CASKIN1
CASK interacting protein 1
Summary
Enables identical protein binding activity. Predicted to be involved in signal transduction. Predicted to be active in cytoplasm; glutamatergic synapse; and postsynapse. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants113 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs761392957 | 16:2,228,556 | C/G | — | uncertain significance |
| rs2545017704 | 16:2,228,622 | C/T | — | uncertain significance |
| rs779842332 | 16:2,228,642 | G/A | — | uncertain significance |
| rs760908481 | 16:2,228,904 | G/A | — | uncertain significance |
| rs2093155846 | 16:2,228,918 | T/A | — | uncertain significance |
| rs2093156348 | 16:2,229,003 | C/A | — | uncertain significance |
| rs1296010908 | 16:2,229,006 | C/T | — | uncertain significance |
| rs1380725979 | 16:2,229,084 | C/T | — | uncertain significance |
| rs1301691459 | 16:2,229,117 | G/A | — | uncertain significance |
| rs1399633425 | 16:2,229,147 | G/A | — | uncertain significance |
| rs1481619236 | 16:2,229,150 | G/A | — | uncertain significance |
| rs1376689037 | 16:2,229,156 | C/T | — | likely benign |
| rs954754613 | 16:2,229,180 | G/A | — | uncertain significance |
| rs964744460 | 16:2,229,182 | G/A | — | uncertain significance |
| rs2545018946 | 16:2,229,203 | G/A | — | uncertain significance |
| rs1454674318 | 16:2,229,290 | G/A | — | uncertain significance |
| rs1176202094 | 16:2,229,318 | G/C | — | uncertain significance |
| rs199978114 | 16:2,229,642 | G/A | — | uncertain significance |
| rs1381181258 | 16:2,229,663 | C/T | — | likely benign |
| rs750787616 | 16:2,229,789 | G/C | — | uncertain significance |
| rs995355275 | 16:2,229,812 | G/T | — | uncertain significance |
| rs2545020224 | 16:2,229,836 | C/T | — | uncertain significance |
| rs967877767 | 16:2,229,874 | C/T | — | likely benign |
| rs1435326377 | 16:2,229,882 | G/A | — | uncertain significance |
| rs769299530 | 16:2,229,909 | C/T | — | uncertain significance |
| rs1243274063 | 16:2,229,930 | T/C | — | uncertain significance |
| rs2545020410 | 16:2,229,939 | C/T | — | uncertain significance |
| rs765428175 | 16:2,229,953 | T/C | — | uncertain significance |
| rs200175101 | 16:2,230,023 | C/G | — | uncertain significance |
| rs2545020665 | 16:2,230,088 | C/T | — | uncertain significance |
| rs1323397210 | 16:2,230,133 | C/T | — | uncertain significance |
| rs767569279 | 16:2,230,134 | G/A | — | uncertain significance |
| rs1407833617 | 16:2,230,143 | T/C | — | uncertain significance |
| rs1412228834 | 16:2,230,169 | C/G | — | uncertain significance |
| rs575231658 | 16:2,230,278 | G/A | — | uncertain significance |
| rs765784613 | 16:2,230,294 | C/G | — | uncertain significance |
| rs563655919 | 16:2,230,314 | C/T | — | uncertain significance |
| rs769767843 | 16:2,230,398 | C/T | — | uncertain significance |
| rs1190303769 | 16:2,230,557 | C/T | — | uncertain significance |
| rs558328556 | 16:2,230,591 | G/A | — | likely benign |
| rs866039831 | 16:2,230,604 | G/A | — | uncertain significance |
| rs1027747328 | 16:2,230,643 | G/A | — | uncertain significance |
| rs2141312245 | 16:2,230,649 | T/C | — | uncertain significance |
| rs778822379 | 16:2,230,658 | G/A | — | uncertain significance |
| rs776265068 | 16:2,230,683 | C/T | — | uncertain significance |
| rs1282304031 | 16:2,230,695 | C/T | — | uncertain significance |
| rs1319296560 | 16:2,230,743 | G/A | — | uncertain significance |
| rs544116870 | 16:2,230,759 | G/C | — | uncertain significance |
