.6017C= (p.Ala2006=)
c.5729C= (p.Ala1910=)
c.3257C= (p.Ala1086=)
19g.35732842C>GCA405427580KMT2Bn.599C>G
c.6227C>G (p.Ala2076Gly)
c.3834C>G (n.3834C>G)
c.1511C>G (p.Ala504Gly)
n.1446C>G
c.1514C>G (p.Ala505Gly)
c.5835C>G
c.6293C>G (p.Ala2098Gly)
c.704+513C>G (n.704+513C>G)
c.3615C>G
c.6017C>G (p.Ala2006Gly)
c.5729C>G (p.Ala1910Gly)
c.3257C>G (p.Ala1086Gly)
19g.35732842C>TCA9385656KMT2Bn.599C>T
c.6227C>T (p.Ala2076Val)
c.3834C>T (n.3834C>T)
c.1511C>T (p.Ala504Val)
n.1446C>T
c.1514C>T (p.Ala505Val)
c.5835C>T
c.6293C>T (p.Ala2098Val)
c.704+513C>T (n.704+513C>T)
c.3615C>T
c.6017C>T (p.Ala2006Val)
c.5729C>T (p.Ala1910Val)
c.3257C>T (p.Ala1086Val)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732843T>ACA507308386KMT2Bn.600T>A
c.6228T>A (p.Ala2076=)
c.3835T>A (n.3835T>A)
c.1512T>A (p.Ala504=)
n.1447T>A
c.1515T>A (p.Ala505=)
c.5836T>A
c.6294T>A (p.Ala2098=)
c.704+514T>A (n.704+514T>A)
c.3616T>A
c.6018T>A (p.Ala2006=)
c.5730T>A (p.Ala1910=)
c.3258T>A (p.Ala1086=)
dbSNP
19g.35732843T>CCA507308394KMT2Bn.600T>C
c.6228T>C (p.Ala2076=)
c.3835T>C (n.3835T>C)
c.1512T>C (p.Ala504=)
n.1447T>C
c.1515T>C (p.Ala505=)
c.5836T>C
c.6294T>C (p.Ala2098=)
c.704+514T>C (n.704+514T>C)
c.3616T>C
c.6018T>C (p.Ala2006=)
c.5730T>C (p.Ala1910=)
c.3258T>C (p.Ala1086=)
ClinVar gnomAD v4
19g.35732843T>GCA507308396KMT2Bn.600T>G
c.6228T>G (p.Ala2076=)
c.3835T>G (n.3835T>G)
c.1512T>G (p.Ala504=)
n.1447T>G
c.1515T>G (p.Ala505=)
c.5836T>G
c.6294T>G (p.Ala2098=)
c.704+514T>G (n.704+514T>G)
c.3616T>G
c.6018T>G (p.Ala2006=)
c.5730T>G (p.Ala1910=)
c.3258T>G (p.Ala1086=)
19g.35732843T=CA2333794528KMT2Bn.600T=
c.6228T= (p.Ala2076=)
c.3835T= (n.3835T=)
c.1512T= (p.Ala504=)
n.1447T=
c.1515T= (p.Ala505=)
c.5836T=
c.6294T= (p.Ala2098=)
c.704+514T= (n.704+514T=)
c.3616T=
c.6018T= (p.Ala2006=)
c.5730T= (p.Ala1910=)
c.3258T= (p.Ala1086=)
19g.35732844G>ACA405427588KMT2Bn.601G>A
c.6229G>A (p.Ala2077Thr)
c.3836G>A (n.3836G>A)
c.1513G>A (p.Ala505Thr)
n.1448G>A
c.1516G>A (p.Ala506Thr)
c.5837G>A
c.6295G>A (p.Ala2099Thr)
c.704+515G>A (n.704+515G>A)
c.3617G>A
c.6019G>A (p.Ala2007Thr)
c.5731G>A (p.Ala1911Thr)
c.3259G>A (p.Ala1087Thr)
dbSNP gnomAD v2 gnomAD v4
19g.35732844G>CCA405427590KMT2Bn.601G>C
c.6229G>C (p.Ala2077Pro)
c.3836G>C (n.3836G>C)
c.1513G>C (p.Ala505Pro)
n.1448G>C
c.1516G>C (p.Ala506Pro)
c.5837G>C
c.6295G>C (p.Ala2099Pro)
