UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.73343634C>A | CA491479807 | HCN4 | c.960G>T (p.Val320=) | |
| 15 | g.73343634C= | CA2187180038 | HCN4 | c.960G= (p.Val320=) | |
| 15 | g.73343634C>G | CA491479806 | HCN4 | c.960G>C (p.Val320=) | |
| 15 | g.73343634C>T | CA491479805 | HCN4 | c.960G>A (p.Val320=) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73343635A>C | CA393095164 | HCN4 | c.959T>G (p.Val320Gly) | |
| 15 | g.73343635A>G | CA393095165 | HCN4 | c.959T>C (p.Val320Ala) | gnomAD v4 |
| 15 | g.73343635A>T | CA393095166 | HCN4 | c.959T>A (p.Val320Glu) | |
| 15 | g.73343636C>A | CA393095167 | HCN4 | c.958G>T (p.Val320Leu) | |
| 15 | g.73343636C>G | CA393095168 | HCN4 | c.958G>C (p.Val320Leu) | |
| 15 | g.73343636C>T | CA393095169 | HCN4 | c.958G>A (p.Val320Met) | COSMIC |
| 15 | g.73343637C>A | CA491479808 | HCN4 | c.957G>T (p.Val319=) | |
| 15 | g.73343637C>G | CA491479810 | HCN4 | c.957G>C (p.Val319=) | gnomAD v4 |
| 15 | g.73343637C>T | CA491479809 | HCN4 | c.957G>A (p.Val319=) | ClinVar |
| 15 | g.73343638A>C | CA393095172 | HCN4 | c.956T>G (p.Val319Gly) | |
| 15 | g.73343638A>G | CA393095170 | HCN4 | c.956T>C (p.Val319Ala) | gnomAD v4 |
| 15 | g.73343638A>T | CA393095171 | HCN4 | c.956T>A (p.Val319Glu) | |
| 15 | g.73343639C>A | CA393095173 | HCN4 | c.955G>T (p.Val319Leu) | gnomAD v4 |
| 15 | g.73343639C= | CA2187180045 | HCN4 | c.955G= (p.Val319=) | |
| 15 | g.73343639C>G | CA393095174 | HCN4 | c.955G>C (p.Val319Leu) | gnomAD v4 |
| 15 | g.73343639C>T | CA7649393 | HCN4 | c.955G>A (p.Val319Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73343640G>A | CA7649394 | HCN4 | c.954C>T (p.Ile318=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73343640G>C | CA7649395 | HCN4 | c.954C>G (p.Ile318Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73343640G= | CA2187180049 | HCN4 | c.954C= (p.Ile318=) | |
| 15 | g.73343640G>T | CA491479811 | HCN4 | c.954C>A (p.Ile318=) | |
| 15 | g.73343641A>C | CA393095175 | HCN4 | c.953T>G (p.Ile318Ser) | |
| 15 | g.73343641A>G | CA393095176 | HCN4 | c.953T>C (p.Ile318Thr) | |
| 15 | g.73343641A>T | CA393095177 | HCN4 | c.953T>A (p.Ile318Asn) | |
| 15 | g.73343642T>A | CA393095178 | HCN4 | c.952A>T (p.Ile318Phe) | |
| 15 | g.73343642T>C | CA7649396 | HCN4 | c.952A>G (p.Ile318Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73343642T>G | CA393095179 | HCN4 | c.952A>C (p.Ile318Leu) | |
| 15 | g.73343642T= | CA2187180052 | HCN4 | c.952A= (p.Ile318=) | |
| 15 | g.73343643C>A | CA491479812 | HCN4 | c.951G>T (p.Gly317=) | |
| 15 | g.73343643C>G | CA491479813 | HCN4 | c.951G>C (p.Gly317=) | |
| 15 | g.73343643C>T | CA491479814 | HCN4 | c.951G>A (p.Gly317=) | |
| 15 | g.73343644C>A | CA393095182 | HCN4 | c.950G>T (p.Gly317Val) | |
| 15 | g.73343644C>G | CA393095181 | HCN4 | c.950G>C (p.Gly317Ala) | |
| 15 | g.73343644C>T | CA393095180 | HCN4 | c.950G>A (p.Gly317Glu) | |
| 15 | g.73343645C>A | CA393095183 | HCN4 | c.949G>T (p.Gly317Trp) | |
| 15 | g.73343645C>G | CA393095184 | HCN4 | c.949G>C (p.Gly317Arg) | |
