Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.118491206C>ACA382834261KMT2Ac.4806C>A (p.Cys1602Ter)
c.483C>A (p.Cys161Ter)
c.4707C>A (p.Cys1569Ter)
c.4593C>A (p.Cys1531Ter)
c.843C>A (p.Cys281Ter)
c.2190C>A (p.Cys730Ter)
c.4803C>A (p.Cys1601Ter)
c.2613C>A (p.Cys871Ter)
c.2289C>A (p.Cys763Ter)
11g.118491206C>GCA382834260KMT2Ac.4806C>G (p.Cys1602Trp)
c.483C>G (p.Cys161Trp)
c.4707C>G (p.Cys1569Trp)
c.4593C>G (p.Cys1531Trp)
c.843C>G (p.Cys281Trp)
c.2190C>G (p.Cys730Trp)
c.4803C>G (p.Cys1601Trp)
c.2613C>G (p.Cys871Trp)
c.2289C>G (p.Cys763Trp)
11g.118491206C>TCA477091614KMT2Ac.4806C>T (p.Cys1602=)
c.483C>T (p.Cys161=)
c.4707C>T (p.Cys1569=)
c.4593C>T (p.Cys1531=)
c.843C>T (p.Cys281=)
c.2190C>T (p.Cys730=)
c.4803C>T (p.Cys1601=)
c.2613C>T (p.Cys871=)
c.2289C>T (p.Cys763=)
11g.118491207C>ACA382834264KMT2Ac.4807C>A (p.Pro1603Thr)
c.484C>A (p.Pro162Thr)
c.4708C>A (p.Pro1570Thr)
c.4594C>A (p.Pro1532Thr)
c.844C>A (p.Pro282Thr)
c.2191C>A (p.Pro731Thr)
c.4804C>A (p.Pro1602Thr)
c.2614C>A (p.Pro872Thr)
c.2290C>A (p.Pro764Thr)
11g.118491207C>GCA382834262KMT2Ac.4807C>G (p.Pro1603Ala)
c.484C>G (p.Pro162Ala)
c.4708C>G (p.Pro1570Ala)
c.4594C>G (p.Pro1532Ala)
c.844C>G (p.Pro282Ala)
c.2191C>G (p.Pro731Ala)
c.4804C>G (p.Pro1602Ala)
c.2614C>G (p.Pro872Ala)
c.2290C>G (p.Pro764Ala)
11g.118491207C>TCA382834263KMT2Ac.4807C>T (p.Pro1603Ser)
c.484C>T (p.Pro162Ser)
c.4708C>T (p.Pro1570Ser)
c.4594C>T (p.Pro1532Ser)
c.844C>T (p.Pro282Ser)
c.2191C>T (p.Pro731Ser)
c.4804C>T (p.Pro1602Ser)
c.2614C>T (p.Pro872Ser)
c.2290C>T (p.Pro764Ser)
11g.118491208C>ACA382834265KMT2Ac.4808C>A (p.Pro1603His)
c.485C>A (p.Pro162His)
c.4709C>A (p.Pro1570His)
c.4595C>A (p.Pro1532His)
c.845C>A (p.Pro282His)
c.2192C>A (p.Pro731His)
c.4805C>A (p.Pro1602His)
c.2615C>A (p.Pro872His)
c.2291C>A (p.Pro764His)
COSMIC COSMIC
11g.118491208C>GCA382834266KMT2Ac.4808C>G (p.Pro1603Arg)
c.485C>G (p.Pro162Arg)
c.4709C>G (p.Pro1570Arg)
c.4595C>G (p.Pro1532Arg)
c.845C>G (p.Pro282Arg)
c.2192C>G (p.Pro731Arg)
c.4805C>G (p.Pro1602Arg)
c.2615C>G (p.Pro872Arg)
c.2291C>G (p.Pro764Arg)
11g.118491208C>TCA382834267KMT2Ac.4808C>T (p.Pro1603Leu)
