Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73322507G>A | CA7648797 | HCN4 | c.3586C>T (p.Arg1196Cys) c.2368C>T (p.Arg790Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
15 | g.73322507G>C | CA393084696 | HCN4 | c.3586C>G (p.Arg1196Gly) c.2368C>G (p.Arg790Gly) | |
15 | g.73322507G= | CA2187186093 | HCN4 | c.3586C= (p.Arg1196=) c.2368C= (p.Arg790=) | |
15 | g.73322507G>T | CA393084699 | HCN4 | c.3586C>A (p.Arg1196Ser) c.2368C>A (p.Arg790Ser) | ClinVar dbSNP gnomAD v4 COSMIC |
15 | g.73322508C>A | CA491477819 | HCN4 | c.3585G>T (p.Val1195=) c.2367G>T (p.Val789=) | gnomAD v4 |
15 | g.73322508C>G | CA491477820 | HCN4 | c.3585G>C (p.Val1195=) c.2367G>C (p.Val789=) | |
15 | g.73322508C>T | CA491477821 | HCN4 | c.3585G>A (p.Val1195=) c.2367G>A (p.Val789=) | |
15 | g.73322509A>C | CA393084701 | HCN4 | c.3584T>G (p.Val1195Gly) c.2366T>G (p.Val789Gly) | |
15 | g.73322509A>G | CA393084704 | HCN4 | c.3584T>C (p.Val1195Ala) c.2366T>C (p.Val789Ala) | |
15 | g.73322509A>T | CA393084707 | HCN4 | c.3584T>A (p.Val1195Glu) c.2366T>A (p.Val789Glu) | gnomAD v4 |
15 | g.73322510C>A | CA7648798 | HCN4 | c.3583G>T (p.Val1195Leu) c.2365G>T (p.Val789Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322510C= | CA2187186098 | HCN4 | c.3583G= (p.Val1195=) c.2365G= (p.Val789=) | |
15 | g.73322510C>G | CA393084711 | HCN4 | c.3583G>C (p.Val1195Leu) c.2365G>C (p.Val789Leu) | |
15 | g.73322510C>T | CA393084714 | HCN4 | c.3583G>A (p.Val1195Met) c.2365G>A (p.Val789Met) | gnomAD v4 |
15 | g.73322511T>A | CA491477824 | HCN4 | c.3582A>T (p.Pro1194=) c.2364A>T (p.Pro788=) | |
15 | g.73322511T>C | CA7648799 | HCN4 | c.3582A>G (p.Pro1194=) c.2364A>G (p.Pro788=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322511T>G | CA491477825 | HCN4 | c.3582A>C (p.Pro1194=) c.2364A>C (p.Pro788=) | |
15 | g.73322511T= | CA2187186104 | HCN4 | c.3582A= (p.Pro1194=) c.2364A= (p.Pro788=) | |
15 | g.73322512G>A | CA7648800 | HCN4 | c.3581C>T (p.Pro1194Leu) c.2363C>T (p.Pro788Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322512G>C | CA393084720 | HCN4 | c.3581C>G (p.Pro1194Arg) c.2363C>G (p.Pro788Arg) | |
15 | g.73322512G= | CA2187186109 | HCN4 | c.3581C= (p.Pro1194=) c.2363C= (p.Pro788=) | |
15 | g.73322512G>T | CA393084719 | HCN4 | c.3581C>A (p.Pro1194Gln) c.2363C>A (p.Pro788Gln) | gnomAD v4 |
15 | g.73322513G>A | CA393084725 | HCN4 | c.3580C>T (p.Pro1194Ser) c.2362C>T (p.Pro788Ser) | gnomAD v4 |
15 | g.73322513G>C | CA393084726 | HCN4 | c.3580C>G (p.Pro1194Ala) c.2362C>G (p.Pro788Ala) | |
15 | g.73322513G>T | CA393084728 | HCN4 | c.3580C>A (p.Pro1194Thr) c.2362C>A (p.Pro788Thr) | gnomAD v4 |
15 | g.73322514C>A | CA393084731 | HCN4 | c.3579G>T (p.Glu1193Asp) c.2361G>T (p.Glu787Asp) | |
15 | g.73322514C= | CA2187186111 | HCN4 | c.3579G= (p.Glu1193=) c.2361G= (p.Glu787=) | |
15 | g.73322514C>G | CA393084734 | HCN4 | c.3579G>C (p.Glu1193Asp) c.2361G>C (p.Glu787Asp) | |
15 | g.73322514C>T | CA491477830 | HCN4 | c.3579G>A (p.Glu1193=) c.2361G>A (p.Glu787=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73322515T>A | CA393084737 | HCN4 | c.3578A>T (p.Glu1193Val) c.2360A>T (p.Glu787Val) | |
15 | g.73322515T>C | CA393084740 | HCN4 | c.3578A>G (p.Glu1193Gly) c.2360A>G (p.Glu787Gly) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322515T>G | CA393084742 | HCN4 | c.3578A>C (p.Glu1193Ala) c.2360A>C (p.Glu787Ala) | |
15 | g.73322515T= | CA2187186117 | HCN4 | c.3578A= (p.Glu1193=) c.2360A= (p.Glu787=) | |
15 | g.73322516C>A | CA7648801 | HCN4 | c.3577G>T (p.Glu1193Ter) c.2359G>T (p.Glu787Ter) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322516C= | CA2187186128 | HCN4 | c.3577G= (p.Glu1193=) c.2359G= (p.Glu787=) | |
15 | g.73322516C>G | CA236695 | HCN4 | c.3577G>C (p.Glu1193Gln) c.2359G>C (p.Glu787Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
15 | g.73322516C>T | CA393084748 | HCN4 | c.3577G>A (p.Glu1193Lys) c.2359G>A (p.Glu787Lys) | gnomAD v4 |
15 | g.73322517A>C | CA491477832 | HCN4 | c.3576T>G (p.Pro1192=) c.2358T>G (p.Pro786=) | |
15 | g.73322517A>G | CA491477833 | HCN4 | c.3576T>C (p.Pro1192=) c.2358T>C (p.Pro786=) | |
15 | g.73322517A>T | CA491477834 | HCN4 | c.3576T>A (p.Pro1192=) c.2358T>A (p.Pro786=) | |
15 | g.73322518G>A | CA7648802 | HCN4 | c.3575C>T (p.Pro1192Leu) c.2357C>T (p.Pro786Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322518G>C | CA393084754 | HCN4 | c.3575C>G (p.Pro1192Arg) c.2357C>G (p.Pro786Arg) | ClinVar |
15 | g.73322518G= | CA2187186131 | HCN4 | c.3575C= (p.Pro1192=) c.2357C= (p.Pro786=) | |
15 | g.73322518G>T | CA393084751 | HCN4 | c.3575C>A (p.Pro1192His) c.2357C>A (p.Pro786His) | gnomAD v4 |
15 | g.73322519G>A | CA7648803 | HCN4 | c.3574C>T (p.Pro1192Ser) c.2356C>T (p.Pro786Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322519G>C | CA393084759 | HCN4 | c.3574C>G (p.Pro1192Ala) c.2356C>G (p.Pro786Ala) | gnomAD v4 |
