Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.45461912A>C | CA444257889 | HCN1 | c.945T>G (p.Leu315=) n.108T>G | |
5 | g.45461912A>G | CA444257891 | HCN1 | c.945T>C (p.Leu315=) n.108T>C | |
5 | g.45461912A>T | CA444257887 | HCN1 | c.945T>A (p.Leu315=) n.108T>A | |
5 | g.45461913A>C | CA359704896 | HCN1 | c.944T>G (p.Leu315Arg) n.107T>G | |
5 | g.45461913A>G | CA359704897 | HCN1 | c.944T>C (p.Leu315Pro) n.107T>C | |
5 | g.45461913A>T | CA359704898 | HCN1 | c.944T>A (p.Leu315His) n.107T>A | |
5 | g.45461914G>A | CA359704899 | HCN1 | c.943C>T (p.Leu315Phe) n.106C>T | |
5 | g.45461914G>C | CA359704900 | HCN1 | c.943C>G (p.Leu315Val) n.106C>G | |
5 | g.45461914G>T | CA359704901 | HCN1 | c.943C>A (p.Leu315Ile) n.106C>A | |
5 | g.45461915A>C | CA359704902 | HCN1 | c.942T>G (p.Cys314Trp) n.105T>G | |
5 | g.45461915A>G | CA444257896 | HCN1 | c.942T>C (p.Cys314=) n.105T>C | |
5 | g.45461915A>T | CA359704903 | HCN1 | c.942T>A (p.Cys314Ter) n.105T>A | |
5 | g.45461916C>A | CA359704906 | HCN1 | c.941G>T (p.Cys314Phe) n.104G>T | COSMIC |
5 | g.45461916C>G | CA359704905 | HCN1 | c.941G>C (p.Cys314Ser) n.104G>C | |
5 | g.45461916C>T | CA359704904 | HCN1 | c.941G>A (p.Cys314Tyr) n.104G>A | |
5 | g.45461917A>C | CA359704907 | HCN1 | c.940T>G (p.Cys314Gly) n.103T>G | |
5 | g.45461917A>G | CA359704908 | HCN1 | c.940T>C (p.Cys314Arg) n.103T>C | |
5 | g.45461917A>T | CA359704909 | HCN1 | c.940T>A (p.Cys314Ser) n.103T>A | |
5 | g.45461918A= | CA1543688320 | HCN1 | c.939T= (p.Gly313=) n.102T= | |
5 | g.45461918A>C | CA444257903 | HCN1 | c.939T>G (p.Gly313=) n.102T>G | |
5 | g.45461918A>G | CA3259391 | HCN1 | c.939T>C (p.Gly313=) n.102T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.45461918A>T | CA444257905 | HCN1 | c.939T>A (p.Gly313=) n.102T>A | |
5 | g.45461919C>A | CA359704910 | HCN1 | c.938G>T (p.Gly313Val) n.101G>T | |
5 | g.45461919C>G | CA359704911 | HCN1 | c.938G>C (p.Gly313Ala) n.101G>C | |
5 | g.45461919C>T | CA359704912 | HCN1 | c.938G>A (p.Gly313Asp) n.101G>A | |
5 | g.45461920C>A | CA359704913 | HCN1 | c.937G>T (p.Gly313Cys) n.100G>T | |
5 | g.45461920C>G | CA359704914 | HCN1 | c.937G>C (p.Gly313Arg) n.100G>C | |
5 | g.45461920C>T | CA359704915 | HCN1 | c.937G>A (p.Gly313Ser) n.100G>A | ClinVar dbSNP |
5 | g.45461921A>C | CA359704916 | HCN1 | c.936T>G (p.Asp312Glu) n.99T>G | |
5 | g.45461921A>G | CA444257912 | HCN1 | c.936T>C (p.Asp312=) n.99T>C | |
5 | g.45461921A>T | CA359704917 | HCN1 | c.936T>A (p.Asp312Glu) n.99T>A | |
5 | g.45461922T>A | CA359704920 | HCN1 | c.935A>T (p.Asp312Val) n.98A>T | ClinVar dbSNP |
5 | g.45461922T>C | CA359704919 | HCN1 | c.935A>G (p.Asp312Gly) n.98A>G | |
5 | g.45461922T>G | CA359704918 | HCN1 | c.935A>C (p.Asp312Ala) n.98A>C | |
5 | g.45461922T= | CA1543688325 | HCN1 | c.935A= (p.Asp312=) n.98A= | |
5 | g.45461923C>A | CA359704921 | HCN1 | c.934G>T (p.Asp312Tyr) n.97G>T | |
5 | g.45461923C>G | CA359704922 | HCN1 | c.934G>C (p.Asp312His) n.97G>C | |
5 | g.45461923C>T | CA359704923 | HCN1 | c.934G>A (p.Asp312Asn) n.97G>A | COSMIC |
5 | g.45461924C>A | CA359704924 | HCN1 | c.933G>T (p.Trp311Cys) n.96G>T | |
5 | g.45461924C>G | CA359704925 | HCN1 | c.933G>C (p.Trp311Cys) n.96G>C | |
5 | g.45461924C>T | CA359704926 | HCN1 | c.933G>A (p.Trp311Ter) n.96G>A | |
