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.73367527C>A | CA393097047 | HCN4 | c.744G>T (p.Lys248Asn) | |
| 15 | g.73367527C>G | CA393097048 | HCN4 | c.744G>C (p.Lys248Asn) | |
| 15 | g.73367527C>T | CA491479243 | HCN4 | c.744G>A (p.Lys248=) | ClinVar |
| 15 | g.73367527_73367528delinsCT | CA2187194435 | HCN4 | c.743_744delinsAG (p.Lys248=) | |
| 15 | g.73367528T>A | CA393097050 | HCN4 | c.743A>T (p.Lys248Met) | |
| 15 | g.73367528T>C | CA7649431 | HCN4 | c.743A>G (p.Lys248Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73367528T>G | CA393097052 | HCN4 | c.743A>C (p.Lys248Thr) | |
| 15 | g.73367528T= | CA2187194436 | HCN4 | c.743A= (p.Lys248=) | |
| 15 | g.73367529del | CA272699944 | HCN4 | c.743del (p.Lys248SerfsTer20) | dbSNP |
| 15 | g.73367529T>A | CA393097053 | HCN4 | c.742A>T (p.Lys248Ter) | |
| 15 | g.73367529T>C | CA393097054 | HCN4 | c.742A>G (p.Lys248Glu) | |
| 15 | g.73367529T>G | CA393097055 | HCN4 | c.742A>C (p.Lys248Gln) | gnomAD v4 |
| 15 | g.73367530G>A | CA491479244 | HCN4 | c.741C>T (p.Val247=) | gnomAD v4 |
| 15 | g.73367530G>C | CA491479245 | HCN4 | c.741C>G (p.Val247=) | dbSNP |
| 15 | g.73367530G= | CA2187194437 | HCN4 | c.741C= (p.Val247=) | |
| 15 | g.73367530G>T | CA491479246 | HCN4 | c.741C>A (p.Val247=) | |
| 15 | g.73367531A>C | CA393097059 | HCN4 | c.740T>G (p.Val247Gly) | |
| 15 | g.73367531A>G | CA393097057 | HCN4 | c.740T>C (p.Val247Ala) | |
| 15 | g.73367531A>T | CA393097056 | HCN4 | c.740T>A (p.Val247Asp) | |
| 15 | g.73367532C>A | CA393097060 | HCN4 | c.739G>T (p.Val247Phe) | |
| 15 | g.73367532C= | CA2187194438 | HCN4 | c.739G= (p.Val247=) | |
| 15 | g.73367532C>G | CA393097061 | HCN4 | c.739G>C (p.Val247Leu) | |
| 15 | g.73367532C>T | CA272699946 | HCN4 | c.739G>A (p.Val247Ile) | dbSNP |
| 15 | g.73367533C>A | CA393097062 | HCN4 | c.738G>T (p.Arg246Ser) | dbSNP |
| 15 | g.73367533C= | CA2187194439 | HCN4 | c.738G= (p.Arg246=) | |
| 15 | g.73367533C>G | CA393097063 | HCN4 | c.738G>C (p.Arg246Ser) | |
| 15 | g.73367533C>T | CA272699948 | HCN4 | c.738G>A (p.Arg246=) | dbSNP gnomAD v4 |
| 15 | g.73367534C>A | CA393097064 | HCN4 | c.737G>T (p.Arg246Met) | |
| 15 | g.73367534C>G | CA393097066 | HCN4 | c.737G>C (p.Arg246Thr) | |
| 15 | g.73367534C>T | CA393097067 | HCN4 | c.737G>A (p.Arg246Lys) | |
| 15 | g.73367535T>A | CA393097069 | HCN4 | c.736A>T (p.Arg246Trp) | |
| 15 | g.73367535T>C | CA393097071 | HCN4 | c.736A>G (p.Arg246Gly) | |
| 15 | g.73367535T>G | CA491479247 | HCN4 | c.736A>C (p.Arg246=) | |
| 15 | g.73367536C>A | CA393097072 | HCN4 | c.735G>T (p.Glu245Asp) | |
| 15 | g.73367536C>G | CA393097073 | HCN4 | c.735G>C (p.Glu245Asp) | |
| 15 | g.73367536C>T | CA491479248 | HCN4 | c.735G>A (p.Glu245=) | |
| 15 | g.73367537T>A | CA393097079 | HCN4 | c.734A>T (p.Glu245Val) | |
| 15 | g.73367537T>C | CA393097077 | HCN4 | c.734A>G (p.Glu245Gly) | |
| 15 | g.73367537T>G | CA393097075 | HCN4 | c.734A>C (p.Glu245Ala) | |
| 15 | g.73367538C>A | CA393097080 | HCN4 | c.733G>T (p.Glu245Ter) | gnomAD v4 |
| 15 | g.73367538C>G | CA393097081 | HCN4 | c.733G>C (p.Glu245Gln) | gnomAD v4 |
| 15 | g.73367538C>T | CA393097083 | HCN4 | c.733G>A (p.Glu245Lys) | |
| 15 | g.73367539C>A | CA393097085 | HCN4 | c.732G>T (p.Gln244His) | |