15 | g.73322519G= | CA2187186138 | HCN4 | c.3574C= (p.Pro1192=) c.2356C= (p.Pro786=) | |
15 | g.73322519G>T | CA393084761 | HCN4 | c.3574C>A (p.Pro1192Thr) c.2356C>A (p.Pro786Thr) | gnomAD v4 |
15 | g.73322520C>A | CA393084764 | HCN4 | c.3573G>T (p.Arg1191Ser) c.2355G>T (p.Arg785Ser) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322520C= | CA2187186142 | HCN4 | c.3573G= (p.Arg1191=) c.2355G= (p.Arg785=) | |
15 | g.73322520C>G | CA393084767 | HCN4 | c.3573G>C (p.Arg1191Ser) c.2355G>C (p.Arg785Ser) | |
15 | g.73322520C>T | CA491477837 | HCN4 | c.3573G>A (p.Arg1191=) c.2355G>A (p.Arg785=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322521C>A | CA393084769 | HCN4 | c.3572G>T (p.Arg1191Met) c.2354G>T (p.Arg785Met) | gnomAD v4 |
15 | g.73322521C= | CA2187186145 | HCN4 | c.3572G= (p.Arg1191=) c.2354G= (p.Arg785=) | |
15 | g.73322521C>G | CA393084772 | HCN4 | c.3572G>C (p.Arg1191Thr) c.2354G>C (p.Arg785Thr) | dbSNP gnomAD v4 |
15 | g.73322521C>T | CA393084774 | HCN4 | c.3572G>A (p.Arg1191Lys) c.2354G>A (p.Arg785Lys) | gnomAD v4 |
15 | g.73322522T>A | CA393084776 | HCN4 | c.3571A>T (p.Arg1191Trp) c.2353A>T (p.Arg785Trp) | |
15 | g.73322522T>C | CA393084777 | HCN4 | c.3571A>G (p.Arg1191Gly) c.2353A>G (p.Arg785Gly) | dbSNP gnomAD v4 |
15 | g.73322522T>G | CA491477839 | HCN4 | c.3571A>C (p.Arg1191=) c.2353A>C (p.Arg785=) | |
15 | g.73322522T= | CA2187186149 | HCN4 | c.3571A= (p.Arg1191=) c.2353A= (p.Arg785=) | |
15 | g.73322523G>A | CA491477840 | HCN4 | c.3570C>T (p.Ala1190=) c.2352C>T (p.Ala784=) | ClinVar dbSNP gnomAD v4 |
15 | g.73322523G>C | CA491477841 | HCN4 | c.3570C>G (p.Ala1190=) c.2352C>G (p.Ala784=) | |
15 | g.73322523G>T | CA491477842 | HCN4 | c.3570C>A (p.Ala1190=) c.2352C>A (p.Ala784=) | |
15 | g.73322524G>A | CA393084780 | HCN4 | c.3569C>T (p.Ala1190Val) c.2351C>T (p.Ala784Val) | gnomAD v4 |
15 | g.73322524G>C | CA393084783 | HCN4 | c.3569C>G (p.Ala1190Gly) c.2351C>G (p.Ala784Gly) | |
15 | g.73322524G>T | CA393084786 | HCN4 | c.3569C>A (p.Ala1190Asp) c.2351C>A (p.Ala784Asp) | gnomAD v4 |
15 | g.73322525C>A | CA393084787 | HCN4 | c.3568G>T (p.Ala1190Ser) c.2350G>T (p.Ala784Ser) | ClinVar gnomAD v4 |
15 | g.73322525C= | CA2187186155 | HCN4 | c.3568G= (p.Ala1190=) c.2350G= (p.Ala784=) | |
15 | g.73322525C>G | CA393084790 | HCN4 | c.3568G>C (p.Ala1190Pro) c.2350G>C (p.Ala784Pro) | |
15 | g.73322525C>T | CA16614725 | HCN4 | c.3568G>A (p.Ala1190Thr) c.2350G>A (p.Ala784Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322528dup | CA2840701777 | HCN4 | c.3568dup (p.Ala1190GlyfsTer4) c.2350dup (p.Ala784GlyfsTer4) | |
15 | g.73322526C>A | CA491477844 | HCN4 | c.3567G>T (p.Gly1189=) c.2349G>T (p.Gly783=) | gnomAD v4 |
15 | g.73322526C= | CA2187186158 | HCN4 | c.3567G= (p.Gly1189=) c.2349G= (p.Gly783=) | |
15 | g.73322526C>G | CA491477845 | HCN4 | c.3567G>C (p.Gly1189=) c.2349G>C (p.Gly783=) | gnomAD v4 |
15 | g.73322526C>T | CA7648804 | HCN4 | c.3567G>A (p.Gly1189=) c.2349G>A (p.Gly783=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322527C>A | CA393084794 | HCN4 | c.3566G>T (p.Gly1189Val) c.2348G>T (p.Gly783Val) | gnomAD v4 |
15 | g.73322527C= | CA2187186161 | HCN4 | c.3566G= (p.Gly1189=) c.2348G= (p.Gly783=) | |
15 | g.73322527C>G | CA393084797 | HCN4 | c.3566G>C (p.Gly1189Ala) c.2348G>C (p.Gly783Ala) | |
15 | g.73322527C>T | CA393084800 | HCN4 | c.3566G>A (p.Gly1189Glu) c.2348G>A (p.Gly783Glu) | dbSNP gnomAD v2 |
15 | g.73322528C>A | CA393084804 | HCN4 | c.3565G>T (p.Gly1189Trp) c.2347G>T (p.Gly783Trp) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322528C= | CA2187186164 | HCN4 | c.3565G= (p.Gly1189=) c.2347G= (p.Gly783=) | |
15 | g.73322528C>G | CA393084806 | HCN4 | c.3565G>C (p.Gly1189Arg) c.2347G>C (p.Gly783Arg) | |
15 | g.73322528C>T | CA393084810 | HCN4 | c.3565G>A (p.Gly1189Arg) c.2347G>A (p.Gly783Arg) | |
15 | g.73322529A>C | CA491477851 | HCN4 | c.3564T>G (p.Pro1188=) c.2346T>G (p.Pro782=) | |
15 | g.73322529A>G | CA491477849 | HCN4 | c.3564T>C (p.Pro1188=) c.2346T>C (p.Pro782=) | ClinVar |
15 | g.73322529A>T | CA491477850 | HCN4 | c.3564T>A (p.Pro1188=) c.2346T>A (p.Pro782=) | |
15 | g.73322530G>A | CA393084813 | HCN4 | c.3563C>T (p.Pro1188Leu) c.2345C>T (p.Pro782Leu) | COSMIC |
15 | g.73322530G>C | CA393084815 | HCN4 | c.3563C>G (p.Pro1188Arg) c.2345C>G (p.Pro782Arg) | gnomAD v4 |
15 | g.73322530G>T | CA393084816 | HCN4 | c.3563C>A (p.Pro1188His) c.2345C>A (p.Pro782His) | |
15 | g.73322531G>A | CA393084819 | HCN4 | c.3562C>T (p.Pro1188Ser) c.2344C>T (p.Pro782Ser) | |
15 | g.73322531G>C | CA393084821 | HCN4 | c.3562C>G (p.Pro1188Ala) c.2344C>G (p.Pro782Ala) | |
15 | g.73322531G>T | CA393084824 | HCN4 | c.3562C>A (p.Pro1188Thr) c.2344C>A (p.Pro782Thr) | gnomAD v4 |
15 | g.73322532T>A | CA393084828 | HCN4 | c.3561A>T (p.Glu1187Asp) c.2343A>T (p.Glu781Asp) | |