5 | g.45461925C>A | CA359704929 | HCN1 | c.932G>T (p.Trp311Leu) n.95G>T | |
5 | g.45461925C>G | CA359704927 | HCN1 | c.932G>C (p.Trp311Ser) n.95G>C | |
5 | g.45461925C>T | CA359704928 | HCN1 | c.932G>A (p.Trp311Ter) n.95G>A | |
5 | g.45461926A>C | CA359704930 | HCN1 | c.931T>G (p.Trp311Gly) n.94T>G | |
5 | g.45461926A>G | CA359704931 | HCN1 | c.931T>C (p.Trp311Arg) n.94T>C | |
5 | g.45461926A>T | CA359704932 | HCN1 | c.931T>A (p.Trp311Arg) n.94T>A | |
5 | g.45461927G>A | CA444257924 | HCN1 | c.930C>T (p.His310=) n.93C>T | dbSNP gnomAD v2 gnomAD v4 COSMIC |
5 | g.45461927G>C | CA359704933 | HCN1 | c.930C>G (p.His310Gln) n.93C>G | |
5 | g.45461927G= | CA1543688328 | HCN1 | c.930C= (p.His310=) n.93C= | |
5 | g.45461927G>T | CA359704934 | HCN1 | c.930C>A (p.His310Gln) n.93C>A | |
5 | g.45461928T>A | CA359704935 | HCN1 | c.929A>T (p.His310Leu) n.92A>T | |
5 | g.45461928T>C | CA359704937 | HCN1 | c.929A>G (p.His310Arg) n.92A>G | |
5 | g.45461928T>G | CA359704936 | HCN1 | c.929A>C (p.His310Pro) n.92A>C | |
5 | g.45461929G>A | CA359704938 | HCN1 | c.928C>T (p.His310Tyr) n.91C>T | ClinVar dbSNP COSMIC |
5 | g.45461929G>C | CA359704939 | HCN1 | c.928C>G (p.His310Asp) n.91C>G | |
5 | g.45461929G>T | CA359704940 | HCN1 | c.928C>A (p.His310Asn) n.91C>A | |
5 | g.45461930G>A | CA444257931 | HCN1 | c.927C>T (p.Cys309=) n.90C>T | gnomAD v4 |
5 | g.45461930G>C | CA359704941 | HCN1 | c.927C>G (p.Cys309Trp) n.90C>G | |
5 | g.45461930G>T | CA359704942 | HCN1 | c.927C>A (p.Cys309Ter) n.90C>A | |
5 | g.45461931C>A | CA359704943 | HCN1 | c.926G>T (p.Cys309Phe) n.89G>T | |
5 | g.45461931C>G | CA359704944 | HCN1 | c.926G>C (p.Cys309Ser) n.89G>C | |
5 | g.45461931C>T | CA359704945 | HCN1 | c.926G>A (p.Cys309Tyr) n.89G>A | |
5 | g.45461932A= | CA1543688331 | HCN1 | c.925T= (p.Cys309=) n.88T= | |
5 | g.45461932A>C | CA359704946 | HCN1 | c.925T>G (p.Cys309Gly) n.88T>G | |
5 | g.45461932A>G | CA359704947 | HCN1 | c.925T>C (p.Cys309Arg) n.88T>C | dbSNP |
5 | g.45461932A>T | CA359704948 | HCN1 | c.925T>A (p.Cys309Ser) n.88T>A | |
5 | g.45461933C>A | CA444257938 | HCN1 | c.924G>T (p.Leu308=) n.87G>T | |
5 | g.45461933C>G | CA444257939 | HCN1 | c.924G>C (p.Leu308=) n.87G>C | |
5 | g.45461933C>T | CA444257936 | HCN1 | c.924G>A (p.Leu308=) n.87G>A | COSMIC |
5 | g.45461934A>C | CA359704949 | HCN1 | c.923T>G (p.Leu308Arg) n.86T>G | |
5 | g.45461934A>G | CA359704951 | HCN1 | c.923T>C (p.Leu308Pro) n.86T>C | |
5 | g.45461934A>T | CA359704950 | HCN1 | c.923T>A (p.Leu308Gln) n.86T>A | |
5 | g.45461935G>A | CA444257943 | HCN1 | c.922C>T (p.Leu308=) n.85C>T | dbSNP gnomAD v4 |
5 | g.45461935G>C | CA359704952 | HCN1 | c.922C>G (p.Leu308Val) n.85C>G | |
5 | g.45461935G>T | CA359704953 | HCN1 | c.922C>A (p.Leu308Met) n.85C>A | |
5 | g.45461936G>A | CA444258162 | HCN1 | c.921C>T (p.Leu307=) n.84C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
5 | g.45461936G>C | CA444258160 | HCN1 | c.921C>G (p.Leu307=) n.84C>G | |
5 | g.45461936G= | CA1543688335 | HCN1 | c.921C= (p.Leu307=) n.84C= | |
5 | g.45461936G>T | CA444258158 | HCN1 | c.921C>A (p.Leu307=) n.84C>A | |
5 | g.45461937A>C | CA359704954 | HCN1 | c.920T>G (p.Leu307Arg) n.83T>G | |
