ZC3H14
zinc finger CCCH-type containing 14
Summary
The protein encoded by this gene is a poly(A)-binding protein that can affect gene expression and poly(A) tail length. The encoded protein may influence mRNA stability, nuclear export, and translation. [provided by RefSeq, May 2016]
Known Variants83 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs199820387 | 14:89,030,006 | G/A | — | likely benign |
| rs774260587 | 14:89,030,009 | G/A | — | likely benign |
| rs201210664 | 14:89,030,056 | G/T | — | uncertain significance |
| rs9743523 | 14:89,032,298 | G/C | — | — |
| rs955426931 | 14:89,034,456 | G/C | — | likely benign |
| rs764670721 | 14:89,034,474 | C/G | — | uncertain significance |
| rs140187818 | 14:89,034,492 | C/T | — | likely benign |
| rs755512386 | 14:89,038,388 | A/G | — | uncertain significance |
| rs765219941 | 14:89,038,402 | C/T | — | likely benign |
| rs755865736 | 14:89,038,420 | C/T | — | likely benign |
| rs80289104 | 14:89,038,424 | C/G | — | benign |
| rs1566896262 | 14:89,038,432 | C/T | — | likely benign |
| rs772949764 | 14:89,038,449 | G/A | — | uncertain significance |
| rs779703453 | 14:89,038,506 | G/A | — | uncertain significance |
| rs144937491 | 14:89,038,567 | C/T | — | likely benign |
| rs77755006 | 14:89,038,919 | T/C | — | likely benign |
| rs2080577589 | 14:89,038,929 | T/C | — | uncertain significance |
| rs185224589 | 14:89,038,931 | C/T | — | likely benign |
| rs886037950 | 14:89,038,950 | C/T | stop gained | no classifications from unflagged records |
| rs369352459 | 14:89,039,124 | A/G | — | uncertain significance |
| rs777903485 | 14:89,039,186 | G/T | — | uncertain significance |
| rs564069379 | 14:89,039,204 | G/A | — | likely benign |
| rs797046115 | 14:89,039,226 | C/G | — | uncertain significance |
| rs144601125 | 14:89,039,234 | T/C | — | likely benign |
| rs761566277 | 14:89,039,305 | C/T | — | uncertain significance |
| rs116690538 | 14:89,039,308 | A/G | — | uncertain significance |
| rs376420911 | 14:89,039,315 | G/A | — | likely benign |
| rs1009281288 | 14:89,039,329 | A/C | — | uncertain significance |
| rs202134673 | 14:89,039,332 | C/T | — | uncertain significance |
| rs145521296 | 14:89,039,343 | A/T | — | conflicting classifications of pathogenicity |
| rs750993458 | 14:89,041,097 | T/A | — | uncertain significance |
| rs746845846 | 14:89,041,130 | G/A | — | uncertain significance |
| rs17124785 | 14:89,041,138 | C/T | — | benign |
| rs1555398661 | 14:89,041,146 | G/A | — | uncertain significance |
| rs143157900 | 14:89,041,173 | C/T | — | uncertain significance |
| rs1469602 | 14:89,042,180 | T/G | — | benign |
| rs147484262 | 14:89,042,232 | G/A | — | likely benign |
| rs1453914882 | 14:89,042,257 | G/A | — | uncertain significance |
| rs778564417 | 14:89,044,338 | A/G | — | uncertain significance |
| rs868558374 | 14:89,044,392 | C/T | — | uncertain significance |
| rs797046114 | 14:89,044,435 | C/T | — | uncertain significance |
| rs201527519 | 14:89,044,437 | C/T | — | uncertain significance |
| rs761958854 | 14:89,044,439 | A/G | — | uncertain significance |
| rs201108116 | 14:89,044,465 | T/G | — | uncertain significance |
| rs1401324807 | 14:89,044,478 | A/C | — | uncertain significance |
| rs200718239 | 14:89,044,493 | T/C | — | uncertain significance |
| rs141805452 | 14:89,058,314 | G/A | — | — |
| rs145362297 | 14:89,061,118 | T/A | — | likely benign |
| rs538186371 | 14:89,061,222 | A/G | — | uncertain significance |
| rs367969370 | 14:89,061,414 | C/G | — | likely benign |
| rs45518831 | 14:89,063,102 | C/T | — | likely benign |
| rs192725167 | 14:89,063,105 | G/A | — | uncertain significance |
| rs2297124 | 14:89,063,167 | A/G | — | benign |
| rs2543028541 | 14:89,068,291 | G/T | — | uncertain significance |
| rs370546299 | 14:89,068,337 | C/T | — | likely benign |
| rs143129413 | 14:89,068,345 | G/A | — | conflicting classifications of pathogenicity |
| rs2543031030 | 14:89,068,368 | G/C | — | uncertain significance |
| rs535112396 | 14:89,069,179 | G/A | — | uncertain significance |
| rs148234290 | 14:89,069,196 | T/C | — | likely benign |
| rs1316245654 | 14:89,069,201 | G/C | — | uncertain significance |
| rs778584454 | 14:89,069,220 | G/A | — | uncertain significance |
| rs2084860116 | 14:89,069,267 | A/T | — | uncertain significance |
| rs573730445 | 14:89,069,403 | C/T | — | likely benign |
| rs765315063 | 14:89,073,587 | C/T | — | uncertain significance |
| rs2543184549 | 14:89,075,636 | G/A | — | uncertain significance |
| rs375580594 | 14:89,075,671 | T/C | — | likely benign |
| rs2543186092 | 14:89,075,705 | A/G | — | uncertain significance |
| rs772791047 | 14:89,075,710 | T/C | — | likely benign |
| rs181607926 | 14:89,075,729 | G/A | — | uncertain significance |
| rs375794726 | 14:89,075,732 | C/T | — | likely benign |
| rs2543196052 | 14:89,076,083 | G/A | — | uncertain significance |
| rs1369427682 | 14:89,076,098 | G/A | — | uncertain significance |
| rs2086565005 | 14:89,077,196 | C/A | — | uncertain significance |
| rs35814324 | 14:89,077,198 | A/G | — | benign |
| rs139980286 | 14:89,077,209 | C/T | — | uncertain significance |
| rs149865117 | 14:89,077,210 | G/A | — | conflicting classifications of pathogenicity |
| rs2543225552 | 14:89,077,251 | G/A | — | uncertain significance |
| rs2543225656 | 14:89,077,256 | G/A | — | uncertain significance |
| rs1442509689 | 14:89,077,264 | A/G | — | likely benign |
| rs191598336 | 14:89,077,288 | A/C | — | benign |
| rs183617466 | 14:89,077,294 | C/G | — | benign |
| rs144843433 | 14:89,078,090 | G/A | — | uncertain significance |
| rs572707604 | 14:89,092,232 | G/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.