Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.35732679_35732702dupCA2333794440KMT2Bn.436_459dup
c.6064_6087dup (p.Ala2029_Thr2030insAlaProGlyLeuAlaProSerAla)
c.3671_3694dup (n.3671_3694dup)
c.1348_1371dup (p.Ala457_Thr458insAlaProGlyLeuAlaProSerAla)
n.1283_1306dup
c.1351_1374dup (p.Ala458_Thr459insAlaProGlyLeuAlaProSerAla)
c.5672_5695dup
c.6130_6153dup (p.Ala2051_Thr2052insAlaProGlyLeuAlaProSerAla)
c.704+350_704+373dup (n.704+350_704+373dup)
c.3452_3475dup
c.5854_5877dup (p.Ala1959_Thr1960insAlaProGlyLeuAlaProSerAla)
c.5566_5589dup (p.Ala1863_Thr1864insAlaProGlyLeuAlaProSerAla)
c.3094_3117dup (p.Ala1039_Thr1040insAlaProGlyLeuAlaProSerAla)
dbSNP
19g.35732697A=CA2333794454KMT2Bn.454A=
c.6082A= (p.Ser2028=)
c.3689A= (n.3689A=)
c.1366A= (p.Ser456=)
n.1301A=
c.1369A= (p.Ser457=)
c.5690A=
c.6148A= (p.Ser2050=)
c.704+368A= (n.704+368A=)
c.3470A=
c.5872A= (p.Ser1958=)
c.5584A= (p.Ser1862=)
c.3112A= (p.Ser1038=)
19g.35732697A>CCA405425867KMT2Bn.454A>C
c.6082A>C (p.Ser2028Arg)
c.3689A>C (n.3689A>C)
c.1366A>C (p.Ser456Arg)
n.1301A>C
c.1369A>C (p.Ser457Arg)
c.5690A>C
c.6148A>C (p.Ser2050Arg)
c.704+368A>C (n.704+368A>C)
c.3470A>C
c.5872A>C (p.Ser1958Arg)
c.5584A>C (p.Ser1862Arg)
c.3112A>C (p.Ser1038Arg)
19g.35732697A>GCA9385616KMT2Bn.454A>G
c.6082A>G (p.Ser2028Gly)
c.3689A>G (n.3689A>G)
c.1366A>G (p.Ser456Gly)
n.1301A>G
c.1369A>G (p.Ser457Gly)
c.5690A>G
c.6148A>G (p.Ser2050Gly)
c.704+368A>G (n.704+368A>G)
c.3470A>G
c.5872A>G (p.Ser1958Gly)
c.5584A>G (p.Ser1862Gly)
c.3112A>G (p.Ser1038Gly)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732697A>TCA405425870KMT2Bn.454A>T
c.6082A>T (p.Ser2028Cys)
c.3689A>T (n.3689A>T)
c.1366A>T (p.Ser456Cys)
n.1301A>T
c.1369A>T (p.Ser457Cys)
c.5690A>T
c.6148A>T (p.Ser2050Cys)
c.704+368A>T (n.704+368A>T)
c.3470A>T
c.5872A>T (p.Ser1958Cys)
c.5584A>T (p.Ser1862Cys)
c.3112A>T (p.Ser1038Cys)
19g.35732698G>ACA405425877KMT2Bn.455G>A
c.6083G>A (p.Ser2028Asn)
c.3690G>A (n.3690G>A)
c.1367G>A (p.Ser456Asn)
n.1302G>A
c.1370G>A (p.Ser457Asn)
c.5691G>A
c.6149G>A (p.Ser2050Asn)
c.704+369G>A (n.704+369G>A)
c.3471G>A
c.5873G>A (p.Ser1958Asn)
c.5585G>A (p.Ser1862Asn)
c.3113G>A (p.Ser1038Asn)
19g.35732698G>CCA405425875KMT2Bn.455G>C
c.6083G>C (p.Ser2028Thr)
c.3690G>C (n.3690G>C)
c.1367G>C (p.Ser456Thr)
n.1302G>C
c.1370G>C (p.Ser457Thr)
c.5691G>C
c.6149G>C (p.Ser2050Thr)
c.704+369G>C (n.704+369G>C)
c.3471G>C
c.5873G>C (p.Ser1958Thr)
c.5585G>C (p.Ser1862Thr)
c.3113G>C (p.Ser1038Thr)
gnomAD v4
19g.35732698G>TCA405425873KMT2Bn.455G>T
c.6083G>T (p.Ser2028Ile)
c.3690G>T (n.3690G>T)
c.1367G>T (p.Ser456Ile)
n.1302G>T
c.1370G>T (p.Ser457Ile)
c.5691G>T
c.6149G>T (p.Ser2050Ile)
c.704+369G>T (n.704+369G>T)
c.3471G>T
c.5873G>T (p.Ser1958Ile)
c.5585G>T (p.Ser1862Ile)
c.3113G>T (p.Ser1038Ile)
19g.35732699C>ACA405425880KMT2Bn.456C>A
c.6084C>A (p.Ser2028Arg)
c.3691C>A (n.3691C>A)
c.1368C>A (p.Ser456Arg)
n.1303C>A
c.1371C>A (p.Ser457Arg)
c.5692C>A
c.6150C>A (p.Ser2050Arg)
c.704+370C>A (n.704+370C>A)
c.3472C>A
c.5874C>A (p.Ser1958Arg)
c.5586C>A (p.Ser1862Arg)
c.3114C>A (p.Ser1038Arg)
gnomAD v4
19g.35732699C=CA2333794455KMT2Bn.456C=
c.6084C= (p.Ser2028=)
c.3691C= (n.3691C=)
c.1368C= (p.Ser456=)
n.1303C=
c.1371C= (p.Ser457=)
c.5692C=
c.6150C= (p.Ser2050=)
c.704+370C= (n.704+370C=)
c.3472C=
c.5874C= (p.Ser1958=)
c.5586C= (p.Ser1862=)
c.3114C= (p.Ser1038=)
19g.35732699C>GCA405425882KMT2Bn.456C>G
c.6084C>G (p.Ser2028Arg)
c.3691C>G (n.3691C>G)
c.1368C>G (p.Ser456Arg)
n.1303C>G
c.1371C>G (p.Ser457Arg)
c.5692C>G
c.6150C>G (p.Ser2050Arg)
c.704+370C>G (n.704+370C>G)
c.3472C>G
c.5874C>G (p.Ser1958Arg)
c.5586C>G (p.Ser1862Arg)
c.3114C>G (p.Ser1038Arg)
19g.35732699C>TCA507308580KMT2Bn.456C>T
c.6084C>T (p.Ser2028=)
c.3691C>T (n.3691C>T)
c.1368C>T (p.Ser456=)
n.1303C>T
c.1371C>T (p.Ser457=)
c.5692C>T
c.6150C>T (p.Ser2050=)
c.704+370C>T (n.704+370C>T)
c.3472C>T
c.5874C>T (p.Ser1958=)
c.5586C>T (p.Ser1862=)
c.3114C>T (p.Ser1038=)
dbSNP gnomAD v3 gnomAD v4
19g.35732700G>ACA9385617KMT2Bn.457G>A
c.6085G>A (p.Ala2029Thr)
c.3692G>A (n.3692G>A)
c.1369G>A (p.Ala457Thr)
n.1304G>A
c.1372G>A (p.Ala458Thr)
c.5693G>A
c.6151G>A (p.Ala2051Thr)
c.704+371G>A (n.704+371G>A)
c.3473G>A
c.5875G>A (p.Ala1959Thr)
c.5587G>A (p.Ala1863Thr)
c.3115G>A (p.Ala1039Thr)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732700G>CCA405425886KMT2Bn.457G>C
c.6085G>C (p.Ala2029Pro)
c.3692G>C (n.3692G>C)
c.1369G>C (p.Ala457Pro)
n.1304G>C
c.1372G>C (p.Ala458Pro)
c.5693G>C
c.6151G>C (p.Ala2051Pro)
c.704+371G>C (n.704+371G>C)
c.3473G>C
c.5875G>C (p.Ala1959Pro)
c.5587G>C (p.Ala1863Pro)
c.3115G>C (p.Ala1039Pro)
19g.35732700G=CA2333794456KMT2Bn.457G=
c.6085G= (p.Ala2029=)
c.3692G= (n.3692G=)
c.1369G= (p.Ala457=)
n.1304G=
c.1372G= (p.Ala458=)
c.5693G=
c.6151G= (p.Ala2051=)
c.704+371G= (n.704+371G=)
c.3473G=
c.5875G= (p.Ala1959=)
c.5587G= (p.Ala1863=)
c.3115G= (p.Ala1039=)
19g.35732700G>TCA405425888KMT2Bn.457G>T
c.6085G>T (p.Ala2029Ser)
c.3692G>T (n.3692G>T)
c.1369G>T (p.Ala457Ser)
n.1304G>T
c.1372G>T (p.Ala458Ser)
c.5693G>T
c.6151G>T (p.Ala2051Ser)
c.704+371G>T (n.704+371G>T)
c.3473G>T
c.5875G>T (p.Ala1959Ser)
c.5587G>T (p.Ala1863Ser)
c.3115G>T (p.Ala1039Ser)
gnomAD v4
19g.35732701C>ACA405425890KMT2Bn.458C>A
c.6086C>A (p.Ala2029Asp)
c.3693C>A (n.3693C>A)
c.1370C>A (p.Ala457Asp)
n.1305C>A
c.1373C>A (p.Ala458Asp)
c.5694C>A
c.6152C>A (p.Ala2051Asp)
c.704+372C>A (n.704+372C>A)
c.3474C>A
c.5876C>A (p.Ala1959Asp)
c.5588C>A (p.Ala1863Asp)
c.3116C>A (p.Ala1039Asp)
19g.35732701C>GCA405425891KMT2Bn.458C>G
c.6086C>G (p.Ala2029Gly)
c.3693C>G (n.3693C>G)
c.1370C>G (p.Ala457Gly)
n.1305C>G
c.1373C>G (p.Ala458Gly)
c.5694C>G
c.6152C>G (p.Ala2051Gly)
c.704+372C>G (n.704+372C>G)
c.3474C>G
c.5876C>G (p.Ala1959Gly)
c.5588C>G (p.Ala1863Gly)
c.3116C>G (p.Ala1039Gly)
19g.35732701C>TCA405425893KMT2Bn.458C>T
c.6086C>T (p.Ala2029Val)
c.3693C>T (n.3693C>T)
c.1370C>T (p.Ala457Val)
n.1305C>T
c.1373C>T (p.Ala458Val)
c.5694C>T
c.6152C>T (p.Ala2051Val)
c.704+372C>T (n.704+372C>T)
c.3474C>T
c.5876C>T (p.Ala1959Val)
c.5588C>T (p.Ala1863Val)
c.3116C>T (p.Ala1039Val)
19g.35732702T>ACA507308582KMT2Bn.459T>A
c.6087T>A (p.Ala2029=)
c.3694T>A (n.3694T>A)
c.1371T>A (p.Ala457=)
n.1306T>A
c.1374T>A (p.Ala458=)
c.5695T>A
c.6153T>A (p.Ala2051=)
c.704+373T>A (n.704+373T>A)
c.3475T>A
c.5877T>A (p.Ala1959=)
c.5589T>A (p.Ala1863=)
c.3117T>A (p.Ala1039=)
dbSNP gnomAD v4
19g.35732702T>CCA507308583KMT2Bn.459T>C
c.6087T>C (p.Ala2029=)
c.3694T>C (n.3694T>C)
c.1371T>C (p.Ala457=)
n.1306T>C
c.1374T>C (p.Ala458=)
c.5695T>C
c.6153T>C (p.Ala2051=)
c.704+373T>C (n.704+373T>C)
c.3475T>C
c.5877T>C (p.Ala1959=)
c.5589T>C (p.Ala1863=)
c.3117T>C (p.Ala1039=)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.35732702T>GCA507308584KMT2Bn.459T>G
c.6087T>G (p.Ala2029=)
c.3694T>G (n.3694T>G)
c.1371T>G (p.Ala457=)
n.1306T>G
c.1374T>G (p.Ala458=)
c.5695T>G
c.6153T>G (p.Ala2051=)
c.704+373T>G (n.704+373T>G)
c.3475T>G
c.5877T>G (p.Ala1959=)
c.5589T>G (p.Ala1863=)
c.3117T>G (p.Ala1039=)
gnomAD v4
19g.35732702T=CA2333794457KMT2Bn.459T=
c.6087T= (p.Ala2029=)
c.3694T= (n.3694T=)
c.1371T= (p.Ala457=)
n.1306T=
c.1374T= (p.Ala458=)
c.5695T=
c.6153T= (p.Ala2051=)
c.704+373T= (n.704+373T=)
c.3475T=
c.5877T= (p.Ala1959=)
c.5589T= (p.Ala1863=)
c.3117T= (p.Ala1039=)
19g.35732702_35732704delinsTACCA2333794458KMT2Bn.459_461delinsTAC
c.6087_6089delinsTAC (p.Ala2029=)
c.3694_3696delinsTAC (n.3694_3696delinsTAC)
c.1371_1373delinsTAC (p.Ala457=)
n.1306_1308delinsTAC
c.1374_1376delinsTAC (p.Ala458=)
c.5695_5697delinsTAC
c.6153_6155delinsTAC (p.Ala2051=)
c.704+373_704+375delinsTAC (n.704+373_704+375delinsTAC)
c.3475_3477delinsTAC
c.5877_5879delinsTAC (p.Ala1959=)
c.5589_5591delinsTAC (p.Ala1863=)
c.3117_3119delinsTAC (p.Ala1039=)
19g.35732703A>CCA405425896KMT2Bn.460A>C
c.6088A>C (p.Thr2030Pro)
c.3695A>C (n.3695A>C)
c.1372A>C (p.Thr458Pro)
n.1307A>C
c.1375A>C (p.Thr459Pro)
c.5696A>C
c.6154A>C (p.Thr2052Pro)
c.704+374A>C (n.704+374A>C)
c.3476A>C
c.5878A>C (p.Thr1960Pro)
c.5590A>C (p.Thr1864Pro)
c.3118A>C (p.Thr1040Pro)
19g.35732703A>GCA405425897KMT2Bn.460A>G
c.6088A>G (p.Thr2030Ala)
c.3695A>G (n.3695A>G)
c.1372A>G (p.Thr458Ala)
n.1307A>G
c.1375A>G (p.Thr459Ala)
c.5696A>G
c.6154A>G (p.Thr2052Ala)
c.704+374A>G (n.704+374A>G)