| rs766721052 | 16:2,230,793 | G/A | — | uncertain significance |
| rs369359969 | 16:2,230,799 | G/A | — | uncertain significance |
| rs1403263137 | 16:2,230,851 | C/T | — | uncertain significance |
| rs757200623 | 16:2,230,899 | G/T | — | uncertain significance |
| rs754466880 | 16:2,230,923 | G/A | — | uncertain significance |
| rs552170346 | 16:2,230,929 | T/G | — | uncertain significance |
| rs199591799 | 16:2,230,946 | G/A | — | uncertain significance |
| rs1434679188 | 16:2,230,967 | G/A | — | uncertain significance |
| rs901159041 | 16:2,230,991 | C/T | — | uncertain significance |
| rs140130801 | 16:2,231,033 | G/A | — | uncertain significance |
| rs752223745 | 16:2,231,079 | G/A | — | uncertain significance |
| rs750979771 | 16:2,231,094 | C/T | — | uncertain significance |
| rs2093166515 | 16:2,231,146 | C/A | — | uncertain significance |
| rs2545022575 | 16:2,231,148 | C/T | — | uncertain significance |
| rs754235888 | 16:2,231,154 | G/A | — | uncertain significance |
| rs770848780 | 16:2,231,174 | C/G | — | uncertain significance |
| rs762662379 | 16:2,231,204 | G/A | — | uncertain significance |
| rs753095859 | 16:2,231,222 | C/T | — | uncertain significance |
| rs758777566 | 16:2,231,229 | G/A | — | uncertain significance |
| rs200142871 | 16:2,231,273 | C/T | — | uncertain significance |
| rs375593225 | 16:2,231,298 | G/A | — | uncertain significance |
| rs369066078 | 16:2,231,312 | G/A | — | uncertain significance |
| rs760868396 | 16:2,231,423 | A/T | — | uncertain significance |
| rs766598978 | 16:2,231,471 | G/A | — | uncertain significance |
| rs556281885 | 16:2,231,520 | G/A | — | uncertain significance |
| rs368506468 | 16:2,231,538 | C/A | — | uncertain significance |
| rs372758880 | 16:2,231,808 | G/A | — | likely benign |
| rs1479864197 | 16:2,231,866 | T/C | — | uncertain significance |
| rs577911589 | 16:2,232,592 | A/C | — | — |
| rs773717553 | 16:2,233,655 | G/A | — | uncertain significance |
| rs769615876 | 16:2,233,715 | G/C | — | uncertain significance |
| rs2545025541 | 16:2,233,746 | G/T | — | uncertain significance |
| rs370914132 | 16:2,233,890 | G/A | — | uncertain significance |
| rs952187650 | 16:2,233,933 | C/G | — | uncertain significance |
| rs563294110 | 16:2,234,812 | G/A | — | uncertain significance |
| rs1263325578 | 16:2,234,819 | C/T | — | uncertain significance |
| rs754489782 | 16:2,234,834 | C/T | — | uncertain significance |
| rs762014225 | 16:2,234,837 | C/T | — | uncertain significance |
| rs758904143 | 16:2,234,842 | G/C | — | uncertain significance |
| rs2545026748 | 16:2,234,855 | G/T | — | uncertain significance |
| rs1242570609 | 16:2,234,966 | G/A | — | uncertain significance |
| rs764696591 | 16:2,234,967 | G/C | — | uncertain significance |
| rs367863057 | 16:2,235,117 | C/T | — | likely benign |
| rs373420687 | 16:2,235,158 | C/T | — | uncertain significance |
| rs201521466 | 16:2,235,317 | G/C | — | uncertain significance |
| rs202081252 | 16:2,235,375 | C/G | — | uncertain significance |
| rs369240172 | 16:2,236,713 | C/T | — | uncertain significance |
| rs954454316 | 16:2,236,759 | G/A | — | uncertain significance |
| rs374094027 | 16:2,236,770 | G/A | — | uncertain significance |
| rs772902793 | 16:2,237,026 | T/C | — | uncertain significance |
| rs770496478 | 16:2,237,032 | A/G | — | uncertain significance |
| rs369964678 | 16:2,237,056 | G/T | — | uncertain significance |
Showing 100 of 113 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.