Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.35732909C>ACA307796700KMT2Bn.666C>A
c.6294C>A (p.Asn2098Lys)
c.3901C>A (n.3901C>A)
c.1578C>A (p.Asn526Lys)
n.1513C>A
c.1581C>A (p.Asn527Lys)
c.5902C>A
c.6360C>A (p.Asn2120Lys)
c.704+580C>A (n.704+580C>A)
c.3682C>A
c.6084C>A (p.Asn2028Lys)
c.5796C>A (p.Asn1932Lys)
c.3324C>A (p.Asn1108Lys)
 dbSNP
19g.35732909C=CA2333794556KMT2Bn.666C=
c.6294C= (p.Asn2098=)
c.3901C= (n.3901C=)
c.1578C= (p.Asn526=)
n.1513C=
c.1581C= (p.Asn527=)
c.5902C=
c.6360C= (p.Asn2120=)
c.704+580C= (n.704+580C=)
c.3682C=
c.6084C= (p.Asn2028=)
c.5796C= (p.Asn1932=)
c.3324C= (p.Asn1108=)
19g.35732909C>GCA405428041KMT2Bn.666C>G
c.6294C>G (p.Asn2098Lys)
c.3901C>G (n.3901C>G)
c.1578C>G (p.Asn526Lys)
n.1513C>G
c.1581C>G (p.Asn527Lys)
c.5902C>G
c.6360C>G (p.Asn2120Lys)
c.704+580C>G (n.704+580C>G)
c.3682C>G
c.6084C>G (p.Asn2028Lys)
c.5796C>G (p.Asn1932Lys)
c.3324C>G (p.Asn1108Lys)
19g.35732909C>TCA507308674KMT2Bn.666C>T
c.6294C>T (p.Asn2098=)
c.3901C>T (n.3901C>T)
c.1578C>T (p.Asn526=)
n.1513C>T
c.1581C>T (p.Asn527=)
c.5902C>T
c.6360C>T (p.Asn2120=)
c.704+580C>T (n.704+580C>T)
c.3682C>T
c.6084C>T (p.Asn2028=)
c.5796C>T (p.Asn1932=)
c.3324C>T (p.Asn1108=)
19g.35732910C>ACA405428046KMT2Bn.667C>A
c.6295C>A (p.Leu2099Ile)
c.3902C>A (n.3902C>A)
c.1579C>A (p.Leu527Ile)
n.1514C>A
c.1582C>A (p.Leu528Ile)
c.5903C>A
c.6361C>A (p.Leu2121Ile)
c.704+581C>A (n.704+581C>A)
c.3683C>A
c.6085C>A (p.Leu2029Ile)
c.5797C>A (p.Leu1933Ile)
c.3325C>A (p.Leu1109Ile)
19g.35732910C=CA2333794557KMT2Bn.667C=
c.6295C= (p.Leu2099=)
c.3902C= (n.3902C=)
c.1579C= (p.Leu527=)
n.1514C=
c.1582C= (p.Leu528=)
c.5903C=
c.6361C= (p.Leu2121=)
c.704+581C= (n.704+581C=)
c.3683C=
c.6085C= (p.Leu2029=)
c.5797C= (p.Leu1933=)
c.3325C= (p.Leu1109=)
19g.35732910C>GCA405428049KMT2Bn.667C>G
c.6295C>G (p.Leu2099Val)
c.3902C>G (n.3902C>G)
c.1579C>G (p.Leu527Val)
n.1514C>G
c.1582C>G (p.Leu528Val)
c.5903C>G
c.6361C>G (p.Leu2121Val)
c.704+581C>G (n.704+581C>G)
c.3683C>G
c.6085C>G (p.Leu2029Val)
c.5797C>G (p.Leu1933Val)
c.3325C>G (p.Leu1109Val)
 gnomAD v4
19g.35732910C>TCA507308676KMT2Bn.667C>T
c.6295C>T (p.Leu2099=)
c.3902C>T (n.3902C>T)
c.1579C>T (p.Leu527=)
n.1514C>T
c.1582C>T (p.Leu528=)
c.5903C>T
c.6361C>T (p.Leu2121=)
c.704+581C>T (n.704+581C>T)
c.3683C>T
c.6085C>T (p.Leu2029=)
c.5797C>T (p.Leu1933=)
c.3325C>T (p.Leu1109=)
 dbSNP gnomAD v4
19g.35732911T>ACA405428053KMT2Bn.668T>A
c.6296T>A (p.Leu2099Gln)
c.3903T>A (n.3903T>A)
c.1580T>A (p.Leu527Gln)
n.1515T>A
c.1583T>A (p.Leu528Gln)
c.5904T>A
c.6362T>A (p.Leu2121Gln)
c.704+582T>A (n.704+582T>A)
c.3684T>A
c.6086T>A (p.Leu2029Gln)
c.5798T>A (p.Leu1933Gln)
c.3326T>A (p.Leu1109Gln)
 gnomAD v4
19g.35732911T>CCA405428055KMT2Bn.668T>C
c.6296T>C (p.Leu2099Pro)
c.3903T>C (n.3903T>C)
c.1580T>C (p.Leu527Pro)
n.1515T>C
c.1583T>C (p.Leu528Pro)
c.5904T>C
c.6362T>C (p.Leu2121Pro)
c.704+582T>C (n.704+582T>C)
c.3684T>C
c.6086T>C (p.Leu2029Pro)
c.5798T>C (p.Leu1933Pro)
c.3326T>C (p.Leu1109Pro)
19g.35732911T>GCA405428058KMT2Bn.668T>G
c.6296T>G (p.Leu2099Arg)
c.3903T>G (n.3903T>G)
c.1580T>G (p.Leu527Arg)
n.1515T>G
c.1583T>G (p.Leu528Arg)
c.5904T>G
c.6362T>G (p.Leu2121Arg)
c.704+582T>G (n.704+582T>G)
c.3684T>G
c.6086T>G (p.Leu2029Arg)
c.5798T>G (p.Leu1933Arg)
c.3326T>G (p.Leu1109Arg)
19g.35732912A=CA2333794558KMT2Bn.669A=
c.6297A= (p.Leu2099=)
c.3904A= (n.3904A=)
c.1581A= (p.Leu527=)
n.1516A=
c.1584A= (p.Leu528=)
c.5905A=
c.6363A= (p.Leu2121=)
c.704+583A= (n.704+583A=)
c.3685A=
c.6087A= (p.Leu2029=)
c.5799A= (p.Leu1933=)
c.3327A= (p.Leu1109=)
19g.35732912A>CCA507308680KMT2Bn.669A>C
c.6297A>C (p.Leu2099=)
c.3904A>C (n.3904A>C)
c.1581A>C (p.Leu527=)
n.1516A>C
c.1584A>C (p.Leu528=)
c.5905A>C
c.6363A>C (p.Leu2121=)
c.704+583A>C (n.704+583A>C)
c.3685A>C
c.6087A>C (p.Leu2029=)
c.5799A>C (p.Leu1933=)
c.3327A>C (p.Leu1109=)
19g.35732912A>GCA507308681KMT2Bn.669A>G
c.6297A>G (p.Leu2099=)
c.3904A>G (n.3904A>G)
c.1581A>G (p.Leu527=)
n.1516A>G
c.1584A>G (p.Leu528=)
c.5905A>G
c.6363A>G (p.Leu2121=)
c.704+583A>G (n.704+583A>G)
c.3685A>G
c.6087A>G (p.Leu2029=)
c.5799A>G (p.Leu1933=)
c.3327A>G (p.Leu1109=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.35732912A>TCA507308682KMT2Bn.669A>T
c.6297A>T (p.Leu2099=)
c.3904A>T (n.3904A>T)
c.1581A>T (p.Leu527=)
n.1516A>T
c.1584A>T (p.Leu528=)
c.5905A>T
c.6363A>T (p.Leu2121=)
c.704+583A>T (n.704+583A>T)
c.3685A>T
c.6087A>T (p.Leu2029=)
c.5799A>T (p.Leu1933=)
c.3327A>T (p.Leu1109=)
 gnomAD v4
19g.35732913G>ACA405428061KMT2Bn.670G>A
c.6298G>A (p.Gly2100Arg)
c.3905G>A (n.3905G>A)
c.1582G>A (p.Gly528Arg)
n.1517G>A
c.1585G>A (p.Gly529Arg)
c.5906G>A
c.6364G>A (p.Gly2122Arg)
c.704+584G>A (n.704+584G>A)
c.3686G>A
c.6088G>A (p.Gly2030Arg)
c.5800G>A (p.Gly1934Arg)
c.3328G>A (p.Gly1110Arg)
19g.35732913G>CCA405428063KMT2Bn.670G>C
c.6298G>C (p.Gly2100Arg)
c.3905G>C (n.3905G>C)
c.1582G>C (p.Gly528Arg)
n.1517G>C
c.1585G>C (p.Gly529Arg)
c.5906G>C
c.6364G>C (p.Gly2122Arg)
c.704+584G>C (n.704+584G>C)
c.3686G>C
c.6088G>C (p.Gly2030Arg)
c.5800G>C (p.Gly1934Arg)
c.3328G>C (p.Gly1110Arg)
19g.35732913G>TCA405428065KMT2Bn.670G>T
c.6298G>T (p.Gly2100Trp)
c.3905G>T (n.3905G>T)
c.1582G>T (p.Gly528Trp)
n.1517G>T
c.1585G>T (p.Gly529Trp)
c.5906G>T
c.6364G>T (p.Gly2122Trp)
c.704+584G>T (n.704+584G>T)
c.3686G>T
c.6088G>T (p.Gly2030Trp)
c.5800G>T (p.Gly1934Trp)
c.3328G>T (p.Gly1110Trp)
19g.35732914G>ACA405428068KMT2Bn.671G>A
c.6299G>A (p.Gly2100Glu)
c.3906G>A (n.3906G>A)
c.1583G>A (p.Gly528Glu)
n.1518G>A
c.1586G>A (p.Gly529Glu)
c.5907G>A
c.6365G>A (p.Gly2122Glu)
c.704+585G>A (n.704+585G>A)
c.3687G>A
c.6089G>A (p.Gly2030Glu)
c.5801G>A (p.Gly1934Glu)
c.3329G>A (p.Gly1110Glu)
 gnomAD v4
19g.35732914G>CCA405428070KMT2Bn.671G>C
c.6299G>C (p.Gly2100Ala)
c.3906G>C (n.3906G>C)
c.1583G>C (p.Gly528Ala)
n.1518G>C
c.1586G>C (p.Gly529Ala)
c.5907G>C
c.6365G>C (p.Gly2122Ala)
c.704+585G>C (n.704+585G>C)
c.3687G>C
c.6089G>C (p.Gly2030Ala)
c.5801G>C (p.Gly1934Ala)
c.3329G>C (p.Gly1110Ala)
19g.35732914G>TCA405428069KMT2Bn.671G>T
c.6299G>T (p.Gly2100Val)
c.3906G>T (n.3906G>T)
c.1583G>T (p.Gly528Val)
n.1518G>T
c.1586G>T (p.Gly529Val)
c.5907G>T
c.6365G>T (p.Gly2122Val)
c.704+585G>T (n.704+585G>T)
c.3687G>T
c.6089G>T (p.Gly2030Val)
c.5801G>T (p.Gly1934Val)
c.3329G>T (p.Gly1110Val)
 gnomAD v4
19g.35732915G>ACA507308690KMT2Bn.672G>A
c.6300G>A (p.Gly2100=)
c.3907G>A (n.3907G>A)
c.1584G>A (p.Gly528=)
n.1519G>A
c.1587G>A (p.Gly529=)
c.5908G>A
c.6366G>A (p.Gly2122=)
c.704+586G>A (n.704+586G>A)
c.3688G>A
c.6090G>A (p.Gly2030=)
c.5802G>A (p.Gly1934=)
c.3330G>A (p.Gly1110=)
19g.35732915G>CCA507308691KMT2Bn.672G>C
c.6300G>C (p.Gly2100=)
c.3907G>C (n.3907G>C)
c.1584G>C (p.Gly528=)
n.1519G>C
c.1587G>C (p.Gly529=)
c.5908G>C
c.6366G>C (p.Gly2122=)
c.704+586G>C (n.704+586G>C)
c.3688G>C
c.6090G>C (p.Gly2030=)
c.5802G>C (p.Gly1934=)
c.3330G>C (p.Gly1110=)
 gnomAD v4
19g.35732915G>TCA507308692KMT2Bn.672G>T
c.6300G>T (p.Gly2100=)
c.3907G>T (n.3907G>T)
c.1584G>T (p.Gly528=)
n.1519G>T
c.1587G>T (p.Gly529=)
c.5908G>T
c.6366G>T (p.Gly2122=)
c.704+586G>T (n.704+586G>T)
c.3688G>T
c.6090G>T (p.Gly2030=)
c.5802G>T (p.Gly1934=)
c.3330G>T (p.Gly1110=)
 gnomAD v4
19g.35732916G>ACA405428073KMT2Bn.673G>A
c.6301G>A (p.Gly2101Ser)
c.3908G>A (n.3908G>A)
c.1585G>A (p.Gly529Ser)
n.1520G>A
c.1588G>A (p.Gly530Ser)
c.5909G>A
c.6367G>A (p.Gly2123Ser)
c.704+587G>A (n.704+587G>A)
c.3689G>A
c.6091G>A (p.Gly2031Ser)
c.5803G>A (p.Gly1935Ser)
c.3331G>A (p.Gly1111Ser)
 dbSNP gnomAD v2 gnomAD v4
19g.35732916G>CCA405428074KMT2Bn.673G>C
c.6301G>C (p.Gly2101Arg)
c.3908G>C (n.3908G>C)
c.1585G>C (p.Gly529Arg)
n.1520G>C
c.1588G>C (p.Gly530Arg)
c.5909G>C
c.6367G>C (p.Gly2123Arg)
c.704+587G>C (n.704+587G>C)
c.3689G>C
c.6091G>C (p.Gly2031Arg)
c.5803G>C (p.Gly1935Arg)
c.3331G>C (p.Gly1111Arg)
19g.35732916G=CA2333794559KMT2Bn.673G=
c.6301G= (p.Gly2101=)
c.3908G= (n.3908G=)
c.1585G= (p.Gly529=)
n.1520G=
c.1588G= (p.Gly530=)
c.5909G=
c.6367G= (p.Gly2123=)
c.704+587G= (n.704+587G=)
c.3689G=
c.6091G= (p.Gly2031=)
c.5803G= (p.Gly1935=)
c.3331G= (p.Gly1111=)
19g.35732916G>TCA405428076KMT2Bn.673G>T
c.6301G>T (p.Gly2101Cys)
c.3908G>T (n.3908G>T)
c.1585G>T (p.Gly529Cys)
n.1520G>T
c.1588G>T (p.Gly530Cys)
c.5909G>T
c.6367G>T (p.Gly2123Cys)
c.704+587G>T (n.704+587G>T)
c.3689G>T
c.6091G>T (p.Gly2031Cys)
c.5803G>T (p.Gly1935Cys)
c.3331G>T (p.Gly1111Cys)
19g.35732917G>ACA405428078KMT2Bn.674G>A
c.6302G>A (p.Gly2101Asp)
c.3909G>A (n.3909G>A)
c.1586G>A (p.Gly529Asp)
n.1521G>A
c.1589G>A (p.Gly530Asp)
c.5910G>A
c.6368G>A (p.Gly2123Asp)
c.704+588G>A (n.704+588G>A)
c.3690G>A
c.6092G>A (p.Gly2031Asp)
c.5804G>A (p.Gly1935Asp)
c.3332G>A (p.Gly1111Asp)
 dbSNP gnomAD v3 gnomAD v4
19g.35732917G>CCA405428079KMT2Bn.674G>C
c.6302G>C (p.Gly2101Ala)
c.3909G>C (n.3909G>C)
c.1586G>C (p.Gly529Ala)
n.1521G>C
c.1589G>C (p.Gly530Ala)
c.5910G>C
c.6368G>C (p.Gly2123Ala)
c.704+588G>C (n.704+588G>C)
c.3690G>C
c.6092G>C (p.Gly2031Ala)
c.5804G>C (p.Gly1935Ala)
c.3332G>C (p.Gly1111Ala)
 gnomAD v4
19g.35732917G=CA2333794560KMT2Bn.674G=
c.6302G= (p.Gly2101=)
c.3909G= (n.3909G=)
c.1586G= (p.Gly529=)
n.1521G=
c.1589G= (p.Gly530=)
c.5910G=
c.6368G= (p.Gly2123=)
c.704+588G= (n.704+588G=)
c.3690G=
c.6092G= (p.Gly2031=)
c.5804G= (p.Gly1935=)
c.3332G= (p.Gly1111=)
19g.35732917G>TCA405428081KMT2Bn.674G>T
c.6302G>T (p.Gly2101Val)
c.3909G>T (n.3909G>T)
c.1586G>T (p.Gly529Val)
n.1521G>T
c.1589G>T (p.Gly530Val)
c.5910G>T
c.6368G>T (p.Gly2123Val)
c.704+588G>T (n.704+588G>T)
c.3690G>T
c.6092G>T (p.Gly2031Val)
c.5804G>T (p.Gly1935Val)
c.3332G>T (p.Gly1111Val)
19g.35732918T>ACA507308699KMT2Bn.675T>A
c.6303T>A (p.Gly2101=)
c.3910T>A (n.3910T>A)
c.1587T>A (p.Gly529=)
n.1522T>A
c.1590T>A (p.Gly530=)
c.5911T>A
c.6369T>A (p.Gly2123=)
c.704+589T>A (n.704+589T>A)
c.3691T>A
c.6093T>A (p.Gly2031=)
c.5805T>A (p.Gly1935=)
c.3333T>A (p.Gly1111=)
19g.35732918T>CCA507308701KMT2Bn.675T>C
c.6303T>C (p.Gly2101=)
c.3910T>C (n.3910T>C)
c.1587T>C (p.Gly529=)
n.1522T>C
c.1590T>C (p.Gly530=)
c.5911T>C
c.6369T>C (p.Gly2123=)
c.704+589T>C (n.704+589T>C)
c.3691T>C
c.6093T>C (p.Gly2031=)
c.5805T>C (p.Gly1935=)
c.3333T>C (p.Gly1111=)
19g.35732918T>GCA507308702KMT2Bn.675T>G
c.6303T>G (p.Gly2101=)
c.3910T>G (n.3910T>G)
c.1587T>G (p.Gly529=)
n.1522T>G
c.1590T>G (p.Gly530=)
c.5911T>G
c.6369T>G (p.Gly2123=)
c.704+589T>G (n.704+589T>G)
c.3691T>G
c.6093T>G (p.Gly2031=)
c.5805T>G (p.Gly1935=)
c.3333T>G (p.Gly1111=)
19g.35732919C>ACA405428083KMT2Bn.676C>A
c.6304C>A (p.Pro2102Thr)
c.3911C>A (n.3911C>A)
c.1588C>A (p.Pro530Thr)
n.1523C>A
c.1591C>A (p.Pro531Thr)
c.5912C>A
c.6370C>A (p.Pro2124Thr)
c.704+590C>A (n.704+590C>A)
c.3692C>A
c.6094C>A (p.Pro2032Thr)
c.5806C>A (p.Pro1936Thr)
c.3334C>A (p.Pro1112Thr)
19g.35732919C=CA2333794561KMT2Bn.676C=
c.6304C= (p.Pro2102=)
c.3911C= (n.3911C=)
c.1588C= (p.Pro530=)
n.1523C=
c.1591C= (p.Pro531=)
c.5912C=
c.6370C= (p.Pro2124=)
c.704+590C= (n.704+590C=)
c.3692C=
c.6094C= (p.Pro2032=)
c.5806C= (p.Pro1936=)
c.3334C= (p.Pro1112=)
19g.35732919C>GCA405428085KMT2Bn.676C>G
c.6304C>G (p.Pro2102Ala)
c.3911C>G (n.3911C>G)
c.1588C>G (p.Pro530Ala)
n.1523C>G
c.1591C>G (p.Pro531Ala)
c.5912C>G
c.6370C>G (p.Pro2124Ala)
c.704+590C>G (n.704+590C>G)
c.3692C>G
c.6094C>G (p.Pro2032Ala)
c.5806C>G (p.Pro1936Ala)
c.3334C>G (p.Pro1112Ala)
 gnomAD v4
19g.35732919C>TCA9385673KMT2Bn.676C>T
c.6304C>T (p.Pro2102Ser)
c.3911C>T (n.3911C>T)
c.1588C>T (p.Pro530Ser)
n.1523C>T
c.1591C>T (p.Pro531Ser)
c.5912C>T
c.6370C>T (p.Pro2124Ser)
c.704+590C>T (n.704+590C>T)
c.3692C>T
c.6094C>T (p.Pro2032Ser)
c.5806C>T (p.Pro1936Ser)
c.3334C>T (p.Pro1112Ser)
 dbSNP ExAC gnomAD v3 gnomAD v4
19g.35732920C>ACA405428092KMT2Bn.677C>A
c.6305C>A (p.Pro2102His)
c.3912C>A (n.3912C>A)
c.1589C>A (p.Pro530His)
n.1524C>A
c.1592C>A (p.Pro531His)
c.5913C>A
c.6371C>A (p.Pro2124His)
c.704+591C>A (n.704+591C>A)
c.3693C>A
c.6095C>A (p.Pro2032His)
c.5807C>A (p.Pro1936His)
c.3335C>A (p.Pro1112His)
19g.35732920C=CA2333794562KMT2Bn.677C=
c.6305C= (p.Pro2102=)
c.3912C= (n.3912C=)
c.1589C= (p.Pro530=)
n.1524C=
c.1592C= (p.Pro531=)
c.5913C=
c.6371C= (p.Pro2124=)
c.704+591C= (n.704+591C=)
c.3693C=
c.6095C= (p.Pro2032=)
c.5807C= (p.Pro1936=)
c.3335C= (p.Pro1112=)
19g.35732920C>GCA405428090KMT2Bn.677C>G
c.6305C>G (p.Pro2102Arg)
c.3912C>G (n.3912C>G)
c.1589C>G (p.Pro530Arg)
n.1524C>G
c.1592C>G (p.Pro531Arg)
c.5913C>G
c.6371C>G (p.Pro2124Arg)
c.704+591C>G (n.704+591C>G)
c.3693C>G
c.6095C>G (p.Pro2032Arg)
c.5807C>G (p.Pro1936Arg)
c.3335C>G (p.Pro1112Arg)
19g.35732920C>TCA405428088KMT2Bn.677C>T
c.6305C>T (p.Pro2102Leu)
c.3912C>T (n.3912C>T)
c.1589C>T (p.Pro530Leu)
n.1524C>T
c.1592C>T (p.Pro531Leu)
c.5913C>T
c.6371C>T (p.Pro2124Leu)
c.704+591C>T (n.704+591C>T)
c.3693C>T
c.6095C>T (p.Pro2032Leu)
c.5807C>T (p.Pro1936Leu)
c.3335C>T (p.Pro1112Leu)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.35732921T>ACA507308704KMT2Bn.678T>A
c.6306T>A (p.Pro2102=)
c.3913T>A (n.3913T>A)
c.1590T>A (p.Pro530=)
n.1525T>A
c.1593T>A (p.Pro531=)
c.5914T>A
c.6372T>A (p.Pro2124=)
c.704+592T>A (n.704+592T>A)
c.3694T>A
c.6096T>A (p.Pro2032=)
c.5808T>A (p.Pro1936=)
c.3336T>A (p.Pro1112=)
19g.35732921T>CCA507308705KMT2Bn.678T>C
c.6306T>C (p.Pro2102=)
c.3913T>C (n.3913T>C)
c.1590T>C (p.Pro530=)
n.1525T>C
c.1593T>C (p.Pro531=)
c.5914T>C
c.6372T>C (p.Pro2124=)
c.704+592T>C (n.704+592T>C)
c.3694T>C
c.6096T>C (p.Pro2032=)
c.5808T>C (p.Pro1936=)
c.3336T>C (p.Pro1112=)
 dbSNP
19g.35732921T>GCA507308707KMT2Bn.678T>G
c.6306T>G (p.Pro2102=)
c.3913T>G (n.3913T>G)
c.1590T>G (p.Pro530=)
n.1525T>G
c.1593T>G (p.Pro531=)
c.5914T>G
c.6372T>G (p.Pro2124=)
c.704+592T>G (n.704+592T>G)