c.485C>T (p.Pro162Leu)
c.4709C>T (p.Pro1570Leu)
c.4595C>T (p.Pro1532Leu)
c.845C>T (p.Pro282Leu)
c.2192C>T (p.Pro731Leu)
c.4805C>T (p.Pro1602Leu)
c.2615C>T (p.Pro872Leu)
c.2291C>T (p.Pro764Leu)
11g.118491209T>ACA477091615KMT2Ac.4809T>A (p.Pro1603=)
c.486T>A (p.Pro162=)
c.4710T>A (p.Pro1570=)
c.4596T>A (p.Pro1532=)
c.846T>A (p.Pro282=)
c.2193T>A (p.Pro731=)
c.4806T>A (p.Pro1602=)
c.2616T>A (p.Pro872=)
c.2292T>A (p.Pro764=)
11g.118491209T>CCA477091616KMT2Ac.4809T>C (p.Pro1603=)
c.486T>C (p.Pro162=)
c.4710T>C (p.Pro1570=)
c.4596T>C (p.Pro1532=)
c.846T>C (p.Pro282=)
c.2193T>C (p.Pro731=)
c.4806T>C (p.Pro1602=)
c.2616T>C (p.Pro872=)
c.2292T>C (p.Pro764=)
dbSNP gnomAD v2 gnomAD v4
11g.118491209T>GCA477091617KMT2Ac.4809T>G (p.Pro1603=)
c.486T>G (p.Pro162=)
c.4710T>G (p.Pro1570=)
c.4596T>G (p.Pro1532=)
c.846T>G (p.Pro282=)
c.2193T>G (p.Pro731=)
c.4806T>G (p.Pro1602=)
c.2616T>G (p.Pro872=)
c.2292T>G (p.Pro764=)
11g.118491209T=CA2003519099KMT2Ac.4809T= (p.Pro1603=)
c.486T= (p.Pro162=)
c.4710T= (p.Pro1570=)
c.4596T= (p.Pro1532=)
c.846T= (p.Pro282=)
c.2193T= (p.Pro731=)
c.4806T= (p.Pro1602=)
c.2616T= (p.Pro872=)
c.2292T= (p.Pro764=)
11g.118491210C>ACA382834270KMT2Ac.4810C>A (p.Leu1604Ile)
c.487C>A (p.Leu163Ile)
c.4711C>A (p.Leu1571Ile)
c.4597C>A (p.Leu1533Ile)
c.847C>A (p.Leu283Ile)
c.2194C>A (p.Leu732Ile)
c.4807C>A (p.Leu1603Ile)
c.2617C>A (p.Leu873Ile)
c.2293C>A (p.Leu765Ile)
11g.118491210C=CA2003519102KMT2Ac.4810C= (p.Leu1604=)
c.487C= (p.Leu163=)
c.4711C= (p.Leu1571=)
c.4597C= (p.Leu1533=)
c.847C= (p.Leu283=)
c.2194C= (p.Leu732=)
c.4807C= (p.Leu1603=)
c.2617C= (p.Leu873=)
c.2293C= (p.Leu765=)
11g.118491210C>GCA382834269KMT2Ac.4810C>G (p.Leu1604Val)
c.487C>G (p.Leu163Val)
c.4711C>G (p.Leu1571Val)
c.4597C>G (p.Leu1533Val)
c.847C>G (p.Leu283Val)
c.2194C>G (p.Leu732Val)
c.4807C>G (p.Leu1603Val)
c.2617C>G (p.Leu873Val)
c.2293C>G (p.Leu765Val)
11g.118491210C>TCA382834268KMT2Ac.4810C>T (p.Leu1604Phe)
c.487C>T (p.Leu163Phe)
c.4711C>T (p.Leu1571Phe)
c.4597C>T (p.Leu1533Phe)
c.847C>T (p.Leu283Phe)
c.2194C>T (p.Leu732Phe)
c.4807C>T (p.Leu1603Phe)
