CCDC154
coiled-coil domain containing 154
Summary
Predicted to be involved in bone mineralization involved in bone maturation. Predicted to act upstream of or within bone resorption; odontogenesis; and sensory perception of sound. Predicted to be located in early endosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants70 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs750721196 | 16:1,484,453 | C/G | — | uncertain significance |
| rs369805573 | 16:1,484,477 | C/T | — | uncertain significance |
| rs565271689 | 16:1,484,491 | C/T | — | likely benign |
| rs1358130787 | 16:1,484,515 | G/C | — | uncertain significance |
| rs918009766 | 16:1,484,527 | C/T | — | uncertain significance |
| rs117318560 | 16:1,484,536 | C/T | — | likely benign |
| rs556514121 | 16:1,484,675 | G/A | — | uncertain significance |
| rs1049201915 | 16:1,484,720 | G/A | — | uncertain significance |
| rs2505789753 | 16:1,484,736 | A/C | — | uncertain significance |
| rs1314775175 | 16:1,484,741 | C/T | — | likely benign |
| rs746911929 | 16:1,484,744 | G/A | — | likely benign |
| rs200299810 | 16:1,484,790 | G/A | — | likely benign |
| rs998380269 | 16:1,484,853 | G/A | — | uncertain significance |
| rs375820770 | 16:1,485,116 | G/A | — | uncertain significance |
| rs370066683 | 16:1,485,138 | C/A | — | uncertain significance |
| rs895531563 | 16:1,485,143 | C/T | — | likely benign |
| rs371380380 | 16:1,485,987 | G/C | — | uncertain significance |
| rs556065475 | 16:1,486,035 | C/T | — | uncertain significance |
| rs2142351059 | 16:1,486,475 | G/T | — | uncertain significance |
| rs112015572 | 16:1,486,700 | G/C | — | uncertain significance |
| rs1435477946 | 16:1,486,722 | G/A | — | uncertain significance |
| rs574311061 | 16:1,486,755 | G/A | — | uncertain significance |
| rs533940963 | 16:1,487,907 | C/T | — | likely benign |
| rs1194249666 | 16:1,487,918 | G/A | — | uncertain significance |
| rs1358649108 | 16:1,487,939 | C/T | — | likely benign |
| rs543092557 | 16:1,487,951 | C/T | — | likely benign |
| rs200441064 | 16:1,488,052 | A/C | — | uncertain significance |
| rs145873417 | 16:1,488,079 | C/T | — | likely benign |
| rs780545865 | 16:1,488,089 | C/T | — | uncertain significance |
| rs749443933 | 16:1,488,121 | T/C | — | uncertain significance |
| rs774763237 | 16:1,488,131 | C/T | — | likely benign |
| rs766229250 | 16:1,488,173 | C/T | — | uncertain significance |
| rs367946151 | 16:1,488,648 | G/A | — | uncertain significance |
| rs1300148280 | 16:1,488,701 | G/A | — | uncertain significance |
| rs1020294579 | 16:1,488,704 | T/A | — | uncertain significance |
| rs1195311926 | 16:1,488,844 | C/T | — | uncertain significance |
| rs867487247 | 16:1,488,890 | C/T | — | uncertain significance |
| rs1036855023 | 16:1,488,892 | C/A | — | uncertain significance |
| rs1030527485 | 16:1,488,895 | C/G | — | uncertain significance |
| rs190211752 | 16:1,488,931 | G/A | — | uncertain significance |
| rs993722067 | 16:1,489,090 | C/T | — | uncertain significance |
| rs1228371732 | 16:1,489,096 | C/T | — | uncertain significance |
| rs755941093 | 16:1,489,112 | G/A | — | uncertain significance |
| rs750460090 | 16:1,492,468 | G/A | — | uncertain significance |
| rs1374174640 | 16:1,492,472 | C/T | — | likely benign |
| rs754724539 | 16:1,492,487 | G/A | — | uncertain significance |
| rs547602890 | 16:1,492,888 | C/T | — | uncertain significance |
| rs758425232 | 16:1,492,900 | C/T | — | uncertain significance |
| rs183290010 | 16:1,493,154 | C/T | — | — |
| rs548421132 | 16:1,493,514 | G/A | — | uncertain significance |
| rs568525805 | 16:1,493,524 | C/T | — | uncertain significance |
| rs992595394 | 16:1,493,538 | G/A | — | uncertain significance |
| rs763953899 | 16:1,493,544 | C/T | — | likely benign |
| rs751331127 | 16:1,493,545 | G/A | — | uncertain significance |
| rs111972266 | 16:1,493,547 | G/A | — | likely benign |
| rs1048052391 | 16:1,493,556 | T/C | — | likely benign |
| rs1294383235 | 16:1,493,593 | G/A | — | uncertain significance |
| rs1305470127 | 16:1,493,598 | C/T | — | uncertain significance |
| rs867422779 | 16:1,493,610 | A/G | — | uncertain significance |
| rs1195669182 | 16:1,493,617 | G/A | — | uncertain significance |
| rs776610240 | 16:1,493,628 | C/T | — | uncertain significance |
| rs571009503 | 16:1,493,631 | G/A | — | uncertain significance |
| rs753466167 | 16:1,493,638 | G/A | — | uncertain significance |
| rs576194066 | 16:1,493,646 | C/T | — | uncertain significance |
| rs200706751 | 16:1,493,837 | C/T | — | uncertain significance |
| rs925240020 | 16:1,493,860 | G/A | — | likely benign |
| rs999513253 | 16:1,493,899 | C/A | — | uncertain significance |
| rs1027416593 | 16:1,493,926 | C/T | — | likely benign |
| rs1157344478 | 16:1,494,008 | C/A | — | uncertain significance |
| rs779080877 | 16:1,494,320 | A/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.