| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.73332164A= | CA2187169761 | HCN4 | c.1338T= (p.Pro446=) c.120T= (p.Pro40=) | |
| 15 | g.73332164A>C | CA7649325 | HCN4 | c.1338T>G (p.Pro446=) c.120T>G (p.Pro40=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73332164A>G | CA491152534 | HCN4 | c.1338T>C (p.Pro446=) c.120T>C (p.Pro40=) | |
| 15 | g.73332164A>T | CA491152533 | HCN4 | c.1338T>A (p.Pro446=) c.120T>A (p.Pro40=) | |
| 15 | g.73332165G>A | CA393094309 | HCN4 | c.1337C>T (p.Pro446Leu) c.119C>T (p.Pro40Leu) | gnomAD v4 |
| 15 | g.73332165G>C | CA393094311 | HCN4 | c.1337C>G (p.Pro446Arg) c.119C>G (p.Pro40Arg) | |
| 15 | g.73332165G>T | CA393094310 | HCN4 | c.1337C>A (p.Pro446His) c.119C>A (p.Pro40His) | |
| 15 | g.73332166G>A | CA393094312 | HCN4 | c.1336C>T (p.Pro446Ser) c.118C>T (p.Pro40Ser) | |
| 15 | g.73332166G>C | CA393094313 | HCN4 | c.1336C>G (p.Pro446Ala) c.118C>G (p.Pro40Ala) | |
| 15 | g.73332166G>T | CA393094314 | HCN4 | c.1336C>A (p.Pro446Thr) c.118C>A (p.Pro40Thr) | |
| 15 | g.73332167G>A | CA491152535 | HCN4 | c.1335C>T (p.Phe445=) c.117C>T (p.Phe39=) | |
| 15 | g.73332167G>C | CA393094315 | HCN4 | c.1335C>G (p.Phe445Leu) c.117C>G (p.Phe39Leu) | gnomAD v4 |
| 15 | g.73332167G>T | CA393094316 | HCN4 | c.1335C>A (p.Phe445Leu) c.117C>A (p.Phe39Leu) | gnomAD v4 |
| 15 | g.73332168A>C | CA393094317 | HCN4 | c.1334T>G (p.Phe445Cys) c.116T>G (p.Phe39Cys) | |
| 15 | g.73332168A>G | CA393094318 | HCN4 | c.1334T>C (p.Phe445Ser) c.116T>C (p.Phe39Ser) | |
| 15 | g.73332168A>T | CA393094319 | HCN4 | c.1334T>A (p.Phe445Tyr) c.116T>A (p.Phe39Tyr) | |
| 15 | g.73332169A>C | CA393094320 | HCN4 | c.1333T>G (p.Phe445Val) c.115T>G (p.Phe39Val) | |
| 15 | g.73332169A>G | CA393094321 | HCN4 | c.1333T>C (p.Phe445Leu) c.115T>C (p.Phe39Leu) | |
| 15 | g.73332169A>T | CA393094322 | HCN4 | c.1333T>A (p.Phe445Ile) c.115T>A (p.Phe39Ile) | |
| 15 | g.73332170G>A | CA491152536 | HCN4 | c.1332C>T (p.Asp444=) c.114C>T (p.Asp38=) | gnomAD v4 |
| 15 | g.73332170G>C | CA393094323 | HCN4 | c.1332C>G (p.Asp444Glu) c.114C>G (p.Asp38Glu) | |
| 15 | g.73332170G>T | CA393094324 | HCN4 | c.1332C>A (p.Asp444Glu) c.114C>A (p.Asp38Glu) | |
| 15 | g.73332171T>A | CA393094325 | HCN4 | c.1331A>T (p.Asp444Val) c.113A>T (p.Asp38Val) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73332171T>C | CA393094326 | HCN4 | c.1331A>G (p.Asp444Gly) c.113A>G (p.Asp38Gly) | |
