MCM9
minichromosome maintenance 9 homologous recombination repair factor
Summary
The protein encoded by this gene is a member of the mini-chromosome maintenance (MCM) protein family that are essential for the initiation of eukaryotic genome replication. Binding of this protein to chromatin has been shown to be a pre-requisite for recruiting the MCM2-7 helicase to DNA replication origins. This protein also binds, and is a positive regulator of, the chromatin licensing and DNA replication factor 1, CDT1. [provided by RefSeq, Nov 2010]
Known Variants110 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs533851347 | 6:119,135,994 | T/C | — | uncertain significance |
| rs573330646 | 6:119,135,999 | T/A | — | uncertain significance |
| rs542454374 | 6:119,136,000 | C/A | — | uncertain significance |
| rs144338608 | 6:119,136,002 | C/T | — | conflicting classifications of pathogenicity |
| rs533379434 | 6:119,136,088 | C/T | — | uncertain significance |
| rs767467581 | 6:119,136,099 | C/T | — | likely benign |
| rs531103567 | 6:119,136,100 | G/A | — | uncertain significance |
| rs1007909127 | 6:119,136,121 | T/C | — | uncertain significance |
| rs748037160 | 6:119,136,129 | C/T | — | uncertain significance |
| rs61742362 | 6:119,136,133 | T/C | — | likely benign |
| rs191076107 | 6:119,136,163 | G/T | — | uncertain significance |
| rs2534090940 | 6:119,136,187 | T/C | — | uncertain significance |
| rs61744508 | 6:119,136,196 | G/A | — | benign |
| rs567816821 | 6:119,136,277 | C/T | — | likely benign |
| rs201828357 | 6:119,136,385 | C/G | — | uncertain significance |
| rs901672093 | 6:119,136,415 | C/T | — | likely benign |
| rs1351910743 | 6:119,136,438 | G/A | — | uncertain significance |
| rs55779481 | 6:119,136,518 | T/C | — | benign |
| rs117470188 | 6:119,136,530 | G/A | — | benign |
| rs1169243600 | 6:119,136,561 | G/C | — | uncertain significance |
| rs751098427 | 6:119,136,579 | T/G | — | uncertain significance |
| rs79301018 | 6:119,136,601 | G/A | — | uncertain significance |
| rs1432753479 | 6:119,136,618 | G/A | — | uncertain significance |
| rs2114487061 | 6:119,136,642 | T/C | — | uncertain significance |
| rs2534093562 | 6:119,136,711 | T/C | — | uncertain significance |
| rs3751444 | 6:119,136,726 | G/A | — | likely benign |
| rs1013234871 | 6:119,136,763 | T/C | — | uncertain significance |
| rs2534094016 | 6:119,136,775 | G/C | — | uncertain significance |
| rs2534094614 | 6:119,136,852 | G/A | — | uncertain significance |
| rs117293145 | 6:119,136,853 | C/T | — | uncertain significance |
| rs777624704 | 6:119,136,875 | C/A | — | likely benign |
| rs772359511 | 6:119,136,924 | G/C | — | uncertain significance |
| rs776836801 | 6:119,136,970 | T/C | — | likely benign |
| rs116048760 | 6:119,136,971 | T/G | — | benign |
| rs187552949 | 6:119,136,985 | C/T | — | uncertain significance |
| rs1773379516 | 6:119,137,006 | C/T | — | uncertain significance |
| rs2534095499 | 6:119,137,027 | C/T | — | uncertain significance |
| rs985121576 | 6:119,137,029 | A/G | — | likely benign |
| rs974602780 | 6:119,137,083 | C/T | — | likely benign |
| rs1489486050 | 6:119,137,090 | A/G | — | uncertain significance |
| rs572521467 | 6:119,137,092 | A/C | — | uncertain significance |
| rs543065031 | 6:119,137,104 | A/G | — | uncertain significance |
| rs2534096003 | 6:119,137,132 | G/A | — | uncertain significance |
| rs1217005643 | 6:119,137,140 | A/C | — | uncertain significance |
| rs2534097271 | 6:119,137,332 | T/C | — | uncertain significance |