| 15 | g.73343645C>T | CA393095185 | HCN4 | c.949G>A (p.Gly317Arg) | COSMIC |
| 15 | g.73343646T>A | CA491479815 | HCN4 | c.948A>T (p.Thr316=) | |
| 15 | g.73343646T>C | CA491479816 | HCN4 | c.948A>G (p.Thr316=) | |
| 15 | g.73343646T>G | CA491479817 | HCN4 | c.948A>C (p.Thr316=) | |
| 15 | g.73343647G>A | CA393095186 | HCN4 | c.947C>T (p.Thr316Ile) | |
| 15 | g.73343647G>C | CA393095187 | HCN4 | c.947C>G (p.Thr316Arg) | |
| 15 | g.73343647G>T | CA393095188 | HCN4 | c.947C>A (p.Thr316Lys) | |
| 15 | g.73343648T>A | CA393095189 | HCN4 | c.946A>T (p.Thr316Ser) | ClinVar dbSNP |
| 15 | g.73343648T>C | CA393095190 | HCN4 | c.946A>G (p.Thr316Ala) | |
| 15 | g.73343648T>G | CA393095191 | HCN4 | c.946A>C (p.Thr316Pro) | |
| 15 | g.73343648T= | CA2187180055 | HCN4 | c.946A= (p.Thr316=) | |
| 15 | g.73343649G>A | CA491479818 | HCN4 | c.945C>T (p.Arg315=) | |
| 15 | g.73343649G>C | CA491479819 | HCN4 | c.945C>G (p.Arg315=) | |
| 15 | g.73343649G>T | CA491479820 | HCN4 | c.945C>A (p.Arg315=) | |
| 15 | g.73343650C>A | CA393095192 | HCN4 | c.944G>T (p.Arg315Leu) | |
| 15 | g.73343650C= | CA2187180059 | HCN4 | c.944G= (p.Arg315=) | |
| 15 | g.73343650C>G | CA393095193 | HCN4 | c.944G>C (p.Arg315Pro) | gnomAD v4 |
| 15 | g.73343650C>T | CA7649397 | HCN4 | c.944G>A (p.Arg315His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73343651G>A | CA393095196 | HCN4 | c.943C>T (p.Arg315Cys) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73343651G>C | CA393095195 | HCN4 | c.943C>G (p.Arg315Gly) | |
| 15 | g.73343651G= | CA2187180062 | HCN4 | c.943C= (p.Arg315=) | |
| 15 | g.73343651G>T | CA393095194 | HCN4 | c.943C>A (p.Arg315Ser) | |
| 15 | g.73343652G>A | CA491479821 | HCN4 | c.942C>T (p.Phe314=) | |
| 15 | g.73343652G>C | CA393095197 | HCN4 | c.942C>G (p.Phe314Leu) | |
| 15 | g.73343652G>T | CA393095198 | HCN4 | c.942C>A (p.Phe314Leu) | |
| 15 | g.73343653A>C | CA393095199 | HCN4 | c.941T>G (p.Phe314Cys) | |
| 15 | g.73343653A>G | CA393095200 | HCN4 | c.941T>C (p.Phe314Ser) | |
| 15 | g.73343653A>T | CA393095201 | HCN4 | c.941T>A (p.Phe314Tyr) | |
| 15 | g.73343654A>C | CA393095202 | HCN4 | c.940T>G (p.Phe314Val) | |
| 15 | g.73343654A>G | CA393095203 | HCN4 | c.940T>C (p.Phe314Leu) | |
| 15 | g.73343654A>T | CA393095204 | HCN4 | c.940T>A (p.Phe314Ile) | |
| 15 | g.73343655G>A | CA491479822 | HCN4 | c.939C>T (p.Asn313=) | |
| 15 | g.73343655G>C | CA393095205 | HCN4 | c.939C>G (p.Asn313Lys) | |
| 15 | g.73343655G>T | CA393095206 | HCN4 | c.939C>A (p.Asn313Lys) | |
| 15 | g.73343656T>A | CA393095207 | HCN4 | c.938A>T (p.Asn313Ile) | |
| 15 | g.73343656T>C | CA393095208 | HCN4 | c.938A>G (p.Asn313Ser) | |
| 15 | g.73343656T>G | CA393095209 | HCN4 | c.938A>C (p.Asn313Thr) | |
| 15 | g.73343657T>A | CA393095211 | HCN4 | c.937A>T (p.Asn313Tyr) | |
| 15 | g.73343657T>C | CA393095212 | HCN4 | c.937A>G (p.Asn313Asp) | COSMIC |
| 15 | g.73343657T>G | CA393095210 | HCN4 | c.937A>C (p.Asn313His) | |
| 15 | g.73343658G>A | CA491479823 | HCN4 | c.936C>T (p.Leu312=) | |
| 15 | g.73343658G>C | CA491479825 | HCN4 | c.936C>G (p.Leu312=) | |