c.704+515G>C (n.704+515G>C)
c.3617G>C
c.6019G>C (p.Ala2007Pro)
c.5731G>C (p.Ala1911Pro)
c.3259G>C (p.Ala1087Pro)
19g.35732844G=CA2333794529KMT2Bn.601G=
c.6229G= (p.Ala2077=)
c.3836G= (n.3836G=)
c.1513G= (p.Ala505=)
n.1448G=
c.1516G= (p.Ala506=)
c.5837G=
c.6295G= (p.Ala2099=)
c.704+515G= (n.704+515G=)
c.3617G=
c.6019G= (p.Ala2007=)
c.5731G= (p.Ala1911=)
c.3259G= (p.Ala1087=)
19g.35732844G>TCA405427585KMT2Bn.601G>T
c.6229G>T (p.Ala2077Ser)
c.3836G>T (n.3836G>T)
c.1513G>T (p.Ala505Ser)
n.1448G>T
c.1516G>T (p.Ala506Ser)
c.5837G>T
c.6295G>T (p.Ala2099Ser)
c.704+515G>T (n.704+515G>T)
c.3617G>T
c.6019G>T (p.Ala2007Ser)
c.5731G>T (p.Ala1911Ser)
c.3259G>T (p.Ala1087Ser)
gnomAD v4
19g.35732845C>ACA405427593KMT2Bn.602C>A
c.6230C>A (p.Ala2077Glu)
c.3837C>A (n.3837C>A)
c.1514C>A (p.Ala505Glu)
n.1449C>A
c.1517C>A (p.Ala506Glu)
c.5838C>A
c.6296C>A (p.Ala2099Glu)
c.704+516C>A (n.704+516C>A)
c.3618C>A
c.6020C>A (p.Ala2007Glu)
c.5732C>A (p.Ala1911Glu)
c.3260C>A (p.Ala1087Glu)
gnomAD v4
19g.35732845C=CA2333794530KMT2Bn.602C=
c.6230C= (p.Ala2077=)
c.3837C= (n.3837C=)
c.1514C= (p.Ala505=)
n.1449C=
c.1517C= (p.Ala506=)
c.5838C=
c.6296C= (p.Ala2099=)
c.704+516C= (n.704+516C=)
c.3618C=
c.6020C= (p.Ala2007=)
c.5732C= (p.Ala1911=)
c.3260C= (p.Ala1087=)
19g.35732845C>GCA405427596KMT2Bn.602C>G
c.6230C>G (p.Ala2077Gly)
c.3837C>G (n.3837C>G)
c.1514C>G (p.Ala505Gly)
n.1449C>G
c.1517C>G (p.Ala506Gly)
c.5838C>G
c.6296C>G (p.Ala2099Gly)
c.704+516C>G (n.704+516C>G)
c.3618C>G
c.6020C>G (p.Ala2007Gly)
c.5732C>G (p.Ala1911Gly)
c.3260C>G (p.Ala1087Gly)
19g.35732845C>TCA9385657KMT2Bn.602C>T
c.6230C>T (p.Ala2077Val)
c.3837C>T (n.3837C>T)
c.1514C>T (p.Ala505Val)
n.1449C>T
c.1517C>T (p.Ala506Val)
c.5838C>T
c.6296C>T (p.Ala2099Val)
c.704+516C>T (n.704+516C>T)
c.3618C>T
c.6020C>T (p.Ala2007Val)
c.5732C>T (p.Ala1911Val)
c.3260C>T (p.Ala1087Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.35732845_35732846delinsTGCA2580096825KMT2Bn.602_603delinsTG
c.6230_6231delinsTG (p.Ala2077Val)
c.3837_3838delinsTG (n.3837_3838delinsTG)
c.1514_1515delinsTG (p.Ala505Val)
n.1449_1450delinsTG
c.1517_1518delinsTG (p.Ala506Val)
c.5838_5839delinsTG
c.6296_6297delinsTG (p.Ala2099Val)
c.704+516_704+517delinsTG (n.704+516_704+517delinsTG)
c.3618_3619delinsTG
c.6020_6021delinsTG (p.Ala2007Val)
c.5732_5733delinsTG (p.Ala1911Val)