15 | g.73322532T>C | CA491477855 | HCN4 | c.3561A>G (p.Glu1187=) c.2343A>G (p.Glu781=) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73322532T>G | CA393084825 | HCN4 | c.3561A>C (p.Glu1187Asp) c.2343A>C (p.Glu781Asp) | |
15 | g.73322532T= | CA2187186167 | HCN4 | c.3561A= (p.Glu1187=) c.2343A= (p.Glu781=) | |
15 | g.73322533T>A | CA393084831 | HCN4 | c.3560A>T (p.Glu1187Val) c.2342A>T (p.Glu781Val) | |
15 | g.73322533T>C | CA393084834 | HCN4 | c.3560A>G (p.Glu1187Gly) c.2342A>G (p.Glu781Gly) | |
15 | g.73322533T>G | CA393084835 | HCN4 | c.3560A>C (p.Glu1187Ala) c.2342A>C (p.Glu781Ala) | |
15 | g.73322534C>A | CA393084839 | HCN4 | c.3559G>T (p.Glu1187Ter) c.2341G>T (p.Glu781Ter) | |
15 | g.73322534C>G | CA393084842 | HCN4 | c.3559G>C (p.Glu1187Gln) c.2341G>C (p.Glu781Gln) | |
15 | g.73322534C>T | CA393084844 | HCN4 | c.3559G>A (p.Glu1187Lys) c.2341G>A (p.Glu781Lys) | |
15 | g.73322535C>A | CA393084849 | HCN4 | c.3558G>T (p.Arg1186Ser) c.2340G>T (p.Arg780Ser) | |
15 | g.73322535C>G | CA393084850 | HCN4 | c.3558G>C (p.Arg1186Ser) c.2340G>C (p.Arg780Ser) | |
15 | g.73322535C>T | CA491477858 | HCN4 | c.3558G>A (p.Arg1186=) c.2340G>A (p.Arg780=) | ClinVar gnomAD v4 |
15 | g.73322536C>A | CA393084851 | HCN4 | c.3557G>T (p.Arg1186Met) c.2339G>T (p.Arg780Met) | |
15 | g.73322536C= | CA2187186169 | HCN4 | c.3557G= (p.Arg1186=) c.2339G= (p.Arg780=) | |
15 | g.73322536C>G | CA393084853 | HCN4 | c.3557G>C (p.Arg1186Thr) c.2339G>C (p.Arg780Thr) | |
15 | g.73322536C>T | CA393084855 | HCN4 | c.3557G>A (p.Arg1186Lys) c.2339G>A (p.Arg780Lys) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322537T>A | CA393084858 | HCN4 | c.3556A>T (p.Arg1186Trp) c.2338A>T (p.Arg780Trp) | |
15 | g.73322537T>C | CA393084859 | HCN4 | c.3556A>G (p.Arg1186Gly) c.2338A>G (p.Arg780Gly) | |
15 | g.73322537T>G | CA491477862 | HCN4 | c.3556A>C (p.Arg1186=) c.2338A>C (p.Arg780=) | |
15 | g.73322538C>A | CA393084867 | HCN4 | c.3555G>T (p.Gln1185His) c.2337G>T (p.Gln779His) | gnomAD v4 |
15 | g.73322538C>G | CA393084864 | HCN4 | c.3555G>C (p.Gln1185His) c.2337G>C (p.Gln779His) | |
15 | g.73322538C>T | CA491477863 | HCN4 | c.3555G>A (p.Gln1185=) c.2337G>A (p.Gln779=) | ClinVar gnomAD v4 |
15 | g.73322539T>A | CA393084870 | HCN4 | c.3554A>T (p.Gln1185Leu) c.2336A>T (p.Gln779Leu) | dbSNP |
15 | g.73322539T>C | CA393084871 | HCN4 | c.3554A>G (p.Gln1185Arg) c.2336A>G (p.Gln779Arg) | |
15 | g.73322539T>G | CA393084873 | HCN4 | c.3554A>C (p.Gln1185Pro) c.2336A>C (p.Gln779Pro) | |
15 | g.73322539T= | CA2187186172 | HCN4 | c.3554A= (p.Gln1185=) c.2336A= (p.Gln779=) | |
15 | g.73322540G>A | CA393084876 | HCN4 | c.3553C>T (p.Gln1185Ter) c.2335C>T (p.Gln779Ter) | |
15 | g.73322540G>C | CA393084879 | HCN4 | c.3553C>G (p.Gln1185Glu) c.2335C>G (p.Gln779Glu) | |
15 | g.73322540G>T | CA393084882 | HCN4 | c.3553C>A (p.Gln1185Lys) c.2335C>A (p.Gln779Lys) | gnomAD v4 |
15 | g.73322541G>A | CA491477866 | HCN4 | c.3552C>T (p.Pro1184=) c.2334C>T (p.Pro778=) | dbSNP gnomAD v2 |
15 | g.73322541G>C | CA491477867 | HCN4 | c.3552C>G (p.Pro1184=) c.2334C>G (p.Pro778=) | |
15 | g.73322541G= | CA2187186175 | HCN4 | c.3552C= (p.Pro1184=) c.2334C= (p.Pro778=) | |
15 | g.73322541G>T | CA491477868 | HCN4 | c.3552C>A (p.Pro1184=) c.2334C>A (p.Pro778=) | |
15 | g.73322542G>A | CA393084890 | HCN4 | c.3551C>T (p.Pro1184Leu) c.2333C>T (p.Pro778Leu) | dbSNP |
15 | g.73322542G>C | CA393084887 | HCN4 | c.3551C>G (p.Pro1184Arg) c.2333C>G (p.Pro778Arg) | ClinVar dbSNP gnomAD v4 |
15 | g.73322542G= | CA2187186183 | HCN4 | c.3551C= (p.Pro1184=) c.2333C= (p.Pro778=) | |
15 | g.73322542G>T | CA393084884 | HCN4 | c.3551C>A (p.Pro1184His) c.2333C>A (p.Pro778His) | gnomAD v4 |
15 | g.73322543G>A | CA393084893 | HCN4 | c.3550C>T (p.Pro1184Ser) c.2332C>T (p.Pro778Ser) | gnomAD v4 COSMIC |
15 | g.73322543G>C | CA393084895 | HCN4 | c.3550C>G (p.Pro1184Ala) c.2332C>G (p.Pro778Ala) | ClinVar |
15 | g.73322543G= | CA2187186186 | HCN4 | c.3550C= (p.Pro1184=) c.2332C= (p.Pro778=) | |
15 | g.73322543G>T | CA272663044 | HCN4 | c.3550C>A (p.Pro1184Thr) c.2332C>A (p.Pro778Thr) | dbSNP gnomAD v4 |
15 | g.73322544T>A | CA491477872 | HCN4 | c.3549A>T (p.Gly1183=) c.2331A>T (p.Gly777=) | |
15 | g.73322544T>C | CA491477873 | HCN4 | c.3549A>G (p.Gly1183=) c.2331A>G (p.Gly777=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73322544T>G | CA491477874 | HCN4 | c.3549A>C (p.Gly1183=) c.2331A>C (p.Gly777=) | |
15 | g.73322544T= | CA2187186189 | HCN4 | c.3549A= (p.Gly1183=) c.2331A= (p.Gly777=) | |
15 | g.73322545C>A | CA393084900 | HCN4 | c.3548G>T (p.Gly1183Val) c.2330G>T (p.Gly777Val) | |
15 | g.73322545C>G | CA393084905 | HCN4 | c.3548G>C (p.Gly1183Ala) c.2330G>C (p.Gly777Ala) | |
15 | g.73322545C>T | CA393084906 | HCN4 | c.3548G>A (p.Gly1183Glu) c.2330G>A (p.Gly777Glu) | |
15 | g.73322546C>A | CA393084909 | HCN4 | c.3547G>T (p.Gly1183Ter) c.2329G>T (p.Gly777Ter) | |
15 | g.73322546C= | CA2187186194 | HCN4 | c.3547G= (p.Gly1183=) c.2329G= (p.Gly777=) | |
