ATAD2B
ATPase family AAA domain containing 2B
Summary
The protein encoded by this gene belongs to the AAA ATPase family. This family member includes an N-terminal bromodomain. It has been found to be localized to the nucleus, partly to replication sites, consistent with a chromatin-related function. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2014]
Known Variants81 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs146831114 | 2:23,903,557 | C/T | intron variant | — |
| rs138299362 | 2:23,903,633 | T/C | intron variant | — |
| rs72796110 | 2:23,905,658 | T/A | intron variant | — |
| rs116821267 | 2:23,907,831 | G/A | intron variant | — |
| rs113831544 | 2:23,912,050 | T/A | intron variant | — |
| rs34964606 | 2:23,916,038 | G/A | — | — |
| rs56152044 | 2:23,927,680 | A/G | intron variant | — |
| rs72796152 | 2:23,933,626 | G/A | downstream gene variant | — |
| rs139389928 | 2:23,933,912 | C/A | downstream gene variant | — |
| rs2113422 | 2:23,939,007 | A/T | — | — |
| rs7608623 | 2:23,948,953 | G/A | — | — |
| rs7575873 | 2:23,962,647 | A/C | — | — |
| rs377110161 | 2:23,963,462 | A/G | — | — |
| rs144333086 | 2:23,963,763 | C/T | intergenic variant | — |
| rs56268260 | 2:23,964,901 | A/C | — | — |
| rs62125861 | 2:23,965,419 | A/T | intergenic variant | — |
| rs2712057 | 2:23,966,524 | G/C | intergenic variant | — |
| rs777638397 | 2:23,974,935 | A/G | — | uncertain significance |
| rs718139 | 2:23,975,911 | G/A | intron variant | — |
| rs200259678 | 2:23,977,552 | C/G | — | uncertain significance |
| rs776141034 | 2:23,977,621 | G/A | — | uncertain significance |
| rs2465759099 | 2:23,980,312 | T/C | — | uncertain significance |
| rs375324464 | 2:23,980,332 | G/A | — | uncertain significance |
| rs941099886 | 2:23,980,401 | G/A | — | likely benign |
| rs765383233 | 2:23,980,404 | G/A | — | uncertain significance |
| rs372015732 | 2:23,980,455 | G/A | — | uncertain significance |
| rs375321718 | 2:23,980,569 | T/C | — | likely benign |
| rs372393038 | 2:23,980,672 | C/G | — | uncertain significance |
| rs763112020 | 2:23,980,753 | T/G | — | uncertain significance |
| rs201429059 | 2:23,980,759 | T/C | — | uncertain significance |
| rs374521897 | 2:23,980,876 | T/A | — | uncertain significance |
| rs1676836080 | 2:23,985,084 | C/T | — | uncertain significance |
| rs1558496515 | 2:23,985,142 | C/G | — | uncertain significance |
| rs367677216 | 2:23,985,148 | C/T | — | uncertain significance |
| rs775849170 | 2:23,985,186 | G/T | — | uncertain significance |
| rs371848643 | 2:23,988,379 | T/C | — | uncertain significance |
| rs781633868 | 2:23,988,397 | T/C | — | uncertain significance |
| rs7569226 | 2:23,992,582 | G/A | regulatory region variant | — |
| rs115457386 | 2:23,998,020 | A/C | intron variant | — |
| rs753646129 | 2:24,005,856 | A/C | — | uncertain significance |
| rs72780191 | 2:24,007,122 | T/C | intron variant | — |
| rs759714301 | 2:24,008,947 | C/T | — | uncertain significance |
| rs1680768947 | 2:24,008,991 | A/G | — | uncertain significance |
| rs774341988 | 2:24,011,433 | C/G | — | uncertain significance |
| rs1469076764 | 2:24,011,435 | T/C | — | uncertain significance |
| rs13009582 | 2:24,018,480 | G/C | — | — |
| rs7569424 | 2:24,036,222 | A/G | intron variant | — |
| rs193002099 | 2:24,042,842 | T/A | intron variant | — |
| rs1230233545 | 2:24,046,184 | G/A | — | uncertain significance |
| rs200578558 | 2:24,046,196 | T/C | — | uncertain significance |
| rs766400706 | 2:24,046,227 | T/C | — | uncertain significance |
| rs372488189 | 2:24,046,278 | C/T | — | uncertain significance |
| rs2467166970 | 2:24,046,280 | A/G | — | uncertain significance |
| rs2467299947 | 2:24,051,770 | T/C | — | uncertain significance |
| rs35832626 | 2:24,054,647 | C/G | — | — |
| rs6719830 | 2:24,061,034 | T/G | — | — |
| rs72786276 | 2:24,062,566 | G/A | intron variant | — |
| rs6718635 | 2:24,066,183 | A/C | regulatory region variant | — |
| rs117735241 | 2:24,077,979 | G/A | intron variant | — |
| rs2468130022 | 2:24,086,339 | T/A | — | uncertain significance |
| rs375884896 | 2:24,086,345 | T/C | — | uncertain significance |
| rs142518269 | 2:24,087,095 | G/A | intron variant | — |
| rs776068430 | 2:24,087,720 | T/G | — | uncertain significance |
| rs1695374869 | 2:24,090,716 | T/G | — | uncertain significance |
| rs2468241356 | 2:24,090,775 | C/T | — | uncertain significance |
| rs150221884 | 2:24,091,099 | C/T | downstream gene variant | — |
| rs891049771 | 2:24,098,707 | G/C | — | uncertain significance |
| rs12988200 | 2:24,100,770 | T/C | — | — |
| rs55682359 | 2:24,101,422 | G/T | intron variant | — |
| rs757248671 | 2:24,110,765 | C/T | — | uncertain significance |
| rs774407808 | 2:24,118,722 | C/T | — | uncertain significance |
| rs372193962 | 2:24,118,786 | G/A | — | uncertain significance |
| rs140521091 | 2:24,129,389 | G/A | intron variant | — |
| rs72796327 | 2:24,140,372 | T/C | intron variant | — |
| rs201165754 | 2:24,144,101 | C/A | — | — |
| rs61739076 | 2:24,149,439 | G/A | — | benign |
| rs1385746254 | 2:24,149,500 | C/A | — | uncertain significance |
| rs550380528 | 2:24,149,522 | G/A | — | uncertain significance |
| rs778862543 | 2:24,149,527 | G/C | — | uncertain significance |
| rs527447797 | 2:24,149,544 | C/T | — | uncertain significance |
| rs754110602 | 2:24,150,032 | C/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.