Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.118503445_118503457delCA2582342478KMT2Ac.7652_7664del (p.Pro2551GlnfsTer4)
c.7643_7655del (p.Pro2548GlnfsTer4)
c.1592_1604del (p.Pro531GlnfsTer4)
c.1850_1862del (p.Pro617GlnfsTer4)
c.7625_7637del (p.Pro2542GlnfsTer4)
c.7544_7556del (p.Pro2515GlnfsTer4)
n.6895_6907del
c.7553_7565del (p.Pro2518GlnfsTer4)
c.7430_7442del (p.Pro2477GlnfsTer4)
n.1680_1692del
c.5036_5048del (p.Pro1679GlnfsTer4)
c.7649_7661del (p.Pro2550GlnfsTer4)
c.5459_5471del (p.Pro1820GlnfsTer4)
c.5135_5147del (p.Pro1712GlnfsTer4)
ClinVar
11g.118503452A=CA2003527905KMT2Ac.7659A= (p.Lys2553=)
c.7650A= (p.Lys2550=)
c.1599A= (p.Lys533=)
c.1857A= (p.Lys619=)
c.7632A= (p.Lys2544=)
c.7551A= (p.Lys2517=)
n.6902A=
c.7560A= (p.Lys2520=)
c.7437A= (p.Lys2479=)
n.1687A=
c.5043A= (p.Lys1681=)
c.7656A= (p.Lys2552=)
c.5466A= (p.Lys1822=)
c.5142A= (p.Lys1714=)
11g.118503452A>CCA382806016KMT2Ac.7659A>C (p.Lys2553Asn)
c.7650A>C (p.Lys2550Asn)
c.1599A>C (p.Lys533Asn)
c.1857A>C (p.Lys619Asn)
c.7632A>C (p.Lys2544Asn)
c.7551A>C (p.Lys2517Asn)
n.6902A>C
c.7560A>C (p.Lys2520Asn)
c.7437A>C (p.Lys2479Asn)
n.1687A>C
c.5043A>C (p.Lys1681Asn)
c.7656A>C (p.Lys2552Asn)
c.5466A>C (p.Lys1822Asn)
c.5142A>C (p.Lys1714Asn)
11g.118503452A>GCA229526913KMT2Ac.7659A>G (p.Lys2553=)
c.7650A>G (p.Lys2550=)
c.1599A>G (p.Lys533=)
c.1857A>G (p.Lys619=)
c.7632A>G (p.Lys2544=)
c.7551A>G (p.Lys2517=)
n.6902A>G
c.7560A>G (p.Lys2520=)
c.7437A>G (p.Lys2479=)
n.1687A>G
c.5043A>G (p.Lys1681=)
c.7656A>G (p.Lys2552=)
c.5466A>G (p.Lys1822=)
c.5142A>G (p.Lys1714=)
dbSNP
11g.118503452A>TCA382806017KMT2Ac.7659A>T (p.Lys2553Asn)
c.7650A>T (p.Lys2550Asn)
c.1599A>T (p.Lys533Asn)
c.1857A>T (p.Lys619Asn)
c.7632A>T (p.Lys2544Asn)
c.7551A>T (p.Lys2517Asn)
n.6902A>T
c.7560A>T (p.Lys2520Asn)
c.7437A>T (p.Lys2479Asn)
n.1687A>T
c.5043A>T (p.Lys1681Asn)
c.7656A>T (p.Lys2552Asn)
c.5466A>T (p.Lys1822Asn)
c.5142A>T (p.Lys1714Asn)
ClinVar
11g.118503453C>ACA382806018KMT2Ac.7660C>A (p.Arg2554Ser)
c.7651C>A (p.Arg2551Ser)
c.1600C>A (p.Arg534Ser)
c.1858C>A (p.Arg620Ser)
c.7633C>A (p.Arg2545Ser)
c.7552C>A (p.Arg2518Ser)
n.6903C>A
c.7561C>A (p.Arg2521Ser)
c.7438C>A (p.Arg2480Ser)
n.1688C>A
c.5044C>A (p.Arg1682Ser)
c.7657C>A (p.Arg2553Ser)
c.5467C>A (p.Arg1823Ser)
c.5143C>A (p.Arg1715Ser)
gnomAD v4