15 | g.73322546C>G | CA393084915 | HCN4 | c.3547G>C (p.Gly1183Arg) c.2329G>C (p.Gly777Arg) | |
15 | g.73322546C>T | CA393084912 | HCN4 | c.3547G>A (p.Gly1183Arg) c.2329G>A (p.Gly777Arg) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322547A>C | CA491477878 | HCN4 | c.3546T>G (p.Ala1182=) c.2328T>G (p.Ala776=) | |
15 | g.73322547A>G | CA491477879 | HCN4 | c.3546T>C (p.Ala1182=) c.2328T>C (p.Ala776=) | gnomAD v4 |
15 | g.73322547A>T | CA491477880 | HCN4 | c.3546T>A (p.Ala1182=) c.2328T>A (p.Ala776=) | |
15 | g.73322548G>A | CA393084916 | HCN4 | c.3545C>T (p.Ala1182Val) c.2327C>T (p.Ala776Val) | dbSNP gnomAD v2 |
15 | g.73322548G>C | CA393084919 | HCN4 | c.3545C>G (p.Ala1182Gly) c.2327C>G (p.Ala776Gly) | |
15 | g.73322548G= | CA2187186202 | HCN4 | c.3545C= (p.Ala1182=) c.2327C= (p.Ala776=) | |
15 | g.73322548G>T | CA393084921 | HCN4 | c.3545C>A (p.Ala1182Asp) c.2327C>A (p.Ala776Asp) | |
15 | g.73322549C>A | CA7648805 | HCN4 | c.3544G>T (p.Ala1182Ser) c.2326G>T (p.Ala776Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322549C= | CA2187186205 | HCN4 | c.3544G= (p.Ala1182=) c.2326G= (p.Ala776=) | |
15 | g.73322549C>G | CA393084926 | HCN4 | c.3544G>C (p.Ala1182Pro) c.2326G>C (p.Ala776Pro) | |
15 | g.73322549C>T | CA393084929 | HCN4 | c.3544G>A (p.Ala1182Thr) c.2326G>A (p.Ala776Thr) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
15 | g.73322552_73322555del | CA2580089966 | HCN4 | c.3541_3544del (p.Thr1181LeufsTer?) c.2323_2326del (p.Thr775LeufsTer?) | ClinVar |
15 | g.73322550A>C | CA491477882 | HCN4 | c.3543T>G (p.Thr1181=) c.2325T>G (p.Thr775=) | |
15 | g.73322550A>G | CA491477883 | HCN4 | c.3543T>C (p.Thr1181=) c.2325T>C (p.Thr775=) | |
15 | g.73322550A>T | CA491477881 | HCN4 | c.3543T>A (p.Thr1181=) c.2325T>A (p.Thr775=) | |
15 | g.73322551G>A | CA393084932 | HCN4 | c.3542C>T (p.Thr1181Ile) c.2324C>T (p.Thr775Ile) | |
15 | g.73322551G>C | CA393084933 | HCN4 | c.3542C>G (p.Thr1181Ser) c.2324C>G (p.Thr775Ser) | |
15 | g.73322551G>T | CA393084934 | HCN4 | c.3542C>A (p.Thr1181Asn) c.2324C>A (p.Thr775Asn) | |
15 | g.73322552T>A | CA393084935 | HCN4 | c.3541A>T (p.Thr1181Ser) c.2323A>T (p.Thr775Ser) | |
15 | g.73322552T>C | CA393084937 | HCN4 | c.3541A>G (p.Thr1181Ala) c.2323A>G (p.Thr775Ala) | gnomAD v4 |
15 | g.73322552T>G | CA7648806 | HCN4 | c.3541A>C (p.Thr1181Pro) c.2323A>C (p.Thr775Pro) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322552T= | CA2187186213 | HCN4 | c.3541A= (p.Thr1181=) c.2323A= (p.Thr775=) | |
15 | g.73322553C>A | CA491477886 | HCN4 | c.3540G>T (p.Leu1180=) c.2322G>T (p.Leu774=) | gnomAD v4 |
15 | g.73322553C= | CA2187186214 | HCN4 | c.3540G= (p.Leu1180=) c.2322G= (p.Leu774=) | |
15 | g.73322553C>G | CA491477884 | HCN4 | c.3540G>C (p.Leu1180=) c.2322G>C (p.Leu774=) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322553C>T | CA491477885 | HCN4 | c.3540G>A (p.Leu1180=) c.2322G>A (p.Leu774=) | |
15 | g.73322557_73322570del | CA2580089967 | HCN4 | c.3527_3540del (p.Gly1176AspfsTer13) c.2309_2322del (p.Gly770AspfsTer13) | ClinVar |
15 | g.73322554A>C | CA393084947 | HCN4 | c.3539T>G (p.Leu1180Arg) c.2321T>G (p.Leu774Arg) | |
15 | g.73322554A>G | CA393084944 | HCN4 | c.3539T>C (p.Leu1180Pro) c.2321T>C (p.Leu774Pro) | |
15 | g.73322554A>T | CA393084943 | HCN4 | c.3539T>A (p.Leu1180Gln) c.2321T>A (p.Leu774Gln) | |
15 | g.73322555G>A | CA491477887 | HCN4 | c.3538C>T (p.Leu1180=) c.2320C>T (p.Leu774=) | |
15 | g.73322555G>C | CA393084953 | HCN4 | c.3538C>G (p.Leu1180Val) c.2320C>G (p.Leu774Val) | |
15 | g.73322555G>T | CA393084952 | HCN4 | c.3538C>A (p.Leu1180Met) c.2320C>A (p.Leu774Met) | |
15 | g.73322556A= | CA2187186218 | HCN4 | c.3537T= (p.Pro1179=) c.2319T= (p.Pro773=) | |
15 | g.73322556A>C | CA491477889 | HCN4 | c.3537T>G (p.Pro1179=) c.2319T>G (p.Pro773=) | |
15 | g.73322556A>G | CA491477890 | HCN4 | c.3537T>C (p.Pro1179=) c.2319T>C (p.Pro773=) | |
15 | g.73322556A>T | CA491477888 | HCN4 | c.3537T>A (p.Pro1179=) c.2319T>A (p.Pro773=) | |
15 | g.73322557G>A | CA393084961 | HCN4 | c.3536C>T (p.Pro1179Leu) c.2318C>T (p.Pro773Leu) | ClinVar COSMIC |
15 | g.73322557G>C | CA393084958 | HCN4 | c.3536C>G (p.Pro1179Arg) c.2318C>G (p.Pro773Arg) | |
15 | g.73322557G>T | CA393084960 | HCN4 | c.3536C>A (p.Pro1179His) c.2318C>A (p.Pro773His) | |
15 | g.73322561dup | CA619410583 | HCN4 | c.3536dup (p.Leu1180SerfsTer14) c.2318dup (p.Leu774SerfsTer14) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322561del | CA645586806 | HCN4 | c.3536del (p.Pro1179LeufsTer2) c.2318del (p.Pro773LeufsTer2) | COSMIC |
15 | g.73322558G>A | CA393084963 | HCN4 | c.3535C>T (p.Pro1179Ser) c.2317C>T (p.Pro773Ser) | gnomAD v4 |
15 | g.73322558G>C | CA393084965 | HCN4 | c.3535C>G (p.Pro1179Ala) c.2317C>G (p.Pro773Ala) | |
15 | g.73322558G>T | CA393084966 | HCN4 | c.3535C>A (p.Pro1179Thr) c.2317C>A (p.Pro773Thr) | |