c.3260_3261delinsTG (p.Ala1087Val)
ClinVar
19g.35732846A=CA2333794531KMT2Bn.603A=
c.6231A= (p.Ala2077=)
c.3838A= (n.3838A=)
c.1515A= (p.Ala505=)
n.1450A=
c.1518A= (p.Ala506=)
c.5839A=
c.6297A= (p.Ala2099=)
c.704+517A= (n.704+517A=)
c.3619A=
c.6021A= (p.Ala2007=)
c.5733A= (p.Ala1911=)
c.3261A= (p.Ala1087=)
19g.35732846A>CCA507308404KMT2Bn.603A>C
c.6231A>C (p.Ala2077=)
c.3838A>C (n.3838A>C)
c.1515A>C (p.Ala505=)
n.1450A>C
c.1518A>C (p.Ala506=)
c.5839A>C
c.6297A>C (p.Ala2099=)
c.704+517A>C (n.704+517A>C)
c.3619A>C
c.6021A>C (p.Ala2007=)
c.5733A>C (p.Ala1911=)
c.3261A>C (p.Ala1087=)
19g.35732846A>GCA9385658KMT2Bn.603A>G
c.6231A>G (p.Ala2077=)
c.3838A>G (n.3838A>G)
c.1515A>G (p.Ala505=)
n.1450A>G
c.1518A>G (p.Ala506=)
c.5839A>G
c.6297A>G (p.Ala2099=)
c.704+517A>G (n.704+517A>G)
c.3619A>G
c.6021A>G (p.Ala2007=)
c.5733A>G (p.Ala1911=)
c.3261A>G (p.Ala1087=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732846A>TCA507308406KMT2Bn.603A>T
c.6231A>T (p.Ala2077=)
c.3838A>T (n.3838A>T)
c.1515A>T (p.Ala505=)
n.1450A>T
c.1518A>T (p.Ala506=)
c.5839A>T
c.6297A>T (p.Ala2099=)
c.704+517A>T (n.704+517A>T)
c.3619A>T
c.6021A>T (p.Ala2007=)
c.5733A>T (p.Ala1911=)
c.3261A>T (p.Ala1087=)
19g.35732847G>ACA405427611KMT2Bn.604G>A
c.6232G>A (p.Gly2078Arg)
c.3839G>A (n.3839G>A)
c.1516G>A (p.Gly506Arg)
n.1451G>A
c.1519G>A (p.Gly507Arg)
c.5840G>A
c.6298G>A (p.Gly2100Arg)
c.704+518G>A (n.704+518G>A)
c.3620G>A
c.6022G>A (p.Gly2008Arg)
c.5734G>A (p.Gly1912Arg)
c.3262G>A (p.Gly1088Arg)
gnomAD v4
19g.35732847G>CCA405427609KMT2Bn.604G>C
c.6232G>C (p.Gly2078Arg)
c.3839G>C (n.3839G>C)
c.1516G>C (p.Gly506Arg)
n.1451G>C
c.1519G>C (p.Gly507Arg)
c.5840G>C
c.6298G>C (p.Gly2100Arg)
c.704+518G>C (n.704+518G>C)
c.3620G>C
c.6022G>C (p.Gly2008Arg)
c.5734G>C (p.Gly1912Arg)
c.3262G>C (p.Gly1088Arg)
19g.35732847G>TCA405427606KMT2Bn.604G>T
c.6232G>T (p.Gly2078Trp)
c.3839G>T (n.3839G>T)
c.1516G>T (p.Gly506Trp)
n.1451G>T
c.1519G>T (p.Gly507Trp)
c.5840G>T
c.6298G>T (p.Gly2100Trp)
c.704+518G>T (n.704+518G>T)
c.3620G>T
c.6022G>T (p.Gly2008Trp)
c.5734G>T (p.Gly1912Trp)
c.3262G>T (p.Gly1088Trp)
gnomAD v4
19g.35732850delCA2580096826KMT2Bn.607del
c.6235del (p.Asp2079ThrfsTer18)
c.3842del (n.3842del)
c.1519del (p.Asp507ThrfsTer18)
n.1454del
c.1522del (p.Asp508ThrfsTer18)
c.5843del
c.6301del (p.Asp2101ThrfsTer18)
c.704+521del (n.704+521del)
c.3623del
