CDK13
cyclin dependent kinase 13
Summary
The protein encoded by this gene is a member of the cyclin-dependent serine/threonine protein kinase family. Members of this family are well known for their essential roles as master switches in cell cycle control. The exact function of this protein has not yet been determined, but it may play a role in mRNA processing and may be involved in regulation of hematopoiesis. Alternatively spliced transcript variants have been described.[provided by RefSeq, Dec 2009]
Known Variants656 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2483665872 | 7:39,990,253 | T/C | — | uncertain significance |
| rs2483665915 | 7:39,990,258 | C/A | — | uncertain significance |
| rs1450916285 | 7:39,990,260 | C/T | — | uncertain significance |
| rs1787122309 | 7:39,990,281 | G/A | — | uncertain significance |
| rs769526109 | 7:39,990,287 | G/C | — | benign |
| rs1011234458 | 7:39,990,288 | C/G | — | uncertain significance |
| rs2483666167 | 7:39,990,291 | G/A | — | uncertain significance |
| rs1022252618 | 7:39,990,300 | G/A | — | likely benign |
| rs571636079 | 7:39,990,310 | G/T | — | uncertain significance |
| rs371265072 | 7:39,990,334 | C/T | — | likely benign |
| rs1390349152 | 7:39,990,337 | T/C | — | benign |
| rs1225471968 | 7:39,990,339 | C/T | — | likely benign |
| rs773857479 | 7:39,990,340 | C/T | — | conflicting classifications of pathogenicity |
| rs756090286 | 7:39,990,355 | C/T | — | likely benign |
| rs1562691317 | 7:39,990,358 | C/T | — | likely benign |
| rs557213181 | 7:39,990,373 | C/A | — | uncertain significance |
| rs918459117 | 7:39,990,382 | C/T | — | uncertain significance |
| rs992749182 | 7:39,990,384 | C/T | — | likely benign |
| rs1378858299 | 7:39,990,386 | T/C | — | uncertain significance |
| rs1787131091 | 7:39,990,389 | A/C | — | uncertain significance |
| rs1318948420 | 7:39,990,409 | C/G | — | uncertain significance |
| rs1255172268 | 7:39,990,412 | C/G | — | uncertain significance |
| rs905637426 | 7:39,990,413 | T/C | — | uncertain significance |
| rs937054016 | 7:39,990,417 | C/T | — | likely benign |
| rs1787135051 | 7:39,990,424 | G/A | — | uncertain significance |
| rs766897511 | 7:39,990,432 | C/G | — | likely benign |
| rs2116049126 | 7:39,990,434 | G/A | — | uncertain significance |
| rs2483667772 | 7:39,990,435 | C/A | — | likely benign |
| rs2483668003 | 7:39,990,449 | C/T | — | uncertain significance |
| rs1047945853 | 7:39,990,450 | A/C | — | likely benign |
| rs2116049843 | 7:39,990,454 | G/A | — | benign |
| rs1021210496 | 7:39,990,458 | C/T | — | uncertain significance |
| rs1282967438 | 7:39,990,464 | C/T | — | uncertain significance |
| rs900164978 | 7:39,990,467 | C/T | — | conflicting classifications of pathogenicity |
| rs902762110 | 7:39,990,469 | T/G | — | likely benign |
| rs998175874 | 7:39,990,471 | C/T | — | likely benign |
| rs1787141502 | 7:39,990,472 | T/A | — | uncertain significance |
| rs1465225798 | 7:39,990,473 | C/T | — | uncertain significance |
| rs1329376938 | 7:39,990,480 | C/T | — | likely benign |
| rs1298081718 | 7:39,990,483 | C/T | — | likely benign |
| rs535997764 | 7:39,990,487 | C/T | — | likely benign |
| rs954023481 | 7:39,990,488 | C/G | — | uncertain significance |
| rs1787143212 | 7:39,990,491 | G/T | — | uncertain significance |
| rs1034818374 | 7:39,990,492 | C/T | — | likely benign |
| rs1562691656 | 7:39,990,493 | C/T | — | benign |
| rs985522324 | 7:39,990,495 | C/T | — | likely benign |
| rs1787148001 | 7:39,990,513 | G/C | — | likely benign |