| 15 | g.73343658G>T | CA491479824 | HCN4 | c.936C>A (p.Leu312=) | |
| 15 | g.73343659A>C | CA393095215 | HCN4 | c.935T>G (p.Leu312Arg) | |
| 15 | g.73343659A>G | CA393095213 | HCN4 | c.935T>C (p.Leu312Pro) | |
| 15 | g.73343659A>T | CA393095214 | HCN4 | c.935T>A (p.Leu312His) | |
| 15 | g.73343660G>A | CA393095216 | HCN4 | c.934C>T (p.Leu312Phe) | dbSNP gnomAD v4 |
| 15 | g.73343660G>C | CA393095217 | HCN4 | c.934C>G (p.Leu312Val) | |
| 15 | g.73343660G= | CA2187180065 | HCN4 | c.934C= (p.Leu312=) | |
| 15 | g.73343660G>T | CA393095218 | HCN4 | c.934C>A (p.Leu312Ile) | |
| 15 | g.73343661G>A | CA491479826 | HCN4 | c.933C>T (p.Val311=) | ClinVar |
| 15 | g.73343661G>C | CA491479827 | HCN4 | c.933C>G (p.Val311=) | |
| 15 | g.73343661G>T | CA491479829 | HCN4 | c.933C>A (p.Val311=) | |
| 15 | g.73343662A>C | CA393095219 | HCN4 | c.932T>G (p.Val311Gly) | |
| 15 | g.73343662A>G | CA393095220 | HCN4 | c.932T>C (p.Val311Ala) | |
| 15 | g.73343662A>T | CA393095221 | HCN4 | c.932T>A (p.Val311Asp) | |
| 15 | g.73343663C>A | CA393095222 | HCN4 | c.931G>T (p.Val311Phe) | |
| 15 | g.73343663C>G | CA393095223 | HCN4 | c.931G>C (p.Val311Leu) | |
| 15 | g.73343663C>T | CA393095224 | HCN4 | c.931G>A (p.Val311Ile) | |
| 15 | g.73343664C>A | CA393095225 | HCN4 | c.930G>T (p.Leu310Phe) | gnomAD v4 |
| 15 | g.73343664C>G | CA393095226 | HCN4 | c.930G>C (p.Leu310Phe) | |
| 15 | g.73343664C>T | CA491479830 | HCN4 | c.930G>A (p.Leu310=) | |
| 15 | g.73343665A>C | CA393095227 | HCN4 | c.929T>G (p.Leu310Trp) | |
| 15 | g.73343665A>G | CA393095229 | HCN4 | c.929T>C (p.Leu310Ser) | COSMIC |
| 15 | g.73343665A>T | CA393095228 | HCN4 | c.929T>A (p.Leu310Ter) | |
| 15 | g.73343666A>C | CA393095230 | HCN4 | c.928T>G (p.Leu310Val) | |
| 15 | g.73343666A>G | CA491479832 | HCN4 | c.928T>C (p.Leu310=) | ClinVar |
| 15 | g.73343666A>T | CA393095231 | HCN4 | c.928T>A (p.Leu310Met) | |
| 15 | g.73343667G>A | CA491479833 | HCN4 | c.927C>T (p.Asp309=) | |
| 15 | g.73343667G>C | CA393095232 | HCN4 | c.927C>G (p.Asp309Glu) | ClinVar dbSNP |
| 15 | g.73343667G>T | CA393095233 | HCN4 | c.927C>A (p.Asp309Glu) | |
| 15 | g.73343668T>A | CA393095234 | HCN4 | c.926A>T (p.Asp309Val) | |
| 15 | g.73343668T>C | CA393095235 | HCN4 | c.926A>G (p.Asp309Gly) | |
| 15 | g.73343668T>G | CA393095236 | HCN4 | c.926A>C (p.Asp309Ala) | |
| 15 | g.73343669C>A | CA393095237 | HCN4 | c.925G>T (p.Asp309Tyr) | gnomAD v4 |
| 15 | g.73343669C>G | CA393095238 | HCN4 | c.925G>C (p.Asp309His) | |
| 15 | g.73343669C>T | CA393095239 | HCN4 | c.925G>A (p.Asp309Asn) | ClinVar gnomAD v4 COSMIC |
| 15 | g.73343670G>A | CA491479835 | HCN4 | c.924C>T (p.Ile308=) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73343670G>C | CA393095240 | HCN4 | c.924C>G (p.Ile308Met) | |
| 15 | g.73343670G= | CA2187180068 | HCN4 | c.924C= (p.Ile308=) | |
| 15 | g.73343670G>T | CA491479836 | HCN4 | c.924C>A (p.Ile308=) | |
| 15 | g.73343671A>C | CA393095242 | HCN4 | c.923T>G (p.Ile308Ser) | |
| 15 | g.73343671A>G | CA393095243 | HCN4 | c.923T>C (p.Ile308Thr) | |
