HCN1
hyperpolarization activated cyclic nucleotide gated potassium channel 1
Summary
The membrane protein encoded by this gene is a hyperpolarization-activated cation channel that contributes to the native pacemaker currents in heart and neurons. The encoded protein can homodimerize or heterodimerize with other pore-forming subunits to form a potassium channel. This channel may act as a receptor for sour tastes. [provided by RefSeq, Oct 2011]
Known Variants738 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2111833509 | 5:45,259,088 | C/A | — | uncertain significance |
| rs12522910 | 5:45,259,363 | T/C | 3 prime UTR variant | — |
| rs1283434459 | 5:45,262,036 | G/A | — | uncertain significance |
| rs757124569 | 5:45,262,037 | C/T | — | likely benign |
| rs775806199 | 5:45,262,042 | C/A | — | uncertain significance |
| rs56377228 | 5:45,262,055 | C/T | — | uncertain significance |
| rs768551046 | 5:45,262,056 | G/T | — | likely benign |
| rs774478577 | 5:45,262,060 | G/C | — | uncertain significance |
| rs761866949 | 5:45,262,061 | G/T | — | conflicting classifications of pathogenicity |
| rs773757463 | 5:45,262,062 | G/T | — | uncertain significance |
| rs2111838008 | 5:45,262,064 | C/G | — | uncertain significance |
| rs1340599360 | 5:45,262,076 | C/G | — | uncertain significance |
| rs199774910 | 5:45,262,081 | G/A | — | uncertain significance |
| rs1744747998 | 5:45,262,084 | G/A | — | uncertain significance |
| rs372807250 | 5:45,262,090 | C/T | — | conflicting classifications of pathogenicity |
| rs1207082922 | 5:45,262,091 | T/C | — | uncertain significance |
| rs1362126619 | 5:45,262,092 | T/C | — | likely benign |
| rs894086520 | 5:45,262,098 | A/G | — | likely benign |
| rs377177102 | 5:45,262,106 | C/T | — | uncertain significance |
| rs756753787 | 5:45,262,115 | G/T | — | conflicting classifications of pathogenicity |
| rs781250348 | 5:45,262,128 | G/T | — | likely benign |
| rs745821900 | 5:45,262,130 | C/T | — | uncertain significance |
| rs1744749557 | 5:45,262,131 | T/C | — | likely benign |
| rs755932633 | 5:45,262,132 | C/T | — | uncertain significance |
| rs2111838209 | 5:45,262,134 | T/G | — | likely benign |
| rs1060500094 | 5:45,262,135 | C/G | — | likely benign |
| rs534013981 | 5:45,262,136 | G/T | — | likely benign |
| rs140186173 | 5:45,262,137 | G/T | — | uncertain significance |
| rs1341530184 | 5:45,262,140 | C/A | — | likely benign |
| rs201368368 | 5:45,262,141 | G/C | — | uncertain significance |
| rs1194036783 | 5:45,262,145 | G/A | — | uncertain significance |
| rs772068771 | 5:45,262,146 | G/T | — | likely benign |
| rs1561078885 | 5:45,262,151 | C/A | — | uncertain significance |
| rs1158586028 | 5:45,262,155 | C/T | — | likely benign |
| rs572698864 | 5:45,262,156 | G/C | — | uncertain significance |
| rs1744751166 | 5:45,262,158 | C/T | — | likely benign |
| rs1477444033 | 5:45,262,159 | G/C | — | uncertain significance |
| rs1373191177 | 5:45,262,168 | C/A | — | uncertain significance |
| rs1046832984 | 5:45,262,169 | G/C | — | uncertain significance |
| rs1328423751 | 5:45,262,181 | C/A | — | uncertain significance |
| rs1561078915 | 5:45,262,182 | G/C | — | likely benign |
| rs368989823 | 5:45,262,189 | G/A | — | conflicting classifications of pathogenicity |
| rs767166082 | 5:45,262,197 | G/T | — | uncertain significance |
| rs199887416 | 5:45,262,201 | C/T | — | uncertain significance |
| rs756131996 | 5:45,262,204 | C/A | — | uncertain significance |
| rs780209007 | 5:45,262,205 | C/T | — | conflicting classifications of pathogenicity |
