USP43
ubiquitin specific peptidase 43
Summary
Predicted to enable ISG15-specific peptidase activity. Predicted to be involved in translesion synthesis. Predicted to be located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants71 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1160942498 | 17:9,548,987 | C/A | — | uncertain significance |
| rs1209634002 | 17:9,549,007 | C/G | — | uncertain significance |
| rs2507745604 | 17:9,549,011 | G/C | — | uncertain significance |
| rs1434204489 | 17:9,549,037 | C/T | — | uncertain significance |
| rs944285870 | 17:9,549,050 | C/A | — | uncertain significance |
| rs891333808 | 17:9,549,061 | C/G | — | uncertain significance |
| rs767001982 | 17:9,549,073 | G/A | — | uncertain significance |
| rs1039977841 | 17:9,549,127 | G/A | — | uncertain significance |
| rs530371655 | 17:9,549,185 | G/A | — | uncertain significance |
| rs755058755 | 17:9,549,233 | C/T | — | uncertain significance |
| rs2507747966 | 17:9,549,359 | C/T | — | uncertain significance |
| rs1479552726 | 17:9,549,387 | G/T | — | uncertain significance |
| rs2507748505 | 17:9,549,448 | T/C | — | uncertain significance |
| rs1442246415 | 17:9,559,756 | A/G | — | uncertain significance |
| rs1210901607 | 17:9,559,822 | G/A | — | uncertain significance |
| rs200451523 | 17:9,570,062 | A/T | — | uncertain significance |
| rs2507825009 | 17:9,578,281 | A/G | — | uncertain significance |
| rs1229223623 | 17:9,580,161 | A/G | — | likely benign |
| rs376716651 | 17:9,580,184 | G/A | — | likely benign |
| rs1303703015 | 17:9,583,573 | G/T | — | uncertain significance |
| rs765887468 | 17:9,583,620 | G/A | — | uncertain significance |
| rs745449130 | 17:9,586,169 | C/T | — | uncertain significance |
| rs2507851520 | 17:9,586,227 | T/C | — | uncertain significance |
| rs779560239 | 17:9,586,265 | C/A | — | uncertain significance |
| rs7219025 | 17:9,587,432 | C/A | intron variant | — |
| rs2139888 | 17:9,587,937 | G/T | — | — |
| rs8079769 | 17:9,588,455 | G/A | regulatory region variant | — |
| rs750749252 | 17:9,590,179 | A/G | — | uncertain significance |
| rs116247935 | 17:9,590,223 | A/T | — | benign |
| rs769838418 | 17:9,596,520 | G/A | — | uncertain significance |
| rs1269171061 | 17:9,603,536 | C/T | — | uncertain significance |
| rs1333072106 | 17:9,604,795 | G/A | — | uncertain significance |
| rs780962461 | 17:9,604,909 | T/C | — | uncertain significance |
| rs186741506 | 17:9,604,922 | C/G | — | uncertain significance |
| rs759529221 | 17:9,604,946 | C/T | — | uncertain significance |
| rs2507916836 | 17:9,613,275 | T/C | — | uncertain significance |
| rs764930248 | 17:9,613,333 | C/T | — | uncertain significance |
| rs201643008 | 17:9,613,339 | G/A | — | uncertain significance |
| rs368374779 | 17:9,613,367 | T/G | — | likely benign |
| rs779316570 | 17:9,613,371 | A/G | — | uncertain significance |
| rs2507917184 | 17:9,613,380 | T/C | — | uncertain significance |
| rs1310314819 | 17:9,615,285 | G/C | — | uncertain significance |
| rs746710515 | 17:9,631,277 | T/G | — | uncertain significance |
| rs2507956243 | 17:9,631,294 | G/A | — | uncertain significance |
| rs200272651 | 17:9,631,298 | G/A | — | uncertain significance |
| rs201063447 | 17:9,631,303 | G/A | — | uncertain significance |
| rs747740075 | 17:9,631,381 | C/T | — | uncertain significance |
| rs76912039 | 17:9,631,397 | C/A | — | uncertain significance |
| rs187057967 | 17:9,631,408 | C/A | — | uncertain significance |
| rs9896179 | 17:9,631,422 | C/T | — | benign |
| rs1465666857 | 17:9,631,462 | C/T | — | uncertain significance |
| rs376910036 | 17:9,631,496 | C/T | — | uncertain significance |
| rs368384262 | 17:9,631,546 | G/A | — | likely benign |
| rs201132961 | 17:9,631,577 | G/A | — | uncertain significance |
| rs199608953 | 17:9,631,628 | A/C | — | uncertain significance |
| rs2507958197 | 17:9,631,636 | C/G | — | uncertain significance |
| rs781092429 | 17:9,631,657 | G/A | — | uncertain significance |
| rs749541896 | 17:9,631,666 | A/G | — | likely benign |
| rs1177672946 | 17:9,631,699 | G/A | — | uncertain significance |
| rs955137421 | 17:9,631,733 | T/G | — | uncertain significance |
| rs772161465 | 17:9,631,772 | G/A | — | uncertain significance |
| rs771240606 | 17:9,631,781 | G/A | — | uncertain significance |
| rs762237784 | 17:9,631,808 | G/A | — | uncertain significance |
| rs2507959528 | 17:9,631,889 | C/T | — | uncertain significance |
| rs781718407 | 17:9,631,906 | C/T | — | uncertain significance |
| rs1216468129 | 17:9,631,939 | G/A | — | uncertain significance |
| rs755033517 | 17:9,631,991 | A/G | — | uncertain significance |
| rs116015543 | 17:9,631,994 | T/C | — | benign |
| rs200626439 | 17:9,632,032 | G/T | — | uncertain significance |
| rs202235190 | 17:9,632,155 | C/T | — | uncertain significance |
| rs370520395 | 17:9,632,276 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.