| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.45645298C>A | CA359707227 | HCN1 | c.736G>T (p.Glu246Ter) | COSMIC |
| 5 | g.45645298C>G | CA359707228 | HCN1 | c.736G>C (p.Glu246Gln) | |
| 5 | g.45645298C>T | CA359707226 | HCN1 | c.736G>A (p.Glu246Lys) | COSMIC |
| 5 | g.45645299A>C | CA444401662 | HCN1 | c.735T>G (p.Ser245=) | |
| 5 | g.45645299A>G | CA444401664 | HCN1 | c.735T>C (p.Ser245=) | |
| 5 | g.45645299A>T | CA444401665 | HCN1 | c.735T>A (p.Ser245=) | |
| 5 | g.45645300G>A | CA359707229 | HCN1 | c.734C>T (p.Ser245Phe) | ClinVar dbSNP gnomAD v4 |
| 5 | g.45645300G>C | CA359707230 | HCN1 | c.734C>G (p.Ser245Cys) | |
| 5 | g.45645300G= | CA1543790389 | HCN1 | c.734C= (p.Ser245=) | |
| 5 | g.45645300G>T | CA359707231 | HCN1 | c.734C>A (p.Ser245Tyr) | COSMIC |
| 5 | g.45645301A= | CA1543790393 | HCN1 | c.733T= (p.Ser245=) | |
| 5 | g.45645301A>C | CA359707232 | HCN1 | c.733T>G (p.Ser245Ala) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.45645301A>G | CA359707233 | HCN1 | c.733T>C (p.Ser245Pro) | |
| 5 | g.45645301A>T | CA359707234 | HCN1 | c.733T>A (p.Ser245Thr) | |
| 5 | g.45645302A>C | CA359707235 | HCN1 | c.732T>G (p.Asp244Glu) | |
| 5 | g.45645302A>G | CA444401672 | HCN1 | c.732T>C (p.Asp244=) | |
| 5 | g.45645302A>T | CA359707236 | HCN1 | c.732T>A (p.Asp244Glu) | |
| 5 | g.45645303T>A | CA359707237 | HCN1 | c.731A>T (p.Asp244Val) | |
| 5 | g.45645303T>C | CA359707238 | HCN1 | c.731A>G (p.Asp244Gly) | ClinVar |
| 5 | g.45645303T>G | CA359707239 | HCN1 | c.731A>C (p.Asp244Ala) | |
| 5 | g.45645304C>A | CA359707242 | HCN1 | c.730G>T (p.Asp244Tyr) | |
| 5 | g.45645304C>G | CA359707241 | HCN1 | c.730G>C (p.Asp244His) | |
| 5 | g.45645304C>T | CA359707240 | HCN1 | c.730G>A (p.Asp244Asn) | COSMIC |
| 5 | g.45645305C>A | CA359707243 | HCN1 | c.729G>T (p.Met243Ile) | |
| 5 | g.45645305C>G | CA359707244 | HCN1 | c.729G>C (p.Met243Ile) | |
| 5 | g.45645305C>T | CA359707245 | HCN1 | c.729G>A (p.Met243Ile) | COSMIC |
| 5 | g.45645306A= | CA1543790394 | HCN1 | c.728T= (p.Met243=) | |
| 5 | g.45645306A>C | CA359707246 | HCN1 | c.728T>G (p.Met243Arg) | ClinVar dbSNP |
| 5 | g.45645306A>G | CA359707247 | HCN1 | c.728T>C (p.Met243Thr) | ClinVar |
| 5 | g.45645306A>T | CA359707248 | HCN1 | c.728T>A (p.Met243Lys) | |
| 5 | g.45645307T>A | CA359707249 | HCN1 | c.727A>T (p.Met243Leu) | |
| 5 | g.45645307T>C | CA359707250 | HCN1 | c.727A>G (p.Met243Val) | ClinVar dbSNP gnomAD v4 |
| 5 | g.45645307T>G | CA359707251 | HCN1 | c.727A>C (p.Met243Leu) | |
| 5 | g.45645307T= | CA1543790400 | HCN1 | c.727A= (p.Met243=) | |
| 5 | g.45645308T>A | CA444401679 | HCN1 | c.726A>T (p.Gly242=) | |
| 5 | g.45645308T>C | CA444401680 | HCN1 | c.726A>G (p.Gly242=) | |
| 5 | g.45645308T>G | CA3259421 | HCN1 | c.726A>C (p.Gly242=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.45645308T= | CA1543790414 | HCN1 | c.726A= (p.Gly242=) | |
| 5 | g.45645309C>A | CA359707252 | HCN1 | c.725G>T (p.Gly242Val) | |
| 5 | g.45645309C>G | CA359707253 | HCN1 | c.725G>C (p.Gly242Ala) | |
| 5 | g.45645309C>T | CA359707254 | HCN1 | c.725G>A (p.Gly242Glu) | gnomAD v4 |
| 5 | g.45645310C>A | CA359707257 | HCN1 | c.724G>T (p.Gly242Ter) | |
