Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73322525C>A | CA393084787 | HCN4 | c.3568G>T (p.Ala1190Ser) c.2350G>T (p.Ala784Ser) | 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.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=) | |
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) |