11g.118503453C=CA2003527912KMT2Ac.7660C= (p.Arg2554=)
c.7651C= (p.Arg2551=)
c.1600C= (p.Arg534=)
c.1858C= (p.Arg620=)
c.7633C= (p.Arg2545=)
c.7552C= (p.Arg2518=)
n.6903C=
c.7561C= (p.Arg2521=)
c.7438C= (p.Arg2480=)
n.1688C=
c.5044C= (p.Arg1682=)
c.7657C= (p.Arg2553=)
c.5467C= (p.Arg1823=)
c.5143C= (p.Arg1715=)
11g.118503453C>GCA382806019KMT2Ac.7660C>G (p.Arg2554Gly)
c.7651C>G (p.Arg2551Gly)
c.1600C>G (p.Arg534Gly)
c.1858C>G (p.Arg620Gly)
c.7633C>G (p.Arg2545Gly)
c.7552C>G (p.Arg2518Gly)
n.6903C>G
c.7561C>G (p.Arg2521Gly)
c.7438C>G (p.Arg2480Gly)
n.1688C>G
c.5044C>G (p.Arg1682Gly)
c.7657C>G (p.Arg2553Gly)
c.5467C>G (p.Arg1823Gly)
c.5143C>G (p.Arg1715Gly)
11g.118503453C>TCA6304413KMT2Ac.7660C>T (p.Arg2554Cys)
c.7651C>T (p.Arg2551Cys)
c.1600C>T (p.Arg534Cys)
c.1858C>T (p.Arg620Cys)
c.7633C>T (p.Arg2545Cys)
c.7552C>T (p.Arg2518Cys)
n.6903C>T
c.7561C>T (p.Arg2521Cys)
c.7438C>T (p.Arg2480Cys)
n.1688C>T
c.5044C>T (p.Arg1682Cys)
c.7657C>T (p.Arg2553Cys)
c.5467C>T (p.Arg1823Cys)
c.5143C>T (p.Arg1715Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.118503454G>ACA382806020KMT2Ac.7661G>A (p.Arg2554His)
c.7652G>A (p.Arg2551His)
c.1601G>A (p.Arg534His)
c.1859G>A (p.Arg620His)
c.7634G>A (p.Arg2545His)
c.7553G>A (p.Arg2518His)
n.6904G>A
c.7562G>A (p.Arg2521His)
c.7439G>A (p.Arg2480His)
n.1689G>A
c.5045G>A (p.Arg1682His)
c.7658G>A (p.Arg2553His)
c.5468G>A (p.Arg1823His)
c.5144G>A (p.Arg1715His)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
11g.118503454G>CCA382806021KMT2Ac.7661G>C (p.Arg2554Pro)
c.7652G>C (p.Arg2551Pro)
c.1601G>C (p.Arg534Pro)
c.1859G>C (p.Arg620Pro)
c.7634G>C (p.Arg2545Pro)
c.7553G>C (p.Arg2518Pro)
n.6904G>C
c.7562G>C (p.Arg2521Pro)
c.7439G>C (p.Arg2480Pro)
n.1689G>C
c.5045G>C (p.Arg1682Pro)
c.7658G>C (p.Arg2553Pro)
c.5468G>C (p.Arg1823Pro)
c.5144G>C (p.Arg1715Pro)
11g.118503454G=CA2003527914KMT2Ac.7661G= (p.Arg2554=)
c.7652G= (p.Arg2551=)
c.1601G= (p.Arg534=)
c.1859G= (p.Arg620=)
c.7634G= (p.Arg2545=)
c.7553G= (p.Arg2518=)
n.6904G=
c.7562G= (p.Arg2521=)
c.7439G= (p.Arg2480=)
n.1689G=
c.5045G= (p.Arg1682=)
c.7658G= (p.Arg2553=)
c.5468G= (p.Arg1823=)
c.5144G= (p.Arg1715=)
11g.118503454G>TCA382806022KMT2Ac.7661G>T (p.Arg2554Leu)
c.7652G>T (p.Arg2551Leu)
c.1601G>T (p.Arg534Leu)
c.1859G>T (p.Arg620Leu)
c.7634G>T (p.Arg2545Leu)
c.7553G>T (p.Arg2518Leu)
n.6904G>T