| 5 | g.45645310C>G | CA359707256 | HCN1 | c.724G>C (p.Gly242Arg) | |
| 5 | g.45645310C>T | CA359707255 | HCN1 | c.724G>A (p.Gly242Arg) | COSMIC |
| 5 | g.45645311T>A | CA359707258 | HCN1 | c.723A>T (p.Lys241Asn) | |
| 5 | g.45645311T>C | CA3259422 | HCN1 | c.723A>G (p.Lys241=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.45645311T>G | CA359707259 | HCN1 | c.723A>C (p.Lys241Asn) | COSMIC |
| 5 | g.45645311T= | CA1543790419 | HCN1 | c.723A= (p.Lys241=) | |
| 5 | g.45645312T>A | CA359707260 | HCN1 | c.722A>T (p.Lys241Ile) | |
| 5 | g.45645312T>C | CA359707261 | HCN1 | c.722A>G (p.Lys241Arg) | |
| 5 | g.45645312T>G | CA359707262 | HCN1 | c.722A>C (p.Lys241Thr) | |
| 5 | g.45645313T>A | CA359707263 | HCN1 | c.721A>T (p.Lys241Ter) | ClinVar |
| 5 | g.45645313T>C | CA359707264 | HCN1 | c.721A>G (p.Lys241Glu) | gnomAD v4 |
| 5 | g.45645313T>G | CA359707265 | HCN1 | c.721A>C (p.Lys241Gln) | |
| 5 | g.45645314T>A | CA359707267 | HCN1 | c.720A>T (p.Glu240Asp) | ClinVar dbSNP |
| 5 | g.45645314T>C | CA444401690 | HCN1 | c.720A>G (p.Glu240=) | dbSNP |
| 5 | g.45645314T>G | CA359707266 | HCN1 | c.720A>C (p.Glu240Asp) | dbSNP |
| 5 | g.45645314T= | CA1543790427 | HCN1 | c.720A= (p.Glu240=) | |
| 5 | g.45645315T>A | CA359707268 | HCN1 | c.719A>T (p.Glu240Val) | |
| 5 | g.45645315T>C | CA359707269 | HCN1 | c.719A>G (p.Glu240Gly) | ClinVar dbSNP |
| 5 | g.45645315T>G | CA359707270 | HCN1 | c.719A>C (p.Glu240Ala) | |
| 5 | g.45645316C>A | CA359707271 | HCN1 | c.718G>T (p.Glu240Ter) | |
| 5 | g.45645316C>G | CA359707272 | HCN1 | c.718G>C (p.Glu240Gln) | |
| 5 | g.45645316C>T | CA359707273 | HCN1 | c.718G>A (p.Glu240Lys) | COSMIC |
| 5 | g.45645317T>A | CA444401692 | HCN1 | c.717A>T (p.Val239=) | |
| 5 | g.45645317T>C | CA444401693 | HCN1 | c.717A>G (p.Val239=) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.45645317T>G | CA444401694 | HCN1 | c.717A>C (p.Val239=) | |
| 5 | g.45645317T= | CA1543790434 | HCN1 | c.717A= (p.Val239=) | |
| 5 | g.45645318A>C | CA359707274 | HCN1 | c.716T>G (p.Val239Gly) | |
| 5 | g.45645318A>G | CA359707276 | HCN1 | c.716T>C (p.Val239Ala) | |
| 5 | g.45645318A>T | CA359707275 | HCN1 | c.716T>A (p.Val239Glu) | |
| 5 | g.45645319C>A | CA359707277 | HCN1 | c.715G>T (p.Val239Leu) | |
| 5 | g.45645319C>G | CA359707278 | HCN1 | c.715G>C (p.Val239Leu) | |
| 5 | g.45645319C>T | CA359707279 | HCN1 | c.715G>A (p.Val239Ile) | |
| 5 | g.45645320A>C | CA359707280 | HCN1 | c.714T>G (p.Ile238Met) | |
| 5 | g.45645320A>G | CA444401697 | HCN1 | c.714T>C (p.Ile238=) | gnomAD v4 |
| 5 | g.45645320A>T | CA444401698 | HCN1 | c.714T>A (p.Ile238=) | |
| 5 | g.45645321A= | CA1543790439 | HCN1 | c.713T= (p.Ile238=) | |
| 5 | g.45645321A>C | CA359707281 | HCN1 | c.713T>G (p.Ile238Ser) | |
| 5 | g.45645321A>G | CA359707282 | HCN1 | c.713T>C (p.Ile238Thr) | |
| 5 | g.45645321A>T | CA359707283 | HCN1 | c.713T>A (p.Ile238Asn) | dbSNP |
| 5 | g.45645322T>A | CA359707284 | HCN1 | c.712A>T (p.Ile238Phe) | |
| 5 | g.45645322T>C | CA359707285 | HCN1 | c.712A>G (p.Ile238Val) | |
| 5 | g.45645322T>G | CA359707286 | HCN1 | c.712A>C (p.Ile238Leu) | dbSNP |