| 15 | g.73343671A>T | CA393095241 | HCN4 | c.923T>A (p.Ile308Asn) | |
| 15 | g.73343672T>A | CA393095244 | HCN4 | c.922A>T (p.Ile308Phe) | |
| 15 | g.73343672T>C | CA393095245 | HCN4 | c.922A>G (p.Ile308Val) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73343672T>G | CA393095246 | HCN4 | c.922A>C (p.Ile308Leu) | |
| 15 | g.73343672T= | CA2187180070 | HCN4 | c.922A= (p.Ile308=) | |
| 15 | g.73343673G>A | CA491479842 | HCN4 | c.921C>T (p.Leu307=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73343673G>C | CA491479841 | HCN4 | c.921C>G (p.Leu307=) | gnomAD v4 |
| 15 | g.73343673G>T | CA491479840 | HCN4 | c.921C>A (p.Leu307=) | |
| 15 | g.73343674A>C | CA393095247 | HCN4 | c.920T>G (p.Leu307Arg) | |
| 15 | g.73343674A>G | CA393095248 | HCN4 | c.920T>C (p.Leu307Pro) | |
| 15 | g.73343674A>T | CA393095249 | HCN4 | c.920T>A (p.Leu307His) | |
| 15 | g.73343675G>A | CA393095250 | HCN4 | c.919C>T (p.Leu307Phe) | |
| 15 | g.73343675G>C | CA393095251 | HCN4 | c.919C>G (p.Leu307Val) | |
| 15 | g.73343675G>T | CA393095252 | HCN4 | c.919C>A (p.Leu307Ile) | |
| 15 | g.73343676G>A | CA491479847 | HCN4 | c.918C>T (p.Phe306=) | ClinVar |
| 15 | g.73343676G>C | CA393095253 | HCN4 | c.918C>G (p.Phe306Leu) | |
| 15 | g.73343676G>T | CA393095254 | HCN4 | c.918C>A (p.Phe306Leu) | |
| 15 | g.73343677A>C | CA393095255 | HCN4 | c.917T>G (p.Phe306Cys) | |
| 15 | g.73343677A>G | CA393095256 | HCN4 | c.917T>C (p.Phe306Ser) | |
| 15 | g.73343677A>T | CA393095257 | HCN4 | c.917T>A (p.Phe306Tyr) | COSMIC |
| 15 | g.73343678A>C | CA393095260 | HCN4 | c.916T>G (p.Phe306Val) | |
| 15 | g.73343678A>G | CA393095259 | HCN4 | c.916T>C (p.Phe306Leu) | |
| 15 | g.73343678A>T | CA393095258 | HCN4 | c.916T>A (p.Phe306Ile) | |
| 15 | g.73343679G>A | CA491479852 | HCN4 | c.915C>T (p.Phe305=) | dbSNP |
| 15 | g.73343679G>C | CA393095261 | HCN4 | c.915C>G (p.Phe305Leu) | |
| 15 | g.73343679G= | CA2187180072 | HCN4 | c.915C= (p.Phe305=) | |
| 15 | g.73343679G>T | CA393095262 | HCN4 | c.915C>A (p.Phe305Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73343680A>C | CA393095263 | HCN4 | c.914T>G (p.Phe305Cys) | |
| 15 | g.73343680A>G | CA393095264 | HCN4 | c.914T>C (p.Phe305Ser) | |
| 15 | g.73343680A>T | CA393095265 | HCN4 | c.914T>A (p.Phe305Tyr) | |
| 15 | g.73343681A= | CA2187180076 | HCN4 | c.913T= (p.Phe305=) | |
| 15 | g.73343681A>C | CA393095266 | HCN4 | c.913T>G (p.Phe305Val) | |
| 15 | g.73343681A>G | CA7649398 | HCN4 | c.913T>C (p.Phe305Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73343681A>T | CA393095267 | HCN4 | c.913T>A (p.Phe305Ile) | |
| 15 | g.73343682T>A | CA491479854 | HCN4 | c.912A>T (p.Thr304=) | |
| 15 | g.73343682T>C | CA491479855 | HCN4 | c.912A>G (p.Thr304=) | |
| 15 | g.73343682T>G | CA491479856 | HCN4 | c.912A>C (p.Thr304=) | |
| 15 | g.73343685_73343686del | CA2629389089 | HCN4 | c.911_912del (p.Thr304IlefsTer30) | gnomAD v4 |
| 15 | g.73343683G>A | CA393095268 | HCN4 | c.911C>T (p.Thr304Ile) | |
| 15 | g.73343683G>C | CA393095269 | HCN4 | c.911C>G (p.Thr304Arg) | |
