CCSER2
coiled-coil serine rich protein 2
Summary
Predicted to enable microtubule binding activity. Predicted to be involved in microtubule bundle formation. Predicted to be located in cytoplasm and cytoskeleton. Predicted to be active in microtubule cytoskeleton. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants51 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1846036221 | 10:86,130,834 | C/G | — | uncertain significance |
| rs772333587 | 10:86,130,873 | C/T | — | uncertain significance |
| rs747964636 | 10:86,130,951 | A/G | — | uncertain significance |
| rs769775447 | 10:86,130,959 | A/G | — | uncertain significance |
| rs1283689282 | 10:86,131,053 | C/T | — | uncertain significance |
| rs1297490735 | 10:86,131,182 | C/G | — | uncertain significance |
| rs757185879 | 10:86,131,187 | C/T | — | uncertain significance |
| rs1345479761 | 10:86,131,193 | A/G | — | uncertain significance |
| rs148835960 | 10:86,131,308 | A/G | — | likely benign |
| rs766154480 | 10:86,131,376 | G/A | — | uncertain significance |
| rs375626713 | 10:86,131,428 | C/A | — | uncertain significance |
| rs1337825020 | 10:86,131,511 | C/G | — | uncertain significance |
| rs759286087 | 10:86,131,518 | C/G | — | uncertain significance |
| rs142860601 | 10:86,131,524 | C/T | — | uncertain significance |
| rs1564607725 | 10:86,131,581 | A/G | — | uncertain significance |
| rs1846080138 | 10:86,131,649 | A/G | — | uncertain significance |
| rs755457843 | 10:86,131,650 | A/G | — | uncertain significance |
| rs145634898 | 10:86,131,742 | A/G | — | uncertain significance |
| rs777493764 | 10:86,131,754 | A/G | — | uncertain significance |
| rs200588575 | 10:86,131,808 | A/G | — | uncertain significance |
| rs771179017 | 10:86,131,824 | A/C | — | uncertain significance |
| rs765789843 | 10:86,132,082 | A/G | — | uncertain significance |
| rs1490157440 | 10:86,132,106 | A/G | — | uncertain significance |
| rs1427009898 | 10:86,132,124 | A/C | — | uncertain significance |
| rs376616118 | 10:86,132,129 | C/T | — | uncertain significance |
| rs140960423 | 10:86,132,148 | A/G | — | uncertain significance |
| rs147804648 | 10:86,132,214 | T/C | — | uncertain significance |
| rs573869341 | 10:86,133,008 | A/G | — | — |
| rs150301166 | 10:86,133,546 | A/G | — | uncertain significance |
| rs75654410 | 10:86,175,805 | C/T | regulatory region variant | — |
| rs2493368458 | 10:86,177,589 | T/A | — | uncertain significance |
| rs1259377452 | 10:86,177,593 | C/T | — | uncertain significance |
| rs149112423 | 10:86,185,507 | C/T | — | uncertain significance |
| rs370948089 | 10:86,185,508 | G/A | — | uncertain significance |
| rs1033141671 | 10:86,185,517 | G/A | — | uncertain significance |
| rs780546894 | 10:86,185,534 | C/T | — | uncertain significance |
| rs141796865 | 10:86,185,549 | G/A | — | uncertain significance |
| rs2493425554 | 10:86,185,558 | A/G | — | uncertain significance |
| rs145429708 | 10:86,185,591 | C/A | — | uncertain significance |
| rs185632970 | 10:86,185,619 | A/G | — | uncertain significance |
| rs563138001 | 10:86,198,290 | C/A | — | uncertain significance |
| rs2493516232 | 10:86,198,327 | T/C | — | uncertain significance |
| rs61743630 | 10:86,198,432 | A/G | — | uncertain significance |
| rs2493741174 | 10:86,230,151 | A/G | — | uncertain significance |
| rs1191437024 | 10:86,259,647 | C/T | — | uncertain significance |
| rs917317849 | 10:86,259,653 | T/C | — | uncertain significance |
| rs145794353 | 10:86,259,662 | G/T | — | uncertain significance |
| rs1168563804 | 10:86,259,707 | G/A | — | uncertain significance |
| rs866188943 | 10:86,273,220 | C/T | — | uncertain significance |
| rs199582393 | 10:86,273,279 | A/G | — | likely benign |
| rs766626465 | 10:86,273,286 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.