| 5 | g.45645322T= | CA1543790446 | HCN1 | c.712A= (p.Ile238=) | |
| 5 | g.45645323A= | CA1543790452 | HCN1 | c.711T= (p.Leu237=) | |
| 5 | g.45645323A>C | CA444401704 | HCN1 | c.711T>G (p.Leu237=) | COSMIC |
| 5 | g.45645323A>G | CA444401703 | HCN1 | c.711T>C (p.Leu237=) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 5 | g.45645323A>T | CA444401701 | HCN1 | c.711T>A (p.Leu237=) | |
| 5 | g.45645324A>C | CA359707289 | HCN1 | c.710T>G (p.Leu237Arg) | |
| 5 | g.45645324A>G | CA359707288 | HCN1 | c.710T>C (p.Leu237Pro) | gnomAD v4 |
| 5 | g.45645324A>T | CA359707287 | HCN1 | c.710T>A (p.Leu237His) | |
| 5 | g.45645325G>A | CA359707290 | HCN1 | c.709C>T (p.Leu237Phe) | |
| 5 | g.45645325G>C | CA359707291 | HCN1 | c.709C>G (p.Leu237Val) | |
| 5 | g.45645325G>T | CA359707292 | HCN1 | c.709C>A (p.Leu237Ile) | |
| 5 | g.45645326A>C | CA359707293 | HCN1 | c.708T>G (p.Phe236Leu) | |
| 5 | g.45645326A>G | CA444401706 | HCN1 | c.708T>C (p.Phe236=) | |
| 5 | g.45645326A>T | CA359707294 | HCN1 | c.708T>A (p.Phe236Leu) | |
| 5 | g.45645327A>C | CA359707295 | HCN1 | c.707T>G (p.Phe236Cys) | |
| 5 | g.45645327A>G | CA359707296 | HCN1 | c.707T>C (p.Phe236Ser) | ClinVar |
| 5 | g.45645327A>T | CA359707297 | HCN1 | c.707T>A (p.Phe236Tyr) | |
| 5 | g.45645328A>C | CA359707298 | HCN1 | c.706T>G (p.Phe236Val) | |
| 5 | g.45645328A>G | CA359707299 | HCN1 | c.706T>C (p.Phe236Leu) | |
| 5 | g.45645328A>T | CA359707300 | HCN1 | c.706T>A (p.Phe236Ile) | |
| 5 | g.45645329G>A | CA444401710 | HCN1 | c.705C>T (p.Ile235=) | dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.45645329G>C | CA359707301 | HCN1 | c.705C>G (p.Ile235Met) | ClinVar |
| 5 | g.45645329G= | CA1543790455 | HCN1 | c.705C= (p.Ile235=) | |
| 5 | g.45645329G>T | CA444401712 | HCN1 | c.705C>A (p.Ile235=) | COSMIC |
| 5 | g.45645330A>C | CA359707303 | HCN1 | c.704T>G (p.Ile235Ser) | |
| 5 | g.45645330A>G | CA359707304 | HCN1 | c.704T>C (p.Ile235Thr) | ClinVar |
| 5 | g.45645330A>T | CA359707302 | HCN1 | c.704T>A (p.Ile235Asn) | |
| 5 | g.45645331T>A | CA359707305 | HCN1 | c.703A>T (p.Ile235Phe) | |
| 5 | g.45645331T>C | CA118324607 | HCN1 | c.703A>G (p.Ile235Val) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.45645331T>G | CA359707306 | HCN1 | c.703A>C (p.Ile235Leu) | |
| 5 | g.45645331T= | CA1543790459 | HCN1 | c.703A= (p.Ile235=) | |
| 5 | g.45645332A= | CA1543790467 | HCN1 | c.702T= (p.Tyr234=) | |
| 5 | g.45645332A>C | CA359707307 | HCN1 | c.702T>G (p.Tyr234Ter) | |
| 5 | g.45645332A>G | CA3259423 | HCN1 | c.702T>C (p.Tyr234=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.45645332A>T | CA359707308 | HCN1 | c.702T>A (p.Tyr234Ter) | |
| 5 | g.45645333T>A | CA359707309 | HCN1 | c.701A>T (p.Tyr234Phe) | ClinVar dbSNP |
| 5 | g.45645333T>C | CA359707311 | HCN1 | c.701A>G (p.Tyr234Cys) | dbSNP |
| 5 | g.45645333T>G | CA359707310 | HCN1 | c.701A>C (p.Tyr234Ser) | |
| 5 | g.45645333T= | CA1543790470 | HCN1 | c.701A= (p.Tyr234=) | |
| 5 | g.45645334A>C | CA359707312 | HCN1 | c.700T>G (p.Tyr234Asp) | |
| 5 | g.45645334A>G | CA359707313 | HCN1 | c.700T>C (p.Tyr234His) | |
| 5 | g.45645334A>T | CA359707314 | HCN1 | c.700T>A (p.Tyr234Asn) | dbSNP |