| 15 | g.73367539C>G | CA393097087 | HCN4 | c.732G>C (p.Gln244His) | |
| 15 | g.73367539C>T | CA491479249 | HCN4 | c.732G>A (p.Gln244=) | gnomAD v4 |
| 15 | g.73367540T>A | CA393097088 | HCN4 | c.731A>T (p.Gln244Leu) | |
| 15 | g.73367540T>C | CA393097090 | HCN4 | c.731A>G (p.Gln244Arg) | |
| 15 | g.73367540T>G | CA393097092 | HCN4 | c.731A>C (p.Gln244Pro) | |
| 15 | g.73367541G>A | CA393097093 | HCN4 | c.730C>T (p.Gln244Ter) | |
| 15 | g.73367541G>C | CA393097094 | HCN4 | c.730C>G (p.Gln244Glu) | |
| 15 | g.73367541G>T | CA393097095 | HCN4 | c.730C>A (p.Gln244Lys) | |
| 15 | g.73367542T>A | CA393097096 | HCN4 | c.729A>T (p.Glu243Asp) | |
| 15 | g.73367542T>C | CA491479250 | HCN4 | c.729A>G (p.Glu243=) | gnomAD v4 |
| 15 | g.73367542T>G | CA393097097 | HCN4 | c.729A>C (p.Glu243Asp) | |
| 15 | g.73367543T>A | CA393097102 | HCN4 | c.728A>T (p.Glu243Val) | |
| 15 | g.73367543T>C | CA393097101 | HCN4 | c.728A>G (p.Glu243Gly) | |
| 15 | g.73367543T>G | CA393097099 | HCN4 | c.728A>C (p.Glu243Ala) | |
| 15 | g.73367544C>A | CA393097103 | HCN4 | c.727G>T (p.Glu243Ter) | |
| 15 | g.73367544C= | CA2187194440 | HCN4 | c.727G= (p.Glu243=) | |
| 15 | g.73367544C>G | CA7649432 | HCN4 | c.727G>C (p.Glu243Gln) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73367544C>T | CA393097105 | HCN4 | c.727G>A (p.Glu243Lys) | COSMIC |
| 15 | g.73367545G>A | CA491479251 | HCN4 | c.726C>T (p.Arg242=) | |
| 15 | g.73367545G>C | CA491479252 | HCN4 | c.726C>G (p.Arg242=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73367545G= | CA2187194441 | HCN4 | c.726C= (p.Arg242=) | |
| 15 | g.73367545G>T | CA491479253 | HCN4 | c.726C>A (p.Arg242=) | |
| 15 | g.73367546C>A | CA393097107 | HCN4 | c.725G>T (p.Arg242Leu) | ClinVar |
| 15 | g.73367546C= | CA2187194442 | HCN4 | c.725G= (p.Arg242=) | |
| 15 | g.73367546C>G | CA393097109 | HCN4 | c.725G>C (p.Arg242Pro) | ClinVar dbSNP |
| 15 | g.73367546C>T | CA393097110 | HCN4 | c.725G>A (p.Arg242His) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73367547G>A | CA7649433 | HCN4 | c.724C>T (p.Arg242Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73367547G>C | CA393097112 | HCN4 | c.724C>G (p.Arg242Gly) | |
| 15 | g.73367547G= | CA2187194443 | HCN4 | c.724C= (p.Arg242=) | |
| 15 | g.73367547G>T | CA393097114 | HCN4 | c.724C>A (p.Arg242Ser) | |
| 15 | g.73367548C>A | CA393097115 | HCN4 | c.723G>T (p.Glu241Asp) | |
| 15 | g.73367548C>G | CA393097116 | HCN4 | c.723G>C (p.Glu241Asp) | |
| 15 | g.73367548C>T | CA491479254 | HCN4 | c.723G>A (p.Glu241=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73367549T>A | CA393097117 | HCN4 | c.722A>T (p.Glu241Val) | |
| 15 | g.73367549T>C | CA393097118 | HCN4 | c.722A>G (p.Glu241Gly) | |
| 15 | g.73367549T>G | CA393097119 | HCN4 | c.722A>C (p.Glu241Ala) | |
| 15 | g.73367550C>A | CA393097122 | HCN4 | c.721G>T (p.Glu241Ter) | |
| 15 | g.73367550C>G | CA393097121 | HCN4 | c.721G>C (p.Glu241Gln) | |
| 15 | g.73367550C>T | CA393097120 | HCN4 | c.721G>A (p.Glu241Lys) | gnomAD v4 |
| 15 | g.73367551C>A | CA491479255 | HCN4 | c.720G>T (p.Val240=) | |
| 15 | g.73367551C>G | CA491479256 | HCN4 | c.720G>C (p.Val240=) | |
| 15 | g.73367551C>T | CA491479257 | HCN4 | c.720G>A (p.Val240=) | |