5 | g.45461937A>G | CA359704956 | HCN1 | c.920T>C (p.Leu307Pro) n.83T>C | |
5 | g.45461937A>T | CA359704955 | HCN1 | c.920T>A (p.Leu307His) n.83T>A | |
5 | g.45461938G>A | CA359704957 | HCN1 | c.919C>T (p.Leu307Phe) n.82C>T | |
5 | g.45461938G>C | CA359704958 | HCN1 | c.919C>G (p.Leu307Val) n.82C>G | |
5 | g.45461938G>T | CA359704959 | HCN1 | c.919C>A (p.Leu307Ile) n.82C>A | |
5 | g.45461939C>A | CA444258172 | HCN1 | c.918G>T (p.Leu306=) n.81G>T | |
5 | g.45461939C>G | CA444258169 | HCN1 | c.918G>C (p.Leu306=) n.81G>C | |
5 | g.45461939C>T | CA444258170 | HCN1 | c.918G>A (p.Leu306=) n.81G>A | |
5 | g.45461940A>C | CA359704960 | HCN1 | c.917T>G (p.Leu306Arg) n.80T>G | |
5 | g.45461940A>G | CA359704961 | HCN1 | c.917T>C (p.Leu306Pro) n.80T>C | |
5 | g.45461940A>T | CA359704962 | HCN1 | c.917T>A (p.Leu306Gln) n.80T>A | |
5 | g.45461941G>A | CA444258176 | HCN1 | c.916C>T (p.Leu306=) n.79C>T | |
5 | g.45461941G>C | CA359704963 | HCN1 | c.916C>G (p.Leu306Val) n.79C>G | |
5 | g.45461941G>T | CA359704964 | HCN1 | c.916C>A (p.Leu306Met) n.79C>A | |
5 | g.45461942C>A | CA359704965 | HCN1 | c.915G>T (p.Met305Ile) n.78G>T | |
5 | g.45461942C>G | CA359704966 | HCN1 | c.915G>C (p.Met305Ile) n.78G>C | |
5 | g.45461942C>T | CA359704967 | HCN1 | c.915G>A (p.Met305Ile) n.78G>A | |
5 | g.45461943A>C | CA359704970 | HCN1 | c.914T>G (p.Met305Arg) n.77T>G | |
5 | g.45461943A>G | CA359704969 | HCN1 | c.914T>C (p.Met305Thr) n.77T>C | |
5 | g.45461943A>T | CA359704968 | HCN1 | c.914T>A (p.Met305Lys) n.77T>A | |
5 | g.45461944T>A | CA16604906 | HCN1 | c.913A>T (p.Met305Leu) n.76A>T | ClinVar dbSNP |
5 | g.45461944T>C | CA359704971 | HCN1 | c.913A>G (p.Met305Val) n.76A>G | |
5 | g.45461944T>G | CA359704972 | HCN1 | c.913A>C (p.Met305Leu) n.76A>C | |
5 | g.45461944T= | CA1543688341 | HCN1 | c.913A= (p.Met305=) n.76A= | |
5 | g.45461945C>A | CA359704973 | HCN1 | c.912G>T (p.Met304Ile) n.75G>T | |
5 | g.45461945C>G | CA359704974 | HCN1 | c.912G>C (p.Met304Ile) n.75G>C | |
5 | g.45461945C>T | CA359704975 | HCN1 | c.912G>A (p.Met304Ile) n.75G>A | |
5 | g.45461946A>C | CA359704976 | HCN1 | c.911T>G (p.Met304Arg) n.74T>G | |
5 | g.45461946A>G | CA359704977 | HCN1 | c.911T>C (p.Met304Thr) n.74T>C | |
5 | g.45461946A>T | CA359704978 | HCN1 | c.911T>A (p.Met304Lys) n.74T>A | |
5 | g.45461947T>A | CA359704979 | HCN1 | c.910A>T (p.Met304Leu) n.73A>T | |
5 | g.45461947T>C | CA359704980 | HCN1 | c.910A>G (p.Met304Val) n.73A>G | |
5 | g.45461947T>G | CA359704981 | HCN1 | c.910A>C (p.Met304Leu) n.73A>C | |
5 | g.45461948G>A | CA444258191 | HCN1 | c.909C>T (p.Gly303=) n.72C>T | |
5 | g.45461948G>C | CA444258193 | HCN1 | c.909C>G (p.Gly303=) n.72C>G | |
5 | g.45461948G= | CA1543688347 | HCN1 | c.909C= (p.Gly303=) n.72C= | |
5 | g.45461948G>T | CA3259392 | HCN1 | c.909C>A (p.Gly303=) n.72C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.45461949C>A | CA359704984 | HCN1 | c.908G>T (p.Gly303Val) n.71G>T | ClinVar |
5 | g.45461949C>G | CA359704982 | HCN1 | c.908G>C (p.Gly303Ala) n.71G>C | |
5 | g.45461949C>T | CA359704983 | HCN1 | c.908G>A (p.Gly303Asp) n.71G>A | |
5 | g.45461950C>A | CA359704985 | HCN1 | c.907G>T (p.Gly303Cys) n.70G>T | |
5 | g.45461950C= | CA1543688351 | HCN1 | c.907G= (p.Gly303=) n.70G= | |