| rs902182209 | 6:119,137,374 | C/T | — | uncertain significance |
| rs759280235 | 6:119,137,422 | C/T | — | likely benign |
| rs75607191 | 6:119,137,423 | A/G | — | likely benign |
| rs368975394 | 6:119,137,435 | G/C | — | uncertain significance |
| rs78791427 | 6:119,137,445 | A/C | — | benign |
| rs554695966 | 6:119,147,400 | G/C | — | uncertain significance |
| rs1351411498 | 6:119,147,429 | A/T | — | uncertain significance |
| rs771690828 | 6:119,147,434 | C/A | — | uncertain significance |
| rs1383853205 | 6:119,147,948 | C/A | — | uncertain significance |
| rs1445557559 | 6:119,147,961 | A/G | — | uncertain significance |
| rs1220828001 | 6:119,147,983 | C/T | — | uncertain significance |
| rs568372543 | 6:119,148,006 | C/T | — | uncertain significance |
| rs1460351219 | 6:119,148,018 | C/T | — | conflicting classifications of pathogenicity |
| rs587777871 | 6:119,149,088 | A/G | — | pathogenic |
| rs935422225 | 6:119,149,123 | G/A | — | uncertain significance |
| rs553491848 | 6:119,149,134 | C/T | — | uncertain significance |
| rs928548799 | 6:119,149,142 | G/A | — | likely benign |
| rs200408257 | 6:119,149,146 | C/T | — | conflicting classifications of pathogenicity |
| rs284921 | 6:119,149,149 | C/G | — | benign |
| rs933243929 | 6:119,149,165 | G/C | — | uncertain significance |
| rs587777873 | 6:119,149,289 | G/T | — | not provided |
| rs772472098 | 6:119,149,300 | G/C | — | likely pathogenic |
| rs9387607 | 6:119,150,218 | T/A | — | benign |
| rs939087744 | 6:119,150,244 | G/T | — | uncertain significance |
| rs533383513 | 6:119,150,252 | T/C | — | uncertain significance |
| rs1060505058 | 6:119,150,256 | C/A | stop gained | pathogenic |
| rs766157559 | 6:119,150,335 | G/A | — | likely benign |
| rs560268904 | 6:119,150,410 | G/A | — | likely benign |
| rs183352104 | 6:119,155,594 | G/A | intron variant | — |
| rs36127776 | 6:119,161,160 | T/C | — | — |
| rs554190089 | 6:119,161,337 | T/A | — | — |
| rs1934923 | 6:119,171,412 | T/C | intron variant | — |
| rs1032388 | 6:119,171,866 | T/A | — | — |
| rs36160966 | 6:119,177,480 | T/A | — | — |
| rs151149424 | 6:119,177,587 | C/T | — | likely benign |
| rs762984976 | 6:119,177,671 | C/G | — | uncertain significance |
| rs1380220881 | 6:119,177,709 | C/T | — | pathogenic |
| rs150141688 | 6:119,178,035 | T/A | intron variant | — |
| rs36151678 | 6:119,193,502 | G/C | — | — |
| rs29001546 | 6:119,211,286 | T/C | upstream gene variant | — |
| rs76967739 | 6:119,232,799 | T/C | — | benign |
| rs746227371 | 6:119,232,826 | G/C | — | uncertain significance |
| rs10456918 | 6:119,233,480 | A/C | downstream gene variant | — |
| rs78231991 | 6:119,234,579 | T/C | — | likely benign |
| rs115751132 | 6:119,238,738 | C/T | — | uncertain significance |
| rs1174482921 | 6:119,238,840 | T/G | — | uncertain significance |
| rs115772624 | 6:119,238,880 | G/A | — | benign |
| rs2534642036 | 6:119,238,893 | T/C | — | uncertain significance |
| rs41292552 | 6:119,238,904 | T/C | — | likely benign |
| rs182397736 | 6:119,245,025 | G/A | — | likely benign |
| rs149844896 | 6:119,245,053 | T/C | — | uncertain significance |
| rs34665713 | 6:119,245,094 | C/T | — | uncertain significance |
| rs969031279 | 6:119,245,125 | C/T | — | uncertain significance |
| rs1651424897 | 6:119,245,166 | T/C | — | uncertain significance |
| rs747476181 | 6:119,245,194 | G/T | — | uncertain significance |
Showing 100 of 110 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.