| 15 | g.73367552A>C | CA393097123 | HCN4 | c.719T>G (p.Val240Gly) | |
| 15 | g.73367552A>G | CA393097124 | HCN4 | c.719T>C (p.Val240Ala) | |
| 15 | g.73367552A>T | CA393097126 | HCN4 | c.719T>A (p.Val240Glu) | |
| 15 | g.73367553C>A | CA393097128 | HCN4 | c.718G>T (p.Val240Leu) | |
| 15 | g.73367553C= | CA2187194444 | HCN4 | c.718G= (p.Val240=) | |
| 15 | g.73367553C>G | CA393097130 | HCN4 | c.718G>C (p.Val240Leu) | |
| 15 | g.73367553C>T | CA393097131 | HCN4 | c.718G>A (p.Val240Met) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73367554G>A | CA491479258 | HCN4 | c.717C>T (p.Ala239=) | |
| 15 | g.73367554G>C | CA491479259 | HCN4 | c.717C>G (p.Ala239=) | COSMIC |
| 15 | g.73367554G>T | CA491479260 | HCN4 | c.717C>A (p.Ala239=) | |
| 15 | g.73367555G>A | CA393097132 | HCN4 | c.716C>T (p.Ala239Val) | |
| 15 | g.73367555G>C | CA393097133 | HCN4 | c.716C>G (p.Ala239Gly) | COSMIC |
| 15 | g.73367555G>T | CA393097135 | HCN4 | c.716C>A (p.Ala239Asp) | |
| 15 | g.73367556C>A | CA393097137 | HCN4 | c.715G>T (p.Ala239Ser) | |
| 15 | g.73367556C>G | CA393097138 | HCN4 | c.715G>C (p.Ala239Pro) | COSMIC |
| 15 | g.73367556C>T | CA393097140 | HCN4 | c.715G>A (p.Ala239Thr) | |
| 15 | g.73367557T>A | CA393097143 | HCN4 | c.714A>T (p.Lys238Asn) | gnomAD v4 COSMIC |
| 15 | g.73367557T>C | CA491479261 | HCN4 | c.714A>G (p.Lys238=) | |
| 15 | g.73367557T>G | CA393097142 | HCN4 | c.714A>C (p.Lys238Asn) | |
| 15 | g.73367558T>A | CA393097145 | HCN4 | c.713A>T (p.Lys238Ile) | |
| 15 | g.73367558T>C | CA393097148 | HCN4 | c.713A>G (p.Lys238Arg) | |
| 15 | g.73367558T>G | CA393097150 | HCN4 | c.713A>C (p.Lys238Thr) | COSMIC |
| 15 | g.73367559T>A | CA393097151 | HCN4 | c.712A>T (p.Lys238Ter) | |
| 15 | g.73367559T>C | CA393097153 | HCN4 | c.712A>G (p.Lys238Glu) | dbSNP |
| 15 | g.73367559T>G | CA393097154 | HCN4 | c.712A>C (p.Lys238Gln) | COSMIC |
| 15 | g.73367559T= | CA2187194445 | HCN4 | c.712A= (p.Lys238=) | |
| 15 | g.73367560C>A | CA393097155 | HCN4 | c.711G>T (p.Gln237His) | |
| 15 | g.73367560C>G | CA393097156 | HCN4 | c.711G>C (p.Gln237His) | COSMIC |
| 15 | g.73367560C>T | CA491479262 | HCN4 | c.711G>A (p.Gln237=) | gnomAD v4 |
| 15 | g.73367561T>A | CA393097157 | HCN4 | c.710A>T (p.Gln237Leu) | |
| 15 | g.73367561T>C | CA393097158 | HCN4 | c.710A>G (p.Gln237Arg) | COSMIC |
| 15 | g.73367561T>G | CA393097159 | HCN4 | c.710A>C (p.Gln237Pro) | |
| 15 | g.73367562G>A | CA393097161 | HCN4 | c.709C>T (p.Gln237Ter) | |
| 15 | g.73367562G>C | CA393097163 | HCN4 | c.709C>G (p.Gln237Glu) | |
| 15 | g.73367562G>T | CA393097164 | HCN4 | c.709C>A (p.Gln237Lys) | COSMIC |
| 15 | g.73367563G>A | CA491479461 | HCN4 | c.708C>T (p.Ser236=) | ClinVar gnomAD v4 |
| 15 | g.73367563G>C | CA393097167 | HCN4 | c.708C>G (p.Ser236Arg) | |
| 15 | g.73367563G>T | CA393097165 | HCN4 | c.708C>A (p.Ser236Arg) | |
| 15 | g.73367564C>A | CA393097168 | HCN4 | c.707G>T (p.Ser236Ile) | |
| 15 | g.73367564C>G | CA393097169 | HCN4 | c.707G>C (p.Ser236Thr) | |
| 15 | g.73367564C>T | CA393097170 | HCN4 | c.707G>A (p.Ser236Asn) | |
| 15 | g.73367565T>A | CA393097172 | HCN4 | c.706A>T (p.Ser236Cys) | |
| 15 | g.73367565T>C | CA393097173 | HCN4 | c.706A>G (p.Ser236Gly) | |
| 15 | g.73367565T>G | CA393097175 | HCN4 | c.706A>C (p.Ser236Arg) | |