15 | g.73322559G>A | CA491477891 | HCN4 | c.3534C>T (p.Pro1178=) c.2316C>T (p.Pro772=) | |
15 | g.73322559G>C | CA491477892 | HCN4 | c.3534C>G (p.Pro1178=) c.2316C>G (p.Pro772=) | |
15 | g.73322559G>T | CA491477894 | HCN4 | c.3534C>A (p.Pro1178=) c.2316C>A (p.Pro772=) | |
15 | g.73322560G>A | CA393084972 | HCN4 | c.3533C>T (p.Pro1178Leu) c.2315C>T (p.Pro772Leu) | ClinVar dbSNP gnomAD v4 COSMIC |
15 | g.73322560G>C | CA393084971 | HCN4 | c.3533C>G (p.Pro1178Arg) c.2315C>G (p.Pro772Arg) | |
15 | g.73322560G= | CA2187186226 | HCN4 | c.3533C= (p.Pro1178=) c.2315C= (p.Pro772=) | |
15 | g.73322560G>T | CA393084969 | HCN4 | c.3533C>A (p.Pro1178His) c.2315C>A (p.Pro772His) | |
15 | g.73322561G>A | CA393084975 | HCN4 | c.3532C>T (p.Pro1178Ser) c.2314C>T (p.Pro772Ser) | ClinVar dbSNP |
15 | g.73322561G>C | CA393084978 | HCN4 | c.3532C>G (p.Pro1178Ala) c.2314C>G (p.Pro772Ala) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73322561G= | CA2187186232 | HCN4 | c.3532C= (p.Pro1178=) c.2314C= (p.Pro772=) | |
15 | g.73322561G>T | CA393084980 | HCN4 | c.3532C>A (p.Pro1178Thr) c.2314C>A (p.Pro772Thr) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322561_73322562delinsGC | CA2187186231 | HCN4 | c.3531_3532delinsGC (p.Gly1177=) c.2313_2314delinsGC (p.Gly771=) | |
15 | g.73322562C>A | CA7648808 | HCN4 | c.3531G>T (p.Gly1177=) c.2313G>T (p.Gly771=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322562C= | CA2187186243 | HCN4 | c.3531G= (p.Gly1177=) c.2313G= (p.Gly771=) | |
15 | g.73322562C>G | CA7648809 | HCN4 | c.3531G>C (p.Gly1177=) c.2313G>C (p.Gly771=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322562C>T | CA491477900 | HCN4 | c.3531G>A (p.Gly1177=) c.2313G>A (p.Gly771=) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
15 | g.73322567dup | CA619410584 | HCN4 | c.3531dup (p.Pro1178AlafsTer16) c.2313dup (p.Pro772AlafsTer16) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
15 | g.73322567del | CA7648807 | HCN4 | c.3531del (p.Pro1179LeufsTer2) c.2313del (p.Pro773LeufsTer2) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
15 | g.73322562_73322563insG | CA491477901 | HCN4 | c.3530_3531insC (p.Pro1178AlafsTer16) c.2312_2313insC (p.Pro772AlafsTer16) | |
15 | g.73322563C>A | CA393084994 | HCN4 | c.3530G>T (p.Gly1177Val) c.2312G>T (p.Gly771Val) | ClinVar |
15 | g.73322563C= | CA2187186249 | HCN4 | c.3530G= (p.Gly1177=) c.2312G= (p.Gly771=) | |
15 | g.73322563C>G | CA393084992 | HCN4 | c.3530G>C (p.Gly1177Ala) c.2312G>C (p.Gly771Ala) | |
15 | g.73322563C>T | CA7648810 | HCN4 | c.3530G>A (p.Gly1177Glu) c.2312G>A (p.Gly771Glu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322564C>A | CA393084997 | HCN4 | c.3529G>T (p.Gly1177Trp) c.2311G>T (p.Gly771Trp) | |
15 | g.73322564C>G | CA393084998 | HCN4 | c.3529G>C (p.Gly1177Arg) c.2311G>C (p.Gly771Arg) | |
15 | g.73322564C>T | CA393085000 | HCN4 | c.3529G>A (p.Gly1177Arg) c.2311G>A (p.Gly771Arg) | ClinVar dbSNP |
15 | g.73322565C>A | CA491477905 | HCN4 | c.3528G>T (p.Gly1176=) c.2310G>T (p.Gly770=) | dbSNP |
15 | g.73322565C>G | CA491477906 | HCN4 | c.3528G>C (p.Gly1176=) c.2310G>C (p.Gly770=) | |
15 | g.73322565C>T | CA491477907 | HCN4 | c.3528G>A (p.Gly1176=) c.2310G>A (p.Gly770=) | COSMIC |
15 | g.73322566C>A | CA393085001 | HCN4 | c.3527G>T (p.Gly1176Val) c.2309G>T (p.Gly770Val) | gnomAD v4 |
15 | g.73322566C= | CA2187186255 | HCN4 | c.3527G= (p.Gly1176=) c.2309G= (p.Gly770=) | |
15 | g.73322566C>G | CA393085003 | HCN4 | c.3527G>C (p.Gly1176Ala) c.2309G>C (p.Gly770Ala) | ClinVar dbSNP gnomAD v4 |
15 | g.73322566C>T | CA393085004 | HCN4 | c.3527G>A (p.Gly1176Glu) c.2309G>A (p.Gly770Glu) | |
15 | g.73322567C>A | CA393085007 | HCN4 | c.3526G>T (p.Gly1176Trp) c.2308G>T (p.Gly770Trp) | ClinVar gnomAD v4 |
15 | g.73322567C= | CA2187186261 | HCN4 | c.3526G= (p.Gly1176=) c.2308G= (p.Gly770=) | |
15 | g.73322567C>G | CA16614912 | HCN4 | c.3526G>C (p.Gly1176Arg) c.2308G>C (p.Gly770Arg) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322567C>T | CA393085008 | HCN4 | c.3526G>A (p.Gly1176Arg) c.2308G>A (p.Gly770Arg) | |
15 | g.73322568A>C | CA491477911 | HCN4 | c.3525T>G (p.Ser1175=) c.2307T>G (p.Ser769=) | |
15 | g.73322568A>G | CA491477912 | HCN4 | c.3525T>C (p.Ser1175=) c.2307T>C (p.Ser769=) | gnomAD v4 |
15 | g.73322568A>T | CA491477913 | HCN4 | c.3525T>A (p.Ser1175=) c.2307T>A (p.Ser769=) | |
15 | g.73322569G>A | CA393085009 | HCN4 | c.3524C>T (p.Ser1175Phe) c.2306C>T (p.Ser769Phe) | gnomAD v4 |
15 | g.73322569G>C | CA393085010 | HCN4 | c.3524C>G (p.Ser1175Cys) c.2306C>G (p.Ser769Cys) | |
15 | g.73322569G>T | CA393085011 | HCN4 | c.3524C>A (p.Ser1175Tyr) c.2306C>A (p.Ser769Tyr) | ClinVar |
15 | g.73322570A>C | CA393085014 | HCN4 | c.3523T>G (p.Ser1175Ala) c.2305T>G (p.Ser769Ala) | |
15 | g.73322570A>G | CA393085017 | HCN4 | c.3523T>C (p.Ser1175Pro) c.2305T>C (p.Ser769Pro) | |
15 | g.73322570A>T | CA393085015 | HCN4 | c.3523T>A (p.Ser1175Thr) c.2305T>A (p.Ser769Thr) | |
