| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.73322976C>A | CA491478073 | HCN4 | c.3117G>T (p.Pro1039=) c.1899G>T (p.Pro633=) | gnomAD v4 |
| 15 | g.73322976C= | CA2187187110 | HCN4 | c.3117G= (p.Pro1039=) c.1899G= (p.Pro633=) | |
| 15 | g.73322976C>G | CA491478074 | HCN4 | c.3117G>C (p.Pro1039=) c.1899G>C (p.Pro633=) | gnomAD v4 |
| 15 | g.73322976C>T | CA7648881 | HCN4 | c.3117G>A (p.Pro1039=) c.1899G>A (p.Pro633=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322977G>A | CA7648882 | HCN4 | c.3116C>T (p.Pro1039Leu) c.1898C>T (p.Pro633Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322977G>C | CA393086182 | HCN4 | c.3116C>G (p.Pro1039Arg) c.1898C>G (p.Pro633Arg) | ClinVar dbSNP |
| 15 | g.73322977G= | CA2187187118 | HCN4 | c.3116C= (p.Pro1039=) c.1898C= (p.Pro633=) | |
| 15 | g.73322977G>T | CA393086183 | HCN4 | c.3116C>A (p.Pro1039Gln) c.1898C>A (p.Pro633Gln) | gnomAD v4 |
| 15 | g.73322978_73322979del | CA2575783827 | HCN4 | c.3115_3116del (p.Pro1039GlufsTer?) c.1897_1898del (p.Pro633GlufsTer?) | |
| 15 | g.73322978G>A | CA393086184 | HCN4 | c.3115C>T (p.Pro1039Ser) c.1897C>T (p.Pro633Ser) | gnomAD v4 COSMIC |
| 15 | g.73322978G>C | CA393086185 | HCN4 | c.3115C>G (p.Pro1039Ala) c.1897C>G (p.Pro633Ala) | |
| 15 | g.73322978G>T | CA393086186 | HCN4 | c.3115C>A (p.Pro1039Thr) c.1897C>A (p.Pro633Thr) | gnomAD v4 |
| 15 | g.73322979G>A | CA491478076 | HCN4 | c.3114C>T (p.Phe1038=) c.1896C>T (p.Phe632=) | |
| 15 | g.73322979G>C | CA393086187 | HCN4 | c.3114C>G (p.Phe1038Leu) c.1896C>G (p.Phe632Leu) | |
| 15 | g.73322979G= | CA2187187131 | HCN4 | c.3114C= (p.Phe1038=) c.1896C= (p.Phe632=) | |
| 15 | g.73322979G>T | CA393086188 | HCN4 | c.3114C>A (p.Phe1038Leu) c.1896C>A (p.Phe632Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322980A>C | CA393086189 | HCN4 | c.3113T>G (p.Phe1038Cys) c.1895T>G (p.Phe632Cys) | |
| 15 | g.73322980A>G | CA393086190 | HCN4 | c.3113T>C (p.Phe1038Ser) c.1895T>C (p.Phe632Ser) | |
| 15 | g.73322980A>T | CA393086191 | HCN4 | c.3113T>A (p.Phe1038Tyr) c.1895T>A (p.Phe632Tyr) | |
| 15 | g.73322981A= | CA2187187135 | HCN4 | c.3112T= (p.Phe1038=) c.1894T= (p.Phe632=) | |
| 15 | g.73322981A>C | CA393086192 | HCN4 | c.3112T>G (p.Phe1038Val) c.1894T>G (p.Phe632Val) | |
| 15 | g.73322981A>G | CA393086193 | HCN4 | c.3112T>C (p.Phe1038Leu) c.1894T>C (p.Phe632Leu) | dbSNP gnomAD v4 |
| 15 | g.73322981A>T | CA393086194 | HCN4 | c.3112T>A (p.Phe1038Ile) c.1894T>A (p.Phe632Ile) | |
| 15 | g.73322982G>A | CA491478079 | HCN4 | c.3111C>T (p.Thr1037=) c.1893C>T (p.Thr631=) | gnomAD v4 |
| 15 | g.73322982G>C | CA491478080 | HCN4 | c.3111C>G (p.Thr1037=) c.1893C>G (p.Thr631=) | |
