ANKRD26
ankyrin repeat domain 26
Summary
This gene encodes a protein containing N-terminal ankyrin repeats which function in protein-protein interactions. Mutations in this gene are associated with autosomal dominant thrombocytopenia-2. Pseudogenes of this gene are found on chromosome 7, 10, 13 and 16. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]
Known Variants942 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs12570065 | 10:27,293,086 | T/C | — | benign |
| rs1355694401 | 10:27,293,168 | C/A | — | uncertain significance |
| rs1264848589 | 10:27,293,276 | T/C | — | uncertain significance |
| rs66931439 | 10:27,293,307 | C/T | — | benign |
| rs10829158 | 10:27,293,344 | G/A | — | benign |
| rs886046938 | 10:27,293,345 | G/C | — | uncertain significance |
| rs886046939 | 10:27,293,349 | C/T | — | uncertain significance |
| rs1589194013 | 10:27,293,350 | G/A | — | uncertain significance |
| rs35446173 | 10:27,293,399 | T/C | — | benign |
| rs1045894805 | 10:27,293,490 | C/T | — | uncertain significance |
| rs540664871 | 10:27,293,507 | G/T | — | benign |
| rs11015449 | 10:27,293,615 | G/T | — | benign |
| rs886046940 | 10:27,293,815 | G/C | — | uncertain significance |
| rs374615840 | 10:27,293,924 | C/T | — | uncertain significance |
| rs149300287 | 10:27,293,953 | C/A | — | uncertain significance |
| rs886046941 | 10:27,293,989 | G/C | — | uncertain significance |
| rs760890734 | 10:27,294,037 | T/G | — | uncertain significance |
| rs377417678 | 10:27,294,349 | C/T | — | uncertain significance |
| rs886046942 | 10:27,294,377 | C/T | — | uncertain significance |
| rs200102083 | 10:27,294,450 | A/G | — | uncertain significance |
| rs886046943 | 10:27,294,511 | C/A | — | uncertain significance |
| rs372479083 | 10:27,294,513 | T/C | — | conflicting classifications of pathogenicity |
| rs754393445 | 10:27,294,522 | G/C | — | uncertain significance |
| rs376466372 | 10:27,294,528 | A/C | — | uncertain significance |
| rs1330485324 | 10:27,294,545 | C/T | — | conflicting classifications of pathogenicity |
| rs1230375690 | 10:27,294,546 | C/G | — | uncertain significance |
| rs749269058 | 10:27,294,551 | C/T | — | uncertain significance |
| rs2538456898 | 10:27,294,554 | A/G | — | uncertain significance |
| rs370943966 | 10:27,294,566 | C/T | — | conflicting classifications of pathogenicity |
| rs749148342 | 10:27,294,567 | T/C | — | likely benign |
| rs373138646 | 10:27,294,592 | T/A | — | conflicting classifications of pathogenicity |
| rs772007481 | 10:27,294,601 | T/C | — | conflicting classifications of pathogenicity |
| rs2538457687 | 10:27,294,624 | T/C | — | uncertain significance |
| rs765715267 | 10:27,294,640 | A/C | — | uncertain significance |
| rs1438822467 | 10:27,294,641 | A/G | — | likely benign |
| rs1233153404 | 10:27,294,659 | T/C | — | likely benign |
| rs116042228 | 10:27,295,564 | G/A | — | likely benign |
| rs2052905041 | 10:27,295,826 | C/G | — | likely benign |
| rs2052905174 | 10:27,295,827 | A/G | — | likely benign |
| rs778711840 | 10:27,295,834 | T/C | — | likely benign |
| rs772061456 | 10:27,295,846 | C/T | — | uncertain significance |
| rs1008531113 | 10:27,295,864 | T/G | — | uncertain significance |
| rs367927114 | 10:27,295,865 | T/C | — | uncertain significance |
| rs2538471914 | 10:27,295,879 | A/C | — | uncertain significance |
| rs764884515 | 10:27,301,804 | A/T | — | likely benign |
| rs368545607 | 10:27,301,808 | A/C | — | conflicting classifications of pathogenicity |
| rs758267677 | 10:27,301,810 | C/A | — | uncertain significance |
| rs2538523988 | 10:27,301,822 | A/G | — | uncertain significance |
| rs199699340 | 10:27,301,840 | T/C | — | uncertain significance |