| rs1258245330 | 7:39,990,518 | C/T | — | conflicting classifications of pathogenicity |
| rs1167686585 | 7:39,990,523 | G/A | — | uncertain significance |
| rs1317210492 | 7:39,990,531 | G/A | — | likely benign |
| rs17496123 | 7:39,990,552 | G/A | — | likely benign |
| rs992864222 | 7:39,990,564 | G/A | — | likely benign |
| rs1787149678 | 7:39,990,565 | C/T | — | uncertain significance |
| rs758702398 | 7:39,990,569 | G/A | — | uncertain significance |
| rs1787150132 | 7:39,990,571 | G/C | — | uncertain significance |
| rs1450928202 | 7:39,990,597 | G/A | — | likely benign |
| rs949933113 | 7:39,990,599 | T/G | — | uncertain significance |
| rs1214793568 | 7:39,990,600 | C/T | — | likely benign |
| rs1202031047 | 7:39,990,610 | C/T | — | uncertain significance |
| rs1430680739 | 7:39,990,612 | C/T | — | likely benign |
| rs2116052719 | 7:39,990,613 | C/T | — | uncertain significance |
| rs1477767717 | 7:39,990,617 | C/A | — | uncertain significance |
| rs973454935 | 7:39,990,633 | T/C | — | likely benign |
| rs1562691800 | 7:39,990,636 | C/G | — | likely benign |
| rs926966364 | 7:39,990,640 | G/A | — | conflicting classifications of pathogenicity |
| rs920813876 | 7:39,990,641 | C/G | — | conflicting classifications of pathogenicity |
| rs1787156957 | 7:39,990,649 | G/C | — | uncertain significance |
| rs895279225 | 7:39,990,659 | T/G | — | uncertain significance |
| rs1787158171 | 7:39,990,660 | G/A | — | likely benign |
| rs1484360053 | 7:39,990,666 | G/A | — | likely benign |
| rs17496130 | 7:39,990,681 | G/C | — | conflicting classifications of pathogenicity |
| rs921732950 | 7:39,990,692 | C/T | — | benign |
| rs1269138380 | 7:39,990,694 | C/T | — | pathogenic |
| rs1279892568 | 7:39,990,698 | C/T | — | conflicting classifications of pathogenicity |
| rs1583892063 | 7:39,990,702 | G/A | — | likely benign |
| rs1339809436 | 7:39,990,708 | G/T | — | likely benign |
| rs1192363832 | 7:39,990,713 | T/C | — | uncertain significance |
| rs1554317112 | 7:39,990,718 | G/C | — | uncertain significance |
| rs2116055386 | 7:39,990,720 | G/A | — | likely benign |
| rs1409394646 | 7:39,990,721 | G/T | — | benign |
| rs902803165 | 7:39,990,722 | G/T | — | uncertain significance |
| rs1216683440 | 7:39,990,725 | C/G | — | conflicting classifications of pathogenicity |
| rs1266918450 | 7:39,990,726 | C/T | — | likely benign |
| rs1297132193 | 7:39,990,729 | C/T | — | likely benign |
| rs1307510038 | 7:39,990,730 | G/A | — | uncertain significance |
| rs998375490 | 7:39,990,738 | G/A | — | likely benign |
| rs2116055945 | 7:39,990,739 | G/A | — | uncertain significance |
| rs999406904 | 7:39,990,741 | G/A | — | likely benign |
| rs1056340771 | 7:39,990,743 | C/T | — | uncertain significance |
| rs2116056085 | 7:39,990,745 | A/G | — | uncertain significance |
| rs1029840854 | 7:39,990,749 | C/T | — | conflicting classifications of pathogenicity |
| rs889792089 | 7:39,990,753 | C/T | — | likely benign |
| rs1263377058 | 7:39,990,756 | G/A | — | likely benign |
| rs995209864 | 7:39,990,761 | C/G | — | uncertain significance |
| rs2116056915 | 7:39,990,772 | G/C | — | uncertain significance |
| rs1341663252 | 7:39,990,776 | G/A | — | uncertain significance |
| rs1295697771 | 7:39,990,785 | C/T | — | uncertain significance |
| rs1787169729 | 7:39,990,787 | T/A | — | uncertain significance |
| rs1787169987 | 7:39,990,789 | C/T | — | likely benign |
| rs1293078589 | 7:39,990,792 | C/T | — | likely benign |
Showing 100 of 656 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.