BANP
BTG3 associated nuclear protein
Summary
This gene encodes a protein that binds to matrix attachment regions. The protein forms a complex with p53 and negatively regulates p53 transcription, and functions as a tumor suppressor and cell cycle regulator. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010]
Known Variants50 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs141103485 | 16:87,983,111 | G/A | upstream gene variant | — |
| rs4843747 | 16:87,991,051 | A/C | intron variant | — |
| rs6540125 | 16:87,993,889 | T/G | intron variant | — |
| rs11117317 | 16:88,000,503 | T/A | — | — |
| rs8052276 | 16:88,004,592 | T/G | — | — |
| rs12931143 | 16:88,006,065 | T/A | — | — |
| rs12927305 | 16:88,006,413 | C/T | intron variant | — |
| rs12932202 | 16:88,006,931 | A/G | intron variant | — |
| rs11117325 | 16:88,007,142 | G/T | — | — |
| rs2509658253 | 16:88,008,782 | G/A | — | uncertain significance |
| rs11117342 | 16:88,011,003 | C/T | intron variant | — |
| rs4843292 | 16:88,013,496 | A/G | intron variant | — |
| rs1243700629 | 16:88,014,677 | G/A | — | uncertain significance |
| rs28599942 | 16:88,017,220 | G/A | regulatory region variant | — |
| rs28690689 | 16:88,017,251 | C/G | regulatory region variant | — |
| rs1294050486 | 16:88,017,731 | A/T | — | uncertain significance |
| rs778185407 | 16:88,017,781 | C/T | — | uncertain significance |
| rs763999087 | 16:88,017,796 | G/A | — | uncertain significance |
| rs1331569719 | 16:88,017,843 | C/G | — | uncertain significance |
| rs34759388 | 16:88,023,556 | A/C | — | — |
| rs141920044 | 16:88,032,189 | C/G | — | — |
| rs552523709 | 16:88,034,329 | C/T | — | — |
| rs1473868674 | 16:88,037,982 | C/G | — | uncertain significance |
| rs773807056 | 16:88,039,710 | G/A | — | uncertain significance |
| rs766622078 | 16:88,039,713 | G/A | — | uncertain significance |
| rs139021637 | 16:88,039,725 | T/C | — | uncertain significance |
| rs778562002 | 16:88,039,834 | C/T | — | likely benign |
| rs1555586650 | 16:88,052,070 | A/G | — | uncertain significance |
| rs200770109 | 16:88,061,168 | G/A | — | benign |
| rs1275748600 | 16:88,061,203 | C/T | — | uncertain significance |
| rs746118781 | 16:88,061,251 | C/T | — | uncertain significance |
| rs2078564683 | 16:88,066,727 | G/T | — | uncertain significance |
| rs373284033 | 16:88,066,754 | C/T | — | uncertain significance |
| rs201270619 | 16:88,066,766 | C/A | — | uncertain significance |
| rs1205198992 | 16:88,066,780 | C/G | — | uncertain significance |
| rs143210504 | 16:88,066,795 | G/T | — | uncertain significance |
| rs766256387 | 16:88,068,987 | C/T | — | uncertain significance |
| rs11641834 | 16:88,070,573 | C/T | intron variant | — |
| rs1466957229 | 16:88,071,612 | G/A | — | uncertain significance |
| rs62046862 | 16:88,073,029 | C/T | — | — |
| rs12922388 | 16:88,073,699 | G/T | intron variant | — |
| rs72818533 | 16:88,073,841 | G/A | intron variant | — |
| rs144169197 | 16:88,099,916 | C/T | intron variant | — |
| rs185736886 | 16:88,101,699 | T/C | intron variant | — |
| rs577190967 | 16:88,105,724 | C/T | — | uncertain significance |
| rs147469146 | 16:88,105,759 | G/A | — | uncertain significance |
| rs371819708 | 16:88,105,805 | C/T | — | uncertain significance |
| rs2545014569 | 16:88,105,817 | A/G | — | uncertain significance |
| rs762644063 | 16:88,110,238 | C/T | — | uncertain significance |
| rs1157702891 | 16:88,110,258 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.