ADPRS
ADP-ribosylserine hydrolase
Summary
This gene encodes a member of the ADP-ribosylglycohydrolase family. The encoded enzyme catalyzes the removal of ADP-ribose from ADP-ribosylated proteins. This enzyme localizes to the mitochondria, in addition to the nucleus and cytoplasm.[provided by RefSeq, Feb 2009]
Known Variants52 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1278943778 | 1:36,554,527 | G/A | — | likely benign |
| rs1326622051 | 1:36,554,528 | C/T | — | likely benign |
| rs777166159 | 1:36,554,531 | C/T | — | uncertain significance |
| rs918091972 | 1:36,554,537 | G/A | — | uncertain significance |
| rs199964084 | 1:36,554,541 | A/G | — | likely benign |
| rs1045143850 | 1:36,554,552 | C/G | — | uncertain significance |
| rs1557732234 | 1:36,554,605 | G/A | — | pathogenic |
| rs1352841148 | 1:36,554,606 | A/G | — | uncertain significance |
| rs1188484640 | 1:36,554,630 | C/T | — | uncertain significance |
| rs749889837 | 1:36,554,641 | G/T | — | uncertain significance |
| rs2524677445 | 1:36,554,671 | C/T | — | likely pathogenic |
| rs3767704 | 1:36,555,817 | A/G | downstream gene variant | — |
| rs768000 | 1:36,556,867 | C/T | — | benign |
| rs1557733311 | 1:36,556,868 | A/C | — | pathogenic |
| rs2524682780 | 1:36,556,871 | G/T | — | uncertain significance |
| rs2524682794 | 1:36,556,875 | T/A | — | uncertain significance |
| rs771257456 | 1:36,556,908 | A/G | — | uncertain significance |
| rs139465196 | 1:36,556,921 | C/T | — | likely benign |
| rs144958655 | 1:36,556,934 | G/A | — | uncertain significance |
| rs368433666 | 1:36,557,226 | C/T | — | likely pathogenic |
| rs764083166 | 1:36,557,252 | G/T | — | uncertain significance |
| rs138995178 | 1:36,557,294 | G/A | — | uncertain significance |
| rs2524683901 | 1:36,557,305 | G/C | — | uncertain significance |
| rs150395881 | 1:36,557,307 | C/T | — | uncertain significance |
| rs866152144 | 1:36,557,376 | C/T | — | uncertain significance |
| rs11538708 | 1:36,557,393 | C/A | — | likely benign |
| rs1570012058 | 1:36,557,395 | T/C | — | likely pathogenic |
| rs139736291 | 1:36,557,401 | A/G | — | uncertain significance |
| rs747584559 | 1:36,557,403 | A/G | — | uncertain significance |
| rs149705523 | 1:36,557,413 | A/G | — | uncertain significance |
| rs1367907346 | 1:36,557,507 | C/G | — | uncertain significance |
| rs759989977 | 1:36,557,517 | C/T | — | uncertain significance |
| rs200626873 | 1:36,557,524 | C/T | — | likely pathogenic |
| rs2124055158 | 1:36,557,538 | C/T | — | uncertain significance |
| rs2524684835 | 1:36,557,539 | A/G | — | likely pathogenic |
| rs201940724 | 1:36,557,547 | T/C | — | uncertain significance |
| rs2124055267 | 1:36,557,558 | C/A | — | likely pathogenic |
| rs146885889 | 1:36,557,577 | G/T | — | uncertain significance |
| rs1015909949 | 1:36,557,607 | G/A | — | uncertain significance |
| rs146990907 | 1:36,557,644 | G/A | — | uncertain significance |
| rs149547220 | 1:36,558,035 | G/A | — | likely benign |
| rs148612837 | 1:36,558,040 | G/A | — | likely benign |
| rs762515954 | 1:36,558,067 | T/A | — | uncertain significance |
| rs756440961 | 1:36,558,751 | C/T | — | uncertain significance |
| rs767594707 | 1:36,558,838 | A/G | — | uncertain significance |
| rs549427499 | 1:36,558,848 | T/C | — | uncertain significance |
| rs1557734377 | 1:36,558,895 | C/T | — | pathogenic |
| rs201735454 | 1:36,558,899 | T/G | — | pathogenic |
| rs200099878 | 1:36,558,902 | C/T | — | uncertain significance |
| rs776682941 | 1:36,558,906 | G/T | — | uncertain significance |
| rs531916765 | 1:36,558,933 | C/G | — | conflicting classifications of pathogenicity |
| rs4641278 | 1:36,559,983 | G/A | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.