| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.45645261C>A | CA359707145 | HCN1 | c.773G>T (p.Arg258Met) n.1G>T | |
| 5 | g.45645261C>G | CA359707146 | HCN1 | c.773G>C (p.Arg258Thr) n.1G>C | |
| 5 | g.45645261C>T | CA359707147 | HCN1 | c.773G>A (p.Arg258Lys) n.1G>A | |
| 5 | g.45645262T>A | CA359707148 | HCN1 | c.772A>T (p.Arg258Trp) | |
| 5 | g.45645262T>C | CA359707149 | HCN1 | c.772A>G (p.Arg258Gly) | |
| 5 | g.45645262T>G | CA444401594 | HCN1 | c.772A>C (p.Arg258=) | gnomAD v4 |
| 5 | g.45645263C>A | CA444401596 | HCN1 | c.771G>T (p.Val257=) | |
| 5 | g.45645263C>G | CA444401599 | HCN1 | c.771G>C (p.Val257=) | |
| 5 | g.45645263C>T | CA444401601 | HCN1 | c.771G>A (p.Val257=) | |
| 5 | g.45645264A>C | CA359707150 | HCN1 | c.770T>G (p.Val257Gly) | |
| 5 | g.45645264A>G | CA359707152 | HCN1 | c.770T>C (p.Val257Ala) | |
| 5 | g.45645264A>T | CA359707151 | HCN1 | c.770T>A (p.Val257Glu) | |
| 5 | g.45645265C>A | CA359707153 | HCN1 | c.769G>T (p.Val257Leu) | |
| 5 | g.45645265C>G | CA359707154 | HCN1 | c.769G>C (p.Val257Leu) | COSMIC |
| 5 | g.45645265C>T | CA359707155 | HCN1 | c.769G>A (p.Val257Met) | |
| 5 | g.45645266A>C | CA359707156 | HCN1 | c.768T>G (p.Ile256Met) | |
| 5 | g.45645266A>G | CA444401604 | HCN1 | c.768T>C (p.Ile256=) | |
| 5 | g.45645266A>T | CA444401607 | HCN1 | c.768T>A (p.Ile256=) | |
| 5 | g.45645267A>C | CA359707157 | HCN1 | c.767T>G (p.Ile256Ser) | |
| 5 | g.45645267A>G | CA359707158 | HCN1 | c.767T>C (p.Ile256Thr) | ClinVar |
| 5 | g.45645267A>T | CA359707159 | HCN1 | c.767T>A (p.Ile256Asn) | |
| 5 | g.45645268T>A | CA359707160 | HCN1 | c.766A>T (p.Ile256Phe) | |
| 5 | g.45645268T>C | CA359707161 | HCN1 | c.766A>G (p.Ile256Val) | |
| 5 | g.45645268T>G | CA359707162 | HCN1 | c.766A>C (p.Ile256Leu) | |
| 5 | g.45645269G>A | CA444401612 | HCN1 | c.765C>T (p.Arg255=) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.45645269G>C | CA444401614 | HCN1 | c.765C>G (p.Arg255=) | |
| 5 | g.45645269G= | CA1543790339 | HCN1 | c.765C= (p.Arg255=) | |
| 5 | g.45645269G>T | CA444401616 | HCN1 | c.765C>A (p.Arg255=) | |
| 5 | g.45645270C>A | CA359707165 | HCN1 | c.764G>T (p.Arg255Leu) | |
| 5 | g.45645270C= | CA1543790342 | HCN1 | c.764G= (p.Arg255=) | |
| 5 | g.45645270C>G | CA359707164 | HCN1 | c.764G>C (p.Arg255Pro) | |
| 5 | g.45645270C>T | CA359707163 | HCN1 | c.764G>A (p.Arg255His) | dbSNP gnomAD v4 |
| 5 | g.45645271G>A | CA359707166 | HCN1 | c.763C>T (p.Arg255Cys) | ClinVar dbSNP COSMIC |
| 5 | g.45645271G>C | CA359707167 | HCN1 | c.763C>G (p.Arg255Gly) | |
| 5 | g.45645271G= | CA1543790348 | HCN1 | c.763C= (p.Arg255=) | |
| 5 | g.45645271G>T | CA359707168 | HCN1 | c.763C>A (p.Arg255Ser) | |
| 5 | g.45645272A>C | CA444401620 | HCN1 | c.762T>G (p.Leu254=) | |
| 5 | g.45645272A>G | CA444401622 | HCN1 | c.762T>C (p.Leu254=) | |
| 5 | g.45645272A>T | CA444401624 | HCN1 | c.762T>A (p.Leu254=) | |
| 5 | g.45645273A>C | CA359707169 | HCN1 | c.761T>G (p.Leu254Arg) | COSMIC |
