Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.103165820delCA227395981DYNC2H1c.4612-78del (p.=)
c.3994-78del (p.=)
c.2205+31401del (p.=)
n.4612-78del (p.=)
dbSNP
11g.103165822G>CCA670953953DYNC2H1c.4612-76G>C (p.=)
c.3994-76G>C (p.=)
c.2205+31403G>C (p.=)
n.4612-76G>C (p.=)
11g.103165822G>TCA670953955DYNC2H1c.4612-76G>T (p.=)
c.3994-76G>T (p.=)
c.2205+31403G>T (p.=)
n.4612-76G>T (p.=)
11g.103165825C>GCA670953958DYNC2H1c.4612-73C>G (p.=)
c.3994-73C>G (p.=)
c.2205+31406C>G (p.=)
n.4612-73C>G (p.=)
11g.103165828T>CCA227395983DYNC2H1c.4612-70T>C (p.=)
c.3994-70T>C (p.=)
c.2205+31409T>C (p.=)
n.4612-70T>C (p.=)
dbSNP
11g.103165833T>CCA670953960DYNC2H1c.4612-65T>C (p.=)
c.3994-65T>C (p.=)
c.2205+31414T>C (p.=)
n.4612-65T>C (p.=)
11g.103165840A>CCA227395987DYNC2H1c.4612-58A>C (p.=)
c.3994-58A>C (p.=)
c.2205+31421A>C (p.=)
n.4612-58A>C (p.=)
dbSNP
11g.103165845A>GCA227396006DYNC2H1c.4612-53A>G (p.=)
c.3994-53A>G (p.=)
c.2205+31426A>G (p.=)
n.4612-53A>G (p.=)
dbSNP
11g.103165862C>ACA670953964DYNC2H1c.4612-36C>A (p.=)
c.3994-36C>A (p.=)
c.2205+31443C>A (p.=)
n.4612-36C>A (p.=)
11g.103165863A>CCA601230149DYNC2H1c.4612-35A>C (p.=)
c.3994-35A>C (p.=)
c.2205+31444A>C (p.=)
n.4612-35A>C (p.=)
gnomAD
11g.103165864C>ACA6253608DYNC2H1c.4612-34C>A (p.=)
c.3994-34C>A (p.=)
c.2205+31445C>A (p.=)
n.4612-34C>A (p.=)
dbSNP ExAC gnomAD
11g.103165865C>ACA6253609DYNC2H1c.4612-33C>A (p.=)
c.3994-33C>A (p.=)
c.2205+31446C>A (p.=)
n.4612-33C>A (p.=)
dbSNP ExAC gnomAD
11g.103165867T>ACA670953973DYNC2H1c.4612-31T>A (p.=)
c.3994-31T>A (p.=)
c.2205+31448T>A (p.=)
n.4612-31T>A (p.=)
11g.103165867T>CCA601230150DYNC2H1c.4612-31T>C (p.=)
c.3994-31T>C (p.=)
c.2205+31448T>C (p.=)
n.4612-31T>C (p.=)
gnomAD
11g.103165877A>CCA6253610DYNC2H1c.4612-21A>C (p.=)
c.3994-21A>C (p.=)
c.2205+31458A>C (p.=)
n.4612-21A>C (p.=)
dbSNP ExAC gnomAD
11g.103165877A>TCA601230151DYNC2H1c.4612-21A>T (p.=)
c.3994-21A>T (p.=)
c.2205+31458A>T (p.=)
n.4612-21A>T (p.=)
gnomAD
11g.103165882T>CCA670953979DYNC2H1c.4612-16T>C (p.=)
c.3994-16T>C (p.=)
c.2205+31463T>C (p.=)
n.4612-16T>C (p.=)
11g.103165894A>GCA6253611DYNC2H1c.4612-4A>G (p.=)
c.3994-4A>G (p.=)
c.2205+31475A>G (p.=)
n.4612-4A>G (p.=)
dbSNP ExAC gnomAD
11g.103165896A>CCA382239294DYNC2H1c.4612-2A>C (p.=)
c.3994-2A>C (p.=)
c.2205+31477A>C (p.=)
n.4612-2A>C (p.=)
11g.103165896A>GCA382239296DYNC2H1c.4612-2A>G (p.=)
c.3994-2A>G (p.=)
c.2205+31477A>G (p.=)
n.4612-2A>G (p.=)
COSMIC
11g.103165896A>TCA382239295DYNC2H1c.4612-2A>T (p.=)
c.3994-2A>T (p.=)
c.2205+31477A>T (p.=)
n.4612-2A>T (p.=)
11g.103165897G>ACA382239297DYNC2H1c.4612-1G>A (p.=)
c.3994-1G>A (p.=)
c.2205+31478G>A (p.=)
n.4612-1G>A (p.=)
11g.103165897G>CCA382239298DYNC2H1c.4612-1G>C (p.=)
c.3994-1G>C (p.=)
c.2205+31478G>C (p.=)
n.4612-1G>C (p.=)
11g.103165897G>TCA382239299DYNC2H1c.4612-1G>T (p.=)
c.3994-1G>T (p.=)
c.2205+31478G>T (p.=)
n.4612-1G>T (p.=)
11g.103165898A>CCA382239300DYNC2H1c.4612A>C (p.Ile1538Leu)
c.3994A>C (p.Ile1332Leu)
c.2205+31479A>C (p.=)
n.4612A>C (p.Ile1538Leu)
11g.103165898A>GCA382239301DYNC2H1c.4612A>G (p.Ile1538Val)
c.3994A>G (p.Ile1332Val)
c.2205+31479A>G (p.=)
n.4612A>G (p.Ile1538Val)