c.3694T>G
c.6096T>G (p.Pro2032=)
c.5808T>G (p.Pro1936=)
c.3336T>G (p.Pro1112=)
19g.35732921T=CA2333794563KMT2Bn.678T=
c.6306T= (p.Pro2102=)
c.3913T= (n.3913T=)
c.1590T= (p.Pro530=)
n.1525T=
c.1593T= (p.Pro531=)
c.5914T=
c.6372T= (p.Pro2124=)
c.704+592T= (n.704+592T=)
c.3694T=
c.6096T= (p.Pro2032=)
c.5808T= (p.Pro1936=)
c.3336T= (p.Pro1112=)
19g.35732922G>ACA405428097KMT2Bn.679G>A
c.6307G>A (p.Gly2103Arg)
c.3914G>A (n.3914G>A)
c.1591G>A (p.Gly531Arg)
n.1526G>A
c.1594G>A (p.Gly532Arg)
c.5915G>A
c.6373G>A (p.Gly2125Arg)
c.704+593G>A (n.704+593G>A)
c.3695G>A
c.6097G>A (p.Gly2033Arg)
c.5809G>A (p.Gly1937Arg)
c.3337G>A (p.Gly1113Arg)
19g.35732922G>CCA405428100KMT2Bn.679G>C
c.6307G>C (p.Gly2103Arg)
c.3914G>C (n.3914G>C)
c.1591G>C (p.Gly531Arg)
n.1526G>C
c.1594G>C (p.Gly532Arg)
c.5915G>C
c.6373G>C (p.Gly2125Arg)
c.704+593G>C (n.704+593G>C)
c.3695G>C
c.6097G>C (p.Gly2033Arg)
c.5809G>C (p.Gly1937Arg)
c.3337G>C (p.Gly1113Arg)
19g.35732922G>TCA405428102KMT2Bn.679G>T
c.6307G>T (p.Gly2103Trp)
c.3914G>T (n.3914G>T)
c.1591G>T (p.Gly531Trp)
n.1526G>T
c.1594G>T (p.Gly532Trp)
c.5915G>T
c.6373G>T (p.Gly2125Trp)
c.704+593G>T (n.704+593G>T)
c.3695G>T
c.6097G>T (p.Gly2033Trp)
c.5809G>T (p.Gly1937Trp)
c.3337G>T (p.Gly1113Trp)
 gnomAD v4
19g.35732923G>ACA405428105KMT2Bn.680G>A
c.6308G>A (p.Gly2103Glu)
c.3915G>A (n.3915G>A)
c.1592G>A (p.Gly531Glu)
n.1527G>A
c.1595G>A (p.Gly532Glu)
c.5916G>A
c.6374G>A (p.Gly2125Glu)
c.704+594G>A (n.704+594G>A)
c.3696G>A
c.6098G>A (p.Gly2033Glu)
c.5810G>A (p.Gly1937Glu)
c.3338G>A (p.Gly1113Glu)
 dbSNP gnomAD v2
19g.35732923G>CCA405428108KMT2Bn.680G>C
c.6308G>C (p.Gly2103Ala)
c.3915G>C (n.3915G>C)
c.1592G>C (p.Gly531Ala)
n.1527G>C
c.1595G>C (p.Gly532Ala)
c.5916G>C
c.6374G>C (p.Gly2125Ala)
c.704+594G>C (n.704+594G>C)
c.3696G>C
c.6098G>C (p.Gly2033Ala)
c.5810G>C (p.Gly1937Ala)
c.3338G>C (p.Gly1113Ala)
19g.35732923G=CA2333794564KMT2Bn.680G=
c.6308G= (p.Gly2103=)
c.3915G= (n.3915G=)
c.1592G= (p.Gly531=)
n.1527G=
c.1595G= (p.Gly532=)
c.5916G=
c.6374G= (p.Gly2125=)
c.704+594G= (n.704+594G=)
c.3696G=
c.6098G= (p.Gly2033=)
c.5810G= (p.Gly1937=)
c.3338G= (p.Gly1113=)
19g.35732923G>TCA405428111KMT2Bn.680G>T
c.6308G>T (p.Gly2103Val)
c.3915G>T (n.3915G>T)
c.1592G>T (p.Gly531Val)
n.1527G>T
c.1595G>T (p.Gly532Val)
c.5916G>T
c.6374G>T (p.Gly2125Val)
c.704+594G>T (n.704+594G>T)
c.3696G>T
c.6098G>T (p.Gly2033Val)
c.5810G>T (p.Gly1937Val)
c.3338G>T (p.Gly1113Val)
19g.35732924G>ACA507308714KMT2Bn.681G>A
c.6309G>A (p.Gly2103=)
c.3916G>A (n.3916G>A)
c.1593G>A (p.Gly531=)
n.1528G>A
c.1596G>A (p.Gly532=)
c.5917G>A
c.6375G>A (p.Gly2125=)
c.704+595G>A (n.704+595G>A)
c.3697G>A
c.6099G>A (p.Gly2033=)
c.5811G>A (p.Gly1937=)
c.3339G>A (p.Gly1113=)
19g.35732924G>CCA507308720KMT2Bn.681G>C
c.6309G>C (p.Gly2103=)
c.3916G>C (n.3916G>C)
c.1593G>C (p.Gly531=)
n.1528G>C
c.1596G>C (p.Gly532=)
c.5917G>C
c.6375G>C (p.Gly2125=)
c.704+595G>C (n.704+595G>C)
c.3697G>C
c.6099G>C (p.Gly2033=)
c.5811G>C (p.Gly1937=)
c.3339G>C (p.Gly1113=)
19g.35732924G>TCA507308717KMT2Bn.681G>T
c.6309G>T (p.Gly2103=)
c.3916G>T (n.3916G>T)
c.1593G>T (p.Gly531=)
n.1528G>T
c.1596G>T (p.Gly532=)
c.5917G>T
c.6375G>T (p.Gly2125=)
c.704+595G>T (n.704+595G>T)
c.3697G>T
c.6099G>T (p.Gly2033=)
c.5811G>T (p.Gly1937=)
c.3339G>T (p.Gly1113=)
19g.35732925G>ACA405428115KMT2Bn.682G>A
c.6310G>A (p.Asp2104Asn)
c.3917G>A (n.3917G>A)
c.1594G>A (p.Asp532Asn)
n.1529G>A
c.1597G>A (p.Asp533Asn)
c.5918G>A
c.6376G>A (p.Asp2126Asn)
c.704+596G>A (n.704+596G>A)
c.3698G>A
c.6100G>A (p.Asp2034Asn)
c.5812G>A (p.Asp1938Asn)
c.3340G>A (p.Asp1114Asn)
 gnomAD v4
19g.35732925G>CCA405428117KMT2Bn.682G>C
c.6310G>C (p.Asp2104His)
c.3917G>C (n.3917G>C)
c.1594G>C (p.Asp532His)
n.1529G>C
c.1597G>C (p.Asp533His)
c.5918G>C
c.6376G>C (p.Asp2126His)
c.704+596G>C (n.704+596G>C)
c.3698G>C
c.6100G>C (p.Asp2034His)
c.5812G>C (p.Asp1938His)
c.3340G>C (p.Asp1114His)
19g.35732925G>TCA405428119KMT2Bn.682G>T
c.6310G>T (p.Asp2104Tyr)
c.3917G>T (n.3917G>T)
c.1594G>T (p.Asp532Tyr)
n.1529G>T
c.1597G>T (p.Asp533Tyr)
c.5918G>T
c.6376G>T (p.Asp2126Tyr)
c.704+596G>T (n.704+596G>T)
c.3698G>T
c.6100G>T (p.Asp2034Tyr)
c.5812G>T (p.Asp1938Tyr)
c.3340G>T (p.Asp1114Tyr)
 gnomAD v4
19g.35732926A>CCA405428123KMT2Bn.683A>C
c.6311A>C (p.Asp2104Ala)
c.3918A>C (n.3918A>C)
c.1595A>C (p.Asp532Ala)
n.1530A>C
c.1598A>C (p.Asp533Ala)
c.5919A>C
c.6377A>C (p.Asp2126Ala)
c.704+597A>C (n.704+597A>C)
c.3699A>C
c.6101A>C (p.Asp2034Ala)
c.5813A>C (p.Asp1938Ala)
c.3341A>C (p.Asp1114Ala)
19g.35732926A>GCA405428125KMT2Bn.683A>G
c.6311A>G (p.Asp2104Gly)
c.3918A>G (n.3918A>G)
c.1595A>G (p.Asp532Gly)
n.1530A>G
c.1598A>G (p.Asp533Gly)
c.5919A>G
c.6377A>G (p.Asp2126Gly)
c.704+597A>G (n.704+597A>G)
c.3699A>G
c.6101A>G (p.Asp2034Gly)
c.5813A>G (p.Asp1938Gly)
c.3341A>G (p.Asp1114Gly)
 gnomAD v4
19g.35732926A>TCA405428128KMT2Bn.683A>T
c.6311A>T (p.Asp2104Val)
c.3918A>T (n.3918A>T)
c.1595A>T (p.Asp532Val)
n.1530A>T
c.1598A>T (p.Asp533Val)
c.5919A>T
c.6377A>T (p.Asp2126Val)
c.704+597A>T (n.704+597A>T)
c.3699A>T
c.6101A>T (p.Asp2034Val)
c.5813A>T (p.Asp1938Val)
c.3341A>T (p.Asp1114Val)
19g.35732927T>ACA405428135KMT2Bn.684T>A
c.6312T>A (p.Asp2104Glu)
c.3919T>A (n.3919T>A)
c.1596T>A (p.Asp532Glu)
n.1531T>A
c.1599T>A (p.Asp533Glu)
c.5920T>A
c.6378T>A (p.Asp2126Glu)
c.704+598T>A (n.704+598T>A)
c.3700T>A
c.6102T>A (p.Asp2034Glu)
c.5814T>A (p.Asp1938Glu)
c.3342T>A (p.Asp1114Glu)
 ClinVar
19g.35732927T>CCA507308722KMT2Bn.684T>C
c.6312T>C (p.Asp2104=)
c.3919T>C (n.3919T>C)
c.1596T>C (p.Asp532=)
n.1531T>C
c.1599T>C (p.Asp533=)
c.5920T>C
c.6378T>C (p.Asp2126=)
c.704+598T>C (n.704+598T>C)
c.3700T>C
c.6102T>C (p.Asp2034=)
c.5814T>C (p.Asp1938=)
c.3342T>C (p.Asp1114=)
19g.35732927T>GCA405428132KMT2Bn.684T>G
c.6312T>G (p.Asp2104Glu)
c.3919T>G (n.3919T>G)
c.1596T>G (p.Asp532Glu)
n.1531T>G
c.1599T>G (p.Asp533Glu)
c.5920T>G
c.6378T>G (p.Asp2126Glu)
c.704+598T>G (n.704+598T>G)
c.3700T>G
c.6102T>G (p.Asp2034Glu)
c.5814T>G (p.Asp1938Glu)
c.3342T>G (p.Asp1114Glu)
19g.35732928G>ACA405428138KMT2Bn.685G>A
c.6313G>A (p.Gly2105Arg)
c.3920G>A (n.3920G>A)
c.1597G>A (p.Gly533Arg)
n.1532G>A
c.1600G>A (p.Gly534Arg)
c.5921G>A
c.6379G>A (p.Gly2127Arg)
c.704+599G>A (n.704+599G>A)
c.3701G>A
c.6103G>A (p.Gly2035Arg)
c.5815G>A (p.Gly1939Arg)
c.3343G>A (p.Gly1115Arg)
19g.35732928G>CCA405428140KMT2Bn.685G>C
c.6313G>C (p.Gly2105Arg)
c.3920G>C (n.3920G>C)
c.1597G>C (p.Gly533Arg)
n.1532G>C
c.1600G>C (p.Gly534Arg)
c.5921G>C
c.6379G>C (p.Gly2127Arg)
c.704+599G>C (n.704+599G>C)
c.3701G>C
c.6103G>C (p.Gly2035Arg)
c.5815G>C (p.Gly1939Arg)
c.3343G>C (p.Gly1115Arg)
19g.35732928G>TCA405428143KMT2Bn.685G>T
c.6313G>T (p.Gly2105Ter)
c.3920G>T (n.3920G>T)
c.1597G>T (p.Gly533Ter)
n.1532G>T
c.1600G>T (p.Gly534Ter)
c.5921G>T
c.6379G>T (p.Gly2127Ter)
c.704+599G>T (n.704+599G>T)
c.3701G>T
c.6103G>T (p.Gly2035Ter)
c.5815G>T (p.Gly1939Ter)
c.3343G>T (p.Gly1115Ter)
19g.35732929G>ACA405428147KMT2Bn.686G>A
c.6314G>A (p.Gly2105Glu)
c.3921G>A (n.3921G>A)
c.1598G>A (p.Gly533Glu)
n.1533G>A
c.1601G>A (p.Gly534Glu)
c.5922G>A
c.6380G>A (p.Gly2127Glu)
c.704+600G>A (n.704+600G>A)
c.3702G>A
c.6104G>A (p.Gly2035Glu)
c.5816G>A (p.Gly1939Glu)
c.3344G>A (p.Gly1115Glu)
19g.35732929G>CCA405428149KMT2Bn.686G>C
c.6314G>C (p.Gly2105Ala)
c.3921G>C (n.3921G>C)
c.1598G>C (p.Gly533Ala)
n.1533G>C
c.1601G>C (p.Gly534Ala)
c.5922G>C
c.6380G>C (p.Gly2127Ala)
c.704+600G>C (n.704+600G>C)
c.3702G>C
c.6104G>C (p.Gly2035Ala)
c.5816G>C (p.Gly1939Ala)
c.3344G>C (p.Gly1115Ala)
19g.35732929G>TCA405428152KMT2Bn.686G>T
c.6314G>T (p.Gly2105Val)
c.3921G>T (n.3921G>T)
c.1598G>T (p.Gly533Val)
n.1533G>T
c.1601G>T (p.Gly534Val)
c.5922G>T
c.6380G>T (p.Gly2127Val)
c.704+600G>T (n.704+600G>T)
c.3702G>T
c.6104G>T (p.Gly2035Val)
c.5816G>T (p.Gly1939Val)
c.3344G>T (p.Gly1115Val)
19g.35732930A=CA2333794565KMT2Bn.687A=
c.6315A= (p.Gly2105=)
c.3922A= (n.3922A=)
c.1599A= (p.Gly533=)
n.1534A=
c.1602A= (p.Gly534=)
c.5923A=
c.6381A= (p.Gly2127=)
c.704+601A= (n.704+601A=)
c.3703A=
c.6105A= (p.Gly2035=)
c.5817A= (p.Gly1939=)
c.3345A= (p.Gly1115=)
19g.35732930A>CCA507308725KMT2Bn.687A>C
c.6315A>C (p.Gly2105=)
c.3922A>C (n.3922A>C)
c.1599A>C (p.Gly533=)
n.1534A>C
c.1602A>C (p.Gly534=)
c.5923A>C
c.6381A>C (p.Gly2127=)
c.704+601A>C (n.704+601A>C)
c.3703A>C
c.6105A>C (p.Gly2035=)
c.5817A>C (p.Gly1939=)
c.3345A>C (p.Gly1115=)
19g.35732930A>GCA9385674KMT2Bn.687A>G
c.6315A>G (p.Gly2105=)
c.3922A>G (n.3922A>G)
c.1599A>G (p.Gly533=)
n.1534A>G
c.1602A>G (p.Gly534=)
c.5923A>G
c.6381A>G (p.Gly2127=)
c.704+601A>G (n.704+601A>G)
c.3703A>G
c.6105A>G (p.Gly2035=)
c.5817A>G (p.Gly1939=)
c.3345A>G (p.Gly1115=)
 dbSNP ExAC gnomAD v4
19g.35732930A>TCA507308726KMT2Bn.687A>T
c.6315A>T (p.Gly2105=)
c.3922A>T (n.3922A>T)
c.1599A>T (p.Gly533=)
n.1534A>T
c.1602A>T (p.Gly534=)
c.5923A>T
c.6381A>T (p.Gly2127=)
c.704+601A>T (n.704+601A>T)
c.3703A>T
c.6105A>T (p.Gly2035=)
c.5817A>T (p.Gly1939=)
c.3345A>T (p.Gly1115=)
19g.35732931G>ACA9385675KMT2Bn.688G>A
c.6316G>A (p.Gly2106Ser)
c.3923G>A (n.3923G>A)
c.1600G>A (p.Gly534Ser)
n.1535G>A
c.1603G>A (p.Gly535Ser)
c.5924G>A
c.6382G>A (p.Gly2128Ser)
c.704+602G>A (n.704+602G>A)
c.3704G>A
c.6106G>A (p.Gly2036Ser)
c.5818G>A (p.Gly1940Ser)
c.3346G>A (p.Gly1116Ser)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732931G>CCA405428160KMT2Bn.688G>C
c.6316G>C (p.Gly2106Arg)
c.3923G>C (n.3923G>C)
c.1600G>C (p.Gly534Arg)
n.1535G>C
c.1603G>C (p.Gly535Arg)
c.5924G>C
c.6382G>C (p.Gly2128Arg)
c.704+602G>C (n.704+602G>C)
c.3704G>C
c.6106G>C (p.Gly2036Arg)
c.5818G>C (p.Gly1940Arg)
c.3346G>C (p.Gly1116Arg)
19g.35732931G=CA2333794566KMT2Bn.688G=
c.6316G= (p.Gly2106=)
c.3923G= (n.3923G=)
c.1600G= (p.Gly534=)
n.1535G=
c.1603G= (p.Gly535=)
c.5924G=
c.6382G= (p.Gly2128=)
c.704+602G= (n.704+602G=)
c.3704G=
c.6106G= (p.Gly2036=)
c.5818G= (p.Gly1940=)
c.3346G= (p.Gly1116=)
19g.35732931G>TCA405428163KMT2Bn.688G>T
c.6316G>T (p.Gly2106Cys)
c.3923G>T (n.3923G>T)
c.1600G>T (p.Gly534Cys)
n.1535G>T
c.1603G>T (p.Gly535Cys)
c.5924G>T
c.6382G>T (p.Gly2128Cys)
c.704+602G>T (n.704+602G>T)
c.3704G>T
c.6106G>T (p.Gly2036Cys)
c.5818G>T (p.Gly1940Cys)
c.3346G>T (p.Gly1116Cys)
19g.35732932G>ACA405428168KMT2Bn.689G>A
c.6317G>A (p.Gly2106Asp)
c.3924G>A (n.3924G>A)
c.1601G>A (p.Gly534Asp)
n.1536G>A
c.1604G>A (p.Gly535Asp)
c.5925G>A
c.6383G>A (p.Gly2128Asp)
c.704+603G>A (n.704+603G>A)
c.3705G>A
c.6107G>A (p.Gly2036Asp)
c.5819G>A (p.Gly1940Asp)
c.3347G>A (p.Gly1116Asp)
 dbSNP gnomAD v2 gnomAD v4
19g.35732932G>CCA405428170KMT2Bn.689G>C
c.6317G>C (p.Gly2106Ala)
c.3924G>C (n.3924G>C)
c.1601G>C (p.Gly534Ala)
n.1536G>C
c.1604G>C (p.Gly535Ala)
c.5925G>C
c.6383G>C (p.Gly2128Ala)
c.704+603G>C (n.704+603G>C)
c.3705G>C
c.6107G>C (p.Gly2036Ala)
c.5819G>C (p.Gly1940Ala)
c.3347G>C (p.Gly1116Ala)
19g.35732932G=CA2333794567KMT2Bn.689G=
c.6317G= (p.Gly2106=)
c.3924G= (n.3924G=)
c.1601G= (p.Gly534=)
n.1536G=
c.1604G= (p.Gly535=)
c.5925G=
c.6383G= (p.Gly2128=)
c.704+603G= (n.704+603G=)
c.3705G=
c.6107G= (p.Gly2036=)
c.5819G= (p.Gly1940=)
c.3347G= (p.Gly1116=)
19g.35732932G>TCA405428175KMT2Bn.689G>T
c.6317G>T (p.Gly2106Val)
c.3924G>T (n.3924G>T)
c.1601G>T (p.Gly534Val)
n.1536G>T
c.1604G>T (p.Gly535Val)
c.5925G>T
c.6383G>T (p.Gly2128Val)
c.704+603G>T (n.704+603G>T)
c.3705G>T
c.6107G>T (p.Gly2036Val)
c.5819G>T (p.Gly1940Val)
c.3347G>T (p.Gly1116Val)
 gnomAD v4
19g.35732933T>ACA507308734KMT2Bn.690T>A
c.6318T>A (p.Gly2106=)
c.3925T>A (n.3925T>A)
c.1602T>A (p.Gly534=)
n.1537T>A
c.1605T>A (p.Gly535=)
c.5926T>A
c.6384T>A (p.Gly2128=)
c.704+604T>A (n.704+604T>A)
c.3706T>A
c.6108T>A (p.Gly2036=)
c.5820T>A (p.Gly1940=)
c.3348T>A (p.Gly1116=)
19g.35732933T>CCA507308735KMT2Bn.690T>C
c.6318T>C (p.Gly2106=)
c.3925T>C (n.3925T>C)
c.1602T>C (p.Gly534=)
n.1537T>C
c.1605T>C (p.Gly535=)
c.5926T>C
c.6384T>C (p.Gly2128=)
c.704+604T>C (n.704+604T>C)
c.3706T>C
c.6108T>C (p.Gly2036=)
c.5820T>C (p.Gly1940=)
c.3348T>C (p.Gly1116=)
19g.35732933T>GCA507308738KMT2Bn.690T>G
c.6318T>G (p.Gly2106=)
c.3925T>G (n.3925T>G)
c.1602T>G (p.Gly534=)
n.1537T>G
c.1605T>G (p.Gly535=)
c.5926T>G
c.6384T>G (p.Gly2128=)
c.704+604T>G (n.704+604T>G)
c.3706T>G
c.6108T>G (p.Gly2036=)
c.5820T>G (p.Gly1940=)
c.3348T>G (p.Gly1116=)
 dbSNP
19g.35732933T=CA2333794568KMT2Bn.690T=
c.6318T= (p.Gly2106=)
c.3925T= (n.3925T=)
c.1602T= (p.Gly534=)
n.1537T=
c.1605T= (p.Gly535=)
c.5926T=
c.6384T= (p.Gly2128=)
c.704+604T= (n.704+604T=)
c.3706T=
c.6108T= (p.Gly2036=)
c.5820T= (p.Gly1940=)
c.3348T= (p.Gly1116=)
19g.35732934G>ACA9385676KMT2Bn.691G>A
c.6319G>A (p.Ala2107Thr)
c.3926G>A (n.3926G>A)
c.1603G>A (p.Ala535Thr)
n.1538G>A
c.1606G>A (p.Ala536Thr)
c.5927G>A
c.6385G>A (p.Ala2129Thr)
c.704+605G>A (n.704+605G>A)
c.3707G>A
c.6109G>A (p.Ala2037Thr)
c.5821G>A (p.Ala1941Thr)
c.3349G>A (p.Ala1117Thr)
 dbSNP ExAC gnomAD v2
19g.35732934G>CCA405428181KMT2Bn.691G>C
c.6319G>C (p.Ala2107Pro)
c.3926G>C (n.3926G>C)
c.1603G>C (p.Ala535Pro)
n.1538G>C
c.1606G>C (p.Ala536Pro)
c.5927G>C
c.6385G>C (p.Ala2129Pro)
c.704+605G>C (n.704+605G>C)
c.3707G>C
c.6109G>C (p.Ala2037Pro)
c.5821G>C (p.Ala1941Pro)
c.3349G>C (p.Ala1117Pro)
19g.35732934G=CA2333794569KMT2Bn.691G=
c.6319G= (p.Ala2107=)
c.3926G= (n.3926G=)
c.1603G= (p.Ala535=)
n.1538G=
c.1606G= (p.Ala536=)
c.5927G=
c.6385G= (p.Ala2129=)
c.704+605G= (n.704+605G=)
c.3707G=
c.6109G= (p.Ala2037=)
c.5821G= (p.Ala1941=)
c.3349G= (p.Ala1117=)
19g.35732934G>TCA405428178KMT2Bn.691G>T
c.6319G>T (p.Ala2107Ser)
c.3926G>T (n.3926G>T)
c.1603G>T (p.Ala535Ser)
n.1538G>T
c.1606G>T (p.Ala536Ser)
c.5927G>T
c.6385G>T (p.Ala2129Ser)
c.704+605G>T (n.704+605G>T)
c.3707G>T
