ZSCAN25
zinc finger and SCAN domain containing 25
Summary
This gene encodes a protein that bears some similarity to zinc finger proteins, which are involved in DNA binding and protein-protein interactions. Multiple alternatively spliced transcript variants have been identified, but the full-length nature for most of them has not been determined. [provided by RefSeq, Jul 2008]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs368474689 | 7:99,217,239 | G/A | — | uncertain significance |
| rs554605817 | 7:99,217,245 | C/T | — | uncertain significance |
| rs760714597 | 7:99,217,251 | A/G | — | uncertain significance |
| rs767644729 | 7:99,217,277 | G/T | — | uncertain significance |
| rs756644497 | 7:99,217,279 | G/A | — | uncertain significance |
| rs778290807 | 7:99,217,281 | A/G | — | likely benign |
| rs752788524 | 7:99,217,375 | G/A | — | uncertain significance |
| rs746507735 | 7:99,217,435 | G/A | — | likely benign |
| rs147649020 | 7:99,217,515 | C/T | — | uncertain significance |
| rs138663458 | 7:99,217,543 | A/G | — | uncertain significance |
| rs200781115 | 7:99,219,032 | G/A | — | uncertain significance |
| rs2484929425 | 7:99,219,054 | A/T | — | uncertain significance |
| rs749364084 | 7:99,219,111 | G/C | — | uncertain significance |
| rs761250562 | 7:99,219,152 | C/T | — | uncertain significance |
| rs137966152 | 7:99,220,177 | C/T | — | uncertain significance |
| rs200142949 | 7:99,220,190 | C/T | — | uncertain significance |
| rs751974406 | 7:99,220,214 | A/G | — | uncertain significance |
| rs1320943015 | 7:99,220,253 | C/T | — | uncertain significance |
| rs750060095 | 7:99,221,762 | T/C | — | uncertain significance |
| rs142244690 | 7:99,226,834 | G/A | — | uncertain significance |
| rs762255222 | 7:99,226,838 | C/T | — | uncertain significance |
| rs2485036238 | 7:99,226,873 | G/C | — | uncertain significance |
| rs1314697023 | 7:99,226,886 | C/T | — | uncertain significance |
| rs369736997 | 7:99,226,898 | G/C | — | uncertain significance |
| rs142763697 | 7:99,226,927 | G/A | — | uncertain significance |
| rs201439642 | 7:99,226,948 | C/G | — | uncertain significance |
| rs775491139 | 7:99,227,008 | C/G | — | uncertain significance |
| rs771385033 | 7:99,227,059 | C/T | — | uncertain significance |
| rs771610970 | 7:99,227,075 | G/C | — | uncertain significance |
| rs2151296962 | 7:99,227,087 | G/A | — | uncertain significance |
| rs751460606 | 7:99,227,218 | G/A | — | uncertain significance |
| rs2485045703 | 7:99,227,343 | C/A | — | uncertain significance |
| rs200089234 | 7:99,227,357 | G/A | — | uncertain significance |
| rs757239096 | 7:99,227,363 | C/T | — | uncertain significance |
| rs1807841452 | 7:99,227,449 | A/G | — | uncertain significance |
| rs746749402 | 7:99,227,630 | C/A | — | uncertain significance |
| rs6465750 | 7:99,235,522 | C/T | downstream gene variant | — |
| rs10242455 | 7:99,240,179 | A/G | upstream gene variant | — |
| rs188845491 | 7:99,286,639 | C/T | intergenic variant | — |
| rs1818797 | 7:99,296,195 | G/C | — | — |
| rs2740563 | 7:99,302,113 | T/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.