15 | g.73322571A= | CA2187186263 | HCN4 | c.3522T= (p.Ser1174=) c.2304T= (p.Ser768=) | |
15 | g.73322571A>C | CA491477916 | HCN4 | c.3522T>G (p.Ser1174=) c.2304T>G (p.Ser768=) | gnomAD v4 |
15 | g.73322571A>G | CA491477917 | HCN4 | c.3522T>C (p.Ser1174=) c.2304T>C (p.Ser768=) | dbSNP gnomAD v4 |
15 | g.73322571A>T | CA491477919 | HCN4 | c.3522T>A (p.Ser1174=) c.2304T>A (p.Ser768=) | |
15 | g.73322572G>A | CA393085018 | HCN4 | c.3521C>T (p.Ser1174Phe) c.2303C>T (p.Ser768Phe) | |
15 | g.73322572G>C | CA393085021 | HCN4 | c.3521C>G (p.Ser1174Cys) c.2303C>G (p.Ser768Cys) | |
15 | g.73322572G>T | CA393085023 | HCN4 | c.3521C>A (p.Ser1174Tyr) c.2303C>A (p.Ser768Tyr) | |
15 | g.73322573A>C | CA393085024 | HCN4 | c.3520T>G (p.Ser1174Ala) c.2302T>G (p.Ser768Ala) | |
15 | g.73322573A>G | CA393085026 | HCN4 | c.3520T>C (p.Ser1174Pro) c.2302T>C (p.Ser768Pro) | |
15 | g.73322573A>T | CA393085027 | HCN4 | c.3520T>A (p.Ser1174Thr) c.2302T>A (p.Ser768Thr) | |
15 | g.73322574G>A | CA7648811 | HCN4 | c.3519C>T (p.Thr1173=) c.2301C>T (p.Thr767=) | dbSNP ExAC gnomAD v3 gnomAD v4 |
15 | g.73322574G>C | CA491477921 | HCN4 | c.3519C>G (p.Thr1173=) c.2301C>G (p.Thr767=) | |
15 | g.73322574G= | CA2187186266 | HCN4 | c.3519C= (p.Thr1173=) c.2301C= (p.Thr767=) | |
15 | g.73322574G>T | CA491477923 | HCN4 | c.3519C>A (p.Thr1173=) c.2301C>A (p.Thr767=) | gnomAD v4 |
15 | g.73322575G>A | CA393085030 | HCN4 | c.3518C>T (p.Thr1173Ile) c.2300C>T (p.Thr767Ile) | gnomAD v4 |
15 | g.73322575G>C | CA393085032 | HCN4 | c.3518C>G (p.Thr1173Ser) c.2300C>G (p.Thr767Ser) | |
15 | g.73322575G>T | CA393085034 | HCN4 | c.3518C>A (p.Thr1173Asn) c.2300C>A (p.Thr767Asn) | gnomAD v4 |
15 | g.73322576T>A | CA393085036 | HCN4 | c.3517A>T (p.Thr1173Ser) c.2299A>T (p.Thr767Ser) | |
15 | g.73322576T>C | CA393085038 | HCN4 | c.3517A>G (p.Thr1173Ala) c.2299A>G (p.Thr767Ala) | |
15 | g.73322576T>G | CA393085039 | HCN4 | c.3517A>C (p.Thr1173Pro) c.2299A>C (p.Thr767Pro) | |
15 | g.73322577G>A | CA491477927 | HCN4 | c.3516C>T (p.Ala1172=) c.2298C>T (p.Ala766=) | |
15 | g.73322577G>C | CA491477928 | HCN4 | c.3516C>G (p.Ala1172=) c.2298C>G (p.Ala766=) | |
15 | g.73322577G>T | CA491477926 | HCN4 | c.3516C>A (p.Ala1172=) c.2298C>A (p.Ala766=) | |
15 | g.73322578G>A | CA393085040 | HCN4 | c.3515C>T (p.Ala1172Val) c.2297C>T (p.Ala766Val) | |
15 | g.73322578G>C | CA393085043 | HCN4 | c.3515C>G (p.Ala1172Gly) c.2297C>G (p.Ala766Gly) | |
15 | g.73322578G>T | CA393085042 | HCN4 | c.3515C>A (p.Ala1172Asp) c.2297C>A (p.Ala766Asp) | |
15 | g.73322579C>A | CA393085045 | HCN4 | c.3514G>T (p.Ala1172Ser) c.2296G>T (p.Ala766Ser) | |
15 | g.73322579C>G | CA393085047 | HCN4 | c.3514G>C (p.Ala1172Pro) c.2296G>C (p.Ala766Pro) | |
15 | g.73322579C>T | CA393085049 | HCN4 | c.3514G>A (p.Ala1172Thr) c.2296G>A (p.Ala766Thr) | gnomAD v4 |
15 | g.73322580T>A | CA393085051 | HCN4 | c.3513A>T (p.Arg1171Ser) c.2295A>T (p.Arg765Ser) | |
15 | g.73322580T>C | CA491477930 | HCN4 | c.3513A>G (p.Arg1171=) c.2295A>G (p.Arg765=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322580T>G | CA393085052 | HCN4 | c.3513A>C (p.Arg1171Ser) c.2295A>C (p.Arg765Ser) | gnomAD v4 |
15 | g.73322580T= | CA2187186274 | HCN4 | c.3513A= (p.Arg1171=) c.2295A= (p.Arg765=) | |
15 | g.73322581C>A | CA301975 | HCN4 | c.3512G>T (p.Arg1171Ile) c.2294G>T (p.Arg765Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322581C= | CA2187186281 | HCN4 | c.3512G= (p.Arg1171=) c.2294G= (p.Arg765=) | |
15 | g.73322581C>G | CA393085054 | HCN4 | c.3512G>C (p.Arg1171Thr) c.2294G>C (p.Arg765Thr) | |
15 | g.73322581C>T | CA393085055 | HCN4 | c.3512G>A (p.Arg1171Lys) c.2294G>A (p.Arg765Lys) | ClinVar dbSNP gnomAD v4 COSMIC |
15 | g.73322582T>A | CA393085056 | HCN4 | c.3511A>T (p.Arg1171Ter) c.2293A>T (p.Arg765Ter) | |
15 | g.73322582T>C | CA393085057 | HCN4 | c.3511A>G (p.Arg1171Gly) c.2293A>G (p.Arg765Gly) | |
15 | g.73322582T>G | CA491477934 | HCN4 | c.3511A>C (p.Arg1171=) c.2293A>C (p.Arg765=) | |
15 | g.73322583T>A | CA491477937 | HCN4 | c.3510A>T (p.Ala1170=) c.2292A>T (p.Ala764=) | |
15 | g.73322583T>C | CA491477935 | HCN4 | c.3510A>G (p.Ala1170=) c.2292A>G (p.Ala764=) | |
15 | g.73322583T>G | CA491477936 | HCN4 | c.3510A>C (p.Ala1170=) c.2292A>C (p.Ala764=) | |
15 | g.73322584G>A | CA393085062 | HCN4 | c.3509C>T (p.Ala1170Val) c.2291C>T (p.Ala764Val) | |
15 | g.73322584G>C | CA393085060 | HCN4 | c.3509C>G (p.Ala1170Gly) c.2291C>G (p.Ala764Gly) | |
15 | g.73322584G>T | CA393085059 | HCN4 | c.3509C>A (p.Ala1170Glu) c.2291C>A (p.Ala764Glu) | |
15 | g.73322585C>A | CA393085064 | HCN4 | c.3508G>T (p.Ala1170Ser) c.2290G>T (p.Ala764Ser) | |
15 | g.73322585C= | CA2187186285 | HCN4 | c.3508G= (p.Ala1170=) c.2290G= (p.Ala764=) | |
15 | g.73322585C>G | CA393085067 | HCN4 | c.3508G>C (p.Ala1170Pro) c.2290G>C (p.Ala764Pro) | |
