ZNF655
zinc finger protein 655
Summary
This gene encodes a zinc finger protein. The zinc finger proteins are involved in DNA binding and protein-protein interactions. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1002844163 | 7:99,158,195 | C/A | — | uncertain significance |
| rs771662591 | 7:99,158,294 | G/A | — | uncertain significance |
| rs182669800 | 7:99,161,491 | C/T | regulatory region variant | — |
| rs11974702 | 7:99,163,951 | A/G | intron variant | — |
| rs766547001 | 7:99,169,343 | C/G | — | uncertain significance |
| rs753484017 | 7:99,169,919 | C/T | — | uncertain significance |
| rs747015316 | 7:99,169,963 | C/T | — | uncertain significance |
| rs754701419 | 7:99,169,966 | G/A | — | uncertain significance |
| rs139434238 | 7:99,170,132 | C/T | — | uncertain significance |
| rs143554866 | 7:99,170,199 | C/T | — | likely benign |
| rs200383277 | 7:99,170,207 | A/G | — | likely benign |
| rs755874656 | 7:99,170,268 | T/G | — | uncertain significance |
| rs369268619 | 7:99,170,360 | A/T | — | uncertain significance |
| rs140597113 | 7:99,170,423 | A/G | — | uncertain significance |
| rs538145078 | 7:99,170,491 | A/C | — | uncertain significance |
| rs372852114 | 7:99,170,529 | A/G | — | likely benign |
| rs760272114 | 7:99,170,567 | C/A | — | uncertain significance |
| rs1271544001 | 7:99,170,752 | C/T | — | uncertain significance |
| rs145746848 | 7:99,170,758 | T/C | — | uncertain significance |
| rs1804209108 | 7:99,170,789 | A/G | — | uncertain significance |
| rs1443966918 | 7:99,170,948 | A/G | — | uncertain significance |
| rs757092547 | 7:99,170,953 | C/G | — | uncertain significance |
| rs1252093062 | 7:99,170,963 | A/G | — | uncertain significance |
| rs765307282 | 7:99,170,987 | A/C | — | uncertain significance |
| rs2484698284 | 7:99,171,059 | G/A | — | uncertain significance |
| rs150697742 | 7:99,171,093 | A/T | — | uncertain significance |
| rs74709169 | 7:99,171,127 | T/G | — | benign |
| rs2484698674 | 7:99,171,148 | T/C | — | uncertain significance |
| rs769968880 | 7:99,171,175 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.