5 | g.45461950C>G | CA359704986 | HCN1 | c.907G>C (p.Gly303Arg) n.70G>C | |
5 | g.45461950C>T | CA359704987 | HCN1 | c.907G>A (p.Gly303Ser) n.70G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.45461951G>A | CA118303545 | HCN1 | c.906C>T (p.Ile302=) n.69C>T | dbSNP gnomAD v4 COSMIC |
5 | g.45461951G>C | CA359704988 | HCN1 | c.906C>G (p.Ile302Met) n.69C>G | |
5 | g.45461951G= | CA1543688357 | HCN1 | c.906C= (p.Ile302=) n.69C= | |
5 | g.45461951G>T | CA444258199 | HCN1 | c.906C>A (p.Ile302=) n.69C>A | |
5 | g.45461952A>C | CA359704989 | HCN1 | c.905T>G (p.Ile302Ser) n.68T>G | |
5 | g.45461952A>G | CA359704991 | HCN1 | c.905T>C (p.Ile302Thr) n.68T>C | |
5 | g.45461952A>T | CA359704990 | HCN1 | c.905T>A (p.Ile302Asn) n.68T>A | |
5 | g.45461953T>A | CA359704992 | HCN1 | c.904A>T (p.Ile302Phe) n.67A>T | COSMIC |
5 | g.45461953T>C | CA359704993 | HCN1 | c.904A>G (p.Ile302Val) n.67A>G | |
5 | g.45461953T>G | CA359704994 | HCN1 | c.904A>C (p.Ile302Leu) n.67A>C | gnomAD v4 |
5 | g.45461954G>A | CA3259393 | HCN1 | c.903C>T (p.Leu301=) n.66C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.45461954G>C | CA444258207 | HCN1 | c.903C>G (p.Leu301=) n.66C>G | |
5 | g.45461954G= | CA1543688364 | HCN1 | c.903C= (p.Leu301=) n.66C= | |
5 | g.45461954G>T | CA444258205 | HCN1 | c.903C>A (p.Leu301=) n.66C>A | |
5 | g.45461955A>C | CA359704995 | HCN1 | c.902T>G (p.Leu301Arg) n.65T>G | |
5 | g.45461955A>G | CA359704997 | HCN1 | c.902T>C (p.Leu301Pro) n.65T>C | |
5 | g.45461955A>T | CA359704996 | HCN1 | c.902T>A (p.Leu301His) n.65T>A | |
5 | g.45461956G>A | CA359704998 | HCN1 | c.901C>T (p.Leu301Phe) n.64C>T | COSMIC |
5 | g.45461956G>C | CA359704999 | HCN1 | c.901C>G (p.Leu301Val) n.64C>G | |
5 | g.45461956G>T | CA359705000 | HCN1 | c.901C>A (p.Leu301Ile) n.64C>A | |
5 | g.45461957A>C | CA359705001 | HCN1 | c.900T>G (p.Asn300Lys) n.63T>G | |
5 | g.45461957A>G | CA444258213 | HCN1 | c.900T>C (p.Asn300=) n.63T>C | gnomAD v3 gnomAD v4 |
5 | g.45461957A>T | CA359705002 | HCN1 | c.900T>A (p.Asn300Lys) n.63T>A | |
5 | g.45461958T>A | CA359705003 | HCN1 | c.899A>T (p.Asn300Ile) n.62A>T | ClinVar |
5 | g.45461958T>C | CA359705004 | HCN1 | c.899A>G (p.Asn300Ser) n.62A>G | |
5 | g.45461958T>G | CA359705005 | HCN1 | c.899A>C (p.Asn300Thr) n.62A>C | |
5 | g.45461959T>A | CA359705006 | HCN1 | c.898A>T (p.Asn300Tyr) n.61A>T | |
5 | g.45461959T>C | CA359705007 | HCN1 | c.898A>G (p.Asn300Asp) n.61A>G | |
5 | g.45461959T>G | CA359705008 | HCN1 | c.898A>C (p.Asn300His) n.61A>C | |
5 | g.45461960A>C | CA359705009 | HCN1 | c.897T>G (p.Phe299Leu) n.60T>G | |
5 | g.45461960A>G | CA444258219 | HCN1 | c.897T>C (p.Phe299=) n.60T>C | |
5 | g.45461960A>T | CA359705010 | HCN1 | c.897T>A (p.Phe299Leu) n.60T>A | |
5 | g.45461964del | CA2573334438 | HCN1 | c.897del (p.Phe299LeufsTer6) n.60del | ClinVar |
5 | g.45461961A>C | CA359705011 | HCN1 | c.896T>G (p.Phe299Cys) n.59T>G | |
5 | g.45461961A>G | CA359705012 | HCN1 | c.896T>C (p.Phe299Ser) n.59T>C | |
5 | g.45461961A>T | CA359705013 | HCN1 | c.896T>A (p.Phe299Tyr) n.59T>A | |
5 | g.45461962A>C | CA359705014 | HCN1 | c.895T>G (p.Phe299Val) n.58T>G | |
5 | g.45461962A>G | CA359705015 | HCN1 | c.895T>C (p.Phe299Leu) n.58T>C | |
5 | g.45461962A>T | CA359705016 | HCN1 | c.895T>A (p.Phe299Ile) n.58T>A | |
