ZNF184
zinc finger protein 184
Summary
The protein encoded by this gene is predicted to be a Kruppel C2H2-type zinc-finger protein family member. Sequence analysis predicts that the protein contains two Kruppel associated box (KRAB) boxes in the N-terminus and highly conserved zinc finger motifs at the C-terminus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2016]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs12525255 | 6:27,377,668 | T/G | — | — |
| rs13196692 | 6:27,379,119 | C/T | downstream gene variant | — |
| rs4711152 | 6:27,380,202 | T/C | downstream gene variant | — |
| rs34953377 | 6:27,381,660 | T/C | intergenic variant | — |
| rs34150729 | 6:27,388,754 | T/C | intergenic variant | — |
| rs551668502 | 6:27,389,935 | G/C | — | — |
| rs13191227 | 6:27,390,115 | G/C | intergenic variant | — |
| rs34185469 | 6:27,391,935 | G/A | intergenic variant | — |
| rs12526495 | 6:27,393,871 | G/T | — | — |
| rs35716472 | 6:27,406,607 | C/G | intergenic variant | — |
| rs76439045 | 6:27,411,729 | A/C | intergenic variant | — |
| rs35394453 | 6:27,413,831 | A/T | downstream gene variant | — |
| rs79225736 | 6:27,414,500 | C/T | downstream gene variant | — |
| rs2481285776 | 6:27,419,190 | G/C | — | uncertain significance |
| rs760994009 | 6:27,419,224 | T/C | — | uncertain significance |
| rs45466497 | 6:27,419,297 | G/A | — | uncertain significance |
| rs73741730 | 6:27,419,334 | C/T | — | benign |
| rs145402588 | 6:27,419,389 | G/A | — | uncertain significance |
| rs2481286986 | 6:27,419,438 | T/G | — | uncertain significance |
| rs1010441463 | 6:27,419,440 | T/G | — | uncertain significance |
| rs774034887 | 6:27,419,468 | G/C | — | uncertain significance |
| rs2481287370 | 6:27,419,513 | T/C | — | uncertain significance |
| rs1202753256 | 6:27,419,896 | T/C | — | uncertain significance |
| rs893193771 | 6:27,419,908 | T/C | — | uncertain significance |
| rs201533442 | 6:27,419,968 | T/C | — | uncertain significance |
| rs2481289638 | 6:27,420,012 | C/T | — | likely benign |
| rs1458588034 | 6:27,420,062 | C/T | — | uncertain significance |
| rs2481291039 | 6:27,420,319 | C/T | — | uncertain significance |
| rs759584230 | 6:27,420,437 | T/G | — | uncertain significance |
| rs927061999 | 6:27,420,509 | G/T | — | uncertain significance |
| rs535511048 | 6:27,420,580 | T/C | — | uncertain significance |
| rs2481292511 | 6:27,420,649 | G/C | — | uncertain significance |
| rs1479336627 | 6:27,420,710 | T/C | — | uncertain significance |
| rs376073172 | 6:27,420,724 | G/A | — | uncertain significance |
| rs182253281 | 6:27,420,781 | C/T | — | uncertain significance |
| rs151024306 | 6:27,421,022 | C/G | — | uncertain significance |
| rs761422824 | 6:27,424,620 | C/T | — | uncertain significance |
| rs1762868491 | 6:27,424,642 | C/A | — | uncertain significance |
| rs77649000 | 6:27,424,872 | T/C | intron variant | — |
| rs193921063 | 6:27,425,151 | G/T | — | uncertain significance |
| rs1310854527 | 6:27,425,172 | T/C | — | uncertain significance |
| rs1353537306 | 6:27,425,187 | T/A | — | uncertain significance |
| rs41269265 | 6:27,425,349 | T/C | intron variant | — |
| rs756596895 | 6:27,435,673 | G/A | — | uncertain significance |
| rs149866169 | 6:27,441,723 | T/A | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.