c.7562G>T (p.Arg2521Leu)
c.7439G>T (p.Arg2480Leu)
n.1689G>T
c.5045G>T (p.Arg1682Leu)
c.7658G>T (p.Arg2553Leu)
c.5468G>T (p.Arg1823Leu)
c.5144G>T (p.Arg1715Leu)
COSMIC COSMIC
11g.118503454_118503455insTTACATGGTCGTTGGCCCA2725065488KMT2Ac.7661_7662insTTACATGGTCGTTGGCC (p.Thr2555TyrfsTer10)
c.7652_7653insTTACATGGTCGTTGGCC (p.Thr2552TyrfsTer10)
c.1601_1602insTTACATGGTCGTTGGCC (p.Thr535TyrfsTer10)
c.1859_1860insTTACATGGTCGTTGGCC (p.Thr621TyrfsTer10)
c.7634_7635insTTACATGGTCGTTGGCC (p.Thr2546TyrfsTer10)
c.7553_7554insTTACATGGTCGTTGGCC (p.Thr2519TyrfsTer10)
n.6904_6905insTTACATGGTCGTTGGCC
c.7562_7563insTTACATGGTCGTTGGCC (p.Thr2522TyrfsTer10)
c.7439_7440insTTACATGGTCGTTGGCC (p.Thr2481TyrfsTer10)
n.1689_1690insTTACATGGTCGTTGGCC
c.5045_5046insTTACATGGTCGTTGGCC (p.Thr1683TyrfsTer10)
c.7658_7659insTTACATGGTCGTTGGCC (p.Thr2554TyrfsTer10)
c.5468_5469insTTACATGGTCGTTGGCC (p.Thr1824TyrfsTer10)
c.5144_5145insTTACATGGTCGTTGGCC (p.Thr1716TyrfsTer10)
dbSNP
11g.118503455C>ACA477359704KMT2Ac.7662C>A (p.Arg2554=)
c.7653C>A (p.Arg2551=)
c.1602C>A (p.Arg534=)
c.1860C>A (p.Arg620=)
c.7635C>A (p.Arg2545=)
c.7554C>A (p.Arg2518=)
n.6905C>A
c.7563C>A (p.Arg2521=)
c.7440C>A (p.Arg2480=)
n.1690C>A
c.5046C>A (p.Arg1682=)
c.7659C>A (p.Arg2553=)
c.5469C>A (p.Arg1823=)
c.5145C>A (p.Arg1715=)
11g.118503455C=CA2003527918KMT2Ac.7662C= (p.Arg2554=)
c.7653C= (p.Arg2551=)
c.1602C= (p.Arg534=)
c.1860C= (p.Arg620=)
c.7635C= (p.Arg2545=)
c.7554C= (p.Arg2518=)
n.6905C=
c.7563C= (p.Arg2521=)
c.7440C= (p.Arg2480=)
n.1690C=
c.5046C= (p.Arg1682=)
c.7659C= (p.Arg2553=)
c.5469C= (p.Arg1823=)
c.5145C= (p.Arg1715=)
11g.118503455C>GCA6304414KMT2Ac.7662C>G (p.Arg2554=)
c.7653C>G (p.Arg2551=)
c.1602C>G (p.Arg534=)
c.1860C>G (p.Arg620=)
c.7635C>G (p.Arg2545=)
c.7554C>G (p.Arg2518=)
n.6905C>G
c.7563C>G (p.Arg2521=)
c.7440C>G (p.Arg2480=)
n.1690C>G
c.5046C>G (p.Arg1682=)
c.7659C>G (p.Arg2553=)
c.5469C>G (p.Arg1823=)
c.5145C>G (p.Arg1715=)
dbSNP ExAC
11g.118503455C>TCA477359707KMT2Ac.7662C>T (p.Arg2554=)
c.7653C>T (p.Arg2551=)
c.1602C>T (p.Arg534=)
c.1860C>T (p.Arg620=)
c.7635C>T (p.Arg2545=)
c.7554C>T (p.Arg2518=)
n.6905C>T
c.7563C>T (p.Arg2521=)
c.7440C>T (p.Arg2480=)
n.1690C>T
c.5046C>T (p.Arg1682=)
c.7659C>T (p.Arg2553=)
c.5469C>T (p.Arg1823=)
c.5145C>T (p.Arg1715=)
ClinVar gnomAD v4