15 | g.73322585C>T | CA393085066 | HCN4 | c.3508G>A (p.Ala1170Thr) c.2290G>A (p.Ala764Thr) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
15 | g.73322586C>A | CA491477939 | HCN4 | c.3507G>T (p.Gly1169=) c.2289G>T (p.Gly763=) | |
15 | g.73322586C>G | CA491477940 | HCN4 | c.3507G>C (p.Gly1169=) c.2289G>C (p.Gly763=) | |
15 | g.73322586C>T | CA491477941 | HCN4 | c.3507G>A (p.Gly1169=) c.2289G>A (p.Gly763=) | COSMIC |
15 | g.73322587C>A | CA393085069 | HCN4 | c.3506G>T (p.Gly1169Val) c.2288G>T (p.Gly763Val) | ClinVar dbSNP gnomAD v4 |
15 | g.73322587C= | CA2187186289 | HCN4 | c.3506G= (p.Gly1169=) c.2288G= (p.Gly763=) | |
15 | g.73322587C>G | CA393085070 | HCN4 | c.3506G>C (p.Gly1169Ala) c.2288G>C (p.Gly763Ala) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322587C>T | CA393085071 | HCN4 | c.3506G>A (p.Gly1169Glu) c.2288G>A (p.Gly763Glu) | |
15 | g.73322587_73322590del | CA2629370523 | HCN4 | c.3503_3506del (p.Phe1168TrpfsTer12) c.2285_2288del (p.Phe762TrpfsTer12) | gnomAD v4 |
15 | g.73322587_73322591delinsCCAAA | CA2187186288 | HCN4 | c.3502_3506delinsTTTGG (p.Phe1168=) c.2284_2288delinsTTTGG (p.Phe762=) | |
15 | g.73322588C>A | CA393085076 | HCN4 | c.3505G>T (p.Gly1169Trp) c.2287G>T (p.Gly763Trp) | |
15 | g.73322588C>G | CA393085077 | HCN4 | c.3505G>C (p.Gly1169Arg) c.2287G>C (p.Gly763Arg) | |
15 | g.73322588C>T | CA393085078 | HCN4 | c.3505G>A (p.Gly1169Arg) c.2287G>A (p.Gly763Arg) | |
15 | g.73322588_73322594delinsCAAACAA | CA2187186298 | HCN4 | c.3499_3505delinsTTGTTTG (p.Leu1167=) c.2281_2287delinsTTGTTTG (p.Leu761=) | |
15 | g.73322592_73322595del | CA199790 | HCN4 | c.3502_3505del (p.Phe1168GlyfsTer12) c.2284_2287del (p.Phe762GlyfsTer12) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322589A= | CA2187186302 | HCN4 | c.3504T= (p.Phe1168=) c.2286T= (p.Phe762=) | |
15 | g.73322589A>C | CA393085082 | HCN4 | c.3504T>G (p.Phe1168Leu) c.2286T>G (p.Phe762Leu) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73322589A>G | CA491477943 | HCN4 | c.3504T>C (p.Phe1168=) c.2286T>C (p.Phe762=) | |
15 | g.73322589A>T | CA393085085 | HCN4 | c.3504T>A (p.Phe1168Leu) c.2286T>A (p.Phe762Leu) | |
15 | g.73322590_73322595del | CA619410585 | HCN4 | c.3499_3504del (p.Leu1167_Phe1168del) c.2281_2286del (p.Leu761_Phe762del) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322590A= | CA2187186304 | HCN4 | c.3503T= (p.Phe1168=) c.2285T= (p.Phe762=) | |
15 | g.73322590A>C | CA393085091 | HCN4 | c.3503T>G (p.Phe1168Cys) c.2285T>G (p.Phe762Cys) | ClinVar dbSNP gnomAD v4 |
15 | g.73322590A>G | CA393085090 | HCN4 | c.3503T>C (p.Phe1168Ser) c.2285T>C (p.Phe762Ser) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73322590A>T | CA393085088 | HCN4 | c.3503T>A (p.Phe1168Tyr) c.2285T>A (p.Phe762Tyr) | |
15 | g.73322591A>C | CA393085093 | HCN4 | c.3502T>G (p.Phe1168Val) c.2284T>G (p.Phe762Val) | |
15 | g.73322591A>G | CA393085095 | HCN4 | c.3502T>C (p.Phe1168Leu) c.2284T>C (p.Phe762Leu) | |
15 | g.73322591A>T | CA393085097 | HCN4 | c.3502T>A (p.Phe1168Ile) c.2284T>A (p.Phe762Ile) | |
15 | g.73322592C>A | CA7648813 | HCN4 | c.3501G>T (p.Leu1167Phe) c.2283G>T (p.Leu761Phe) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
15 | g.73322592C= | CA2187186305 | HCN4 | c.3501G= (p.Leu1167=) c.2283G= (p.Leu761=) | |
15 | g.73322592C>G | CA7648812 | HCN4 | c.3501G>C (p.Leu1167Phe) c.2283G>C (p.Leu761Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322592C>T | CA491477947 | HCN4 | c.3501G>A (p.Leu1167=) c.2283G>A (p.Leu761=) | |
15 | g.73322592_73322596delinsCAAAG | CA2187186306 | HCN4 | c.3497_3501delinsCTTTG (p.Ser1166=) c.2279_2283delinsCTTTG (p.Ser760=) | |
15 | g.73322593A= | CA2187186307 | HCN4 | c.3500T= (p.Leu1167=) c.2282T= (p.Leu761=) | |
15 | g.73322593A>C | CA393085101 | HCN4 | c.3500T>G (p.Leu1167Trp) c.2282T>G (p.Leu761Trp) | |
15 | g.73322593A>G | CA7648814 | HCN4 | c.3500T>C (p.Leu1167Ser) c.2282T>C (p.Leu761Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322593A>T | CA393085104 | HCN4 | c.3500T>A (p.Leu1167Ter) c.2282T>A (p.Leu761Ter) | |
15 | g.73322594_73322597del | CA301968 | HCN4 | c.3497_3500del (p.Ser1166CysfsTer14) c.2279_2282del (p.Ser760CysfsTer14) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322593_73322594insCACCC | CA2804726809 | HCN4 | c.3499_3500insGGGTG (p.Leu1167TrpfsTer16) c.2281_2282insGGGTG (p.Leu761TrpfsTer16) | |
15 | g.73322594A>C | CA393085107 | HCN4 | c.3499T>G (p.Leu1167Val) c.2281T>G (p.Leu761Val) | |
15 | g.73322594A>G | CA491477951 | HCN4 | c.3499T>C (p.Leu1167=) c.2281T>C (p.Leu761=) | |
15 | g.73322594A>T | CA393085109 | HCN4 | c.3499T>A (p.Leu1167Met) c.2281T>A (p.Leu761Met) | |
15 | g.73322595_73322596insCCAAACACACCCAA | CA2804726810 | HCN4 | c.3499_3500insGGGTGTGTTTGGTT (p.Leu1167TrpfsTer19) c.2281_2282insGGGTGTGTTTGGTT (p.Leu761TrpfsTer19) | |
15 | g.73322595A>C | CA491477952 | HCN4 | c.3498T>G (p.Ser1166=) c.2280T>G (p.Ser760=) | |
