CABLES2
Cdk5 and Abl enzyme substrate 2
Summary
Predicted to be involved in cell division and regulation of cell cycle. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants50 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs751635728 | 20:60,966,043 | A/G | — | uncertain significance |
| rs2516383073 | 20:60,966,085 | A/G | — | uncertain significance |
| rs762899891 | 20:60,966,121 | A/G | — | uncertain significance |
| rs2516383507 | 20:60,966,366 | A/C | — | uncertain significance |
| rs766614146 | 20:60,966,462 | G/T | — | uncertain significance |
| rs200810639 | 20:60,966,492 | C/T | — | uncertain significance |
| rs756963039 | 20:60,966,493 | G/A | — | uncertain significance |
| rs778553140 | 20:60,966,495 | A/G | — | uncertain significance |
| rs750044349 | 20:60,967,496 | G/T | — | uncertain significance |
| rs779965934 | 20:60,967,510 | C/A | — | uncertain significance |
| rs1044079708 | 20:60,967,533 | C/T | — | uncertain significance |
| rs770984242 | 20:60,967,545 | C/T | — | uncertain significance |
| rs377753672 | 20:60,968,001 | C/T | — | uncertain significance |
| rs779628073 | 20:60,968,507 | C/T | — | uncertain significance |
| rs769583416 | 20:60,968,528 | G/A | — | uncertain significance |
| rs772962793 | 20:60,968,541 | G/A | — | likely benign |
| rs765488829 | 20:60,968,658 | C/T | — | uncertain significance |
| rs778885001 | 20:60,969,269 | C/T | — | likely benign |
| rs2427308 | 20:60,969,451 | C/T | intron variant | — |
| rs746103333 | 20:60,970,039 | A/G | — | uncertain significance |
| rs2427313 | 20:60,970,675 | G/A | regulatory region variant | — |
| rs1451057881 | 20:60,971,399 | T/G | — | uncertain significance |
| rs771723662 | 20:60,971,416 | G/A | — | uncertain significance |
| rs555344970 | 20:60,971,628 | C/T | — | uncertain significance |
| rs774214864 | 20:60,971,643 | C/T | — | uncertain significance |
| rs1162057875 | 20:60,974,883 | C/T | — | — |
| rs6061512 | 20:60,976,929 | G/A | intron variant | — |
| rs6061235 | 20:60,978,524 | C/G | intron variant | — |
| rs146975578 | 20:60,982,024 | C/T | — | benign |
| rs1988309465 | 20:60,982,119 | G/A | — | uncertain significance |
| rs952349966 | 20:60,982,122 | G/T | — | uncertain significance |
| rs1434874404 | 20:60,982,170 | T/C | — | uncertain significance |
| rs755759738 | 20:60,982,182 | A/C | — | uncertain significance |
| rs868316661 | 20:60,982,199 | C/A | — | uncertain significance |
| rs1182332496 | 20:60,982,210 | G/C | — | uncertain significance |
| rs979108950 | 20:60,982,224 | G/C | — | uncertain significance |
| rs1988313269 | 20:60,982,229 | G/A | — | uncertain significance |
| rs1327552563 | 20:60,982,265 | G/T | — | uncertain significance |
| rs1397827980 | 20:60,982,266 | C/T | — | uncertain significance |
| rs943878486 | 20:60,982,275 | G/A | — | uncertain significance |
| rs897926945 | 20:60,982,284 | C/T | — | uncertain significance |
| rs887809337 | 20:60,982,295 | G/T | — | uncertain significance |
| rs1250790930 | 20:60,982,298 | G/A | — | uncertain significance |
| rs1002455567 | 20:60,982,299 | G/A | — | uncertain significance |
| rs1365270055 | 20:60,982,304 | G/T | — | uncertain significance |
| rs1468540907 | 20:60,982,305 | G/T | — | uncertain significance |
| rs1988318428 | 20:60,982,307 | G/A | — | uncertain significance |
| rs1384379941 | 20:60,982,314 | C/T | — | uncertain significance |
| rs1222512037 | 20:60,982,322 | G/A | — | uncertain significance |
| rs187505351 | 20:60,982,419 | C/T | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.