| 5 | g.45645273A>G | CA359707170 | HCN1 | c.761T>C (p.Leu254Pro) | |
| 5 | g.45645273A>T | CA359707171 | HCN1 | c.761T>A (p.Leu254His) | |
| 5 | g.45645274G>A | CA359707172 | HCN1 | c.760C>T (p.Leu254Phe) | |
| 5 | g.45645274G>C | CA359707173 | HCN1 | c.760C>G (p.Leu254Val) | COSMIC |
| 5 | g.45645274G>T | CA359707174 | HCN1 | c.760C>A (p.Leu254Ile) | |
| 5 | g.45645275T>A | CA444401626 | HCN1 | c.759A>T (p.Ala253=) | |
| 5 | g.45645275T>C | CA444401627 | HCN1 | c.759A>G (p.Ala253=) | |
| 5 | g.45645275T>G | CA444401628 | HCN1 | c.759A>C (p.Ala253=) | |
| 5 | g.45645276G>A | CA359707175 | HCN1 | c.758C>T (p.Ala253Val) | |
| 5 | g.45645276G>C | CA359707176 | HCN1 | c.758C>G (p.Ala253Gly) | |
| 5 | g.45645276G>T | CA359707177 | HCN1 | c.758C>A (p.Ala253Glu) | |
| 5 | g.45645277C>A | CA359707180 | HCN1 | c.757G>T (p.Ala253Ser) | |
| 5 | g.45645277C>G | CA359707179 | HCN1 | c.757G>C (p.Ala253Pro) | |
| 5 | g.45645277C>T | CA359707178 | HCN1 | c.757G>A (p.Ala253Thr) | |
| 5 | g.45645278C>A | CA359707181 | HCN1 | c.756G>T (p.Arg252Ser) | |
| 5 | g.45645278C= | CA1543790352 | HCN1 | c.756G= (p.Arg252=) | |
| 5 | g.45645278C>G | CA359707182 | HCN1 | c.756G>C (p.Arg252Ser) | |
| 5 | g.45645278C>T | CA444401630 | HCN1 | c.756G>A (p.Arg252=) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.45645279C>A | CA359707183 | HCN1 | c.755G>T (p.Arg252Met) | |
| 5 | g.45645279C>G | CA359707184 | HCN1 | c.755G>C (p.Arg252Thr) | |
| 5 | g.45645279C>T | CA359707185 | HCN1 | c.755G>A (p.Arg252Lys) | |
| 5 | g.45645280T>A | CA3259419 | HCN1 | c.754A>T (p.Arg252Trp) | dbSNP ExAC gnomAD v2 |
| 5 | g.45645280T>C | CA359707186 | HCN1 | c.754A>G (p.Arg252Gly) | |
| 5 | g.45645280T>G | CA444401634 | HCN1 | c.754A>C (p.Arg252=) | |
| 5 | g.45645280T= | CA1543790356 | HCN1 | c.754A= (p.Arg252=) | |
| 5 | g.45645281G>A | CA444401637 | HCN1 | c.753C>T (p.Ala251=) | |
| 5 | g.45645281G>C | CA444401636 | HCN1 | c.753C>G (p.Ala251=) | |
| 5 | g.45645281G>T | CA444401635 | HCN1 | c.753C>A (p.Ala251=) | |
| 5 | g.45645282G>A | CA359707187 | HCN1 | c.752C>T (p.Ala251Val) | |
| 5 | g.45645282G>C | CA359707188 | HCN1 | c.752C>G (p.Ala251Gly) | |
| 5 | g.45645282G>T | CA359707189 | HCN1 | c.752C>A (p.Ala251Asp) | |
| 5 | g.45645283C>A | CA359707190 | HCN1 | c.751G>T (p.Ala251Ser) | COSMIC |
| 5 | g.45645283C>G | CA359707191 | HCN1 | c.751G>C (p.Ala251Pro) | |
| 5 | g.45645283C>T | CA359707192 | HCN1 | c.751G>A (p.Ala251Thr) | |
| 5 | g.45645284T>A | CA444401639 | HCN1 | c.750A>T (p.Thr250=) | |
| 5 | g.45645284T>C | CA444401640 | HCN1 | c.750A>G (p.Thr250=) | dbSNP gnomAD v4 |
| 5 | g.45645284T>G | CA444401641 | HCN1 | c.750A>C (p.Thr250=) | |
| 5 | g.45645284T= | CA1543790359 | HCN1 | c.750A= (p.Thr250=) | |
| 5 | g.45645285G>A | CA359707194 | HCN1 | c.749C>T (p.Thr250Ile) | |
| 5 | g.45645285G>C | CA359707195 | HCN1 | c.749C>G (p.Thr250Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.45645285G= | CA1543790366 | HCN1 | c.749C= (p.Thr250=) | |
