Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.29495646T>A | CA399193721 | TAOK1 | c.918T>A (p.Asn306Lys) n.766T>A | |
17 | g.29495646T>C | CA289645001 | TAOK1 | c.918T>C (p.Asn306=) n.766T>C | dbSNP |
17 | g.29495646T>G | CA399193724 | TAOK1 | c.918T>G (p.Asn306Lys) n.766T>G | |
17 | g.29495646T= | CA2254790972 | TAOK1 | c.918T= (p.Asn306=) n.766T= | |
17 | g.29495647C>A | CA399193728 | TAOK1 | c.919C>A (p.Leu307Met) n.767C>A | |
17 | g.29495647C>G | CA399193726 | TAOK1 | c.919C>G (p.Leu307Val) n.767C>G | |
17 | g.29495647C>T | CA499309078 | TAOK1 | c.919C>T (p.Leu307=) n.767C>T | |
17 | g.29495648T>A | CA399193730 | TAOK1 | c.920T>A (p.Leu307Gln) n.768T>A | gnomAD v4 |
17 | g.29495648T>C | CA399193732 | TAOK1 | c.920T>C (p.Leu307Pro) n.768T>C | |
17 | g.29495648T>G | CA399193734 | TAOK1 | c.920T>G (p.Leu307Arg) n.768T>G | |
17 | g.29495649G>A | CA8474560 | TAOK1 | c.921G>A (p.Leu307=) n.769G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.29495649G>C | CA499309085 | TAOK1 | c.921G>C (p.Leu307=) n.769G>C | |
17 | g.29495649G= | CA2254790973 | TAOK1 | c.921G= (p.Leu307=) n.769G= | |
17 | g.29495649G>T | CA499309083 | TAOK1 | c.921G>T (p.Leu307=) n.769G>T | dbSNP gnomAD v4 |
17 | g.29495650C>A | CA399193738 | TAOK1 | c.922C>A (p.Gln308Lys) n.770C>A | |
17 | g.29495650C>G | CA399193740 | TAOK1 | c.922C>G (p.Gln308Glu) n.770C>G | |
17 | g.29495650C>T | CA399193742 | TAOK1 | c.922C>T (p.Gln308Ter) n.770C>T | |
17 | g.29495651A>C | CA399193744 | TAOK1 | c.923A>C (p.Gln308Pro) n.771A>C | |
17 | g.29495651A>G | CA399193746 | TAOK1 | c.923A>G (p.Gln308Arg) n.771A>G | |
17 | g.29495651A>T | CA399193748 | TAOK1 | c.923A>T (p.Gln308Leu) n.771A>T | |
17 | g.29495652G>A | CA499309092 | TAOK1 | c.924G>A (p.Gln308=) n.772G>A | |
17 | g.29495652G>C | CA399193750 | TAOK1 | c.924G>C (p.Gln308His) n.772G>C | dbSNP |
17 | g.29495652G= | CA2254790974 | TAOK1 | c.924G= (p.Gln308=) n.772G= | |
17 | g.29495652G>T | CA399193752 | TAOK1 | c.924G>T (p.Gln308His) n.772G>T | |
17 | g.29495653T>A | CA399193755 | TAOK1 | c.925T>A (p.Tyr309Asn) n.773T>A | |
17 | g.29495653T>C | CA399193757 | TAOK1 | c.925T>C (p.Tyr309His) n.773T>C | |
17 | g.29495653T>G | CA399193754 | TAOK1 | c.925T>G (p.Tyr309Asp) n.773T>G | |
17 | g.29495654A>C | CA399193760 | TAOK1 | c.926A>C (p.Tyr309Ser) n.774A>C | |
17 | g.29495654A>G | CA399193762 | TAOK1 | c.926A>G (p.Tyr309Cys) n.774A>G | dbSNP |
17 | g.29495654A>T | CA399193764 | TAOK1 | c.926A>T (p.Tyr309Phe) n.774A>T | |
17 | g.29495655T>A | CA399193766 | TAOK1 | c.927T>A (p.Tyr309Ter) n.775T>A | |
17 | g.29495655T>C | CA499309101 | TAOK1 | c.927T>C (p.Tyr309=) n.775T>C | |
17 | g.29495655T>G | CA399193768 | TAOK1 | c.927T>G (p.Tyr309Ter) n.775T>G | |
17 | g.29495656C>A | CA499309103 | TAOK1 | c.928C>A (p.Arg310=) n.776C>A | dbSNP |
17 | g.29495656C= | CA2254790975 | TAOK1 | c.928C= (p.Arg310=) n.776C= | |
17 | g.29495656C>G | CA399193771 | TAOK1 | c.928C>G (p.Arg310Gly) n.776C>G | |
17 | g.29495656C>T | CA289645002 | TAOK1 | c.928C>T (p.Arg310Ter) n.776C>T | ClinVar dbSNP |
17 | g.29495657G>A | CA8474561 | TAOK1 | c.929G>A (p.Arg310Gln) n.777G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.29495657G>C | CA399193774 | TAOK1 | c.929G>C (p.Arg310Pro) n.777G>C | |
17 | g.29495657G= | CA2254790976 | TAOK1 | c.929G= (p.Arg310=) n.777G= | |
17 | g.29495657G>T | CA399193777 | TAOK1 | c.929G>T (p.Arg310Leu) n.777G>T | |
17 | g.29495658A>C | CA499309108 | TAOK1 | c.930A>C (p.Arg310=) n.778A>C | |
17 | g.29495658A>G | CA499309109 | TAOK1 | c.930A>G (p.Arg310=) n.778A>G | |
17 | g.29495658A>T | CA499309111 | TAOK1 | c.930A>T (p.Arg310=) n.778A>T | |
17 | g.29495659A>C | CA399193780 | TAOK1 | c.931A>C (p.Lys311Gln) n.779A>C | |
17 | g.29495659A>G | CA399193782 | TAOK1 | c.931A>G (p.Lys311Glu) n.779A>G | |
17 | g.29495659A>T | CA399193784 | TAOK1 | c.931A>T (p.Lys311Ter) n.779A>T | |
17 | g.29495660A>C | CA399193790 | TAOK1 | c.932A>C (p.Lys311Thr) n.780A>C | |
17 | g.29495660A>G | CA399193788 | TAOK1 | c.932A>G (p.Lys311Arg) n.780A>G | |
17 | g.29495660A>T | CA399193786 | TAOK1 | c.932A>T (p.Lys311Met) n.780A>T |