5 | g.45461963A= | CA1543688370 | HCN1 | c.894T= (p.Ile298=) n.57T= | |
5 | g.45461963A>C | CA359705017 | HCN1 | c.894T>G (p.Ile298Met) n.57T>G | ClinVar COSMIC |
5 | g.45461963A>G | CA444258225 | HCN1 | c.894T>C (p.Ile298=) n.57T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.45461963A>T | CA444258226 | HCN1 | c.894T>A (p.Ile298=) n.57T>A | |
5 | g.45461964A>C | CA359705020 | HCN1 | c.893T>G (p.Ile298Ser) n.56T>G | |
5 | g.45461964A>G | CA359705018 | HCN1 | c.893T>C (p.Ile298Thr) n.56T>C | |
5 | g.45461964A>T | CA359705019 | HCN1 | c.893T>A (p.Ile298Asn) n.56T>A | |
5 | g.45461965T>A | CA359705021 | HCN1 | c.892A>T (p.Ile298Phe) n.55A>T | |
5 | g.45461965T>C | CA359705022 | HCN1 | c.892A>G (p.Ile298Val) n.55A>G | |
5 | g.45461965T>G | CA359705023 | HCN1 | c.892A>C (p.Ile298Leu) n.55A>C | |
5 | g.45461966T>A | CA359705024 | HCN1 | c.891A>T (p.Arg297Ser) n.54A>T | |
5 | g.45461966T>C | CA444258230 | HCN1 | c.891A>G (p.Arg297=) n.54A>G | gnomAD v4 |
5 | g.45461966T>G | CA359705025 | HCN1 | c.891A>C (p.Arg297Ser) n.54A>C | COSMIC |
5 | g.45461967C>A | CA359705026 | HCN1 | c.890G>T (p.Arg297Ile) n.53G>T | |
5 | g.45461967C= | CA1543688382 | HCN1 | c.890G= (p.Arg297=) n.53G= | |
5 | g.45461967C>G | CA163274 | HCN1 | c.890G>C (p.Arg297Thr) n.53G>C | ClinVar dbSNP |
5 | g.45461967C>T | CA359705027 | HCN1 | c.890G>A (p.Arg297Lys) n.53G>A | dbSNP gnomAD v2 gnomAD v4 |
5 | g.45461968T>A | CA359705028 | HCN1 | c.889A>T (p.Arg297Ter) n.52A>T | |
5 | g.45461968T>C | CA359705029 | HCN1 | c.889A>G (p.Arg297Gly) n.52A>G | |
5 | g.45461968T>G | CA444258233 | HCN1 | c.889A>C (p.Arg297=) n.52A>C | |
5 | g.45461969C>A | CA444258234 | HCN1 | c.888G>T (p.Val296=) n.51G>T | |
5 | g.45461969C>G | CA444258235 | HCN1 | c.888G>C (p.Val296=) n.51G>C | |
5 | g.45461969C>T | CA444258236 | HCN1 | c.888G>A (p.Val296=) n.51G>A | |
5 | g.45461970A= | CA1543688395 | HCN1 | c.887T= (p.Val296=) n.50T= | |
5 | g.45461970A>C | CA3259394 | HCN1 | c.887T>G (p.Val296Gly) n.50T>G | dbSNP ExAC gnomAD v2 |
5 | g.45461970A>G | CA359705030 | HCN1 | c.887T>C (p.Val296Ala) n.50T>C | |
5 | g.45461970A>T | CA359705031 | HCN1 | c.887T>A (p.Val296Glu) n.50T>A | |
5 | g.45461971C>A | CA359705032 | HCN1 | c.886G>T (p.Val296Leu) n.49G>T | |
5 | g.45461971C>G | CA359705033 | HCN1 | c.886G>C (p.Val296Leu) n.49G>C | |
5 | g.45461971C>T | CA359705034 | HCN1 | c.886G>A (p.Val296Met) n.49G>A | |
5 | g.45461972C>A | CA444258241 | HCN1 | c.885G>T (p.Val295=) n.48G>T | |
5 | g.45461972C= | CA1543688398 | HCN1 | c.885G= (p.Val295=) n.48G= | |
5 | g.45461972C>G | CA444258243 | HCN1 | c.885G>C (p.Val295=) n.48G>C | |
5 | g.45461972C>T | CA444258244 | HCN1 | c.885G>A (p.Val295=) n.48G>A | dbSNP gnomAD v3 gnomAD v4 |
5 | g.45461973A>C | CA359705035 | HCN1 | c.884T>G (p.Val295Gly) n.47T>G | |
5 | g.45461973A>G | CA359705036 | HCN1 | c.884T>C (p.Val295Ala) n.47T>C | |
5 | g.45461973A>T | CA359705037 | HCN1 | c.884T>A (p.Val295Glu) n.47T>A | |
5 | g.45461974C>A | CA359705038 | HCN1 | c.883G>T (p.Val295Leu) n.46G>T | |
5 | g.45461974C>G | CA359705040 | HCN1 | c.883G>C (p.Val295Leu) n.46G>C | |
5 | g.45461974C>T | CA359705039 | HCN1 | c.883G>A (p.Val295Met) n.46G>A | ClinVar |