11g.118503456A>CCA382806023KMT2Ac.7663A>C (p.Thr2555Pro)
c.7654A>C (p.Thr2552Pro)
c.1603A>C (p.Thr535Pro)
c.1861A>C (p.Thr621Pro)
c.7636A>C (p.Thr2546Pro)
c.7555A>C (p.Thr2519Pro)
n.6906A>C
c.7564A>C (p.Thr2522Pro)
c.7441A>C (p.Thr2481Pro)
n.1691A>C
c.5047A>C (p.Thr1683Pro)
c.7660A>C (p.Thr2554Pro)
c.5470A>C (p.Thr1824Pro)
c.5146A>C (p.Thr1716Pro)
11g.118503456A>GCA382806024KMT2Ac.7663A>G (p.Thr2555Ala)
c.7654A>G (p.Thr2552Ala)
c.1603A>G (p.Thr535Ala)
c.1861A>G (p.Thr621Ala)
c.7636A>G (p.Thr2546Ala)
c.7555A>G (p.Thr2519Ala)
n.6906A>G
c.7564A>G (p.Thr2522Ala)
c.7441A>G (p.Thr2481Ala)
n.1691A>G
c.5047A>G (p.Thr1683Ala)
c.7660A>G (p.Thr2554Ala)
c.5470A>G (p.Thr1824Ala)
c.5146A>G (p.Thr1716Ala)
gnomAD v4
11g.118503456A>TCA382806025KMT2Ac.7663A>T (p.Thr2555Ser)
c.7654A>T (p.Thr2552Ser)
c.1603A>T (p.Thr535Ser)
c.1861A>T (p.Thr621Ser)
c.7636A>T (p.Thr2546Ser)
c.7555A>T (p.Thr2519Ser)
n.6906A>T
c.7564A>T (p.Thr2522Ser)
c.7441A>T (p.Thr2481Ser)
n.1691A>T
c.5047A>T (p.Thr1683Ser)
c.7660A>T (p.Thr2554Ser)
c.5470A>T (p.Thr1824Ser)
c.5146A>T (p.Thr1716Ser)
11g.118503456_118503460delinsACAGTCA2003527921KMT2Ac.7663_7667delinsACAGT (p.Thr2555=)
c.7654_7658delinsACAGT (p.Thr2552=)
c.1603_1607delinsACAGT (p.Thr535=)
c.1861_1865delinsACAGT (p.Thr621=)
c.7636_7640delinsACAGT (p.Thr2546=)
c.7555_7559delinsACAGT (p.Thr2519=)
n.6906_6910delinsACAGT
c.7564_7568delinsACAGT (p.Thr2522=)
c.7441_7445delinsACAGT (p.Thr2481=)
n.1691_1695delinsACAGT
c.5047_5051delinsACAGT (p.Thr1683=)
c.7660_7664delinsACAGT (p.Thr2554=)
c.5470_5474delinsACAGT (p.Thr1824=)
c.5146_5150delinsACAGT (p.Thr1716=)
11g.118503457C>ACA382806028KMT2Ac.7664C>A (p.Thr2555Lys)
c.7655C>A (p.Thr2552Lys)
c.1604C>A (p.Thr535Lys)
c.1862C>A (p.Thr621Lys)
c.7637C>A (p.Thr2546Lys)
c.7556C>A (p.Thr2519Lys)
n.6907C>A
c.7565C>A (p.Thr2522Lys)
c.7442C>A (p.Thr2481Lys)
n.1692C>A
c.5048C>A (p.Thr1683Lys)
c.7661C>A (p.Thr2554Lys)
c.5471C>A (p.Thr1824Lys)
c.5147C>A (p.Thr1716Lys)
11g.118503457C>GCA382806027KMT2Ac.7664C>G (p.Thr2555Arg)
c.7655C>G (p.Thr2552Arg)
c.1604C>G (p.Thr535Arg)
c.1862C>G (p.Thr621Arg)
c.7637C>G (p.Thr2546Arg)
c.7556C>G (p.Thr2519Arg)
n.6907C>G
c.7565C>G (p.Thr2522Arg)
c.7442C>G (p.Thr2481Arg)
n.1692C>G
c.5048C>G (p.Thr1683Arg)
c.7661C>G (p.Thr2554Arg)
c.5471C>G (p.Thr1824Arg)
c.5147C>G (p.Thr1716Arg)
gnomAD v4