| rs184369322 | 10:27,301,848 | C/T | — | conflicting classifications of pathogenicity |
| rs368507197 | 10:27,301,849 | G/A | — | uncertain significance |
| rs915022204 | 10:27,301,863 | G/T | — | uncertain significance |
| rs1346412801 | 10:27,301,864 | A/G | — | conflicting classifications of pathogenicity |
| rs2538524789 | 10:27,301,866 | A/T | — | uncertain significance |
| rs572143624 | 10:27,301,885 | G/A | — | conflicting classifications of pathogenicity |
| rs372371136 | 10:27,301,888 | T/G | — | uncertain significance |
| rs926308913 | 10:27,301,898 | G/A | — | likely benign |
| rs769629179 | 10:27,301,906 | C/A | — | uncertain significance |
| rs375363190 | 10:27,301,918 | T/A | — | conflicting classifications of pathogenicity |
| rs2538525514 | 10:27,301,920 | A/C | — | uncertain significance |
| rs766114521 | 10:27,301,928 | C/T | — | likely benign |
| rs751471164 | 10:27,301,930 | C/T | — | uncertain significance |
| rs1267753506 | 10:27,301,933 | A/C | — | uncertain significance |
| rs2538525746 | 10:27,301,936 | G/T | — | uncertain significance |
| rs1464218339 | 10:27,301,944 | A/C | — | uncertain significance |
| rs2538525878 | 10:27,301,946 | G/A | — | likely benign |
| rs886046944 | 10:27,301,956 | G/C | — | uncertain significance |
| rs756257659 | 10:27,301,969 | T/C | — | uncertain significance |
| rs749494441 | 10:27,301,979 | T/A | — | uncertain significance |
| rs746318386 | 10:27,301,985 | C/G | — | uncertain significance |
| rs1436380295 | 10:27,301,988 | C/T | — | likely benign |
| rs1236531019 | 10:27,301,993 | T/G | — | uncertain significance |
| rs778242497 | 10:27,302,002 | G/A | — | uncertain significance |
| rs187507221 | 10:27,302,028 | C/T | — | uncertain significance |
| rs769313376 | 10:27,302,032 | C/G | — | uncertain significance |
| rs2538527228 | 10:27,302,033 | A/C | — | uncertain significance |
| rs369868995 | 10:27,302,049 | T/C | — | uncertain significance |
| rs373529426 | 10:27,302,054 | G/A | — | conflicting classifications of pathogenicity |
| rs772539619 | 10:27,303,412 | T/C | — | uncertain significance |
| rs780591166 | 10:27,303,418 | C/G | — | uncertain significance |
| rs2134925272 | 10:27,303,421 | A/T | — | uncertain significance |
| rs1205847358 | 10:27,303,426 | G/T | — | conflicting classifications of pathogenicity |
| rs1250389794 | 10:27,303,432 | T/C | — | uncertain significance |
| rs2538539659 | 10:27,303,438 | G/A | — | uncertain significance |
| rs369676324 | 10:27,303,440 | C/T | — | likely benign |
| rs1237696600 | 10:27,303,449 | T/C | — | likely benign |
| rs953922597 | 10:27,303,454 | C/T | — | uncertain significance |
| rs200392387 | 10:27,303,463 | C/T | — | uncertain significance |
| rs557821284 | 10:27,303,471 | T/C | — | uncertain significance |
| rs2538540493 | 10:27,303,488 | T/C | — | likely benign |
| rs373586187 | 10:27,303,496 | C/T | — | conflicting classifications of pathogenicity |
| rs377587261 | 10:27,303,497 | G/A | — | likely benign |
| rs760534554 | 10:27,303,503 | A/G | — | likely benign |
| rs370491617 | 10:27,303,506 | A/C | — | conflicting classifications of pathogenicity |
| rs2053227182 | 10:27,303,508 | A/G | — | uncertain significance |
| rs753924410 | 10:27,303,511 | C/G | — | conflicting classifications of pathogenicity |
| rs374895454 | 10:27,303,531 | T/C | — | uncertain significance |
| rs1250283542 | 10:27,303,534 | G/T | — | uncertain significance |
| rs377464823 | 10:27,303,538 | G/A | — | uncertain significance |
| rs1042409642 | 10:27,303,547 | C/T | — | uncertain significance |
Showing 100 of 942 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.