5 | g.45461975T>A | CA444258249 | HCN1 | c.882A>T (p.Ala294=) n.45A>T | |
5 | g.45461975T>C | CA118303546 | HCN1 | c.882A>G (p.Ala294=) n.45A>G | ClinVar dbSNP |
5 | g.45461975T>G | CA444258251 | HCN1 | c.882A>C (p.Ala294=) n.45A>C | |
5 | g.45461975T= | CA1543688405 | HCN1 | c.882A= (p.Ala294=) n.45A= | |
5 | g.45461976G>A | CA359705041 | HCN1 | c.881C>T (p.Ala294Val) n.44C>T | ClinVar |
5 | g.45461976G>C | CA359705042 | HCN1 | c.881C>G (p.Ala294Gly) n.44C>G | |
5 | g.45461976G>T | CA359705043 | HCN1 | c.881C>A (p.Ala294Glu) n.44C>A | |
5 | g.45461977C>A | CA359705044 | HCN1 | c.880G>T (p.Ala294Ser) n.43G>T | |
5 | g.45461977C>G | CA359705045 | HCN1 | c.880G>C (p.Ala294Pro) n.43G>C | |
5 | g.45461977C>T | CA359705046 | HCN1 | c.880G>A (p.Ala294Thr) n.43G>A | |
5 | g.45461978A= | CA1543688409 | HCN1 | c.879T= (p.Ser293=) n.42T= | |
5 | g.45461978A>C | CA359705047 | HCN1 | c.879T>G (p.Ser293Arg) n.42T>G | |
5 | g.45461978A>G | CA444258257 | HCN1 | c.879T>C (p.Ser293=) n.42T>C | dbSNP gnomAD v4 |
5 | g.45461978A>T | CA359705048 | HCN1 | c.879T>A (p.Ser293Arg) n.42T>A | |
5 | g.45461979C>A | CA359705049 | HCN1 | c.878G>T (p.Ser293Ile) n.41G>T | |
5 | g.45461979C>G | CA359705050 | HCN1 | c.878G>C (p.Ser293Thr) n.41G>C | |
5 | g.45461979C>T | CA359705051 | HCN1 | c.878G>A (p.Ser293Asn) n.41G>A | |
5 | g.45461980T>A | CA359705054 | HCN1 | c.877A>T (p.Ser293Cys) n.40A>T | |
5 | g.45461980T>C | CA359705053 | HCN1 | c.877A>G (p.Ser293Gly) n.40A>G | |
5 | g.45461980T>G | CA359705052 | HCN1 | c.877A>C (p.Ser293Arg) n.40A>C | |
5 | g.45461981G>A | CA444258263 | HCN1 | c.876C>T (p.Ala292=) n.39C>T | ClinVar dbSNP gnomAD v4 COSMIC |
5 | g.45461981G>C | CA444258265 | HCN1 | c.876C>G (p.Ala292=) n.39C>G | |
5 | g.45461981G= | CA1543688416 | HCN1 | c.876C= (p.Ala292=) n.39C= | |
5 | g.45461981G>T | CA444258266 | HCN1 | c.876C>A (p.Ala292=) n.39C>A | |
5 | g.45461982G>A | CA359705055 | HCN1 | c.875C>T (p.Ala292Val) n.38C>T | |
5 | g.45461982G>C | CA359705056 | HCN1 | c.875C>G (p.Ala292Gly) n.38C>G | |
5 | g.45461982G>T | CA359705057 | HCN1 | c.875C>A (p.Ala292Asp) n.38C>A | |
5 | g.45461983C>A | CA359705058 | HCN1 | c.874G>T (p.Ala292Ser) n.37G>T | |
5 | g.45461983C= | CA1543688422 | HCN1 | c.874G= (p.Ala292=) n.37G= | |
5 | g.45461983C>G | CA359705059 | HCN1 | c.874G>C (p.Ala292Pro) n.37G>C | COSMIC |
5 | g.45461983C>T | CA359705060 | HCN1 | c.874G>A (p.Ala292Thr) n.37G>A | ClinVar dbSNP gnomAD v4 COSMIC |
5 | g.45461984G>A | CA3259395 | HCN1 | c.873C>T (p.Leu291=) n.36C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.45461984G>C | CA444258274 | HCN1 | c.873C>G (p.Leu291=) n.36C>G | dbSNP |
5 | g.45461984G= | CA1543688427 | HCN1 | c.873C= (p.Leu291=) n.36C= | |
5 | g.45461984G>T | CA444258272 | HCN1 | c.873C>A (p.Leu291=) n.36C>A | |
5 | g.45461985A>C | CA359705061 | HCN1 | c.872T>G (p.Leu291Arg) n.35T>G | COSMIC |
5 | g.45461985A>G | CA359705062 | HCN1 | c.872T>C (p.Leu291Pro) n.35T>C | |
5 | g.45461985A>T | CA359705063 | HCN1 | c.872T>A (p.Leu291His) n.35T>A | |
5 | g.45461986G>A | CA359705064 | HCN1 | c.871C>T (p.Leu291Phe) n.34C>T | dbSNP gnomAD v2 gnomAD v4 |
5 | g.45461986G>C | CA359705065 | HCN1 | c.871C>G (p.Leu291Val) n.34C>G | |
5 | g.45461986G= | CA1543688432 | HCN1 | c.871C= (p.Leu291=) n.34C= | |
