ZC3H12C
zinc finger CCCH-type containing 12C
Summary
Predicted to enable RNA endonuclease activity and mRNA binding activity. Predicted to be active in cytoplasmic ribonucleoprotein granule and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants50 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs4561177 | 11:109,962,432 | A/G | upstream gene variant | — |
| rs4356188 | 11:109,963,745 | C/G | regulatory region variant | — |
| rs768813122 | 11:109,964,150 | G/C | — | uncertain significance |
| rs7116683 | 11:109,964,257 | A/C | — | — |
| rs10891054 | 11:109,966,513 | A/C | regulatory region variant | — |
| rs6589112 | 11:109,971,929 | T/C | intron variant | — |
| rs7128556 | 11:109,972,228 | G/A | intron variant | — |
| rs746463 | 11:109,995,944 | C/G | — | — |
| rs201314969 | 11:110,007,394 | G/A | — | uncertain significance |
| rs760670937 | 11:110,007,448 | C/T | — | uncertain significance |
| rs368225431 | 11:110,007,449 | G/A | — | likely benign |
| rs766223495 | 11:110,007,485 | A/G | — | uncertain significance |
| rs752698103 | 11:110,007,493 | G/A | — | likely benign |
| rs757729109 | 11:110,007,611 | A/G | — | uncertain significance |
| rs2496709338 | 11:110,007,640 | G/A | — | uncertain significance |
| rs368637944 | 11:110,007,706 | A/G | — | uncertain significance |
| rs775161683 | 11:110,007,721 | C/G | — | uncertain significance |
| rs182300452 | 11:110,007,743 | T/C | — | uncertain significance |
| rs750859968 | 11:110,007,746 | A/T | — | uncertain significance |
| rs778011615 | 11:110,007,748 | C/T | — | uncertain significance |
| rs1565260394 | 11:110,007,753 | C/G | — | uncertain significance |
| rs377391499 | 11:110,007,764 | G/T | — | uncertain significance |
| rs1325841742 | 11:110,007,811 | T/A | — | uncertain significance |
| rs200420973 | 11:110,007,835 | G/A | — | uncertain significance |
| rs762024976 | 11:110,007,845 | G/A | — | uncertain significance |
| rs751932671 | 11:110,007,893 | A/G | — | uncertain significance |
| rs779618188 | 11:110,008,078 | G/T | — | uncertain significance |
| rs769984848 | 11:110,008,135 | A/G | — | uncertain significance |
| rs368667714 | 11:110,023,658 | A/C | — | uncertain significance |
| rs200240485 | 11:110,029,996 | G/A | — | uncertain significance |
| rs747122949 | 11:110,030,073 | G/A | — | uncertain significance |
| rs895276058 | 11:110,030,213 | C/G | — | uncertain significance |
| rs1383017256 | 11:110,034,102 | A/T | — | uncertain significance |
| rs769365245 | 11:110,035,171 | C/T | — | uncertain significance |
| rs1862540042 | 11:110,035,227 | A/G | — | uncertain significance |
| rs757239149 | 11:110,035,374 | G/A | — | uncertain significance |
| rs2496758926 | 11:110,035,432 | G/A | — | uncertain significance |
| rs957424554 | 11:110,035,494 | A/G | — | uncertain significance |
| rs1862547459 | 11:110,035,566 | G/A | — | uncertain significance |
| rs199586562 | 11:110,035,576 | A/G | — | uncertain significance |
| rs779988811 | 11:110,035,747 | G/A | — | uncertain significance |
| rs377669177 | 11:110,035,770 | C/T | — | uncertain significance |
| rs770955983 | 11:110,035,834 | C/T | — | uncertain significance |
| rs1163990721 | 11:110,035,886 | C/G | — | uncertain significance |
| rs779103613 | 11:110,036,007 | C/T | — | uncertain significance |
| rs2496760440 | 11:110,036,068 | A/C | — | uncertain significance |
| rs1345351899 | 11:110,036,112 | T/A | — | uncertain significance |
| rs751878934 | 11:110,036,233 | C/T | — | uncertain significance |
| rs553171095 | 11:110,036,361 | C/A | — | uncertain significance |
| rs774369678 | 11:110,036,400 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.