MACROD2
mono-ADP ribosylhydrolase 2
Summary
The protein encoded by this gene is a deacetylase involved in removing ADP-ribose from mono-ADP-ribosylated proteins. The encoded protein has been shown to translocate from the nucleus to the cytoplasm upon DNA damage. [provided by RefSeq, May 2017]
Known Variants88 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs200598669 | 20:13,976,404 | G/A | — | likely benign |
| rs2052743339 | 20:13,982,990 | A/T | — | uncertain significance |
| rs759161223 | 20:13,983,001 | C/A | — | uncertain significance |
| rs77520851 | 20:14,041,062 | A/G | intron variant | — |
| rs6110154 | 20:14,044,408 | C/G | intron variant | — |
| rs2990505 | 20:14,066,276 | T/C | — | benign |
| rs2208454 | 20:14,265,415 | G/T | intron variant | — |
| rs6079395 | 20:14,327,899 | G/A | intron variant | — |
| rs566462617 | 20:14,356,980 | T/C | — | — |
| rs6110278 | 20:14,388,215 | C/T | intron variant | — |
| rs8122234 | 20:14,431,463 | A/C | intron variant | — |
| rs13038351 | 20:14,467,387 | A/T | intron variant | — |
| rs2515144396 | 20:14,474,149 | G/A | — | uncertain significance |
| rs6074747 | 20:14,497,884 | C/T | intron variant | — |
| rs6079469 | 20:14,501,141 | T/A | intron variant | — |
| rs11698330 | 20:14,507,909 | G/T | intron variant | — |
| rs2224291 | 20:14,535,045 | G/T | coding sequence variant | — |
| rs62202889 | 20:14,544,626 | G/A | intron variant | — |
| rs62202906 | 20:14,580,279 | G/A | intron variant | — |
| rs185734295 | 20:14,594,260 | C/T | intron variant | — |
| rs55771103 | 20:14,616,908 | C/T | intron variant | — |
| rs73100693 | 20:14,624,598 | T/A | intron variant | — |
| rs1932957 | 20:14,631,935 | G/A | intron variant | — |
| rs62202941 | 20:14,653,919 | G/T | regulatory region variant | — |
| rs201978764 | 20:14,665,545 | C/G | — | uncertain significance |
| rs2515454220 | 20:14,665,592 | C/A | — | uncertain significance |
| rs6135229 | 20:14,683,029 | C/A | intron variant | — |
| rs11908351 | 20:14,686,509 | A/C | — | — |
| rs550086140 | 20:14,697,501 | T/G | — | — |
| rs6074776 | 20:14,697,914 | C/T | intron variant | — |
| rs6135234 | 20:14,701,557 | G/T | intron variant | — |
| rs6034019 | 20:14,702,915 | A/G | regulatory region variant | — |
| rs4141463 | 20:14,747,471 | T/C | intron variant | — |
| rs743134 | 20:14,804,964 | G/A | intron variant | — |
| rs2024900 | 20:14,827,827 | C/T | intron variant | — |
| rs385678 | 20:14,835,172 | A/T | intron variant | — |
| rs8182773 | 20:14,835,640 | C/T | intron variant | — |
| rs13043001 | 20:14,843,361 | A/G | — | — |
| rs367798757 | 20:14,855,804 | G/A | — | — |
| rs1408430 | 20:14,917,048 | C/G | upstream gene variant | — |
| rs11087123 | 20:15,120,744 | A/G | intron variant | — |
| rs199307 | 20:15,177,580 | A/G | intron variant | — |
| rs17773241 | 20:15,185,604 | G/A | intron variant | — |
| rs769941282 | 20:15,210,616 | G/A | — | uncertain significance |
| rs189533691 | 20:15,210,624 | A/G | — | likely benign |
| rs1292698569 | 20:15,210,639 | A/G | — | uncertain significance |
| rs750028619 | 20:15,210,645 | G/T | — | uncertain significance |
| rs2076945732 | 20:15,210,650 | T/G | — | likely benign |
| rs7267421 | 20:15,227,636 | G/A | intron variant | — |
| rs6110577 | 20:15,335,754 | T/C | intron variant | — |
| rs778184364 | 20:15,480,430 | G/A | — | uncertain significance |
| rs200224844 | 20:15,480,458 | C/T | — | uncertain significance |
| rs117214008 | 20:15,675,362 | T/G | intron variant | — |
| rs6514610 | 20:15,739,440 | G/A | intron variant | — |
| rs55677435 | 20:15,752,536 | T/A | — | — |
| rs10460644 | 20:15,768,237 | G/T | — | — |
| rs6131710 | 20:15,776,241 | C/T | intron variant | — |
| rs73246158 | 20:15,783,377 | G/T | — | — |
| rs6135551 | 20:15,795,175 | T/C | intron variant | — |
| rs6135555 | 20:15,796,237 | C/A | intron variant | — |
| rs73898513 | 20:15,806,210 | C/T | intron variant | — |
| rs73898514 | 20:15,806,261 | T/G | intron variant | — |
| rs8118253 | 20:15,819,926 | T/A | intron variant | — |
| rs175804 | 20:15,832,299 | A/T | intron variant | — |
| rs747679634 | 20:15,843,407 | C/A | — | uncertain significance |
| rs769250469 | 20:15,843,454 | A/G | — | likely benign |
| rs778645787 | 20:15,866,411 | G/A | — | uncertain significance |
| rs373690455 | 20:15,913,928 | C/T | — | likely benign |
| rs776889043 | 20:15,913,950 | G/A | — | conflicting classifications of pathogenicity |
| rs2514835063 | 20:15,913,980 | G/T | — | uncertain significance |
| rs566607934 | 20:15,918,132 | A/G | — | likely benign |
| rs760177995 | 20:15,918,147 | G/A | — | likely benign |
| rs73597733 | 20:15,941,137 | G/A | intron variant | — |
| rs150617904 | 20:15,948,230 | G/A | — | benign |
| rs41275442 | 20:15,967,390 | C/T | — | benign |
| rs748972891 | 20:15,967,716 | T/C | — | uncertain significance |
| rs138229827 | 20:15,967,722 | A/G | — | uncertain significance |
| rs748015755 | 20:15,967,724 | C/G | — | uncertain significance |
| rs561276144 | 20:15,967,752 | C/T | — | uncertain significance |
| rs147212262 | 20:15,967,795 | G/A | — | uncertain significance |
| rs6080100 | 20:16,003,406 | T/C | intron variant | — |
| rs114484322 | 20:16,021,855 | A/T | — | benign |
| rs201701473 | 20:16,025,206 | C/T | — | likely benign |
| rs139092334 | 20:16,025,279 | T/A | — | benign |
| rs80044408 | 20:16,025,289 | T/G | — | benign |
| rs374569449 | 20:16,030,485 | A/G | — | likely benign |
| rs146842863 | 20:16,030,519 | T/A | — | uncertain significance |
| rs146233573 | 20:16,030,533 | A/G | 3 prime UTR variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.