5 | g.45461986G>T | CA359705066 | HCN1 | c.871C>A (p.Leu291Ile) n.34C>A | |
5 | g.45461987A= | CA1543688444 | HCN1 | c.870T= (p.Asp290=) n.33T= | |
5 | g.45461987A>C | CA359705068 | HCN1 | c.870T>G (p.Asp290Glu) n.33T>G | ClinVar |
5 | g.45461987A>G | CA3259396 | HCN1 | c.870T>C (p.Asp290=) n.33T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.45461987A>T | CA359705067 | HCN1 | c.870T>A (p.Asp290Glu) n.33T>A | |
5 | g.45461988T>A | CA359705070 | HCN1 | c.869A>T (p.Asp290Val) n.32A>T | |
5 | g.45461988T>C | CA359705069 | HCN1 | c.869A>G (p.Asp290Gly) n.32A>G | |
5 | g.45461988T>G | CA359705071 | HCN1 | c.869A>C (p.Asp290Ala) n.32A>C | |
5 | g.45461989C>A | CA359705072 | HCN1 | c.868G>T (p.Asp290Tyr) n.31G>T | |
5 | g.45461989C>G | CA359705074 | HCN1 | c.868G>C (p.Asp290His) n.31G>C | |
5 | g.45461989C>T | CA359705073 | HCN1 | c.868G>A (p.Asp290Asn) n.31G>A | COSMIC |
5 | g.45461990A>C | CA359705075 | HCN1 | c.867T>G (p.Tyr289Ter) n.30T>G | |
5 | g.45461990A>G | CA444258280 | HCN1 | c.867T>C (p.Tyr289=) n.30T>C | |
5 | g.45461990A>T | CA359705076 | HCN1 | c.867T>A (p.Tyr289Ter) n.30T>A | |
5 | g.45461991T>A | CA359705077 | HCN1 | c.866A>T (p.Tyr289Phe) n.29A>T | |
5 | g.45461991T>C | CA359705078 | HCN1 | c.866A>G (p.Tyr289Cys) n.29A>G | |
5 | g.45461991T>G | CA359705079 | HCN1 | c.866A>C (p.Tyr289Ser) n.29A>C | |
5 | g.45461992A>C | CA359705080 | HCN1 | c.865T>G (p.Tyr289Asp) n.28T>G | |
5 | g.45461992A>G | CA359705081 | HCN1 | c.865T>C (p.Tyr289His) n.28T>C | |
5 | g.45461992A>T | CA359705082 | HCN1 | c.865T>A (p.Tyr289Asn) n.28T>A | |
5 | g.45461993T>A | CA444258282 | HCN1 | c.864A>T (p.Thr288=) n.27A>T | |
5 | g.45461993T>C | CA3259397 | HCN1 | c.864A>G (p.Thr288=) n.27A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.45461993T>G | CA444258281 | HCN1 | c.864A>C (p.Thr288=) n.27A>C | |
5 | g.45461993T= | CA1543688451 | HCN1 | c.864A= (p.Thr288=) n.27A= | |
5 | g.45461994G>A | CA359705083 | HCN1 | c.863C>T (p.Thr288Ile) n.26C>T | |
5 | g.45461994G>C | CA359705084 | HCN1 | c.863C>G (p.Thr288Arg) n.26C>G | |
5 | g.45461994G>T | CA359705085 | HCN1 | c.863C>A (p.Thr288Lys) n.26C>A | |
5 | g.45461995T>A | CA359705088 | HCN1 | c.862A>T (p.Thr288Ser) n.25A>T | |
5 | g.45461995T>C | CA359705087 | HCN1 | c.862A>G (p.Thr288Ala) n.25A>G | |
5 | g.45461995T>G | CA359705086 | HCN1 | c.862A>C (p.Thr288Pro) n.25A>C | |
5 | g.45461997_45462008del | CA2499217867 | HCN1 | c.851_862del n.14_25del | ClinVar dbSNP |
5 | g.45461996C>A | CA359705089 | HCN1 | c.861G>T (p.Met287Ile) n.24G>T | |
5 | g.45461996C= | CA1543688458 | HCN1 | c.861G= (p.Met287=) n.24G= | |
5 | g.45461996C>G | CA359705090 | HCN1 | c.861G>C (p.Met287Ile) n.24G>C | |
5 | g.45461996C>T | CA118303547 | HCN1 | c.861G>A (p.Met287Ile) n.24G>A | dbSNP |
5 | g.45461997A>C | CA359705091 | HCN1 | c.860T>G (p.Met287Arg) n.23T>G | |
5 | g.45461997A>G | CA359705092 | HCN1 | c.860T>C (p.Met287Thr) n.23T>C | COSMIC |
5 | g.45461997A>T | CA359705093 | HCN1 | c.860T>A (p.Met287Lys) n.23T>A | |
5 | g.45461998T>A | CA359705094 | HCN1 | c.859A>T (p.Met287Leu) n.22A>T | |
5 | g.45461998T>C | CA359705095 | HCN1 | c.859A>G (p.Met287Val) n.22A>G | |
5 | g.45461998T>G | CA359705096 | HCN1 | c.859A>C (p.Met287Leu) n.22A>C | ClinVar |