| 15 | g.73322982G>T | CA491478081 | HCN4 | c.3111C>A (p.Thr1037=) c.1893C>A (p.Thr631=) | ClinVar gnomAD v4 |
| 15 | g.73322983G>A | CA393086196 | HCN4 | c.3110C>T (p.Thr1037Ile) c.1892C>T (p.Thr631Ile) | |
| 15 | g.73322983G>C | CA393086197 | HCN4 | c.3110C>G (p.Thr1037Ser) c.1892C>G (p.Thr631Ser) | |
| 15 | g.73322983G>T | CA393086195 | HCN4 | c.3110C>A (p.Thr1037Asn) c.1892C>A (p.Thr631Asn) | ClinVar gnomAD v4 |
| 15 | g.73322984T>A | CA393086198 | HCN4 | c.3109A>T (p.Thr1037Ser) c.1891A>T (p.Thr631Ser) | |
| 15 | g.73322984T>C | CA393086199 | HCN4 | c.3109A>G (p.Thr1037Ala) c.1891A>G (p.Thr631Ala) | gnomAD v4 |
| 15 | g.73322984T>G | CA393086200 | HCN4 | c.3109A>C (p.Thr1037Pro) c.1891A>C (p.Thr631Pro) | |
| 15 | g.73322985T>A | CA393086201 | HCN4 | c.3108A>T (p.Arg1036Ser) c.1890A>T (p.Arg630Ser) | ClinVar |
| 15 | g.73322985T>C | CA491478084 | HCN4 | c.3108A>G (p.Arg1036=) c.1890A>G (p.Arg630=) | |
| 15 | g.73322985T>G | CA393086202 | HCN4 | c.3108A>C (p.Arg1036Ser) c.1890A>C (p.Arg630Ser) | |
| 15 | g.73322986C>A | CA393086205 | HCN4 | c.3107G>T (p.Arg1036Ile) c.1889G>T (p.Arg630Ile) | gnomAD v4 |
| 15 | g.73322986C>G | CA393086203 | HCN4 | c.3107G>C (p.Arg1036Thr) c.1889G>C (p.Arg630Thr) | |
| 15 | g.73322986C>T | CA393086204 | HCN4 | c.3107G>A (p.Arg1036Lys) c.1889G>A (p.Arg630Lys) | |
| 15 | g.73322987T>A | CA393086206 | HCN4 | c.3106A>T (p.Arg1036Ter) c.1888A>T (p.Arg630Ter) | |
| 15 | g.73322987T>C | CA393086207 | HCN4 | c.3106A>G (p.Arg1036Gly) c.1888A>G (p.Arg630Gly) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322987T>G | CA491478088 | HCN4 | c.3106A>C (p.Arg1036=) c.1888A>C (p.Arg630=) | |
| 15 | g.73322987T= | CA2187187138 | HCN4 | c.3106A= (p.Arg1036=) c.1888A= (p.Arg630=) | |
| 15 | g.73322988T>A | CA491478089 | HCN4 | c.3105A>T (p.Pro1035=) c.1887A>T (p.Pro629=) | |
| 15 | g.73322988T>C | CA491478090 | HCN4 | c.3105A>G (p.Pro1035=) c.1887A>G (p.Pro629=) | gnomAD v4 |
| 15 | g.73322988T>G | CA491478092 | HCN4 | c.3105A>C (p.Pro1035=) c.1887A>C (p.Pro629=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73322988T= | CA2187187144 | HCN4 | c.3105A= (p.Pro1035=) c.1887A= (p.Pro629=) | |
| 15 | g.73322989G>A | CA393086208 | HCN4 | c.3104C>T (p.Pro1035Leu) c.1886C>T (p.Pro629Leu) | gnomAD v4 COSMIC |
| 15 | g.73322989G>C | CA393086209 | HCN4 | c.3104C>G (p.Pro1035Arg) c.1886C>G (p.Pro629Arg) | |
| 15 | g.73322989G>T | CA393086210 | HCN4 | c.3104C>A (p.Pro1035Gln) c.1886C>A (p.Pro629Gln) | gnomAD v4 |
| 15 | g.73322994dup | CA619410589 | HCN4 | c.3104dup (p.Arg1036LysfsTer?) c.1886dup (p.Arg630LysfsTer?) | dbSNP gnomAD v2 gnomAD v4 |