ZNF385B
zinc finger protein 385B
Summary
Enables p53 binding activity. Involved in intrinsic apoptotic signaling pathway by p53 class mediator. Located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs35165565 | 2:180,308,010 | G/A | — | benign |
| rs1463570303 | 2:180,308,012 | C/T | — | uncertain significance |
| rs756682404 | 2:180,308,063 | C/A | — | uncertain significance |
| rs774281320 | 2:180,308,171 | T/C | — | uncertain significance |
| rs779574586 | 2:180,309,616 | G/C | — | uncertain significance |
| rs2468439217 | 2:180,309,664 | T/A | — | uncertain significance |
| rs760630158 | 2:180,309,668 | C/T | — | uncertain significance |
| rs183122712 | 2:180,309,708 | A/G | — | benign |
| rs1216250114 | 2:180,310,353 | C/G | — | uncertain significance |
| rs372754906 | 2:180,310,408 | T/C | — | uncertain significance |
| rs1321394353 | 2:180,311,329 | T/C | — | uncertain significance |
| rs1160724623 | 2:180,311,384 | G/C | — | uncertain significance |
| rs775577501 | 2:180,311,393 | C/T | — | uncertain significance |
| rs763544764 | 2:180,311,422 | G/C | — | uncertain significance |
| rs771636656 | 2:180,311,423 | A/C | — | uncertain significance |
| rs757181258 | 2:180,311,464 | C/T | — | uncertain significance |
| rs780051817 | 2:180,348,046 | G/A | — | uncertain significance |
| rs1458585133 | 2:180,348,113 | T/A | — | uncertain significance |
| rs1389138012 | 2:180,348,115 | A/G | — | uncertain significance |
| rs146036736 | 2:180,383,268 | C/T | — | uncertain significance |
| rs531960671 | 2:180,397,741 | A/G | — | — |
| rs75024049 | 2:180,405,223 | C/A | intron variant | — |
| rs984503184 | 2:180,409,694 | T/C | — | uncertain significance |
| rs563885038 | 2:180,435,221 | G/A | — | — |
| rs2222030 | 2:180,493,998 | C/G | intron variant | — |
| rs6718154 | 2:180,497,923 | C/G | — | — |
| rs16866933 | 2:180,566,678 | G/A | regulatory region variant | — |
| rs11885327 | 2:180,568,073 | C/T | intron variant | — |
| rs73973711 | 2:180,579,238 | A/G | intron variant | — |
| rs1964081 | 2:180,591,421 | T/A | — | — |
| rs148987445 | 2:180,634,235 | C/A | — | benign |
| rs756106583 | 2:180,634,272 | G/A | — | uncertain significance |
| rs762392705 | 2:180,634,297 | C/T | — | likely benign |
| rs61744327 | 2:180,634,321 | G/A | — | benign |
| rs61747266 | 2:180,634,432 | G/A | — | benign |
| rs757231529 | 2:180,634,460 | C/T | — | uncertain significance |
| rs367921783 | 2:180,657,289 | A/G | — | — |
| rs1296008867 | 2:180,657,293 | A/G | — | — |
| rs551168461 | 2:180,675,510 | G/A | — | — |
| rs13407401 | 2:180,715,706 | T/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.