| 15 | g.73367566G>A | CA491479462 | HCN4 | c.705C>T (p.Gly235=) | |
| 15 | g.73367566G>C | CA7649434 | HCN4 | c.705C>G (p.Gly235=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73367566G= | CA2187194446 | HCN4 | c.705C= (p.Gly235=) | |
| 15 | g.73367566G>T | CA491479463 | HCN4 | c.705C>A (p.Gly235=) | |
| 15 | g.73367567C>A | CA393097178 | HCN4 | c.704G>T (p.Gly235Val) | |
| 15 | g.73367567C>G | CA393097179 | HCN4 | c.704G>C (p.Gly235Ala) | |
| 15 | g.73367567C>T | CA393097181 | HCN4 | c.704G>A (p.Gly235Asp) | |
| 15 | g.73367568C>A | CA393097182 | HCN4 | c.703G>T (p.Gly235Cys) | |
| 15 | g.73367568C>G | CA393097184 | HCN4 | c.703G>C (p.Gly235Arg) | |
| 15 | g.73367568C>T | CA393097185 | HCN4 | c.703G>A (p.Gly235Ser) | |
| 15 | g.73367569G>A | CA7649435 | HCN4 | c.702C>T (p.Phe234=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73367569G>C | CA393097189 | HCN4 | c.702C>G (p.Phe234Leu) | |
| 15 | g.73367569G= | CA2187194447 | HCN4 | c.702C= (p.Phe234=) | |
| 15 | g.73367569G>T | CA393097188 | HCN4 | c.702C>A (p.Phe234Leu) | ClinVar |
| 15 | g.73367570A>C | CA393097190 | HCN4 | c.701T>G (p.Phe234Cys) | |
| 15 | g.73367570A>G | CA393097192 | HCN4 | c.701T>C (p.Phe234Ser) | |
| 15 | g.73367570A>T | CA393097191 | HCN4 | c.701T>A (p.Phe234Tyr) | |
| 15 | g.73367571A>C | CA393097193 | HCN4 | c.700T>G (p.Phe234Val) | |
| 15 | g.73367571A>G | CA393097196 | HCN4 | c.700T>C (p.Phe234Leu) | |
| 15 | g.73367571A>T | CA393097195 | HCN4 | c.700T>A (p.Phe234Ile) | |
| 15 | g.73367572C>A | CA393097198 | HCN4 | c.699G>T (p.Met233Ile) | |
| 15 | g.73367572C= | CA2187194448 | HCN4 | c.699G= (p.Met233=) | |
| 15 | g.73367572C>G | CA393097201 | HCN4 | c.699G>C (p.Met233Ile) | |
| 15 | g.73367572C>T | CA393097199 | HCN4 | c.699G>A (p.Met233Ile) | ClinVar dbSNP |
| 15 | g.73367573A= | CA2187194449 | HCN4 | c.698T= (p.Met233=) | |
| 15 | g.73367573A>C | CA393097203 | HCN4 | c.698T>G (p.Met233Arg) | |
| 15 | g.73367573A>G | CA393097205 | HCN4 | c.698T>C (p.Met233Thr) | dbSNP |
| 15 | g.73367573A>T | CA393097206 | HCN4 | c.698T>A (p.Met233Lys) | |
| 15 | g.73367574T>A | CA7649436 | HCN4 | c.697A>T (p.Met233Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73367574T>C | CA393097207 | HCN4 | c.697A>G (p.Met233Val) | dbSNP gnomAD v4 |
| 15 | g.73367574T>G | CA393097208 | HCN4 | c.697A>C (p.Met233Leu) | |
| 15 | g.73367574T= | CA2187194450 | HCN4 | c.697A= (p.Met233=) | |
| 15 | g.73367575C>A | CA393097209 | HCN4 | c.696G>T (p.Arg232Ser) | gnomAD v4 |
| 15 | g.73367575C>G | CA393097210 | HCN4 | c.696G>C (p.Arg232Ser) | |
| 15 | g.73367575C>T | CA491479464 | HCN4 | c.696G>A (p.Arg232=) | gnomAD v4 |
| 15 | g.73367576C>A | CA7649437 | HCN4 | c.695G>T (p.Arg232Met) | dbSNP ExAC |
| 15 | g.73367576C= | CA2187194451 | HCN4 | c.695G= (p.Arg232=) | |
| 15 | g.73367576C>G | CA393097211 | HCN4 | c.695G>C (p.Arg232Thr) | ClinVar dbSNP |
| 15 | g.73367576C>T | CA393097212 | HCN4 | c.695G>A (p.Arg232Lys) | gnomAD v4 |
| 15 | g.73367577T>A | CA393097213 | HCN4 | c.694A>T (p.Arg232Trp) | |
| 15 | g.73367577T>C | CA393097214 | HCN4 | c.694A>G (p.Arg232Gly) | |
| 15 | g.73367577T>G | CA491479465 | HCN4 | c.694A>C (p.Arg232=) | |
| 15 | g.73367578T>A | CA491479466 | HCN4 | c.693A>T (p.Leu231=) | dbSNP |