c.6025del (p.Asp2009ThrfsTer18)
c.5737del (p.Asp1913ThrfsTer18)
c.3265del (p.Asp1089ThrfsTer18)
ClinVar
19g.35732848G>ACA405427620KMT2Bn.605G>A
c.6233G>A (p.Gly2078Glu)
c.3840G>A (n.3840G>A)
c.1517G>A (p.Gly506Glu)
n.1452G>A
c.1520G>A (p.Gly507Glu)
c.5841G>A
c.6299G>A (p.Gly2100Glu)
c.704+519G>A (n.704+519G>A)
c.3621G>A
c.6023G>A (p.Gly2008Glu)
c.5735G>A (p.Gly1912Glu)
c.3263G>A (p.Gly1088Glu)
gnomAD v4
19g.35732848G>CCA405427623KMT2Bn.605G>C
c.6233G>C (p.Gly2078Ala)
c.3840G>C (n.3840G>C)
c.1517G>C (p.Gly506Ala)
n.1452G>C
c.1520G>C (p.Gly507Ala)
c.5841G>C
c.6299G>C (p.Gly2100Ala)
c.704+519G>C (n.704+519G>C)
c.3621G>C
c.6023G>C (p.Gly2008Ala)
c.5735G>C (p.Gly1912Ala)
c.3263G>C (p.Gly1088Ala)
19g.35732848G>TCA405427625KMT2Bn.605G>T
c.6233G>T (p.Gly2078Val)
c.3840G>T (n.3840G>T)
c.1517G>T (p.Gly506Val)
n.1452G>T
c.1520G>T (p.Gly507Val)
c.5841G>T
c.6299G>T (p.Gly2100Val)
c.704+519G>T (n.704+519G>T)
c.3621G>T
c.6023G>T (p.Gly2008Val)
c.5735G>T (p.Gly1912Val)
c.3263G>T (p.Gly1088Val)
19g.35732849G>ACA507308417KMT2Bn.606G>A
c.6234G>A (p.Gly2078=)
c.3841G>A (n.3841G>A)
c.1518G>A (p.Gly506=)
n.1453G>A
c.1521G>A (p.Gly507=)
c.5842G>A
c.6300G>A (p.Gly2100=)
c.704+520G>A (n.704+520G>A)
c.3622G>A
c.6024G>A (p.Gly2008=)
c.5736G>A (p.Gly1912=)
c.3264G>A (p.Gly1088=)
dbSNP gnomAD v4
19g.35732849G>CCA507308422KMT2Bn.606G>C
c.6234G>C (p.Gly2078=)
c.3841G>C (n.3841G>C)
c.1518G>C (p.Gly506=)
n.1453G>C
c.1521G>C (p.Gly507=)
c.5842G>C
c.6300G>C (p.Gly2100=)
c.704+520G>C (n.704+520G>C)
c.3622G>C
c.6024G>C (p.Gly2008=)
c.5736G>C (p.Gly1912=)
c.3264G>C (p.Gly1088=)
19g.35732849G=CA2333794532KMT2Bn.606G=
c.6234G= (p.Gly2078=)
c.3841G= (n.3841G=)
c.1518G= (p.Gly506=)
n.1453G=
c.1521G= (p.Gly507=)
c.5842G=
c.6300G= (p.Gly2100=)
c.704+520G= (n.704+520G=)
c.3622G=
c.6024G= (p.Gly2008=)
c.5736G= (p.Gly1912=)
c.3264G= (p.Gly1088=)
19g.35732849G>TCA507308415KMT2Bn.606G>T
c.6234G>T (p.Gly2078=)
c.3841G>T (n.3841G>T)
c.1518G>T (p.Gly506=)
n.1453G>T
c.1521G>T (p.Gly507=)
c.5842G>T
c.6300G>T (p.Gly2100=)
c.704+520G>T (n.704+520G>T)
c.3622G>T
c.6024G>T (p.Gly2008=)
c.5736G>T (p.Gly1912=)
c.3264G>T (p.Gly1088=)
gnomAD v4
19g.35732850G>ACA9385660KMT2Bn.607G>A
c.6235G>A (p.Asp2079Asn)
c.3842G>A (n.3842G>A)
c.1519G>A (p.Asp507Asn)
n.1454G>A
c.1522G>A (p.Asp508Asn)
c.5843G>A
c.6301G>A (p.Asp2101Asn)
c.704+521G>A (n.704+521G>A)