| 15 | g.73343683G>T | CA393095270 | HCN4 | c.911C>A (p.Thr304Lys) | |
| 15 | g.73343684T>A | CA393095271 | HCN4 | c.910A>T (p.Thr304Ser) | |
| 15 | g.73343684T>C | CA393095272 | HCN4 | c.910A>G (p.Thr304Ala) | |
| 15 | g.73343684T>G | CA393095273 | HCN4 | c.910A>C (p.Thr304Pro) | |
| 15 | g.73343685G>A | CA491479858 | HCN4 | c.909C>T (p.Asp303=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73343685G>C | CA393095274 | HCN4 | c.909C>G (p.Asp303Glu) | |
| 15 | g.73343685G= | CA2187180078 | HCN4 | c.909C= (p.Asp303=) | |
| 15 | g.73343685G>T | CA393095275 | HCN4 | c.909C>A (p.Asp303Glu) | |
| 15 | g.73343686T>A | CA393095276 | HCN4 | c.908A>T (p.Asp303Val) | |
| 15 | g.73343686T>C | CA393095278 | HCN4 | c.908A>G (p.Asp303Gly) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73343686T>G | CA393095277 | HCN4 | c.908A>C (p.Asp303Ala) | |
| 15 | g.73343686T= | CA2187180080 | HCN4 | c.908A= (p.Asp303=) | |
| 15 | g.73343687C>A | CA393095279 | HCN4 | c.907G>T (p.Asp303Tyr) | |
| 15 | g.73343687C>G | CA393095281 | HCN4 | c.907G>C (p.Asp303His) | |
| 15 | g.73343687C>T | CA393095280 | HCN4 | c.907G>A (p.Asp303Asn) | |
| 15 | g.73343688T>A | CA491479861 | HCN4 | c.906A>T (p.Ser302=) | |
| 15 | g.73343688T>C | CA491479862 | HCN4 | c.906A>G (p.Ser302=) | |
| 15 | g.73343688T>G | CA491479863 | HCN4 | c.906A>C (p.Ser302=) | |
| 15 | g.73343689G>A | CA393095282 | HCN4 | c.905C>T (p.Ser302Leu) | |
| 15 | g.73343689G>C | CA393095283 | HCN4 | c.905C>G (p.Ser302Ter) | |
| 15 | g.73343689G>T | CA393095284 | HCN4 | c.905C>A (p.Ser302Ter) | |
| 15 | g.73343690A= | CA2187180082 | HCN4 | c.904T= (p.Ser302=) | |
| 15 | g.73343690A>C | CA393095285 | HCN4 | c.904T>G (p.Ser302Ala) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73343690A>G | CA393095286 | HCN4 | c.904T>C (p.Ser302Pro) | |
| 15 | g.73343690A>T | CA393095287 | HCN4 | c.904T>A (p.Ser302Thr) | |
| 15 | g.73343691C>A | CA491479864 | HCN4 | c.903G>T (p.Val301=) | gnomAD v4 |
| 15 | g.73343691C= | CA2187180085 | HCN4 | c.903G= (p.Val301=) | |
| 15 | g.73343691C>G | CA491479865 | HCN4 | c.903G>C (p.Val301=) | |
| 15 | g.73343691C>T | CA7649399 | HCN4 | c.903G>A (p.Val301=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73343692A>C | CA393095288 | HCN4 | c.902T>G (p.Val301Gly) | |
| 15 | g.73343692A>G | CA393095289 | HCN4 | c.902T>C (p.Val301Ala) | |
| 15 | g.73343692A>T | CA393095290 | HCN4 | c.902T>A (p.Val301Glu) | |
| 15 | g.73343693C>A | CA393095291 | HCN4 | c.901G>T (p.Val301Leu) | |
| 15 | g.73343693C>G | CA393095292 | HCN4 | c.901G>C (p.Val301Leu) | |
| 15 | g.73343693C>T | CA393095293 | HCN4 | c.901G>A (p.Val301Met) | |
| 15 | g.73343694C>A | CA491479872 | HCN4 | c.900G>T (p.Val300=) | ClinVar gnomAD v4 |
| 15 | g.73343694C>G | CA491479873 | HCN4 | c.900G>C (p.Val300=) | |
| 15 | g.73343694C>T | CA491479874 | HCN4 | c.900G>A (p.Val300=) | |
| 15 | g.73343695A>C | CA393095294 | HCN4 | c.899T>G (p.Val300Gly) | |
| 15 | g.73343695A>G | CA393095296 | HCN4 | c.899T>C (p.Val300Ala) | |
| 15 | g.73343695A>T | CA393095295 | HCN4 | c.899T>A (p.Val300Glu) | |