| 15 | g.73367578T>C | CA491479467 | HCN4 | c.693A>G (p.Leu231=) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73367578T>G | CA491479468 | HCN4 | c.693A>C (p.Leu231=) | |
| 15 | g.73367578T= | CA2187194452 | HCN4 | c.693A= (p.Leu231=) | |
| 15 | g.73367579A>C | CA393097215 | HCN4 | c.692T>G (p.Leu231Arg) | |
| 15 | g.73367579A>G | CA393097216 | HCN4 | c.692T>C (p.Leu231Pro) | |
| 15 | g.73367579A>T | CA393097217 | HCN4 | c.692T>A (p.Leu231Gln) | |
| 15 | g.73367580G>A | CA491479469 | HCN4 | c.691C>T (p.Leu231=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73367580G>C | CA393097218 | HCN4 | c.691C>G (p.Leu231Val) | ClinVar |
| 15 | g.73367580G= | CA2187194453 | HCN4 | c.691C= (p.Leu231=) | |
| 15 | g.73367580G>T | CA393097219 | HCN4 | c.691C>A (p.Leu231Ile) | |
| 15 | g.73367581G>A | CA7649438 | HCN4 | c.690C>T (p.Ser230=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73367581G>C | CA491479470 | HCN4 | c.690C>G (p.Ser230=) | |
| 15 | g.73367581G= | CA2187194454 | HCN4 | c.690C= (p.Ser230=) | |
| 15 | g.73367581G>T | CA491479471 | HCN4 | c.690C>A (p.Ser230=) | |
| 15 | g.73367582G>A | CA393097220 | HCN4 | c.689C>T (p.Ser230Phe) | |
| 15 | g.73367582G>C | CA393097221 | HCN4 | c.689C>G (p.Ser230Cys) | |
| 15 | g.73367582G>T | CA393097222 | HCN4 | c.689C>A (p.Ser230Tyr) | |
| 15 | g.73367583A>C | CA393097225 | HCN4 | c.688T>G (p.Ser230Ala) | |
| 15 | g.73367583A>G | CA393097227 | HCN4 | c.688T>C (p.Ser230Pro) | |
| 15 | g.73367583A>T | CA393097223 | HCN4 | c.688T>A (p.Ser230Thr) | |
| 15 | g.73367584G>A | CA491479472 | HCN4 | c.687C>T (p.Phe229=) | gnomAD v4 |
| 15 | g.73367584G>C | CA393097228 | HCN4 | c.687C>G (p.Phe229Leu) | gnomAD v4 |
| 15 | g.73367584G>T | CA393097230 | HCN4 | c.687C>A (p.Phe229Leu) | |
| 15 | g.73367585A>C | CA393097231 | HCN4 | c.686T>G (p.Phe229Cys) | |
| 15 | g.73367585A>G | CA393097232 | HCN4 | c.686T>C (p.Phe229Ser) | |
| 15 | g.73367585A>T | CA393097233 | HCN4 | c.686T>A (p.Phe229Tyr) | |
| 15 | g.73367586A>C | CA393097236 | HCN4 | c.685T>G (p.Phe229Val) | |
| 15 | g.73367586A>G | CA393097234 | HCN4 | c.685T>C (p.Phe229Leu) | |
| 15 | g.73367586A>T | CA393097235 | HCN4 | c.685T>A (p.Phe229Ile) | |
| 15 | g.73367587T>A | CA393097238 | HCN4 | c.684A>T (p.Lys228Asn) | |
| 15 | g.73367587T>C | CA491479473 | HCN4 | c.684A>G (p.Lys228=) | |
| 15 | g.73367587T>G | CA393097240 | HCN4 | c.684A>C (p.Lys228Asn) | |
| 15 | g.73367588T>A | CA393097241 | HCN4 | c.683A>T (p.Lys228Ile) | |
| 15 | g.73367588T>C | CA393097243 | HCN4 | c.683A>G (p.Lys228Arg) | ClinVar |
| 15 | g.73367588T>G | CA393097244 | HCN4 | c.683A>C (p.Lys228Thr) | |
| 15 | g.73367589T>A | CA393097246 | HCN4 | c.682A>T (p.Lys228Ter) | |
| 15 | g.73367589T>C | CA393097249 | HCN4 | c.682A>G (p.Lys228Glu) | |
| 15 | g.73367589T>G | CA393097248 | HCN4 | c.682A>C (p.Lys228Gln) | |
| 15 | g.73367590G>A | CA491479474 | HCN4 | c.681C>T (p.Asn227=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73367590G>C | CA393097250 | HCN4 | c.681C>G (p.Asn227Lys) | ClinVar |
| 15 | g.73367590G= | CA2187194455 | HCN4 | c.681C= (p.Asn227=) | |
| 15 | g.73367590G>T | CA393097251 | HCN4 | c.681C>A (p.Asn227Lys) | |
| 15 | g.73367591T>A | CA393097253 | HCN4 | c.680A>T (p.Asn227Ile) | |
