ZNF398
zinc finger protein 398
Summary
This gene encodes a member of the Kruppel family of C2H2-type zinc-finger transcription factor proteins. The encoded protein acts as a transcriptional activator. Two transcript variants encoding distinct isoforms have been identified for this gene. Other transcript variants have been described, but their full length sequence has not been determined. [provided by RefSeq, Jul 2008]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs144723593 | 7:148,840,186 | T/C | upstream gene variant | — |
| rs1794918591 | 7:148,851,172 | G/C | — | uncertain significance |
| rs1794920820 | 7:148,851,286 | C/A | — | uncertain significance |
| rs982829410 | 7:148,851,331 | G/A | — | uncertain significance |
| rs2535711839 | 7:148,851,403 | C/T | — | uncertain significance |
| rs12672745 | 7:148,852,434 | C/A | intron variant | — |
| rs1585532294 | 7:148,863,356 | A/G | — | uncertain significance |
| rs1295774572 | 7:148,863,917 | A/G | — | uncertain significance |
| rs2535746078 | 7:148,873,619 | G/A | — | uncertain significance |
| rs749782587 | 7:148,873,644 | A/C | — | uncertain significance |
| rs117490281 | 7:148,873,662 | G/A | — | uncertain significance |
| rs746687315 | 7:148,875,751 | G/A | — | uncertain significance |
| rs776343314 | 7:148,875,765 | A/T | — | uncertain significance |
| rs765158679 | 7:148,875,782 | C/T | — | uncertain significance |
| rs769646143 | 7:148,875,874 | A/G | — | likely benign |
| rs775243051 | 7:148,875,878 | C/T | — | uncertain significance |
| rs546325784 | 7:148,875,929 | G/A | — | uncertain significance |
| rs372016731 | 7:148,875,970 | C/A | — | uncertain significance |
| rs200631421 | 7:148,875,995 | C/T | — | uncertain significance |
| rs2535750140 | 7:148,876,075 | C/T | — | uncertain significance |
| rs762423694 | 7:148,876,138 | C/T | — | uncertain significance |
| rs1260044228 | 7:148,876,157 | C/T | — | uncertain significance |
| rs758415968 | 7:148,876,192 | C/T | — | uncertain significance |
| rs183707865 | 7:148,876,205 | C/T | — | uncertain significance |
| rs780321918 | 7:148,876,286 | G/A | — | uncertain significance |
| rs757002812 | 7:148,876,330 | C/T | — | uncertain significance |
| rs751484212 | 7:148,876,387 | C/T | — | uncertain significance |
| rs140891075 | 7:148,876,432 | A/G | — | uncertain significance |
| rs2535751358 | 7:148,876,465 | C/T | — | uncertain significance |
| rs774912149 | 7:148,876,589 | C/T | — | uncertain significance |
| rs369333287 | 7:148,876,658 | G/A | — | uncertain significance |
| rs532116376 | 7:148,876,694 | G/A | — | uncertain significance |
| rs116863926 | 7:148,876,736 | A/G | — | likely benign |
| rs188035814 | 7:148,876,763 | C/T | — | uncertain significance |
| rs201807737 | 7:148,876,783 | C/G | — | uncertain significance |
| rs143085255 | 7:148,876,786 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.