| 15 | g.73343696C>A | CA393095297 | HCN4 | c.898G>T (p.Val300Leu) | |
| 15 | g.73343696C>G | CA393095298 | HCN4 | c.898G>C (p.Val300Leu) | |
| 15 | g.73343696C>T | CA393095299 | HCN4 | c.898G>A (p.Val300Met) | |
| 15 | g.73343697A= | CA2187180087 | HCN4 | c.897T= (p.Asn299=) | |
| 15 | g.73343697A>C | CA393095300 | HCN4 | c.897T>G (p.Asn299Lys) | |
| 15 | g.73343697A>G | CA7649400 | HCN4 | c.897T>C (p.Asn299=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73343697A>T | CA393095301 | HCN4 | c.897T>A (p.Asn299Lys) | |
| 15 | g.73343698T>A | CA393095302 | HCN4 | c.896A>T (p.Asn299Ile) | |
| 15 | g.73343698T>C | CA16043025 | HCN4 | c.896A>G (p.Asn299Ser) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73343698T>G | CA393095303 | HCN4 | c.896A>C (p.Asn299Thr) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73343698T= | CA2187180089 | HCN4 | c.896A= (p.Asn299=) | |
| 15 | g.73343699T>A | CA393095306 | HCN4 | c.895A>T (p.Asn299Tyr) | |
| 15 | g.73343699T>C | CA393095305 | HCN4 | c.895A>G (p.Asn299Asp) | |
| 15 | g.73343699T>G | CA393095304 | HCN4 | c.895A>C (p.Asn299His) | |
| 15 | g.73343700G>A | CA491479882 | HCN4 | c.894C>T (p.Phe298=) | gnomAD v4 |
| 15 | g.73343700G>C | CA393095307 | HCN4 | c.894C>G (p.Phe298Leu) | |
| 15 | g.73343700G>T | CA393095308 | HCN4 | c.894C>A (p.Phe298Leu) | |
| 15 | g.73343701A>C | CA393095309 | HCN4 | c.893T>G (p.Phe298Cys) | |
| 15 | g.73343701A>G | CA393095310 | HCN4 | c.893T>C (p.Phe298Ser) | |
| 15 | g.73343701A>T | CA393095311 | HCN4 | c.893T>A (p.Phe298Tyr) | |
| 15 | g.73343702A>C | CA393095312 | HCN4 | c.892T>G (p.Phe298Val) | |
| 15 | g.73343702A>G | CA393095313 | HCN4 | c.892T>C (p.Phe298Leu) | |
| 15 | g.73343702A>T | CA393095314 | HCN4 | c.892T>A (p.Phe298Ile) | |
| 15 | g.73343703G>A | CA491479886 | HCN4 | c.891C>T (p.Val297=) | |
| 15 | g.73343703G>C | CA491479887 | HCN4 | c.891C>G (p.Val297=) | |
| 15 | g.73343703G>T | CA491479888 | HCN4 | c.891C>A (p.Val297=) | |
| 15 | g.73343704A>C | CA393095315 | HCN4 | c.890T>G (p.Val297Gly) | |
| 15 | g.73343704A>G | CA393095316 | HCN4 | c.890T>C (p.Val297Ala) | |
| 15 | g.73343704A>T | CA393095317 | HCN4 | c.890T>A (p.Val297Asp) | |
| 15 | g.73343705C>A | CA393095320 | HCN4 | c.889G>T (p.Val297Phe) | |
| 15 | g.73343705C>G | CA393095319 | HCN4 | c.889G>C (p.Val297Leu) | |
| 15 | g.73343705C>T | CA393095318 | HCN4 | c.889G>A (p.Val297Ile) | |
| 15 | g.73343706A>C | CA393095321 | HCN4 | c.888T>G (p.Ile296Met) | |
| 15 | g.73343706A>G | CA491479895 | HCN4 | c.888T>C (p.Ile296=) | ClinVar gnomAD v4 |
| 15 | g.73343706A>T | CA491479894 | HCN4 | c.888T>A (p.Ile296=) | |
| 15 | g.73343707A>C | CA393095322 | HCN4 | c.887T>G (p.Ile296Ser) | |
| 15 | g.73343707A>G | CA393095323 | HCN4 | c.887T>C (p.Ile296Thr) | |
| 15 | g.73343707A>T | CA393095324 | HCN4 | c.887T>A (p.Ile296Asn) | |
| 15 | g.73343708T>A | CA393095325 | HCN4 | c.886A>T (p.Ile296Phe) | |
| 15 | g.73343708T>C | CA393095326 | HCN4 | c.886A>G (p.Ile296Val) | ClinVar gnomAD v4 |