11g.103165898A>TCA382239302DYNC2H1c.4612A>T (p.Ile1538Phe)
c.3994A>T (p.Ile1332Phe)
c.2205+31479A>T (p.=)
n.4612A>T (p.Ile1538Phe)
11g.103165899T>ACA382239303DYNC2H1c.4613T>A (p.Ile1538Asn)
c.3995T>A (p.Ile1332Asn)
c.2205+31480T>A (p.=)
n.4613T>A (p.Ile1538Asn)
11g.103165899T>CCA382239304DYNC2H1c.4613T>C (p.Ile1538Thr)
c.3995T>C (p.Ile1332Thr)
c.2205+31480T>C (p.=)
n.4613T>C (p.Ile1538Thr)
11g.103165899T>GCA382239305DYNC2H1c.4613T>G (p.Ile1538Ser)
c.3995T>G (p.Ile1332Ser)
c.2205+31480T>G (p.=)
n.4613T>G (p.Ile1538Ser)
11g.103165900T>ACA476600313DYNC2H1c.4614T>A (p.Ile1538=)
c.3996T>A (p.Ile1332=)
c.2205+31481T>A (p.=)
n.4614T>A (p.Ile1538=)
11g.103165900T>CCA476600316DYNC2H1c.4614T>C (p.Ile1538=)
c.3996T>C (p.Ile1332=)
c.2205+31481T>C (p.=)
n.4614T>C (p.Ile1538=)
11g.103165900T>GCA382239306DYNC2H1c.4614T>G (p.Ile1538Met)
c.3996T>G (p.Ile1332Met)
c.2205+31481T>G (p.=)
n.4614T>G (p.Ile1538Met)
11g.103165901T>ACA382239307DYNC2H1c.4615T>A (p.Leu1539Ile)
c.3997T>A (p.Leu1333Ile)
c.2205+31482T>A (p.=)
n.4615T>A (p.Leu1539Ile)
11g.103165901T>CCA476600323DYNC2H1c.4615T>C (p.Leu1539=)
c.3997T>C (p.Leu1333=)
c.2205+31482T>C (p.=)
n.4615T>C (p.Leu1539=)
11g.103165901T>GCA382239308DYNC2H1c.4615T>G (p.Leu1539Val)
c.3997T>G (p.Leu1333Val)
c.2205+31482T>G (p.=)
n.4615T>G (p.Leu1539Val)
11g.103165902T>ACA382239310DYNC2H1c.4616T>A (p.Leu1539Ter)
c.3998T>A (p.Leu1333Ter)
c.2205+31483T>A (p.=)
n.4616T>A (p.Leu1539Ter)
11g.103165902T>CCA382239311DYNC2H1c.4616T>C (p.Leu1539Ser)
c.3998T>C (p.Leu1333Ser)
c.2205+31483T>C (p.=)
n.4616T>C (p.Leu1539Ser)
COSMIC
11g.103165902T>GCA382239309DYNC2H1c.4616T>G (p.Leu1539Ter)
c.3998T>G (p.Leu1333Ter)
c.2205+31483T>G (p.=)
n.4616T>G (p.Leu1539Ter)
11g.103165903A>CCA382239313DYNC2H1c.4617A>C (p.Leu1539Phe)
c.3999A>C (p.Leu1333Phe)
c.2205+31484A>C (p.=)
n.4617A>C (p.Leu1539Phe)
11g.103165903A>GCA227396023DYNC2H1c.4617A>G (p.Leu1539=)
c.3999A>G (p.Leu1333=)
c.2205+31484A>G (p.=)
n.4617A>G (p.Leu1539=)
dbSNP gnomAD
11g.103165903A>TCA382239312DYNC2H1c.4617A>T (p.Leu1539Phe)
c.3999A>T (p.Leu1333Phe)
c.2205+31484A>T (p.=)
n.4617A>T (p.Leu1539Phe)
11g.103165904T>ACA382239316DYNC2H1c.4618T>A (p.Cys1540Ser)
c.4000T>A (p.Cys1334Ser)
c.2205+31485T>A (p.=)
n.4618T>A (p.Cys1540Ser)
11g.103165904T>CCA382239314DYNC2H1c.4618T>C (p.Cys1540Arg)
c.4000T>C (p.Cys1334Arg)
c.2205+31485T>C (p.=)
n.4618T>C (p.Cys1540Arg)
11g.103165904T>GCA382239315DYNC2H1c.4618T>G (p.Cys1540Gly)
c.4000T>G (p.Cys1334Gly)
c.2205+31485T>G (p.=)
n.4618T>G (p.Cys1540Gly)
11g.103165905G>ACA227396026DYNC2H1c.4619G>A (p.Cys1540Tyr)
c.4001G>A (p.Cys1334Tyr)
c.2205+31486G>A (p.=)
n.4619G>A (p.Cys1540Tyr)
dbSNP
11g.103165905G>CCA382239317DYNC2H1c.4619G>C (p.Cys1540Ser)
c.4001G>C (p.Cys1334Ser)
c.2205+31486G>C (p.=)
n.4619G>C (p.Cys1540Ser)
11g.103165905G>TCA382239318DYNC2H1c.4619G>T (p.Cys1540Phe)
c.4001G>T (p.Cys1334Phe)
c.2205+31486G>T (p.=)
n.4619G>T (p.Cys1540Phe)
11g.103165906C>ACA382239319DYNC2H1c.4620C>A (p.Cys1540Ter)
c.4002C>A (p.Cys1334Ter)
c.2205+31487C>A (p.=)
n.4620C>A (p.Cys1540Ter)
11g.103165906C>GCA382239320DYNC2H1c.4620C>G (p.Cys1540Trp)
c.4002C>G (p.Cys1334Trp)
c.2205+31487C>G (p.=)
n.4620C>G (p.Cys1540Trp)

Number of alleles fetched