c.2617C>T (p.Leu873Phe)
c.2293C>T (p.Leu765Phe)
dbSNP
11g.118491211T>ACA382834271KMT2Ac.4811T>A (p.Leu1604His)
c.488T>A (p.Leu163His)
c.4712T>A (p.Leu1571His)
c.4598T>A (p.Leu1533His)
c.848T>A (p.Leu283His)
c.2195T>A (p.Leu732His)
c.4808T>A (p.Leu1603His)
c.2618T>A (p.Leu873His)
c.2294T>A (p.Leu765His)
11g.118491211T>CCA382834272KMT2Ac.4811T>C (p.Leu1604Pro)
c.488T>C (p.Leu163Pro)
c.4712T>C (p.Leu1571Pro)
c.4598T>C (p.Leu1533Pro)
c.848T>C (p.Leu283Pro)
c.2195T>C (p.Leu732Pro)
c.4808T>C (p.Leu1603Pro)
c.2618T>C (p.Leu873Pro)
c.2294T>C (p.Leu765Pro)
11g.118491211T>GCA382834273KMT2Ac.4811T>G (p.Leu1604Arg)
c.488T>G (p.Leu163Arg)
c.4712T>G (p.Leu1571Arg)
c.4598T>G (p.Leu1533Arg)
c.848T>G (p.Leu283Arg)
c.2195T>G (p.Leu732Arg)
c.4808T>G (p.Leu1603Arg)
c.2618T>G (p.Leu873Arg)
c.2294T>G (p.Leu765Arg)
11g.118491212C>ACA477091618KMT2Ac.4812C>A (p.Leu1604=)
c.489C>A (p.Leu163=)
c.4713C>A (p.Leu1571=)
c.4599C>A (p.Leu1533=)
c.849C>A (p.Leu283=)
c.2196C>A (p.Leu732=)
c.4809C>A (p.Leu1603=)
c.2619C>A (p.Leu873=)
c.2295C>A (p.Leu765=)
11g.118491212C>GCA477091619KMT2Ac.4812C>G (p.Leu1604=)
c.489C>G (p.Leu163=)
c.4713C>G (p.Leu1571=)
c.4599C>G (p.Leu1533=)
c.849C>G (p.Leu283=)
c.2196C>G (p.Leu732=)
c.4809C>G (p.Leu1603=)
c.2619C>G (p.Leu873=)
c.2295C>G (p.Leu765=)
11g.118491212C>TCA477091620KMT2Ac.4812C>T (p.Leu1604=)
c.489C>T (p.Leu163=)
c.4713C>T (p.Leu1571=)
c.4599C>T (p.Leu1533=)
c.849C>T (p.Leu283=)
c.2196C>T (p.Leu732=)
c.4809C>T (p.Leu1603=)
c.2619C>T (p.Leu873=)
c.2295C>T (p.Leu765=)
11g.118491213T>ACA382834274KMT2Ac.4813T>A (p.Cys1605Ser)
c.490T>A (p.Cys164Ser)
c.4714T>A (p.Cys1572Ser)
c.4600T>A (p.Cys1534Ser)
c.850T>A (p.Cys284Ser)
c.2197T>A (p.Cys733Ser)
c.4810T>A (p.Cys1604Ser)
c.2620T>A (p.Cys874Ser)
c.2296T>A (p.Cys766Ser)
11g.118491213T>CCA382834275KMT2Ac.4813T>C (p.Cys1605Arg)
c.490T>C (p.Cys164Arg)
c.4714T>C (p.Cys1572Arg)
c.4600T>C (p.Cys1534Arg)
c.850T>C (p.Cys284Arg)
c.2197T>C (p.Cys733Arg)
c.4810T>C (p.Cys1604Arg)
c.2620T>C (p.Cys874Arg)
c.2296T>C (p.Cys766Arg)
11g.118491213T>GCA382834276KMT2Ac.4813T>G (p.Cys1605Gly)
c.490T>G (p.Cys164Gly)