11g.118503457C>TCA382806026KMT2Ac.7664C>T (p.Thr2555Ile)
c.7655C>T (p.Thr2552Ile)
c.1604C>T (p.Thr535Ile)
c.1862C>T (p.Thr621Ile)
c.7637C>T (p.Thr2546Ile)
c.7556C>T (p.Thr2519Ile)
n.6907C>T
c.7565C>T (p.Thr2522Ile)
c.7442C>T (p.Thr2481Ile)
n.1692C>T
c.5048C>T (p.Thr1683Ile)
c.7661C>T (p.Thr2554Ile)
c.5471C>T (p.Thr1824Ile)
c.5147C>T (p.Thr1716Ile)
dbSNP COSMIC COSMIC
11g.118503459_118503462delCA236389KMT2Ac.7666_7669del (p.Val2556LysfsTer2)
c.7657_7660del (p.Val2553LysfsTer2)
c.1606_1609del (p.Val536LysfsTer2)
c.1864_1867del (p.Val622LysfsTer2)
c.7639_7642del (p.Val2547LysfsTer2)
c.7558_7561del (p.Val2520LysfsTer2)
n.6909_6912del
c.7567_7570del (p.Val2523LysfsTer2)
c.7444_7447del (p.Val2482LysfsTer2)
n.1694_1697del
c.5050_5053del (p.Val1684LysfsTer2)
c.7663_7666del (p.Val2555LysfsTer2)
c.5473_5476del (p.Val1825LysfsTer2)
c.5149_5152del (p.Val1717LysfsTer2)
ClinVar dbSNP
11g.118503458A=CA2003527931KMT2Ac.7665A= (p.Thr2555=)
c.7656A= (p.Thr2552=)
c.1605A= (p.Thr535=)
c.1863A= (p.Thr621=)
c.7638A= (p.Thr2546=)
c.7557A= (p.Thr2519=)
n.6908A=
c.7566A= (p.Thr2522=)
c.7443A= (p.Thr2481=)
n.1693A=
c.5049A= (p.Thr1683=)
c.7662A= (p.Thr2554=)
c.5472A= (p.Thr1824=)
c.5148A= (p.Thr1716=)
11g.118503458A>CCA477359710KMT2Ac.7665A>C (p.Thr2555=)
c.7656A>C (p.Thr2552=)
c.1605A>C (p.Thr535=)
c.1863A>C (p.Thr621=)
c.7638A>C (p.Thr2546=)
c.7557A>C (p.Thr2519=)
n.6908A>C
c.7566A>C (p.Thr2522=)
c.7443A>C (p.Thr2481=)
n.1693A>C
c.5049A>C (p.Thr1683=)
c.7662A>C (p.Thr2554=)
c.5472A>C (p.Thr1824=)
c.5148A>C (p.Thr1716=)
11g.118503458A>GCA477359711KMT2Ac.7665A>G (p.Thr2555=)
c.7656A>G (p.Thr2552=)
c.1605A>G (p.Thr535=)
c.1863A>G (p.Thr621=)
c.7638A>G (p.Thr2546=)
c.7557A>G (p.Thr2519=)
n.6908A>G
c.7566A>G (p.Thr2522=)
c.7443A>G (p.Thr2481=)
n.1693A>G
c.5049A>G (p.Thr1683=)
c.7662A>G (p.Thr2554=)
c.5472A>G (p.Thr1824=)
c.5148A>G (p.Thr1716=)
dbSNP gnomAD v3 gnomAD v4
11g.118503458A>TCA477359713KMT2Ac.7665A>T (p.Thr2555=)
c.7656A>T (p.Thr2552=)
c.1605A>T (p.Thr535=)
c.1863A>T (p.Thr621=)
c.7638A>T (p.Thr2546=)
c.7557A>T (p.Thr2519=)
n.6908A>T
c.7566A>T (p.Thr2522=)
c.7443A>T (p.Thr2481=)
n.1693A>T
c.5049A>T (p.Thr1683=)
c.7662A>T (p.Thr2554=)
c.5472A>T (p.Thr1824=)
c.5148A>T (p.Thr1716=)
11g.118503459G>ACA382806029KMT2Ac.7666G>A (p.Val2556Ile)
c.7657G>A (p.Val2553Ile)
c.1606G>A (p.Val536Ile)
