Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.50343117_50343129dupCA1047834370ZMYND10c.588_599+1dup
c.459_470+1dup
c.*340_*351+1dup
n.40_52dup
c.351_362+1dup
 dbSNP gnomAD v3 gnomAD v4
3g.50343127_50343128delCA214444ZMYND10c.593_594del (p.Val198GlyfsTer13)
c.593_594del (p.Val198GlyfsTer?)
c.464_465del (p.Val155GlyfsTer13)
c.*345_*346del (n.*345_*346del)
n.45_46del
c.356_357del (p.Val119GlyfsTer13)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.50343127C>ACA352942062ZMYND10c.590G>T (p.Cys197Phe)
c.461G>T (p.Cys154Phe)
c.*342G>T (n.*342G>T)
n.42G>T
c.353G>T (p.Cys118Phe)
 gnomAD v4
3g.50343127C=CA1363903263ZMYND10c.590G= (p.Cys197=)
c.461G= (p.Cys154=)
c.*342G= (n.*342G=)
n.42G=
c.353G= (p.Cys118=)
3g.50343127C>GCA352942063ZMYND10c.590G>C (p.Cys197Ser)
c.461G>C (p.Cys154Ser)
c.*342G>C (n.*342G>C)
n.42G>C
c.353G>C (p.Cys118Ser)
3g.50343127C>TCA352942064ZMYND10c.590G>A (p.Cys197Tyr)
c.461G>A (p.Cys154Tyr)
c.*342G>A (n.*342G>A)
n.42G>A
c.353G>A (p.Cys118Tyr)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.50343128A>CCA352942065ZMYND10c.589T>G (p.Cys197Gly)
c.460T>G (p.Cys154Gly)
c.*341T>G (n.*341T>G)
n.41T>G
c.352T>G (p.Cys118Gly)
3g.50343128A>GCA352942066ZMYND10c.589T>C (p.Cys197Arg)
c.460T>C (p.Cys154Arg)
c.*341T>C (n.*341T>C)
n.41T>C
c.352T>C (p.Cys118Arg)
 gnomAD v4
3g.50343128A>TCA352942067ZMYND10c.589T>A (p.Cys197Ser)
c.460T>A (p.Cys154Ser)
c.*341T>A (n.*341T>A)
n.41T>A
c.352T>A (p.Cys118Ser)
3g.50343129G>ACA2417166ZMYND10c.588C>T (p.Asp196=)
c.459C>T (p.Asp153=)
c.*340C>T (n.*340C>T)
n.40C>T
c.351C>T (p.Asp117=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
3g.50343129G>CCA352942068ZMYND10c.588C>G (p.Asp196Glu)
c.459C>G (p.Asp153Glu)
c.*340C>G (n.*340C>G)
n.40C>G
c.351C>G (p.Asp117Glu)
3g.50343129G=CA1363903267ZMYND10c.588C= (p.Asp196=)
c.459C= (p.Asp153=)
c.*340C= (n.*340C=)
n.40C=
c.351C= (p.Asp117=)
3g.50343129G>TCA352942069ZMYND10c.588C>A (p.Asp196Glu)
c.459C>A (p.Asp153Glu)
c.*340C>A (n.*340C>A)
n.40C>A
c.351C>A (p.Asp117Glu)
3g.50343130T>ACA352942072ZMYND10c.587A>T (p.Asp196Val)
c.458A>T (p.Asp153Val)
c.*339A>T (n.*339A>T)
n.39A>T
c.350A>T (p.Asp117Val)
3g.50343130T>CCA352942074ZMYND10c.587A>G (p.Asp196Gly)
c.458A>G (p.Asp153Gly)
c.*339A>G (n.*339A>G)
n.39A>G
c.350A>G (p.Asp117Gly)
3g.50343130T>GCA352942075ZMYND10c.587A>C (p.Asp196Ala)