c.3623G>A
c.6025G>A (p.Asp2009Asn)
c.5737G>A (p.Asp1913Asn)
c.3265G>A (p.Asp1089Asn)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.35732850G>CCA9385659KMT2Bn.607G>C
c.6235G>C (p.Asp2079His)
c.3842G>C (n.3842G>C)
c.1519G>C (p.Asp507His)
n.1454G>C
c.1522G>C (p.Asp508His)
c.5843G>C
c.6301G>C (p.Asp2101His)
c.704+521G>C (n.704+521G>C)
c.3623G>C
c.6025G>C (p.Asp2009His)
c.5737G>C (p.Asp1913His)
c.3265G>C (p.Asp1089His)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.35732850G=CA2333794533KMT2Bn.607G=
c.6235G= (p.Asp2079=)
c.3842G= (n.3842G=)
c.1519G= (p.Asp507=)
n.1454G=
c.1522G= (p.Asp508=)
c.5843G=
c.6301G= (p.Asp2101=)
c.704+521G= (n.704+521G=)
c.3623G=
c.6025G= (p.Asp2009=)
c.5737G= (p.Asp1913=)
c.3265G= (p.Asp1089=)
19g.35732850G>TCA405427633KMT2Bn.607G>T
c.6235G>T (p.Asp2079Tyr)
c.3842G>T (n.3842G>T)
c.1519G>T (p.Asp507Tyr)
n.1454G>T
c.1522G>T (p.Asp508Tyr)
c.5843G>T
c.6301G>T (p.Asp2101Tyr)
c.704+521G>T (n.704+521G>T)
c.3623G>T
c.6025G>T (p.Asp2009Tyr)
c.5737G>T (p.Asp1913Tyr)
c.3265G>T (p.Asp1089Tyr)
gnomAD v4
19g.35732851A>CCA405427642KMT2Bn.608A>C
c.6236A>C (p.Asp2079Ala)
c.3843A>C (n.3843A>C)
c.1520A>C (p.Asp507Ala)
n.1455A>C
c.1523A>C (p.Asp508Ala)
c.5844A>C
c.6302A>C (p.Asp2101Ala)
c.704+522A>C (n.704+522A>C)
c.3624A>C
c.6026A>C (p.Asp2009Ala)
c.5738A>C (p.Asp1913Ala)
c.3266A>C (p.Asp1089Ala)
19g.35732851A>GCA405427639KMT2Bn.608A>G
c.6236A>G (p.Asp2079Gly)
c.3843A>G (n.3843A>G)
c.1520A>G (p.Asp507Gly)
n.1455A>G
c.1523A>G (p.Asp508Gly)
c.5844A>G
c.6302A>G (p.Asp2101Gly)
c.704+522A>G (n.704+522A>G)
c.3624A>G
c.6026A>G (p.Asp2009Gly)
c.5738A>G (p.Asp1913Gly)
c.3266A>G (p.Asp1089Gly)
19g.35732851A>TCA405427636KMT2Bn.608A>T
c.6236A>T (p.Asp2079Val)
c.3843A>T (n.3843A>T)
c.1520A>T (p.Asp507Val)
n.1455A>T
c.1523A>T (p.Asp508Val)
c.5844A>T
c.6302A>T (p.Asp2101Val)
c.704+522A>T (n.704+522A>T)
c.3624A>T
c.6026A>T (p.Asp2009Val)
c.5738A>T (p.Asp1913Val)
c.3266A>T (p.Asp1089Val)
19g.35732852C>ACA405427645KMT2Bn.609C>A
c.6237C>A (p.Asp2079Glu)
c.3844C>A (n.3844C>A)
c.1521C>A (p.Asp507Glu)
n.1456C>A
c.1524C>A (p.Asp508Glu)
c.5845C>A
c.6303C>A (p.Asp2101Glu)
c.704+523C>A (n.704+523C>A)
c.3625C>A
c.6027C>A (p.Asp2009Glu)
c.5739C>A (p.Asp1913Glu)
c.3267C>A (p.Asp1089Glu)
19g.35732852C=CA2333794534KMT2Bn.609C=
c.6237C= (p.Asp2079=)
c.3844C= (n.3844C=)
c.1521C= (p.Asp507=)
