ZC3H3
zinc finger CCCH-type containing 3
Summary
Predicted to enable DNA binding activity; R-SMAD binding activity; and zinc ion binding activity. Predicted to be involved in mRNA transport. Predicted to act upstream of or within mRNA 3'-end processing and positive regulation of activin receptor signaling pathway. Located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants91 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs755614487 | 8:144,522,215 | G/A | — | likely benign |
| rs112624965 | 8:144,522,222 | G/C | — | uncertain significance |
| rs115456950 | 8:144,522,247 | C/A | — | benign |
| rs147697502 | 8:144,522,278 | C/G | — | conflicting classifications of pathogenicity |
| rs562469901 | 8:144,522,336 | G/T | — | uncertain significance |
| rs200152789 | 8:144,522,399 | G/A | — | uncertain significance |
| rs141703643 | 8:144,522,474 | G/C | — | uncertain significance |
| rs759555801 | 8:144,522,489 | G/A | — | uncertain significance |
| rs146240989 | 8:144,522,529 | G/A | — | likely benign |
| rs756631579 | 8:144,523,172 | G/A | — | uncertain significance |
| rs376452593 | 8:144,523,193 | C/T | — | likely benign |
| rs776331845 | 8:144,523,194 | G/A | — | uncertain significance |
| rs759395862 | 8:144,523,196 | T/A | — | uncertain significance |
| rs368841712 | 8:144,523,205 | C/T | — | uncertain significance |
| rs373236426 | 8:144,523,232 | C/T | — | uncertain significance |
| rs754359844 | 8:144,523,241 | G/A | — | likely benign |
| rs1002361809 | 8:144,523,242 | C/A | — | uncertain significance |
| rs190324157 | 8:144,537,022 | G/C | regulatory region variant | — |
| rs138004837 | 8:144,539,721 | C/T | intron variant | — |
| rs113716075 | 8:144,547,942 | C/T | — | uncertain significance |
| rs367545625 | 8:144,550,607 | G/A | — | uncertain significance |
| rs746306450 | 8:144,550,799 | C/T | — | uncertain significance |
| rs202075905 | 8:144,557,573 | C/T | — | uncertain significance |
| rs149988955 | 8:144,557,582 | G/T | — | uncertain significance |
| rs763445850 | 8:144,557,583 | G/A | — | uncertain significance |
| rs373613798 | 8:144,557,594 | G/A | — | uncertain significance |
| rs763733445 | 8:144,557,595 | C/T | — | uncertain significance |
| rs2537728150 | 8:144,557,669 | T/C | — | uncertain significance |
| rs147928863 | 8:144,557,699 | G/A | — | uncertain significance |
| rs380904 | 8:144,565,905 | A/G | intron variant | — |
| rs410836 | 8:144,576,849 | A/C | — | — |
| rs574135193 | 8:144,585,902 | A/G | — | — |
| rs188617864 | 8:144,588,521 | C/G | intron variant | — |
| rs142965748 | 8:144,589,932 | G/A | — | uncertain significance |
| rs149025999 | 8:144,589,985 | G/A | — | likely benign |
| rs7826922 | 8:144,600,768 | C/T | regulatory region variant | — |
| rs6558369 | 8:144,604,786 | C/A | — | — |
| rs921667 | 8:144,610,033 | T/C | regulatory region variant | — |
| rs2382955 | 8:144,613,172 | C/T | — | — |
| rs6558370 | 8:144,617,691 | A/G | intron variant | — |
| rs149514479 | 8:144,618,434 | G/C | — | likely benign |
| rs1822792391 | 8:144,618,438 | G/A | — | uncertain significance |
| rs527397487 | 8:144,618,442 | G/A | — | uncertain significance |
| rs2537834312 | 8:144,618,447 | G/A | — | uncertain significance |
| rs757727180 | 8:144,618,451 | G/A | — | uncertain significance |
| rs531200439 | 8:144,618,465 | C/T | — | uncertain significance |
| rs771961082 | 8:144,618,466 | G/A | — | likely benign |
| rs907942932 | 8:144,618,474 | C/T | — | uncertain significance |
| rs770813041 | 8:144,618,547 | C/T | — | uncertain significance |
| rs762712152 | 8:144,618,559 | G/A | — | uncertain significance |
| rs4874147 | 8:144,620,183 | T/A | missense variant | — |
| rs753785236 | 8:144,620,224 | G/A | — | uncertain significance |
| rs754913575 | 8:144,620,225 | C/A | — | uncertain significance |
| rs2130521284 | 8:144,620,249 | G/A | — | uncertain significance |
| rs1371031135 | 8:144,620,291 | A/T | — | uncertain significance |
| rs1344195461 | 8:144,620,294 | G/C | — | uncertain significance |
| rs145312531 | 8:144,620,334 | C/G | — | likely benign |
| rs2537839324 | 8:144,620,336 | T/C | — | uncertain significance |
| rs752249331 | 8:144,620,429 | G/T | — | uncertain significance |
| rs2537840025 | 8:144,620,456 | G/A | — | uncertain significance |
| rs777810790 | 8:144,620,471 | C/T | — | uncertain significance |
| rs867932072 | 8:144,620,504 | C/T | — | uncertain significance |
| rs778569392 | 8:144,620,563 | C/T | — | uncertain significance |
| rs770790299 | 8:144,620,572 | C/G | — | uncertain significance |
| rs139016238 | 8:144,620,618 | G/A | — | uncertain significance |
| rs2537840851 | 8:144,620,642 | C/T | — | uncertain significance |
| rs777874268 | 8:144,620,668 | C/A | — | uncertain significance |
| rs1822886217 | 8:144,620,704 | G/A | — | likely benign |
| rs765556938 | 8:144,620,824 | C/T | — | uncertain significance |
| rs150666715 | 8:144,620,837 | C/T | — | likely benign |
| rs2537841931 | 8:144,620,847 | G/C | — | uncertain significance |
| rs2537842097 | 8:144,620,884 | G/A | — | uncertain significance |
| rs560861663 | 8:144,620,888 | G/A | — | uncertain significance |
| rs139064874 | 8:144,620,891 | G/A | — | uncertain significance |
| rs186238217 | 8:144,620,899 | C/T | — | uncertain significance |
| rs758053909 | 8:144,620,902 | G/C | — | uncertain significance |
| rs776589420 | 8:144,620,985 | A/C | — | uncertain significance |
| rs547169616 | 8:144,621,007 | G/T | — | uncertain significance |
| rs774684604 | 8:144,621,041 | G/A | — | uncertain significance |
| rs755125057 | 8:144,621,110 | G/A | — | uncertain significance |
| rs748458246 | 8:144,621,115 | G/A | — | likely benign |
| rs754433835 | 8:144,621,210 | A/C | — | uncertain significance |
| rs757255382 | 8:144,621,241 | C/T | — | uncertain significance |
| rs754166703 | 8:144,621,245 | C/G | — | uncertain significance |
| rs200115197 | 8:144,621,256 | G/A | — | uncertain significance |
| rs146214248 | 8:144,621,294 | C/A | — | likely benign |
| rs185805345 | 8:144,621,302 | G/A | — | uncertain significance |
| rs201808943 | 8:144,621,356 | C/T | missense variant | — |
| rs571985943 | 8:144,621,361 | C/T | — | uncertain significance |
| rs201294393 | 8:144,621,371 | G/A | — | uncertain significance |
| rs762378930 | 8:144,621,452 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.