| 15 | g.73367591T>C | CA393097254 | HCN4 | c.680A>G (p.Asn227Ser) | |
| 15 | g.73367591T>G | CA393097256 | HCN4 | c.680A>C (p.Asn227Thr) | |
| 15 | g.73367592T>A | CA393097257 | HCN4 | c.679A>T (p.Asn227Tyr) | |
| 15 | g.73367592T>C | CA393097258 | HCN4 | c.679A>G (p.Asn227Asp) | |
| 15 | g.73367592T>G | CA393097259 | HCN4 | c.679A>C (p.Asn227His) | |
| 15 | g.73367593G>A | CA491479475 | HCN4 | c.678C>T (p.Val226=) | |
| 15 | g.73367593G>C | CA491479476 | HCN4 | c.678C>G (p.Val226=) | |
| 15 | g.73367593G>T | CA491479477 | HCN4 | c.678C>A (p.Val226=) | COSMIC |
| 15 | g.73367594A>C | CA393097260 | HCN4 | c.677T>G (p.Val226Gly) | |
| 15 | g.73367594A>G | CA393097262 | HCN4 | c.677T>C (p.Val226Ala) | ClinVar dbSNP |
| 15 | g.73367594A>T | CA393097263 | HCN4 | c.677T>A (p.Val226Asp) | |
| 15 | g.73367595C>A | CA393097264 | HCN4 | c.676G>T (p.Val226Phe) | |
| 15 | g.73367595C= | CA2187194456 | HCN4 | c.676G= (p.Val226=) | |
| 15 | g.73367595C>G | CA393097265 | HCN4 | c.676G>C (p.Val226Leu) | |
| 15 | g.73367595C>T | CA7649439 | HCN4 | c.676G>A (p.Val226Ile) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73367596C>A | CA491479478 | HCN4 | c.675G>T (p.Gly225=) | gnomAD v4 |
| 15 | g.73367596C= | CA2187194457 | HCN4 | c.675G= (p.Gly225=) | |
| 15 | g.73367596C>G | CA491479479 | HCN4 | c.675G>C (p.Gly225=) | gnomAD v4 |
| 15 | g.73367596C>T | CA491479480 | HCN4 | c.675G>A (p.Gly225=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73367597C>A | CA393097270 | HCN4 | c.674G>T (p.Gly225Val) | dbSNP |
| 15 | g.73367597C= | CA2187194458 | HCN4 | c.674G= (p.Gly225=) | |
| 15 | g.73367597C>G | CA393097267 | HCN4 | c.674G>C (p.Gly225Ala) | |
| 15 | g.73367597C>T | CA393097269 | HCN4 | c.674G>A (p.Gly225Glu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73367598C>A | CA393097271 | HCN4 | c.673G>T (p.Gly225Trp) | |
| 15 | g.73367598C= | CA2187194459 | HCN4 | c.673G= (p.Gly225=) | |
| 15 | g.73367598C>G | CA393097272 | HCN4 | c.673G>C (p.Gly225Arg) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73367598C>T | CA7649440 | HCN4 | c.673G>A (p.Gly225Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73367599G>A | CA491479481 | HCN4 | c.672C>T (p.Pro224=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73367599G>C | CA491479482 | HCN4 | c.672C>G (p.Pro224=) | gnomAD v4 |
| 15 | g.73367599G= | CA2187194460 | HCN4 | c.672C= (p.Pro224=) | |
| 15 | g.73367599G>T | CA491479483 | HCN4 | c.672C>A (p.Pro224=) | |
| 15 | g.73367600G>A | CA393097274 | HCN4 | c.671C>T (p.Pro224Leu) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73367600G>C | CA393097275 | HCN4 | c.671C>G (p.Pro224Arg) | |
| 15 | g.73367600G= | CA2187194461 | HCN4 | c.671C= (p.Pro224=) | |
| 15 | g.73367600G>T | CA393097277 | HCN4 | c.671C>A (p.Pro224His) | COSMIC |
| 15 | g.73367601G>A | CA393097279 | HCN4 | c.670C>T (p.Pro224Ser) | |
| 15 | g.73367601G>C | CA393097280 | HCN4 | c.670C>G (p.Pro224Ala) | |
| 15 | g.73367601G>T | CA393097281 | HCN4 | c.670C>A (p.Pro224Thr) | |
| 15 | g.73367602T>A | CA393097283 | HCN4 | c.669A>T (p.Gln223His) | |
| 15 | g.73367602T>C | CA491479484 | HCN4 | c.669A>G (p.Gln223=) | |
| 15 | g.73367602T>G | CA393097285 | HCN4 | c.669A>C (p.Gln223His) | |
