| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.73322967C>A | CA491478059 | HCN4 | c.3126G>T (p.Pro1042=) c.1908G>T (p.Pro636=) | gnomAD v4 |
| 15 | g.73322967C= | CA2187187078 | HCN4 | c.3126G= (p.Pro1042=) c.1908G= (p.Pro636=) | |
| 15 | g.73322967C>G | CA491478060 | HCN4 | c.3126G>C (p.Pro1042=) c.1908G>C (p.Pro636=) | gnomAD v4 |
| 15 | g.73322967C>T | CA16606777 | HCN4 | c.3126G>A (p.Pro1042=) c.1908G>A (p.Pro636=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322968G>A | CA393086163 | HCN4 | c.3125C>T (p.Pro1042Leu) c.1907C>T (p.Pro636Leu) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73322968G>C | CA393086164 | HCN4 | c.3125C>G (p.Pro1042Arg) c.1907C>G (p.Pro636Arg) | gnomAD v4 |
| 15 | g.73322968G= | CA2187187085 | HCN4 | c.3125C= (p.Pro1042=) c.1907C= (p.Pro636=) | |
| 15 | g.73322968G>T | CA393086165 | HCN4 | c.3125C>A (p.Pro1042Gln) c.1907C>A (p.Pro636Gln) | gnomAD v4 |
| 15 | g.73322971del | CA2575783825 | HCN4 | c.3125del (p.Pro1042ArgfsTer?) c.1907del (p.Pro636ArgfsTer?) | gnomAD v4 |
| 15 | g.73322970_73322971del | CA2575783826 | HCN4 | c.3124_3125del (p.Pro1042AlafsTer?) c.1906_1907del (p.Pro636AlafsTer?) | |
| 15 | g.73322969G>A | CA393086167 | HCN4 | c.3124C>T (p.Pro1042Ser) c.1906C>T (p.Pro636Ser) | gnomAD v4 |
| 15 | g.73322969G>C | CA393086168 | HCN4 | c.3124C>G (p.Pro1042Ala) c.1906C>G (p.Pro636Ala) | dbSNP |
| 15 | g.73322969G= | CA2187187088 | HCN4 | c.3124C= (p.Pro1042=) c.1906C= (p.Pro636=) | |
| 15 | g.73322969G>T | CA393086166 | HCN4 | c.3124C>A (p.Pro1042Thr) c.1906C>A (p.Pro636Thr) | gnomAD v4 |
| 15 | g.73322970G>A | CA491478063 | HCN4 | c.3123C>T (p.Ala1041=) c.1905C>T (p.Ala635=) | gnomAD v4 |
| 15 | g.73322970G>C | CA491478064 | HCN4 | c.3123C>G (p.Ala1041=) c.1905C>G (p.Ala635=) | |
| 15 | g.73322970G>T | CA491478065 | HCN4 | c.3123C>A (p.Ala1041=) c.1905C>A (p.Ala635=) | gnomAD v4 |
| 15 | g.73322971G>A | CA393086169 | HCN4 | c.3122C>T (p.Ala1041Val) c.1904C>T (p.Ala635Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322971G>C | CA393086170 | HCN4 | c.3122C>G (p.Ala1041Gly) c.1904C>G (p.Ala635Gly) | |
| 15 | g.73322971G= | CA2187187092 | HCN4 | c.3122C= (p.Ala1041=) c.1904C= (p.Ala635=) | |
| 15 | g.73322971G>T | CA393086171 | HCN4 | c.3122C>A (p.Ala1041Asp) c.1904C>A (p.Ala635Asp) | gnomAD v4 |
| 15 | g.73322972C>A | CA393086172 | HCN4 | c.3121G>T (p.Ala1041Ser) c.1903G>T (p.Ala635Ser) | gnomAD v4 |
| 15 | g.73322972C= | CA2187187100 | HCN4 | c.3121G= (p.Ala1041=) c.1903G= (p.Ala635=) | |
| 15 | g.73322972C>G | CA393086173 | HCN4 | c.3121G>C (p.Ala1041Pro) c.1903G>C (p.Ala635Pro) | |
| 15 | g.73322972C>T | CA7648880 | HCN4 | c.3121G>A (p.Ala1041Thr) c.1903G>A (p.Ala635Thr) | dbSNP ExAC gnomAD v4 |
| 15 | g.73322973A>C | CA393086174 | HCN4 | c.3120T>G (p.Ser1040Arg) c.1902T>G (p.Ser634Arg) | |
| 15 | g.73322973A>G | CA491478069 | HCN4 | c.3120T>C (p.Ser1040=) c.1902T>C (p.Ser634=) | gnomAD v4 |
| 15 | g.73322973A>T | CA393086175 | HCN4 | c.3120T>A (p.Ser1040Arg) c.1902T>A (p.Ser634Arg) | COSMIC |
| 15 | g.73322974C>A | CA393086176 | HCN4 | c.3119G>T (p.Ser1040Ile) c.1901G>T (p.Ser634Ile) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73322974C= | CA2187187103 | HCN4 | c.3119G= (p.Ser1040=) c.1901G= (p.Ser634=) | |
| 15 | g.73322974C>G | CA393086177 | HCN4 | c.3119G>C (p.Ser1040Thr) c.1901G>C (p.Ser634Thr) | |
| 15 | g.73322974C>T | CA393086178 | HCN4 | c.3119G>A (p.Ser1040Asn) c.1901G>A (p.Ser634Asn) | |
| 15 | g.73322975T>A | CA393086179 | HCN4 | c.3118A>T (p.Ser1040Cys) c.1900A>T (p.Ser634Cys) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73322975T>C | CA393086180 | HCN4 | c.3118A>G (p.Ser1040Gly) c.1900A>G (p.Ser634Gly) | gnomAD v4 |
| 15 | g.73322975T>G | CA393086181 | HCN4 | c.3118A>C (p.Ser1040Arg) c.1900A>C (p.Ser634Arg) | |
| 15 | g.73322975T= | CA2187187106 | HCN4 | c.3118A= (p.Ser1040=) c.1900A= (p.Ser634=) | |
| 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) |