| 15 | g.73343708T>G | CA393095327 | HCN4 | c.886A>C (p.Ile296Leu) | |
| 15 | g.73343709C>A | CA393095328 | HCN4 | c.885G>T (p.Trp295Cys) | |
| 15 | g.73343709C>G | CA393095329 | HCN4 | c.885G>C (p.Trp295Cys) | |
| 15 | g.73343709C>T | CA393095330 | HCN4 | c.885G>A (p.Trp295Ter) | |
| 15 | g.73343710C>A | CA393095331 | HCN4 | c.884G>T (p.Trp295Leu) | |
| 15 | g.73343710C>G | CA393095332 | HCN4 | c.884G>C (p.Trp295Ser) | |
| 15 | g.73343710C>T | CA393095333 | HCN4 | c.884G>A (p.Trp295Ter) | |
| 15 | g.73343711A>C | CA393095335 | HCN4 | c.883T>G (p.Trp295Gly) | |
| 15 | g.73343711A>G | CA393095336 | HCN4 | c.883T>C (p.Trp295Arg) | gnomAD v4 |
| 15 | g.73343711A>T | CA393095334 | HCN4 | c.883T>A (p.Trp295Arg) | |
| 15 | g.73343712G>A | CA491479899 | HCN4 | c.882C>T (p.Pro294=) | |
| 15 | g.73343712G>C | CA7649401 | HCN4 | c.882C>G (p.Pro294=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73343712G= | CA2187180093 | HCN4 | c.882C= (p.Pro294=) | |
| 15 | g.73343712G>T | CA491479902 | HCN4 | c.882C>A (p.Pro294=) | |
| 15 | g.73343714del | CA2629389090 | HCN4 | c.882del (p.Trp295GlyfsTer?) | gnomAD v4 |
| 15 | g.73343713G>A | CA393095337 | HCN4 | c.881C>T (p.Pro294Leu) | ClinVar COSMIC |
| 15 | g.73343713G>C | CA393095338 | HCN4 | c.881C>G (p.Pro294Arg) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73343713G= | CA2187180096 | HCN4 | c.881C= (p.Pro294=) | |
| 15 | g.73343713G>T | CA393095339 | HCN4 | c.881C>A (p.Pro294His) | |
| 15 | g.73343714G>A | CA393095340 | HCN4 | c.880C>T (p.Pro294Ser) | |
| 15 | g.73343714G>C | CA393095341 | HCN4 | c.880C>G (p.Pro294Ala) | |
| 15 | g.73343714G>T | CA393095342 | HCN4 | c.880C>A (p.Pro294Thr) | |
| 15 | g.73343715T>A | CA491479907 | HCN4 | c.879A>T (p.Thr293=) | |
| 15 | g.73343715T>C | CA491479908 | HCN4 | c.879A>G (p.Thr293=) | gnomAD v4 |
| 15 | g.73343715T>G | CA491479909 | HCN4 | c.879A>C (p.Thr293=) | |
| 15 | g.73343716G>A | CA393095343 | HCN4 | c.878C>T (p.Thr293Ile) | |
| 15 | g.73343716G>C | CA393095344 | HCN4 | c.878C>G (p.Thr293Arg) | |
| 15 | g.73343716G>T | CA393095345 | HCN4 | c.878C>A (p.Thr293Lys) | |
| 15 | g.73343717T>A | CA393095346 | HCN4 | c.877A>T (p.Thr293Ser) | |
| 15 | g.73343717T>C | CA393095347 | HCN4 | c.877A>G (p.Thr293Ala) | gnomAD v4 |
| 15 | g.73343717T>G | CA393095348 | HCN4 | c.877A>C (p.Thr293Pro) | |
| 15 | g.73343718G>A | CA491479915 | HCN4 | c.876C>T (p.Thr292=) | gnomAD v4 |
| 15 | g.73343718G>C | CA491479917 | HCN4 | c.876C>G (p.Thr292=) | |
| 15 | g.73343718G>T | CA491479916 | HCN4 | c.876C>A (p.Thr292=) | |
| 15 | g.73343719G>A | CA393095350 | HCN4 | c.875C>T (p.Thr292Ile) | COSMIC |
| 15 | g.73343719G>C | CA393095351 | HCN4 | c.875C>G (p.Thr292Ser) | |
| 15 | g.73343719G>T | CA393095349 | HCN4 | c.875C>A (p.Thr292Asn) | |
| 15 | g.73343720T>A | CA393095352 | HCN4 | c.874A>T (p.Thr292Ser) | |
| 15 | g.73343720T>C | CA393095353 | HCN4 | c.874A>G (p.Thr292Ala) | |
| 15 | g.73343720T>G | CA393095354 | HCN4 | c.874A>C (p.Thr292Pro) | |
| 15 | g.73343721G>A | CA491479922 | HCN4 | c.873C>T (p.Asn291=) | gnomAD v4 |