c.6109G>T (p.Ala2037Ser)
c.5821G>T (p.Ala1941Ser)
c.3349G>T (p.Ala1117Ser)
19g.35732935C>ACA405428184KMT2Bn.692C>A
c.6320C>A (p.Ala2107Asp)
c.3927C>A (n.3927C>A)
c.1604C>A (p.Ala535Asp)
n.1539C>A
c.1607C>A (p.Ala536Asp)
c.5928C>A
c.6386C>A (p.Ala2129Asp)
c.704+606C>A (n.704+606C>A)
c.3708C>A
c.6110C>A (p.Ala2037Asp)
c.5822C>A (p.Ala1941Asp)
c.3350C>A (p.Ala1117Asp)
19g.35732935C>GCA405428186KMT2Bn.692C>G
c.6320C>G (p.Ala2107Gly)
c.3927C>G (n.3927C>G)
c.1604C>G (p.Ala535Gly)
n.1539C>G
c.1607C>G (p.Ala536Gly)
c.5928C>G
c.6386C>G (p.Ala2129Gly)
c.704+606C>G (n.704+606C>G)
c.3708C>G
c.6110C>G (p.Ala2037Gly)
c.5822C>G (p.Ala1941Gly)
c.3350C>G (p.Ala1117Gly)
19g.35732935C>TCA405428189KMT2Bn.692C>T
c.6320C>T (p.Ala2107Val)
c.3927C>T (n.3927C>T)
c.1604C>T (p.Ala535Val)
n.1539C>T
c.1607C>T (p.Ala536Val)
c.5928C>T
c.6386C>T (p.Ala2129Val)
c.704+606C>T (n.704+606C>T)
c.3708C>T
c.6110C>T (p.Ala2037Val)
c.5822C>T (p.Ala1941Val)
c.3350C>T (p.Ala1117Val)
19g.35732936T>ACA507308742KMT2Bn.693T>A
c.6321T>A (p.Ala2107=)
c.3928T>A (n.3928T>A)
c.1605T>A (p.Ala535=)
n.1540T>A
c.1608T>A (p.Ala536=)
c.5929T>A
c.6387T>A (p.Ala2129=)
c.704+607T>A (n.704+607T>A)
c.3709T>A
c.6111T>A (p.Ala2037=)
c.5823T>A (p.Ala1941=)
c.3351T>A (p.Ala1117=)
19g.35732936T>CCA507308744KMT2Bn.693T>C
c.6321T>C (p.Ala2107=)
c.3928T>C (n.3928T>C)
c.1605T>C (p.Ala535=)
n.1540T>C
c.1608T>C (p.Ala536=)
c.5929T>C
c.6387T>C (p.Ala2129=)
c.704+607T>C (n.704+607T>C)
c.3709T>C
c.6111T>C (p.Ala2037=)
c.5823T>C (p.Ala1941=)
c.3351T>C (p.Ala1117=)
19g.35732936T>GCA507308745KMT2Bn.693T>G
c.6321T>G (p.Ala2107=)
c.3928T>G (n.3928T>G)
c.1605T>G (p.Ala535=)
n.1540T>G
c.1608T>G (p.Ala536=)
c.5929T>G
c.6387T>G (p.Ala2129=)
c.704+607T>G (n.704+607T>G)
c.3709T>G
c.6111T>G (p.Ala2037=)
c.5823T>G (p.Ala1941=)
c.3351T>G (p.Ala1117=)
19g.35732937G>ACA405428193KMT2Bn.694G>A
c.6322G>A (p.Gly2108Ser)
c.3929G>A (n.3929G>A)
c.1606G>A (p.Gly536Ser)
n.1541G>A
c.1609G>A (p.Gly537Ser)
c.5930G>A
c.6388G>A (p.Gly2130Ser)
c.704+608G>A (n.704+608G>A)
c.3710G>A
c.6112G>A (p.Gly2038Ser)
c.5824G>A (p.Gly1942Ser)
c.3352G>A (p.Gly1118Ser)
19g.35732937G>CCA405428194KMT2Bn.694G>C
c.6322G>C (p.Gly2108Arg)
c.3929G>C (n.3929G>C)
c.1606G>C (p.Gly536Arg)
n.1541G>C
c.1609G>C (p.Gly537Arg)
c.5930G>C
c.6388G>C (p.Gly2130Arg)
c.704+608G>C (n.704+608G>C)
c.3710G>C
c.6112G>C (p.Gly2038Arg)
c.5824G>C (p.Gly1942Arg)
c.3352G>C (p.Gly1118Arg)
19g.35732937G>TCA405428198KMT2Bn.694G>T
c.6322G>T (p.Gly2108Cys)
c.3929G>T (n.3929G>T)
c.1606G>T (p.Gly536Cys)
n.1541G>T
c.1609G>T (p.Gly537Cys)
c.5930G>T
c.6388G>T (p.Gly2130Cys)
c.704+608G>T (n.704+608G>T)
c.3710G>T
c.6112G>T (p.Gly2038Cys)
c.5824G>T (p.Gly1942Cys)
c.3352G>T (p.Gly1118Cys)
19g.35732938G>ACA405428202KMT2Bn.695G>A
c.6323G>A (p.Gly2108Asp)
c.3930G>A (n.3930G>A)
c.1607G>A (p.Gly536Asp)
n.1542G>A
c.1610G>A (p.Gly537Asp)
c.5931G>A
c.6389G>A (p.Gly2130Asp)
c.704+609G>A (n.704+609G>A)
c.3711G>A
c.6113G>A (p.Gly2038Asp)
c.5825G>A (p.Gly1942Asp)
c.3353G>A (p.Gly1118Asp)
 gnomAD v4
19g.35732938G>CCA405428206KMT2Bn.695G>C
c.6323G>C (p.Gly2108Ala)
c.3930G>C (n.3930G>C)
c.1607G>C (p.Gly536Ala)
n.1542G>C
c.1610G>C (p.Gly537Ala)
c.5931G>C
c.6389G>C (p.Gly2130Ala)
c.704+609G>C (n.704+609G>C)
c.3711G>C
c.6113G>C (p.Gly2038Ala)
c.5825G>C (p.Gly1942Ala)
c.3353G>C (p.Gly1118Ala)
19g.35732938G>TCA405428208KMT2Bn.695G>T
c.6323G>T (p.Gly2108Val)
c.3930G>T (n.3930G>T)
c.1607G>T (p.Gly536Val)
n.1542G>T
c.1610G>T (p.Gly537Val)
c.5931G>T
c.6389G>T (p.Gly2130Val)
c.704+609G>T (n.704+609G>T)
c.3711G>T
c.6113G>T (p.Gly2038Val)
c.5825G>T (p.Gly1942Val)
c.3353G>T (p.Gly1118Val)
 gnomAD v4
19g.35732939C>ACA507308751KMT2Bn.696C>A
c.6324C>A (p.Gly2108=)
c.3931C>A (n.3931C>A)
c.1608C>A (p.Gly536=)
n.1543C>A
c.1611C>A (p.Gly537=)
c.5932C>A
c.6390C>A (p.Gly2130=)
c.704+610C>A (n.704+610C>A)
c.3712C>A
c.6114C>A (p.Gly2038=)
c.5826C>A (p.Gly1942=)
c.3354C>A (p.Gly1118=)
 gnomAD v4
19g.35732939C>GCA507308752KMT2Bn.696C>G
c.6324C>G (p.Gly2108=)
c.3931C>G (n.3931C>G)
c.1608C>G (p.Gly536=)
n.1543C>G
c.1611C>G (p.Gly537=)
c.5932C>G
c.6390C>G (p.Gly2130=)
c.704+610C>G (n.704+610C>G)
c.3712C>G
c.6114C>G (p.Gly2038=)
c.5826C>G (p.Gly1942=)
c.3354C>G (p.Gly1118=)
19g.35732939C>TCA507308753KMT2Bn.696C>T
c.6324C>T (p.Gly2108=)
c.3931C>T (n.3931C>T)
c.1608C>T (p.Gly536=)
n.1543C>T
c.1611C>T (p.Gly537=)
c.5932C>T
c.6390C>T (p.Gly2130=)
c.704+610C>T (n.704+610C>T)
c.3712C>T
c.6114C>T (p.Gly2038=)
c.5826C>T (p.Gly1942=)
c.3354C>T (p.Gly1118=)
 gnomAD v4
19g.35732940C>ACA405428212KMT2Bn.697C>A
c.6325C>A (p.Pro2109Thr)
c.3932C>A (n.3932C>A)
c.1609C>A (p.Pro537Thr)
n.1544C>A
c.1612C>A (p.Pro538Thr)
c.5933C>A
c.6391C>A (p.Pro2131Thr)
c.704+611C>A (n.704+611C>A)
c.3713C>A
c.6115C>A (p.Pro2039Thr)
c.5827C>A (p.Pro1943Thr)
c.3355C>A (p.Pro1119Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.35732940C=CA2333794570KMT2Bn.697C=
c.6325C= (p.Pro2109=)
c.3932C= (n.3932C=)
c.1609C= (p.Pro537=)
n.1544C=
c.1612C= (p.Pro538=)
c.5933C=
c.6391C= (p.Pro2131=)
c.704+611C= (n.704+611C=)
c.3713C=
c.6115C= (p.Pro2039=)
c.5827C= (p.Pro1943=)
c.3355C= (p.Pro1119=)
19g.35732940C>GCA405428214KMT2Bn.697C>G
c.6325C>G (p.Pro2109Ala)
c.3932C>G (n.3932C>G)
c.1609C>G (p.Pro537Ala)
n.1544C>G
c.1612C>G (p.Pro538Ala)
c.5933C>G
c.6391C>G (p.Pro2131Ala)
c.704+611C>G (n.704+611C>G)
c.3713C>G
c.6115C>G (p.Pro2039Ala)
c.5827C>G (p.Pro1943Ala)
c.3355C>G (p.Pro1119Ala)
19g.35732940C>TCA405428217KMT2Bn.697C>T
c.6325C>T (p.Pro2109Ser)
c.3932C>T (n.3932C>T)
c.1609C>T (p.Pro537Ser)
n.1544C>T
c.1612C>T (p.Pro538Ser)
c.5933C>T
c.6391C>T (p.Pro2131Ser)
c.704+611C>T (n.704+611C>T)
c.3713C>T
c.6115C>T (p.Pro2039Ser)
c.5827C>T (p.Pro1943Ser)
c.3355C>T (p.Pro1119Ser)
 gnomAD v4
19g.35732941C>ACA405428222KMT2Bn.698C>A
c.6326C>A (p.Pro2109His)
c.3933C>A (n.3933C>A)
c.1610C>A (p.Pro537His)
n.1545C>A
c.1613C>A (p.Pro538His)
c.5934C>A
c.6392C>A (p.Pro2131His)
c.704+612C>A (n.704+612C>A)
c.3714C>A
c.6116C>A (p.Pro2039His)
c.5828C>A (p.Pro1943His)
c.3356C>A (p.Pro1119His)
19g.35732941C=CA2333794571KMT2Bn.698C=
c.6326C= (p.Pro2109=)
c.3933C= (n.3933C=)
c.1610C= (p.Pro537=)
n.1545C=
c.1613C= (p.Pro538=)
c.5934C=
c.6392C= (p.Pro2131=)
c.704+612C= (n.704+612C=)
c.3714C=
c.6116C= (p.Pro2039=)
c.5828C= (p.Pro1943=)
c.3356C= (p.Pro1119=)
19g.35732941C>GCA405428226KMT2Bn.698C>G
c.6326C>G (p.Pro2109Arg)
c.3933C>G (n.3933C>G)
c.1610C>G (p.Pro537Arg)
n.1545C>G
c.1613C>G (p.Pro538Arg)
c.5934C>G
c.6392C>G (p.Pro2131Arg)
c.704+612C>G (n.704+612C>G)
c.3714C>G
c.6116C>G (p.Pro2039Arg)
c.5828C>G (p.Pro1943Arg)
c.3356C>G (p.Pro1119Arg)
 ClinVar dbSNP gnomAD v3 gnomAD v4
19g.35732941C>TCA405428229KMT2Bn.698C>T
c.6326C>T (p.Pro2109Leu)
c.3933C>T (n.3933C>T)
c.1610C>T (p.Pro537Leu)
n.1545C>T
c.1613C>T (p.Pro538Leu)
c.5934C>T
c.6392C>T (p.Pro2131Leu)
c.704+612C>T (n.704+612C>T)
c.3714C>T
c.6116C>T (p.Pro2039Leu)
c.5828C>T (p.Pro1943Leu)
c.3356C>T (p.Pro1119Leu)
 gnomAD v4
19g.35732942T>ACA507308761KMT2Bn.699T>A
c.6327T>A (p.Pro2109=)
c.3934T>A (n.3934T>A)
c.1611T>A (p.Pro537=)
n.1546T>A
c.1614T>A (p.Pro538=)
c.5935T>A
c.6393T>A (p.Pro2131=)
c.704+613T>A (n.704+613T>A)
c.3715T>A
c.6117T>A (p.Pro2039=)
c.5829T>A (p.Pro1943=)
c.3357T>A (p.Pro1119=)
19g.35732942T>CCA507308764KMT2Bn.699T>C
c.6327T>C (p.Pro2109=)
c.3934T>C (n.3934T>C)
c.1611T>C (p.Pro537=)
n.1546T>C
c.1614T>C (p.Pro538=)
c.5935T>C
c.6393T>C (p.Pro2131=)
c.704+613T>C (n.704+613T>C)
c.3715T>C
c.6117T>C (p.Pro2039=)
c.5829T>C (p.Pro1943=)
c.3357T>C (p.Pro1119=)
 gnomAD v4
19g.35732942T>GCA507308765KMT2Bn.699T>G
c.6327T>G (p.Pro2109=)
c.3934T>G (n.3934T>G)
c.1611T>G (p.Pro537=)
n.1546T>G
c.1614T>G (p.Pro538=)
c.5935T>G
c.6393T>G (p.Pro2131=)
c.704+613T>G (n.704+613T>G)
c.3715T>G
c.6117T>G (p.Pro2039=)
c.5829T>G (p.Pro1943=)
c.3357T>G (p.Pro1119=)
19g.35732943A>CCA507308769KMT2Bn.700A>C
c.6328A>C (p.Arg2110=)
c.3935A>C (n.3935A>C)
c.1612A>C (p.Arg538=)
n.1547A>C
c.1615A>C (p.Arg539=)
c.5936A>C
c.6394A>C (p.Arg2132=)
c.704+614A>C (n.704+614A>C)
c.3716A>C
c.6118A>C (p.Arg2040=)
c.5830A>C (p.Arg1944=)
c.3358A>C (p.Arg1120=)
19g.35732943A>GCA405428233KMT2Bn.700A>G
c.6328A>G (p.Arg2110Gly)
c.3935A>G (n.3935A>G)
c.1612A>G (p.Arg538Gly)
n.1547A>G
c.1615A>G (p.Arg539Gly)
c.5936A>G
c.6394A>G (p.Arg2132Gly)
c.704+614A>G (n.704+614A>G)
c.3716A>G
c.6118A>G (p.Arg2040Gly)
c.5830A>G (p.Arg1944Gly)
c.3358A>G (p.Arg1120Gly)
19g.35732943A>TCA405428234KMT2Bn.700A>T
c.6328A>T (p.Arg2110Ter)
c.3935A>T (n.3935A>T)
c.1612A>T (p.Arg538Ter)
n.1547A>T
c.1615A>T (p.Arg539Ter)
c.5936A>T
c.6394A>T (p.Arg2132Ter)
c.704+614A>T (n.704+614A>T)
c.3716A>T
c.6118A>T (p.Arg2040Ter)
c.5830A>T (p.Arg1944Ter)
c.3358A>T (p.Arg1120Ter)
19g.35732944G>ACA9385677KMT2Bn.701G>A
c.6329G>A (p.Arg2110Lys)
c.3936G>A (n.3936G>A)
c.1613G>A (p.Arg538Lys)
n.1548G>A
c.1616G>A (p.Arg539Lys)
c.5937G>A
c.6395G>A (p.Arg2132Lys)
c.704+615G>A (n.704+615G>A)
c.3717G>A
c.6119G>A (p.Arg2040Lys)
c.5831G>A (p.Arg1944Lys)
c.3359G>A (p.Arg1120Lys)
 dbSNP ExAC gnomAD v2
19g.35732944G>CCA405428237KMT2Bn.701G>C
c.6329G>C (p.Arg2110Thr)
c.3936G>C (n.3936G>C)
c.1613G>C (p.Arg538Thr)
n.1548G>C
c.1616G>C (p.Arg539Thr)
c.5937G>C
c.6395G>C (p.Arg2132Thr)
c.704+615G>C (n.704+615G>C)
c.3717G>C
c.6119G>C (p.Arg2040Thr)
c.5831G>C (p.Arg1944Thr)
c.3359G>C (p.Arg1120Thr)
19g.35732944G=CA2333794572KMT2Bn.701G=
c.6329G= (p.Arg2110=)
c.3936G= (n.3936G=)
c.1613G= (p.Arg538=)
n.1548G=
c.1616G= (p.Arg539=)
c.5937G=
c.6395G= (p.Arg2132=)
c.704+615G= (n.704+615G=)
c.3717G=
c.6119G= (p.Arg2040=)
c.5831G= (p.Arg1944=)
c.3359G= (p.Arg1120=)
19g.35732944G>TCA405428241KMT2Bn.701G>T
c.6329G>T (p.Arg2110Ile)
c.3936G>T (n.3936G>T)
c.1613G>T (p.Arg538Ile)
n.1548G>T
c.1616G>T (p.Arg539Ile)
c.5937G>T
c.6395G>T (p.Arg2132Ile)
c.704+615G>T (n.704+615G>T)
c.3717G>T
c.6119G>T (p.Arg2040Ile)
c.5831G>T (p.Arg1944Ile)
c.3359G>T (p.Arg1120Ile)
 gnomAD v4
19g.35732945A>CCA405428244KMT2Bn.702A>C
c.6330A>C (p.Arg2110Ser)
c.3937A>C (n.3937A>C)
c.1614A>C (p.Arg538Ser)
n.1549A>C
c.1617A>C (p.Arg539Ser)
c.5938A>C
c.6396A>C (p.Arg2132Ser)
c.704+616A>C (n.704+616A>C)
c.3718A>C
c.6120A>C (p.Arg2040Ser)
c.5832A>C (p.Arg1944Ser)
c.3360A>C (p.Arg1120Ser)
19g.35732945A>GCA507308770KMT2Bn.702A>G
c.6330A>G (p.Arg2110=)
c.3937A>G (n.3937A>G)
c.1614A>G (p.Arg538=)
n.1549A>G
c.1617A>G (p.Arg539=)
c.5938A>G
c.6396A>G (p.Arg2132=)
c.704+616A>G (n.704+616A>G)
c.3718A>G
c.6120A>G (p.Arg2040=)
c.5832A>G (p.Arg1944=)
c.3360A>G (p.Arg1120=)
19g.35732945A>TCA405428246KMT2Bn.702A>T
c.6330A>T (p.Arg2110Ser)
c.3937A>T (n.3937A>T)
c.1614A>T (p.Arg538Ser)
n.1549A>T
c.1617A>T (p.Arg539Ser)
c.5938A>T
c.6396A>T (p.Arg2132Ser)
c.704+616A>T (n.704+616A>T)
c.3718A>T
c.6120A>T (p.Arg2040Ser)
c.5832A>T (p.Arg1944Ser)
c.3360A>T (p.Arg1120Ser)
19g.35732946G>ACA405428250KMT2Bn.703G>A
c.6331G>A (p.Glu2111Lys)
c.3938G>A (n.3938G>A)
c.1615G>A (p.Glu539Lys)
n.1550G>A
c.1618G>A (p.Glu540Lys)
c.5939G>A
c.6397G>A (p.Glu2133Lys)
c.704+617G>A (n.704+617G>A)
c.3719G>A
c.6121G>A (p.Glu2041Lys)
c.5833G>A (p.Glu1945Lys)
c.3361G>A (p.Glu1121Lys)
19g.35732946G>CCA405428253KMT2Bn.703G>C
c.6331G>C (p.Glu2111Gln)
c.3938G>C (n.3938G>C)
c.1615G>C (p.Glu539Gln)
n.1550G>C
c.1618G>C (p.Glu540Gln)
c.5939G>C
c.6397G>C (p.Glu2133Gln)
c.704+617G>C (n.704+617G>C)
c.3719G>C
c.6121G>C (p.Glu2041Gln)
c.5833G>C (p.Glu1945Gln)
c.3361G>C (p.Glu1121Gln)
19g.35732946G>TCA405428255KMT2Bn.703G>T
c.6331G>T (p.Glu2111Ter)
c.3938G>T (n.3938G>T)
c.1615G>T (p.Glu539Ter)
n.1550G>T
c.1618G>T (p.Glu540Ter)
c.5939G>T
c.6397G>T (p.Glu2133Ter)
c.704+617G>T (n.704+617G>T)
c.3719G>T
c.6121G>T (p.Glu2041Ter)
c.5833G>T (p.Glu1945Ter)
c.3361G>T (p.Glu1121Ter)
19g.35732949_35732951delCA2814254940KMT2Bn.706_708del
c.6334_6336del (p.Glu2112del)
c.3941_3943del (n.3941_3943del)
c.1618_1620del (p.Glu540del)
n.1553_1555del
c.1621_1623del (p.Glu541del)
c.5942_5944del
c.6400_6402del (p.Glu2134del)
c.704+620_704+622del (n.704+620_704+622del)
c.3722_3724del
c.6124_6126del (p.Glu2042del)
c.5836_5838del (p.Glu1946del)
c.3364_3366del (p.Glu1122del)
19g.35732947A=CA2333794573KMT2Bn.704A=
c.6332A= (p.Glu2111=)
c.3939A= (n.3939A=)
c.1616A= (p.Glu539=)
n.1551A=
c.1619A= (p.Glu540=)
c.5940A=
c.6398A= (p.Glu2133=)
c.704+618A= (n.704+618A=)
c.3720A=
c.6122A= (p.Glu2041=)
c.5834A= (p.Glu1945=)
c.3362A= (p.Glu1121=)
19g.35732947A>CCA405428259KMT2Bn.704A>C
c.6332A>C (p.Glu2111Ala)
c.3939A>C (n.3939A>C)
c.1616A>C (p.Glu539Ala)
n.1551A>C
c.1619A>C (p.Glu540Ala)
c.5940A>C
c.6398A>C (p.Glu2133Ala)
c.704+618A>C (n.704+618A>C)
c.3720A>C
c.6122A>C (p.Glu2041Ala)
c.5834A>C (p.Glu1945Ala)
c.3362A>C (p.Glu1121Ala)
19g.35732947A>GCA405428262KMT2Bn.704A>G
c.6332A>G (p.Glu2111Gly)
c.3939A>G (n.3939A>G)
c.1616A>G (p.Glu539Gly)
n.1551A>G
c.1619A>G (p.Glu540Gly)
c.5940A>G
c.6398A>G (p.Glu2133Gly)
c.704+618A>G (n.704+618A>G)
c.3720A>G
c.6122A>G (p.Glu2041Gly)
c.5834A>G (p.Glu1945Gly)
c.3362A>G (p.Glu1121Gly)
 dbSNP
19g.35732947A>TCA405428265KMT2Bn.704A>T
c.6332A>T (p.Glu2111Val)
c.3939A>T (n.3939A>T)
c.1616A>T (p.Glu539Val)
n.1551A>T
c.1619A>T (p.Glu540Val)
c.5940A>T
c.6398A>T (p.Glu2133Val)
c.704+618A>T (n.704+618A>T)
c.3720A>T
c.6122A>T (p.Glu2041Val)
c.5834A>T (p.Glu1945Val)
c.3362A>T (p.Glu1121Val)
19g.35732948G>ACA507308788KMT2Bn.705G>A
c.6333G>A (p.Glu2111=)
c.3940G>A (n.3940G>A)
c.1617G>A (p.Glu539=)
n.1552G>A
c.1620G>A (p.Glu540=)
c.5941G>A
c.6399G>A (p.Glu2133=)
c.704+619G>A (n.704+619G>A)
c.3721G>A
c.6123G>A (p.Glu2041=)
c.5835G>A (p.Glu1945=)
c.3363G>A (p.Glu1121=)
 gnomAD v4
19g.35732948G>CCA405428269KMT2Bn.705G>C
c.6333G>C (p.Glu2111Asp)
c.3940G>C (n.3940G>C)