| 15 | g.73332171T>G | CA393094327 | HCN4 | c.1331A>C (p.Asp444Ala) c.113A>C (p.Asp38Ala) | |
| 15 | g.73332171T= | CA2187169765 | HCN4 | c.1331A= (p.Asp444=) c.113A= (p.Asp38=) | |
| 15 | g.73332172C>A | CA393094328 | HCN4 | c.1330G>T (p.Asp444Tyr) c.112G>T (p.Asp38Tyr) | |
| 15 | g.73332172C>G | CA393094329 | HCN4 | c.1330G>C (p.Asp444His) c.112G>C (p.Asp38His) | |
| 15 | g.73332172C>T | CA393094330 | HCN4 | c.1330G>A (p.Asp444Asn) c.112G>A (p.Asp38Asn) | |
| 15 | g.73332173C>A | CA393094332 | HCN4 | c.1329G>T (p.Gln443His) c.111G>T (p.Gln37His) | |
| 15 | g.73332173C>G | CA393094331 | HCN4 | c.1329G>C (p.Gln443His) c.111G>C (p.Gln37His) | |
| 15 | g.73332173C>T | CA491152537 | HCN4 | c.1329G>A (p.Gln443=) c.111G>A (p.Gln37=) | |
| 15 | g.73332174T>A | CA393094333 | HCN4 | c.1328A>T (p.Gln443Leu) c.110A>T (p.Gln37Leu) | COSMIC |
| 15 | g.73332174T>C | CA393094334 | HCN4 | c.1328A>G (p.Gln443Arg) c.110A>G (p.Gln37Arg) | gnomAD v4 |
| 15 | g.73332174T>G | CA393094335 | HCN4 | c.1328A>C (p.Gln443Pro) c.110A>C (p.Gln37Pro) | |
| 15 | g.73332175G>A | CA393094336 | HCN4 | c.1327C>T (p.Gln443Ter) c.109C>T (p.Gln37Ter) | |
| 15 | g.73332175G>C | CA393094337 | HCN4 | c.1327C>G (p.Gln443Glu) c.109C>G (p.Gln37Glu) | |
| 15 | g.73332175G>T | CA393094338 | HCN4 | c.1327C>A (p.Gln443Lys) c.109C>A (p.Gln37Lys) | |
| 15 | g.73332176T>A | CA491152538 | HCN4 | c.1326A>T (p.Leu442=) c.108A>T (p.Leu36=) | |
| 15 | g.73332176T>C | CA491152539 | HCN4 | c.1326A>G (p.Leu442=) c.108A>G (p.Leu36=) | dbSNP |
| 15 | g.73332176T>G | CA491152540 | HCN4 | c.1326A>C (p.Leu442=) c.108A>C (p.Leu36=) | |
| 15 | g.73332176T= | CA2187169769 | HCN4 | c.1326A= (p.Leu442=) c.108A= (p.Leu36=) | |
| 15 | g.73332177A>C | CA393094339 | HCN4 | c.1325T>G (p.Leu442Arg) c.107T>G (p.Leu36Arg) | |
| 15 | g.73332177A>G | CA393094341 | HCN4 | c.1325T>C (p.Leu442Pro) c.107T>C (p.Leu36Pro) | |
| 15 | g.73332177A>T | CA393094340 | HCN4 | c.1325T>A (p.Leu442Gln) c.107T>A (p.Leu36Gln) | |
| 15 | g.73332178G>A | CA491152541 | HCN4 | c.1324C>T (p.Leu442=) c.106C>T (p.Leu36=) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73332178G>C | CA393094342 | HCN4 | c.1324C>G (p.Leu442Val) c.106C>G (p.Leu36Val) | |
| 15 | g.73332178G= | CA2187169774 | HCN4 | c.1324C= (p.Leu442=) c.106C= (p.Leu36=) | |
| 15 | g.73332178G>T | CA393094343 | HCN4 | c.1324C>A (p.Leu442Ile) c.106C>A (p.Leu36Ile) | |
| 15 | g.73332179C>A | CA393094344 | HCN4 | c.1323G>T (p.Met441Ile) c.105G>T (p.Met35Ile) |