5 | g.45461999G>A | CA3259398 | HCN1 | c.858C>T (p.His286=) n.21C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.45461999G>C | CA359705097 | HCN1 | c.858C>G (p.His286Gln) n.21C>G | |
5 | g.45461999G= | CA1543688463 | HCN1 | c.858C= (p.His286=) n.21C= | |
5 | g.45461999G>T | CA359705098 | HCN1 | c.858C>A (p.His286Gln) n.21C>A | ClinVar dbSNP COSMIC |
5 | g.45462000T>A | CA359705100 | HCN1 | c.857A>T (p.His286Leu) n.20A>T | |
5 | g.45462000T>C | CA359705101 | HCN1 | c.857A>G (p.His286Arg) n.20A>G | |
5 | g.45462000T>G | CA359705099 | HCN1 | c.857A>C (p.His286Pro) n.20A>C | |
5 | g.45462001G>A | CA359705102 | HCN1 | c.856C>T (p.His286Tyr) n.19C>T | |
5 | g.45462001G>C | CA359705103 | HCN1 | c.856C>G (p.His286Asp) n.19C>G | |
5 | g.45462001G>T | CA359705104 | HCN1 | c.856C>A (p.His286Asn) n.19C>A | |
5 | g.45462002G>A | CA444258296 | HCN1 | c.855C>T (p.Phe285=) n.18C>T | |
5 | g.45462002G>C | CA359705105 | HCN1 | c.855C>G (p.Phe285Leu) n.18C>G | |
5 | g.45462002G>T | CA359705106 | HCN1 | c.855C>A (p.Phe285Leu) n.18C>A | |
5 | g.45462003A= | CA1543688467 | HCN1 | c.854T= (p.Phe285=) n.17T= | |
5 | g.45462003A>C | CA359705107 | HCN1 | c.854T>G (p.Phe285Cys) n.17T>G | |
5 | g.45462003A>G | CA359705108 | HCN1 | c.854T>C (p.Phe285Ser) n.17T>C | |
5 | g.45462003A>T | CA359705109 | HCN1 | c.854T>A (p.Phe285Tyr) n.17T>A | dbSNP gnomAD v2 gnomAD v4 |
5 | g.45462004A>C | CA359705110 | HCN1 | c.853T>G (p.Phe285Val) n.16T>G | |
5 | g.45462004A>G | CA359705111 | HCN1 | c.853T>C (p.Phe285Leu) n.16T>C | |
5 | g.45462004A>T | CA359705112 | HCN1 | c.853T>A (p.Phe285Ile) n.16T>A | |
5 | g.45462005T>A | CA444258303 | HCN1 | c.852A>T (p.Ile284=) n.15A>T | |
5 | g.45462005T>C | CA359705113 | HCN1 | c.852A>G (p.Ile284Met) n.15A>G | |
5 | g.45462005T>G | CA444258305 | HCN1 | c.852A>C (p.Ile284=) n.15A>C | |
5 | g.45462006A= | CA1543688475 | HCN1 | c.851T= (p.Ile284=) n.14T= | |
5 | g.45462006A>C | CA359705116 | HCN1 | c.851T>G (p.Ile284Arg) n.14T>G | |
5 | g.45462006A>G | CA359705114 | HCN1 | c.851T>C (p.Ile284Thr) n.14T>C | ClinVar dbSNP |
5 | g.45462006A>T | CA359705115 | HCN1 | c.851T>A (p.Ile284Lys) n.14T>A | |
5 | g.45462007T>A | CA359705117 | HCN1 | c.850A>T (p.Ile284Leu) n.13A>T | dbSNP gnomAD v3 gnomAD v4 |
5 | g.45462007T>C | CA359705118 | HCN1 | c.850A>G (p.Ile284Val) n.13A>G | gnomAD v4 |
5 | g.45462007T>G | CA359705119 | HCN1 | c.850A>C (p.Ile284Leu) n.13A>C | |
5 | g.45462007T= | CA1543688487 | HCN1 | c.850A= (p.Ile284=) n.13A= | |
5 | g.45462008C>A | CA359705120 | HCN1 | c.850-1G>T (n.850-1G>T) n.13-1G>T | COSMIC |
5 | g.45462008C>G | CA359705121 | HCN1 | c.850-1G>C (n.850-1G>C) n.13-1G>C | |
5 | g.45462008C>T | CA359705122 | HCN1 | c.850-1G>A (n.850-1G>A) n.13-1G>A | |
5 | g.45462009T>A | CA359705123 | HCN1 | c.850-2A>T (n.850-2A>T) n.13-2A>T | |
5 | g.45462009T>C | CA359705124 | HCN1 | c.850-2A>G (n.850-2A>G) n.13-2A>G | |
5 | g.45462009T>G | CA359705125 | HCN1 | c.850-2A>C (n.850-2A>C) n.13-2A>C | |
5 | g.45462010G>A | CA811095470 | HCN1 | c.850-3C>T (n.850-3C>T) n.13-3C>T | dbSNP |
5 | g.45462010G= | CA1543688491 | HCN1 | c.850-3C= (n.850-3C=) n.13-3C= | |
5 | g.45462012T>G | CA2503742193 | HCN1 | c.850-5A>C (n.850-5A>C) n.13-5A>C | ClinVar gnomAD v4 |