c.4714T>G (p.Cys1572Gly)
c.4600T>G (p.Cys1534Gly)
c.850T>G (p.Cys284Gly)
c.2197T>G (p.Cys733Gly)
c.4810T>G (p.Cys1604Gly)
c.2620T>G (p.Cys874Gly)
c.2296T>G (p.Cys766Gly)
11g.118491214G>ACA382834277KMT2Ac.4814G>A (p.Cys1605Tyr)
c.491G>A (p.Cys164Tyr)
c.4715G>A (p.Cys1572Tyr)
c.4601G>A (p.Cys1534Tyr)
c.851G>A (p.Cys284Tyr)
c.2198G>A (p.Cys733Tyr)
c.4811G>A (p.Cys1604Tyr)
c.2621G>A (p.Cys874Tyr)
c.2297G>A (p.Cys766Tyr)
COSMIC COSMIC
11g.118491214G>CCA382834279KMT2Ac.4814G>C (p.Cys1605Ser)
c.491G>C (p.Cys164Ser)
c.4715G>C (p.Cys1572Ser)
c.4601G>C (p.Cys1534Ser)
c.851G>C (p.Cys284Ser)
c.2198G>C (p.Cys733Ser)
c.4811G>C (p.Cys1604Ser)
c.2621G>C (p.Cys874Ser)
c.2297G>C (p.Cys766Ser)
11g.118491214G>TCA382834278KMT2Ac.4814G>T (p.Cys1605Phe)
c.491G>T (p.Cys164Phe)
c.4715G>T (p.Cys1572Phe)
c.4601G>T (p.Cys1534Phe)
c.851G>T (p.Cys284Phe)
c.2198G>T (p.Cys733Phe)
c.4811G>T (p.Cys1604Phe)
c.2621G>T (p.Cys874Phe)
c.2297G>T (p.Cys766Phe)
11g.118491215T>ACA382834280KMT2Ac.4815T>A (p.Cys1605Ter)
c.492T>A (p.Cys164Ter)
c.4716T>A (p.Cys1572Ter)
c.4602T>A (p.Cys1534Ter)
c.852T>A (p.Cys284Ter)
c.2199T>A (p.Cys733Ter)
c.4812T>A (p.Cys1604Ter)
c.2622T>A (p.Cys874Ter)
c.2298T>A (p.Cys766Ter)
11g.118491215T>CCA477091621KMT2Ac.4815T>C (p.Cys1605=)
c.492T>C (p.Cys164=)
c.4716T>C (p.Cys1572=)
c.4602T>C (p.Cys1534=)
c.852T>C (p.Cys284=)
c.2199T>C (p.Cys733=)
c.4812T>C (p.Cys1604=)
c.2622T>C (p.Cys874=)
c.2298T>C (p.Cys766=)
gnomAD v4
11g.118491215T>GCA382834281KMT2Ac.4815T>G (p.Cys1605Trp)
c.492T>G (p.Cys164Trp)
c.4716T>G (p.Cys1572Trp)
c.4602T>G (p.Cys1534Trp)
c.852T>G (p.Cys284Trp)
c.2199T>G (p.Cys733Trp)
c.4812T>G (p.Cys1604Trp)
c.2622T>G (p.Cys874Trp)
c.2298T>G (p.Cys766Trp)
11g.118491216G>ACA382834282KMT2Ac.4816G>A (p.Asp1606Asn)
c.493G>A (p.Asp165Asn)
c.4717G>A (p.Asp1573Asn)
c.4603G>A (p.Asp1535Asn)
c.853G>A (p.Asp285Asn)
c.2200G>A (p.Asp734Asn)
c.4813G>A (p.Asp1605Asn)
c.2623G>A (p.Asp875Asn)
c.2299G>A (p.Asp767Asn)
dbSNP
11g.118491216G>CCA382834283KMT2Ac.4816G>C (p.Asp1606His)
c.493G>C (p.Asp165His)
c.4717G>C (p.Asp1573His)
c.4603G>C (p.Asp1535His)
