CCDC97
coiled-coil domain containing 97
Summary
Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs143841115 | 19:41,822,429 | G/T | — | uncertain significance |
| rs75624130 | 19:41,822,570 | C/T | — | uncertain significance |
| rs559582361 | 19:41,822,589 | G/A | — | uncertain significance |
| rs2513362271 | 19:41,822,610 | T/A | — | uncertain significance |
| rs200401151 | 19:41,822,622 | G/A | — | uncertain significance |
| rs551538141 | 19:41,822,633 | C/A | — | uncertain significance |
| rs750870913 | 19:41,822,634 | G/A | — | uncertain significance |
| rs200711332 | 19:41,822,637 | C/T | — | uncertain significance |
| rs745757074 | 19:41,822,664 | G/A | — | likely benign |
| rs143157411 | 19:41,822,678 | C/T | — | uncertain significance |
| rs756362212 | 19:41,822,711 | C/T | — | uncertain significance |
| rs575323158 | 19:41,825,484 | G/A | — | uncertain significance |
| rs749474375 | 19:41,825,520 | C/T | — | uncertain significance |
| rs752926768 | 19:41,825,596 | C/A | — | uncertain significance |
| rs759164631 | 19:41,825,616 | G/A | — | uncertain significance |
| rs774895639 | 19:41,825,631 | C/T | — | uncertain significance |
| rs764377967 | 19:41,825,661 | G/A | — | uncertain significance |
| rs1805661437 | 19:41,825,743 | A/G | — | uncertain significance |
| rs56254331 | 19:41,826,020 | A/G | — | — |
| rs759691177 | 19:41,826,281 | C/T | — | uncertain significance |
| rs760667676 | 19:41,826,284 | G/A | — | uncertain significance |
| rs368555031 | 19:41,826,293 | G/A | — | uncertain significance |
| rs2513365414 | 19:41,826,321 | C/T | — | uncertain significance |
| rs768577577 | 19:41,826,338 | C/T | — | uncertain significance |
| rs372224178 | 19:41,826,339 | G/A | — | uncertain significance |
| rs755824909 | 19:41,826,372 | A/G | — | uncertain significance |
| rs2513366745 | 19:41,828,513 | A/G | — | uncertain significance |
| rs778386811 | 19:41,828,519 | G/A | — | uncertain significance |
| rs35135271 | 19:41,828,525 | G/A | — | uncertain significance |
| rs201740650 | 19:41,828,540 | G/A | — | uncertain significance |
| rs2513366827 | 19:41,828,589 | A/G | — | uncertain significance |
| rs2513366829 | 19:41,828,590 | T/A | — | uncertain significance |
| rs1197555394 | 19:41,828,600 | C/A | — | uncertain significance |
| rs2241718 | 19:41,829,606 | G/C | — | — |
| rs6957 | 19:41,830,606 | T/C | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.