| 5 | g.45645285G>T | CA359707193 | HCN1 | c.749C>A (p.Thr250Lys) | |
| 5 | g.45645286T>A | CA359707198 | HCN1 | c.748A>T (p.Thr250Ser) | |
| 5 | g.45645286T>C | CA359707196 | HCN1 | c.748A>G (p.Thr250Ala) | |
| 5 | g.45645286T>G | CA359707197 | HCN1 | c.748A>C (p.Thr250Pro) | |
| 5 | g.45645287C>A | CA359707199 | HCN1 | c.747G>T (p.Lys249Asn) | |
| 5 | g.45645287C= | CA1543790370 | HCN1 | c.747G= (p.Lys249=) | |
| 5 | g.45645287C>G | CA359707200 | HCN1 | c.747G>C (p.Lys249Asn) | ClinVar |
| 5 | g.45645287C>T | CA3259420 | HCN1 | c.747G>A (p.Lys249=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.45645288T>A | CA359707201 | HCN1 | c.746A>T (p.Lys249Met) | |
| 5 | g.45645288T>C | CA359707202 | HCN1 | c.746A>G (p.Lys249Arg) | gnomAD v4 |
| 5 | g.45645288T>G | CA359707203 | HCN1 | c.746A>C (p.Lys249Thr) | |
| 5 | g.45645289T>A | CA359707204 | HCN1 | c.745A>T (p.Lys249Ter) | |
| 5 | g.45645289T>C | CA359707205 | HCN1 | c.745A>G (p.Lys249Glu) | |
| 5 | g.45645289T>G | CA359707206 | HCN1 | c.745A>C (p.Lys249Gln) | |
| 5 | g.45645290G>A | CA444401645 | HCN1 | c.744C>T (p.Tyr248=) | |
| 5 | g.45645290G>C | CA359707207 | HCN1 | c.744C>G (p.Tyr248Ter) | |
| 5 | g.45645290G>T | CA359707208 | HCN1 | c.744C>A (p.Tyr248Ter) | COSMIC |
| 5 | g.45645291T>A | CA359707211 | HCN1 | c.743A>T (p.Tyr248Phe) | COSMIC |
| 5 | g.45645291T>C | CA359707210 | HCN1 | c.743A>G (p.Tyr248Cys) | dbSNP |
| 5 | g.45645291T>G | CA359707209 | HCN1 | c.743A>C (p.Tyr248Ser) | |
| 5 | g.45645291T= | CA1543790377 | HCN1 | c.743A= (p.Tyr248=) | |
| 5 | g.45645292A>C | CA359707212 | HCN1 | c.742T>G (p.Tyr248Asp) | |
| 5 | g.45645292A>G | CA359707213 | HCN1 | c.742T>C (p.Tyr248His) | |
| 5 | g.45645292A>T | CA359707214 | HCN1 | c.742T>A (p.Tyr248Asn) | |
| 5 | g.45645293A>C | CA444401650 | HCN1 | c.741T>G (p.Val247=) | |
| 5 | g.45645293A>G | CA444401652 | HCN1 | c.741T>C (p.Val247=) | |
| 5 | g.45645293A>T | CA444401651 | HCN1 | c.741T>A (p.Val247=) | |
| 5 | g.45645294A>C | CA359707215 | HCN1 | c.740T>G (p.Val247Gly) | |
| 5 | g.45645294A>G | CA359707216 | HCN1 | c.740T>C (p.Val247Ala) | |
| 5 | g.45645294A>T | CA359707217 | HCN1 | c.740T>A (p.Val247Asp) | |
| 5 | g.45645295C>A | CA359707218 | HCN1 | c.739G>T (p.Val247Phe) | |
| 5 | g.45645295C>G | CA359707219 | HCN1 | c.739G>C (p.Val247Leu) | |
| 5 | g.45645295C>T | CA359707220 | HCN1 | c.739G>A (p.Val247Ile) | |
| 5 | g.45645296T>A | CA359707221 | HCN1 | c.738A>T (p.Glu246Asp) | |
| 5 | g.45645296T>C | CA444401658 | HCN1 | c.738A>G (p.Glu246=) | dbSNP |
| 5 | g.45645296T>G | CA359707222 | HCN1 | c.738A>C (p.Glu246Asp) | |
| 5 | g.45645297T>A | CA359707223 | HCN1 | c.737A>T (p.Glu246Val) | |
| 5 | g.45645297T>C | CA359707224 | HCN1 | c.737A>G (p.Glu246Gly) | |
| 5 | g.45645297T>G | CA359707225 | HCN1 | c.737A>C (p.Glu246Ala) | ClinVar dbSNP |
| 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) |