| 5 | g.45645335A>C | CA359707315 | HCN1 | c.699T>G (p.Asp233Glu) | |
| 5 | g.45645335A>G | CA444401723 | HCN1 | c.699T>C (p.Asp233=) | |
| 5 | g.45645335A>T | CA359707316 | HCN1 | c.699T>A (p.Asp233Glu) | |
| 5 | g.45645336T>A | CA359707319 | HCN1 | c.698A>T (p.Asp233Val) | |
| 5 | g.45645336T>C | CA359707318 | HCN1 | c.698A>G (p.Asp233Gly) | |
| 5 | g.45645336T>G | CA359707317 | HCN1 | c.698A>C (p.Asp233Ala) | |
| 5 | g.45645337C>A | CA359707320 | HCN1 | c.697G>T (p.Asp233Tyr) | gnomAD v4 |
| 5 | g.45645337C>G | CA359707321 | HCN1 | c.697G>C (p.Asp233His) | |
| 5 | g.45645337C>T | CA359707322 | HCN1 | c.697G>A (p.Asp233Asn) | COSMIC |
| 5 | g.45645338C>A | CA444401725 | HCN1 | c.696G>T (p.Val232=) | |
| 5 | g.45645338C>G | CA444401727 | HCN1 | c.696G>C (p.Val232=) | |
| 5 | g.45645338C>T | CA444401728 | HCN1 | c.696G>A (p.Val232=) | |
| 5 | g.45645339A>C | CA359707323 | HCN1 | c.695T>G (p.Val232Gly) | |
| 5 | g.45645339A>G | CA359707324 | HCN1 | c.695T>C (p.Val232Ala) | |
| 5 | g.45645339A>T | CA359707325 | HCN1 | c.695T>A (p.Val232Glu) | |
| 5 | g.45645340C>A | CA359707328 | HCN1 | c.694G>T (p.Val232Leu) | COSMIC |
| 5 | g.45645340C= | CA1543790475 | HCN1 | c.694G= (p.Val232=) | |
| 5 | g.45645340C>G | CA359707327 | HCN1 | c.694G>C (p.Val232Leu) | |
| 5 | g.45645340C>T | CA359707326 | HCN1 | c.694G>A (p.Val232Met) | ClinVar dbSNP |
| 5 | g.45645341T>A | CA444401730 | HCN1 | c.693A>T (p.Pro231=) | |
| 5 | g.45645341T>C | CA444401731 | HCN1 | c.693A>G (p.Pro231=) | dbSNP gnomAD v2 |
| 5 | g.45645341T>G | CA444401733 | HCN1 | c.693A>C (p.Pro231=) | dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.45645341T= | CA1543790478 | HCN1 | c.693A= (p.Pro231=) | |
| 5 | g.45645342G>A | CA359707329 | HCN1 | c.692C>T (p.Pro231Leu) | |
| 5 | g.45645342G>C | CA359707330 | HCN1 | c.692C>G (p.Pro231Arg) | |
| 5 | g.45645342G>T | CA359707331 | HCN1 | c.692C>A (p.Pro231Gln) | COSMIC |
| 5 | g.45645343G>A | CA359707332 | HCN1 | c.691C>T (p.Pro231Ser) | |
| 5 | g.45645343G>C | CA359707333 | HCN1 | c.691C>G (p.Pro231Ala) | |
| 5 | g.45645343G>T | CA359707334 | HCN1 | c.691C>A (p.Pro231Thr) | |
| 5 | g.45645344G>A | CA444401734 | HCN1 | c.690C>T (p.Ile230=) | dbSNP gnomAD v4 |
| 5 | g.45645344G>C | CA359707335 | HCN1 | c.690C>G (p.Ile230Met) | |
| 5 | g.45645344G= | CA1543790485 | HCN1 | c.690C= (p.Ile230=) | |
| 5 | g.45645344G>T | CA444401736 | HCN1 | c.690C>A (p.Ile230=) | dbSNP |
| 5 | g.45645345A>C | CA359707336 | HCN1 | c.689T>G (p.Ile230Ser) | |
| 5 | g.45645345A>G | CA359707338 | HCN1 | c.689T>C (p.Ile230Thr) | |
| 5 | g.45645345A>T | CA359707337 | HCN1 | c.689T>A (p.Ile230Asn) | |
| 5 | g.45645346T>A | CA359707339 | HCN1 | c.688A>T (p.Ile230Phe) | |
| 5 | g.45645346T>C | CA359707340 | HCN1 | c.688A>G (p.Ile230Val) | |
| 5 | g.45645346T>G | CA359707341 | HCN1 | c.688A>C (p.Ile230Leu) | |
| 5 | g.45645347G>A | CA444401740 | HCN1 | c.687C>T (p.Ser229=) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 5 | g.45645347G>C | CA444401741 | HCN1 | c.687C>G (p.Ser229=) | gnomAD v4 |
| 5 | g.45645347G= | CA1543790489 | HCN1 | c.687C= (p.Ser229=) | |
| 5 | g.45645347G>T | CA444401743 | HCN1 | c.687C>A (p.Ser229=) | ClinVar dbSNP |