c.3476A>G
c.5878A>G (p.Thr1960Ala)
c.5590A>G (p.Thr1864Ala)
c.3118A>G (p.Thr1040Ala)
19g.35732703A>TCA405425899KMT2Bn.460A>T
c.6088A>T (p.Thr2030Ser)
c.3695A>T (n.3695A>T)
c.1372A>T (p.Thr458Ser)
n.1307A>T
c.1375A>T (p.Thr459Ser)
c.5696A>T
c.6154A>T (p.Thr2052Ser)
c.704+374A>T (n.704+374A>T)
c.3476A>T
c.5878A>T (p.Thr1960Ser)
c.5590A>T (p.Thr1864Ser)
c.3118A>T (p.Thr1040Ser)
19g.35732703_35732704delCA2333794459KMT2Bn.460_461del
c.6088_6089del (p.Thr2030ProfsTer7)
c.3695_3696del (n.3695_3696del)
c.1372_1373del (p.Thr458ProfsTer7)
n.1307_1308del
c.1375_1376del (p.Thr459ProfsTer7)
c.5696_5697del
c.6154_6155del (p.Thr2052ProfsTer7)
c.704+374_704+375del (n.704+374_704+375del)
c.3476_3477del
c.5878_5879del (p.Thr1960ProfsTer7)
c.5590_5591del (p.Thr1864ProfsTer7)
c.3118_3119del (p.Thr1040ProfsTer7)
dbSNP
19g.35732704C>ACA307796349KMT2Bn.461C>A
c.6089C>A (p.Thr2030Asn)
c.3696C>A (n.3696C>A)
c.1373C>A (p.Thr458Asn)
n.1308C>A
c.1376C>A (p.Thr459Asn)
c.5697C>A
c.6155C>A (p.Thr2052Asn)
c.704+375C>A (n.704+375C>A)
c.3477C>A
c.5879C>A (p.Thr1960Asn)
c.5591C>A (p.Thr1864Asn)
c.3119C>A (p.Thr1040Asn)
dbSNP gnomAD v3 gnomAD v4
19g.35732704C=CA2333794460KMT2Bn.461C=
c.6089C= (p.Thr2030=)
c.3696C= (n.3696C=)
c.1373C= (p.Thr458=)
n.1308C=
c.1376C= (p.Thr459=)
c.5697C=
c.6155C= (p.Thr2052=)
c.704+375C= (n.704+375C=)
c.3477C=
c.5879C= (p.Thr1960=)
c.5591C= (p.Thr1864=)
c.3119C= (p.Thr1040=)
19g.35732704C>GCA405425905KMT2Bn.461C>G
c.6089C>G (p.Thr2030Ser)
c.3696C>G (n.3696C>G)
c.1373C>G (p.Thr458Ser)
n.1308C>G
c.1376C>G (p.Thr459Ser)
c.5697C>G
c.6155C>G (p.Thr2052Ser)
c.704+375C>G (n.704+375C>G)
c.3477C>G
c.5879C>G (p.Thr1960Ser)
c.5591C>G (p.Thr1864Ser)
c.3119C>G (p.Thr1040Ser)
19g.35732704C>TCA405425902KMT2Bn.461C>T
c.6089C>T (p.Thr2030Ile)
c.3696C>T (n.3696C>T)
c.1373C>T (p.Thr458Ile)
n.1308C>T
c.1376C>T (p.Thr459Ile)
c.5697C>T
c.6155C>T (p.Thr2052Ile)
c.704+375C>T (n.704+375C>T)
c.3477C>T
c.5879C>T (p.Thr1960Ile)
c.5591C>T (p.Thr1864Ile)
c.3119C>T (p.Thr1040Ile)
dbSNP gnomAD v4
19g.35732705C>ACA507308596KMT2Bn.462C>A
c.6090C>A (p.Thr2030=)
c.3697C>A (n.3697C>A)
c.1374C>A (p.Thr458=)
n.1309C>A
c.1377C>A (p.Thr459=)
c.5698C>A
c.6156C>A (p.Thr2052=)
c.704+376C>A (n.704+376C>A)
c.3478C>A
c.5880C>A (p.Thr1960=)
c.5592C>A (p.Thr1864=)
c.3120C>A (p.Thr1040=)
19g.35732705C=CA2333794461KMT2Bn.462C=
c.6090C= (p.Thr2030=)
c.3697C= (n.3697C=)
c.1374C= (p.Thr458=)
n.1309C=
c.1377C= (p.Thr459=)
c.5698C=
c.6156C= (p.Thr2052=)
c.704+376C= (n.704+376C=)
c.3478C=
c.5880C= (p.Thr1960=)
c.5592C= (p.Thr1864=)
c.3120C= (p.Thr1040=)
19g.35732705C>GCA9385618KMT2Bn.462C>G
c.6090C>G (p.Thr2030=)
c.3697C>G (n.3697C>G)
c.1374C>G (p.Thr458=)
n.1309C>G
c.1377C>G (p.Thr459=)
c.5698C>G
c.6156C>G (p.Thr2052=)
c.704+376C>G (n.704+376C>G)
c.3478C>G
c.5880C>G (p.Thr1960=)
c.5592C>G (p.Thr1864=)
c.3120C>G (p.Thr1040=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.35732705C>TCA507308595KMT2Bn.462C>T
c.6090C>T (p.Thr2030=)
c.3697C>T (n.3697C>T)
c.1374C>T (p.Thr458=)
n.1309C>T
c.1377C>T (p.Thr459=)
c.5698C>T
c.6156C>T (p.Thr2052=)
c.704+376C>T (n.704+376C>T)
c.3478C>T
c.5880C>T (p.Thr1960=)
c.5592C>T (p.Thr1864=)
c.3120C>T (p.Thr1040=)
dbSNP gnomAD v4
19g.35732706C>ACA405425912KMT2Bn.463C>A
c.6091C>A (p.Pro2031Thr)
c.3698C>A (n.3698C>A)
c.1375C>A (p.Pro459Thr)
n.1310C>A
c.1378C>A (p.Pro460Thr)
c.5699C>A
c.6157C>A (p.Pro2053Thr)
c.704+377C>A (n.704+377C>A)
c.3479C>A
c.5881C>A (p.Pro1961Thr)
c.5593C>A (p.Pro1865Thr)
c.3121C>A (p.Pro1041Thr)
gnomAD v4
19g.35732706C=CA2333794462KMT2Bn.463C=
c.6091C= (p.Pro2031=)
c.3698C= (n.3698C=)
c.1375C= (p.Pro459=)
n.1310C=
c.1378C= (p.Pro460=)
c.5699C=
c.6157C= (p.Pro2053=)
c.704+377C= (n.704+377C=)
c.3479C=
c.5881C= (p.Pro1961=)
c.5593C= (p.Pro1865=)
c.3121C= (p.Pro1041=)
19g.35732706C>GCA405425913KMT2Bn.463C>G
c.6091C>G (p.Pro2031Ala)
c.3698C>G (n.3698C>G)
c.1375C>G (p.Pro459Ala)
n.1310C>G
c.1378C>G (p.Pro460Ala)
c.5699C>G
c.6157C>G (p.Pro2053Ala)
c.704+377C>G (n.704+377C>G)
c.3479C>G
c.5881C>G (p.Pro1961Ala)
c.5593C>G (p.Pro1865Ala)
c.3121C>G (p.Pro1041Ala)
19g.35732706C>TCA307796362KMT2Bn.463C>T
c.6091C>T (p.Pro2031Ser)
c.3698C>T (n.3698C>T)
c.1375C>T (p.Pro459Ser)
n.1310C>T
c.1378C>T (p.Pro460Ser)
c.5699C>T
c.6157C>T (p.Pro2053Ser)
c.704+377C>T (n.704+377C>T)
c.3479C>T
c.5881C>T (p.Pro1961Ser)
c.5593C>T (p.Pro1865Ser)
c.3121C>T (p.Pro1041Ser)
dbSNP gnomAD v2 gnomAD v4
19g.35732707C>ACA9385619KMT2Bn.464C>A
c.6092C>A (p.Pro2031His)
c.3699C>A (n.3699C>A)
c.1376C>A (p.Pro459His)
n.1311C>A
c.1379C>A (p.Pro460His)
c.5700C>A
c.6158C>A (p.Pro2053His)
c.704+378C>A (n.704+378C>A)
c.3480C>A
c.5882C>A (p.Pro1961His)
c.5594C>A (p.Pro1865His)
c.3122C>A (p.Pro1041His)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732707C=CA2333794463KMT2Bn.464C=
c.6092C= (p.Pro2031=)
c.3699C= (n.3699C=)
c.1376C= (p.Pro459=)
n.1311C=
c.1379C= (p.Pro460=)
c.5700C=
c.6158C= (p.Pro2053=)
c.704+378C= (n.704+378C=)
c.3480C=
c.5882C= (p.Pro1961=)
c.5594C= (p.Pro1865=)
c.3122C= (p.Pro1041=)
19g.35732707C>GCA405425919KMT2Bn.464C>G
c.6092C>G (p.Pro2031Arg)
c.3699C>G (n.3699C>G)
c.1376C>G (p.Pro459Arg)
n.1311C>G
c.1379C>G (p.Pro460Arg)
c.5700C>G
c.6158C>G (p.Pro2053Arg)
c.704+378C>G (n.704+378C>G)
c.3480C>G
c.5882C>G (p.Pro1961Arg)
c.5594C>G (p.Pro1865Arg)
c.3122C>G (p.Pro1041Arg)
19g.35732707C>TCA405425921KMT2Bn.464C>T
c.6092C>T (p.Pro2031Leu)
c.3699C>T (n.3699C>T)
c.1376C>T (p.Pro459Leu)
n.1311C>T
c.1379C>T (p.Pro460Leu)
c.5700C>T
c.6158C>T (p.Pro2053Leu)
c.704+378C>T (n.704+378C>T)
c.3480C>T
c.5882C>T (p.Pro1961Leu)
c.5594C>T (p.Pro1865Leu)
c.3122C>T (p.Pro1041Leu)
dbSNP gnomAD v3 gnomAD v4
19g.35732708T>ACA507308599KMT2Bn.465T>A
c.6093T>A (p.Pro2031=)
c.3700T>A (n.3700T>A)
c.1377T>A (p.Pro459=)
n.1312T>A
c.1380T>A (p.Pro460=)
c.5701T>A
c.6159T>A (p.Pro2053=)
c.704+379T>A (n.704+379T>A)
c.3481T>A
c.5883T>A (p.Pro1961=)
c.5595T>A (p.Pro1865=)
c.3123T>A (p.Pro1041=)
19g.35732708T>CCA507308600KMT2Bn.465T>C
c.6093T>C (p.Pro2031=)
c.3700T>C (n.3700T>C)
c.1377T>C (p.Pro459=)
n.1312T>C
c.1380T>C (p.Pro460=)
c.5701T>C
c.6159T>C (p.Pro2053=)
c.704+379T>C (n.704+379T>C)
c.3481T>C
c.5883T>C (p.Pro1961=)
c.5595T>C (p.Pro1865=)
c.3123T>C (p.Pro1041=)
19g.35732708T>GCA507308601KMT2Bn.465T>G
c.6093T>G (p.Pro2031=)
c.3700T>G (n.3700T>G)
c.1377T>G (p.Pro459=)
n.1312T>G
c.1380T>G (p.Pro460=)
c.5701T>G
c.6159T>G (p.Pro2053=)
c.704+379T>G (n.704+379T>G)
c.3481T>G
c.5883T>G (p.Pro1961=)
c.5595T>G (p.Pro1865=)
c.3123T>G (p.Pro1041=)
19g.35732709G>ACA405425924KMT2Bn.466G>A
c.6094G>A (p.Gly2032Arg)
c.3701G>A (n.3701G>A)
c.1378G>A (p.Gly460Arg)
n.1313G>A
c.1381G>A (p.Gly461Arg)
c.5702G>A
c.6160G>A (p.Gly2054Arg)
c.704+380G>A (n.704+380G>A)
c.3482G>A
c.5884G>A (p.Gly1962Arg)
c.5596G>A (p.Gly1866Arg)
c.3124G>A (p.Gly1042Arg)
dbSNP gnomAD v2 gnomAD v4 COSMIC
19g.35732709G>CCA405425926KMT2Bn.466G>C
c.6094G>C (p.Gly2032Arg)
c.3701G>C (n.3701G>C)
c.1378G>C (p.Gly460Arg)
n.1313G>C
c.1381G>C (p.Gly461Arg)
c.5702G>C
c.6160G>C (p.Gly2054Arg)
c.704+380G>C (n.704+380G>C)
c.3482G>C
c.5884G>C (p.Gly1962Arg)
c.5596G>C (p.Gly1866Arg)
c.3124G>C (p.Gly1042Arg)
19g.35732709G=CA2333794464KMT2Bn.466G=
c.6094G= (p.Gly2032=)
c.3701G= (n.3701G=)
c.1378G= (p.Gly460=)
n.1313G=
c.1381G= (p.Gly461=)
c.5702G=
c.6160G= (p.Gly2054=)
c.704+380G= (n.704+380G=)
c.3482G=
c.5884G= (p.Gly1962=)
c.5596G= (p.Gly1866=)
c.3124G= (p.Gly1042=)
19g.35732709G>TCA405425928KMT2Bn.466G>T
c.6094G>T (p.Gly2032Ter)
c.3701G>T (n.3701G>T)
c.1378G>T (p.Gly460Ter)
n.1313G>T
c.1381G>T (p.Gly461Ter)
c.5702G>T
c.6160G>T (p.Gly2054Ter)
c.704+380G>T (n.704+380G>T)
c.3482G>T
c.5884G>T (p.Gly1962Ter)
c.5596G>T (p.Gly1866Ter)
c.3124G>T (p.Gly1042Ter)
19g.35732710G>ACA405425931KMT2Bn.467G>A
c.6095G>A (p.Gly2032Glu)
c.3702G>A (n.3702G>A)
c.1379G>A (p.Gly460Glu)
n.1314G>A
c.1382G>A (p.Gly461Glu)
c.5703G>A
c.6161G>A (p.Gly2054Glu)
c.704+381G>A (n.704+381G>A)
c.3483G>A
c.5885G>A (p.Gly1962Glu)
c.5597G>A (p.Gly1866Glu)
c.3125G>A (p.Gly1042Glu)
19g.35732710G>CCA405425933KMT2Bn.467G>C
c.6095G>C (p.Gly2032Ala)
c.3702G>C (n.3702G>C)
c.1379G>C (p.Gly460Ala)
n.1314G>C
c.1382G>C (p.Gly461Ala)
c.5703G>C
c.6161G>C (p.Gly2054Ala)
c.704+381G>C (n.704+381G>C)
c.3483G>C
c.5885G>C (p.Gly1962Ala)
c.5597G>C (p.Gly1866Ala)