c.1864G>A (p.Val622Ile)
c.7639G>A (p.Val2547Ile)
c.7558G>A (p.Val2520Ile)
n.6909G>A
c.7567G>A (p.Val2523Ile)
c.7444G>A (p.Val2482Ile)
n.1694G>A
c.5050G>A (p.Val1684Ile)
c.7663G>A (p.Val2555Ile)
c.5473G>A (p.Val1825Ile)
c.5149G>A (p.Val1717Ile)
11g.118503459G>CCA382806030KMT2Ac.7666G>C (p.Val2556Leu)
c.7657G>C (p.Val2553Leu)
c.1606G>C (p.Val536Leu)
c.1864G>C (p.Val622Leu)
c.7639G>C (p.Val2547Leu)
c.7558G>C (p.Val2520Leu)
n.6909G>C
c.7567G>C (p.Val2523Leu)
c.7444G>C (p.Val2482Leu)
n.1694G>C
c.5050G>C (p.Val1684Leu)
c.7663G>C (p.Val2555Leu)
c.5473G>C (p.Val1825Leu)
c.5149G>C (p.Val1717Leu)
11g.118503459G>TCA382806031KMT2Ac.7666G>T (p.Val2556Phe)
c.7657G>T (p.Val2553Phe)
c.1606G>T (p.Val536Phe)
c.1864G>T (p.Val622Phe)
c.7639G>T (p.Val2547Phe)
c.7558G>T (p.Val2520Phe)
n.6909G>T
c.7567G>T (p.Val2523Phe)
c.7444G>T (p.Val2482Phe)
n.1694G>T
c.5050G>T (p.Val1684Phe)
c.7663G>T (p.Val2555Phe)
c.5473G>T (p.Val1825Phe)
c.5149G>T (p.Val1717Phe)
11g.118503460T>ACA382806032KMT2Ac.7667T>A (p.Val2556Asp)
c.7658T>A (p.Val2553Asp)
c.1607T>A (p.Val536Asp)
c.1865T>A (p.Val622Asp)
c.7640T>A (p.Val2547Asp)
c.7559T>A (p.Val2520Asp)
n.6910T>A
c.7568T>A (p.Val2523Asp)
c.7445T>A (p.Val2482Asp)
n.1695T>A
c.5051T>A (p.Val1684Asp)
c.7664T>A (p.Val2555Asp)
c.5474T>A (p.Val1825Asp)
c.5150T>A (p.Val1717Asp)
dbSNP
11g.118503460T>CCA382806033KMT2Ac.7667T>C (p.Val2556Ala)
c.7658T>C (p.Val2553Ala)
c.1607T>C (p.Val536Ala)
c.1865T>C (p.Val622Ala)
c.7640T>C (p.Val2547Ala)
c.7559T>C (p.Val2520Ala)
n.6910T>C
c.7568T>C (p.Val2523Ala)
c.7445T>C (p.Val2482Ala)
n.1695T>C
c.5051T>C (p.Val1684Ala)
c.7664T>C (p.Val2555Ala)
c.5474T>C (p.Val1825Ala)
c.5150T>C (p.Val1717Ala)
11g.118503460T>GCA382806034KMT2Ac.7667T>G (p.Val2556Gly)
c.7658T>G (p.Val2553Gly)
c.1607T>G (p.Val536Gly)
c.1865T>G (p.Val622Gly)
c.7640T>G (p.Val2547Gly)
c.7559T>G (p.Val2520Gly)
n.6910T>G
c.7568T>G (p.Val2523Gly)
c.7445T>G (p.Val2482Gly)
n.1695T>G
c.5051T>G (p.Val1684Gly)
c.7664T>G (p.Val2555Gly)
c.5474T>G (p.Val1825Gly)
c.5150T>G (p.Val1717Gly)
11g.118503461C>ACA477359720KMT2Ac.7668C>A (p.Val2556=)
c.7659C>A (p.Val2553=)
c.1608C>A (p.Val536=)
c.1866C>A (p.Val622=)
c.7641C>A (p.Val2547=)
c.7560C>A (p.Val2520=)
n.6911C>A
c.7569C>A (p.Val2523=)
c.7446C>A (p.Val2482=)
n.1696C>A
c.5052C>A (p.Val1684=)
c.7665C>A (p.Val2555=)
c.5475C>A (p.Val1825=)