c.1617G>C (p.Glu539Asp)
n.1552G>C
c.1620G>C (p.Glu540Asp)
c.5941G>C
c.6399G>C (p.Glu2133Asp)
c.704+619G>C (n.704+619G>C)
c.3721G>C
c.6123G>C (p.Glu2041Asp)
c.5835G>C (p.Glu1945Asp)
c.3363G>C (p.Glu1121Asp)
19g.35732948G>TCA405428272KMT2Bn.705G>T
c.6333G>T (p.Glu2111Asp)
c.3940G>T (n.3940G>T)
c.1617G>T (p.Glu539Asp)
n.1552G>T
c.1620G>T (p.Glu540Asp)
c.5941G>T
c.6399G>T (p.Glu2133Asp)
c.704+619G>T (n.704+619G>T)
c.3721G>T
c.6123G>T (p.Glu2041Asp)
c.5835G>T (p.Glu1945Asp)
c.3363G>T (p.Glu1121Asp)
 gnomAD v4
19g.35732949G>ACA405428275KMT2Bn.706G>A
c.6334G>A (p.Glu2112Lys)
c.3941G>A (n.3941G>A)
c.1618G>A (p.Glu540Lys)
n.1553G>A
c.1621G>A (p.Glu541Lys)
c.5942G>A
c.6400G>A (p.Glu2134Lys)
c.704+620G>A (n.704+620G>A)
c.3722G>A
c.6124G>A (p.Glu2042Lys)
c.5836G>A (p.Glu1946Lys)
c.3364G>A (p.Glu1122Lys)
 gnomAD v4
19g.35732949G>CCA405428281KMT2Bn.706G>C
c.6334G>C (p.Glu2112Gln)
c.3941G>C (n.3941G>C)
c.1618G>C (p.Glu540Gln)
n.1553G>C
c.1621G>C (p.Glu541Gln)
c.5942G>C
c.6400G>C (p.Glu2134Gln)
c.704+620G>C (n.704+620G>C)
c.3722G>C
c.6124G>C (p.Glu2042Gln)
c.5836G>C (p.Glu1946Gln)
c.3364G>C (p.Glu1122Gln)
 dbSNP gnomAD v2 gnomAD v4
19g.35732949G=CA2333794574KMT2Bn.706G=
c.6334G= (p.Glu2112=)
c.3941G= (n.3941G=)
c.1618G= (p.Glu540=)
n.1553G=
c.1621G= (p.Glu541=)
c.5942G=
c.6400G= (p.Glu2134=)
c.704+620G= (n.704+620G=)
c.3722G=
c.6124G= (p.Glu2042=)
c.5836G= (p.Glu1946=)
c.3364G= (p.Glu1122=)
19g.35732949G>TCA405428278KMT2Bn.706G>T
c.6334G>T (p.Glu2112Ter)
c.3941G>T (n.3941G>T)
c.1618G>T (p.Glu540Ter)
n.1553G>T
c.1621G>T (p.Glu541Ter)
c.5942G>T
c.6400G>T (p.Glu2134Ter)
c.704+620G>T (n.704+620G>T)
c.3722G>T
c.6124G>T (p.Glu2042Ter)
c.5836G>T (p.Glu1946Ter)
c.3364G>T (p.Glu1122Ter)
 COSMIC
19g.35732950A>CCA405428285KMT2Bn.707A>C
c.6335A>C (p.Glu2112Ala)
c.3942A>C (n.3942A>C)
c.1619A>C (p.Glu540Ala)
n.1554A>C
c.1622A>C (p.Glu541Ala)
c.5943A>C
c.6401A>C (p.Glu2134Ala)
c.704+621A>C (n.704+621A>C)
c.3723A>C
c.6125A>C (p.Glu2042Ala)
c.5837A>C (p.Glu1946Ala)
c.3365A>C (p.Glu1122Ala)
19g.35732950A>GCA405428288KMT2Bn.707A>G
c.6335A>G (p.Glu2112Gly)
c.3942A>G (n.3942A>G)
c.1619A>G (p.Glu540Gly)
n.1554A>G
c.1622A>G (p.Glu541Gly)
c.5943A>G
c.6401A>G (p.Glu2134Gly)
c.704+621A>G (n.704+621A>G)
c.3723A>G
c.6125A>G (p.Glu2042Gly)
c.5837A>G (p.Glu1946Gly)
c.3365A>G (p.Glu1122Gly)
19g.35732950A>TCA405428291KMT2Bn.707A>T
c.6335A>T (p.Glu2112Val)
c.3942A>T (n.3942A>T)
c.1619A>T (p.Glu540Val)
n.1554A>T
c.1622A>T (p.Glu541Val)
c.5943A>T
c.6401A>T (p.Glu2134Val)
c.704+621A>T (n.704+621A>T)
c.3723A>T
c.6125A>T (p.Glu2042Val)
c.5837A>T (p.Glu1946Val)
c.3365A>T (p.Glu1122Val)
19g.35732951G>ACA507308799KMT2Bn.708G>A
c.6336G>A (p.Glu2112=)
c.3943G>A (n.3943G>A)
c.1620G>A (p.Glu540=)
n.1555G>A
c.1623G>A (p.Glu541=)
c.5944G>A
c.6402G>A (p.Glu2134=)
c.704+622G>A (n.704+622G>A)
c.3724G>A
c.6126G>A (p.Glu2042=)
c.5838G>A (p.Glu1946=)
c.3366G>A (p.Glu1122=)
19g.35732951G>CCA405428295KMT2Bn.708G>C
c.6336G>C (p.Glu2112Asp)
c.3943G>C (n.3943G>C)
c.1620G>C (p.Glu540Asp)
n.1555G>C
c.1623G>C (p.Glu541Asp)
c.5944G>C
c.6402G>C (p.Glu2134Asp)
c.704+622G>C (n.704+622G>C)
c.3724G>C
c.6126G>C (p.Glu2042Asp)
c.5838G>C (p.Glu1946Asp)
c.3366G>C (p.Glu1122Asp)
19g.35732951G>TCA405428298KMT2Bn.708G>T
c.6336G>T (p.Glu2112Asp)
c.3943G>T (n.3943G>T)
c.1620G>T (p.Glu540Asp)
n.1555G>T
c.1623G>T (p.Glu541Asp)
c.5944G>T
c.6402G>T (p.Glu2134Asp)
c.704+622G>T (n.704+622G>T)
c.3724G>T
c.6126G>T (p.Glu2042Asp)
c.5838G>T (p.Glu1946Asp)
c.3366G>T (p.Glu1122Asp)
19g.35732952T>ACA405428302KMT2Bn.709T>A
c.6337T>A (p.Ser2113Thr)
c.3944T>A (n.3944T>A)
c.1621T>A (p.Ser541Thr)
n.1556T>A
c.1624T>A (p.Ser542Thr)
c.5945T>A
c.6403T>A (p.Ser2135Thr)
c.704+623T>A (n.704+623T>A)
c.3725T>A
c.6127T>A (p.Ser2043Thr)
c.5839T>A (p.Ser1947Thr)
c.3367T>A (p.Ser1123Thr)
19g.35732952T>CCA405428303KMT2Bn.709T>C
c.6337T>C (p.Ser2113Pro)
c.3944T>C (n.3944T>C)
c.1621T>C (p.Ser541Pro)
n.1556T>C
c.1624T>C (p.Ser542Pro)
c.5945T>C
c.6403T>C (p.Ser2135Pro)
c.704+623T>C (n.704+623T>C)
c.3725T>C
c.6127T>C (p.Ser2043Pro)
c.5839T>C (p.Ser1947Pro)
c.3367T>C (p.Ser1123Pro)
19g.35732952T>GCA405428307KMT2Bn.709T>G
c.6337T>G (p.Ser2113Ala)
c.3944T>G (n.3944T>G)
c.1621T>G (p.Ser541Ala)
n.1556T>G
c.1624T>G (p.Ser542Ala)
c.5945T>G
c.6403T>G (p.Ser2135Ala)
c.704+623T>G (n.704+623T>G)
c.3725T>G
c.6127T>G (p.Ser2043Ala)
c.5839T>G (p.Ser1947Ala)
c.3367T>G (p.Ser1123Ala)
19g.35732953C>ACA405428311KMT2Bn.710C>A
c.6338C>A (p.Ser2113Ter)
c.3945C>A (n.3945C>A)
c.1622C>A (p.Ser541Ter)
n.1557C>A
c.1625C>A (p.Ser542Ter)
c.5946C>A
c.6404C>A (p.Ser2135Ter)
c.704+624C>A (n.704+624C>A)
c.3726C>A
c.6128C>A (p.Ser2043Ter)
c.5840C>A (p.Ser1947Ter)
c.3368C>A (p.Ser1123Ter)
19g.35732953C>GCA405428312KMT2Bn.710C>G
c.6338C>G (p.Ser2113Ter)
c.3945C>G (n.3945C>G)
c.1622C>G (p.Ser541Ter)
n.1557C>G
c.1625C>G (p.Ser542Ter)
c.5946C>G
c.6404C>G (p.Ser2135Ter)
c.704+624C>G (n.704+624C>G)
c.3726C>G
c.6128C>G (p.Ser2043Ter)
c.5840C>G (p.Ser1947Ter)
c.3368C>G (p.Ser1123Ter)
19g.35732953C>TCA405428316KMT2Bn.710C>T
c.6338C>T (p.Ser2113Leu)
c.3945C>T (n.3945C>T)
c.1622C>T (p.Ser541Leu)
n.1557C>T
c.1625C>T (p.Ser542Leu)
c.5946C>T
c.6404C>T (p.Ser2135Leu)
c.704+624C>T (n.704+624C>T)
c.3726C>T
c.6128C>T (p.Ser2043Leu)
c.5840C>T (p.Ser1947Leu)
c.3368C>T (p.Ser1123Leu)
19g.35732954A=CA2333794575KMT2Bn.711A=
c.6339A= (p.Ser2113=)
c.3946A= (n.3946A=)
c.1623A= (p.Ser541=)
n.1558A=
c.1626A= (p.Ser542=)
c.5947A=
c.6405A= (p.Ser2135=)
c.704+625A= (n.704+625A=)
c.3727A=
c.6129A= (p.Ser2043=)
c.5841A= (p.Ser1947=)
c.3369A= (p.Ser1123=)
19g.35732954A>CCA507308803KMT2Bn.711A>C
c.6339A>C (p.Ser2113=)
c.3946A>C (n.3946A>C)
c.1623A>C (p.Ser541=)
n.1558A>C
c.1626A>C (p.Ser542=)
c.5947A>C
c.6405A>C (p.Ser2135=)
c.704+625A>C (n.704+625A>C)
c.3727A>C
c.6129A>C (p.Ser2043=)
c.5841A>C (p.Ser1947=)
c.3369A>C (p.Ser1123=)
19g.35732954A>GCA9385678KMT2Bn.711A>G
c.6339A>G (p.Ser2113=)
c.3946A>G (n.3946A>G)
c.1623A>G (p.Ser541=)
n.1558A>G
c.1626A>G (p.Ser542=)
c.5947A>G
c.6405A>G (p.Ser2135=)
c.704+625A>G (n.704+625A>G)
c.3727A>G
c.6129A>G (p.Ser2043=)
c.5841A>G (p.Ser1947=)
c.3369A>G (p.Ser1123=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.35732954A>TCA507308807KMT2Bn.711A>T
c.6339A>T (p.Ser2113=)
c.3946A>T (n.3946A>T)
c.1623A>T (p.Ser541=)
n.1558A>T
c.1626A>T (p.Ser542=)
c.5947A>T
c.6405A>T (p.Ser2135=)
c.704+625A>T (n.704+625A>T)
c.3727A>T
c.6129A>T (p.Ser2043=)
c.5841A>T (p.Ser1947=)
c.3369A>T (p.Ser1123=)
19g.35732954_35732955delinsACCA2333794576KMT2Bn.711_712delinsAC
c.6339_6340delinsAC (p.Ser2113=)
c.3946_3947delinsAC (n.3946_3947delinsAC)
c.1623_1624delinsAC (p.Ser541=)
n.1558_1559delinsAC
c.1626_1627delinsAC (p.Ser542=)
c.5947_5948delinsAC
c.6405_6406delinsAC (p.Ser2135=)
c.704+625_704+626delinsAC (n.704+625_704+626delinsAC)
c.3727_3728delinsAC
c.6129_6130delinsAC (p.Ser2043=)
c.5841_5842delinsAC (p.Ser1947=)
c.3369_3370delinsAC (p.Ser1123=)
19g.35732955delCA16043946KMT2Bn.712del
c.6340del (p.Leu2114SerfsTer17)
c.3947del (n.3947del)
c.1624del (p.Leu542SerfsTer17)
n.1559del
c.1627del (p.Leu543SerfsTer17)
c.5948del
c.6406del (p.Leu2136SerfsTer17)
c.704+626del (n.704+626del)
c.3728del
c.6130del (p.Leu2044SerfsTer17)
c.5842del (p.Leu1948SerfsTer17)
c.3370del (p.Leu1124SerfsTer17)
 ClinVar dbSNP
19g.35732955C>ACA405428329KMT2Bn.712C>A
c.6340C>A (p.Leu2114Ile)
c.3947C>A (n.3947C>A)
c.1624C>A (p.Leu542Ile)
n.1559C>A
c.1627C>A (p.Leu543Ile)
c.5948C>A
c.6406C>A (p.Leu2136Ile)
c.704+626C>A (n.704+626C>A)
c.3728C>A
c.6130C>A (p.Leu2044Ile)
c.5842C>A (p.Leu1948Ile)
c.3370C>A (p.Leu1124Ile)
19g.35732955C>GCA405428327KMT2Bn.712C>G
c.6340C>G (p.Leu2114Val)
c.3947C>G (n.3947C>G)
c.1624C>G (p.Leu542Val)
n.1559C>G
c.1627C>G (p.Leu543Val)
c.5948C>G
c.6406C>G (p.Leu2136Val)
c.704+626C>G (n.704+626C>G)
c.3728C>G
c.6130C>G (p.Leu2044Val)
c.5842C>G (p.Leu1948Val)
c.3370C>G (p.Leu1124Val)
19g.35732955C>TCA405428324KMT2Bn.712C>T
c.6340C>T (p.Leu2114Phe)
c.3947C>T (n.3947C>T)
c.1624C>T (p.Leu542Phe)
n.1559C>T
c.1627C>T (p.Leu543Phe)
c.5948C>T
c.6406C>T (p.Leu2136Phe)
c.704+626C>T (n.704+626C>T)
c.3728C>T
c.6130C>T (p.Leu2044Phe)
c.5842C>T (p.Leu1948Phe)
c.3370C>T (p.Leu1124Phe)
 gnomAD v4
19g.35732956T>ACA405428332KMT2Bn.713T>A
c.6341T>A (p.Leu2114His)
c.3948T>A (n.3948T>A)
c.1625T>A (p.Leu542His)
n.1560T>A
c.1628T>A (p.Leu543His)
c.5949T>A
c.6407T>A (p.Leu2136His)
c.704+627T>A (n.704+627T>A)
c.3729T>A
c.6131T>A (p.Leu2044His)
c.5843T>A (p.Leu1948His)
c.3371T>A (p.Leu1124His)
 COSMIC
19g.35732956T>CCA405428335KMT2Bn.713T>C
c.6341T>C (p.Leu2114Pro)
c.3948T>C (n.3948T>C)
c.1625T>C (p.Leu542Pro)
n.1560T>C
c.1628T>C (p.Leu543Pro)
c.5949T>C
c.6407T>C (p.Leu2136Pro)
c.704+627T>C (n.704+627T>C)
c.3729T>C
c.6131T>C (p.Leu2044Pro)
c.5843T>C (p.Leu1948Pro)
c.3371T>C (p.Leu1124Pro)
 gnomAD v4
19g.35732956T>GCA405428337KMT2Bn.713T>G
c.6341T>G (p.Leu2114Arg)
c.3948T>G (n.3948T>G)
c.1625T>G (p.Leu542Arg)
n.1560T>G
c.1628T>G (p.Leu543Arg)
c.5949T>G
c.6407T>G (p.Leu2136Arg)
c.704+627T>G (n.704+627T>G)
c.3729T>G
c.6131T>G (p.Leu2044Arg)
c.5843T>G (p.Leu1948Arg)
c.3371T>G (p.Leu1124Arg)
 gnomAD v4
19g.35732956T=CA2333794577KMT2Bn.713T=
c.6341T= (p.Leu2114=)
c.3948T= (n.3948T=)
c.1625T= (p.Leu542=)
n.1560T=
c.1628T= (p.Leu543=)
c.5949T=
c.6407T= (p.Leu2136=)
c.704+627T= (n.704+627T=)
c.3729T=
c.6131T= (p.Leu2044=)
c.5843T= (p.Leu1948=)
c.3371T= (p.Leu1124=)
19g.35732957C>ACA507308829KMT2Bn.714C>A
c.6342C>A (p.Leu2114=)
c.3949C>A (n.3949C>A)
c.1626C>A (p.Leu542=)
n.1561C>A
c.1629C>A (p.Leu543=)
c.5950C>A
c.6408C>A (p.Leu2136=)
c.704+628C>A (n.704+628C>A)
c.3730C>A
c.6132C>A (p.Leu2044=)
c.5844C>A (p.Leu1948=)
c.3372C>A (p.Leu1124=)
19g.35732957C=CA2333794578KMT2Bn.714C=
c.6342C= (p.Leu2114=)
c.3949C= (n.3949C=)
c.1626C= (p.Leu542=)
n.1561C=
c.1629C= (p.Leu543=)
c.5950C=
c.6408C= (p.Leu2136=)
c.704+628C= (n.704+628C=)
c.3730C=
c.6132C= (p.Leu2044=)
c.5844C= (p.Leu1948=)
c.3372C= (p.Leu1124=)
19g.35732957C>GCA507308831KMT2Bn.714C>G
c.6342C>G (p.Leu2114=)
c.3949C>G (n.3949C>G)
c.1626C>G (p.Leu542=)
n.1561C>G
c.1629C>G (p.Leu543=)
c.5950C>G
c.6408C>G (p.Leu2136=)
c.704+628C>G (n.704+628C>G)
c.3730C>G
c.6132C>G (p.Leu2044=)
c.5844C>G (p.Leu1948=)
c.3372C>G (p.Leu1124=)
 dbSNP
19g.35732957C>TCA507308832KMT2Bn.714C>T
c.6342C>T (p.Leu2114=)
c.3949C>T (n.3949C>T)
c.1626C>T (p.Leu542=)
n.1561C>T
c.1629C>T (p.Leu543=)
c.5950C>T
c.6408C>T (p.Leu2136=)
c.704+628C>T (n.704+628C>T)
c.3730C>T
c.6132C>T (p.Leu2044=)
c.5844C>T (p.Leu1948=)
c.3372C>T (p.Leu1124=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
19g.35732962dupCA9385679KMT2Bn.719dup
c.6347dup (p.Ala2117GlyfsTer6)
c.3954dup (n.3954dup)
c.1631dup (p.Ala545GlyfsTer6)
n.1566dup
c.1634dup (p.Ala546GlyfsTer6)
c.5955dup
c.6413dup (p.Ala2139GlyfsTer6)
c.704+633dup (n.704+633dup)
c.3735dup
c.6137dup (p.Ala2047GlyfsTer6)
c.5849dup (p.Ala1951GlyfsTer6)
c.3377dup (p.Ala1127GlyfsTer6)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.35732962delCA645604595KMT2Bn.719del
c.6347del (p.Pro2116ArgfsTer15)
c.3954del (n.3954del)
c.1631del (p.Pro544ArgfsTer15)
n.1566del
c.1634del (p.Pro545ArgfsTer15)
c.5955del
c.6413del (p.Pro2138ArgfsTer15)
c.704+633del (n.704+633del)
c.3735del
c.6137del (p.Pro2046ArgfsTer15)
c.5849del (p.Pro1950ArgfsTer15)
c.3377del (p.Pro1126ArgfsTer15)
 gnomAD v4 COSMIC
19g.35732958C>ACA405428343KMT2Bn.715C>A
c.6343C>A (p.Pro2115Thr)
c.3950C>A (n.3950C>A)
c.1627C>A (p.Pro543Thr)
n.1562C>A
c.1630C>A (p.Pro544Thr)
c.5951C>A
c.6409C>A (p.Pro2137Thr)
c.704+629C>A (n.704+629C>A)
c.3731C>A
c.6133C>A (p.Pro2045Thr)
c.5845C>A (p.Pro1949Thr)
c.3373C>A (p.Pro1125Thr)
 gnomAD v4
19g.35732958C=CA2333794579KMT2Bn.715C=
c.6343C= (p.Pro2115=)
c.3950C= (n.3950C=)
c.1627C= (p.Pro543=)
n.1562C=
c.1630C= (p.Pro544=)
c.5951C=
c.6409C= (p.Pro2137=)
c.704+629C= (n.704+629C=)
c.3731C=
c.6133C= (p.Pro2045=)
c.5845C= (p.Pro1949=)
c.3373C= (p.Pro1125=)
19g.35732958C>GCA405428345KMT2Bn.715C>G
c.6343C>G (p.Pro2115Ala)
c.3950C>G (n.3950C>G)
c.1627C>G (p.Pro543Ala)
n.1562C>G
c.1630C>G (p.Pro544Ala)
c.5951C>G
c.6409C>G (p.Pro2137Ala)
c.704+629C>G (n.704+629C>G)
c.3731C>G
c.6133C>G (p.Pro2045Ala)
c.5845C>G (p.Pro1949Ala)
c.3373C>G (p.Pro1125Ala)
 ClinVar gnomAD v4
19g.35732958C>TCA9385680KMT2Bn.715C>T
c.6343C>T (p.Pro2115Ser)
c.3950C>T (n.3950C>T)
c.1627C>T (p.Pro543Ser)
n.1562C>T
c.1630C>T (p.Pro544Ser)
c.5951C>T
c.6409C>T (p.Pro2137Ser)
c.704+629C>T (n.704+629C>T)
c.3731C>T
c.6133C>T (p.Pro2045Ser)
c.5845C>T (p.Pro1949Ser)
c.3373C>T (p.Pro1125Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732959C>ACA405428351KMT2Bn.716C>A
c.6344C>A (p.Pro2115His)
c.3951C>A (n.3951C>A)
c.1628C>A (p.Pro543His)
n.1563C>A
c.1631C>A (p.Pro544His)
c.5952C>A
c.6410C>A (p.Pro2137His)
c.704+630C>A (n.704+630C>A)
c.3732C>A
c.6134C>A (p.Pro2045His)
c.5846C>A (p.Pro1949His)
c.3374C>A (p.Pro1125His)
19g.35732959C>GCA405428353KMT2Bn.716C>G
c.6344C>G (p.Pro2115Arg)
c.3951C>G (n.3951C>G)
c.1628C>G (p.Pro543Arg)
n.1563C>G
c.1631C>G (p.Pro544Arg)
c.5952C>G
c.6410C>G (p.Pro2137Arg)
c.704+630C>G (n.704+630C>G)
c.3732C>G
c.6134C>G (p.Pro2045Arg)
c.5846C>G (p.Pro1949Arg)
c.3374C>G (p.Pro1125Arg)
19g.35732959C>TCA405428355KMT2Bn.716C>T
c.6344C>T (p.Pro2115Leu)
c.3951C>T (n.3951C>T)
c.1628C>T (p.Pro543Leu)
n.1563C>T
c.1631C>T (p.Pro544Leu)
c.5952C>T
c.6410C>T (p.Pro2137Leu)
c.704+630C>T (n.704+630C>T)
c.3732C>T
c.6134C>T (p.Pro2045Leu)
c.5846C>T (p.Pro1949Leu)
c.3374C>T (p.Pro1125Leu)
19g.35732960C>ACA9385681KMT2Bn.717C>A
c.6345C>A (p.Pro2115=)
c.3952C>A (n.3952C>A)
c.1629C>A (p.Pro543=)
n.1564C>A
c.1632C>A (p.Pro544=)
c.5953C>A