| 5 | g.45645348G>A | CA359707342 | HCN1 | c.686C>T (p.Ser229Phe) | COSMIC |
| 5 | g.45645348G>C | CA359707343 | HCN1 | c.686C>G (p.Ser229Cys) | |
| 5 | g.45645348G>T | CA359707344 | HCN1 | c.686C>A (p.Ser229Tyr) | |
| 5 | g.45645349A= | CA1543790497 | HCN1 | c.685T= (p.Ser229=) | |
| 5 | g.45645349A>C | CA359707345 | HCN1 | c.685T>G (p.Ser229Ala) | |
| 5 | g.45645349A>G | CA359707346 | HCN1 | c.685T>C (p.Ser229Pro) | |
| 5 | g.45645349A>T | CA359707347 | HCN1 | c.685T>A (p.Ser229Thr) | ClinVar dbSNP |
| 5 | g.45645350T>A | CA444401749 | HCN1 | c.684A>T (p.Ser228=) | |
| 5 | g.45645350T>C | CA444401751 | HCN1 | c.684A>G (p.Ser228=) | |
| 5 | g.45645350T>G | CA444401750 | HCN1 | c.684A>C (p.Ser228=) | |
| 5 | g.45645351G>A | CA359707348 | HCN1 | c.683C>T (p.Ser228Leu) | |
| 5 | g.45645351G>C | CA359707349 | HCN1 | c.683C>G (p.Ser228Ter) | |
| 5 | g.45645351G>T | CA359707350 | HCN1 | c.683C>A (p.Ser228Ter) | |
| 5 | g.45645352A>C | CA359707353 | HCN1 | c.682T>G (p.Ser228Ala) | |
| 5 | g.45645352A>G | CA359707351 | HCN1 | c.682T>C (p.Ser228Pro) | |
| 5 | g.45645352A>T | CA359707352 | HCN1 | c.682T>A (p.Ser228Thr) | |
| 5 | g.45645353G>A | CA444401756 | HCN1 | c.681C>T (p.Ile227=) | |
| 5 | g.45645353G>C | CA359707354 | HCN1 | c.681C>G (p.Ile227Met) | |
| 5 | g.45645353G>T | CA444401757 | HCN1 | c.681C>A (p.Ile227=) | ClinVar dbSNP |
| 5 | g.45645354A>C | CA359707355 | HCN1 | c.680T>G (p.Ile227Ser) | |
| 5 | g.45645354A>G | CA359707356 | HCN1 | c.680T>C (p.Ile227Thr) | ClinVar dbSNP |
| 5 | g.45645354A>T | CA359707357 | HCN1 | c.680T>A (p.Ile227Asn) | |
| 5 | g.45645355T>A | CA359707358 | HCN1 | c.679A>T (p.Ile227Phe) | |
| 5 | g.45645355T>C | CA359707359 | HCN1 | c.679A>G (p.Ile227Val) | dbSNP gnomAD v2 |
| 5 | g.45645355T>G | CA359707360 | HCN1 | c.679A>C (p.Ile227Leu) | |
| 5 | g.45645355T= | CA1543790500 | HCN1 | c.679A= (p.Ile227=) | |
| 5 | g.45645356G>A | CA444401762 | HCN1 | c.678C>T (p.Phe226=) | |
| 5 | g.45645356G>C | CA3259424 | HCN1 | c.678C>G (p.Phe226Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.45645356G= | CA1543790505 | HCN1 | c.678C= (p.Phe226=) | |
| 5 | g.45645356G>T | CA359707361 | HCN1 | c.678C>A (p.Phe226Leu) | COSMIC |
| 5 | g.45645357A>C | CA359707362 | HCN1 | c.677T>G (p.Phe226Cys) | |
| 5 | g.45645357A>G | CA359707363 | HCN1 | c.677T>C (p.Phe226Ser) | |
| 5 | g.45645357A>T | CA359707364 | HCN1 | c.677T>A (p.Phe226Tyr) | |
| 5 | g.45645358A>C | CA359707365 | HCN1 | c.676T>G (p.Phe226Val) | |
| 5 | g.45645358A>G | CA359707366 | HCN1 | c.676T>C (p.Phe226Leu) | |
| 5 | g.45645358A>T | CA359707367 | HCN1 | c.676T>A (p.Phe226Ile) | |
| 5 | g.45645359G>A | CA444401764 | HCN1 | c.675C>T (p.Asp225=) | |
| 5 | g.45645359G>C | CA359707368 | HCN1 | c.675C>G (p.Asp225Glu) | |
| 5 | g.45645359G>T | CA359707369 | HCN1 | c.675C>A (p.Asp225Glu) | |
| 5 | g.45645360T>A | CA359707370 | HCN1 | c.674A>T (p.Asp225Val) | |
| 5 | g.45645360T>C | CA359707371 | HCN1 | c.674A>G (p.Asp225Gly) | |
| 5 | g.45645360T>G | CA359707372 | HCN1 | c.674A>C (p.Asp225Ala) | |
