ZC3H7B
zinc finger CCCH-type containing 7B
Summary
This gene encodes a protein that contains a tetratricopeptide repeat domain. The encoded protein also interacts with the rotavirus non-structural protein NSP3. [provided by RefSeq, Jul 2008]
Known Variants58 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1883826 | 22:41,703,428 | G/T | — | — |
| rs34011394 | 22:41,704,872 | C/T | regulatory region variant | — |
| rs9611550 | 22:41,707,054 | C/A | intron variant | — |
| rs9611555 | 22:41,713,111 | G/A | intron variant | — |
| rs2518091435 | 22:41,716,709 | G/T | — | uncertain significance |
| rs6002333 | 22:41,719,469 | C/T | intron variant | — |
| rs5751077 | 22:41,720,728 | G/C | intron variant | — |
| rs73176674 | 22:41,721,792 | A/G | — | uncertain significance |
| rs151077891 | 22:41,721,853 | C/T | — | likely benign |
| rs202146852 | 22:41,721,870 | G/A | — | uncertain significance |
| rs1569234786 | 22:41,721,902 | G/T | — | uncertain significance |
| rs3927 | 22:41,722,864 | T/C | intron variant | — |
| rs367879359 | 22:41,723,295 | G/A | — | uncertain significance |
| rs201720517 | 22:41,723,316 | G/A | — | uncertain significance |
| rs1229210488 | 22:41,726,055 | A/G | — | uncertain significance |
| rs774333614 | 22:41,728,196 | C/T | — | uncertain significance |
| rs148237320 | 22:41,728,205 | G/A | — | uncertain significance |
| rs191143984 | 22:41,728,239 | C/T | — | likely benign |
| rs375805232 | 22:41,735,832 | G/C | — | uncertain significance |
| rs2518106678 | 22:41,735,859 | A/G | — | uncertain significance |
| rs2518106733 | 22:41,735,908 | T/C | — | uncertain significance |
| rs139915247 | 22:41,736,000 | G/A | — | uncertain significance |
| rs746678633 | 22:41,736,037 | C/T | — | uncertain significance |
| rs776136179 | 22:41,736,042 | G/A | — | uncertain significance |
| rs570655747 | 22:41,736,075 | C/T | — | uncertain significance |
| rs376029308 | 22:41,737,115 | C/T | — | uncertain significance |
| rs2518108143 | 22:41,737,124 | A/G | — | uncertain significance |
| rs2518108170 | 22:41,737,140 | C/T | — | uncertain significance |
| rs137940372 | 22:41,737,145 | C/A | — | uncertain significance |
| rs150687294 | 22:41,739,473 | G/A | — | uncertain significance |
| rs1470482736 | 22:41,739,475 | G/T | — | uncertain significance |
| rs780582712 | 22:41,739,524 | G/A | — | uncertain significance |
| rs374299866 | 22:41,742,024 | G/A | — | uncertain significance |
| rs766418434 | 22:41,742,030 | A/C | — | uncertain significance |
| rs757989990 | 22:41,742,084 | A/G | — | uncertain significance |
| rs373304213 | 22:41,742,126 | G/T | — | uncertain significance |
| rs759659032 | 22:41,742,130 | C/T | — | uncertain significance |
| rs1427262961 | 22:41,745,140 | G/A | — | uncertain significance |
| rs2518114497 | 22:41,745,196 | G/T | — | uncertain significance |
| rs764885694 | 22:41,745,246 | G/A | — | uncertain significance |
| rs2281333 | 22:41,749,630 | T/C | intron variant | — |
| rs570159570 | 22:41,751,480 | C/T | — | uncertain significance |
| rs776863330 | 22:41,751,574 | C/A | — | uncertain significance |
| rs200542050 | 22:41,751,599 | C/T | — | uncertain significance |
| rs764761875 | 22:41,751,844 | G/A | — | uncertain significance |
| rs2518119849 | 22:41,752,352 | G/C | — | uncertain significance |
| rs758659694 | 22:41,752,374 | T/C | — | uncertain significance |
| rs2036718171 | 22:41,752,453 | G/C | — | uncertain significance |
| rs1031873824 | 22:41,752,461 | C/T | — | uncertain significance |
| rs761842811 | 22:41,752,470 | C/T | — | uncertain significance |
| rs12484074 | 22:41,752,747 | G/A | synonymous variant | — |
| rs1373535528 | 22:41,752,751 | G/A | — | uncertain significance |
| rs143415211 | 22:41,752,753 | C/A | — | uncertain significance |
| rs2036724163 | 22:41,752,755 | G/A | — | uncertain significance |
| rs372991434 | 22:41,752,800 | G/A | — | uncertain significance |
| rs2518120836 | 22:41,753,203 | C/G | — | uncertain significance |
| rs774972968 | 22:41,753,331 | C/A | — | uncertain significance |
| rs147270928 | 22:41,753,369 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.