c.6411C>A (p.Pro2137=)
c.704+631C>A (n.704+631C>A)
c.3733C>A
c.6135C>A (p.Pro2045=)
c.5847C>A (p.Pro1949=)
c.3375C>A (p.Pro1125=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732960C=CA2333794580KMT2Bn.717C=
c.6345C= (p.Pro2115=)
c.3952C= (n.3952C=)
c.1629C= (p.Pro543=)
n.1564C=
c.1632C= (p.Pro544=)
c.5953C=
c.6411C= (p.Pro2137=)
c.704+631C= (n.704+631C=)
c.3733C=
c.6135C= (p.Pro2045=)
c.5847C= (p.Pro1949=)
c.3375C= (p.Pro1125=)
19g.35732960C>GCA507308847KMT2Bn.717C>G
c.6345C>G (p.Pro2115=)
c.3952C>G (n.3952C>G)
c.1629C>G (p.Pro543=)
n.1564C>G
c.1632C>G (p.Pro544=)
c.5953C>G
c.6411C>G (p.Pro2137=)
c.704+631C>G (n.704+631C>G)
c.3733C>G
c.6135C>G (p.Pro2045=)
c.5847C>G (p.Pro1949=)
c.3375C>G (p.Pro1125=)
 dbSNP gnomAD v3 gnomAD v4
19g.35732960C>TCA507308845KMT2Bn.717C>T
c.6345C>T (p.Pro2115=)
c.3952C>T (n.3952C>T)
c.1629C>T (p.Pro543=)
n.1564C>T
c.1632C>T (p.Pro544=)
c.5953C>T
c.6411C>T (p.Pro2137=)
c.704+631C>T (n.704+631C>T)
c.3733C>T
c.6135C>T (p.Pro2045=)
c.5847C>T (p.Pro1949=)
c.3375C>T (p.Pro1125=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.35732961C>ACA9385682KMT2Bn.718C>A
c.6346C>A (p.Pro2116Thr)
c.3953C>A (n.3953C>A)
c.1630C>A (p.Pro544Thr)
n.1565C>A
c.1633C>A (p.Pro545Thr)
c.5954C>A
c.6412C>A (p.Pro2138Thr)
c.704+632C>A (n.704+632C>A)
c.3734C>A
c.6136C>A (p.Pro2046Thr)
c.5848C>A (p.Pro1950Thr)
c.3376C>A (p.Pro1126Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732961C=CA2333794581KMT2Bn.718C=
c.6346C= (p.Pro2116=)
c.3953C= (n.3953C=)
c.1630C= (p.Pro544=)
n.1565C=
c.1633C= (p.Pro545=)
c.5954C=
c.6412C= (p.Pro2138=)
c.704+632C= (n.704+632C=)
c.3734C=
c.6136C= (p.Pro2046=)
c.5848C= (p.Pro1950=)
c.3376C= (p.Pro1126=)
19g.35732961C>GCA405428363KMT2Bn.718C>G
c.6346C>G (p.Pro2116Ala)
c.3953C>G (n.3953C>G)
c.1630C>G (p.Pro544Ala)
n.1565C>G
c.1633C>G (p.Pro545Ala)
c.5954C>G
c.6412C>G (p.Pro2138Ala)
c.704+632C>G (n.704+632C>G)
c.3734C>G
c.6136C>G (p.Pro2046Ala)
c.5848C>G (p.Pro1950Ala)
c.3376C>G (p.Pro1126Ala)
19g.35732961C>TCA405428360KMT2Bn.718C>T
c.6346C>T (p.Pro2116Ser)
c.3953C>T (n.3953C>T)
c.1630C>T (p.Pro544Ser)
n.1565C>T
c.1633C>T (p.Pro545Ser)
c.5954C>T
c.6412C>T (p.Pro2138Ser)
c.704+632C>T (n.704+632C>T)
c.3734C>T
c.6136C>T (p.Pro2046Ser)
c.5848C>T (p.Pro1950Ser)
c.3376C>T (p.Pro1126Ser)
 dbSNP gnomAD v3 gnomAD v4
19g.35732962C>ACA9385683KMT2Bn.719C>A
c.6347C>A (p.Pro2116Gln)
c.3954C>A (n.3954C>A)
c.1631C>A (p.Pro544Gln)
n.1566C>A
c.1634C>A (p.Pro545Gln)
c.5955C>A
c.6413C>A (p.Pro2138Gln)
c.704+633C>A (n.704+633C>A)
c.3735C>A
c.6137C>A (p.Pro2046Gln)
c.5849C>A (p.Pro1950Gln)
c.3377C>A (p.Pro1126Gln)
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.35732962C=CA2333794582KMT2Bn.719C=
c.6347C= (p.Pro2116=)
c.3954C= (n.3954C=)
c.1631C= (p.Pro544=)
n.1566C=
c.1634C= (p.Pro545=)
c.5955C=
c.6413C= (p.Pro2138=)
c.704+633C= (n.704+633C=)
c.3735C=
c.6137C= (p.Pro2046=)
c.5849C= (p.Pro1950=)
c.3377C= (p.Pro1126=)
19g.35732962C>GCA9385685KMT2Bn.719C>G
c.6347C>G (p.Pro2116Arg)
c.3954C>G (n.3954C>G)
c.1631C>G (p.Pro544Arg)
n.1566C>G
c.1634C>G (p.Pro545Arg)
c.5955C>G
c.6413C>G (p.Pro2138Arg)
c.704+633C>G (n.704+633C>G)
c.3735C>G
c.6137C>G (p.Pro2046Arg)
c.5849C>G (p.Pro1950Arg)
c.3377C>G (p.Pro1126Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732962C>TCA9385684KMT2Bn.719C>T
c.6347C>T (p.Pro2116Leu)
c.3954C>T (n.3954C>T)
c.1631C>T (p.Pro544Leu)
n.1566C>T
c.1634C>T (p.Pro545Leu)
c.5955C>T
c.6413C>T (p.Pro2138Leu)
c.704+633C>T (n.704+633C>T)
c.3735C>T
c.6137C>T (p.Pro2046Leu)
c.5849C>T (p.Pro1950Leu)
c.3377C>T (p.Pro1126Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732963G>ACA9385686KMT2Bn.720G>A
c.6348G>A (p.Pro2116=)
c.3955G>A (n.3955G>A)
c.1632G>A (p.Pro544=)
n.1567G>A
c.1635G>A (p.Pro545=)
c.5956G>A
c.6414G>A (p.Pro2138=)
c.705-634G>A (n.705-634G>A)
c.3736G>A
c.6138G>A (p.Pro2046=)
c.5850G>A (p.Pro1950=)
c.3378G>A (p.Pro1126=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732963G>CCA507308861KMT2Bn.720G>C
c.6348G>C (p.Pro2116=)
c.3955G>C (n.3955G>C)
c.1632G>C (p.Pro544=)
n.1567G>C
c.1635G>C (p.Pro545=)
c.5956G>C
c.6414G>C (p.Pro2138=)
c.705-634G>C (n.705-634G>C)
c.3736G>C
c.6138G>C (p.Pro2046=)
c.5850G>C (p.Pro1950=)
c.3378G>C (p.Pro1126=)
19g.35732963G=CA2333794583KMT2Bn.720G=
c.6348G= (p.Pro2116=)
c.3955G= (n.3955G=)
c.1632G= (p.Pro544=)
n.1567G=
c.1635G= (p.Pro545=)
c.5956G=
c.6414G= (p.Pro2138=)
c.705-634G= (n.705-634G=)
c.3736G=
c.6138G= (p.Pro2046=)
c.5850G= (p.Pro1950=)
c.3378G= (p.Pro1126=)
19g.35732963G>TCA507308864KMT2Bn.720G>T
c.6348G>T (p.Pro2116=)
c.3955G>T (n.3955G>T)
c.1632G>T (p.Pro544=)
n.1567G>T
c.1635G>T (p.Pro545=)
c.5956G>T
c.6414G>T (p.Pro2138=)
c.705-634G>T (n.705-634G>T)
c.3736G>T
c.6138G>T (p.Pro2046=)
c.5850G>T (p.Pro1950=)
c.3378G>T (p.Pro1126=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.35732964G>ACA405428380KMT2Bn.721G>A
c.6349G>A (p.Ala2117Thr)
c.3956G>A (n.3956G>A)
c.1633G>A (p.Ala545Thr)
n.1568G>A
c.1636G>A (p.Ala546Thr)
c.5957G>A
c.6415G>A (p.Ala2139Thr)
c.705-633G>A (n.705-633G>A)
c.3737G>A
c.6139G>A (p.Ala2047Thr)
c.5851G>A (p.Ala1951Thr)
c.3379G>A (p.Ala1127Thr)
19g.35732964G>CCA405428377KMT2Bn.721G>C
c.6349G>C (p.Ala2117Pro)
c.3956G>C (n.3956G>C)
c.1633G>C (p.Ala545Pro)
n.1568G>C
c.1636G>C (p.Ala546Pro)
c.5957G>C
c.6415G>C (p.Ala2139Pro)
c.705-633G>C (n.705-633G>C)
c.3737G>C
c.6139G>C (p.Ala2047Pro)
c.5851G>C (p.Ala1951Pro)
c.3379G>C (p.Ala1127Pro)
19g.35732964G=CA2333794584KMT2Bn.721G=
c.6349G= (p.Ala2117=)
c.3956G= (n.3956G=)
c.1633G= (p.Ala545=)
n.1568G=
c.1636G= (p.Ala546=)
c.5957G=
c.6415G= (p.Ala2139=)
c.705-633G= (n.705-633G=)
c.3737G=
c.6139G= (p.Ala2047=)
c.5851G= (p.Ala1951=)
c.3379G= (p.Ala1127=)
19g.35732964G>TCA405428382KMT2Bn.721G>T
c.6349G>T (p.Ala2117Ser)
c.3956G>T (n.3956G>T)
c.1633G>T (p.Ala545Ser)
n.1568G>T
c.1636G>T (p.Ala546Ser)
c.5957G>T
c.6415G>T (p.Ala2139Ser)
c.705-633G>T (n.705-633G>T)
c.3737G>T
c.6139G>T (p.Ala2047Ser)
c.5851G>T (p.Ala1951Ser)
c.3379G>T (p.Ala1127Ser)
 dbSNP gnomAD v3 gnomAD v4
19g.35732965C>ACA405428387KMT2Bn.722C>A
c.6350C>A (p.Ala2117Glu)
c.3957C>A (n.3957C>A)
c.1634C>A (p.Ala545Glu)
n.1569C>A
c.1637C>A (p.Ala546Glu)
c.5958C>A
c.6416C>A (p.Ala2139Glu)
c.705-632C>A (n.705-632C>A)
c.3738C>A
c.6140C>A (p.Ala2047Glu)
c.5852C>A (p.Ala1951Glu)
c.3380C>A (p.Ala1127Glu)
 gnomAD v4
19g.35732965C=CA2333794585KMT2Bn.722C=
c.6350C= (p.Ala2117=)
c.3957C= (n.3957C=)
c.1634C= (p.Ala545=)
n.1569C=
c.1637C= (p.Ala546=)
c.5958C=
c.6416C= (p.Ala2139=)
c.705-632C= (n.705-632C=)
c.3738C=
c.6140C= (p.Ala2047=)
c.5852C= (p.Ala1951=)
c.3380C= (p.Ala1127=)
19g.35732965C>GCA405428388KMT2Bn.722C>G
c.6350C>G (p.Ala2117Gly)
c.3957C>G (n.3957C>G)
c.1634C>G (p.Ala545Gly)
n.1569C>G
c.1637C>G (p.Ala546Gly)
c.5958C>G
c.6416C>G (p.Ala2139Gly)
c.705-632C>G (n.705-632C>G)
c.3738C>G
c.6140C>G (p.Ala2047Gly)
c.5852C>G (p.Ala1951Gly)
c.3380C>G (p.Ala1127Gly)
 dbSNP gnomAD v2
19g.35732965C>TCA405428390KMT2Bn.722C>T
c.6350C>T (p.Ala2117Val)
c.3957C>T (n.3957C>T)
c.1634C>T (p.Ala545Val)
n.1569C>T
c.1637C>T (p.Ala546Val)
c.5958C>T
c.6416C>T (p.Ala2139Val)
c.705-632C>T (n.705-632C>T)
c.3738C>T
c.6140C>T (p.Ala2047Val)
c.5852C>T (p.Ala1951Val)
c.3380C>T (p.Ala1127Val)
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.35732966G>ACA507308873KMT2Bn.723G>A
c.6351G>A (p.Ala2117=)
c.3958G>A (n.3958G>A)
c.1635G>A (p.Ala545=)
n.1570G>A
c.1638G>A (p.Ala546=)
c.5959G>A
c.6417G>A (p.Ala2139=)
c.705-631G>A (n.705-631G>A)
c.3739G>A
c.6141G>A (p.Ala2047=)
c.5853G>A (p.Ala1951=)
c.3381G>A (p.Ala1127=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.35732966G>CCA507308884KMT2Bn.723G>C
c.6351G>C (p.Ala2117=)
c.3958G>C (n.3958G>C)
c.1635G>C (p.Ala545=)
n.1570G>C
c.1638G>C (p.Ala546=)
c.5959G>C
c.6417G>C (p.Ala2139=)
c.705-631G>C (n.705-631G>C)
c.3739G>C
c.6141G>C (p.Ala2047=)
c.5853G>C (p.Ala1951=)
c.3381G>C (p.Ala1127=)
19g.35732966G=CA2333794586KMT2Bn.723G=
c.6351G= (p.Ala2117=)
c.3958G= (n.3958G=)
c.1635G= (p.Ala545=)
n.1570G=
c.1638G= (p.Ala546=)
c.5959G=
c.6417G= (p.Ala2139=)
c.705-631G= (n.705-631G=)
c.3739G=
c.6141G= (p.Ala2047=)
c.5853G= (p.Ala1951=)
c.3381G= (p.Ala1127=)
19g.35732966G>TCA507308882KMT2Bn.723G>T
c.6351G>T (p.Ala2117=)
c.3958G>T (n.3958G>T)
c.1635G>T (p.Ala545=)
n.1570G>T
c.1638G>T (p.Ala546=)
c.5959G>T
c.6417G>T (p.Ala2139=)
c.705-631G>T (n.705-631G>T)
c.3739G>T
c.6141G>T (p.Ala2047=)
c.5853G>T (p.Ala1951=)
c.3381G>T (p.Ala1127=)
 dbSNP gnomAD v3 gnomAD v4
19g.35732967C>ACA405428393KMT2Bn.724C>A
c.6352C>A (p.Pro2118Thr)
c.3959C>A (n.3959C>A)
c.1636C>A (p.Pro546Thr)
n.1571C>A
c.1639C>A (p.Pro547Thr)
c.5960C>A
c.6418C>A (p.Pro2140Thr)
c.705-630C>A (n.705-630C>A)
c.3740C>A
c.6142C>A (p.Pro2048Thr)
c.5854C>A (p.Pro1952Thr)
c.3382C>A (p.Pro1128Thr)
19g.35732967C>GCA405428396KMT2Bn.724C>G
c.6352C>G (p.Pro2118Ala)
c.3959C>G (n.3959C>G)
c.1636C>G (p.Pro546Ala)
n.1571C>G
c.1639C>G (p.Pro547Ala)
c.5960C>G
c.6418C>G (p.Pro2140Ala)
c.705-630C>G (n.705-630C>G)
c.3740C>G
c.6142C>G (p.Pro2048Ala)
c.5854C>G (p.Pro1952Ala)
c.3382C>G (p.Pro1128Ala)
19g.35732967C>TCA405428399KMT2Bn.724C>T
c.6352C>T (p.Pro2118Ser)
c.3959C>T (n.3959C>T)
c.1636C>T (p.Pro546Ser)
n.1571C>T
c.1639C>T (p.Pro547Ser)
c.5960C>T
c.6418C>T (p.Pro2140Ser)
c.705-630C>T (n.705-630C>T)
c.3740C>T
c.6142C>T (p.Pro2048Ser)
c.5854C>T (p.Pro1952Ser)
c.3382C>T (p.Pro1128Ser)
19g.35732968C>ACA405428401KMT2Bn.725C>A
c.6353C>A (p.Pro2118His)
c.3960C>A (n.3960C>A)
c.1637C>A (p.Pro546His)
n.1572C>A
c.1640C>A (p.Pro547His)
c.5961C>A
c.6419C>A (p.Pro2140His)
c.705-629C>A (n.705-629C>A)
c.3741C>A
c.6143C>A (p.Pro2048His)
c.5855C>A (p.Pro1952His)
c.3383C>A (p.Pro1128His)
19g.35732968C>GCA405428403KMT2Bn.725C>G
c.6353C>G (p.Pro2118Arg)
c.3960C>G (n.3960C>G)
c.1637C>G (p.Pro546Arg)
n.1572C>G
c.1640C>G (p.Pro547Arg)
c.5961C>G
c.6419C>G (p.Pro2140Arg)
c.705-629C>G (n.705-629C>G)
c.3741C>G
c.6143C>G (p.Pro2048Arg)
c.5855C>G (p.Pro1952Arg)
c.3383C>G (p.Pro1128Arg)
19g.35732968C>TCA405428406KMT2Bn.725C>T
c.6353C>T (p.Pro2118Leu)
c.3960C>T (n.3960C>T)
c.1637C>T (p.Pro546Leu)
n.1572C>T
c.1640C>T (p.Pro547Leu)
c.5961C>T
c.6419C>T (p.Pro2140Leu)
c.705-629C>T (n.705-629C>T)
c.3741C>T
c.6143C>T (p.Pro2048Leu)
c.5855C>T (p.Pro1952Leu)
c.3383C>T (p.Pro1128Leu)
19g.35732969T>ACA507308892KMT2Bn.726T>A
c.6354T>A (p.Pro2118=)
c.3961T>A (n.3961T>A)
c.1638T>A (p.Pro546=)
n.1573T>A
c.1641T>A (p.Pro547=)
c.5962T>A
c.6420T>A (p.Pro2140=)
c.705-628T>A (n.705-628T>A)
c.3742T>A
c.6144T>A (p.Pro2048=)
c.5856T>A (p.Pro1952=)
c.3384T>A (p.Pro1128=)
 gnomAD v4
19g.35732969T>CCA507308894KMT2Bn.726T>C
c.6354T>C (p.Pro2118=)
c.3961T>C (n.3961T>C)
c.1638T>C (p.Pro546=)
n.1573T>C
c.1641T>C (p.Pro547=)
c.5962T>C
c.6420T>C (p.Pro2140=)
c.705-628T>C (n.705-628T>C)
c.3742T>C
c.6144T>C (p.Pro2048=)
c.5856T>C (p.Pro1952=)
c.3384T>C (p.Pro1128=)
 dbSNP gnomAD v4
19g.35732969T>GCA507308897KMT2Bn.726T>G
c.6354T>G (p.Pro2118=)
c.3961T>G (n.3961T>G)
c.1638T>G (p.Pro546=)
n.1573T>G
c.1641T>G (p.Pro547=)
c.5962T>G
c.6420T>G (p.Pro2140=)
c.705-628T>G (n.705-628T>G)
c.3742T>G
c.6144T>G (p.Pro2048=)
c.5856T>G (p.Pro1952=)
c.3384T>G (p.Pro1128=)
19g.35732969T=CA2333794587KMT2Bn.726T=
c.6354T= (p.Pro2118=)
c.3961T= (n.3961T=)
c.1638T= (p.Pro546=)
n.1573T=
c.1641T= (p.Pro547=)
c.5962T=
c.6420T= (p.Pro2140=)
c.705-628T= (n.705-628T=)
c.3742T=
c.6144T= (p.Pro2048=)
c.5856T= (p.Pro1952=)
c.3384T= (p.Pro1128=)
19g.35732970C>ACA405428410KMT2Bn.727C>A
c.6355C>A (p.Pro2119Thr)
c.3962C>A (n.3962C>A)
c.1639C>A (p.Pro547Thr)
n.1574C>A
c.1642C>A (p.Pro548Thr)
c.5963C>A
c.6421C>A (p.Pro2141Thr)
c.705-627C>A (n.705-627C>A)
c.3743C>A
c.6145C>A (p.Pro2049Thr)
c.5857C>A (p.Pro1953Thr)
c.3385C>A (p.Pro1129Thr)
 gnomAD v4
19g.35732970C=CA2333794588KMT2Bn.727C=
c.6355C= (p.Pro2119=)
c.3962C= (n.3962C=)
c.1639C= (p.Pro547=)
n.1574C=
c.1642C= (p.Pro548=)
c.5963C=
c.6421C= (p.Pro2141=)
c.705-627C= (n.705-627C=)
c.3743C=
c.6145C= (p.Pro2049=)
c.5857C= (p.Pro1953=)
c.3385C= (p.Pro1129=)
19g.35732970C>GCA405428412KMT2Bn.727C>G
c.6355C>G (p.Pro2119Ala)
c.3962C>G (n.3962C>G)
c.1639C>G (p.Pro547Ala)
n.1574C>G
c.1642C>G (p.Pro548Ala)
c.5963C>G
c.6421C>G (p.Pro2141Ala)
c.705-627C>G (n.705-627C>G)
c.3743C>G
c.6145C>G (p.Pro2049Ala)
c.5857C>G (p.Pro1953Ala)
c.3385C>G (p.Pro1129Ala)
 dbSNP gnomAD v3 gnomAD v4
19g.35732970C>TCA405428414KMT2Bn.727C>T
c.6355C>T (p.Pro2119Ser)
c.3962C>T (n.3962C>T)
c.1639C>T (p.Pro547Ser)
n.1574C>T
c.1642C>T (p.Pro548Ser)
c.5963C>T
c.6421C>T (p.Pro2141Ser)
c.705-627C>T (n.705-627C>T)
c.3743C>T
c.6145C>T (p.Pro2049Ser)
c.5857C>T (p.Pro1953Ser)
c.3385C>T (p.Pro1129Ser)
 gnomAD v4
19g.35732973delCA2584575163KMT2Bn.730del
c.6358del (p.Leu2120TrpfsTer11)
c.3965del (n.3965del)
c.1642del (p.Leu548TrpfsTer11)
n.1577del
c.1645del (p.Leu549TrpfsTer11)
c.5966del
c.6424del (p.Leu2142TrpfsTer11)
c.705-624del (n.705-624del)
c.3746del
c.6148del (p.Leu2050TrpfsTer11)
c.5860del (p.Leu1954TrpfsTer11)
c.3388del (p.Leu1130TrpfsTer11)
 gnomAD v4
19g.35732971C>ACA405428424KMT2Bn.728C>A
c.6356C>A (p.Pro2119His)
c.3963C>A (n.3963C>A)
c.1640C>A (p.Pro547His)
n.1575C>A
c.1643C>A (p.Pro548His)
c.5964C>A
c.6422C>A (p.Pro2141His)
c.705-626C>A (n.705-626C>A)
c.3744C>A
c.6146C>A (p.Pro2049His)
c.5858C>A (p.Pro1953His)
c.3386C>A (p.Pro1129His)
 gnomAD v4
19g.35732971C=CA2333794589KMT2Bn.728C=
c.6356C= (p.Pro2119=)
c.3963C= (n.3963C=)
c.1640C= (p.Pro547=)
n.1575C=
c.1643C= (p.Pro548=)
c.5964C=
c.6422C= (p.Pro2141=)
c.705-626C= (n.705-626C=)
c.3744C=
c.6146C= (p.Pro2049=)
c.5858C= (p.Pro1953=)
c.3386C= (p.Pro1129=)
19g.35732971C>GCA405428419KMT2Bn.728C>G
