CCDC13
coiled-coil domain containing 13
Summary
Acts upstream of or within DNA damage response; cytoplasmic microtubule organization; and non-motile cilium assembly. Located in centriolar satellite. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants49 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs367554932 | 3:42,750,527 | T/C | — | uncertain significance |
| rs187826060 | 3:42,750,552 | G/A | — | uncertain significance |
| rs368701943 | 3:42,751,254 | C/A | — | uncertain significance |
| rs1203640992 | 3:42,751,255 | C/T | — | uncertain significance |
| rs339661 | 3:42,753,904 | G/T | — | — |
| rs901736657 | 3:42,754,681 | G/C | — | uncertain significance |
| rs747995879 | 3:42,754,726 | G/T | — | uncertain significance |
| rs754506293 | 3:42,754,801 | C/T | — | uncertain significance |
| rs11718476 | 3:42,764,838 | C/A | — | — |
| rs9830553 | 3:42,767,465 | T/A | intron variant | — |
| rs142035542 | 3:42,769,533 | C/T | upstream gene variant | — |
| rs200289473 | 3:42,771,960 | G/A | — | uncertain significance |
| rs1438914919 | 3:42,771,984 | C/T | — | uncertain significance |
| rs138907128 | 3:42,771,992 | C/T | — | uncertain significance |
| rs199605259 | 3:42,771,993 | G/A | — | uncertain significance |
| rs763112794 | 3:42,772,076 | G/A | — | likely benign |
| rs1157132821 | 3:42,774,413 | G/A | — | uncertain significance |
| rs371554766 | 3:42,774,418 | G/A | — | uncertain significance |
| rs1467134628 | 3:42,774,443 | G/A | — | uncertain significance |
| rs1431076265 | 3:42,775,040 | G/A | — | uncertain significance |
| rs199503570 | 3:42,775,061 | C/T | — | uncertain significance |
| rs201282842 | 3:42,775,064 | C/A | — | uncertain significance |
| rs1399769535 | 3:42,775,068 | T/C | — | uncertain significance |
| rs1298724722 | 3:42,775,095 | G/A | — | uncertain significance |
| rs777005407 | 3:42,777,297 | G/A | — | uncertain significance |
| rs1326648307 | 3:42,781,131 | G/C | — | uncertain significance |
| rs750273952 | 3:42,781,221 | T/G | — | uncertain significance |
| rs752988457 | 3:42,781,232 | C/T | — | likely benign |
| rs772674988 | 3:42,781,287 | G/A | — | uncertain significance |
| rs780440894 | 3:42,784,407 | T/C | — | uncertain significance |
| rs147740813 | 3:42,788,771 | T/C | — | uncertain significance |
| rs756581513 | 3:42,793,472 | C/T | — | uncertain significance |
| rs747912716 | 3:42,794,089 | C/T | — | uncertain significance |
| rs547999003 | 3:42,794,090 | G/A | — | uncertain significance |
| rs776853041 | 3:42,794,146 | C/T | — | uncertain significance |
| rs762089355 | 3:42,794,147 | G/A | — | uncertain significance |
| rs530423995 | 3:42,794,186 | C/A | — | uncertain significance |
| rs201462906 | 3:42,794,198 | C/T | — | uncertain significance |
| rs373266481 | 3:42,794,201 | C/T | — | uncertain significance |
| rs376549796 | 3:42,798,617 | C/G | — | uncertain significance |
| rs778801415 | 3:42,798,696 | C/T | — | uncertain significance |
| rs34234072 | 3:42,799,674 | C/T | — | benign |
| rs1417933269 | 3:42,799,704 | T/A | — | uncertain significance |
| rs778360015 | 3:42,799,720 | G/A | — | uncertain significance |
| rs2471497152 | 3:42,799,755 | T/G | — | uncertain significance |
| rs144956988 | 3:42,799,780 | C/T | — | uncertain significance |
| rs1187176348 | 3:42,799,828 | C/T | — | uncertain significance |
| rs148570614 | 3:42,799,830 | G/A | — | uncertain significance |
| rs339665 | 3:42,808,071 | C/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.