| 5 | g.45645361C>A | CA359707373 | HCN1 | c.673G>T (p.Asp225Tyr) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 5 | g.45645361C= | CA1543790509 | HCN1 | c.673G= (p.Asp225=) | |
| 5 | g.45645361C>G | CA359707374 | HCN1 | c.673G>C (p.Asp225His) | |
| 5 | g.45645361C>T | CA359707375 | HCN1 | c.673G>A (p.Asp225Asn) | |
| 5 | g.45645362A= | CA1543790516 | HCN1 | c.672T= (p.Val224=) | |
| 5 | g.45645362A>C | CA444401769 | HCN1 | c.672T>G (p.Val224=) | |
| 5 | g.45645362A>G | CA444401770 | HCN1 | c.672T>C (p.Val224=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.45645362A>T | CA444401771 | HCN1 | c.672T>A (p.Val224=) | |
| 5 | g.45645363A>C | CA359707376 | HCN1 | c.671T>G (p.Val224Gly) | |
| 5 | g.45645363A>G | CA359707377 | HCN1 | c.671T>C (p.Val224Ala) | |
| 5 | g.45645363A>T | CA359707378 | HCN1 | c.671T>A (p.Val224Asp) | |
| 5 | g.45645364C>A | CA359707379 | HCN1 | c.670G>T (p.Val224Phe) | ClinVar |
| 5 | g.45645364C>G | CA359707380 | HCN1 | c.670G>C (p.Val224Leu) | |
| 5 | g.45645364C>T | CA359707381 | HCN1 | c.670G>A (p.Val224Ile) | |
| 5 | g.45645365C>A | CA444401776 | HCN1 | c.669G>T (p.Val223=) | |
| 5 | g.45645365C>G | CA444401773 | HCN1 | c.669G>C (p.Val223=) | |
| 5 | g.45645365C>T | CA444401775 | HCN1 | c.669G>A (p.Val223=) | |
| 5 | g.45645366A>C | CA359707382 | HCN1 | c.668T>G (p.Val223Gly) | |
| 5 | g.45645366A>G | CA359707384 | HCN1 | c.668T>C (p.Val223Ala) | |
| 5 | g.45645366A>T | CA359707383 | HCN1 | c.668T>A (p.Val223Glu) | dbSNP |
| 5 | g.45645367C>A | CA359707385 | HCN1 | c.667G>T (p.Val223Leu) | COSMIC |
| 5 | g.45645367C>G | CA359707386 | HCN1 | c.667G>C (p.Val223Leu) | |
| 5 | g.45645367C>T | CA359707387 | HCN1 | c.667G>A (p.Val223Met) | |
| 5 | g.45645368A>C | CA359707388 | HCN1 | c.666T>G (p.Phe222Leu) | |
| 5 | g.45645368A>G | CA444401781 | HCN1 | c.666T>C (p.Phe222=) | |
| 5 | g.45645368A>T | CA359707389 | HCN1 | c.666T>A (p.Phe222Leu) | |
| 5 | g.45645369A>C | CA359707392 | HCN1 | c.665T>G (p.Phe222Cys) | |
| 5 | g.45645369A>G | CA359707391 | HCN1 | c.665T>C (p.Phe222Ser) | |
| 5 | g.45645369A>T | CA359707390 | HCN1 | c.665T>A (p.Phe222Tyr) | |
| 5 | g.45645370A>C | CA359707393 | HCN1 | c.664T>G (p.Phe222Val) | |
| 5 | g.45645370A>G | CA359707394 | HCN1 | c.664T>C (p.Phe222Leu) | |
| 5 | g.45645370A>T | CA359707395 | HCN1 | c.664T>A (p.Phe222Ile) | |
| 5 | g.45645371C>A | CA359707396 | HCN1 | c.663G>T (p.Trp221Cys) | |
| 5 | g.45645371C>G | CA359707397 | HCN1 | c.663G>C (p.Trp221Cys) | |
| 5 | g.45645371C>T | CA359707398 | HCN1 | c.663G>A (p.Trp221Ter) | |
| 5 | g.45645372C>A | CA359707401 | HCN1 | c.662G>T (p.Trp221Leu) | ClinVar dbSNP COSMIC |
| 5 | g.45645372C>G | CA359707399 | HCN1 | c.662G>C (p.Trp221Ser) | |
| 5 | g.45645372C>T | CA359707400 | HCN1 | c.662G>A (p.Trp221Ter) | COSMIC |
| 5 | g.45645373_45645374insAACACACCCAACACA | CA2766121198 | HCN1 | c.662_663insTGTTGGGTGTGTTTG (p.Ser220_Trp221insCysValGlyCysVal) | |
| 5 | g.45645373A= | CA1543790521 | HCN1 | c.661T= (p.Trp221=) | |
| 5 | g.45645373A>C | CA359707402 | HCN1 | c.661T>G (p.Trp221Gly) | |
| 5 | g.45645373A>G | CA359707403 | HCN1 | c.661T>C (p.Trp221Arg) | ClinVar dbSNP |
| 5 | g.45645373A>T | CA359707404 | HCN1 | c.661T>A (p.Trp221Arg) | |