c.3125G>C (p.Gly1042Ala)
19g.35732710G>TCA405425935KMT2Bn.467G>T
c.6095G>T (p.Gly2032Val)
c.3702G>T (n.3702G>T)
c.1379G>T (p.Gly460Val)
n.1314G>T
c.1382G>T (p.Gly461Val)
c.5703G>T
c.6161G>T (p.Gly2054Val)
c.704+381G>T (n.704+381G>T)
c.3483G>T
c.5885G>T (p.Gly1962Val)
c.5597G>T (p.Gly1866Val)
c.3125G>T (p.Gly1042Val)
19g.35732711A>CCA507308607KMT2Bn.468A>C
c.6096A>C (p.Gly2032=)
c.3703A>C (n.3703A>C)
c.1380A>C (p.Gly460=)
n.1315A>C
c.1383A>C (p.Gly461=)
c.5704A>C
c.6162A>C (p.Gly2054=)
c.704+382A>C (n.704+382A>C)
c.3484A>C
c.5886A>C (p.Gly1962=)
c.5598A>C (p.Gly1866=)
c.3126A>C (p.Gly1042=)
19g.35732711A>GCA507308615KMT2Bn.468A>G
c.6096A>G (p.Gly2032=)
c.3703A>G (n.3703A>G)
c.1380A>G (p.Gly460=)
n.1315A>G
c.1383A>G (p.Gly461=)
c.5704A>G
c.6162A>G (p.Gly2054=)
c.704+382A>G (n.704+382A>G)
c.3484A>G
c.5886A>G (p.Gly1962=)
c.5598A>G (p.Gly1866=)
c.3126A>G (p.Gly1042=)
19g.35732711A>TCA507308612KMT2Bn.468A>T
c.6096A>T (p.Gly2032=)
c.3703A>T (n.3703A>T)
c.1380A>T (p.Gly460=)
n.1315A>T
c.1383A>T (p.Gly461=)
c.5704A>T
c.6162A>T (p.Gly2054=)
c.704+382A>T (n.704+382A>T)
c.3484A>T
c.5886A>T (p.Gly1962=)
c.5598A>T (p.Gly1866=)
c.3126A>T (p.Gly1042=)
19g.35732712G>ACA405425940KMT2Bn.469G>A
c.6097G>A (p.Ala2033Thr)
c.3704G>A (n.3704G>A)
c.1381G>A (p.Ala461Thr)
n.1316G>A
c.1384G>A (p.Ala462Thr)
c.5705G>A
c.6163G>A (p.Ala2055Thr)
c.704+383G>A (n.704+383G>A)
c.3485G>A
c.5887G>A (p.Ala1963Thr)
c.5599G>A (p.Ala1867Thr)
c.3127G>A (p.Ala1043Thr)
gnomAD v4
19g.35732712G>CCA9385621KMT2Bn.469G>C
c.6097G>C (p.Ala2033Pro)
c.3704G>C (n.3704G>C)
c.1381G>C (p.Ala461Pro)
n.1316G>C
c.1384G>C (p.Ala462Pro)
c.5705G>C
c.6163G>C (p.Ala2055Pro)
c.704+383G>C (n.704+383G>C)
c.3485G>C
c.5887G>C (p.Ala1963Pro)
c.5599G>C (p.Ala1867Pro)
c.3127G>C (p.Ala1043Pro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732712G=CA2333794465KMT2Bn.469G=
c.6097G= (p.Ala2033=)
c.3704G= (n.3704G=)
c.1381G= (p.Ala461=)
n.1316G=
c.1384G= (p.Ala462=)
c.5705G=
c.6163G= (p.Ala2055=)
c.704+383G= (n.704+383G=)
c.3485G=
c.5887G= (p.Ala1963=)
c.5599G= (p.Ala1867=)
c.3127G= (p.Ala1043=)
19g.35732712G>TCA405425938KMT2Bn.469G>T
c.6097G>T (p.Ala2033Ser)
c.3704G>T (n.3704G>T)
c.1381G>T (p.Ala461Ser)
n.1316G>T
c.1384G>T (p.Ala462Ser)
c.5705G>T
c.6163G>T (p.Ala2055Ser)
c.704+383G>T (n.704+383G>T)
c.3485G>T
c.5887G>T (p.Ala1963Ser)
c.5599G>T (p.Ala1867Ser)
c.3127G>T (p.Ala1043Ser)
gnomAD v4
19g.35732713C>ACA405425943KMT2Bn.470C>A
c.6098C>A (p.Ala2033Asp)
c.3705C>A (n.3705C>A)
c.1382C>A (p.Ala461Asp)
n.1317C>A
c.1385C>A (p.Ala462Asp)
c.5706C>A
c.6164C>A (p.Ala2055Asp)
c.704+384C>A (n.704+384C>A)
c.3486C>A
c.5888C>A (p.Ala1963Asp)
c.5600C>A (p.Ala1867Asp)
c.3128C>A (p.Ala1043Asp)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.35732713C=CA2333794466KMT2Bn.470C=
c.6098C= (p.Ala2033=)
c.3705C= (n.3705C=)
c.1382C= (p.Ala461=)
n.1317C=
c.1385C= (p.Ala462=)
c.5706C=
c.6164C= (p.Ala2055=)
c.704+384C= (n.704+384C=)
c.3486C=
c.5888C= (p.Ala1963=)
c.5600C= (p.Ala1867=)
c.3128C= (p.Ala1043=)
19g.35732713C>GCA405425945KMT2Bn.470C>G
c.6098C>G (p.Ala2033Gly)
c.3705C>G (n.3705C>G)
c.1382C>G (p.Ala461Gly)
n.1317C>G
c.1385C>G (p.Ala462Gly)
c.5706C>G
c.6164C>G (p.Ala2055Gly)
c.704+384C>G (n.704+384C>G)
c.3486C>G
c.5888C>G (p.Ala1963Gly)
c.5600C>G (p.Ala1867Gly)
c.3128C>G (p.Ala1043Gly)
19g.35732713C>TCA405425948KMT2Bn.470C>T
c.6098C>T (p.Ala2033Val)
c.3705C>T (n.3705C>T)
c.1382C>T (p.Ala461Val)
n.1317C>T
c.1385C>T (p.Ala462Val)
c.5706C>T
c.6164C>T (p.Ala2055Val)
c.704+384C>T (n.704+384C>T)
c.3486C>T
c.5888C>T (p.Ala1963Val)
c.5600C>T (p.Ala1867Val)
c.3128C>T (p.Ala1043Val)
COSMIC
19g.35732718dupCA9385620KMT2Bn.475dup
c.6103dup (p.Arg2035ProfsTer3)
c.3710dup (n.3710dup)
c.1387dup (p.Arg463ProfsTer3)
n.1322dup
c.1390dup (p.Arg464ProfsTer3)
c.5711dup
c.6169dup (p.Arg2057ProfsTer3)
c.704+389dup (n.704+389dup)
c.3491dup
c.5893dup (p.Arg1965ProfsTer3)
c.5605dup (p.Arg1869ProfsTer3)
c.3133dup (p.Arg1045ProfsTer3)
dbSNP ExAC gnomAD v4
19g.35732717_35732718dupCA2814254938KMT2Bn.474_475dup
c.6102_6103dup (p.Arg2035ProfsTer?)
c.3709_3710dup (n.3709_3710dup)
c.1386_1387dup (p.Arg463ProfsTer?)
n.1321_1322dup
c.1389_1390dup (p.Arg464ProfsTer?)
c.5710_5711dup
c.6168_6169dup (p.Arg2057ProfsTer?)
c.704+388_704+389dup (n.704+388_704+389dup)
c.3490_3491dup
c.5892_5893dup (p.Arg1965ProfsTer?)
c.5604_5605dup (p.Arg1869ProfsTer?)
c.3132_3133dup (p.Arg1045ProfsTer?)
19g.35732714C>ACA507308645KMT2Bn.471C>A
c.6099C>A (p.Ala2033=)
c.3706C>A (n.3706C>A)
c.1383C>A (p.Ala461=)
n.1318C>A
c.1386C>A (p.Ala462=)
c.5707C>A
c.6165C>A (p.Ala2055=)
c.704+385C>A (n.704+385C>A)
c.3487C>A
c.5889C>A (p.Ala1963=)
c.5601C>A (p.Ala1867=)
c.3129C>A (p.Ala1043=)
dbSNP gnomAD v4
19g.35732714C=CA2333794467KMT2Bn.471C=
c.6099C= (p.Ala2033=)
c.3706C= (n.3706C=)
c.1383C= (p.Ala461=)
n.1318C=
c.1386C= (p.Ala462=)
c.5707C=
c.6165C= (p.Ala2055=)
c.704+385C= (n.704+385C=)
c.3487C=
c.5889C= (p.Ala1963=)
c.5601C= (p.Ala1867=)
c.3129C= (p.Ala1043=)
19g.35732714C>GCA9385622KMT2Bn.471C>G
c.6099C>G (p.Ala2033=)
c.3706C>G (n.3706C>G)
c.1383C>G (p.Ala461=)
n.1318C>G
c.1386C>G (p.Ala462=)
c.5707C>G
c.6165C>G (p.Ala2055=)
c.704+385C>G (n.704+385C>G)
c.3487C>G
c.5889C>G (p.Ala1963=)
c.5601C>G (p.Ala1867=)
c.3129C>G (p.Ala1043=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732714C>TCA507308642KMT2Bn.471C>T
c.6099C>T (p.Ala2033=)
c.3706C>T (n.3706C>T)
c.1383C>T (p.Ala461=)
n.1318C>T
c.1386C>T (p.Ala462=)
c.5707C>T
c.6165C>T (p.Ala2055=)
c.704+385C>T (n.704+385C>T)
c.3487C>T
c.5889C>T (p.Ala1963=)
c.5601C>T (p.Ala1867=)
c.3129C>T (p.Ala1043=)
19g.35732715C>ACA405425951KMT2Bn.472C>A
c.6100C>A (p.Pro2034Thr)
c.3707C>A (n.3707C>A)
c.1384C>A (p.Pro462Thr)
n.1319C>A
c.1387C>A (p.Pro463Thr)
c.5708C>A
c.6166C>A (p.Pro2056Thr)
c.704+386C>A (n.704+386C>A)
c.3488C>A
c.5890C>A (p.Pro1964Thr)
c.5602C>A (p.Pro1868Thr)
c.3130C>A (p.Pro1044Thr)
19g.35732715C=CA2333794468KMT2Bn.472C=
c.6100C= (p.Pro2034=)
c.3707C= (n.3707C=)
c.1384C= (p.Pro462=)
n.1319C=
c.1387C= (p.Pro463=)
c.5708C=
c.6166C= (p.Pro2056=)
c.704+386C= (n.704+386C=)
c.3488C=
c.5890C= (p.Pro1964=)
c.5602C= (p.Pro1868=)
c.3130C= (p.Pro1044=)
19g.35732715C>GCA405425952KMT2Bn.472C>G
c.6100C>G (p.Pro2034Ala)
c.3707C>G (n.3707C>G)
c.1384C>G (p.Pro462Ala)
n.1319C>G
c.1387C>G (p.Pro463Ala)
c.5708C>G
c.6166C>G (p.Pro2056Ala)
c.704+386C>G (n.704+386C>G)
c.3488C>G
c.5890C>G (p.Pro1964Ala)
c.5602C>G (p.Pro1868Ala)
c.3130C>G (p.Pro1044Ala)
19g.35732715C>TCA405425955KMT2Bn.472C>T
c.6100C>T (p.Pro2034Ser)
c.3707C>T (n.3707C>T)
c.1384C>T (p.Pro462Ser)
n.1319C>T
c.1387C>T (p.Pro463Ser)
c.5708C>T
c.6166C>T (p.Pro2056Ser)
c.704+386C>T (n.704+386C>T)
c.3488C>T
c.5890C>T (p.Pro1964Ser)
c.5602C>T (p.Pro1868Ser)
c.3130C>T (p.Pro1044Ser)
dbSNP gnomAD v2 gnomAD v4
19g.35732716C>ACA405425958KMT2Bn.473C>A
c.6101C>A (p.Pro2034His)
c.3708C>A (n.3708C>A)
c.1385C>A (p.Pro462His)
n.1320C>A
c.1388C>A (p.Pro463His)
c.5709C>A
c.6167C>A (p.Pro2056His)
c.704+387C>A (n.704+387C>A)
c.3489C>A
c.5891C>A (p.Pro1964His)
c.5603C>A (p.Pro1868His)
c.3131C>A (p.Pro1044His)
19g.35732716C=CA2333794469KMT2Bn.473C=
c.6101C= (p.Pro2034=)
c.3708C= (n.3708C=)
c.1385C= (p.Pro462=)
n.1320C=
c.1388C= (p.Pro463=)
c.5709C=
c.6167C= (p.Pro2056=)
c.704+387C= (n.704+387C=)
c.3489C=
c.5891C= (p.Pro1964=)
c.5603C= (p.Pro1868=)
c.3131C= (p.Pro1044=)
19g.35732716C>GCA405425960KMT2Bn.473C>G
c.6101C>G (p.Pro2034Arg)
c.3708C>G (n.3708C>G)
c.1385C>G (p.Pro462Arg)
n.1320C>G
c.1388C>G (p.Pro463Arg)
c.5709C>G
c.6167C>G (p.Pro2056Arg)
c.704+387C>G (n.704+387C>G)
c.3489C>G
c.5891C>G (p.Pro1964Arg)
c.5603C>G (p.Pro1868Arg)
c.3131C>G (p.Pro1044Arg)
19g.35732716C>TCA405425962KMT2Bn.473C>T
c.6101C>T (p.Pro2034Leu)
c.3708C>T (n.3708C>T)
c.1385C>T (p.Pro462Leu)
n.1320C>T
c.1388C>T (p.Pro463Leu)
c.5709C>T
c.6167C>T (p.Pro2056Leu)
c.704+387C>T (n.704+387C>T)
c.3489C>T
c.5891C>T (p.Pro1964Leu)
c.5603C>T (p.Pro1868Leu)
c.3131C>T (p.Pro1044Leu)
dbSNP gnomAD v2
19g.35732717C>ACA507308652KMT2Bn.474C>A
c.6102C>A (p.Pro2034=)
c.3709C>A (n.3709C>A)
c.1386C>A (p.Pro462=)
n.1321C>A
c.1389C>A (p.Pro463=)
c.5710C>A
c.6168C>A (p.Pro2056=)
c.704+388C>A (n.704+388C>A)
c.3490C>A
c.5892C>A (p.Pro1964=)
c.5604C>A (p.Pro1868=)
c.3132C>A (p.Pro1044=)
