CDCA7L
cell division cycle associated 7 like
Summary
Acts upstream of or within positive regulation of cell population proliferation. Located in cytosol; fibrillar center; and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants28 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs141309943 | 7:21,941,954 | C/A | — | uncertain significance |
| rs2534187562 | 7:21,942,705 | T/C | — | uncertain significance |
| rs768924803 | 7:21,943,766 | G/A | — | uncertain significance |
| rs777278383 | 7:21,943,844 | T/C | — | uncertain significance |
| rs2534199408 | 7:21,945,149 | C/T | — | uncertain significance |
| rs1785112982 | 7:21,945,191 | T/C | — | uncertain significance |
| rs775830609 | 7:21,945,225 | G/A | — | uncertain significance |
| rs371749596 | 7:21,945,239 | C/T | — | likely benign |
| rs780113859 | 7:21,945,926 | C/T | — | uncertain significance |
| rs746650414 | 7:21,945,948 | C/G | — | uncertain significance |
| rs145238615 | 7:21,946,053 | C/T | — | uncertain significance |
| rs115917503 | 7:21,946,266 | C/G | — | benign |
| rs758630757 | 7:21,947,773 | A/G | — | uncertain significance |
| rs1289023037 | 7:21,947,800 | C/G | — | uncertain significance |
| rs563675406 | 7:21,947,819 | G/A | — | uncertain significance |
| rs1785203275 | 7:21,947,890 | A/G | — | uncertain significance |
| rs201734057 | 7:21,947,917 | C/T | — | likely benign |
| rs750462397 | 7:21,947,960 | G/A | — | likely benign |
| rs749722138 | 7:21,947,972 | G/C | — | uncertain significance |
| rs141140287 | 7:21,948,001 | C/T | — | uncertain significance |
| rs137919998 | 7:21,948,065 | C/G | — | uncertain significance |
| rs142981617 | 7:21,948,077 | C/T | — | uncertain significance |
| rs2534208927 | 7:21,948,107 | T/A | — | uncertain significance |
| rs2534217913 | 7:21,951,275 | G/A | — | uncertain significance |
| rs200336698 | 7:21,951,353 | G/C | — | uncertain significance |
| rs144827468 | 7:21,956,437 | G/A | — | uncertain significance |
| rs9692388 | 7:21,976,001 | C/G | intron variant | — |
| rs185017010 | 7:21,984,018 | G/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.