CCDC102A
coiled-coil domain containing 102A
Summary
Predicted to be part of myosin complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1169210613 | 16:57,546,661 | C/T | — | uncertain significance |
| rs750089033 | 16:57,546,709 | C/T | — | uncertain significance |
| rs377282751 | 16:57,546,718 | C/T | — | uncertain significance |
| rs2543676498 | 16:57,546,726 | A/G | — | uncertain significance |
| rs144990758 | 16:57,546,739 | G/A | — | uncertain significance |
| rs2031890404 | 16:57,546,757 | G/C | — | uncertain significance |
| rs2543678570 | 16:57,549,265 | T/G | — | uncertain significance |
| rs756313654 | 16:57,549,308 | C/G | — | uncertain significance |
| rs1454961554 | 16:57,550,326 | T/A | — | uncertain significance |
| rs2031957910 | 16:57,550,374 | T/G | — | uncertain significance |
| rs150464217 | 16:57,551,997 | G/A | — | uncertain significance |
| rs762305485 | 16:57,551,999 | G/T | — | uncertain significance |
| rs780307321 | 16:57,552,000 | C/T | — | uncertain significance |
| rs749467074 | 16:57,552,014 | C/T | — | uncertain significance |
| rs761170137 | 16:57,552,033 | C/T | — | uncertain significance |
| rs752427469 | 16:57,552,039 | C/T | — | uncertain significance |
| rs144945819 | 16:57,552,081 | C/T | — | uncertain significance |
| rs2031990330 | 16:57,552,120 | C/T | — | uncertain significance |
| rs777842983 | 16:57,552,140 | C/T | — | uncertain significance |
| rs201621400 | 16:57,552,149 | C/T | — | uncertain significance |
| rs765040571 | 16:57,552,171 | C/T | — | uncertain significance |
| rs1304993808 | 16:57,555,042 | G/A | — | uncertain significance |
| rs1418758928 | 16:57,555,062 | A/T | — | uncertain significance |
| rs1455477131 | 16:57,559,845 | A/C | — | uncertain significance |
| rs138430955 | 16:57,559,853 | G/A | — | uncertain significance |
| rs372606995 | 16:57,559,867 | G/A | — | uncertain significance |
| rs563952674 | 16:57,559,891 | G/A | — | uncertain significance |
| rs751465724 | 16:57,559,948 | C/T | — | uncertain significance |
| rs780252323 | 16:57,559,954 | C/T | — | uncertain significance |
| rs767427086 | 16:57,560,022 | C/G | — | uncertain significance |
| rs778992550 | 16:57,562,531 | C/T | — | uncertain significance |
| rs759249270 | 16:57,562,578 | C/T | — | uncertain significance |
| rs2032189287 | 16:57,562,588 | C/T | — | uncertain significance |
| rs992326781 | 16:57,562,593 | A/C | — | uncertain significance |
| rs2032189834 | 16:57,562,600 | G/A | — | uncertain significance |
| rs1356475083 | 16:57,562,620 | A/G | — | uncertain significance |
| rs757839319 | 16:57,562,632 | C/G | — | uncertain significance |
| rs767457149 | 16:57,562,875 | C/T | — | uncertain significance |
| rs766862771 | 16:57,562,896 | G/A | — | uncertain significance |
| rs2543695049 | 16:57,562,956 | C/A | — | uncertain significance |
| rs2543695057 | 16:57,562,960 | T/G | — | uncertain significance |
| rs79928291 | 16:57,562,973 | C/T | synonymous variant | — |
| rs775536376 | 16:57,563,052 | G/A | — | uncertain significance |
| rs8052123 | 16:57,563,671 | T/C | regulatory region variant | — |
| rs9928663 | 16:57,570,562 | C/G | — | — |
| rs9939347 | 16:57,570,704 | A/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.