19g.35732717C=CA2333794470KMT2Bn.474C=
c.6102C= (p.Pro2034=)
c.3709C= (n.3709C=)
c.1386C= (p.Pro462=)
n.1321C=
c.1389C= (p.Pro463=)
c.5710C=
c.6168C= (p.Pro2056=)
c.704+388C= (n.704+388C=)
c.3490C=
c.5892C= (p.Pro1964=)
c.5604C= (p.Pro1868=)
c.3132C= (p.Pro1044=)
19g.35732717C>GCA507308655KMT2Bn.474C>G
c.6102C>G (p.Pro2034=)
c.3709C>G (n.3709C>G)
c.1386C>G (p.Pro462=)
n.1321C>G
c.1389C>G (p.Pro463=)
c.5710C>G
c.6168C>G (p.Pro2056=)
c.704+388C>G (n.704+388C>G)
c.3490C>G
c.5892C>G (p.Pro1964=)
c.5604C>G (p.Pro1868=)
c.3132C>G (p.Pro1044=)
19g.35732717C>TCA507308653KMT2Bn.474C>T
c.6102C>T (p.Pro2034=)
c.3709C>T (n.3709C>T)
c.1386C>T (p.Pro462=)
n.1321C>T
c.1389C>T (p.Pro463=)
c.5710C>T
c.6168C>T (p.Pro2056=)
c.704+388C>T (n.704+388C>T)
c.3490C>T
c.5892C>T (p.Pro1964=)
c.5604C>T (p.Pro1868=)
c.3132C>T (p.Pro1044=)
dbSNP
19g.35732718C>ACA9385623KMT2Bn.475C>A
c.6103C>A (p.Arg2035Ser)
c.3710C>A (n.3710C>A)
c.1387C>A (p.Arg463Ser)
n.1322C>A
c.1390C>A (p.Arg464Ser)
c.5711C>A
c.6169C>A (p.Arg2057Ser)
c.704+389C>A (n.704+389C>A)
c.3491C>A
c.5893C>A (p.Arg1965Ser)
c.5605C>A (p.Arg1869Ser)
c.3133C>A (p.Arg1045Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732718C=CA2333794471KMT2Bn.475C=
c.6103C= (p.Arg2035=)
c.3710C= (n.3710C=)
c.1387C= (p.Arg463=)
n.1322C=
c.1390C= (p.Arg464=)
c.5711C=
c.6169C= (p.Arg2057=)
c.704+389C= (n.704+389C=)
c.3491C=
c.5893C= (p.Arg1965=)
c.5605C= (p.Arg1869=)
c.3133C= (p.Arg1045=)
19g.35732718C>GCA405425966KMT2Bn.475C>G
c.6103C>G (p.Arg2035Gly)
c.3710C>G (n.3710C>G)
c.1387C>G (p.Arg463Gly)
n.1322C>G
c.1390C>G (p.Arg464Gly)
c.5711C>G
c.6169C>G (p.Arg2057Gly)
c.704+389C>G (n.704+389C>G)
c.3491C>G
c.5893C>G (p.Arg1965Gly)
c.5605C>G (p.Arg1869Gly)
c.3133C>G (p.Arg1045Gly)
dbSNP
19g.35732718C>TCA9385624KMT2Bn.475C>T
c.6103C>T (p.Arg2035Cys)
c.3710C>T (n.3710C>T)
c.1387C>T (p.Arg463Cys)
n.1322C>T
c.1390C>T (p.Arg464Cys)
c.5711C>T
c.6169C>T (p.Arg2057Cys)
c.704+389C>T (n.704+389C>T)
c.3491C>T
c.5893C>T (p.Arg1965Cys)
c.5605C>T (p.Arg1869Cys)
c.3133C>T (p.Arg1045Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732719G>ACA405425971KMT2Bn.476G>A
c.6104G>A (p.Arg2035His)
c.3711G>A (n.3711G>A)
c.1388G>A (p.Arg463His)
n.1323G>A
c.1391G>A (p.Arg464His)
c.5712G>A
c.6170G>A (p.Arg2057His)
c.704+390G>A (n.704+390G>A)
c.3492G>A
c.5894G>A (p.Arg1965His)
c.5606G>A (p.Arg1869His)
c.3134G>A (p.Arg1045His)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.35732719G>CCA307796379KMT2Bn.476G>C
c.6104G>C (p.Arg2035Pro)
c.3711G>C (n.3711G>C)
c.1388G>C (p.Arg463Pro)
n.1323G>C
c.1391G>C (p.Arg464Pro)
c.5712G>C
c.6170G>C (p.Arg2057Pro)
c.704+390G>C (n.704+390G>C)
c.3492G>C
c.5894G>C (p.Arg1965Pro)
c.5606G>C (p.Arg1869Pro)
c.3134G>C (p.Arg1045Pro)
dbSNP
19g.35732719G=CA2333794472KMT2Bn.476G=
c.6104G= (p.Arg2035=)
c.3711G= (n.3711G=)
c.1388G= (p.Arg463=)
n.1323G=
c.1391G= (p.Arg464=)
c.5712G=
c.6170G= (p.Arg2057=)
c.704+390G= (n.704+390G=)
c.3492G=
c.5894G= (p.Arg1965=)
c.5606G= (p.Arg1869=)
c.3134G= (p.Arg1045=)
19g.35732719G>TCA9385625KMT2Bn.476G>T
c.6104G>T (p.Arg2035Leu)
c.3711G>T (n.3711G>T)
c.1388G>T (p.Arg463Leu)
n.1323G>T
c.1391G>T (p.Arg464Leu)
c.5712G>T
c.6170G>T (p.Arg2057Leu)
c.704+390G>T (n.704+390G>T)
c.3492G>T
c.5894G>T (p.Arg1965Leu)
c.5606G>T (p.Arg1869Leu)
c.3134G>T (p.Arg1045Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.35732720C>ACA507308661KMT2Bn.477C>A
c.6105C>A (p.Arg2035=)
c.3712C>A (n.3712C>A)
c.1389C>A (p.Arg463=)
n.1324C>A
c.1392C>A (p.Arg464=)
c.5713C>A
c.6171C>A (p.Arg2057=)
c.704+391C>A (n.704+391C>A)
c.3493C>A
c.5895C>A (p.Arg1965=)
c.5607C>A (p.Arg1869=)
c.3135C>A (p.Arg1045=)
19g.35732720C=CA2333794473KMT2Bn.477C=
c.6105C= (p.Arg2035=)
c.3712C= (n.3712C=)
c.1389C= (p.Arg463=)
n.1324C=
c.1392C= (p.Arg464=)
c.5713C=
c.6171C= (p.Arg2057=)
c.704+391C= (n.704+391C=)
c.3493C=
c.5895C= (p.Arg1965=)
c.5607C= (p.Arg1869=)
c.3135C= (p.Arg1045=)
19g.35732720C>GCA507308663KMT2Bn.477C>G
c.6105C>G (p.Arg2035=)
c.3712C>G (n.3712C>G)
c.1389C>G (p.Arg463=)
n.1324C>G
c.1392C>G (p.Arg464=)
c.5713C>G
c.6171C>G (p.Arg2057=)
c.704+391C>G (n.704+391C>G)
c.3493C>G
c.5895C>G (p.Arg1965=)
c.5607C>G (p.Arg1869=)
c.3135C>G (p.Arg1045=)
19g.35732720C>TCA507308664KMT2Bn.477C>T
c.6105C>T (p.Arg2035=)
c.3712C>T (n.3712C>T)
c.1389C>T (p.Arg463=)
n.1324C>T
c.1392C>T (p.Arg464=)
c.5713C>T
c.6171C>T (p.Arg2057=)
c.704+391C>T (n.704+391C>T)
c.3493C>T
c.5895C>T (p.Arg1965=)
c.5607C>T (p.Arg1869=)
c.3135C>T (p.Arg1045=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.35732721A=CA2333794474KMT2Bn.478A=
c.6106A= (p.Ile2036=)
c.3713A= (n.3713A=)
c.1390A= (p.Ile464=)
n.1325A=
c.1393A= (p.Ile465=)
c.5714A=
c.6172A= (p.Ile2058=)
c.704+392A= (n.704+392A=)
c.3494A=
c.5896A= (p.Ile1966=)
c.5608A= (p.Ile1870=)
c.3136A= (p.Ile1046=)
19g.35732721A>CCA405425972KMT2Bn.478A>C
c.6106A>C (p.Ile2036Leu)
c.3713A>C (n.3713A>C)
c.1390A>C (p.Ile464Leu)
n.1325A>C
c.1393A>C (p.Ile465Leu)
c.5714A>C
c.6172A>C (p.Ile2058Leu)
c.704+392A>C (n.704+392A>C)
c.3494A>C
c.5896A>C (p.Ile1966Leu)
c.5608A>C (p.Ile1870Leu)
c.3136A>C (p.Ile1046Leu)
19g.35732721A>GCA9385626KMT2Bn.478A>G
c.6106A>G (p.Ile2036Val)
c.3713A>G (n.3713A>G)
c.1390A>G (p.Ile464Val)
n.1325A>G
c.1393A>G (p.Ile465Val)
c.5714A>G
c.6172A>G (p.Ile2058Val)
c.704+392A>G (n.704+392A>G)
c.3494A>G
c.5896A>G (p.Ile1966Val)
c.5608A>G (p.Ile1870Val)
c.3136A>G (p.Ile1046Val)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.35732721A>TCA405425973KMT2Bn.478A>T
c.6106A>T (p.Ile2036Phe)
c.3713A>T (n.3713A>T)
c.1390A>T (p.Ile464Phe)
n.1325A>T
c.1393A>T (p.Ile465Phe)
c.5714A>T
c.6172A>T (p.Ile2058Phe)
c.704+392A>T (n.704+392A>T)
c.3494A>T
c.5896A>T (p.Ile1966Phe)
c.5608A>T (p.Ile1870Phe)
c.3136A>T (p.Ile1046Phe)
19g.35732722T>ACA405425974KMT2Bn.479T>A
c.6107T>A (p.Ile2036Asn)
c.3714T>A (n.3714T>A)
c.1391T>A (p.Ile464Asn)
n.1326T>A
c.1394T>A (p.Ile465Asn)
c.5715T>A
c.6173T>A (p.Ile2058Asn)
c.704+393T>A (n.704+393T>A)
c.3495T>A
c.5897T>A (p.Ile1966Asn)
c.5609T>A (p.Ile1870Asn)
c.3137T>A (p.Ile1046Asn)
19g.35732722T>CCA405425975KMT2Bn.479T>C
c.6107T>C (p.Ile2036Thr)
c.3714T>C (n.3714T>C)
c.1391T>C (p.Ile464Thr)
n.1326T>C
c.1394T>C (p.Ile465Thr)
c.5715T>C
c.6173T>C (p.Ile2058Thr)
c.704+393T>C (n.704+393T>C)
c.3495T>C
c.5897T>C (p.Ile1966Thr)
c.5609T>C (p.Ile1870Thr)
c.3137T>C (p.Ile1046Thr)
dbSNP gnomAD v3 gnomAD v4
19g.35732722T>GCA405425976KMT2Bn.479T>G
c.6107T>G (p.Ile2036Ser)
c.3714T>G (n.3714T>G)
c.1391T>G (p.Ile464Ser)
n.1326T>G
c.1394T>G (p.Ile465Ser)
c.5715T>G
c.6173T>G (p.Ile2058Ser)
c.704+393T>G (n.704+393T>G)
c.3495T>G
c.5897T>G (p.Ile1966Ser)
c.5609T>G (p.Ile1870Ser)
c.3137T>G (p.Ile1046Ser)
19g.35732722T=CA2333794475KMT2Bn.479T=
c.6107T= (p.Ile2036=)
c.3714T= (n.3714T=)
c.1391T= (p.Ile464=)
n.1326T=
c.1394T= (p.Ile465=)
c.5715T=
c.6173T= (p.Ile2058=)
c.704+393T= (n.704+393T=)
c.3495T=
c.5897T= (p.Ile1966=)
c.5609T= (p.Ile1870=)
c.3137T= (p.Ile1046=)
19g.35732723T>ACA507308672KMT2Bn.480T>A
c.6108T>A (p.Ile2036=)
c.3715T>A (n.3715T>A)
c.1392T>A (p.Ile464=)
n.1327T>A
c.1395T>A (p.Ile465=)
c.5716T>A
c.6174T>A (p.Ile2058=)
c.704+394T>A (n.704+394T>A)
c.3496T>A
c.5898T>A (p.Ile1966=)
c.5610T>A (p.Ile1870=)
c.3138T>A (p.Ile1046=)
gnomAD v4
19g.35732723T>CCA307796395KMT2Bn.480T>C
c.6108T>C (p.Ile2036=)
c.3715T>C (n.3715T>C)
c.1392T>C (p.Ile464=)
n.1327T>C
c.1395T>C (p.Ile465=)
c.5716T>C
c.6174T>C (p.Ile2058=)
c.704+394T>C (n.704+394T>C)
c.3496T>C
c.5898T>C (p.Ile1966=)
c.5610T>C (p.Ile1870=)
c.3138T>C (p.Ile1046=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.35732723T>GCA405425977KMT2Bn.480T>G
c.6108T>G (p.Ile2036Met)
c.3715T>G (n.3715T>G)
c.1392T>G (p.Ile464Met)
n.1327T>G
c.1395T>G (p.Ile465Met)
c.5716T>G
c.6174T>G (p.Ile2058Met)
c.704+394T>G (n.704+394T>G)
c.3496T>G
c.5898T>G (p.Ile1966Met)
c.5610T>G (p.Ile1870Met)
c.3138T>G (p.Ile1046Met)
19g.35732723T=CA2333794476KMT2Bn.480T=
c.6108T= (p.Ile2036=)
c.3715T= (n.3715T=)
c.1392T= (p.Ile464=)
n.1327T=
c.1395T= (p.Ile465=)
c.5716T=
c.6174T= (p.Ile2058=)
c.704+394T= (n.704+394T=)
c.3496T=
c.5898T= (p.Ile1966=)
c.5610T= (p.Ile1870=)
c.3138T= (p.Ile1046=)
19g.35732724G>ACA405425978KMT2Bn.481G>A
c.6109G>A (p.Glu2037Lys)
c.3716G>A (n.3716G>A)
c.1393G>A (p.Glu465Lys)
n.1328G>A
c.1396G>A (p.Glu466Lys)
c.5717G>A
c.6175G>A (p.Glu2059Lys)
c.704+395G>A (n.704+395G>A)
c.3497G>A
c.5899G>A (p.Glu1967Lys)
c.5611G>A (p.Glu1871Lys)
c.3139G>A (p.Glu1047Lys)
gnomAD v4
19g.35732724G>CCA405425979KMT2Bn.481G>C
c.6109G>C (p.Glu2037Gln)
c.3716G>C (n.3716G>C)
c.1393G>C (p.Glu465Gln)
n.1328G>C
c.1396G>C (p.Glu466Gln)
c.5717G>C
c.6175G>C (p.Glu2059Gln)
c.704+395G>C (n.704+395G>C)
c.3497G>C
c.5899G>C (p.Glu1967Gln)
c.5611G>C (p.Glu1871Gln)
c.3139G>C (p.Glu1047Gln)
19g.35732724G>TCA405425980KMT2Bn.481G>T
c.6109G>T (p.Glu2037Ter)
c.3716G>T (n.3716G>T)
c.1393G>T (p.Glu465Ter)
n.1328G>T
c.1396G>T (p.Glu466Ter)
c.5717G>T
c.6175G>T (p.Glu2059Ter)
c.704+395G>T (n.704+395G>T)
c.3497G>T
c.5899G>T (p.Glu1967Ter)
c.5611G>T (p.Glu1871Ter)
c.3139G>T (p.Glu1047Ter)
19g.35732725A>CCA405425981KMT2Bn.482A>C
c.6110A>C (p.Glu2037Ala)
c.3717A>C (n.3717A>C)
c.1394A>C (p.Glu465Ala)
n.1329A>C
c.1397A>C (p.Glu466Ala)
c.5718A>C
c.6176A>C (p.Glu2059Ala)
c.704+396A>C (n.704+396A>C)
c.3498A>C
c.5900A>C (p.Glu1967Ala)
c.5612A>C (p.Glu1871Ala)
c.3140A>C (p.Glu1047Ala)
19g.35732725A>GCA405425982KMT2Bn.482A>G
c.6110A>G (p.Glu2037Gly)
c.3717A>G (n.3717A>G)
c.1394A>G (p.Glu465Gly)
n.1329A>G
c.1397A>G (p.Glu466Gly)
c.5718A>G
c.6176A>G (p.Glu2059Gly)
c.704+396A>G (n.704+396A>G)
c.3498A>G
c.5900A>G (p.Glu1967Gly)
c.5612A>G (p.Glu1871Gly)
c.3140A>G (p.Glu1047Gly)
19g.35732725A>TCA405425983KMT2Bn.482A>T
c.6110A>T (p.Glu2037Val)
c.3717A>T (n.3717A>T)
c.1394A>T (p.Glu465Val)
n.1329A>T
c.1397A>T (p.Glu466Val)
c.5718A>T
c.6176A>T (p.Glu2059Val)
c.704+396A>T (n.704+396A>T)
c.3498A>T
c.5900A>T (p.Glu1967Val)
c.5612A>T (p.Glu1871Val)
c.3140A>T (p.Glu1047Val)
19g.35732726A>CCA405425984KMT2Bn.483A>C
c.6111A>C (p.Glu2037Asp)
c.3718A>C (n.3718A>C)
c.1395A>C (p.Glu465Asp)
n.1330A>C
c.1398A>C (p.Glu466Asp)
c.5719A>C
c.6177A>C (p.Glu2059Asp)
c.704+397A>C (n.704+397A>C)
c.3499A>C
c.5901A>C (p.Glu1967Asp)
c.5613A>C (p.Glu1871Asp)
c.3141A>C (p.Glu1047Asp)
19g.35732726A>GCA507308683KMT2Bn.483A>G
c.6111A>G (p.Glu2037=)
c.3718A>G (n.3718A>G)
c.1395A>G (p.Glu465=)
n.1330A>G
c.1398A>G (p.Glu466=)
c.5719A>G
c.6177A>G (p.Glu2059=)
c.704+397A>G (n.704+397A>G)
c.3499A>G
c.5901A>G (p.Glu1967=)
c.5613A>G (p.Glu1871=)
c.3141A>G (p.Glu1047=)
19g.35732726A>TCA405425985KMT2Bn.483A>T
c.6111A>T (p.Glu2037Asp)
c.3718A>T (n.3718A>T)
c.1395A>T (p.Glu465Asp)
n.1330A>T
c.1398A>T (p.Glu466Asp)
c.5719A>T
c.6177A>T (p.Glu2059Asp)
c.704+397A>T (n.704+397A>T)
c.3499A>T
c.5901A>T (p.Glu1967Asp)
c.5613A>T (p.Glu1871Asp)
c.3141A>T (p.Glu1047Asp)
19g.35732727C>ACA405425986KMT2Bn.484C>A
c.6112C>A (p.Gln2038Lys)
c.3719C>A (n.3719C>A)
c.1396C>A (p.Gln466Lys)
n.1331C>A
c.1399C>A (p.Gln467Lys)
c.5720C>A
c.6178C>A (p.Gln2060Lys)
c.704+398C>A (n.704+398C>A)
c.3500C>A
c.5902C>A (p.Gln1968Lys)
c.5614C>A (p.Gln1872Lys)
c.3142C>A (p.Gln1048Lys)
19g.35732727C=CA2333794477KMT2Bn.484C=
c.6112C= (p.Gln2038=)
c.3719C= (n.3719C=)
c.1396C= (p.Gln466=)
n.1331C=
c.1399C= (p.Gln467=)
c.5720C=
c.6178C= (p.Gln2060=)
c.704+398C= (n.704+398C=)
c.3500C=
c.5902C= (p.Gln1968=)
c.5614C= (p.Gln1872=)
c.3142C= (p.Gln1048=)
19g.35732727C>GCA405425987KMT2Bn.484C>G
c.6112C>G (p.Gln2038Glu)
c.3719C>G (n.3719C>G)
c.1396C>G (p.Gln466Glu)
n.1331C>G
c.1399C>G (p.Gln467Glu)
c.5720C>G
c.6178C>G (p.Gln2060Glu)
c.704+398C>G (n.704+398C>G)
c.3500C>G
c.5902C>G (p.Gln1968Glu)
c.5614C>G (p.Gln1872Glu)
c.3142C>G (p.Gln1048Glu)
dbSNP gnomAD v2 gnomAD v4
19g.35732727C>TCA405425988KMT2Bn.484C>T
c.6112C>T (p.Gln2038Ter)
c.3719C>T (n.3719C>T)
c.1396C>T (p.Gln466Ter)
n.1331C>T
c.1399C>T (p.Gln467Ter)
c.5720C>T
c.6178C>T (p.Gln2060Ter)
c.704+398C>T (n.704+398C>T)
c.3500C>T
c.5902C>T (p.Gln1968Ter)
c.5614C>T (p.Gln1872Ter)
c.3142C>T (p.Gln1048Ter)
dbSNP gnomAD v2
19g.35732728A>CCA405425989KMT2Bn.485A>C
c.6113A>C (p.Gln2038Pro)
c.3720A>C (n.3720A>C)
c.1397A>C (p.Gln466Pro)
n.1332A>C
c.1400A>C (p.Gln467Pro)
c.5721A>C
c.6179A>C (p.Gln2060Pro)
c.704+399A>C (n.704+399A>C)
c.3501A>C
c.5903A>C (p.Gln1968Pro)
c.5615A>C (p.Gln1872Pro)
c.3143A>C (p.Gln1048Pro)
19g.35732728A>GCA405425990KMT2Bn.485A>G
c.6113A>G (p.Gln2038Arg)
c.3720A>G (n.3720A>G)
c.1397A>G (p.Gln466Arg)
n.1332A>G
c.1400A>G (p.Gln467Arg)
c.5721A>G
c.6179A>G (p.Gln2060Arg)
c.704+399A>G (n.704+399A>G)
c.3501A>G
c.5903A>G (p.Gln1968Arg)
c.5615A>G (p.Gln1872Arg)
c.3143A>G (p.Gln1048Arg)
gnomAD v4
19g.35732728A>TCA405425991KMT2Bn.485A>T
c.6113A>T (p.Gln2038Leu)
c.3720A>T (n.3720A>T)
c.1397A>T (p.Gln466Leu)
n.1332A>T
c.1400A>T (p.Gln467Leu)
c.5721A>T
c.6179A>T (p.Gln2060Leu)
c.704+399A>T (n.704+399A>T)
c.3501A>T
c.5903A>T (p.Gln1968Leu)
c.5615A>T (p.Gln1872Leu)
c.3143A>T (p.Gln1048Leu)
19g.35732729G>ACA507308689KMT2Bn.486G>A
c.6114G>A (p.Gln2038=)
c.3721G>A (n.3721G>A)
c.1398G>A (p.Gln466=)
n.1333G>A
c.1401G>A (p.Gln467=)
c.5722G>A
c.6180G>A (p.Gln2060=)
c.704+400G>A (n.704+400G>A)
c.3502G>A
c.5904G>A (p.Gln1968=)
c.5616G>A (p.Gln1872=)
c.3144G>A (p.Gln1048=)
19g.35732729G>CCA405425993KMT2Bn.486G>C
c.6114G>C (p.Gln2038His)
c.3721G>C (n.3721G>C)
c.1398G>C (p.Gln466His)
n.1333G>C
c.1401G>C (p.Gln467His)
c.5722G>C
c.6180G>C (p.Gln2060His)
c.704+400G>C (n.704+400G>C)
c.3502G>C
c.5904G>C (p.Gln1968His)
c.5616G>C (p.Gln1872His)
c.3144G>C (p.Gln1048His)
19g.35732729G>TCA405425992KMT2Bn.486G>T
c.6114G>T (p.Gln2038His)
c.3721G>T (n.3721G>T)
c.1398G>T (p.Gln466His)
n.1333G>T
c.1401G>T (p.Gln467His)
c.5722G>T
c.6180G>T (p.Gln2060His)
c.704+400G>T (n.704+400G>T)
c.3502G>T
c.5904G>T (p.Gln1968His)
c.5616G>T (p.Gln1872His)
c.3144G>T (p.Gln1048His)
19g.35732730C>ACA405425994KMT2Bn.487C>A
c.6115C>A (p.Leu2039Met)
c.3722C>A (n.3722C>A)
c.1399C>A (p.Leu467Met)
n.1334C>A
c.1402C>A (p.Leu468Met)
c.5723C>A
c.6181C>A (p.Leu2061Met)
c.704+401C>A (n.704+401C>A)
c.3503C>A
c.5905C>A (p.Leu1969Met)
c.5617C>A (p.Leu1873Met)
c.3145C>A (p.Leu1049Met)
gnomAD v4
19g.35732730C=CA2333794478KMT2Bn.487C=
c.6115C= (p.Leu2039=)
c.3722C= (n.3722C=)
c.1399C= (p.Leu467=)
n.1334C=
c.1402C= (p.Leu468=)
c.5723C=
c.6181C= (p.Leu2061=)
c.704+401C= (n.704+401C=)
c.3503C=
c.5905C= (p.Leu1969=)
c.5617C= (p.Leu1873=)
c.3145C= (p.Leu1049=)
19g.35732730C>GCA9385627KMT2Bn.487C>G
c.6115C>G (p.Leu2039Val)
c.3722C>G (n.3722C>G)
c.1399C>G (p.Leu467Val)
n.1334C>G
c.1402C>G (p.Leu468Val)
c.5723C>G
c.6181C>G (p.Leu2061Val)
c.704+401C>G (n.704+401C>G)
c.3503C>G
c.5905C>G (p.Leu1969Val)
c.5617C>G (p.Leu1873Val)
c.3145C>G (p.Leu1049Val)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732730C>TCA507308694KMT2Bn.487C>T
c.6115C>T (p.Leu2039=)
c.3722C>T (n.3722C>T)
c.1399C>T (p.Leu467=)
n.1334C>T
c.1402C>T (p.Leu468=)
c.5723C>T
c.6181C>T (p.Leu2061=)
c.704+401C>T (n.704+401C>T)
c.3503C>T
c.5905C>T (p.Leu1969=)
c.5617C>T (p.Leu1873=)
c.3145C>T (p.Leu1049=)
19g.35732731T>ACA405425995KMT2Bn.488T>A
c.6116T>A (p.Leu2039Gln)
c.3723T>A (n.3723T>A)
c.1400T>A (p.Leu467Gln)
n.1335T>A
c.1403T>A (p.Leu468Gln)
c.5724T>A
c.6182T>A (p.Leu2061Gln)
c.704+402T>A (n.704+402T>A)
c.3504T>A
c.5906T>A (p.Leu1969Gln)
c.5618T>A (p.Leu1873Gln)
c.3146T>A (p.Leu1049Gln)
19g.35732731T>CCA405425996KMT2Bn.488T>C
c.6116T>C (p.Leu2039Pro)
c.3723T>C (n.3723T>C)
c.1400T>C (p.Leu467Pro)
n.1335T>C
c.1403T>C (p.Leu468Pro)
c.5724T>C
c.6182T>C (p.Leu2061Pro)
c.704+402T>C (n.704+402T>C)
c.3504T>C
c.5906T>C (p.Leu1969Pro)
c.5618T>C (p.Leu1873Pro)
c.3146T>C (p.Leu1049Pro)
19g.35732731T>GCA405425997KMT2Bn.488T>G
c.6116T>G (p.Leu2039Arg)
c.3723T>G (n.3723T>G)
c.1400T>G (p.Leu467Arg)
n.1335T>G
c.1403T>G (p.Leu468Arg)
c.5724T>G
c.6182T>G (p.Leu2061Arg)
c.704+402T>G (n.704+402T>G)
c.3504T>G
c.5906T>G (p.Leu1969Arg)
c.5618T>G (p.Leu1873Arg)
c.3146T>G (p.Leu1049Arg)
19g.35732732G>ACA307796397KMT2Bn.489G>A
c.6117G>A (p.Leu2039=)
c.3724G>A (n.3724G>A)
c.1401G>A (p.Leu467=)
n.1336G>A
c.1404G>A (p.Leu468=)
c.5725G>A
c.6183G>A (p.Leu2061=)
c.704+403G>A (n.704+403G>A)
c.3505G>A
c.5907G>A (p.Leu1969=)
c.5619G>A (p.Leu1873=)
c.3147G>A (p.Leu1049=)
dbSNP gnomAD v2 gnomAD v4
19g.35732732G>CCA507308695KMT2Bn.489G>C
c.6117G>C (p.Leu2039=)
c.3724G>C (n.3724G>C)
c.1401G>C (p.Leu467=)
n.1336G>C
c.1404G>C (p.Leu468=)
c.5725G>C
c.6183G>C (p.Leu2061=)
c.704+403G>C (n.704+403G>C)
c.3505G>C
c.5907G>C (p.Leu1969=)
c.5619G>C (p.Leu1873=)
c.3147G>C (p.Leu1049=)
19g.35732732G=CA2333794479KMT2Bn.489G=
c.6117G= (p.Leu2039=)
c.3724G= (n.3724G=)
c.1401G= (p.Leu467=)
n.1336G=
c.1404G= (p.Leu468=)
c.5725G=
c.6183G= (p.Leu2061=)
c.704+403G= (n.704+403G=)
c.3505G=
c.5907G= (p.Leu1969=)
c.5619G= (p.Leu1873=)
c.3147G= (p.Leu1049=)
19g.35732732G>TCA507308697KMT2Bn.489G>T
c.6117G>T (p.Leu2039=)
c.3724G>T (n.3724G>T)
c.1401G>T (p.Leu467=)
n.1336G>T
c.1404G>T (p.Leu468=)
c.5725G>T
c.6183G>T (p.Leu2061=)
c.704+403G>T (n.704+403G>T)
c.3505G>T
c.5907G>T (p.Leu1969=)
c.5619G>T (p.Leu1873=)
c.3147G>T (p.Leu1049=)
19g.35732733G>ACA405425998KMT2Bn.490G>A
c.6118G>A (p.Asp2040Asn)
c.3725G>A (n.3725G>A)
c.1402G>A (p.Asp468Asn)
n.1337G>A
c.1405G>A (p.Asp469Asn)
c.5726G>A
c.6184G>A (p.Asp2062Asn)
c.704+404G>A (n.704+404G>A)
c.3506G>A
c.5908G>A (p.Asp1970Asn)
c.5620G>A (p.Asp1874Asn)
c.3148G>A (p.Asp1050Asn)
19g.35732733G>CCA405426000KMT2Bn.490G>C
c.6118G>C (p.Asp2040His)
c.3725G>C (n.3725G>C)
c.1402G>C (p.Asp468His)
n.1337G>C
c.1405G>C (p.Asp469His)
c.5726G>C
c.6184G>C (p.Asp2062His)
c.704+404G>C (n.704+404G>C)
c.3506G>C
c.5908G>C (p.Asp1970His)
c.5620G>C (p.Asp1874His)
c.3148G>C (p.Asp1050His)
19g.35732733G>TCA405425999KMT2Bn.490G>T
c.6118G>T (p.Asp2040Tyr)
c.3725G>T (n.3725G>T)
c.1402G>T (p.Asp468Tyr)
n.1337G>T
c.1405G>T (p.Asp469Tyr)
c.5726G>T
c.6184G>T (p.Asp2062Tyr)
c.704+404G>T (n.704+404G>T)
c.3506G>T
c.5908G>T (p.Asp1970Tyr)
c.5620G>T (p.Asp1874Tyr)
c.3148G>T (p.Asp1050Tyr)
gnomAD v4
19g.35732734A>CCA405426001KMT2Bn.491A>C
c.6119A>C (p.Asp2040Ala)
c.3726A>C (n.3726A>C)
c.1403A>C (p.Asp468Ala)
n.1338A>C
c.1406A>C (p.Asp469Ala)
c.5727A>C
c.6185A>C (p.Asp2062Ala)
c.704+405A>C (n.704+405A>C)
c.3507A>C
c.5909A>C (p.Asp1970Ala)
c.5621A>C (p.Asp1874Ala)
c.3149A>C (p.Asp1050Ala)
19g.35732734A>GCA405426002KMT2Bn.491A>G
c.6119A>G (p.Asp2040Gly)
c.3726A>G (n.3726A>G)
c.1403A>G (p.Asp468Gly)
n.1338A>G
c.1406A>G (p.Asp469Gly)
c.5727A>G
c.6185A>G (p.Asp2062Gly)
c.704+405A>G (n.704+405A>G)
c.3507A>G
c.5909A>G (p.Asp1970Gly)
c.5621A>G (p.Asp1874Gly)
c.3149A>G (p.Asp1050Gly)
19g.35732734A>TCA405426003KMT2Bn.491A>T
c.6119A>T (p.Asp2040Val)
c.3726A>T (n.3726A>T)
c.1403A>T (p.Asp468Val)
n.1338A>T
c.1406A>T (p.Asp469Val)
c.5727A>T
c.6185A>T (p.Asp2062Val)
c.704+405A>T (n.704+405A>T)
c.3507A>T
c.5909A>T (p.Asp1970Val)
c.5621A>T (p.Asp1874Val)
c.3149A>T (p.Asp1050Val)
19g.35732735C>ACA405426004KMT2Bn.492C>A
c.6120C>A (p.Asp2040Glu)
c.3727C>A (n.3727C>A)
c.1404C>A (p.Asp468Glu)
n.1339C>A
c.1407C>A (p.Asp469Glu)
c.5728C>A
c.6186C>A (p.Asp2062Glu)
c.704+406C>A (n.704+406C>A)
c.3508C>A
c.5910C>A (p.Asp1970Glu)
c.5622C>A (p.Asp1874Glu)
c.3150C>A (p.Asp1050Glu)
19g.35732735C=CA2333794480KMT2Bn.492C=
c.6120C= (p.Asp2040=)
c.3727C= (n.3727C=)
c.1404C= (p.Asp468=)
n.1339C=
c.1407C= (p.Asp469=)
c.5728C=
c.6186C= (p.Asp2062=)
c.704+406C= (n.704+406C=)
c.3508C=
c.5910C= (p.Asp1970=)
c.5622C= (p.Asp1874=)
c.3150C= (p.Asp1050=)
19g.35732735C>GCA405426005KMT2Bn.492C>G
c.6120C>G (p.Asp2040Glu)
c.3727C>G (n.3727C>G)
c.1404C>G (p.Asp468Glu)
n.1339C>G
c.1407C>G (p.Asp469Glu)
c.5728C>G
c.6186C>G (p.Asp2062Glu)
c.704+406C>G (n.704+406C>G)
c.3508C>G
c.5910C>G (p.Asp1970Glu)
c.5622C>G (p.Asp1874Glu)
c.3150C>G (p.Asp1050Glu)
19g.35732735C>TCA9385628KMT2Bn.492C>T
c.6120C>T (p.Asp2040=)
c.3727C>T (n.3727C>T)
c.1404C>T (p.Asp468=)
n.1339C>T
c.1407C>T (p.Asp469=)
c.5728C>T
c.6186C>T (p.Asp2062=)
c.704+406C>T (n.704+406C>T)
c.3508C>T
c.5910C>T (p.Asp1970=)
c.5622C>T (p.Asp1874=)
c.3150C>T (p.Asp1050=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.35732736G>ACA405426006KMT2Bn.493G>A
c.6121G>A (p.Gly2041Ser)
c.3728G>A (n.3728G>A)
c.1405G>A (p.Gly469Ser)
n.1340G>A
c.1408G>A (p.Gly470Ser)
c.5729G>A
c.6187G>A (p.Gly2063Ser)
c.704+407G>A (n.704+407G>A)
c.3509G>A
c.5911G>A (p.Gly1971Ser)
c.5623G>A (p.Gly1875Ser)
c.3151G>A (p.Gly1051Ser)
gnomAD v4
19g.35732736G>CCA405426007KMT2Bn.493G>C
c.6121G>C (p.Gly2041Arg)
c.3728G>C (n.3728G>C)
c.1405G>C (p.Gly469Arg)
n.1340G>C
c.1408G>C (p.Gly470Arg)
c.5729G>C
c.6187G>C (p.Gly2063Arg)
c.704+407G>C (n.704+407G>C)
c.3509G>C
c.5911G>C (p.Gly1971Arg)
c.5623G>C (p.Gly1875Arg)
c.3151G>C (p.Gly1051Arg)
19g.35732736G>TCA405426008KMT2Bn.493G>T
c.6121G>T (p.Gly2041Cys)
c.3728G>T (n.3728G>T)
c.1405G>T (p.Gly469Cys)
n.1340G>T
c.1408G>T (p.Gly470Cys)
c.5729G>T
c.6187G>T (p.Gly2063Cys)
c.704+407G>T (n.704+407G>T)
c.3509G>T
c.5911G>T (p.Gly1971Cys)
c.5623G>T (p.Gly1875Cys)
c.3151G>T (p.Gly1051Cys)
19g.35732737G>ACA405426009KMT2Bn.494G>A
c.6122G>A (p.Gly2041Asp)
c.3729G>A (n.3729G>A)
c.1406G>A (p.Gly469Asp)
n.1341G>A
c.1409G>A (p.Gly470Asp)
c.5730G>A
c.6188G>A (p.Gly2063Asp)
c.704+408G>A (n.704+408G>A)
c.3510G>A
c.5912G>A (p.Gly1971Asp)
c.5624G>A (p.Gly1875Asp)
c.3152G>A (p.Gly1051Asp)
19g.35732737G>CCA405426010KMT2Bn.494G>C
c.6122G>C (p.Gly2041Ala)
c.3729G>C (n.3729G>C)
c.1406G>C (p.Gly469Ala)
n.1341G>C
c.1409G>C (p.Gly470Ala)
c.5730G>C
c.6188G>C (p.Gly2063Ala)
c.704+408G>C (n.704+408G>C)
c.3510G>C
c.5912G>C (p.Gly1971Ala)
c.5624G>C (p.Gly1875Ala)
c.3152G>C (p.Gly1051Ala)
19g.35732737G>TCA405426011KMT2Bn.494G>T
c.6122G>T (p.Gly2041Val)
c.3729G>T (n.3729G>T)
c.1406G>T (p.Gly469Val)
n.1341G>T
c.1409G>T (p.Gly470Val)
c.5730G>T
c.6188G>T (p.Gly2063Val)
c.704+408G>T (n.704+408G>T)
c.3510G>T
c.5912G>T (p.Gly1971Val)
c.5624G>T (p.Gly1875Val)
c.3152G>T (p.Gly1051Val)
19g.35732738C>ACA507308709KMT2Bn.495C>A
c.6123C>A (p.Gly2041=)
c.3730C>A (n.3730C>A)
c.1407C>A (p.Gly469=)
n.1342C>A
c.1410C>A (p.Gly470=)
c.5731C>A
c.6189C>A (p.Gly2063=)
c.704+409C>A (n.704+409C>A)
c.3511C>A
c.5913C>A (p.Gly1971=)
c.5625C>A (p.Gly1875=)
c.3153C>A (p.Gly1051=)
19g.35732738C=CA2333794481KMT2Bn.495C=
c.6123C= (p.Gly2041=)
c.3730C= (n.3730C=)
c.1407C= (p.Gly469=)
n.1342C=
c.1410C= (p.Gly470=)
c.5731C=
c.6189C= (p.Gly2063=)
c.704+409C= (n.704+409C=)
c.3511C=
c.5913C= (p.Gly1971=)
c.5625C= (p.Gly1875=)
c.3153C= (p.Gly1051=)
19g.35732738C>GCA507308710KMT2Bn.495C>G
c.6123C>G (p.Gly2041=)
c.3730C>G (n.3730C>G)
c.1407C>G (p.Gly469=)
n.1342C>G
c.1410C>G (p.Gly470=)
c.5731C>G
c.6189C>G (p.Gly2063=)
c.704+409C>G (n.704+409C>G)
c.3511C>G
c.5913C>G (p.Gly1971=)
c.5625C>G (p.Gly1875=)
c.3153C>G (p.Gly1051=)
19g.35732738C>TCA9385629KMT2Bn.495C>T
c.6123C>T (p.Gly2041=)
c.3730C>T (n.3730C>T)
c.1407C>T (p.Gly469=)
n.1342C>T
c.1410C>T (p.Gly470=)
c.5731C>T
c.6189C>T (p.Gly2063=)
c.704+409C>T (n.704+409C>T)
c.3511C>T
c.5913C>T (p.Gly1971=)
c.5625C>T (p.Gly1875=)
c.3153C>T (p.Gly1051=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732739G>ACA405426013KMT2Bn.496G>A
c.6124G>A (p.Val2042Met)
c.3731G>A (n.3731G>A)
c.1408G>A (p.Val470Met)
n.1343G>A
c.1411G>A (p.Val471Met)
c.5732G>A
c.6190G>A (p.Val2064Met)
c.704+410G>A (n.704+410G>A)
c.3512G>A
c.5914G>A (p.Val1972Met)
c.5626G>A (p.Val1876Met)
c.3154G>A (p.Val1052Met)
gnomAD v4
19g.35732739G>CCA405426012KMT2Bn.496G>C
c.6124G>C (p.Val2042Leu)
c.3731G>C (n.3731G>C)
c.1408G>C (p.Val470Leu)
n.1343G>C
c.1411G>C (p.Val471Leu)
c.5732G>C
c.6190G>C (p.Val2064Leu)
c.704+410G>C (n.704+410G>C)
c.3512G>C
c.5914G>C (p.Val1972Leu)
c.5626G>C (p.Val1876Leu)
c.3154G>C (p.Val1052Leu)
19g.35732739G>TCA405426014KMT2Bn.496G>T
c.6124G>T (p.Val2042Leu)
c.3731G>T (n.3731G>T)
c.1408G>T (p.Val470Leu)
n.1343G>T
c.1411G>T (p.Val471Leu)
c.5732G>T
c.6190G>T (p.Val2064Leu)
c.704+410G>T (n.704+410G>T)
c.3512G>T
c.5914G>T (p.Val1972Leu)
c.5626G>T (p.Val1876Leu)
c.3154G>T (p.Val1052Leu)
gnomAD v4
19g.35732740T>ACA405426015KMT2Bn.497T>A
c.6125T>A (p.Val2042Glu)
c.3732T>A (n.3732T>A)
c.1409T>A (p.Val470Glu)
n.1344T>A
c.1412T>A (p.Val471Glu)
c.5733T>A
c.6191T>A (p.Val2064Glu)
c.704+411T>A (n.704+411T>A)
c.3513T>A
c.5915T>A (p.Val1972Glu)
c.5627T>A (p.Val1876Glu)
c.3155T>A (p.Val1052Glu)
gnomAD v4
19g.35732740T>CCA405426017KMT2Bn.497T>C
c.6125T>C (p.Val2042Ala)
c.3732T>C (n.3732T>C)
c.1409T>C (p.Val470Ala)
n.1344T>C
c.1412T>C (p.Val471Ala)
c.5733T>C
c.6191T>C (p.Val2064Ala)
c.704+411T>C (n.704+411T>C)
c.3513T>C
c.5915T>C (p.Val1972Ala)
c.5627T>C (p.Val1876Ala)
c.3155T>C (p.Val1052Ala)
19g.35732740T>GCA405426016KMT2Bn.497T>G
c.6125T>G (p.Val2042Gly)
c.3732T>G (n.3732T>G)
c.1409T>G (p.Val470Gly)
n.1344T>G
c.1412T>G (p.Val471Gly)
c.5733T>G
c.6191T>G (p.Val2064Gly)
c.704+411T>G (n.704+411T>G)
c.3513T>G
c.5915T>G (p.Val1972Gly)
c.5627T>G (p.Val1876Gly)
c.3155T>G (p.Val1052Gly)
19g.35732741G>ACA507308715KMT2Bn.498G>A
c.6126G>A (p.Val2042=)
c.3733G>A (n.3733G>A)
c.1410G>A (p.Val470=)
n.1345G>A
c.1413G>A (p.Val471=)
c.5734G>A
c.6192G>A (p.Val2064=)
c.704+412G>A (n.704+412G>A)
c.3514G>A
c.5916G>A (p.Val1972=)
c.5628G>A (p.Val1876=)
c.3156G>A (p.Val1052=)
dbSNP gnomAD v2
19g.35732741G>CCA507308718KMT2Bn.498G>C
c.6126G>C (p.Val2042=)
c.3733G>C (n.3733G>C)
c.1410G>C (p.Val470=)
n.1345G>C
c.1413G>C (p.Val471=)
c.5734G>C
c.6192G>C (p.Val2064=)
c.704+412G>C (n.704+412G>C)
c.3514G>C
c.5916G>C (p.Val1972=)
c.5628G>C (p.Val1876=)
c.3156G>C (p.Val1052=)
19g.35732741G=CA2333794482KMT2Bn.498G=
c.6126G= (p.Val2042=)
c.3733G= (n.3733G=)
c.1410G= (p.Val470=)
n.1345G=
c.1413G= (p.Val471=)
c.5734G=
c.6192G= (p.Val2064=)
c.704+412G= (n.704+412G=)
c.3514G=
c.5916G= (p.Val1972=)
c.5628G= (p.Val1876=)
c.3156G= (p.Val1052=)
19g.35732741G>TCA507308721KMT2Bn.498G>T
c.6126G>T (p.Val2042=)
c.3733G>T (n.3733G>T)
c.1410G>T (p.Val470=)
n.1345G>T
c.1413G>T (p.Val471=)
c.5734G>T
c.6192G>T (p.Val2064=)
c.704+412G>T (n.704+412G>T)
c.3514G>T
c.5916G>T (p.Val1972=)
c.5628G>T (p.Val1876=)
c.3156G>T (p.Val1052=)
gnomAD v4
19g.35732742G>ACA405426018KMT2Bn.499G>A
c.6127G>A (p.Asp2043Asn)
c.3734G>A (n.3734G>A)
c.1411G>A (p.Asp471Asn)
n.1346G>A
c.1414G>A (p.Asp472Asn)
c.5735G>A
c.6193G>A (p.Asp2065Asn)
c.704+413G>A (n.704+413G>A)
c.3515G>A
c.5917G>A (p.Asp1973Asn)
c.5629G>A (p.Asp1877Asn)
c.3157G>A (p.Asp1053Asn)
19g.35732742G>CCA405426020KMT2Bn.499G>C
c.6127G>C (p.Asp2043His)
c.3734G>C (n.3734G>C)
c.1411G>C (p.Asp471His)
n.1346G>C
c.1414G>C (p.Asp472His)
c.5735G>C
c.6193G>C (p.Asp2065His)
c.704+413G>C (n.704+413G>C)
c.3515G>C
c.5917G>C (p.Asp1973His)
c.5629G>C (p.Asp1877His)
c.3157G>C (p.Asp1053His)
ClinVar
19g.35732742G>TCA405426019KMT2Bn.499G>T
c.6127G>T (p.Asp2043Tyr)
c.3734G>T (n.3734G>T)
c.1411G>T (p.Asp471Tyr)
n.1346G>T
c.1414G>T (p.Asp472Tyr)
c.5735G>T
c.6193G>T (p.Asp2065Tyr)
c.704+413G>T (n.704+413G>T)
c.3515G>T
c.5917G>T (p.Asp1973Tyr)
c.5629G>T (p.Asp1877Tyr)
c.3157G>T (p.Asp1053Tyr)
19g.35732743A=CA2333794483KMT2Bn.500A=
c.6128A= (p.Asp2043=)
c.3735A= (n.3735A=)
c.1412A= (p.Asp471=)
n.1347A=
c.1415A= (p.Asp472=)
c.5736A=
c.6194A= (p.Asp2065=)
c.704+414A= (n.704+414A=)
c.3516A=
c.5918A= (p.Asp1973=)
c.5630A= (p.Asp1877=)
c.3158A= (p.Asp1053=)
19g.35732743A>CCA405426021KMT2Bn.500A>C
c.6128A>C (p.Asp2043Ala)
c.3735A>C (n.3735A>C)
c.1412A>C (p.Asp471Ala)
n.1347A>C
c.1415A>C (p.Asp472Ala)
c.5736A>C
c.6194A>C (p.Asp2065Ala)
c.704+414A>C (n.704+414A>C)
c.3516A>C
c.5918A>C (p.Asp1973Ala)
c.5630A>C (p.Asp1877Ala)
c.3158A>C (p.Asp1053Ala)
19g.35732743A>GCA405426023KMT2Bn.500A>G
c.6128A>G (p.Asp2043Gly)
c.3735A>G (n.3735A>G)
c.1412A>G (p.Asp471Gly)
n.1347A>G
c.1415A>G (p.Asp472Gly)
c.5736A>G
c.6194A>G (p.Asp2065Gly)
c.704+414A>G (n.704+414A>G)
c.3516A>G
c.5918A>G (p.Asp1973Gly)
c.5630A>G (p.Asp1877Gly)
c.3158A>G (p.Asp1053Gly)
dbSNP
19g.35732743A>TCA405426022KMT2Bn.500A>T
c.6128A>T (p.Asp2043Val)
c.3735A>T (n.3735A>T)
c.1412A>T (p.Asp471Val)
n.1347A>T
c.1415A>T (p.Asp472Val)
c.5736A>T
c.6194A>T (p.Asp2065Val)
c.704+414A>T (n.704+414A>T)
c.3516A>T
c.5918A>T (p.Asp1973Val)
c.5630A>T (p.Asp1877Val)
c.3158A>T (p.Asp1053Val)
19g.35732744C>ACA405426024KMT2Bn.501C>A
c.6129C>A (p.Asp2043Glu)
c.3736C>A (n.3736C>A)
c.1413C>A (p.Asp471Glu)
n.1348C>A
c.1416C>A (p.Asp472Glu)
c.5737C>A
c.6195C>A (p.Asp2065Glu)
c.704+415C>A (n.704+415C>A)
c.3517C>A
c.5919C>A (p.Asp1973Glu)
c.5631C>A (p.Asp1877Glu)
c.3159C>A (p.Asp1053Glu)
19g.35732744C=CA2333794484KMT2Bn.501C=
c.6129C= (p.Asp2043=)
c.3736C= (n.3736C=)
c.1413C= (p.Asp471=)
n.1348C=
c.1416C= (p.Asp472=)
c.5737C=
c.6195C= (p.Asp2065=)
c.704+415C= (n.704+415C=)
c.3517C=
c.5919C= (p.Asp1973=)
c.5631C= (p.Asp1877=)
c.3159C= (p.Asp1053=)
19g.35732744C>GCA307796421KMT2Bn.501C>G
c.6129C>G (p.Asp2043Glu)
c.3736C>G (n.3736C>G)
c.1413C>G (p.Asp471Glu)
n.1348C>G
c.1416C>G (p.Asp472Glu)
c.5737C>G
c.6195C>G (p.Asp2065Glu)
c.704+415C>G (n.704+415C>G)
c.3517C>G
c.5919C>G (p.Asp1973Glu)
c.5631C>G (p.Asp1877Glu)
c.3159C>G (p.Asp1053Glu)
dbSNP gnomAD v3 gnomAD v4
19g.35732744C>TCA9385630KMT2Bn.501C>T
c.6129C>T (p.Asp2043=)
c.3736C>T (n.3736C>T)
c.1413C>T (p.Asp471=)
n.1348C>T
c.1416C>T (p.Asp472=)
c.5737C>T
c.6195C>T (p.Asp2065=)
c.704+415C>T (n.704+415C>T)
c.3517C>T
c.5919C>T (p.Asp1973=)
c.5631C>T (p.Asp1877=)
c.3159C>T (p.Asp1053=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.35732745G>ACA9385631KMT2Bn.502G>A
c.6130G>A (p.Asp2044Asn)
c.3737G>A (n.3737G>A)
c.1414G>A (p.Asp472Asn)
n.1349G>A
c.1417G>A (p.Asp473Asn)
c.5738G>A
c.6196G>A (p.Asp2066Asn)
c.704+416G>A (n.704+416G>A)
c.3518G>A
c.5920G>A (p.Asp1974Asn)
c.5632G>A (p.Asp1878Asn)
c.3160G>A (p.Asp1054Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732745G>CCA405426025KMT2Bn.502G>C
c.6130G>C (p.Asp2044His)
c.3737G>C (n.3737G>C)
c.1414G>C (p.Asp472His)
n.1349G>C
c.1417G>C (p.Asp473His)
c.5738G>C
c.6196G>C (p.Asp2066His)
c.704+416G>C (n.704+416G>C)
c.3518G>C
c.5920G>C (p.Asp1974His)
c.5632G>C (p.Asp1878His)
c.3160G>C (p.Asp1054His)
19g.35732745G=CA2333794485KMT2Bn.502G=
c.6130G= (p.Asp2044=)
c.3737G= (n.3737G=)
c.1414G= (p.Asp472=)
n.1349G=
c.1417G= (p.Asp473=)
c.5738G=
c.6196G= (p.Asp2066=)
c.704+416G= (n.704+416G=)
c.3518G=
c.5920G= (p.Asp1974=)
c.5632G= (p.Asp1878=)
c.3160G= (p.Asp1054=)
19g.35732745G>TCA307796432KMT2Bn.502G>T
c.6130G>T (p.Asp2044Tyr)
c.3737G>T (n.3737G>T)
c.1414G>T (p.Asp472Tyr)
n.1349G>T
c.1417G>T (p.Asp473Tyr)
c.5738G>T
c.6196G>T (p.Asp2066Tyr)
c.704+416G>T (n.704+416G>T)
c.3518G>T
c.5920G>T (p.Asp1974Tyr)
c.5632G>T (p.Asp1878Tyr)
c.3160G>T (p.Asp1054Tyr)
dbSNP gnomAD v4
19g.35732746A>CCA405426026KMT2Bn.503A>C
c.6131A>C (p.Asp2044Ala)
c.3738A>C (n.3738A>C)
c.1415A>C (p.Asp472Ala)
n.1350A>C
c.1418A>C (p.Asp473Ala)
c.5739A>C
c.6197A>C (p.Asp2066Ala)
c.704+417A>C (n.704+417A>C)
c.3519A>C
c.5921A>C (p.Asp1974Ala)
c.5633A>C (p.Asp1878Ala)
c.3161A>C (p.Asp1054Ala)
19g.35732746A>GCA405426027KMT2Bn.503A>G
c.6131A>G (p.Asp2044Gly)
c.3738A>G (n.3738A>G)
c.1415A>G (p.Asp472Gly)
n.1350A>G
c.1418A>G (p.Asp473Gly)
c.5739A>G
c.6197A>G (p.Asp2066Gly)
c.704+417A>G (n.704+417A>G)
c.3519A>G
c.5921A>G (p.Asp1974Gly)
c.5633A>G (p.Asp1878Gly)
c.3161A>G (p.Asp1054Gly)
19g.35732746A>TCA405426028KMT2Bn.503A>T
c.6131A>T (p.Asp2044Val)
c.3738A>T (n.3738A>T)
c.1415A>T (p.Asp472Val)
n.1350A>T
c.1418A>T (p.Asp473Val)
c.5739A>T
c.6197A>T (p.Asp2066Val)
c.704+417A>T (n.704+417A>T)
c.3519A>T
c.5921A>T (p.Asp1974Val)
c.5633A>T (p.Asp1878Val)
c.3161A>T (p.Asp1054Val)
19g.35732747C>ACA405426029KMT2Bn.504C>A
c.6132C>A (p.Asp2044Glu)
c.3739C>A (n.3739C>A)
c.1416C>A (p.Asp472Glu)
n.1351C>A
c.1419C>A (p.Asp473Glu)
c.5740C>A
c.6198C>A (p.Asp2066Glu)
c.704+418C>A (n.704+418C>A)
c.3520C>A
c.5922C>A (p.Asp1974Glu)
c.5634C>A (p.Asp1878Glu)
c.3162C>A (p.Asp1054Glu)
19g.35732747C=CA2333794486KMT2Bn.504C=
c.6132C= (p.Asp2044=)
c.3739C= (n.3739C=)
c.1416C= (p.Asp472=)
n.1351C=
c.1419C= (p.Asp473=)
c.5740C=
c.6198C= (p.Asp2066=)
c.704+418C= (n.704+418C=)
c.3520C=
c.5922C= (p.Asp1974=)
c.5634C= (p.Asp1878=)
c.3162C= (p.Asp1054=)
19g.35732747C>GCA405426030KMT2Bn.504C>G
c.6132C>G (p.Asp2044Glu)
c.3739C>G (n.3739C>G)
c.1416C>G (p.Asp472Glu)
n.1351C>G
c.1419C>G (p.Asp473Glu)
c.5740C>G
c.6198C>G (p.Asp2066Glu)
c.704+418C>G (n.704+418C>G)
c.3520C>G
c.5922C>G (p.Asp1974Glu)
c.5634C>G (p.Asp1878Glu)
c.3162C>G (p.Asp1054Glu)
gnomAD v4
19g.35732747C>TCA9385632KMT2Bn.504C>T
c.6132C>T (p.Asp2044=)
c.3739C>T (n.3739C>T)
c.1416C>T (p.Asp472=)
n.1351C>T
c.1419C>T (p.Asp473=)
c.5740C>T
c.6198C>T (p.Asp2066=)
c.704+418C>T (n.704+418C>T)
c.3520C>T
c.5922C>T (p.Asp1974=)
c.5634C>T (p.Asp1878=)
c.3162C>T (p.Asp1054=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732748G>ACA9385633KMT2Bn.505G>A
c.6133G>A (p.Gly2045Ser)
c.3740G>A (n.3740G>A)
c.1417G>A (p.Gly473Ser)
n.1352G>A
c.1420G>A (p.Gly474Ser)
c.5741G>A
c.6199G>A (p.Gly2067Ser)
c.704+419G>A (n.704+419G>A)
c.3521G>A
c.5923G>A (p.Gly1975Ser)
c.5635G>A (p.Gly1879Ser)
c.3163G>A (p.Gly1055Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732748G>CCA405426031KMT2Bn.505G>C
c.6133G>C (p.Gly2045Arg)
c.3740G>C (n.3740G>C)
c.1417G>C (p.Gly473Arg)
n.1352G>C
c.1420G>C (p.Gly474Arg)
c.5741G>C
c.6199G>C (p.Gly2067Arg)
c.704+419G>C (n.704+419G>C)
c.3521G>C
c.5923G>C (p.Gly1975Arg)
c.5635G>C (p.Gly1879Arg)
c.3163G>C (p.Gly1055Arg)
19g.35732748G=CA2333794487KMT2Bn.505G=
c.6133G= (p.Gly2045=)
c.3740G= (n.3740G=)
c.1417G= (p.Gly473=)
n.1352G=
c.1420G= (p.Gly474=)
c.5741G=
c.6199G= (p.Gly2067=)
c.704+419G= (n.704+419G=)
c.3521G=
c.5923G= (p.Gly1975=)
c.5635G= (p.Gly1879=)
c.3163G= (p.Gly1055=)
19g.35732748G>TCA307796438KMT2Bn.505G>T
c.6133G>T (p.Gly2045Cys)
c.3740G>T (n.3740G>T)
c.1417G>T (p.Gly473Cys)
n.1352G>T
c.1420G>T (p.Gly474Cys)
c.5741G>T
c.6199G>T (p.Gly2067Cys)
c.704+419G>T (n.704+419G>T)
c.3521G>T
c.5923G>T (p.Gly1975Cys)
c.5635G>T (p.Gly1879Cys)
c.3163G>T (p.Gly1055Cys)
dbSNP
19g.35732749G>ACA9385634KMT2Bn.506G>A
c.6134G>A (p.Gly2045Asp)
c.3741G>A (n.3741G>A)
c.1418G>A (p.Gly473Asp)
n.1353G>A
c.1421G>A (p.Gly474Asp)
c.5742G>A
c.6200G>A (p.Gly2067Asp)
c.704+420G>A (n.704+420G>A)
c.3522G>A
c.5924G>A (p.Gly1975Asp)
c.5636G>A (p.Gly1879Asp)
c.3164G>A (p.Gly1055Asp)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.35732749G>CCA405426032KMT2Bn.506G>C
c.6134G>C (p.Gly2045Ala)
c.3741G>C (n.3741G>C)
c.1418G>C (p.Gly473Ala)
n.1353G>C
c.1421G>C (p.Gly474Ala)
c.5742G>C
c.6200G>C (p.Gly2067Ala)
c.704+420G>C (n.704+420G>C)
c.3522G>C
c.5924G>C (p.Gly1975Ala)
c.5636G>C (p.Gly1879Ala)
c.3164G>C (p.Gly1055Ala)
19g.35732749G=CA2333794488KMT2Bn.506G=
c.6134G= (p.Gly2045=)
c.3741G= (n.3741G=)
c.1418G= (p.Gly473=)
n.1353G=
c.1421G= (p.Gly474=)
c.5742G=
c.6200G= (p.Gly2067=)
c.704+420G= (n.704+420G=)
c.3522G=
c.5924G= (p.Gly1975=)
c.5636G= (p.Gly1879=)
c.3164G= (p.Gly1055=)
19g.35732749G>TCA307796454KMT2Bn.506G>T
c.6134G>T (p.Gly2045Val)
c.3741G>T (n.3741G>T)
c.1418G>T (p.Gly473Val)
n.1353G>T
c.1421G>T (p.Gly474Val)
c.5742G>T
c.6200G>T (p.Gly2067Val)
c.704+420G>T (n.704+420G>T)
c.3522G>T
c.5924G>T (p.Gly1975Val)
c.5636G>T (p.Gly1879Val)
c.3164G>T (p.Gly1055Val)
dbSNP gnomAD v4
19g.35732750C>ACA507308737KMT2Bn.507C>A
c.6135C>A (p.Gly2045=)
c.3742C>A (n.3742C>A)
c.1419C>A (p.Gly473=)
n.1354C>A
c.1422C>A (p.Gly474=)
c.5743C>A
c.6201C>A (p.Gly2067=)
c.704+421C>A (n.704+421C>A)
c.3523C>A
c.5925C>A (p.Gly1975=)
c.5637C>A (p.Gly1879=)
c.3165C>A (p.Gly1055=)
19g.35732750C=CA2333794489KMT2Bn.507C=
c.6135C= (p.Gly2045=)
c.3742C= (n.3742C=)
c.1419C= (p.Gly473=)
n.1354C=
c.1422C= (p.Gly474=)
c.5743C=
c.6201C= (p.Gly2067=)
c.704+421C= (n.704+421C=)
c.3523C=
c.5925C= (p.Gly1975=)
c.5637C= (p.Gly1879=)
c.3165C= (p.Gly1055=)
19g.35732750C>GCA507308739KMT2Bn.507C>G
c.6135C>G (p.Gly2045=)
c.3742C>G (n.3742C>G)
c.1419C>G (p.Gly473=)
n.1354C>G
c.1422C>G (p.Gly474=)
c.5743C>G
c.6201C>G (p.Gly2067=)
c.704+421C>G (n.704+421C>G)
c.3523C>G
c.5925C>G (p.Gly1975=)
c.5637C>G (p.Gly1879=)
c.3165C>G (p.Gly1055=)
19g.35732750C>TCA9385635KMT2Bn.507C>T
c.6135C>T (p.Gly2045=)
c.3742C>T (n.3742C>T)
c.1419C>T (p.Gly473=)
n.1354C>T
c.1422C>T (p.Gly474=)
c.5743C>T
c.6201C>T (p.Gly2067=)
c.704+421C>T (n.704+421C>T)
c.3523C>T
c.5925C>T (p.Gly1975=)
c.5637C>T (p.Gly1879=)
c.3165C>T (p.Gly1055=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732751A>CCA405426033KMT2Bn.508A>C
c.6136A>C (p.Thr2046Pro)
c.3743A>C (n.3743A>C)
c.1420A>C (p.Thr474Pro)
n.1355A>C
c.1423A>C (p.Thr475Pro)
c.5744A>C
c.6202A>C (p.Thr2068Pro)
c.704+422A>C (n.704+422A>C)
c.3524A>C
c.5926A>C (p.Thr1976Pro)
c.5638A>C (p.Thr1880Pro)
c.3166A>C (p.Thr1056Pro)
19g.35732751A>GCA405426034KMT2Bn.508A>G
c.6136A>G (p.Thr2046Ala)
c.3743A>G (n.3743A>G)
c.1420A>G (p.Thr474Ala)
n.1355A>G
c.1423A>G (p.Thr475Ala)
c.5744A>G
c.6202A>G (p.Thr2068Ala)
c.704+422A>G (n.704+422A>G)
c.3524A>G
c.5926A>G (p.Thr1976Ala)
c.5638A>G (p.Thr1880Ala)
c.3166A>G (p.Thr1056Ala)
19g.35732751A>TCA405426035KMT2Bn.508A>T
c.6136A>T (p.Thr2046Ser)
c.3743A>T (n.3743A>T)
c.1420A>T (p.Thr474Ser)
n.1355A>T
c.1423A>T (p.Thr475Ser)
c.5744A>T
c.6202A>T (p.Thr2068Ser)
c.704+422A>T (n.704+422A>T)
c.3524A>T
c.5926A>T (p.Thr1976Ser)
c.5638A>T (p.Thr1880Ser)
c.3166A>T (p.Thr1056Ser)
19g.35732752C>ACA405426036KMT2Bn.509C>A
c.6137C>A (p.Thr2046Asn)
c.3744C>A (n.3744C>A)
c.1421C>A (p.Thr474Asn)
n.1356C>A
c.1424C>A (p.Thr475Asn)
c.5745C>A
c.6203C>A (p.Thr2068Asn)
c.704+423C>A (n.704+423C>A)
c.3525C>A
c.5927C>A (p.Thr1976Asn)
c.5639C>A (p.Thr1880Asn)
c.3167C>A (p.Thr1056Asn)
19g.35732752C=CA2333794490KMT2Bn.509C=
c.6137C= (p.Thr2046=)
c.3744C= (n.3744C=)
c.1421C= (p.Thr474=)
n.1356C=
c.1424C= (p.Thr475=)
c.5745C=
c.6203C= (p.Thr2068=)
c.704+423C= (n.704+423C=)
c.3525C=
c.5927C= (p.Thr1976=)
c.5639C= (p.Thr1880=)
c.3167C= (p.Thr1056=)
19g.35732752C>GCA405426037KMT2Bn.509C>G
c.6137C>G (p.Thr2046Ser)
c.3744C>G (n.3744C>G)
c.1421C>G (p.Thr474Ser)
n.1356C>G
c.1424C>G (p.Thr475Ser)
c.5745C>G
c.6203C>G (p.Thr2068Ser)
c.704+423C>G (n.704+423C>G)
c.3525C>G
c.5927C>G (p.Thr1976Ser)
c.5639C>G (p.Thr1880Ser)
c.3167C>G (p.Thr1056Ser)
19g.35732752C>TCA405426038KMT2Bn.509C>T
c.6137C>T (p.Thr2046Ile)
c.3744C>T (n.3744C>T)
c.1421C>T (p.Thr474Ile)
n.1356C>T
c.1424C>T (p.Thr475Ile)
c.5745C>T
c.6203C>T (p.Thr2068Ile)
c.704+423C>T (n.704+423C>T)
c.3525C>T
c.5927C>T (p.Thr1976Ile)
c.5639C>T (p.Thr1880Ile)
c.3167C>T (p.Thr1056Ile)
dbSNP gnomAD v2
19g.35732753T>ACA507308741KMT2Bn.510T>A
c.6138T>A (p.Thr2046=)
c.3745T>A (n.3745T>A)
c.1422T>A (p.Thr474=)
n.1357T>A
c.1425T>A (p.Thr475=)
c.5746T>A
c.6204T>A (p.Thr2068=)
c.704+424T>A (n.704+424T>A)
c.3526T>A
c.5928T>A (p.Thr1976=)
c.5640T>A (p.Thr1880=)
c.3168T>A (p.Thr1056=)
gnomAD v4
19g.35732753T>CCA507308743KMT2Bn.510T>C
c.6138T>C (p.Thr2046=)
c.3745T>C (n.3745T>C)
c.1422T>C (p.Thr474=)
n.1357T>C
c.1425T>C (p.Thr475=)
c.5746T>C
c.6204T>C (p.Thr2068=)
c.704+424T>C (n.704+424T>C)
c.3526T>C
c.5928T>C (p.Thr1976=)
c.5640T>C (p.Thr1880=)
c.3168T>C (p.Thr1056=)
gnomAD v4
19g.35732753T>GCA507308746KMT2Bn.510T>G
c.6138T>G (p.Thr2046=)
c.3745T>G (n.3745T>G)
c.1422T>G (p.Thr474=)
n.1357T>G
c.1425T>G (p.Thr475=)
c.5746T>G
c.6204T>G (p.Thr2068=)
c.704+424T>G (n.704+424T>G)
c.3526T>G
c.5928T>G (p.Thr1976=)
c.5640T>G (p.Thr1880=)
c.3168T>G (p.Thr1056=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.35732753T=CA2333794491KMT2Bn.510T=
c.6138T= (p.Thr2046=)
c.3745T= (n.3745T=)
c.1422T= (p.Thr474=)
n.1357T=
c.1425T= (p.Thr475=)
c.5746T=
c.6204T= (p.Thr2068=)
c.704+424T= (n.704+424T=)
c.3526T=
c.5928T= (p.Thr1976=)
c.5640T= (p.Thr1880=)
c.3168T= (p.Thr1056=)
19g.35732754G>ACA405426040KMT2Bn.511G>A
c.6139G>A (p.Asp2047Asn)
c.3746G>A (n.3746G>A)
c.1423G>A (p.Asp475Asn)
n.1358G>A
c.1426G>A (p.Asp476Asn)
c.5747G>A
c.6205G>A (p.Asp2069Asn)
c.704+425G>A (n.704+425G>A)
c.3527G>A
c.5929G>A (p.Asp1977Asn)
c.5641G>A (p.Asp1881Asn)
c.3169G>A (p.Asp1057Asn)
19g.35732754G>CCA405426041KMT2Bn.511G>C
c.6139G>C (p.Asp2047His)
c.3746G>C (n.3746G>C)
c.1423G>C (p.Asp475His)
n.1358G>C
c.1426G>C (p.Asp476His)
c.5747G>C
c.6205G>C (p.Asp2069His)
c.704+425G>C (n.704+425G>C)
c.3527G>C
c.5929G>C (p.Asp1977His)
c.5641G>C (p.Asp1881His)
c.3169G>C (p.Asp1057His)
COSMIC
19g.35732754G>TCA405426039KMT2Bn.511G>T
c.6139G>T (p.Asp2047Tyr)
c.3746G>T (n.3746G>T)
c.1423G>T (p.Asp475Tyr)
n.1358G>T
c.1426G>T (p.Asp476Tyr)
c.5747G>T
c.6205G>T (p.Asp2069Tyr)
c.704+425G>T (n.704+425G>T)
c.3527G>T
c.5929G>T (p.Asp1977Tyr)
c.5641G>T (p.Asp1881Tyr)
c.3169G>T (p.Asp1057Tyr)
19g.35732755A>CCA405426042KMT2Bn.512A>C
c.6140A>C (p.Asp2047Ala)
c.3747A>C (n.3747A>C)
c.1424A>C (p.Asp475Ala)
n.1359A>C
c.1427A>C (p.Asp476Ala)
c.5748A>C
c.6206A>C (p.Asp2069Ala)
c.704+426A>C (n.704+426A>C)
c.3528A>C
c.5930A>C (p.Asp1977Ala)
c.5642A>C (p.Asp1881Ala)
c.3170A>C (p.Asp1057Ala)
19g.35732755A>GCA405426043KMT2Bn.512A>G
c.6140A>G (p.Asp2047Gly)
c.3747A>G (n.3747A>G)
c.1424A>G (p.Asp475Gly)
n.1359A>G
c.1427A>G (p.Asp476Gly)
c.5748A>G
c.6206A>G (p.Asp2069Gly)
c.704+426A>G (n.704+426A>G)
c.3528A>G
c.5930A>G (p.Asp1977Gly)
c.5642A>G (p.Asp1881Gly)
c.3170A>G (p.Asp1057Gly)
19g.35732755A>TCA405426044KMT2Bn.512A>T
c.6140A>T (p.Asp2047Val)
c.3747A>T (n.3747A>T)
c.1424A>T (p.Asp475Val)
n.1359A>T
c.1427A>T (p.Asp476Val)
c.5748A>T
c.6206A>T (p.Asp2069Val)
c.704+426A>T (n.704+426A>T)
c.3528A>T
c.5930A>T (p.Asp1977Val)
c.5642A>T (p.Asp1881Val)
c.3170A>T (p.Asp1057Val)
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

Number of alleles fetched