NIBAN1
niban apoptosis regulator 1
Summary
This gene encodes a member of the family with sequence similarity 129 protein family. This gene is highly expressed in several cancer cells and may serve as a prognostic marker for certain cancers. The encoded protein may play a role in regulating p53-mediated apoptosis. [provided by RefSeq, Sep 2016]
Known Variants70 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs682331 | 1:184,761,365 | A/T | — | — |
| rs775947562 | 1:184,764,116 | C/T | — | uncertain significance |
| rs201437304 | 1:184,764,167 | C/T | — | uncertain significance |
| rs147815528 | 1:184,764,181 | G/C | stop gained | — |
| rs547469636 | 1:184,764,272 | C/T | — | uncertain significance |
| rs749884547 | 1:184,764,286 | G/A | — | likely benign |
| rs141961108 | 1:184,764,287 | C/A | — | uncertain significance |
| rs760760777 | 1:184,764,336 | A/T | — | uncertain significance |
| rs35601690 | 1:184,764,410 | C/T | — | benign |
| rs578139767 | 1:184,764,455 | G/A | — | uncertain significance |
| rs769046244 | 1:184,764,462 | C/A | — | uncertain significance |
| rs773090679 | 1:184,764,466 | A/T | — | uncertain significance |
| rs2526489515 | 1:184,764,470 | G/A | — | uncertain significance |
| rs1231766756 | 1:184,764,488 | T/C | — | uncertain significance |
| rs776359250 | 1:184,764,520 | C/T | — | uncertain significance |
| rs769669832 | 1:184,764,527 | C/A | — | uncertain significance |
| rs1230607359 | 1:184,764,548 | C/G | — | uncertain significance |
| rs140276880 | 1:184,764,680 | C/T | — | likely benign |
| rs201876014 | 1:184,764,697 | G/A | — | uncertain significance |
| rs373614339 | 1:184,764,727 | A/G | — | uncertain significance |
| rs367621751 | 1:184,764,781 | G/A | — | uncertain significance |
| rs941929346 | 1:184,764,788 | T/C | — | uncertain significance |
| rs770359056 | 1:184,764,821 | C/G | — | uncertain significance |
| rs141082620 | 1:184,764,832 | G/T | — | uncertain significance |
| rs2526492202 | 1:184,764,869 | G/A | — | uncertain significance |
| rs894082811 | 1:184,764,874 | C/A | — | uncertain significance |
| rs75030920 | 1:184,764,908 | C/A | — | uncertain significance |
| rs760951913 | 1:184,764,922 | C/T | — | uncertain significance |
| rs762095918 | 1:184,772,720 | G/T | — | uncertain significance |
| rs1202172632 | 1:184,772,769 | G/T | — | uncertain significance |
| rs550538767 | 1:184,773,621 | G/T | — | — |
| rs371316368 | 1:184,775,090 | C/T | — | uncertain significance |
| rs139993256 | 1:184,775,133 | C/T | — | uncertain significance |
| rs777265482 | 1:184,775,142 | G/C | — | uncertain significance |
| rs764411941 | 1:184,775,169 | T/G | — | uncertain significance |
| rs141805525 | 1:184,777,287 | C/T | — | uncertain significance |
| rs200832703 | 1:184,777,288 | G/A | — | uncertain significance |
| rs369740091 | 1:184,777,344 | G/A | — | uncertain significance |
| rs771081777 | 1:184,777,360 | G/A | — | uncertain significance |
| rs1305419937 | 1:184,787,804 | G/T | — | uncertain significance |
| rs765565397 | 1:184,787,851 | A/G | — | uncertain significance |
| rs753085116 | 1:184,787,852 | C/A | — | uncertain significance |
| rs144571721 | 1:184,787,906 | G/C | — | uncertain significance |
| rs377436763 | 1:184,787,944 | G/A | — | uncertain significance |
| rs199974297 | 1:184,792,315 | A/G | — | likely benign |
| rs148732242 | 1:184,792,357 | C/T | — | uncertain significance |
| rs1443056845 | 1:184,792,381 | G/A | — | uncertain significance |
| rs746584140 | 1:184,792,457 | C/T | — | uncertain significance |
| rs376713721 | 1:184,792,822 | G/T | — | uncertain significance |
| rs756581844 | 1:184,800,986 | T/C | — | likely benign |
| rs780521763 | 1:184,800,997 | G/A | — | uncertain significance |
| rs200108989 | 1:184,801,022 | G/A | — | uncertain significance |
| rs144689007 | 1:184,801,036 | C/T | — | uncertain significance |
| rs200052631 | 1:184,801,049 | C/T | — | uncertain significance |
| rs495530 | 1:184,804,718 | C/G | — | — |
| rs116820598 | 1:184,853,810 | C/T | — | benign |
| rs748954236 | 1:184,853,811 | C/A | — | uncertain significance |
| rs112268696 | 1:184,853,857 | A/G | — | benign |
| rs373711868 | 1:184,853,889 | T/C | — | uncertain significance |
| rs140191774 | 1:184,853,890 | T/C | — | likely benign |
| rs763916159 | 1:184,859,254 | G/A | — | uncertain significance |
| rs201304773 | 1:184,863,215 | A/T | — | uncertain significance |
| rs760547105 | 1:184,863,244 | T/G | — | uncertain significance |
| rs151291324 | 1:184,863,250 | C/G | — | uncertain significance |
| rs1352445758 | 1:184,863,328 | G/A | — | uncertain significance |
| rs234640 | 1:184,867,830 | C/G | — | — |
| rs759605713 | 1:184,868,313 | T/G | — | uncertain significance |
| rs763675642 | 1:184,868,334 | G/A | — | uncertain significance |
| rs370523132 | 1:184,868,368 | C/T | — | uncertain significance |
| rs2525784352 | 1:184,943,461 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.