ISOC2
isochorismatase domain containing 2
Summary
Involved in protein destabilization. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants26 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs945499813 | 19:55,966,370 | G/T | — | uncertain significance |
| rs551380020 | 19:55,966,444 | C/T | — | uncertain significance |
| rs761217454 | 19:55,966,631 | G/A | — | uncertain significance |
| rs779830218 | 19:55,966,663 | T/G | — | uncertain significance |
| rs202116366 | 19:55,966,670 | C/T | — | uncertain significance |
| rs555676504 | 19:55,966,672 | C/T | — | uncertain significance |
| rs140943962 | 19:55,966,673 | G/A | missense variant | — |
| rs1448712116 | 19:55,966,695 | G/T | — | uncertain significance |
| rs2514212445 | 19:55,966,696 | T/G | — | uncertain significance |
| rs1599881790 | 19:55,966,705 | T/G | — | uncertain significance |
| rs2514212475 | 19:55,966,706 | A/T | — | uncertain significance |
| rs2514212494 | 19:55,966,708 | A/T | — | uncertain significance |
| rs369547081 | 19:55,966,743 | G/C | — | uncertain significance |
| rs372768676 | 19:55,967,043 | G/A | — | uncertain significance |
| rs150695554 | 19:55,967,047 | G/A | — | uncertain significance |
| rs538150462 | 19:55,967,058 | C/T | — | uncertain significance |
| rs147467798 | 19:55,967,092 | T/C | — | uncertain significance |
| rs2514213740 | 19:55,967,100 | C/A | — | uncertain significance |
| rs749732792 | 19:55,967,115 | G/A | — | uncertain significance |
| rs769034749 | 19:55,967,119 | G/A | — | uncertain significance |
| rs373813460 | 19:55,967,148 | G/A | — | uncertain significance |
| rs375030964 | 19:55,967,726 | C/T | — | uncertain significance |
| rs201886494 | 19:55,967,733 | C/G | — | uncertain significance |
| rs144270874 | 19:55,967,747 | T/A | — | uncertain significance |
| rs374642327 | 19:55,967,825 | C/T | — | uncertain significance |
| rs200823817 | 19:55,967,849 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.