c.5151C>A (p.Val1717=)
11g.118503461C>GCA477359721KMT2Ac.7668C>G (p.Val2556=)
c.7659C>G (p.Val2553=)
c.1608C>G (p.Val536=)
c.1866C>G (p.Val622=)
c.7641C>G (p.Val2547=)
c.7560C>G (p.Val2520=)
n.6911C>G
c.7569C>G (p.Val2523=)
c.7446C>G (p.Val2482=)
n.1696C>G
c.5052C>G (p.Val1684=)
c.7665C>G (p.Val2555=)
c.5475C>G (p.Val1825=)
c.5151C>G (p.Val1717=)
dbSNP
11g.118503461C>TCA477359722KMT2Ac.7668C>T (p.Val2556=)
c.7659C>T (p.Val2553=)
c.1608C>T (p.Val536=)
c.1866C>T (p.Val622=)
c.7641C>T (p.Val2547=)
c.7560C>T (p.Val2520=)
n.6911C>T
c.7569C>T (p.Val2523=)
c.7446C>T (p.Val2482=)
n.1696C>T
c.5052C>T (p.Val1684=)
c.7665C>T (p.Val2555=)
c.5475C>T (p.Val1825=)
c.5151C>T (p.Val1717=)
11g.118503462A>CCA382806037KMT2Ac.7669A>C (p.Lys2557Gln)
c.7660A>C (p.Lys2554Gln)
c.1609A>C (p.Lys537Gln)
c.1867A>C (p.Lys623Gln)
c.7642A>C (p.Lys2548Gln)
c.7561A>C (p.Lys2521Gln)
n.6912A>C
c.7570A>C (p.Lys2524Gln)
c.7447A>C (p.Lys2483Gln)
n.1697A>C
c.5053A>C (p.Lys1685Gln)
c.7666A>C (p.Lys2556Gln)
c.5476A>C (p.Lys1826Gln)
c.5152A>C (p.Lys1718Gln)
11g.118503462A>GCA382806035KMT2Ac.7669A>G (p.Lys2557Glu)
c.7660A>G (p.Lys2554Glu)
c.1609A>G (p.Lys537Glu)
c.1867A>G (p.Lys623Glu)
c.7642A>G (p.Lys2548Glu)
c.7561A>G (p.Lys2521Glu)
n.6912A>G
c.7570A>G (p.Lys2524Glu)
c.7447A>G (p.Lys2483Glu)
n.1697A>G
c.5053A>G (p.Lys1685Glu)
c.7666A>G (p.Lys2556Glu)
c.5476A>G (p.Lys1826Glu)
c.5152A>G (p.Lys1718Glu)
gnomAD v4
11g.118503462A>TCA382806036KMT2Ac.7669A>T (p.Lys2557Ter)
c.7660A>T (p.Lys2554Ter)
c.1609A>T (p.Lys537Ter)
c.1867A>T (p.Lys623Ter)
c.7642A>T (p.Lys2548Ter)
c.7561A>T (p.Lys2521Ter)
n.6912A>T
c.7570A>T (p.Lys2524Ter)
c.7447A>T (p.Lys2483Ter)
n.1697A>T
c.5053A>T (p.Lys1685Ter)
c.7666A>T (p.Lys2556Ter)
c.5476A>T (p.Lys1826Ter)
c.5152A>T (p.Lys1718Ter)
11g.118503463A>CCA382806038KMT2Ac.7670A>C (p.Lys2557Thr)
c.7661A>C (p.Lys2554Thr)
c.1610A>C (p.Lys537Thr)
c.1868A>C (p.Lys623Thr)
c.7643A>C (p.Lys2548Thr)
c.7562A>C (p.Lys2521Thr)
n.6913A>C
c.7571A>C (p.Lys2524Thr)
c.7448A>C (p.Lys2483Thr)
n.1698A>C
c.5054A>C (p.Lys1685Thr)
c.7667A>C (p.Lys2556Thr)
c.5477A>C (p.Lys1826Thr)
c.5153A>C (p.Lys1718Thr)
11g.118503463A>GCA382806039KMT2Ac.7670A>G (p.Lys2557Arg)
c.7661A>G (p.Lys2554Arg)
c.1610A>G (p.Lys537Arg)
c.1868A>G (p.Lys623Arg)
c.7643A>G (p.Lys2548Arg)
c.7562A>G (p.Lys2521Arg)
n.6913A>G