| 15 | g.73367603T>A | CA393097287 | HCN4 | c.668A>T (p.Gln223Leu) | |
| 15 | g.73367603T>C | CA393097290 | HCN4 | c.668A>G (p.Gln223Arg) | gnomAD v4 |
| 15 | g.73367603T>G | CA393097288 | HCN4 | c.668A>C (p.Gln223Pro) | |
| 15 | g.73367604G>A | CA393097292 | HCN4 | c.667C>T (p.Gln223Ter) | gnomAD v4 |
| 15 | g.73367604G>C | CA393097293 | HCN4 | c.667C>G (p.Gln223Glu) | |
| 15 | g.73367604G>T | CA393097295 | HCN4 | c.667C>A (p.Gln223Lys) | |
| 15 | g.73367605G>A | CA491479486 | HCN4 | c.666C>T (p.Leu222=) | |
| 15 | g.73367605G>C | CA7649441 | HCN4 | c.666C>G (p.Leu222=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73367605G= | CA2187194462 | HCN4 | c.666C= (p.Leu222=) | |
| 15 | g.73367605G>T | CA491479485 | HCN4 | c.666C>A (p.Leu222=) | |
| 15 | g.73367606A>C | CA393097297 | HCN4 | c.665T>G (p.Leu222Arg) | |
| 15 | g.73367606A>G | CA393097298 | HCN4 | c.665T>C (p.Leu222Pro) | |
| 15 | g.73367606A>T | CA393097300 | HCN4 | c.665T>A (p.Leu222His) | |
| 15 | g.73367607G>A | CA393097302 | HCN4 | c.664C>T (p.Leu222Phe) | |
| 15 | g.73367607G>C | CA393097303 | HCN4 | c.664C>G (p.Leu222Val) | gnomAD v4 |
| 15 | g.73367607G>T | CA393097304 | HCN4 | c.664C>A (p.Leu222Ile) | |
| 15 | g.73367608C>A | CA393097308 | HCN4 | c.663G>T (p.Met221Ile) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73367608C= | CA2187194463 | HCN4 | c.663G= (p.Met221=) | |
| 15 | g.73367608C>G | CA393097309 | HCN4 | c.663G>C (p.Met221Ile) | |
| 15 | g.73367608C>T | CA393097306 | HCN4 | c.663G>A (p.Met221Ile) | |
| 15 | g.73367609A>C | CA393097311 | HCN4 | c.662T>G (p.Met221Arg) | |
| 15 | g.73367609A>G | CA393097312 | HCN4 | c.662T>C (p.Met221Thr) | |
| 15 | g.73367609A>T | CA393097313 | HCN4 | c.662T>A (p.Met221Lys) | |
| 15 | g.73367610T>A | CA393097314 | HCN4 | c.661A>T (p.Met221Leu) | |
| 15 | g.73367610T>C | CA7649442 | HCN4 | c.661A>G (p.Met221Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73367610T>G | CA393097315 | HCN4 | c.661A>C (p.Met221Leu) | |
| 15 | g.73367610T= | CA2187194464 | HCN4 | c.661A= (p.Met221=) | |
| 15 | g.73367611G>A | CA491479487 | HCN4 | c.660C>T (p.Ala220=) | |
| 15 | g.73367611G>C | CA491479489 | HCN4 | c.660C>G (p.Ala220=) | |
| 15 | g.73367611G>T | CA491479488 | HCN4 | c.660C>A (p.Ala220=) | |
| 15 | g.73367612G>A | CA393097317 | HCN4 | c.659C>T (p.Ala220Val) | |
| 15 | g.73367612G>C | CA393097318 | HCN4 | c.659C>G (p.Ala220Gly) | |
| 15 | g.73367612G>T | CA393097320 | HCN4 | c.659C>A (p.Ala220Asp) | |
| 15 | g.73367613C>A | CA272700028 | HCN4 | c.658G>T (p.Ala220Ser) | ClinVar dbSNP gnomAD v2 |
| 15 | g.73367613C= | CA2187194465 | HCN4 | c.658G= (p.Ala220=) | |
| 15 | g.73367613C>G | CA393097321 | HCN4 | c.658G>C (p.Ala220Pro) | |
| 15 | g.73367613C>T | CA393097322 | HCN4 | c.658G>A (p.Ala220Thr) | dbSNP |
| 15 | g.73367614C>A | CA491479490 | HCN4 | c.657G>T (p.Gly219=) | |
| 15 | g.73367614C>G | CA491479491 | HCN4 | c.657G>C (p.Gly219=) | |
| 15 | g.73367614C>T | CA491479492 | HCN4 | c.657G>A (p.Gly219=) | |
| 15 | g.73367615C>A | CA393097326 | HCN4 | c.656G>T (p.Gly219Val) | |
| 15 | g.73367615C= | CA2187194466 | HCN4 | c.656G= (p.Gly219=) | |
| 15 | g.73367615C>G | CA393097327 | HCN4 | c.656G>C (p.Gly219Ala) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73367615C>T | CA393097324 | HCN4 | c.656G>A (p.Gly219Glu) | |