c.6356C>G (p.Pro2119Arg)
c.3963C>G (n.3963C>G)
c.1640C>G (p.Pro547Arg)
n.1575C>G
c.1643C>G (p.Pro548Arg)
c.5964C>G
c.6422C>G (p.Pro2141Arg)
c.705-626C>G (n.705-626C>G)
c.3744C>G
c.6146C>G (p.Pro2049Arg)
c.5858C>G (p.Pro1953Arg)
c.3386C>G (p.Pro1129Arg)
 dbSNP
19g.35732971C>TCA405428420KMT2Bn.728C>T
c.6356C>T (p.Pro2119Leu)
c.3963C>T (n.3963C>T)
c.1640C>T (p.Pro547Leu)
n.1575C>T
c.1643C>T (p.Pro548Leu)
c.5964C>T
c.6422C>T (p.Pro2141Leu)
c.705-626C>T (n.705-626C>T)
c.3744C>T
c.6146C>T (p.Pro2049Leu)
c.5858C>T (p.Pro1953Leu)
c.3386C>T (p.Pro1129Leu)
19g.35732972C>ACA507308902KMT2Bn.729C>A
c.6357C>A (p.Pro2119=)
c.3964C>A (n.3964C>A)
c.1641C>A (p.Pro547=)
n.1576C>A
c.1644C>A (p.Pro548=)
c.5965C>A
c.6423C>A (p.Pro2141=)
c.705-625C>A (n.705-625C>A)
c.3745C>A
c.6147C>A (p.Pro2049=)
c.5859C>A (p.Pro1953=)
c.3387C>A (p.Pro1129=)
 gnomAD v4
19g.35732972C>GCA507308904KMT2Bn.729C>G
c.6357C>G (p.Pro2119=)
c.3964C>G (n.3964C>G)
c.1641C>G (p.Pro547=)
n.1576C>G
c.1644C>G (p.Pro548=)
c.5965C>G
c.6423C>G (p.Pro2141=)
c.705-625C>G (n.705-625C>G)
c.3745C>G
c.6147C>G (p.Pro2049=)
c.5859C>G (p.Pro1953=)
c.3387C>G (p.Pro1129=)
19g.35732972C>TCA507308905KMT2Bn.729C>T
c.6357C>T (p.Pro2119=)
c.3964C>T (n.3964C>T)
c.1641C>T (p.Pro547=)
n.1576C>T
c.1644C>T (p.Pro548=)
c.5965C>T
c.6423C>T (p.Pro2141=)
c.705-625C>T (n.705-625C>T)
c.3745C>T
c.6147C>T (p.Pro2049=)
c.5859C>T (p.Pro1953=)
c.3387C>T (p.Pro1129=)
19g.35732973C>ACA405428427KMT2Bn.730C>A
c.6358C>A (p.Leu2120Met)
c.3965C>A (n.3965C>A)
c.1642C>A (p.Leu548Met)
n.1577C>A
c.1645C>A (p.Leu549Met)
c.5966C>A
c.6424C>A (p.Leu2142Met)
c.705-624C>A (n.705-624C>A)
c.3746C>A
c.6148C>A (p.Leu2050Met)
c.5860C>A (p.Leu1954Met)
c.3388C>A (p.Leu1130Met)
 gnomAD v4
19g.35732973C=CA2333794590KMT2Bn.730C=
c.6358C= (p.Leu2120=)
c.3965C= (n.3965C=)
c.1642C= (p.Leu548=)
n.1577C=
c.1645C= (p.Leu549=)
c.5966C=
c.6424C= (p.Leu2142=)
c.705-624C= (n.705-624C=)
c.3746C=
c.6148C= (p.Leu2050=)
c.5860C= (p.Leu1954=)
c.3388C= (p.Leu1130=)
19g.35732973C>GCA405428429KMT2Bn.730C>G
c.6358C>G (p.Leu2120Val)
c.3965C>G (n.3965C>G)
c.1642C>G (p.Leu548Val)
n.1577C>G
c.1645C>G (p.Leu549Val)
c.5966C>G
c.6424C>G (p.Leu2142Val)
c.705-624C>G (n.705-624C>G)
c.3746C>G
c.6148C>G (p.Leu2050Val)
c.5860C>G (p.Leu1954Val)
c.3388C>G (p.Leu1130Val)
 gnomAD v4
19g.35732973C>TCA507308908KMT2Bn.730C>T
c.6358C>T (p.Leu2120=)
c.3965C>T (n.3965C>T)
c.1642C>T (p.Leu548=)
n.1577C>T
c.1645C>T (p.Leu549=)
c.5966C>T
c.6424C>T (p.Leu2142=)
c.705-624C>T (n.705-624C>T)
c.3746C>T
c.6148C>T (p.Leu2050=)
c.5860C>T (p.Leu1954=)
c.3388C>T (p.Leu1130=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.35732974T>ACA405428431KMT2Bn.731T>A
c.6359T>A (p.Leu2120Gln)
c.3966T>A (n.3966T>A)
c.1643T>A (p.Leu548Gln)
n.1578T>A
c.1646T>A (p.Leu549Gln)
c.5967T>A
c.6425T>A (p.Leu2142Gln)
c.705-623T>A (n.705-623T>A)
c.3747T>A
c.6149T>A (p.Leu2050Gln)
c.5861T>A (p.Leu1954Gln)
c.3389T>A (p.Leu1130Gln)
 gnomAD v4
19g.35732974T>CCA405428434KMT2Bn.731T>C
c.6359T>C (p.Leu2120Pro)
c.3966T>C (n.3966T>C)
c.1643T>C (p.Leu548Pro)
n.1578T>C
c.1646T>C (p.Leu549Pro)
c.5967T>C
c.6425T>C (p.Leu2142Pro)
c.705-623T>C (n.705-623T>C)
c.3747T>C
c.6149T>C (p.Leu2050Pro)
c.5861T>C (p.Leu1954Pro)
c.3389T>C (p.Leu1130Pro)
 ClinVar gnomAD v4
19g.35732974T>GCA405428437KMT2Bn.731T>G
c.6359T>G (p.Leu2120Arg)
c.3966T>G (n.3966T>G)
c.1643T>G (p.Leu548Arg)
n.1578T>G
c.1646T>G (p.Leu549Arg)
c.5967T>G
c.6425T>G (p.Leu2142Arg)
c.705-623T>G (n.705-623T>G)
c.3747T>G
c.6149T>G (p.Leu2050Arg)
c.5861T>G (p.Leu1954Arg)
c.3389T>G (p.Leu1130Arg)
19g.35732975G>ACA507308912KMT2Bn.732G>A
c.6360G>A (p.Leu2120=)
c.3967G>A (n.3967G>A)
c.1644G>A (p.Leu548=)
n.1579G>A
c.1647G>A (p.Leu549=)
c.5968G>A
c.6426G>A (p.Leu2142=)
c.705-622G>A (n.705-622G>A)
c.3748G>A
c.6150G>A (p.Leu2050=)
c.5862G>A (p.Leu1954=)
c.3390G>A (p.Leu1130=)
 gnomAD v4
19g.35732975G>CCA507308913KMT2Bn.732G>C
c.6360G>C (p.Leu2120=)
c.3967G>C (n.3967G>C)
c.1644G>C (p.Leu548=)
n.1579G>C
c.1647G>C (p.Leu549=)
c.5968G>C
c.6426G>C (p.Leu2142=)
c.705-622G>C (n.705-622G>C)
c.3748G>C
c.6150G>C (p.Leu2050=)
c.5862G>C (p.Leu1954=)
c.3390G>C (p.Leu1130=)
19g.35732975G>TCA507308914KMT2Bn.732G>T
c.6360G>T (p.Leu2120=)
c.3967G>T (n.3967G>T)
c.1644G>T (p.Leu548=)
n.1579G>T
c.1647G>T (p.Leu549=)
c.5968G>T
c.6426G>T (p.Leu2142=)
c.705-622G>T (n.705-622G>T)
c.3748G>T
c.6150G>T (p.Leu2050=)
c.5862G>T (p.Leu1954=)
c.3390G>T (p.Leu1130=)
19g.35732976G>ACA405428440KMT2Bn.733G>A
c.6361G>A (p.Ala2121Thr)
c.3968G>A (n.3968G>A)
c.1645G>A (p.Ala549Thr)
n.1580G>A
c.1648G>A (p.Ala550Thr)
c.5969G>A
c.6427G>A (p.Ala2143Thr)
c.705-621G>A (n.705-621G>A)
c.3749G>A
c.6151G>A (p.Ala2051Thr)
c.5863G>A (p.Ala1955Thr)
c.3391G>A (p.Ala1131Thr)
 dbSNP gnomAD v2
19g.35732976G>CCA9385687KMT2Bn.733G>C
c.6361G>C (p.Ala2121Pro)
c.3968G>C (n.3968G>C)
c.1645G>C (p.Ala549Pro)
n.1580G>C
c.1648G>C (p.Ala550Pro)
c.5969G>C
c.6427G>C (p.Ala2143Pro)
c.705-621G>C (n.705-621G>C)
c.3749G>C
c.6151G>C (p.Ala2051Pro)
c.5863G>C (p.Ala1955Pro)
c.3391G>C (p.Ala1131Pro)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.35732976G=CA2333794591KMT2Bn.733G=
c.6361G= (p.Ala2121=)
c.3968G= (n.3968G=)
c.1645G= (p.Ala549=)
n.1580G=
c.1648G= (p.Ala550=)
c.5969G=
c.6427G= (p.Ala2143=)
c.705-621G= (n.705-621G=)
c.3749G=
c.6151G= (p.Ala2051=)
c.5863G= (p.Ala1955=)
c.3391G= (p.Ala1131=)
19g.35732976G>TCA405428445KMT2Bn.733G>T
c.6361G>T (p.Ala2121Ser)
c.3968G>T (n.3968G>T)
c.1645G>T (p.Ala549Ser)
n.1580G>T
c.1648G>T (p.Ala550Ser)
c.5969G>T
c.6427G>T (p.Ala2143Ser)
c.705-621G>T (n.705-621G>T)
c.3749G>T
c.6151G>T (p.Ala2051Ser)
c.5863G>T (p.Ala1955Ser)
c.3391G>T (p.Ala1131Ser)
 gnomAD v4
19g.35732977C>ACA307796795KMT2Bn.734C>A
c.6362C>A (p.Ala2121Asp)
c.3969C>A (n.3969C>A)
c.1646C>A (p.Ala549Asp)
n.1581C>A
c.1649C>A (p.Ala550Asp)
c.5970C>A
c.6428C>A (p.Ala2143Asp)
c.705-620C>A (n.705-620C>A)
c.3750C>A
c.6152C>A (p.Ala2051Asp)
c.5864C>A (p.Ala1955Asp)
c.3392C>A (p.Ala1131Asp)
 dbSNP gnomAD v4
19g.35732977C=CA2333794592KMT2Bn.734C=
c.6362C= (p.Ala2121=)
c.3969C= (n.3969C=)
c.1646C= (p.Ala549=)
n.1581C=
c.1649C= (p.Ala550=)
c.5970C=
c.6428C= (p.Ala2143=)
c.705-620C= (n.705-620C=)
c.3750C=
c.6152C= (p.Ala2051=)
c.5864C= (p.Ala1955=)
c.3392C= (p.Ala1131=)
19g.35732977C>GCA405428447KMT2Bn.734C>G
c.6362C>G (p.Ala2121Gly)
c.3969C>G (n.3969C>G)
c.1646C>G (p.Ala549Gly)
n.1581C>G
c.1649C>G (p.Ala550Gly)
c.5970C>G
c.6428C>G (p.Ala2143Gly)
c.705-620C>G (n.705-620C>G)
c.3750C>G
c.6152C>G (p.Ala2051Gly)
c.5864C>G (p.Ala1955Gly)
c.3392C>G (p.Ala1131Gly)
 gnomAD v4
19g.35732977C>TCA405428452KMT2Bn.734C>T
c.6362C>T (p.Ala2121Val)
c.3969C>T (n.3969C>T)
c.1646C>T (p.Ala549Val)
n.1581C>T
c.1649C>T (p.Ala550Val)
c.5970C>T
c.6428C>T (p.Ala2143Val)
c.705-620C>T (n.705-620C>T)
c.3750C>T
c.6152C>T (p.Ala2051Val)
c.5864C>T (p.Ala1955Val)
c.3392C>T (p.Ala1131Val)
 dbSNP gnomAD v4
19g.35732978T>ACA507308920KMT2Bn.735T>A
c.6363T>A (p.Ala2121=)
c.3970T>A (n.3970T>A)
c.1647T>A (p.Ala549=)
n.1582T>A
c.1650T>A (p.Ala550=)
c.5971T>A
c.6429T>A (p.Ala2143=)
c.705-619T>A (n.705-619T>A)
c.3751T>A
c.6153T>A (p.Ala2051=)
c.5865T>A (p.Ala1955=)
c.3393T>A (p.Ala1131=)
19g.35732978T>CCA507308922KMT2Bn.735T>C
c.6363T>C (p.Ala2121=)
c.3970T>C (n.3970T>C)
c.1647T>C (p.Ala549=)
n.1582T>C
c.1650T>C (p.Ala550=)
c.5971T>C
c.6429T>C (p.Ala2143=)
c.705-619T>C (n.705-619T>C)
c.3751T>C
c.6153T>C (p.Ala2051=)
c.5865T>C (p.Ala1955=)
c.3393T>C (p.Ala1131=)
 dbSNP gnomAD v2 gnomAD v4
19g.35732978T>GCA507308924KMT2Bn.735T>G
c.6363T>G (p.Ala2121=)
c.3970T>G (n.3970T>G)
c.1647T>G (p.Ala549=)
n.1582T>G
c.1650T>G (p.Ala550=)
c.5971T>G
c.6429T>G (p.Ala2143=)
c.705-619T>G (n.705-619T>G)
c.3751T>G
c.6153T>G (p.Ala2051=)
c.5865T>G (p.Ala1955=)
c.3393T>G (p.Ala1131=)
19g.35732978T=CA2333794593KMT2Bn.735T=
c.6363T= (p.Ala2121=)
c.3970T= (n.3970T=)
c.1647T= (p.Ala549=)
n.1582T=
c.1650T= (p.Ala550=)
c.5971T=
c.6429T= (p.Ala2143=)
c.705-619T= (n.705-619T=)
c.3751T=
c.6153T= (p.Ala2051=)
c.5865T= (p.Ala1955=)
c.3393T= (p.Ala1131=)
19g.35732979A=CA2333794594KMT2Bn.736A=
c.6364A= (p.Asn2122=)
c.3971A= (n.3971A=)
c.1648A= (p.Asn550=)
n.1583A=
c.1651A= (p.Asn551=)
c.5972A=
c.6430A= (p.Asn2144=)
c.705-618A= (n.705-618A=)
c.3752A=
c.6154A= (p.Asn2052=)
c.5866A= (p.Asn1956=)
c.3394A= (p.Asn1132=)
19g.35732979A>CCA405428458KMT2Bn.736A>C
c.6364A>C (p.Asn2122His)
c.3971A>C (n.3971A>C)
c.1648A>C (p.Asn550His)
n.1583A>C
c.1651A>C (p.Asn551His)
c.5972A>C
c.6430A>C (p.Asn2144His)
c.705-618A>C (n.705-618A>C)
c.3752A>C
c.6154A>C (p.Asn2052His)
c.5866A>C (p.Asn1956His)
c.3394A>C (p.Asn1132His)
19g.35732979A>GCA405428456KMT2Bn.736A>G
c.6364A>G (p.Asn2122Asp)
c.3971A>G (n.3971A>G)
c.1648A>G (p.Asn550Asp)
n.1583A>G
c.1651A>G (p.Asn551Asp)
c.5972A>G
c.6430A>G (p.Asn2144Asp)
c.705-618A>G (n.705-618A>G)
c.3752A>G
c.6154A>G (p.Asn2052Asp)
c.5866A>G (p.Asn1956Asp)
c.3394A>G (p.Asn1132Asp)
 dbSNP gnomAD v4
19g.35732979A>TCA405428454KMT2Bn.736A>T
c.6364A>T (p.Asn2122Tyr)
c.3971A>T (n.3971A>T)
c.1648A>T (p.Asn550Tyr)
n.1583A>T
c.1651A>T (p.Asn551Tyr)
c.5972A>T
c.6430A>T (p.Asn2144Tyr)
c.705-618A>T (n.705-618A>T)
c.3752A>T
c.6154A>T (p.Asn2052Tyr)
c.5866A>T (p.Asn1956Tyr)
c.3394A>T (p.Asn1132Tyr)
19g.35732980A>CCA405428461KMT2Bn.737A>C
c.6365A>C (p.Asn2122Thr)
c.3972A>C (n.3972A>C)
c.1649A>C (p.Asn550Thr)
n.1584A>C
c.1652A>C (p.Asn551Thr)
c.5973A>C
c.6431A>C (p.Asn2144Thr)
c.705-617A>C (n.705-617A>C)
c.3753A>C
c.6155A>C (p.Asn2052Thr)
c.5867A>C (p.Asn1956Thr)
c.3395A>C (p.Asn1132Thr)
19g.35732980A>GCA405428462KMT2Bn.737A>G
c.6365A>G (p.Asn2122Ser)
c.3972A>G (n.3972A>G)
c.1649A>G (p.Asn550Ser)
n.1584A>G
c.1652A>G (p.Asn551Ser)
c.5973A>G
c.6431A>G (p.Asn2144Ser)
c.705-617A>G (n.705-617A>G)
c.3753A>G
c.6155A>G (p.Asn2052Ser)
c.5867A>G (p.Asn1956Ser)
c.3395A>G (p.Asn1132Ser)
19g.35732980A>TCA405428465KMT2Bn.737A>T
c.6365A>T (p.Asn2122Ile)
c.3972A>T (n.3972A>T)
c.1649A>T (p.Asn550Ile)
n.1584A>T
c.1652A>T (p.Asn551Ile)
c.5973A>T
c.6431A>T (p.Asn2144Ile)
c.705-617A>T (n.705-617A>T)
c.3753A>T
c.6155A>T (p.Asn2052Ile)
c.5867A>T (p.Asn1956Ile)
c.3395A>T (p.Asn1132Ile)
19g.35732981T>ACA405428466KMT2Bn.738T>A
c.6366T>A (p.Asn2122Lys)
c.3973T>A (n.3973T>A)
c.1650T>A (p.Asn550Lys)
n.1585T>A
c.1653T>A (p.Asn551Lys)
c.5974T>A
c.6432T>A (p.Asn2144Lys)
c.705-616T>A (n.705-616T>A)
c.3754T>A
c.6156T>A (p.Asn2052Lys)
c.5868T>A (p.Asn1956Lys)
c.3396T>A (p.Asn1132Lys)
19g.35732981T>CCA507308934KMT2Bn.738T>C
c.6366T>C (p.Asn2122=)
c.3973T>C (n.3973T>C)
c.1650T>C (p.Asn550=)
n.1585T>C
c.1653T>C (p.Asn551=)
c.5974T>C
c.6432T>C (p.Asn2144=)
c.705-616T>C (n.705-616T>C)
c.3754T>C
c.6156T>C (p.Asn2052=)
c.5868T>C (p.Asn1956=)
c.3396T>C (p.Asn1132=)
 gnomAD v4
19g.35732981T>GCA405428467KMT2Bn.738T>G
c.6366T>G (p.Asn2122Lys)
c.3973T>G (n.3973T>G)
c.1650T>G (p.Asn550Lys)
n.1585T>G
c.1653T>G (p.Asn551Lys)
c.5974T>G
c.6432T>G (p.Asn2144Lys)
c.705-616T>G (n.705-616T>G)
c.3754T>G
c.6156T>G (p.Asn2052Lys)
c.5868T>G (p.Asn1956Lys)
c.3396T>G (p.Asn1132Lys)
19g.35732982G>ACA405428473KMT2Bn.739G>A
c.6367G>A (p.Gly2123Ser)
c.3974G>A (n.3974G>A)
c.1651G>A (p.Gly551Ser)
n.1586G>A
c.1654G>A (p.Gly552Ser)
c.5975G>A
c.6433G>A (p.Gly2145Ser)
c.705-615G>A (n.705-615G>A)
c.3755G>A
c.6157G>A (p.Gly2053Ser)
c.5869G>A (p.Gly1957Ser)
c.3397G>A (p.Gly1133Ser)
 dbSNP gnomAD v2
19g.35732982G>CCA405428471KMT2Bn.739G>C
c.6367G>C (p.Gly2123Arg)
c.3974G>C (n.3974G>C)
c.1651G>C (p.Gly551Arg)
n.1586G>C
c.1654G>C (p.Gly552Arg)
c.5975G>C
c.6433G>C (p.Gly2145Arg)
c.705-615G>C (n.705-615G>C)
c.3755G>C
c.6157G>C (p.Gly2053Arg)
c.5869G>C (p.Gly1957Arg)
c.3397G>C (p.Gly1133Arg)
19g.35732982G=CA2333794595KMT2Bn.739G=
c.6367G= (p.Gly2123=)
c.3974G= (n.3974G=)
c.1651G= (p.Gly551=)
n.1586G=
c.1654G= (p.Gly552=)
c.5975G=
c.6433G= (p.Gly2145=)
c.705-615G= (n.705-615G=)
c.3755G=
c.6157G= (p.Gly2053=)
c.5869G= (p.Gly1957=)
c.3397G= (p.Gly1133=)
19g.35732982G>TCA405428469KMT2Bn.739G>T
c.6367G>T (p.Gly2123Cys)
c.3974G>T (n.3974G>T)
c.1651G>T (p.Gly551Cys)
n.1586G>T
c.1654G>T (p.Gly552Cys)
c.5975G>T
c.6433G>T (p.Gly2145Cys)
c.705-615G>T (n.705-615G>T)
c.3755G>T
c.6157G>T (p.Gly2053Cys)
c.5869G>T (p.Gly1957Cys)
c.3397G>T (p.Gly1133Cys)
 gnomAD v4
19g.35732983G>ACA405428476KMT2Bn.740G>A
c.6368G>A (p.Gly2123Asp)
c.3975G>A (n.3975G>A)
c.1652G>A (p.Gly551Asp)
n.1587G>A
c.1655G>A (p.Gly552Asp)
c.5976G>A
c.6434G>A (p.Gly2145Asp)
c.705-614G>A (n.705-614G>A)
c.3756G>A
c.6158G>A (p.Gly2053Asp)
c.5870G>A (p.Gly1957Asp)
c.3398G>A (p.Gly1133Asp)
 gnomAD v4
19g.35732983G>CCA405428479KMT2Bn.740G>C
c.6368G>C (p.Gly2123Ala)
c.3975G>C (n.3975G>C)
c.1652G>C (p.Gly551Ala)
n.1587G>C
c.1655G>C (p.Gly552Ala)
c.5976G>C
c.6434G>C (p.Gly2145Ala)
c.705-614G>C (n.705-614G>C)
c.3756G>C
c.6158G>C (p.Gly2053Ala)
c.5870G>C (p.Gly1957Ala)
c.3398G>C (p.Gly1133Ala)
19g.35732983G=CA2333794596KMT2Bn.740G=
c.6368G= (p.Gly2123=)
c.3975G= (n.3975G=)
c.1652G= (p.Gly551=)
n.1587G=
c.1655G= (p.Gly552=)
c.5976G=
c.6434G= (p.Gly2145=)
c.705-614G= (n.705-614G=)
c.3756G=
c.6158G= (p.Gly2053=)
c.5870G= (p.Gly1957=)
c.3398G= (p.Gly1133=)
19g.35732983G>TCA405428480KMT2Bn.740G>T
c.6368G>T (p.Gly2123Val)
c.3975G>T (n.3975G>T)
c.1652G>T (p.Gly551Val)
n.1587G>T
c.1655G>T (p.Gly552Val)
c.5976G>T
c.6434G>T (p.Gly2145Val)
c.705-614G>T (n.705-614G>T)
c.3756G>T
c.6158G>T (p.Gly2053Val)
c.5870G>T (p.Gly1957Val)
c.3398G>T (p.Gly1133Val)
 dbSNP gnomAD v2 gnomAD v4
19g.35732984C>ACA507308943KMT2Bn.741C>A
c.6369C>A (p.Gly2123=)
c.3976C>A (n.3976C>A)
c.1653C>A (p.Gly551=)
n.1588C>A
c.1656C>A (p.Gly552=)
c.5977C>A
c.6435C>A (p.Gly2145=)
c.705-613C>A (n.705-613C>A)