c.853G>C (p.Asp285His)
c.2200G>C (p.Asp734His)
c.4813G>C (p.Asp1605His)
c.2623G>C (p.Asp875His)
c.2299G>C (p.Asp767His)
11g.118491216G>TCA382834284KMT2Ac.4816G>T (p.Asp1606Tyr)
c.493G>T (p.Asp165Tyr)
c.4717G>T (p.Asp1573Tyr)
c.4603G>T (p.Asp1535Tyr)
c.853G>T (p.Asp285Tyr)
c.2200G>T (p.Asp734Tyr)
c.4813G>T (p.Asp1605Tyr)
c.2623G>T (p.Asp875Tyr)
c.2299G>T (p.Asp767Tyr)
11g.118491217A>CCA382834285KMT2Ac.4817A>C (p.Asp1606Ala)
c.494A>C (p.Asp165Ala)
c.4718A>C (p.Asp1573Ala)
c.4604A>C (p.Asp1535Ala)
c.854A>C (p.Asp285Ala)
c.2201A>C (p.Asp734Ala)
c.4814A>C (p.Asp1605Ala)
c.2624A>C (p.Asp875Ala)
c.2300A>C (p.Asp767Ala)
11g.118491217A>GCA382834286KMT2Ac.4817A>G (p.Asp1606Gly)
c.494A>G (p.Asp165Gly)
c.4718A>G (p.Asp1573Gly)
c.4604A>G (p.Asp1535Gly)
c.854A>G (p.Asp285Gly)
c.2201A>G (p.Asp734Gly)
c.4814A>G (p.Asp1605Gly)
c.2624A>G (p.Asp875Gly)
c.2300A>G (p.Asp767Gly)
11g.118491217A>TCA382834287KMT2Ac.4817A>T (p.Asp1606Val)
c.494A>T (p.Asp165Val)
c.4718A>T (p.Asp1573Val)
c.4604A>T (p.Asp1535Val)
c.854A>T (p.Asp285Val)
c.2201A>T (p.Asp734Val)
c.4814A>T (p.Asp1605Val)
c.2624A>T (p.Asp875Val)
c.2300A>T (p.Asp767Val)
11g.118491218C>ACA382834288KMT2Ac.4818C>A (p.Asp1606Glu)
c.495C>A (p.Asp165Glu)
c.4719C>A (p.Asp1573Glu)
c.4605C>A (p.Asp1535Glu)
c.855C>A (p.Asp285Glu)
c.2202C>A (p.Asp734Glu)
c.4815C>A (p.Asp1605Glu)
c.2625C>A (p.Asp875Glu)
c.2301C>A (p.Asp767Glu)
11g.118491218C>GCA382834289KMT2Ac.4818C>G (p.Asp1606Glu)
c.495C>G (p.Asp165Glu)
c.4719C>G (p.Asp1573Glu)
c.4605C>G (p.Asp1535Glu)
c.855C>G (p.Asp285Glu)
c.2202C>G (p.Asp734Glu)
c.4815C>G (p.Asp1605Glu)
c.2625C>G (p.Asp875Glu)
c.2301C>G (p.Asp767Glu)
11g.118491218C>TCA477091623KMT2Ac.4818C>T (p.Asp1606=)
c.495C>T (p.Asp165=)
c.4719C>T (p.Asp1573=)
c.4605C>T (p.Asp1535=)
c.855C>T (p.Asp285=)
c.2202C>T (p.Asp734=)
c.4815C>T (p.Asp1605=)
c.2625C>T (p.Asp875=)
c.2301C>T (p.Asp767=)
gnomAD v4
11g.118491219A>CCA382834292KMT2Ac.4819A>C (p.Lys1607Gln)
c.496A>C (p.Lys166Gln)
c.4720A>C (p.Lys1574Gln)
c.4606A>C (p.Lys1536Gln)
c.856A>C (p.Lys286Gln)
c.2203A>C (p.Lys735Gln)
c.4816A>C (p.Lys1606Gln)
c.2626A>C (p.Lys876Gln)