| 5 | g.45645374G>A | CA444401790 | HCN1 | c.660C>T (p.Ser220=) | ClinVar dbSNP |
| 5 | g.45645374G>C | CA359707405 | HCN1 | c.660C>G (p.Ser220Arg) | |
| 5 | g.45645374G= | CA1543790527 | HCN1 | c.660C= (p.Ser220=) | |
| 5 | g.45645374G>T | CA359707406 | HCN1 | c.660C>A (p.Ser220Arg) | |
| 5 | g.45645375C>A | CA359707407 | HCN1 | c.659G>T (p.Ser220Ile) | COSMIC |
| 5 | g.45645375C>G | CA359707408 | HCN1 | c.659G>C (p.Ser220Thr) | |
| 5 | g.45645375C>T | CA359707409 | HCN1 | c.659G>A (p.Ser220Asn) | |
| 5 | g.45645376T>A | CA359707410 | HCN1 | c.658A>T (p.Ser220Cys) | |
| 5 | g.45645376T>C | CA359707411 | HCN1 | c.658A>G (p.Ser220Gly) | dbSNP gnomAD v3 gnomAD v4 |
| 5 | g.45645376T>G | CA359707412 | HCN1 | c.658A>C (p.Ser220Arg) | |
| 5 | g.45645376T= | CA1543790536 | HCN1 | c.658A= (p.Ser220=) | |
| 5 | g.45645377T>A | CA359707413 | HCN1 | c.657A>T (p.Lys219Asn) | |
| 5 | g.45645377T>C | CA444401794 | HCN1 | c.657A>G (p.Lys219=) | |
| 5 | g.45645377T>G | CA359707414 | HCN1 | c.657A>C (p.Lys219Asn) | |
| 5 | g.45645378T>A | CA359707415 | HCN1 | c.656A>T (p.Lys219Ile) | |
| 5 | g.45645378T>C | CA359707417 | HCN1 | c.656A>G (p.Lys219Arg) | |
| 5 | g.45645378T>G | CA359707416 | HCN1 | c.656A>C (p.Lys219Thr) | |
| 5 | g.45645379T>A | CA359707418 | HCN1 | c.655A>T (p.Lys219Ter) | |
| 5 | g.45645379T>C | CA359707419 | HCN1 | c.655A>G (p.Lys219Glu) | |
| 5 | g.45645379T>G | CA359707420 | HCN1 | c.655A>C (p.Lys219Gln) | |
| 5 | g.45645380T>A | CA359707421 | HCN1 | c.654A>T (p.Leu218Phe) | |
| 5 | g.45645380T>C | CA444401798 | HCN1 | c.654A>G (p.Leu218=) | ClinVar dbSNP gnomAD v4 |
| 5 | g.45645380T>G | CA359707422 | HCN1 | c.654A>C (p.Leu218Phe) | |
| 5 | g.45645380T= | CA1543790540 | HCN1 | c.654A= (p.Leu218=) | |
| 5 | g.45645381A= | CA1543790546 | HCN1 | c.653T= (p.Leu218=) | |
| 5 | g.45645381A>C | CA359707423 | HCN1 | c.653T>G (p.Leu218Ter) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.45645381A>G | CA359707424 | HCN1 | c.653T>C (p.Leu218Ser) | |
| 5 | g.45645381A>T | CA359707425 | HCN1 | c.653T>A (p.Leu218Ter) | |
| 5 | g.45645382A>C | CA359707426 | HCN1 | c.652T>G (p.Leu218Val) | |
| 5 | g.45645382A>G | CA444401800 | HCN1 | c.652T>C (p.Leu218=) | |
| 5 | g.45645382A>T | CA359707427 | HCN1 | c.652T>A (p.Leu218Ile) | |
| 5 | g.45645383A= | CA1543790549 | HCN1 | c.651T= (p.Tyr217=) | |
| 5 | g.45645383A>C | CA359707428 | HCN1 | c.651T>G (p.Tyr217Ter) | |
| 5 | g.45645383A>G | CA444401801 | HCN1 | c.651T>C (p.Tyr217=) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.45645383A>T | CA359707429 | HCN1 | c.651T>A (p.Tyr217Ter) | |
| 5 | g.45645384T>A | CA359707432 | HCN1 | c.650A>T (p.Tyr217Phe) | |
| 5 | g.45645384T>C | CA359707430 | HCN1 | c.650A>G (p.Tyr217Cys) | |
| 5 | g.45645384T>G | CA359707431 | HCN1 | c.650A>C (p.Tyr217Ser) | |
| 5 | g.45645385A>C | CA359707433 | HCN1 | c.649T>G (p.Tyr217Asp) | |
| 5 | g.45645385A>G | CA359707434 | HCN1 | c.649T>C (p.Tyr217His) | |
| 5 | g.45645385A>T | CA359707435 | HCN1 | c.649T>A (p.Tyr217Asn) | |
| 5 | g.45645386A>C | CA359707436 | HCN1 | c.648T>G (p.Asn216Lys) | |
| 5 | g.45645386A>G | CA444401805 | HCN1 | c.648T>C (p.Asn216=) | |