15 | g.73322595A>G | CA491477954 | HCN4 | c.3498T>C (p.Ser1166=) c.2280T>C (p.Ser760=) | |
15 | g.73322595A>T | CA491477956 | HCN4 | c.3498T>A (p.Ser1166=) c.2280T>A (p.Ser760=) | |
15 | g.73322598_73322601del | CA2573151172 | HCN4 | c.3495_3498del (p.Ser1166CysfsTer14) c.2277_2280del (p.Ser760CysfsTer14) | ClinVar dbSNP |
15 | g.73322596G>A | CA393085113 | HCN4 | c.3497C>T (p.Ser1166Phe) c.2279C>T (p.Ser760Phe) | |
15 | g.73322596G>C | CA393085114 | HCN4 | c.3497C>G (p.Ser1166Cys) c.2279C>G (p.Ser760Cys) | |
15 | g.73322596G>T | CA393085111 | HCN4 | c.3497C>A (p.Ser1166Tyr) c.2279C>A (p.Ser760Tyr) | |
15 | g.73322597A>C | CA393085115 | HCN4 | c.3496T>G (p.Ser1166Ala) c.2278T>G (p.Ser760Ala) | |
15 | g.73322597A>G | CA393085116 | HCN4 | c.3496T>C (p.Ser1166Pro) c.2278T>C (p.Ser760Pro) | |
15 | g.73322597A>T | CA393085117 | HCN4 | c.3496T>A (p.Ser1166Thr) c.2278T>A (p.Ser760Thr) | |
15 | g.73322598C>A | CA491477959 | HCN4 | c.3495G>T (p.Leu1165=) c.2277G>T (p.Leu759=) | |
15 | g.73322598C= | CA2187186308 | HCN4 | c.3495G= (p.Leu1165=) c.2277G= (p.Leu759=) | |
15 | g.73322598C>G | CA491477961 | HCN4 | c.3495G>C (p.Leu1165=) c.2277G>C (p.Leu759=) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322598C>T | CA491477960 | HCN4 | c.3495G>A (p.Leu1165=) c.2277G>A (p.Leu759=) | |
15 | g.73322599A= | CA2187186309 | HCN4 | c.3494T= (p.Leu1165=) c.2276T= (p.Leu759=) | |
15 | g.73322599A>C | CA393085119 | HCN4 | c.3494T>G (p.Leu1165Arg) c.2276T>G (p.Leu759Arg) | |
15 | g.73322599A>G | CA393085121 | HCN4 | c.3494T>C (p.Leu1165Pro) c.2276T>C (p.Leu759Pro) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322599A>T | CA393085123 | HCN4 | c.3494T>A (p.Leu1165Gln) c.2276T>A (p.Leu759Gln) | |
15 | g.73322601_73322602del | CA2697549178 | HCN4 | c.3493_3494del (p.Leu1165ValfsTer28) c.2275_2276del (p.Leu759ValfsTer28) | ClinVar |
15 | g.73322600G>A | CA491477965 | HCN4 | c.3493C>T (p.Leu1165=) c.2275C>T (p.Leu759=) | COSMIC |
15 | g.73322600G>C | CA393085126 | HCN4 | c.3493C>G (p.Leu1165Val) c.2275C>G (p.Leu759Val) | |
15 | g.73322600G>T | CA393085124 | HCN4 | c.3493C>A (p.Leu1165Met) c.2275C>A (p.Leu759Met) | |
15 | g.73322601A>C | CA491477966 | HCN4 | c.3492T>G (p.Pro1164=) c.2274T>G (p.Pro758=) | |
15 | g.73322601A>G | CA491477967 | HCN4 | c.3492T>C (p.Pro1164=) c.2274T>C (p.Pro758=) | ClinVar |
15 | g.73322601A>T | CA491477968 | HCN4 | c.3492T>A (p.Pro1164=) c.2274T>A (p.Pro758=) | |
15 | g.73322602G>A | CA393085128 | HCN4 | c.3491C>T (p.Pro1164Leu) c.2273C>T (p.Pro758Leu) | |
15 | g.73322602G>C | CA393085129 | HCN4 | c.3491C>G (p.Pro1164Arg) c.2273C>G (p.Pro758Arg) | |
15 | g.73322602G>T | CA393085131 | HCN4 | c.3491C>A (p.Pro1164His) c.2273C>A (p.Pro758His) | |
15 | g.73322606del | CA491477970 | HCN4 | c.3491del (p.Pro1164LeufsTer17) c.2273del (p.Pro758LeufsTer17) | gnomAD v4 COSMIC |
15 | g.73322603G>A | CA393085133 | HCN4 | c.3490C>T (p.Pro1164Ser) c.2272C>T (p.Pro758Ser) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322603G>C | CA7648815 | HCN4 | c.3490C>G (p.Pro1164Ala) c.2272C>G (p.Pro758Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322603G= | CA2187186310 | HCN4 | c.3490C= (p.Pro1164=) c.2272C= (p.Pro758=) | |
15 | g.73322603G>T | CA393085135 | HCN4 | c.3490C>A (p.Pro1164Thr) c.2272C>A (p.Pro758Thr) | gnomAD v4 |
15 | g.73322604G>A | CA491477971 | HCN4 | c.3489C>T (p.Pro1163=) c.2271C>T (p.Pro757=) | |
15 | g.73322604G>C | CA491477972 | HCN4 | c.3489C>G (p.Pro1163=) c.2271C>G (p.Pro757=) | |
15 | g.73322604G>T | CA491477973 | HCN4 | c.3489C>A (p.Pro1163=) c.2271C>A (p.Pro757=) | ClinVar |
15 | g.73322605G>A | CA272663151 | HCN4 | c.3488C>T (p.Pro1163Leu) c.2270C>T (p.Pro757Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322605G>C | CA393085139 | HCN4 | c.3488C>G (p.Pro1163Arg) c.2270C>G (p.Pro757Arg) | |
15 | g.73322605G= | CA2187186311 | HCN4 | c.3488C= (p.Pro1163=) c.2270C= (p.Pro757=) | |
15 | g.73322605G>T | CA7648816 | HCN4 | c.3488C>A (p.Pro1163His) c.2270C>A (p.Pro757His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
15 | g.73322606G>A | CA393085141 | HCN4 | c.3487C>T (p.Pro1163Ser) c.2269C>T (p.Pro757Ser) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322606G>C | CA393085143 | HCN4 | c.3487C>G (p.Pro1163Ala) c.2269C>G (p.Pro757Ala) | |
15 | g.73322606G= | CA2187186312 | HCN4 | c.3487C= (p.Pro1163=) c.2269C= (p.Pro757=) | |
15 | g.73322606G>T | CA7648817 | HCN4 | c.3487C>A (p.Pro1163Thr) c.2269C>A (p.Pro757Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322607T>A | CA491477978 | HCN4 | c.3486A>T (p.Pro1162=) c.2268A>T (p.Pro756=) | |
15 | g.73322607T>C | CA491477979 | HCN4 | c.3486A>G (p.Pro1162=) c.2268A>G (p.Pro756=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322607T>G | CA491477977 | HCN4 | c.3486A>C (p.Pro1162=) c.2268A>C (p.Pro756=) | |
15 | g.73322607T= | CA2187186313 | HCN4 | c.3486A= (p.Pro1162=) c.2268A= (p.Pro756=) |