CFDP1
craniofacial development protein 1
Summary
Predicted to be involved in chromatin remodeling. Predicted to act upstream of or within several processes, including cell adhesion; negative regulation of fibroblast apoptotic process; and regulation of cell shape. Predicted to be located in kinetochore. Predicted to be part of Swr1 complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants67 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs4888378 | 16:75,298,143 | A/G | intron variant | — |
| rs2507589670 | 16:75,327,937 | G/C | — | uncertain significance |
| rs11647088 | 16:75,331,064 | C/A | — | — |
| rs11646852 | 16:75,331,178 | G/T | — | — |
| rs752675935 | 16:75,338,926 | C/T | — | uncertain significance |
| rs762736889 | 16:75,338,934 | C/A | — | uncertain significance |
| rs149995941 | 16:75,339,005 | C/T | — | likely benign |
| rs145593544 | 16:75,339,006 | T/C | — | uncertain significance |
| rs4888379 | 16:75,340,231 | A/G | — | — |
| rs8057535 | 16:75,347,941 | C/T | intron variant | — |
| rs3975148 | 16:75,364,879 | A/C | — | — |
| rs3863446 | 16:75,385,735 | G/A | intron variant | — |
| rs4888383 | 16:75,386,349 | C/G | — | — |
| rs3851738 | 16:75,387,533 | G/A | — | — |
| rs3851740 | 16:75,387,578 | T/A | — | — |
| rs2865531 | 16:75,390,316 | T/C | — | — |
| rs2059256 | 16:75,395,835 | G/T | intron variant | — |
| rs1364077 | 16:75,396,991 | C/A | — | — |
| rs192611749 | 16:75,398,337 | A/C | intron variant | — |
| rs11642921 | 16:75,401,569 | A/T | intron variant | — |
| rs8057203 | 16:75,404,974 | T/C | regulatory region variant | — |
| rs11646677 | 16:75,408,981 | T/C | downstream gene variant | — |
| rs11858992 | 16:75,411,445 | A/G | — | — |
| rs4146810 | 16:75,415,831 | A/C | — | — |
| rs570960460 | 16:75,416,760 | G/A | — | — |
| rs1808435 | 16:75,425,819 | T/G | — | — |
| rs559305355 | 16:75,426,083 | C/G | — | — |
| rs146975317 | 16:75,428,991 | G/A | — | uncertain significance |
| rs371488344 | 16:75,428,996 | G/A | — | likely benign |
| rs142200520 | 16:75,429,016 | C/G | — | uncertain significance |
| rs772094397 | 16:75,429,039 | T/G | — | uncertain significance |
| rs2507185132 | 16:75,429,083 | T/C | — | likely benign |
| rs202002820 | 16:75,429,091 | C/T | — | uncertain significance |
| rs2285221 | 16:75,429,626 | A/G | intron variant | — |
| rs77246010 | 16:75,429,853 | T/A | — | — |
| rs11864587 | 16:75,431,263 | G/A | intron variant | — |
| rs59867374 | 16:75,432,682 | G/A | intron variant | — |
| rs4888408 | 16:75,432,824 | G/C | — | — |
| rs7184525 | 16:75,437,186 | A/G | intron variant | — |
| rs8046696 | 16:75,442,143 | T/G | downstream gene variant | — |
| rs8046697 | 16:75,442,144 | T/C | downstream gene variant | — |
| rs4888411 | 16:75,443,183 | T/A | downstream gene variant | — |
| rs35261357 | 16:75,444,572 | C/G | — | — |
| rs72787160 | 16:75,445,162 | G/A | — | — |
| rs247436 | 16:75,445,971 | T/G | upstream gene variant | — |
| rs201209631 | 16:75,446,435 | T/C | — | uncertain significance |
| rs763357455 | 16:75,446,510 | T/C | — | uncertain significance |
| rs1314683218 | 16:75,446,543 | T/C | — | uncertain significance |
| rs1162980394 | 16:75,446,558 | C/A | — | uncertain significance |
| rs370354614 | 16:75,446,565 | T/C | — | likely benign |
| rs202202039 | 16:75,446,584 | C/T | — | uncertain significance |
| rs143082831 | 16:75,446,636 | C/T | — | uncertain significance |
| rs6564260 | 16:75,447,426 | A/T | — | — |
| rs16963331 | 16:75,448,480 | C/T | — | likely benign |
| rs532522214 | 16:75,448,490 | C/G | — | uncertain significance |
| rs569392299 | 16:75,448,546 | C/G | — | uncertain significance |
| rs4888415 | 16:75,448,921 | C/G | — | — |
| rs12444589 | 16:75,454,404 | T/A | intron variant | — |
| rs180710836 | 16:75,456,385 | C/T | intron variant | — |
| rs62062572 | 16:75,457,654 | C/G | — | — |
| rs11861810 | 16:75,461,829 | A/T | — | — |
| rs12930452 | 16:75,462,055 | A/C | — | — |
| rs12449170 | 16:75,463,012 | C/T | intron variant | — |
| rs4888421 | 16:75,465,339 | A/T | — | — |
| rs3743609 | 16:75,467,021 | G/C | regulatory region variant | — |
| rs754680010 | 16:75,467,191 | C/A | — | likely benign |
| rs75511445 | 16:75,467,223 | A/G | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.