HCN3
hyperpolarization activated cyclic nucleotide gated potassium channel 3
Summary
This gene encodes a multi-pass membrane protein that functions as a voltage gated cation channel. The encoded protein is a member of a family of closely related cyclic adenosine monophosphate-binding channel proteins. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1673858245 | 1:155,247,417 | C/A | — | uncertain significance |
| rs780507850 | 1:155,247,466 | C/T | — | uncertain significance |
| rs2525126973 | 1:155,247,488 | C/G | — | uncertain significance |
| rs931272117 | 1:155,247,583 | C/T | — | uncertain significance |
| rs11264349 | 1:155,248,113 | A/C | — | — |
| rs559374581 | 1:155,250,058 | T/A | — | — |
| rs960904131 | 1:155,252,239 | G/A | — | uncertain significance |
| rs764405079 | 1:155,252,288 | A/C | — | uncertain significance |
| rs765836236 | 1:155,252,305 | G/A | — | uncertain significance |
| rs1172005432 | 1:155,252,354 | A/G | — | uncertain significance |
| rs2525183275 | 1:155,253,778 | C/A | — | uncertain significance |
| rs765123608 | 1:155,253,814 | A/C | — | uncertain significance |
| rs750317134 | 1:155,253,816 | C/A | — | uncertain significance |
| rs2525184942 | 1:155,253,913 | T/C | — | uncertain significance |
| rs753984470 | 1:155,254,432 | G/C | — | uncertain significance |
| rs199623311 | 1:155,254,437 | G/T | — | uncertain significance |
| rs201298503 | 1:155,255,022 | G/A | — | uncertain significance |
| rs774674306 | 1:155,255,037 | C/T | — | uncertain significance |
| rs867092241 | 1:155,255,054 | G/A | — | uncertain significance |
| rs772287358 | 1:155,255,092 | C/T | — | uncertain significance |
| rs112470069 | 1:155,255,098 | G/A | — | uncertain significance |
| rs576680898 | 1:155,255,536 | C/T | — | uncertain significance |
| rs752440221 | 1:155,255,539 | G/A | — | uncertain significance |
| rs781614213 | 1:155,255,597 | T/C | — | uncertain significance |
| rs753739215 | 1:155,255,641 | G/A | — | uncertain significance |
| rs141817871 | 1:155,255,673 | G/A | — | uncertain significance |
| rs151135773 | 1:155,255,701 | G/A | — | uncertain significance |
| rs137971983 | 1:155,255,719 | C/T | — | uncertain significance |
| rs41264937 | 1:155,257,087 | G/C | — | uncertain significance |
| rs144688517 | 1:155,257,113 | C/T | — | uncertain significance |
| rs774471370 | 1:155,257,122 | C/T | — | uncertain significance |
| rs139768739 | 1:155,257,596 | G/T | — | uncertain significance |
| rs897179968 | 1:155,257,727 | C/T | — | uncertain significance |
| rs569376899 | 1:155,257,860 | G/A | — | uncertain significance |
| rs149880612 | 1:155,257,935 | C/T | — | uncertain significance |
| rs577533643 | 1:155,257,991 | C/T | — | likely benign |
| rs2525237554 | 1:155,258,015 | C/A | — | uncertain significance |
| rs763111047 | 1:155,258,051 | C/G | — | uncertain significance |
| rs770306788 | 1:155,258,052 | G/A | — | uncertain significance |
| rs369748993 | 1:155,258,057 | C/T | — | uncertain significance |
| rs200468064 | 1:155,258,141 | C/T | — | uncertain significance |
| rs757620410 | 1:155,258,172 | C/G | — | uncertain significance |
| rs754284796 | 1:155,258,222 | C/T | — | uncertain significance |
| rs376990594 | 1:155,258,225 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.