c.3757C>A
c.6159C>A (p.Gly2053=)
c.5871C>A (p.Gly1957=)
c.3399C>A (p.Gly1133=)
 gnomAD v4
19g.35732984C=CA2333794597KMT2Bn.741C=
c.6369C= (p.Gly2123=)
c.3976C= (n.3976C=)
c.1653C= (p.Gly551=)
n.1588C=
c.1656C= (p.Gly552=)
c.5977C=
c.6435C= (p.Gly2145=)
c.705-613C= (n.705-613C=)
c.3757C=
c.6159C= (p.Gly2053=)
c.5871C= (p.Gly1957=)
c.3399C= (p.Gly1133=)
19g.35732984C>GCA507308945KMT2Bn.741C>G
c.6369C>G (p.Gly2123=)
c.3976C>G (n.3976C>G)
c.1653C>G (p.Gly551=)
n.1588C>G
c.1656C>G (p.Gly552=)
c.5977C>G
c.6435C>G (p.Gly2145=)
c.705-613C>G (n.705-613C>G)
c.3757C>G
c.6159C>G (p.Gly2053=)
c.5871C>G (p.Gly1957=)
c.3399C>G (p.Gly1133=)
19g.35732984C>TCA507308946KMT2Bn.741C>T
c.6369C>T (p.Gly2123=)
c.3976C>T (n.3976C>T)
c.1653C>T (p.Gly551=)
n.1588C>T
c.1656C>T (p.Gly552=)
c.5977C>T
c.6435C>T (p.Gly2145=)
c.705-613C>T (n.705-613C>T)
c.3757C>T
c.6159C>T (p.Gly2053=)
c.5871C>T (p.Gly1957=)
c.3399C>T (p.Gly1133=)
 ClinVar dbSNP
19g.35732985A>CCA405428482KMT2Bn.742A>C
c.6370A>C (p.Ser2124Arg)
c.3977A>C (n.3977A>C)
c.1654A>C (p.Ser552Arg)
n.1589A>C
c.1657A>C (p.Ser553Arg)
c.5978A>C
c.6436A>C (p.Ser2146Arg)
c.705-612A>C (n.705-612A>C)
c.3758A>C
c.6160A>C (p.Ser2054Arg)
c.5872A>C (p.Ser1958Arg)
c.3400A>C (p.Ser1134Arg)
19g.35732985A>GCA405428485KMT2Bn.742A>G
c.6370A>G (p.Ser2124Gly)
c.3977A>G (n.3977A>G)
c.1654A>G (p.Ser552Gly)
n.1589A>G
c.1657A>G (p.Ser553Gly)
c.5978A>G
c.6436A>G (p.Ser2146Gly)
c.705-612A>G (n.705-612A>G)
c.3758A>G
c.6160A>G (p.Ser2054Gly)
c.5872A>G (p.Ser1958Gly)
c.3400A>G (p.Ser1134Gly)
19g.35732985A>TCA405428487KMT2Bn.742A>T
c.6370A>T (p.Ser2124Cys)
c.3977A>T (n.3977A>T)
c.1654A>T (p.Ser552Cys)
n.1589A>T
c.1657A>T (p.Ser553Cys)
c.5978A>T
c.6436A>T (p.Ser2146Cys)
c.705-612A>T (n.705-612A>T)
c.3758A>T
c.6160A>T (p.Ser2054Cys)
c.5872A>T (p.Ser1958Cys)
c.3400A>T (p.Ser1134Cys)
19g.35732986G>ACA405428489KMT2Bn.743G>A
c.6371G>A (p.Ser2124Asn)
c.3978G>A (n.3978G>A)
c.1655G>A (p.Ser552Asn)
n.1590G>A
c.1658G>A (p.Ser553Asn)
c.5979G>A
c.6437G>A (p.Ser2146Asn)
c.705-611G>A (n.705-611G>A)
c.3759G>A
c.6161G>A (p.Ser2054Asn)
c.5873G>A (p.Ser1958Asn)
c.3401G>A (p.Ser1134Asn)
 dbSNP gnomAD v2 gnomAD v4
19g.35732986G>CCA405428492KMT2Bn.743G>C
c.6371G>C (p.Ser2124Thr)
c.3978G>C (n.3978G>C)
c.1655G>C (p.Ser552Thr)
n.1590G>C
c.1658G>C (p.Ser553Thr)
c.5979G>C
c.6437G>C (p.Ser2146Thr)
c.705-611G>C (n.705-611G>C)
c.3759G>C
c.6161G>C (p.Ser2054Thr)
c.5873G>C (p.Ser1958Thr)
c.3401G>C (p.Ser1134Thr)
19g.35732986G=CA2333794598KMT2Bn.743G=
c.6371G= (p.Ser2124=)
c.3978G= (n.3978G=)
c.1655G= (p.Ser552=)
n.1590G=
c.1658G= (p.Ser553=)
c.5979G=
c.6437G= (p.Ser2146=)
c.705-611G= (n.705-611G=)
c.3759G=
c.6161G= (p.Ser2054=)
c.5873G= (p.Ser1958=)
c.3401G= (p.Ser1134=)
19g.35732986G>TCA405428491KMT2Bn.743G>T
c.6371G>T (p.Ser2124Ile)
c.3978G>T (n.3978G>T)
c.1655G>T (p.Ser552Ile)
n.1590G>T
c.1658G>T (p.Ser553Ile)
c.5979G>T
c.6437G>T (p.Ser2146Ile)
c.705-611G>T (n.705-611G>T)
c.3759G>T
c.6161G>T (p.Ser2054Ile)
c.5873G>T (p.Ser1958Ile)
c.3401G>T (p.Ser1134Ile)
 gnomAD v4
19g.35732987C>ACA405428496KMT2Bn.744C>A
c.6372C>A (p.Ser2124Arg)
c.3979C>A (n.3979C>A)
c.1656C>A (p.Ser552Arg)
n.1591C>A
c.1659C>A (p.Ser553Arg)
c.5980C>A
c.6438C>A (p.Ser2146Arg)
c.705-610C>A (n.705-610C>A)
c.3760C>A
c.6162C>A (p.Ser2054Arg)
c.5874C>A (p.Ser1958Arg)
c.3402C>A (p.Ser1134Arg)
 gnomAD v4
19g.35732987C>GCA405428499KMT2Bn.744C>G
c.6372C>G (p.Ser2124Arg)
c.3979C>G (n.3979C>G)
c.1656C>G (p.Ser552Arg)
n.1591C>G
c.1659C>G (p.Ser553Arg)
c.5980C>G
c.6438C>G (p.Ser2146Arg)
c.705-610C>G (n.705-610C>G)
c.3760C>G
c.6162C>G (p.Ser2054Arg)
c.5874C>G (p.Ser1958Arg)
c.3402C>G (p.Ser1134Arg)
19g.35732987C>TCA507308953KMT2Bn.744C>T
c.6372C>T (p.Ser2124=)
c.3979C>T (n.3979C>T)
c.1656C>T (p.Ser552=)
n.1591C>T
c.1659C>T (p.Ser553=)
c.5980C>T
c.6438C>T (p.Ser2146=)
c.705-610C>T (n.705-610C>T)
c.3760C>T
c.6162C>T (p.Ser2054=)
c.5874C>T (p.Ser1958=)
c.3402C>T (p.Ser1134=)
 gnomAD v4
19g.35732988C>ACA405428501KMT2Bn.745C>A
c.6373C>A (p.Gln2125Lys)
c.3980C>A (n.3980C>A)
c.1657C>A (p.Gln553Lys)
n.1592C>A
c.1660C>A (p.Gln554Lys)
c.5981C>A
c.6439C>A (p.Gln2147Lys)
c.705-609C>A (n.705-609C>A)
c.3761C>A
c.6163C>A (p.Gln2055Lys)
c.5875C>A (p.Gln1959Lys)
c.3403C>A (p.Gln1135Lys)
19g.35732988C>GCA405428503KMT2Bn.745C>G
c.6373C>G (p.Gln2125Glu)
c.3980C>G (n.3980C>G)
c.1657C>G (p.Gln553Glu)
n.1592C>G
c.1660C>G (p.Gln554Glu)
c.5981C>G
c.6439C>G (p.Gln2147Glu)
c.705-609C>G (n.705-609C>G)
c.3761C>G
c.6163C>G (p.Gln2055Glu)
c.5875C>G (p.Gln1959Glu)
c.3403C>G (p.Gln1135Glu)
19g.35732988C>TCA405428505KMT2Bn.745C>T
c.6373C>T (p.Gln2125Ter)
c.3980C>T (n.3980C>T)
c.1657C>T (p.Gln553Ter)
n.1592C>T
c.1660C>T (p.Gln554Ter)
c.5981C>T
c.6439C>T (p.Gln2147Ter)
c.705-609C>T (n.705-609C>T)
c.3761C>T
c.6163C>T (p.Gln2055Ter)
c.5875C>T (p.Gln1959Ter)
c.3403C>T (p.Gln1135Ter)
 ClinVar dbSNP
19g.35732989A>CCA405428508KMT2Bn.746A>C
c.6374A>C (p.Gln2125Pro)
c.3981A>C (n.3981A>C)
c.1658A>C (p.Gln553Pro)
n.1593A>C
c.1661A>C (p.Gln554Pro)
c.5982A>C
c.6440A>C (p.Gln2147Pro)
c.705-608A>C (n.705-608A>C)
c.3762A>C
c.6164A>C (p.Gln2055Pro)
c.5876A>C (p.Gln1959Pro)
c.3404A>C (p.Gln1135Pro)
19g.35732989A>GCA405428511KMT2Bn.746A>G
c.6374A>G (p.Gln2125Arg)
c.3981A>G (n.3981A>G)
c.1658A>G (p.Gln553Arg)
n.1593A>G
c.1661A>G (p.Gln554Arg)
c.5982A>G
c.6440A>G (p.Gln2147Arg)
c.705-608A>G (n.705-608A>G)
c.3762A>G
c.6164A>G (p.Gln2055Arg)
c.5876A>G (p.Gln1959Arg)
c.3404A>G (p.Gln1135Arg)
19g.35732989A>TCA405428512KMT2Bn.746A>T
c.6374A>T (p.Gln2125Leu)
c.3981A>T (n.3981A>T)
c.1658A>T (p.Gln553Leu)
n.1593A>T
c.1661A>T (p.Gln554Leu)
c.5982A>T
c.6440A>T (p.Gln2147Leu)
c.705-608A>T (n.705-608A>T)
c.3762A>T
c.6164A>T (p.Gln2055Leu)
c.5876A>T (p.Gln1959Leu)
c.3404A>T (p.Gln1135Leu)
19g.35732990G>ACA507308972KMT2Bn.747G>A
c.6375G>A (p.Gln2125=)
c.3982G>A (n.3982G>A)
c.1659G>A (p.Gln553=)
n.1594G>A
c.1662G>A (p.Gln554=)
c.5983G>A
c.6441G>A (p.Gln2147=)
c.705-607G>A (n.705-607G>A)
c.3763G>A
c.6165G>A (p.Gln2055=)
c.5877G>A (p.Gln1959=)
c.3405G>A (p.Gln1135=)
19g.35732990G>CCA405428515KMT2Bn.747G>C
c.6375G>C (p.Gln2125His)
c.3982G>C (n.3982G>C)
c.1659G>C (p.Gln553His)
n.1594G>C
c.1662G>C (p.Gln554His)
c.5983G>C
c.6441G>C (p.Gln2147His)
c.705-607G>C (n.705-607G>C)
c.3763G>C
c.6165G>C (p.Gln2055His)
c.5877G>C (p.Gln1959His)
c.3405G>C (p.Gln1135His)
19g.35732990G>TCA405428518KMT2Bn.747G>T
c.6375G>T (p.Gln2125His)
c.3982G>T (n.3982G>T)
c.1659G>T (p.Gln553His)
n.1594G>T
c.1662G>T (p.Gln554His)
c.5983G>T
c.6441G>T (p.Gln2147His)
c.705-607G>T (n.705-607G>T)
c.3763G>T
c.6165G>T (p.Gln2055His)
c.5877G>T (p.Gln1959His)
c.3405G>T (p.Gln1135His)
19g.35732991C>ACA405428526KMT2Bn.748C>A
c.6376C>A (p.Pro2126Thr)
c.3983C>A (n.3983C>A)
c.1660C>A (p.Pro554Thr)
n.1595C>A
c.1663C>A (p.Pro555Thr)
c.5984C>A
c.6442C>A (p.Pro2148Thr)
c.705-606C>A (n.705-606C>A)
c.3764C>A
c.6166C>A (p.Pro2056Thr)
c.5878C>A (p.Pro1960Thr)
c.3406C>A (p.Pro1136Thr)
 gnomAD v4
19g.35732991C=CA2333794599KMT2Bn.748C=
c.6376C= (p.Pro2126=)
c.3983C= (n.3983C=)
c.1660C= (p.Pro554=)
n.1595C=
c.1663C= (p.Pro555=)
c.5984C=
c.6442C= (p.Pro2148=)
c.705-606C= (n.705-606C=)
c.3764C=
c.6166C= (p.Pro2056=)
c.5878C= (p.Pro1960=)
c.3406C= (p.Pro1136=)
19g.35732991C>GCA405428523KMT2Bn.748C>G
c.6376C>G (p.Pro2126Ala)
c.3983C>G (n.3983C>G)
c.1660C>G (p.Pro554Ala)
n.1595C>G
c.1663C>G (p.Pro555Ala)
c.5984C>G
c.6442C>G (p.Pro2148Ala)
c.705-606C>G (n.705-606C>G)
c.3764C>G
c.6166C>G (p.Pro2056Ala)
c.5878C>G (p.Pro1960Ala)
c.3406C>G (p.Pro1136Ala)
19g.35732991C>TCA405428522KMT2Bn.748C>T
c.6376C>T (p.Pro2126Ser)
c.3983C>T (n.3983C>T)
c.1660C>T (p.Pro554Ser)
n.1595C>T
c.1663C>T (p.Pro555Ser)
c.5984C>T
c.6442C>T (p.Pro2148Ser)
c.705-606C>T (n.705-606C>T)
c.3764C>T
c.6166C>T (p.Pro2056Ser)
c.5878C>T (p.Pro1960Ser)
c.3406C>T (p.Pro1136Ser)
 dbSNP gnomAD v2 gnomAD v4
19g.35732992C>ACA405428529KMT2Bn.749C>A
c.6377C>A (p.Pro2126His)
c.3984C>A (n.3984C>A)
c.1661C>A (p.Pro554His)
n.1596C>A
c.1664C>A (p.Pro555His)
c.5985C>A
c.6443C>A (p.Pro2148His)
c.705-605C>A (n.705-605C>A)
c.3765C>A
c.6167C>A (p.Pro2056His)
c.5879C>A (p.Pro1960His)
c.3407C>A (p.Pro1136His)
 gnomAD v4
19g.35732992C=CA2333794600KMT2Bn.749C=
c.6377C= (p.Pro2126=)
c.3984C= (n.3984C=)
c.1661C= (p.Pro554=)
n.1596C=
c.1664C= (p.Pro555=)
c.5985C=
c.6443C= (p.Pro2148=)
c.705-605C= (n.705-605C=)
c.3765C=
c.6167C= (p.Pro2056=)
c.5879C= (p.Pro1960=)
c.3407C= (p.Pro1136=)
19g.35732992C>GCA9385688KMT2Bn.749C>G
c.6377C>G (p.Pro2126Arg)
c.3984C>G (n.3984C>G)
c.1661C>G (p.Pro554Arg)
n.1596C>G
c.1664C>G (p.Pro555Arg)
c.5985C>G
c.6443C>G (p.Pro2148Arg)
c.705-605C>G (n.705-605C>G)
c.3765C>G
c.6167C>G (p.Pro2056Arg)
c.5879C>G (p.Pro1960Arg)
c.3407C>G (p.Pro1136Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35732992C>TCA405428539KMT2Bn.749C>T
c.6377C>T (p.Pro2126Leu)
c.3984C>T (n.3984C>T)
c.1661C>T (p.Pro554Leu)
n.1596C>T
c.1664C>T (p.Pro555Leu)
c.5985C>T
c.6443C>T (p.Pro2148Leu)
c.705-605C>T (n.705-605C>T)
c.3765C>T
c.6167C>T (p.Pro2056Leu)
c.5879C>T (p.Pro1960Leu)
c.3407C>T (p.Pro1136Leu)
 gnomAD v4
19g.35732993C>ACA507308978KMT2Bn.750C>A
c.6378C>A (p.Pro2126=)
c.3985C>A (n.3985C>A)
c.1662C>A (p.Pro554=)
n.1597C>A
c.1665C>A (p.Pro555=)
c.5986C>A
c.6444C>A (p.Pro2148=)
c.705-604C>A (n.705-604C>A)
c.3766C>A
c.6168C>A (p.Pro2056=)
c.5880C>A (p.Pro1960=)
c.3408C>A (p.Pro1136=)
 gnomAD v4
19g.35732993C>GCA507308980KMT2Bn.750C>G
c.6378C>G (p.Pro2126=)
c.3985C>G (n.3985C>G)
c.1662C>G (p.Pro554=)
n.1597C>G
c.1665C>G (p.Pro555=)
c.5986C>G
c.6444C>G (p.Pro2148=)
c.705-604C>G (n.705-604C>G)
c.3766C>G
c.6168C>G (p.Pro2056=)
c.5880C>G (p.Pro1960=)
c.3408C>G (p.Pro1136=)
19g.35732993C>TCA507308979KMT2Bn.750C>T
c.6378C>T (p.Pro2126=)
c.3985C>T (n.3985C>T)
c.1662C>T (p.Pro554=)
n.1597C>T
c.1665C>T (p.Pro555=)
c.5986C>T
c.6444C>T (p.Pro2148=)
c.705-604C>T (n.705-604C>T)
c.3766C>T
c.6168C>T (p.Pro2056=)
c.5880C>T (p.Pro1960=)
c.3408C>T (p.Pro1136=)
 gnomAD v4
19g.35732994T>ACA405428544KMT2Bn.751T>A
c.6379T>A (p.Ser2127Thr)
c.3986T>A (n.3986T>A)
c.1663T>A (p.Ser555Thr)
n.1598T>A
c.1666T>A (p.Ser556Thr)
c.5987T>A
c.6445T>A (p.Ser2149Thr)
c.705-603T>A (n.705-603T>A)
c.3767T>A
c.6169T>A (p.Ser2057Thr)
c.5881T>A (p.Ser1961Thr)
c.3409T>A (p.Ser1137Thr)
19g.35732994T>CCA405428545KMT2Bn.751T>C
c.6379T>C (p.Ser2127Pro)
c.3986T>C (n.3986T>C)
c.1663T>C (p.Ser555Pro)
n.1598T>C
c.1666T>C (p.Ser556Pro)
c.5987T>C
c.6445T>C (p.Ser2149Pro)
c.705-603T>C (n.705-603T>C)
c.3767T>C
c.6169T>C (p.Ser2057Pro)
c.5881T>C (p.Ser1961Pro)
c.3409T>C (p.Ser1137Pro)
19g.35732994T>GCA405428546KMT2Bn.751T>G
c.6379T>G (p.Ser2127Ala)
c.3986T>G (n.3986T>G)
c.1663T>G (p.Ser555Ala)
n.1598T>G
c.1666T>G (p.Ser556Ala)
c.5987T>G
c.6445T>G (p.Ser2149Ala)
c.705-603T>G (n.705-603T>G)
c.3767T>G
c.6169T>G (p.Ser2057Ala)
c.5881T>G (p.Ser1961Ala)
c.3409T>G (p.Ser1137Ala)
19g.35732995C>ACA405428550KMT2Bn.752C>A
c.6380C>A (p.Ser2127Tyr)
c.3987C>A (n.3987C>A)
c.1664C>A (p.Ser555Tyr)
n.1599C>A
c.1667C>A (p.Ser556Tyr)
c.5988C>A
c.6446C>A (p.Ser2149Tyr)
c.705-602C>A (n.705-602C>A)
c.3768C>A
c.6170C>A (p.Ser2057Tyr)
c.5882C>A (p.Ser1961Tyr)
c.3410C>A (p.Ser1137Tyr)
19g.35732995C>GCA405428548KMT2Bn.752C>G
c.6380C>G (p.Ser2127Cys)
c.3987C>G (n.3987C>G)
c.1664C>G (p.Ser555Cys)
n.1599C>G
c.1667C>G (p.Ser556Cys)
c.5988C>G
c.6446C>G (p.Ser2149Cys)
c.705-602C>G (n.705-602C>G)
c.3768C>G
c.6170C>G (p.Ser2057Cys)
c.5882C>G (p.Ser1961Cys)
c.3410C>G (p.Ser1137Cys)
19g.35732995C>TCA405428547KMT2Bn.752C>T
c.6380C>T (p.Ser2127Phe)
c.3987C>T (n.3987C>T)
c.1664C>T (p.Ser555Phe)
n.1599C>T
c.1667C>T (p.Ser556Phe)
c.5988C>T
c.6446C>T (p.Ser2149Phe)
c.705-602C>T (n.705-602C>T)
c.3768C>T
c.6170C>T (p.Ser2057Phe)
c.5882C>T (p.Ser1961Phe)
c.3410C>T (p.Ser1137Phe)
 gnomAD v4 COSMIC
19g.35732997delCA645604596KMT2Bn.754del
c.6382del (p.Gln2128LysfsTer3)
c.3989del (n.3989del)
c.1666del (p.Gln556LysfsTer3)
n.1601del
c.1669del (p.Gln557LysfsTer3)
c.5990del
c.6448del (p.Gln2150LysfsTer3)
c.705-600del (n.705-600del)
c.3770del
c.6172del (p.Gln2058LysfsTer3)
c.5884del (p.Gln1962LysfsTer3)
c.3412del (p.Gln1138LysfsTer3)
 COSMIC
19g.35732996C>ACA507308985KMT2Bn.753C>A
c.6381C>A (p.Ser2127=)
c.3988C>A (n.3988C>A)
c.1665C>A (p.Ser555=)
n.1600C>A
c.1668C>A (p.Ser556=)
c.5989C>A
c.6447C>A (p.Ser2149=)
c.705-601C>A (n.705-601C>A)
c.3769C>A
c.6171C>A (p.Ser2057=)
c.5883C>A (p.Ser1961=)
c.3411C>A (p.Ser1137=)
19g.35732996C>GCA507308988KMT2Bn.753C>G
c.6381C>G (p.Ser2127=)
c.3988C>G (n.3988C>G)
c.1665C>G (p.Ser555=)
n.1600C>G
c.1668C>G (p.Ser556=)
c.5989C>G
c.6447C>G (p.Ser2149=)
c.705-601C>G (n.705-601C>G)
c.3769C>G
c.6171C>G (p.Ser2057=)
c.5883C>G (p.Ser1961=)
c.3411C>G (p.Ser1137=)
19g.35732996C>TCA507308990KMT2Bn.753C>T
c.6381C>T (p.Ser2127=)
c.3988C>T (n.3988C>T)
c.1665C>T (p.Ser555=)
n.1600C>T
c.1668C>T (p.Ser556=)
c.5989C>T
c.6447C>T (p.Ser2149=)
c.705-601C>T (n.705-601C>T)
c.3769C>T
c.6171C>T (p.Ser2057=)
c.5883C>T (p.Ser1961=)
c.3411C>T (p.Ser1137=)
 gnomAD v4
19g.35732997C>ACA405428554KMT2Bn.754C>A
c.6382C>A (p.Gln2128Lys)
c.3989C>A (n.3989C>A)
c.1666C>A (p.Gln556Lys)
n.1601C>A
c.1669C>A (p.Gln557Lys)
c.5990C>A
c.6448C>A (p.Gln2150Lys)
c.705-600C>A (n.705-600C>A)
c.3770C>A
c.6172C>A (p.Gln2058Lys)
c.5884C>A (p.Gln1962Lys)
c.3412C>A (p.Gln1138Lys)
 gnomAD v4
19g.35732997C>GCA405428557KMT2Bn.754C>G
c.6382C>G (p.Gln2128Glu)
c.3989C>G (n.3989C>G)
c.1666C>G (p.Gln556Glu)
n.1601C>G
c.1669C>G (p.Gln557Glu)
c.5990C>G
c.6448C>G (p.Gln2150Glu)
c.705-600C>G (n.705-600C>G)
c.3770C>G
c.6172C>G (p.Gln2058Glu)
c.5884C>G (p.Gln1962Glu)
c.3412C>G (p.Gln1138Glu)
 gnomAD v4