c.458A>C (p.Asp153Ala)
c.*339A>C (n.*339A>C)
n.39A>C
c.350A>C (p.Asp117Ala)
3g.50343131C>ACA352942076ZMYND10c.586G>T (p.Asp196Tyr)
c.457G>T (p.Asp153Tyr)
c.*338G>T (n.*338G>T)
n.38G>T
c.349G>T (p.Asp117Tyr)
3g.50343131C>GCA352942078ZMYND10c.586G>C (p.Asp196His)
c.457G>C (p.Asp153His)
c.*338G>C (n.*338G>C)
n.38G>C
c.349G>C (p.Asp117His)
 gnomAD v4
3g.50343131C>TCA352942080ZMYND10c.586G>A (p.Asp196Asn)
c.457G>A (p.Asp153Asn)
c.*338G>A (n.*338G>A)
n.38G>A
c.349G>A (p.Asp117Asn)
3g.50343132T>ACA433709318ZMYND10c.585A>T (p.Thr195=)
c.456A>T (p.Thr152=)
c.*337A>T (n.*337A>T)
n.37A>T
c.348A>T (p.Thr116=)
3g.50343132T>CCA433709320ZMYND10c.585A>G (p.Thr195=)
c.456A>G (p.Thr152=)
c.*337A>G (n.*337A>G)
n.37A>G
c.348A>G (p.Thr116=)
3g.50343132T>GCA433709322ZMYND10c.585A>C (p.Thr195=)
c.456A>C (p.Thr152=)
c.*337A>C (n.*337A>C)
n.37A>C
c.348A>C (p.Thr116=)
3g.50343133G>ACA74632272ZMYND10c.584C>T (p.Thr195Ile)
c.455C>T (p.Thr152Ile)
c.*336C>T (n.*336C>T)
n.36C>T
c.347C>T (p.Thr116Ile)
 ClinVar dbSNP
3g.50343133G>CCA352942082ZMYND10c.584C>G (p.Thr195Arg)
c.455C>G (p.Thr152Arg)
c.*336C>G (n.*336C>G)
n.36C>G
c.347C>G (p.Thr116Arg)
3g.50343133G=CA1363903269ZMYND10c.584C= (p.Thr195=)
c.455C= (p.Thr152=)
c.*336C= (n.*336C=)
n.36C=
c.347C= (p.Thr116=)
3g.50343133G>TCA352942083ZMYND10c.584C>A (p.Thr195Lys)
c.455C>A (p.Thr152Lys)
c.*336C>A (n.*336C>A)
n.36C>A
c.347C>A (p.Thr116Lys)
3g.50343134delCA2665853743ZMYND10c.583del (p.Thr195GlnfsTer12)
c.583del (p.Thr195GlnfsTer19)
c.454del (p.Thr152GlnfsTer12)
c.*335del (n.*335del)
n.35del
c.346del (p.Thr116GlnfsTer12)
 gnomAD v4
3g.50343134T>ACA352942086ZMYND10c.583A>T (p.Thr195Ser)
c.454A>T (p.Thr152Ser)
c.*335A>T (n.*335A>T)
n.35A>T
c.346A>T (p.Thr116Ser)
3g.50343134T>CCA352942087ZMYND10c.583A>G (p.Thr195Ala)
c.454A>G (p.Thr152Ala)
c.*335A>G (n.*335A>G)
n.35A>G
c.346A>G (p.Thr116Ala)
3g.50343134T>GCA352942089ZMYND10c.583A>C (p.Thr195Pro)
c.454A>C (p.Thr152Pro)
c.*335A>C (n.*335A>C)
n.35A>C
c.346A>C (p.Thr116Pro)
3g.50343135G>ACA433709328ZMYND10c.582C>T (p.Ile194=)
c.453C>T (p.Ile151=)
c.*334C>T (n.*334C>T)
n.34C>T
c.345C>T (p.Ile115=)
3g.50343135G>CCA352942090ZMYND10c.582C>G (p.Ile194Met)
c.453C>G (p.Ile151Met)
c.*334C>G (n.*334C>G)
n.34C>G
c.345C>G (p.Ile115Met)
3g.50343135G>TCA433709331ZMYND10c.582C>A (p.Ile194=)
c.453C>A (p.Ile151=)
c.*334C>A (n.*334C>A)