c.2302A>C (p.Lys768Gln)
11g.118491219A>GCA382834291KMT2Ac.4819A>G (p.Lys1607Glu)
c.496A>G (p.Lys166Glu)
c.4720A>G (p.Lys1574Glu)
c.4606A>G (p.Lys1536Glu)
c.856A>G (p.Lys286Glu)
c.2203A>G (p.Lys735Glu)
c.4816A>G (p.Lys1606Glu)
c.2626A>G (p.Lys876Glu)
c.2302A>G (p.Lys768Glu)
gnomAD v4
11g.118491219A>TCA382834290KMT2Ac.4819A>T (p.Lys1607Ter)
c.496A>T (p.Lys166Ter)
c.4720A>T (p.Lys1574Ter)
c.4606A>T (p.Lys1536Ter)
c.856A>T (p.Lys286Ter)
c.2203A>T (p.Lys735Ter)
c.4816A>T (p.Lys1606Ter)
c.2626A>T (p.Lys876Ter)
c.2302A>T (p.Lys768Ter)
11g.118491220A=CA2003519106KMT2Ac.4820A= (p.Lys1607=)
c.497A= (p.Lys166=)
c.4721A= (p.Lys1574=)
c.4607A= (p.Lys1536=)
c.857A= (p.Lys286=)
c.2204A= (p.Lys735=)
c.4817A= (p.Lys1606=)
c.2627A= (p.Lys876=)
c.2303A= (p.Lys768=)
11g.118491220A>CCA382834293KMT2Ac.4820A>C (p.Lys1607Thr)
c.497A>C (p.Lys166Thr)
c.4721A>C (p.Lys1574Thr)
c.4607A>C (p.Lys1536Thr)
c.857A>C (p.Lys286Thr)
c.2204A>C (p.Lys735Thr)
c.4817A>C (p.Lys1606Thr)
c.2627A>C (p.Lys876Thr)
c.2303A>C (p.Lys768Thr)
11g.118491220A>GCA382834294KMT2Ac.4820A>G (p.Lys1607Arg)
c.497A>G (p.Lys166Arg)
c.4721A>G (p.Lys1574Arg)
c.4607A>G (p.Lys1536Arg)
c.857A>G (p.Lys286Arg)
c.2204A>G (p.Lys735Arg)
c.4817A>G (p.Lys1606Arg)
c.2627A>G (p.Lys876Arg)
c.2303A>G (p.Lys768Arg)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC
11g.118491220A>TCA382834295KMT2Ac.4820A>T (p.Lys1607Ile)
c.497A>T (p.Lys166Ile)
c.4721A>T (p.Lys1574Ile)
c.4607A>T (p.Lys1536Ile)
c.857A>T (p.Lys286Ile)
c.2204A>T (p.Lys735Ile)
c.4817A>T (p.Lys1606Ile)
c.2627A>T (p.Lys876Ile)
c.2303A>T (p.Lys768Ile)
11g.118491221A>CCA382834296KMT2Ac.4821A>C (p.Lys1607Asn)
c.498A>C (p.Lys166Asn)
c.4722A>C (p.Lys1574Asn)
c.4608A>C (p.Lys1536Asn)
c.858A>C (p.Lys286Asn)
c.2205A>C (p.Lys735Asn)
c.4818A>C (p.Lys1606Asn)
c.2628A>C (p.Lys876Asn)
c.2304A>C (p.Lys768Asn)
11g.118491221A>GCA477091624KMT2Ac.4821A>G (p.Lys1607=)
c.498A>G (p.Lys166=)
c.4722A>G (p.Lys1574=)
c.4608A>G (p.Lys1536=)
c.858A>G (p.Lys286=)
c.2205A>G (p.Lys735=)
c.4818A>G (p.Lys1606=)
c.2628A>G (p.Lys876=)
c.2304A>G (p.Lys768=)
gnomAD v4

Number of alleles fetched