| 5 | g.45645386A>T | CA359707437 | HCN1 | c.648T>A (p.Asn216Lys) | |
| 5 | g.45645387T>A | CA359707438 | HCN1 | c.647A>T (p.Asn216Ile) | |
| 5 | g.45645387T>C | CA359707439 | HCN1 | c.647A>G (p.Asn216Ser) | gnomAD v4 |
| 5 | g.45645387T>G | CA359707440 | HCN1 | c.647A>C (p.Asn216Thr) | |
| 5 | g.45645388T>A | CA359707441 | HCN1 | c.646A>T (p.Asn216Tyr) | |
| 5 | g.45645388T>C | CA359707442 | HCN1 | c.646A>G (p.Asn216Asp) | |
| 5 | g.45645388T>G | CA359707443 | HCN1 | c.646A>C (p.Asn216His) | |
| 5 | g.45645389C>A | CA359707446 | HCN1 | c.645G>T (p.Met215Ile) | dbSNP gnomAD v2 COSMIC |
| 5 | g.45645389C= | CA1543790554 | HCN1 | c.645G= (p.Met215=) | |
| 5 | g.45645389C>G | CA359707444 | HCN1 | c.645G>C (p.Met215Ile) | |
| 5 | g.45645389C>T | CA359707445 | HCN1 | c.645G>A (p.Met215Ile) | COSMIC |
| 5 | g.45645390A>C | CA359707447 | HCN1 | c.644T>G (p.Met215Arg) | gnomAD v4 |
| 5 | g.45645390A>G | CA359707449 | HCN1 | c.644T>C (p.Met215Thr) | gnomAD v3 gnomAD v4 |
| 5 | g.45645390A>T | CA359707448 | HCN1 | c.644T>A (p.Met215Lys) | |
| 5 | g.45645391T>A | CA359707450 | HCN1 | c.643A>T (p.Met215Leu) | COSMIC |
| 5 | g.45645391T>C | CA118324608 | HCN1 | c.643A>G (p.Met215Val) | ClinVar dbSNP gnomAD v4 COSMIC |
| 5 | g.45645391T>G | CA359707451 | HCN1 | c.643A>C (p.Met215Leu) | |
| 5 | g.45645391T= | CA1543790557 | HCN1 | c.643A= (p.Met215=) | |
| 5 | g.45645392C>A | CA359707452 | HCN1 | c.642G>T (p.Lys214Asn) | COSMIC |
| 5 | g.45645392C>G | CA359707453 | HCN1 | c.642G>C (p.Lys214Asn) | |
| 5 | g.45645392C>T | CA444401806 | HCN1 | c.642G>A (p.Lys214=) | |
| 5 | g.45645393T>A | CA359707454 | HCN1 | c.641A>T (p.Lys214Met) | |
| 5 | g.45645393T>C | CA118324609 | HCN1 | c.641A>G (p.Lys214Arg) | dbSNP |
| 5 | g.45645393T>G | CA359707455 | HCN1 | c.641A>C (p.Lys214Thr) | |
| 5 | g.45645393T= | CA1543790559 | HCN1 | c.641A= (p.Lys214=) | |
| 5 | g.45645394T>A | CA359707456 | HCN1 | c.640A>T (p.Lys214Ter) | |
| 5 | g.45645394T>C | CA359707457 | HCN1 | c.640A>G (p.Lys214Glu) | |
| 5 | g.45645394T>G | CA359707458 | HCN1 | c.640A>C (p.Lys214Gln) | |
| 5 | g.45645395G>A | CA444401807 | HCN1 | c.639C>T (p.Ile213=) | |
| 5 | g.45645395G>C | CA359707459 | HCN1 | c.639C>G (p.Ile213Met) | |
| 5 | g.45645395G= | CA1543790564 | HCN1 | c.639C= (p.Ile213=) | |
| 5 | g.45645395G>T | CA3259425 | HCN1 | c.639C>A (p.Ile213=) | ClinVar dbSNP ExAC gnomAD v2 |
| 5 | g.45645396A>C | CA359707462 | HCN1 | c.638T>G (p.Ile213Ser) | |
| 5 | g.45645396A>G | CA359707461 | HCN1 | c.638T>C (p.Ile213Thr) | |
| 5 | g.45645396A>T | CA359707460 | HCN1 | c.638T>A (p.Ile213Asn) | |
| 5 | g.45645397T>A | CA359707463 | HCN1 | c.637A>T (p.Ile213Phe) | COSMIC |
| 5 | g.45645397T>C | CA359707464 | HCN1 | c.637A>G (p.Ile213Val) | |
| 5 | g.45645397T>G | CA359707465 | HCN1 | c.637A>C (p.Ile213Leu) | |
| 5 | g.45645398C>A | CA3259426 | HCN1 | c.636G>T (p.Val212=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.45645398C= | CA1543790569 | HCN1 | c.636G= (p.Val212=) | |
| 5 | g.45645398C>G | CA444401808 | HCN1 | c.636G>C (p.Val212=) | |
| 5 | g.45645398C>T | CA3259427 | HCN1 | c.636G>A (p.Val212=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |