| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.73323744C>A | CA393089064 | HCN4 | c.2349G>T (p.Gln783His) c.1131G>T (p.Gln377His) | |
| 15 | g.73323744C= | CA2187188631 | HCN4 | c.2349G= (p.Gln783=) c.1131G= (p.Gln377=) | |
| 15 | g.73323744C>G | CA393089065 | HCN4 | c.2349G>C (p.Gln783His) c.1131G>C (p.Gln377His) | |
| 15 | g.73323744C>T | CA7649043 | HCN4 | c.2349G>A (p.Gln783=) c.1131G>A (p.Gln377=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323745T>A | CA393089066 | HCN4 | c.2348A>T (p.Gln783Leu) c.1130A>T (p.Gln377Leu) | |
| 15 | g.73323745T>C | CA393089067 | HCN4 | c.2348A>G (p.Gln783Arg) c.1130A>G (p.Gln377Arg) | |
| 15 | g.73323745T>G | CA393089068 | HCN4 | c.2348A>C (p.Gln783Pro) c.1130A>C (p.Gln377Pro) | |
| 15 | g.73323746G>A | CA393089069 | HCN4 | c.2347C>T (p.Gln783Ter) c.1129C>T (p.Gln377Ter) | gnomAD v4 |
| 15 | g.73323746G>C | CA393089070 | HCN4 | c.2347C>G (p.Gln783Glu) c.1129C>G (p.Gln377Glu) | |
| 15 | g.73323746G>T | CA393089071 | HCN4 | c.2347C>A (p.Gln783Lys) c.1129C>A (p.Gln377Lys) | gnomAD v4 |
| 15 | g.73323747C>A | CA272664904 | HCN4 | c.2346G>T (p.Leu782=) c.1128G>T (p.Leu376=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323747C= | CA2187188632 | HCN4 | c.2346G= (p.Leu782=) c.1128G= (p.Leu376=) | |
| 15 | g.73323747C>G | CA491478618 | HCN4 | c.2346G>C (p.Leu782=) c.1128G>C (p.Leu376=) | |
| 15 | g.73323747C>T | CA491478616 | HCN4 | c.2346G>A (p.Leu782=) c.1128G>A (p.Leu376=) | |
| 15 | g.73323748A= | CA2187188633 | HCN4 | c.2345T= (p.Leu782=) c.1127T= (p.Leu376=) | |
| 15 | g.73323748A>C | CA393089072 | HCN4 | c.2345T>G (p.Leu782Arg) c.1127T>G (p.Leu376Arg) | ClinVar dbSNP |
| 15 | g.73323748A>G | CA393089073 | HCN4 | c.2345T>C (p.Leu782Pro) c.1127T>C (p.Leu376Pro) | |
| 15 | g.73323748A>T | CA393089074 | HCN4 | c.2345T>A (p.Leu782Gln) c.1127T>A (p.Leu376Gln) | |
| 15 | g.73323749G>A | CA491478622 | HCN4 | c.2344C>T (p.Leu782=) c.1126C>T (p.Leu376=) | |
| 15 | g.73323749G>C | CA393089076 | HCN4 | c.2344C>G (p.Leu782Val) c.1126C>G (p.Leu376Val) | |
| 15 | g.73323749G>T | CA393089075 | HCN4 | c.2344C>A (p.Leu782Met) c.1126C>A (p.Leu376Met) | gnomAD v4 |
| 15 | g.73323750T>A | CA491478624 | HCN4 | c.2343A>T (p.Pro781=) c.1125A>T (p.Pro375=) | |
| 15 | g.73323750T>C | CA491478626 | HCN4 | c.2343A>G (p.Pro781=) c.1125A>G (p.Pro375=) | dbSNP |
| 15 | g.73323750T>G | CA491478628 | HCN4 | c.2343A>C (p.Pro781=) c.1125A>C (p.Pro375=) | |
| 15 | g.73323750T= | CA2187188634 | HCN4 | c.2343A= (p.Pro781=) c.1125A= (p.Pro375=) | |
| 15 | g.73323751G>A | CA393089077 | HCN4 | c.2342C>T (p.Pro781Leu) c.1124C>T (p.Pro375Leu) | |
| 15 | g.73323751G>C | CA393089079 | HCN4 | c.2342C>G (p.Pro781Arg) c.1124C>G (p.Pro375Arg) | |
| 15 | g.73323751G>T | CA393089078 | HCN4 | c.2342C>A (p.Pro781Gln) c.1124C>A (p.Pro375Gln) | gnomAD v4 |
| 15 | g.73323752G>A | CA393089080 | HCN4 | c.2341C>T (p.Pro781Ser) c.1123C>T (p.Pro375Ser) | |
| 15 | g.73323752G>C | CA393089081 | HCN4 | c.2341C>G (p.Pro781Ala) c.1123C>G (p.Pro375Ala) | COSMIC |
| 15 | g.73323752G>T | CA393089082 | HCN4 | c.2341C>A (p.Pro781Thr) c.1123C>A (p.Pro375Thr) | |
| 15 | g.73323753T>A | CA491478632 | HCN4 | c.2340A>T (p.Ala780=) c.1122A>T (p.Ala374=) | |
| 15 | g.73323753T>C | CA491478633 | HCN4 | c.2340A>G (p.Ala780=) c.1122A>G (p.Ala374=) | |
| 15 | g.73323753T>G | CA491478634 | HCN4 | c.2340A>C (p.Ala780=) c.1122A>C (p.Ala374=) | |
| 15 | g.73323754G>A | CA393089083 | HCN4 | c.2339C>T (p.Ala780Val) c.1121C>T (p.Ala374Val) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323754G>C | CA393089084 | HCN4 | c.2339C>G (p.Ala780Gly) c.1121C>G (p.Ala374Gly) | |
| 15 | g.73323754G= | CA2187188635 | HCN4 | c.2339C= (p.Ala780=) c.1121C= (p.Ala374=) | |
| 15 | g.73323754G>T | CA393089085 | HCN4 | c.2339C>A (p.Ala780Glu) c.1121C>A (p.Ala374Glu) | gnomAD v4 |
| 15 | g.73323755C>A | CA393089086 | HCN4 | c.2338G>T (p.Ala780Ser) c.1120G>T (p.Ala374Ser) | gnomAD v4 COSMIC |
| 15 | g.73323755C>G | CA393089087 | HCN4 | c.2338G>C (p.Ala780Pro) c.1120G>C (p.Ala374Pro) | |
| 15 | g.73323755C>T | CA393089088 | HCN4 | c.2338G>A (p.Ala780Thr) c.1120G>A (p.Ala374Thr) | |
| 15 | g.73323756C>A | CA393089089 | HCN4 | c.2337G>T (p.Gln779His) c.1119G>T (p.Gln373His) | gnomAD v4 |
| 15 | g.73323756C= | CA2187188636 | HCN4 | c.2337G= (p.Gln779=) c.1119G= (p.Gln373=) | |
| 15 | g.73323756C>G | CA393089090 | HCN4 | c.2337G>C (p.Gln779His) c.1119G>C (p.Gln373His) | |
| 15 | g.73323756C>T | CA491478637 | HCN4 | c.2337G>A (p.Gln779=) c.1119G>A (p.Gln373=) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323757T>A | CA393089093 | HCN4 | c.2336A>T (p.Gln779Leu) c.1118A>T (p.Gln373Leu) | |
| 15 | g.73323757T>C | CA393089092 | HCN4 | c.2336A>G (p.Gln779Arg) c.1118A>G (p.Gln373Arg) | gnomAD v4 |
| 15 | g.73323757T>G | CA393089091 | HCN4 | c.2336A>C (p.Gln779Pro) c.1118A>C (p.Gln373Pro) | |
| 15 | g.73323758G>A | CA393089094 | HCN4 | c.2335C>T (p.Gln779Ter) c.1117C>T (p.Gln373Ter) | |
| 15 | g.73323758G>C | CA393089095 | HCN4 | c.2335C>G (p.Gln779Glu) c.1117C>G (p.Gln373Glu) |