INO80D
INO80 complex subunit D
Summary
Involved in several processes, including chromatin remodeling; regulation of chromosome organization; and regulation of nucleobase-containing compound metabolic process. Part of Ino80 complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants52 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs759356199 | 2:206,869,123 | T/C | — | uncertain significance |
| rs1410696557 | 2:206,869,324 | G/C | — | uncertain significance |
| rs777518928 | 2:206,869,367 | C/T | — | uncertain significance |
| rs202107782 | 2:206,869,373 | C/T | — | uncertain significance |
| rs761951615 | 2:206,869,408 | G/A | — | uncertain significance |
| rs1315597888 | 2:206,869,480 | T/C | — | uncertain significance |
| rs1687979621 | 2:206,869,535 | C/T | — | uncertain significance |
| rs542653405 | 2:206,869,675 | T/C | — | uncertain significance |
| rs374462979 | 2:206,869,828 | T/C | — | uncertain significance |
| rs2469601149 | 2:206,869,837 | A/G | — | uncertain significance |
| rs2469601769 | 2:206,869,915 | C/A | — | uncertain significance |
| rs781503649 | 2:206,869,939 | G/A | — | uncertain significance |
| rs775445232 | 2:206,870,056 | C/T | — | uncertain significance |
| rs768886465 | 2:206,870,110 | C/T | — | uncertain significance |
| rs779232035 | 2:206,870,144 | C/G | — | uncertain significance |
| rs748552208 | 2:206,870,164 | A/G | — | uncertain significance |
| rs818022 | 2:206,871,458 | C/G | — | — |
| rs201681502 | 2:206,872,113 | T/C | — | likely benign |
| rs557304541 | 2:206,874,302 | G/A | — | uncertain significance |
| rs144598064 | 2:206,874,307 | T/C | — | benign |
| rs368082888 | 2:206,874,395 | G/A | — | uncertain significance |
| rs769913280 | 2:206,874,490 | C/T | — | uncertain significance |
| rs539232439 | 2:206,876,110 | T/C | — | — |
| rs77534600 | 2:206,876,813 | G/A | upstream gene variant | — |
| rs754767138 | 2:206,884,517 | C/T | — | uncertain significance |
| rs369566340 | 2:206,884,520 | T/A | — | uncertain significance |
| rs770510485 | 2:206,884,568 | T/C | — | uncertain significance |
| rs147537311 | 2:206,891,281 | A/T | downstream gene variant | — |
| rs1163915802 | 2:206,892,887 | A/T | — | uncertain significance |
| rs200519220 | 2:206,892,937 | C/T | — | uncertain significance |
| rs2469703567 | 2:206,893,036 | C/T | — | uncertain significance |
| rs774297499 | 2:206,911,229 | C/T | — | likely benign |
| rs1689199329 | 2:206,911,249 | G/T | — | uncertain significance |
| rs376007552 | 2:206,911,255 | C/T | — | uncertain significance |
| rs767743342 | 2:206,911,277 | A/G | — | uncertain significance |
| rs376594097 | 2:206,911,289 | G/C | — | uncertain significance |
| rs755751160 | 2:206,911,294 | G/A | — | uncertain significance |
| rs1189105383 | 2:206,911,316 | T/C | — | uncertain significance |
| rs1575851053 | 2:206,915,607 | G/C | — | — |
| rs200755221 | 2:206,920,966 | C/T | — | uncertain significance |
| rs144619437 | 2:206,920,990 | C/T | — | benign |
| rs2469815028 | 2:206,921,004 | G/C | — | uncertain significance |
| rs200938296 | 2:206,921,053 | G/C | — | uncertain significance |
| rs774994130 | 2:206,921,117 | G/C | — | uncertain significance |
| rs533369239 | 2:206,921,122 | G/A | — | uncertain significance |
| rs371646344 | 2:206,921,218 | G/A | — | uncertain significance |
| rs2469818581 | 2:206,921,465 | G/A | — | uncertain significance |
| rs202127822 | 2:206,921,503 | C/G | — | uncertain significance |
| rs778667830 | 2:206,921,588 | C/T | — | uncertain significance |
| rs1409578530 | 2:206,921,667 | C/G | — | uncertain significance |
| rs1689722743 | 2:206,927,596 | T/C | — | uncertain significance |
| rs745458624 | 2:206,927,721 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.