19g.35732997C>TCA405428560KMT2Bn.754C>T
c.6382C>T (p.Gln2128Ter)
c.3989C>T (n.3989C>T)
c.1666C>T (p.Gln556Ter)
n.1601C>T
c.1669C>T (p.Gln557Ter)
c.5990C>T
c.6448C>T (p.Gln2150Ter)
c.705-600C>T (n.705-600C>T)
c.3770C>T
c.6172C>T (p.Gln2058Ter)
c.5884C>T (p.Gln1962Ter)
c.3412C>T (p.Gln1138Ter)
19g.35732998A=CA2333794601KMT2Bn.755A=
c.6383A= (p.Gln2128=)
c.3990A= (n.3990A=)
c.1667A= (p.Gln556=)
n.1602A=
c.1670A= (p.Gln557=)
c.5991A=
c.6449A= (p.Gln2150=)
c.705-599A= (n.705-599A=)
c.3771A=
c.6173A= (p.Gln2058=)
c.5885A= (p.Gln1962=)
c.3413A= (p.Gln1138=)
19g.35732998A>CCA405428563KMT2Bn.755A>C
c.6383A>C (p.Gln2128Pro)
c.3990A>C (n.3990A>C)
c.1667A>C (p.Gln556Pro)
n.1602A>C
c.1670A>C (p.Gln557Pro)
c.5991A>C
c.6449A>C (p.Gln2150Pro)
c.705-599A>C (n.705-599A>C)
c.3771A>C
c.6173A>C (p.Gln2058Pro)
c.5885A>C (p.Gln1962Pro)
c.3413A>C (p.Gln1138Pro)
19g.35732998A>GCA405428566KMT2Bn.755A>G
c.6383A>G (p.Gln2128Arg)
c.3990A>G (n.3990A>G)
c.1667A>G (p.Gln556Arg)
n.1602A>G
c.1670A>G (p.Gln557Arg)
c.5991A>G
c.6449A>G (p.Gln2150Arg)
c.705-599A>G (n.705-599A>G)
c.3771A>G
c.6173A>G (p.Gln2058Arg)
c.5885A>G (p.Gln1962Arg)
c.3413A>G (p.Gln1138Arg)
 dbSNP
19g.35732998A>TCA405428569KMT2Bn.755A>T
c.6383A>T (p.Gln2128Leu)
c.3990A>T (n.3990A>T)
c.1667A>T (p.Gln556Leu)
n.1602A>T
c.1670A>T (p.Gln557Leu)
c.5991A>T
c.6449A>T (p.Gln2150Leu)
c.705-599A>T (n.705-599A>T)
c.3771A>T
c.6173A>T (p.Gln2058Leu)
c.5885A>T (p.Gln1962Leu)
c.3413A>T (p.Gln1138Leu)
19g.35732999A=CA2333794602KMT2Bn.756A=
c.6384A= (p.Gln2128=)
c.3991A= (n.3991A=)
c.1668A= (p.Gln556=)
n.1603A=
c.1671A= (p.Gln557=)
c.5992A=
c.6450A= (p.Gln2150=)
c.705-598A= (n.705-598A=)
c.3772A=
c.6174A= (p.Gln2058=)
c.5886A= (p.Gln1962=)
c.3414A= (p.Gln1138=)
19g.35732999A>CCA9385689KMT2Bn.756A>C
c.6384A>C (p.Gln2128His)
c.3991A>C (n.3991A>C)
c.1668A>C (p.Gln556His)
n.1603A>C
c.1671A>C (p.Gln557His)
c.5992A>C
c.6450A>C (p.Gln2150His)
c.705-598A>C (n.705-598A>C)
c.3772A>C
c.6174A>C (p.Gln2058His)
c.5886A>C (p.Gln1962His)
c.3414A>C (p.Gln1138His)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
19g.35732999A>GCA9385690KMT2Bn.756A>G
c.6384A>G (p.Gln2128=)
c.3991A>G (n.3991A>G)
c.1668A>G (p.Gln556=)
n.1603A>G
c.1671A>G (p.Gln557=)
c.5992A>G
c.6450A>G (p.Gln2150=)
c.705-598A>G (n.705-598A>G)
c.3772A>G
c.6174A>G (p.Gln2058=)
c.5886A>G (p.Gln1962=)
c.3414A>G (p.Gln1138=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.35732999A>TCA405428575KMT2Bn.756A>T
c.6384A>T (p.Gln2128His)
c.3991A>T (n.3991A>T)
c.1668A>T (p.Gln556His)
n.1603A>T
c.1671A>T (p.Gln557His)
c.5992A>T
c.6450A>T (p.Gln2150His)
c.705-598A>T (n.705-598A>T)
c.3772A>T
c.6174A>T (p.Gln2058His)
c.5886A>T (p.Gln1962His)
c.3414A>T (p.Gln1138His)
19g.35733000G>ACA405428580KMT2Bn.757G>A
c.6385G>A (p.Gly2129Ser)
c.3992G>A (n.3992G>A)
c.1669G>A (p.Gly557Ser)
n.1604G>A
c.1672G>A (p.Gly558Ser)
c.5993G>A
c.6451G>A (p.Gly2151Ser)
c.705-597G>A (n.705-597G>A)
c.3773G>A
c.6175G>A (p.Gly2059Ser)
c.5887G>A (p.Gly1963Ser)
c.3415G>A (p.Gly1139Ser)
19g.35733000G>CCA405428590KMT2Bn.757G>C
c.6385G>C (p.Gly2129Arg)
c.3992G>C (n.3992G>C)
c.1669G>C (p.Gly557Arg)
n.1604G>C
c.1672G>C (p.Gly558Arg)
c.5993G>C
c.6451G>C (p.Gly2151Arg)
c.705-597G>C (n.705-597G>C)
c.3773G>C
c.6175G>C (p.Gly2059Arg)
c.5887G>C (p.Gly1963Arg)
c.3415G>C (p.Gly1139Arg)
19g.35733000G>TCA405428596KMT2Bn.757G>T
c.6385G>T (p.Gly2129Cys)
c.3992G>T (n.3992G>T)
c.1669G>T (p.Gly557Cys)
n.1604G>T
c.1672G>T (p.Gly558Cys)
c.5993G>T
c.6451G>T (p.Gly2151Cys)
c.705-597G>T (n.705-597G>T)
c.3773G>T
c.6175G>T (p.Gly2059Cys)
c.5887G>T (p.Gly1963Cys)
c.3415G>T (p.Gly1139Cys)
19g.35733001G>ACA9385691KMT2Bn.758G>A
c.6386G>A (p.Gly2129Asp)
c.3993G>A (n.3993G>A)
c.1670G>A (p.Gly557Asp)
n.1605G>A
c.1673G>A (p.Gly558Asp)
c.5994G>A
c.6452G>A (p.Gly2151Asp)
c.705-596G>A (n.705-596G>A)
c.3774G>A
c.6176G>A (p.Gly2059Asp)
c.5888G>A (p.Gly1963Asp)
c.3416G>A (p.Gly1139Asp)
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.35733001G>CCA405428602KMT2Bn.758G>C
c.6386G>C (p.Gly2129Ala)
c.3993G>C (n.3993G>C)
c.1670G>C (p.Gly557Ala)
n.1605G>C
c.1673G>C (p.Gly558Ala)
c.5994G>C
c.6452G>C (p.Gly2151Ala)
c.705-596G>C (n.705-596G>C)
c.3774G>C
c.6176G>C (p.Gly2059Ala)
c.5888G>C (p.Gly1963Ala)
c.3416G>C (p.Gly1139Ala)
19g.35733001G=CA2333794603KMT2Bn.758G=
c.6386G= (p.Gly2129=)
c.3993G= (n.3993G=)
c.1670G= (p.Gly557=)
n.1605G=
c.1673G= (p.Gly558=)
c.5994G=
c.6452G= (p.Gly2151=)
c.705-596G= (n.705-596G=)
c.3774G=
c.6176G= (p.Gly2059=)
c.5888G= (p.Gly1963=)
c.3416G= (p.Gly1139=)
19g.35733001G>TCA405428604KMT2Bn.758G>T
c.6386G>T (p.Gly2129Val)
c.3993G>T (n.3993G>T)
c.1670G>T (p.Gly557Val)
n.1605G>T
c.1673G>T (p.Gly558Val)
c.5994G>T
c.6452G>T (p.Gly2151Val)
c.705-596G>T (n.705-596G>T)
c.3774G>T
c.6176G>T (p.Gly2059Val)
c.5888G>T (p.Gly1963Val)
c.3416G>T (p.Gly1139Val)
 gnomAD v4
19g.35733002C>ACA507309011KMT2Bn.759C>A
c.6387C>A (p.Gly2129=)
c.3994C>A (n.3994C>A)
c.1671C>A (p.Gly557=)
n.1606C>A
c.1674C>A (p.Gly558=)
c.5995C>A
c.6453C>A (p.Gly2151=)
c.705-595C>A (n.705-595C>A)
c.3775C>A
c.6177C>A (p.Gly2059=)
c.5889C>A (p.Gly1963=)
c.3417C>A (p.Gly1139=)
19g.35733002C=CA2333794604KMT2Bn.759C=
c.6387C= (p.Gly2129=)
c.3994C= (n.3994C=)
c.1671C= (p.Gly557=)
n.1606C=
c.1674C= (p.Gly558=)
c.5995C=
c.6453C= (p.Gly2151=)
c.705-595C= (n.705-595C=)
c.3775C=
c.6177C= (p.Gly2059=)
c.5889C= (p.Gly1963=)
c.3417C= (p.Gly1139=)
19g.35733002C>GCA507309012KMT2Bn.759C>G
c.6387C>G (p.Gly2129=)
c.3994C>G (n.3994C>G)
c.1671C>G (p.Gly557=)
n.1606C>G
c.1674C>G (p.Gly558=)
c.5995C>G
c.6453C>G (p.Gly2151=)
c.705-595C>G (n.705-595C>G)
c.3775C>G
c.6177C>G (p.Gly2059=)
c.5889C>G (p.Gly1963=)
c.3417C>G (p.Gly1139=)
19g.35733002C>TCA507309013KMT2Bn.759C>T
c.6387C>T (p.Gly2129=)
c.3994C>T (n.3994C>T)
c.1671C>T (p.Gly557=)
n.1606C>T
c.1674C>T (p.Gly558=)
c.5995C>T
c.6453C>T (p.Gly2151=)
c.705-595C>T (n.705-595C>T)
c.3775C>T
c.6177C>T (p.Gly2059=)
c.5889C>T (p.Gly1963=)
c.3417C>T (p.Gly1139=)
 dbSNP gnomAD v3 gnomAD v4
19g.35733003C>ACA405428608KMT2Bn.760C>A
c.6388C>A (p.Leu2130Met)
c.3995C>A (n.3995C>A)
c.1672C>A (p.Leu558Met)
n.1607C>A
c.1675C>A (p.Leu559Met)
c.5996C>A
c.6454C>A (p.Leu2152Met)
c.705-594C>A (n.705-594C>A)
c.3776C>A
c.6178C>A (p.Leu2060Met)
c.5890C>A (p.Leu1964Met)
c.3418C>A (p.Leu1140Met)
 gnomAD v4
19g.35733003C>GCA405428611KMT2Bn.760C>G
c.6388C>G (p.Leu2130Val)
c.3995C>G (n.3995C>G)
c.1672C>G (p.Leu558Val)
n.1607C>G
c.1675C>G (p.Leu559Val)
c.5996C>G
c.6454C>G (p.Leu2152Val)
c.705-594C>G (n.705-594C>G)
c.3776C>G
c.6178C>G (p.Leu2060Val)
c.5890C>G (p.Leu1964Val)
c.3418C>G (p.Leu1140Val)
19g.35733003C>TCA507309015KMT2Bn.760C>T
c.6388C>T (p.Leu2130=)
c.3995C>T (n.3995C>T)
c.1672C>T (p.Leu558=)
n.1607C>T
c.1675C>T (p.Leu559=)
c.5996C>T
c.6454C>T (p.Leu2152=)
c.705-594C>T (n.705-594C>T)
c.3776C>T
c.6178C>T (p.Leu2060=)
c.5890C>T (p.Leu1964=)
c.3418C>T (p.Leu1140=)
19g.35733004T>ACA405428615KMT2Bn.761T>A
c.6389T>A (p.Leu2130Gln)
c.3996T>A (n.3996T>A)
c.1673T>A (p.Leu558Gln)
n.1608T>A
c.1676T>A (p.Leu559Gln)
c.5997T>A
c.6455T>A (p.Leu2152Gln)
c.705-593T>A (n.705-593T>A)
c.3777T>A
c.6179T>A (p.Leu2060Gln)
c.5891T>A (p.Leu1964Gln)
c.3419T>A (p.Leu1140Gln)
19g.35733004T>CCA405428617KMT2Bn.761T>C
c.6389T>C (p.Leu2130Pro)
c.3996T>C (n.3996T>C)
c.1673T>C (p.Leu558Pro)
n.1608T>C
c.1676T>C (p.Leu559Pro)
c.5997T>C
c.6455T>C (p.Leu2152Pro)
c.705-593T>C (n.705-593T>C)
c.3777T>C
c.6179T>C (p.Leu2060Pro)
c.5891T>C (p.Leu1964Pro)
c.3419T>C (p.Leu1140Pro)
 gnomAD v4
19g.35733004T>GCA405428618KMT2Bn.761T>G
c.6389T>G (p.Leu2130Arg)
c.3996T>G (n.3996T>G)
c.1673T>G (p.Leu558Arg)
n.1608T>G
c.1676T>G (p.Leu559Arg)
c.5997T>G
c.6455T>G (p.Leu2152Arg)
c.705-593T>G (n.705-593T>G)
c.3777T>G
c.6179T>G (p.Leu2060Arg)
c.5891T>G (p.Leu1964Arg)
c.3419T>G (p.Leu1140Arg)
19g.35733005G>ACA507309022KMT2Bn.762G>A
c.6390G>A (p.Leu2130=)
c.3997G>A (n.3997G>A)
c.1674G>A (p.Leu558=)
n.1609G>A
c.1677G>A (p.Leu559=)
c.5998G>A
c.6456G>A (p.Leu2152=)
c.705-592G>A (n.705-592G>A)
c.3778G>A
c.6180G>A (p.Leu2060=)
c.5892G>A (p.Leu1964=)
c.3420G>A (p.Leu1140=)
19g.35733005G>CCA507309023KMT2Bn.762G>C
c.6390G>C (p.Leu2130=)
c.3997G>C (n.3997G>C)
c.1674G>C (p.Leu558=)
n.1609G>C
c.1677G>C (p.Leu559=)
c.5998G>C
c.6456G>C (p.Leu2152=)
c.705-592G>C (n.705-592G>C)
c.3778G>C
c.6180G>C (p.Leu2060=)
c.5892G>C (p.Leu1964=)
c.3420G>C (p.Leu1140=)
19g.35733005G>TCA507309024KMT2Bn.762G>T
c.6390G>T (p.Leu2130=)
c.3997G>T (n.3997G>T)
c.1674G>T (p.Leu558=)
n.1609G>T
c.1677G>T (p.Leu559=)
c.5998G>T
c.6456G>T (p.Leu2152=)
c.705-592G>T (n.705-592G>T)
c.3778G>T
c.6180G>T (p.Leu2060=)
c.5892G>T (p.Leu1964=)
c.3420G>T (p.Leu1140=)
 gnomAD v4
19g.35733005_35733006delCA2507100180KMT2Bn.762_763del
c.6390_6391del (p.Thr2131ArgfsTer5)
c.3997_3998del (n.3997_3998del)
c.1674_1675del (p.Thr559ArgfsTer5)
n.1609_1610del
c.1677_1678del (p.Thr560ArgfsTer5)
c.5998_5999del
c.6456_6457del (p.Thr2153ArgfsTer5)
c.705-592_705-591del (n.705-592_705-591del)
c.3778_3779del
c.6180_6181del (p.Thr2061ArgfsTer5)
c.5892_5893del (p.Thr1965ArgfsTer5)
c.3420_3421del (p.Thr1141ArgfsTer5)
19g.35733006A=CA2333794605KMT2Bn.763A=
c.6391A= (p.Thr2131=)
c.3998A= (n.3998A=)
c.1675A= (p.Thr559=)
n.1610A=
c.1678A= (p.Thr560=)
c.5999A=
c.6457A= (p.Thr2153=)
c.705-591A= (n.705-591A=)
c.3779A=
c.6181A= (p.Thr2061=)
c.5893A= (p.Thr1965=)
c.3421A= (p.Thr1141=)
19g.35733006A>CCA405428622KMT2Bn.763A>C
c.6391A>C (p.Thr2131Pro)
c.3998A>C (n.3998A>C)
c.1675A>C (p.Thr559Pro)
n.1610A>C
c.1678A>C (p.Thr560Pro)
c.5999A>C
c.6457A>C (p.Thr2153Pro)
c.705-591A>C (n.705-591A>C)
c.3779A>C
c.6181A>C (p.Thr2061Pro)
c.5893A>C (p.Thr1965Pro)
c.3421A>C (p.Thr1141Pro)
19g.35733006A>GCA405428629KMT2Bn.763A>G
c.6391A>G (p.Thr2131Ala)
c.3998A>G (n.3998A>G)
c.1675A>G (p.Thr559Ala)
n.1610A>G
c.1678A>G (p.Thr560Ala)
c.5999A>G
c.6457A>G (p.Thr2153Ala)
c.705-591A>G (n.705-591A>G)
c.3779A>G
c.6181A>G (p.Thr2061Ala)
c.5893A>G (p.Thr1965Ala)
c.3421A>G (p.Thr1141Ala)
 dbSNP gnomAD v2 gnomAD v4
19g.35733006A>TCA405428626KMT2Bn.763A>T
c.6391A>T (p.Thr2131Ser)
c.3998A>T (n.3998A>T)
c.1675A>T (p.Thr559Ser)
n.1610A>T
c.1678A>T (p.Thr560Ser)
c.5999A>T
c.6457A>T (p.Thr2153Ser)
c.705-591A>T (n.705-591A>T)
c.3779A>T
c.6181A>T (p.Thr2061Ser)
c.5893A>T (p.Thr1965Ser)
c.3421A>T (p.Thr1141Ser)
19g.35733007C>ACA405428630KMT2Bn.764C>A
c.6392C>A (p.Thr2131Asn)
c.3999C>A (n.3999C>A)
c.1676C>A (p.Thr559Asn)
n.1611C>A
c.1679C>A (p.Thr560Asn)
c.6000C>A
c.6458C>A (p.Thr2153Asn)
c.705-590C>A (n.705-590C>A)
c.3780C>A
c.6182C>A (p.Thr2061Asn)
c.5894C>A (p.Thr1965Asn)
c.3422C>A (p.Thr1141Asn)
 gnomAD v4
19g.35733007C>GCA405428631KMT2Bn.764C>G
c.6392C>G (p.Thr2131Ser)
c.3999C>G (n.3999C>G)
c.1676C>G (p.Thr559Ser)
n.1611C>G
c.1679C>G (p.Thr560Ser)
c.6000C>G
c.6458C>G (p.Thr2153Ser)
c.705-590C>G (n.705-590C>G)
c.3780C>G
c.6182C>G (p.Thr2061Ser)
c.5894C>G (p.Thr1965Ser)
c.3422C>G (p.Thr1141Ser)
19g.35733007C>TCA405428632KMT2Bn.764C>T
c.6392C>T (p.Thr2131Ile)
c.3999C>T (n.3999C>T)
c.1676C>T (p.Thr559Ile)
n.1611C>T
c.1679C>T (p.Thr560Ile)
c.6000C>T
c.6458C>T (p.Thr2153Ile)
c.705-590C>T (n.705-590C>T)
c.3780C>T
c.6182C>T (p.Thr2061Ile)
c.5894C>T (p.Thr1965Ile)
c.3422C>T (p.Thr1141Ile)
 gnomAD v4
19g.35733008C>ACA507309037KMT2Bn.765C>A
c.6393C>A (p.Thr2131=)
c.4000C>A (n.4000C>A)
c.1677C>A (p.Thr559=)
n.1612C>A
c.1680C>A (p.Thr560=)
c.6001C>A
c.6459C>A (p.Thr2153=)
c.705-589C>A (n.705-589C>A)
c.3781C>A
c.6183C>A (p.Thr2061=)
c.5895C>A (p.Thr1965=)
c.3423C>A (p.Thr1141=)
 gnomAD v4
19g.35733008C=CA2333794606KMT2Bn.765C=
c.6393C= (p.Thr2131=)
c.4000C= (n.4000C=)
c.1677C= (p.Thr559=)
n.1612C=
c.1680C= (p.Thr560=)
c.6001C=
c.6459C= (p.Thr2153=)
c.705-589C= (n.705-589C=)
c.3781C=
c.6183C= (p.Thr2061=)
c.5895C= (p.Thr1965=)
c.3423C= (p.Thr1141=)
19g.35733008C>GCA507309042KMT2Bn.765C>G
c.6393C>G (p.Thr2131=)
c.4000C>G (n.4000C>G)
c.1677C>G (p.Thr559=)
n.1612C>G
c.1680C>G (p.Thr560=)
c.6001C>G
c.6459C>G (p.Thr2153=)
c.705-589C>G (n.705-589C>G)
c.3781C>G
c.6183C>G (p.Thr2061=)
c.5895C>G (p.Thr1965=)
c.3423C>G (p.Thr1141=)
19g.35733008C>TCA9385692KMT2Bn.765C>T
c.6393C>T (p.Thr2131=)
c.4000C>T (n.4000C>T)
c.1677C>T (p.Thr559=)
n.1612C>T
c.1680C>T (p.Thr560=)
c.6001C>T
c.6459C>T (p.Thr2153=)
c.705-589C>T (n.705-589C>T)
c.3781C>T
c.6183C>T (p.Thr2061=)
c.5895C>T (p.Thr1965=)
c.3423C>T (p.Thr1141=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35733009G>ACA9385693KMT2Bn.766G>A
c.6394G>A (p.Ala2132Thr)
c.4001G>A (n.4001G>A)
c.1678G>A (p.Ala560Thr)
n.1613G>A
c.1681G>A (p.Ala561Thr)
c.6002G>A
c.6460G>A (p.Ala2154Thr)
c.705-588G>A (n.705-588G>A)
c.3782G>A
c.6184G>A (p.Ala2062Thr)
c.5896G>A (p.Ala1966Thr)
c.3424G>A (p.Ala1142Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.35733009G>CCA405428639KMT2Bn.766G>C
c.6394G>C (p.Ala2132Pro)
c.4001G>C (n.4001G>C)
c.1678G>C (p.Ala560Pro)
n.1613G>C
c.1681G>C (p.Ala561Pro)
c.6002G>C
c.6460G>C (p.Ala2154Pro)
c.705-588G>C (n.705-588G>C)
c.3782G>C
c.6184G>C (p.Ala2062Pro)
c.5896G>C (p.Ala1966Pro)
c.3424G>C (p.Ala1142Pro)
19g.35733009G=CA2333794607KMT2Bn.766G=
c.6394G= (p.Ala2132=)
c.4001G= (n.4001G=)
c.1678G= (p.Ala560=)
n.1613G=
c.1681G= (p.Ala561=)
c.6002G=
c.6460G= (p.Ala2154=)
c.705-588G= (n.705-588G=)
c.3782G=
c.6184G= (p.Ala2062=)
c.5896G= (p.Ala1966=)
c.3424G= (p.Ala1142=)
19g.35733009G>TCA405428642KMT2Bn.766G>T
c.6394G>T (p.Ala2132Ser)
c.4001G>T (n.4001G>T)
c.1678G>T (p.Ala560Ser)
n.1613G>T
c.1681G>T (p.Ala561Ser)
c.6002G>T
c.6460G>T (p.Ala2154Ser)
c.705-588G>T (n.705-588G>T)
c.3782G>T
c.6184G>T (p.Ala2062Ser)
c.5896G>T (p.Ala1966Ser)
c.3424G>T (p.Ala1142Ser)
 gnomAD v4

Number of alleles fetched