| rs2111838550 | 5:45,262,207 | C/T | — | uncertain significance |
| rs1484753978 | 5:45,262,208 | C/T | — | uncertain significance |
| rs1744753344 | 5:45,262,209 | T/C | — | likely benign |
| rs2111838570 | 5:45,262,218 | G/A | — | likely benign |
| rs1204287489 | 5:45,262,219 | C/T | — | uncertain significance |
| rs753637793 | 5:45,262,221 | C/G | — | likely benign |
| rs142485423 | 5:45,262,227 | G/A | — | likely benign |
| rs371602396 | 5:45,262,234 | G/A | — | conflicting classifications of pathogenicity |
| rs1197215604 | 5:45,262,241 | C/T | — | uncertain significance |
| rs747153982 | 5:45,262,242 | G/A | — | likely benign |
| rs2111838689 | 5:45,262,245 | T/C | — | likely benign |
| rs1413473165 | 5:45,262,249 | G/C | — | uncertain significance |
| rs375360013 | 5:45,262,251 | G/T | — | likely benign |
| rs2111838716 | 5:45,262,254 | G/A | — | likely benign |
| rs1356149824 | 5:45,262,257 | G/T | — | likely benign |
| rs777158203 | 5:45,262,258 | G/A | — | uncertain significance |
| rs2478181447 | 5:45,262,263 | G/A | — | likely benign |
| rs1744755026 | 5:45,262,266 | C/T | — | likely benign |
| rs727503956 | 5:45,262,268 | C/G | — | uncertain significance |
| rs774013410 | 5:45,262,269 | G/A | — | likely benign |
| rs1244303801 | 5:45,262,276 | G/C | — | conflicting classifications of pathogenicity |
| rs1035068089 | 5:45,262,277 | T/C | — | uncertain significance |
| rs1744759169 | 5:45,262,291 | G/C | — | uncertain significance |
| rs1461281527 | 5:45,262,292 | A/G | — | uncertain significance |
| rs766397326 | 5:45,262,300 | G/A | — | uncertain significance |
| rs2478181588 | 5:45,262,305 | C/T | — | likely benign |
| rs150936707 | 5:45,262,306 | A/C | — | conflicting classifications of pathogenicity |
| rs2111838849 | 5:45,262,308 | C/T | — | likely benign |
| rs754764304 | 5:45,262,314 | G/A | — | likely benign |
| rs1579762540 | 5:45,262,317 | C/T | — | likely benign |
| rs140758934 | 5:45,262,321 | G/A | — | uncertain significance |
| rs948061807 | 5:45,262,332 | G/A | — | likely benign |
| rs778039525 | 5:45,262,343 | G/A | — | conflicting classifications of pathogenicity |
| rs2111838926 | 5:45,262,345 | C/T | — | uncertain significance |
| rs1338055183 | 5:45,262,350 | T/C | — | likely benign |
| rs781686163 | 5:45,262,355 | G/C | — | likely benign |
| rs2478181744 | 5:45,262,357 | G/A | — | uncertain significance |
| rs1307516754 | 5:45,262,367 | T/C | — | uncertain significance |
| rs770127695 | 5:45,262,368 | G/A | — | likely benign |
| rs2111838973 | 5:45,262,370 | T/C | — | likely benign |
| rs149702217 | 5:45,262,375 | A/G | — | likely benign |
| rs1232040161 | 5:45,262,378 | G/C | — | uncertain significance |
| rs975750493 | 5:45,262,382 | G/C | — | uncertain significance |
| rs749727167 | 5:45,262,386 | G/A | — | likely benign |
| rs773048153 | 5:45,262,390 | T/C | — | likely benign |
| rs1561079128 | 5:45,262,393 | T/G | — | uncertain significance |
| rs760215449 | 5:45,262,394 | G/C | — | uncertain significance |
| rs776567935 | 5:45,262,400 | C/T | — | uncertain significance |
| rs933648147 | 5:45,262,401 | A/G | — | likely benign |
| rs1437053801 | 5:45,262,408 | G/C | — | uncertain significance |
| rs2478181891 | 5:45,262,409 | G/A | — | uncertain significance |
| rs2111839064 | 5:45,262,412 | T/A | — | uncertain significance |
| rs1744761859 | 5:45,262,417 | C/G | — | uncertain significance |
| rs1579762677 | 5:45,262,426 | G/A | — | likely benign |
Showing 100 of 738 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.