| 15 | g.73343721G>C | CA393095355 | HCN4 | c.873C>G (p.Asn291Lys) | |
| 15 | g.73343721G>T | CA393095356 | HCN4 | c.873C>A (p.Asn291Lys) | |
| 15 | g.73343722T>A | CA393095359 | HCN4 | c.872A>T (p.Asn291Ile) | |
| 15 | g.73343722T>C | CA393095357 | HCN4 | c.872A>G (p.Asn291Ser) | |
| 15 | g.73343722T>G | CA393095358 | HCN4 | c.872A>C (p.Asn291Thr) | |
| 15 | g.73343723T>A | CA393095360 | HCN4 | c.871A>T (p.Asn291Tyr) | |
| 15 | g.73343723T>C | CA393095361 | HCN4 | c.871A>G (p.Asn291Asp) | |
| 15 | g.73343723T>G | CA393095362 | HCN4 | c.871A>C (p.Asn291His) | |
| 15 | g.73343724C>A | CA393095363 | HCN4 | c.870G>T (p.Glu290Asp) | |
| 15 | g.73343724C>G | CA393095364 | HCN4 | c.870G>C (p.Glu290Asp) | |
| 15 | g.73343724C>T | CA491479926 | HCN4 | c.870G>A (p.Glu290=) | |
| 15 | g.73343725T>A | CA393095367 | HCN4 | c.869A>T (p.Glu290Val) | |
| 15 | g.73343725T>C | CA393095366 | HCN4 | c.869A>G (p.Glu290Gly) | |
| 15 | g.73343725T>G | CA393095365 | HCN4 | c.869A>C (p.Glu290Ala) | |
| 15 | g.73343726C>A | CA393095368 | HCN4 | c.868G>T (p.Glu290Ter) | |
| 15 | g.73343726C>G | CA393095369 | HCN4 | c.868G>C (p.Glu290Gln) | |
| 15 | g.73343726C>T | CA393095370 | HCN4 | c.868G>A (p.Glu290Lys) | |
| 15 | g.73343727A>C | CA393095371 | HCN4 | c.867T>G (p.Asp289Glu) | gnomAD v4 |
| 15 | g.73343727A>G | CA491479931 | HCN4 | c.867T>C (p.Asp289=) | |
| 15 | g.73343727A>T | CA393095372 | HCN4 | c.867T>A (p.Asp289Glu) | |
| 15 | g.73343728T>A | CA393095373 | HCN4 | c.866A>T (p.Asp289Val) | |
| 15 | g.73343728T>C | CA393095374 | HCN4 | c.866A>G (p.Asp289Gly) | |
| 15 | g.73343728T>G | CA393095375 | HCN4 | c.866A>C (p.Asp289Ala) | |
| 15 | g.73343729C>A | CA393095376 | HCN4 | c.865G>T (p.Asp289Tyr) | |
| 15 | g.73343729C>G | CA393095377 | HCN4 | c.865G>C (p.Asp289His) | |
| 15 | g.73343729C>T | CA393095378 | HCN4 | c.865G>A (p.Asp289Asn) | |
| 15 | g.73343730C>A | CA393095379 | HCN4 | c.864G>T (p.Lys288Asn) | gnomAD v4 |
| 15 | g.73343730C= | CA2187180099 | HCN4 | c.864G= (p.Lys288=) | |
| 15 | g.73343730C>G | CA393095380 | HCN4 | c.864G>C (p.Lys288Asn) | |
| 15 | g.73343730C>T | CA491479936 | HCN4 | c.864G>A (p.Lys288=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73343731T>A | CA393095382 | HCN4 | c.863A>T (p.Lys288Met) | |
| 15 | g.73343731T>C | CA393095383 | HCN4 | c.863A>G (p.Lys288Arg) | COSMIC |
| 15 | g.73343731T>G | CA393095381 | HCN4 | c.863A>C (p.Lys288Thr) | |
| 15 | g.73343732T>A | CA393095384 | HCN4 | c.862A>T (p.Lys288Ter) | |
| 15 | g.73343732T>C | CA393095385 | HCN4 | c.862A>G (p.Lys288Glu) | |
| 15 | g.73343732T>G | CA393095386 | HCN4 | c.862A>C (p.Lys288Gln) | |
| 15 | g.73343733G>A | CA491479940 | HCN4 | c.861C>T (p.Phe287=) | |
| 15 | g.73343733G>C | CA393095387 | HCN4 | c.861C>G (p.Phe287Leu) | |
| 15 | g.73343733G>T | CA393095388 | HCN4 | c.861C>A (p.Phe287Leu) | |
| 15 | g.73343734A>C | CA393095391 | HCN4 | c.860T>G (p.Phe287Cys) | gnomAD v4 |
| 15 | g.73343734A>G | CA393095389 | HCN4 | c.860T>C (p.Phe287Ser) | |
| 15 | g.73343734A>T | CA393095390 | HCN4 | c.860T>A (p.Phe287Tyr) |