c.7571A>G (p.Lys2524Arg)
c.7448A>G (p.Lys2483Arg)
n.1698A>G
c.5054A>G (p.Lys1685Arg)
c.7667A>G (p.Lys2556Arg)
c.5477A>G (p.Lys1826Arg)
c.5153A>G (p.Lys1718Arg)
11g.118503463A>TCA382806040KMT2Ac.7670A>T (p.Lys2557Ile)
c.7661A>T (p.Lys2554Ile)
c.1610A>T (p.Lys537Ile)
c.1868A>T (p.Lys623Ile)
c.7643A>T (p.Lys2548Ile)
c.7562A>T (p.Lys2521Ile)
n.6913A>T
c.7571A>T (p.Lys2524Ile)
c.7448A>T (p.Lys2483Ile)
n.1698A>T
c.5054A>T (p.Lys1685Ile)
c.7667A>T (p.Lys2556Ile)
c.5477A>T (p.Lys1826Ile)
c.5153A>T (p.Lys1718Ile)
11g.118503464A>CCA382806041KMT2Ac.7671A>C (p.Lys2557Asn)
c.7662A>C (p.Lys2554Asn)
c.1611A>C (p.Lys537Asn)
c.1869A>C (p.Lys623Asn)
c.7644A>C (p.Lys2548Asn)
c.7563A>C (p.Lys2521Asn)
n.6914A>C
c.7572A>C (p.Lys2524Asn)
c.7449A>C (p.Lys2483Asn)
n.1699A>C
c.5055A>C (p.Lys1685Asn)
c.7668A>C (p.Lys2556Asn)
c.5478A>C (p.Lys1826Asn)
c.5154A>C (p.Lys1718Asn)
11g.118503464A>GCA477359727KMT2Ac.7671A>G (p.Lys2557=)
c.7662A>G (p.Lys2554=)
c.1611A>G (p.Lys537=)
c.1869A>G (p.Lys623=)
c.7644A>G (p.Lys2548=)
c.7563A>G (p.Lys2521=)
n.6914A>G
c.7572A>G (p.Lys2524=)
c.7449A>G (p.Lys2483=)
n.1699A>G
c.5055A>G (p.Lys1685=)
c.7668A>G (p.Lys2556=)
c.5478A>G (p.Lys1826=)
c.5154A>G (p.Lys1718=)
11g.118503464A>TCA382806042KMT2Ac.7671A>T (p.Lys2557Asn)
c.7662A>T (p.Lys2554Asn)
c.1611A>T (p.Lys537Asn)
c.1869A>T (p.Lys623Asn)
c.7644A>T (p.Lys2548Asn)
c.7563A>T (p.Lys2521Asn)
n.6914A>T
c.7572A>T (p.Lys2524Asn)
c.7449A>T (p.Lys2483Asn)
n.1699A>T
c.5055A>T (p.Lys1685Asn)
c.7668A>T (p.Lys2556Asn)
c.5478A>T (p.Lys1826Asn)
c.5154A>T (p.Lys1718Asn)
11g.118503465G>ACA382806043KMT2Ac.7672G>A (p.Val2558Met)
c.7663G>A (p.Val2555Met)
c.1612G>A (p.Val538Met)
c.1870G>A (p.Val624Met)
c.7645G>A (p.Val2549Met)
c.7564G>A (p.Val2522Met)
n.6915G>A
c.7573G>A (p.Val2525Met)
c.7450G>A (p.Val2484Met)
n.1700G>A
c.5056G>A (p.Val1686Met)
c.7669G>A (p.Val2557Met)
c.5479G>A (p.Val1827Met)
c.5155G>A (p.Val1719Met)
gnomAD v4 COSMIC COSMIC
11g.118503465G>CCA382806045KMT2Ac.7672G>C (p.Val2558Leu)
c.7663G>C (p.Val2555Leu)
c.1612G>C (p.Val538Leu)
c.1870G>C (p.Val624Leu)
c.7645G>C (p.Val2549Leu)
c.7564G>C (p.Val2522Leu)
n.6915G>C
c.7573G>C (p.Val2525Leu)
c.7450G>C (p.Val2484Leu)
n.1700G>C
c.5056G>C (p.Val1686Leu)
c.7669G>C (p.Val2557Leu)
c.5479G>C (p.Val1827Leu)
c.5155G>C (p.Val1719Leu)
gnomAD v4

Number of alleles fetched