| 15 | g.73367616C>A | CA393097329 | HCN4 | c.655G>T (p.Gly219Trp) | dbSNP |
| 15 | g.73367616C= | CA2187194467 | HCN4 | c.655G= (p.Gly219=) | |
| 15 | g.73367616C>G | CA393097330 | HCN4 | c.655G>C (p.Gly219Arg) | |
| 15 | g.73367616C>T | CA393097331 | HCN4 | c.655G>A (p.Gly219Arg) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73367617G>A | CA7649443 | HCN4 | c.654C>T (p.Phe218=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73367617G>C | CA393097332 | HCN4 | c.654C>G (p.Phe218Leu) | |
| 15 | g.73367617G= | CA2187194468 | HCN4 | c.654C= (p.Phe218=) | |
| 15 | g.73367617G>T | CA393097333 | HCN4 | c.654C>A (p.Phe218Leu) | |
| 15 | g.73367618A= | CA2187194469 | HCN4 | c.653T= (p.Phe218=) | |
| 15 | g.73367618A>C | CA393097335 | HCN4 | c.653T>G (p.Phe218Cys) | |
| 15 | g.73367618A>G | CA393097338 | HCN4 | c.653T>C (p.Phe218Ser) | |
| 15 | g.73367618A>T | CA393097336 | HCN4 | c.653T>A (p.Phe218Tyr) | dbSNP |
| 15 | g.73367619A= | CA2187194470 | HCN4 | c.652T= (p.Phe218=) | |
| 15 | g.73367619A>C | CA393097340 | HCN4 | c.652T>G (p.Phe218Val) | dbSNP |
| 15 | g.73367619A>G | CA393097341 | HCN4 | c.652T>C (p.Phe218Leu) | |
| 15 | g.73367619A>T | CA393097343 | HCN4 | c.652T>A (p.Phe218Ile) | |
| 15 | g.73367620C>A | CA393097346 | HCN4 | c.651G>T (p.Gln217His) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73367620C= | CA2187194471 | HCN4 | c.651G= (p.Gln217=) | |
| 15 | g.73367620C>G | CA393097347 | HCN4 | c.651G>C (p.Gln217His) | gnomAD v4 |
| 15 | g.73367620C>T | CA491479493 | HCN4 | c.651G>A (p.Gln217=) | |
| 15 | g.73367621T>A | CA393097351 | HCN4 | c.650A>T (p.Gln217Leu) | gnomAD v4 |
| 15 | g.73367621T>C | CA393097352 | HCN4 | c.650A>G (p.Gln217Arg) | |
| 15 | g.73367621T>G | CA393097349 | HCN4 | c.650A>C (p.Gln217Pro) | |
| 15 | g.73367622G>A | CA393097355 | HCN4 | c.649C>T (p.Gln217Ter) | |
| 15 | g.73367622G>C | CA393097354 | HCN4 | c.649C>G (p.Gln217Glu) | |
| 15 | g.73367622G>T | CA393097357 | HCN4 | c.649C>A (p.Gln217Lys) | |
| 15 | g.73367623G>A | CA491479494 | HCN4 | c.648C>T (p.Arg216=) | |
| 15 | g.73367623G>C | CA491479495 | HCN4 | c.648C>G (p.Arg216=) | |
| 15 | g.73367623G>T | CA491479496 | HCN4 | c.648C>A (p.Arg216=) | |
| 15 | g.73367624C>A | CA393097359 | HCN4 | c.647G>T (p.Arg216Leu) | |
| 15 | g.73367624C>G | CA393097361 | HCN4 | c.647G>C (p.Arg216Pro) | |
| 15 | g.73367624C>T | CA393097362 | HCN4 | c.647G>A (p.Arg216His) | |
| 15 | g.73367625G>A | CA272700035 | HCN4 | c.646C>T (p.Arg216Cys) | dbSNP |
| 15 | g.73367625G>C | CA393097365 | HCN4 | c.646C>G (p.Arg216Gly) | ClinVar dbSNP |
| 15 | g.73367625G= | CA2187194472 | HCN4 | c.646C= (p.Arg216=) | |
| 15 | g.73367625G>T | CA393097366 | HCN4 | c.646C>A (p.Arg216Ser) | |
| 15 | g.73367626C>A | CA393097367 | HCN4 | c.645G>T (p.Gln215His) | |
| 15 | g.73367626C>G | CA393097368 | HCN4 | c.645G>C (p.Gln215His) | |
| 15 | g.73367626C>T | CA491479497 | HCN4 | c.645G>A (p.Gln215=) | |
| 15 | g.73367627T>A | CA393097371 | HCN4 | c.644A>T (p.Gln215Leu) | |
| 15 | g.73367627T>C | CA393097373 | HCN4 | c.644A>G (p.Gln215Arg) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73367627T>G | CA393097374 | HCN4 | c.644A>C (p.Gln215Pro) |