CCDC144A
coiled-coil domain containing 144A
Summary
Predicted to enable calcium oxalate binding activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants52 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs530262939 | 17:16,574,090 | C/T | — | — |
| rs747697017 | 17:16,593,812 | G/A | — | likely benign |
| rs1910991625 | 17:16,593,845 | A/G | — | uncertain significance |
| rs761254619 | 17:16,608,515 | A/C | — | uncertain significance |
| rs764713137 | 17:16,608,516 | A/G | — | uncertain significance |
| rs1352599190 | 17:16,608,615 | G/C | — | uncertain significance |
| rs752953255 | 17:16,608,621 | A/T | — | uncertain significance |
| rs761128361 | 17:16,608,629 | A/C | — | uncertain significance |
| rs531081500 | 17:16,608,662 | C/T | — | uncertain significance |
| rs534183012 | 17:16,610,814 | A/G | — | likely benign |
| rs765491212 | 17:16,612,126 | C/A | — | uncertain significance |
| rs368503677 | 17:16,612,133 | G/A | — | uncertain significance |
| rs371860754 | 17:16,612,146 | G/A | — | uncertain significance |
| rs376203443 | 17:16,612,162 | C/G | — | uncertain significance |
| rs200353361 | 17:16,612,182 | C/T | — | uncertain significance |
| rs376339930 | 17:16,612,251 | G/A | — | likely benign |
| rs2544464861 | 17:16,612,401 | T/C | — | uncertain significance |
| rs200444506 | 17:16,612,452 | T/C | — | uncertain significance |
| rs993127122 | 17:16,612,456 | C/A | — | uncertain significance |
| rs2143120140 | 17:16,612,639 | A/G | — | uncertain significance |
| rs925763310 | 17:16,612,772 | A/C | — | uncertain significance |
| rs2544466161 | 17:16,612,852 | A/T | — | uncertain significance |
| rs1242084498 | 17:16,612,909 | T/C | — | uncertain significance |
| rs1912457394 | 17:16,615,006 | T/C | — | uncertain significance |
| rs1170666638 | 17:16,615,042 | G/T | — | uncertain significance |
| rs560068310 | 17:16,615,079 | T/G | — | uncertain significance |
| rs769142301 | 17:16,630,853 | T/C | — | uncertain significance |
| rs762948246 | 17:16,630,974 | T/A | — | likely benign |
| rs1377143446 | 17:16,630,978 | C/G | — | uncertain significance |
| rs754974502 | 17:16,631,027 | A/G | — | uncertain significance |
| rs753431696 | 17:16,635,892 | A/G | — | uncertain significance |
| rs2544496562 | 17:16,638,033 | T/A | — | uncertain significance |
| rs946961343 | 17:16,638,148 | G/C | — | uncertain significance |
| rs1039973331 | 17:16,638,182 | T/G | — | uncertain significance |
| rs1913922233 | 17:16,638,200 | A/T | — | uncertain significance |
| rs745887947 | 17:16,638,245 | A/G | — | uncertain significance |
| rs1205573998 | 17:16,638,359 | G/A | — | likely benign |
| rs962740133 | 17:16,638,424 | T/G | — | uncertain significance |
| rs2544497280 | 17:16,638,451 | G/T | — | likely benign |
| rs1023268141 | 17:16,638,455 | A/G | — | uncertain significance |
| rs776647456 | 17:16,638,491 | C/T | — | uncertain significance |
| rs550372444 | 17:16,638,653 | T/A | — | likely benign |
| rs552510172 | 17:16,638,793 | A/G | — | uncertain significance |
| rs1356792288 | 17:16,638,884 | A/C | — | uncertain significance |
| rs1282090779 | 17:16,638,893 | T/C | — | uncertain significance |
| rs2544497745 | 17:16,638,946 | G/T | — | uncertain significance |
| rs1915364933 | 17:16,664,767 | T/C | — | likely benign |
| rs1464045002 | 17:16,665,701 | G/A | — | uncertain significance |
| rs2544528418 | 17:16,665,717 | G/A | — | likely benign |
| rs755565950 | 17:16,665,719 | T/A | — | uncertain significance |
| rs56371417 | 17:16,665,774 | G/A | — | uncertain significance |
| rs770511297 | 17:16,676,811 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.