n.1456C=
c.1524C= (p.Asp508=)
c.5845C=
c.6303C= (p.Asp2101=)
c.704+523C= (n.704+523C=)
c.3625C=
c.6027C= (p.Asp2009=)
c.5739C= (p.Asp1913=)
c.3267C= (p.Asp1089=)
19g.35732852C>GCA405427647KMT2Bn.609C>G
c.6237C>G (p.Asp2079Glu)
c.3844C>G (n.3844C>G)
c.1521C>G (p.Asp507Glu)
n.1456C>G
c.1524C>G (p.Asp508Glu)
c.5845C>G
c.6303C>G (p.Asp2101Glu)
c.704+523C>G (n.704+523C>G)
c.3625C>G
c.6027C>G (p.Asp2009Glu)
c.5739C>G (p.Asp1913Glu)
c.3267C>G (p.Asp1089Glu)
19g.35732852C>TCA9385661KMT2Bn.609C>T
c.6237C>T (p.Asp2079=)
c.3844C>T (n.3844C>T)
c.1521C>T (p.Asp507=)
n.1456C>T
c.1524C>T (p.Asp508=)
c.5845C>T
c.6303C>T (p.Asp2101=)
c.704+523C>T (n.704+523C>T)
c.3625C>T
c.6027C>T (p.Asp2009=)
c.5739C>T (p.Asp1913=)
c.3267C>T (p.Asp1089=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.35732853A=CA2333794535KMT2Bn.610A=
c.6238A= (p.Arg2080=)
c.3845A= (n.3845A=)
c.1522A= (p.Arg508=)
n.1457A=
c.1525A= (p.Arg509=)
c.5846A=
c.6304A= (p.Arg2102=)
c.704+524A= (n.704+524A=)
c.3626A=
c.6028A= (p.Arg2010=)
c.5740A= (p.Arg1914=)
c.3268A= (p.Arg1090=)
19g.35732853A>CCA507308438KMT2Bn.610A>C
c.6238A>C (p.Arg2080=)
c.3845A>C (n.3845A>C)
c.1522A>C (p.Arg508=)
n.1457A>C
c.1525A>C (p.Arg509=)
c.5846A>C
c.6304A>C (p.Arg2102=)
c.704+524A>C (n.704+524A>C)
c.3626A>C
c.6028A>C (p.Arg2010=)
c.5740A>C (p.Arg1914=)
c.3268A>C (p.Arg1090=)
19g.35732853A>GCA9385662KMT2Bn.610A>G
c.6238A>G (p.Arg2080Gly)
c.3845A>G (n.3845A>G)
c.1522A>G (p.Arg508Gly)
n.1457A>G
c.1525A>G (p.Arg509Gly)
c.5846A>G
c.6304A>G (p.Arg2102Gly)
c.704+524A>G (n.704+524A>G)
c.3626A>G
c.6028A>G (p.Arg2010Gly)
c.5740A>G (p.Arg1914Gly)
c.3268A>G (p.Arg1090Gly)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.35732853A>TCA405427651KMT2Bn.610A>T
c.6238A>T (p.Arg2080Trp)
c.3845A>T (n.3845A>T)
c.1522A>T (p.Arg508Trp)
n.1457A>T
c.1525A>T (p.Arg509Trp)
c.5846A>T
c.6304A>T (p.Arg2102Trp)
c.704+524A>T (n.704+524A>T)
c.3626A>T
c.6028A>T (p.Arg2010Trp)
c.5740A>T (p.Arg1914Trp)
c.3268A>T (p.Arg1090Trp)
19g.35732854G>ACA405427659KMT2Bn.611G>A
c.6239G>A (p.Arg2080Lys)
c.3846G>A (n.3846G>A)
c.1523G>A (p.Arg508Lys)
n.1458G>A
c.1526G>A (p.Arg509Lys)
c.5847G>A
c.6305G>A (p.Arg2102Lys)
c.704+525G>A (n.704+525G>A)
c.3627G>A
c.6029G>A (p.Arg2010Lys)
c.5741G>A (p.Arg1914Lys)
c.3269G>A (p.Arg1090Lys)
19g.35732854G>CCA405427665KMT2Bn.611G>C
c.6239G>C (p.Arg2080Thr)