n.34C>A
c.345C>A (p.Ile115=)
3g.50343136A=CA1363903271ZMYND10c.581T= (p.Ile194=)
c.452T= (p.Ile151=)
c.*333T= (n.*333T=)
n.33T=
c.344T= (p.Ile115=)
3g.50343136A>CCA352942096ZMYND10c.581T>G (p.Ile194Ser)
c.452T>G (p.Ile151Ser)
c.*333T>G (n.*333T>G)
n.33T>G
c.344T>G (p.Ile115Ser)
3g.50343136A>GCA352942092ZMYND10c.581T>C (p.Ile194Thr)
c.452T>C (p.Ile151Thr)
c.*333T>C (n.*333T>C)
n.33T>C
c.344T>C (p.Ile115Thr)
 dbSNP
3g.50343136A>TCA352942094ZMYND10c.581T>A (p.Ile194Asn)
c.452T>A (p.Ile151Asn)
c.*333T>A (n.*333T>A)
n.33T>A
c.344T>A (p.Ile115Asn)
3g.50343137T>ACA352942097ZMYND10c.580A>T (p.Ile194Phe)
c.451A>T (p.Ile151Phe)
c.*332A>T (n.*332A>T)
n.32A>T
c.343A>T (p.Ile115Phe)
3g.50343137T>CCA352942098ZMYND10c.580A>G (p.Ile194Val)
c.451A>G (p.Ile151Val)
c.*332A>G (n.*332A>G)
n.32A>G
c.343A>G (p.Ile115Val)
3g.50343137T>GCA352942099ZMYND10c.580A>C (p.Ile194Leu)
c.451A>C (p.Ile151Leu)
c.*332A>C (n.*332A>C)
n.32A>C
c.343A>C (p.Ile115Leu)
3g.50343138G>ACA2417167ZMYND10c.579C>T (p.Tyr193=)
c.450C>T (p.Tyr150=)
c.*331C>T (n.*331C>T)
n.31C>T
c.342C>T (p.Tyr114=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.50343138G>CCA352942102ZMYND10c.579C>G (p.Tyr193Ter)
c.450C>G (p.Tyr150Ter)
c.*331C>G (n.*331C>G)
n.31C>G
c.342C>G (p.Tyr114Ter)
3g.50343138G=CA1363903273ZMYND10c.579C= (p.Tyr193=)
c.450C= (p.Tyr150=)
c.*331C= (n.*331C=)
n.31C=
c.342C= (p.Tyr114=)
3g.50343138G>TCA352942101ZMYND10c.579C>A (p.Tyr193Ter)
c.450C>A (p.Tyr150Ter)
c.*331C>A (n.*331C>A)
n.31C>A
c.342C>A (p.Tyr114Ter)
3g.50343139T>ACA352942105ZMYND10c.578A>T (p.Tyr193Phe)
c.449A>T (p.Tyr150Phe)
c.*330A>T (n.*330A>T)
n.30A>T
c.341A>T (p.Tyr114Phe)
3g.50343139T>CCA352942106ZMYND10c.578A>G (p.Tyr193Cys)
c.449A>G (p.Tyr150Cys)
c.*330A>G (n.*330A>G)
n.30A>G
c.341A>G (p.Tyr114Cys)
 ClinVar gnomAD v4
3g.50343139T>GCA352942107ZMYND10c.578A>C (p.Tyr193Ser)
c.449A>C (p.Tyr150Ser)
c.*330A>C (n.*330A>C)
n.30A>C
c.341A>C (p.Tyr114Ser)
3g.50343140A=CA1363903275ZMYND10c.577T= (p.Tyr193=)
c.448T= (p.Tyr150=)
c.*329T= (n.*329T=)
n.29T=
c.340T= (p.Tyr114=)
3g.50343140A>CCA352942109ZMYND10c.577T>G (p.Tyr193Asp)
c.448T>G (p.Tyr150Asp)
c.*329T>G (n.*329T>G)
n.29T>G
c.340T>G (p.Tyr114Asp)
3g.50343140A>GCA352942111ZMYND10c.577T>C (p.Tyr193His)
c.448T>C (p.Tyr150His)
c.*329T>C (n.*329T>C)
n.29T>C
c.340T>C (p.Tyr114His)

Number of alleles fetched