c.3846G>C (n.3846G>C)
c.1523G>C (p.Arg508Thr)
n.1458G>C
c.1526G>C (p.Arg509Thr)
c.5847G>C
c.6305G>C (p.Arg2102Thr)
c.704+525G>C (n.704+525G>C)
c.3627G>C
c.6029G>C (p.Arg2010Thr)
c.5741G>C (p.Arg1914Thr)
c.3269G>C (p.Arg1090Thr)
19g.35732854G>TCA405427662KMT2Bn.611G>T
c.6239G>T (p.Arg2080Met)
c.3846G>T (n.3846G>T)
c.1523G>T (p.Arg508Met)
n.1458G>T
c.1526G>T (p.Arg509Met)
c.5847G>T
c.6305G>T (p.Arg2102Met)
c.704+525G>T (n.704+525G>T)
c.3627G>T
c.6029G>T (p.Arg2010Met)
c.5741G>T (p.Arg1914Met)
c.3269G>T (p.Arg1090Met)
COSMIC
19g.35732855G>ACA507308441KMT2Bn.612G>A
c.6240G>A (p.Arg2080=)
c.3847G>A (n.3847G>A)
c.1524G>A (p.Arg508=)
n.1459G>A
c.1527G>A (p.Arg509=)
c.5848G>A
c.6306G>A (p.Arg2102=)
c.704+526G>A (n.704+526G>A)
c.3628G>A
c.6030G>A (p.Arg2010=)
c.5742G>A (p.Arg1914=)
c.3270G>A (p.Arg1090=)
gnomAD v4
19g.35732855G>CCA405427668KMT2Bn.612G>C
c.6240G>C (p.Arg2080Ser)
c.3847G>C (n.3847G>C)
c.1524G>C (p.Arg508Ser)
n.1459G>C
c.1527G>C (p.Arg509Ser)
c.5848G>C
c.6306G>C (p.Arg2102Ser)
c.704+526G>C (n.704+526G>C)
c.3628G>C
c.6030G>C (p.Arg2010Ser)
c.5742G>C (p.Arg1914Ser)
c.3270G>C (p.Arg1090Ser)
19g.35732855G>TCA405427671KMT2Bn.612G>T
c.6240G>T (p.Arg2080Ser)
c.3847G>T (n.3847G>T)
c.1524G>T (p.Arg508Ser)
n.1459G>T
c.1527G>T (p.Arg509Ser)
c.5848G>T
c.6306G>T (p.Arg2102Ser)
c.704+526G>T (n.704+526G>T)
c.3628G>T
c.6030G>T (p.Arg2010Ser)
c.5742G>T (p.Arg1914Ser)
c.3270G>T (p.Arg1090Ser)
19g.35732856G>ACA405427674KMT2Bn.613G>A
c.6241G>A (p.Ala2081Thr)
c.3848G>A (n.3848G>A)
c.1525G>A (p.Ala509Thr)
n.1460G>A
c.1528G>A (p.Ala510Thr)
c.5849G>A
c.6307G>A (p.Ala2103Thr)
c.704+527G>A (n.704+527G>A)
c.3629G>A
c.6031G>A (p.Ala2011Thr)
c.5743G>A (p.Ala1915Thr)
c.3271G>A (p.Ala1091Thr)
19g.35732856G>CCA405427676KMT2Bn.613G>C
c.6241G>C (p.Ala2081Pro)
c.3848G>C (n.3848G>C)
c.1525G>C (p.Ala509Pro)
n.1460G>C
c.1528G>C (p.Ala510Pro)
c.5849G>C
c.6307G>C (p.Ala2103Pro)
c.704+527G>C (n.704+527G>C)
c.3629G>C
c.6031G>C (p.Ala2011Pro)
c.5743G>C (p.Ala1915Pro)
c.3271G>C (p.Ala1091Pro)
19g.35732856G>TCA405427679KMT2Bn.613G>T
c.6241G>T (p.Ala2081Ser)
c.3848G>T (n.3848G>T)
c.1525G>T (p.Ala509Ser)
n.1460G>T
c.1528G>T (p.Ala510Ser)
c.5849G>T
c.6307G>T (p.Ala2103Ser)
c.704+527G>T (n.704+527G>T)
c.3629G>T
c.6031G>T (p.Ala2011Ser)
c.5743G>T (p.Ala1915Ser)
c.3271G>T (p.Ala1091Ser)
gnomAD v4

Number of alleles fetched