ClinVar Miner

List of variants in gene ANKRD26 reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 48
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_014915.3(ANKRD26):c.-113A>C rs886046949 0.00038
NM_014915.3(ANKRD26):c.*566G>A rs149300287 0.00033
NM_014915.3(ANKRD26):c.1327G>A (p.Gly443Arg) rs199787000 0.00017
NM_014915.3(ANKRD26):c.*482A>C rs760890734 0.00009
NM_014915.2(ANKRD26):c.-172A>T rs886046951 0.00006
NM_014915.3(ANKRD26):c.4725-15C>T rs373529426 0.00006
NM_014915.3(ANKRD26):c.-135A>C rs373811579 0.00004
NM_014915.3(ANKRD26):c.4676A>G (p.Tyr1559Cys) rs557821284 0.00003
NM_014915.3(ANKRD26):c.739A>T (p.Arg247Trp) rs765170468 0.00003
NM_014915.3(ANKRD26):c.*1243A>G rs1264848589 0.00001
NM_014915.3(ANKRD26):c.*1351G>T rs1355694401 0.00001
NM_014915.3(ANKRD26):c.*530C>G rs886046941 0.00001
NM_014915.3(ANKRD26):c.*69T>C rs200102083 0.00001
NM_014915.3(ANKRD26):c.*704C>G rs886046940 0.00001
NM_014915.3(ANKRD26):c.*8G>T rs886046943 0.00001
NM_014915.3(ANKRD26):c.-138C>G rs886046950 0.00001
NM_014915.3(ANKRD26):c.1176T>C (p.Tyr392=) rs368451975 0.00001
NM_014915.3(ANKRD26):c.1439T>C (p.Val480Ala) rs886046947 0.00001
NM_014915.3(ANKRD26):c.1492-6A>G rs946903113 0.00001
NM_014915.3(ANKRD26):c.1754G>C (p.Arg585Thr) rs1293742057 0.00001
NM_014915.3(ANKRD26):c.426G>A (p.Ala142=) rs746957045 0.00001
NM_014915.3(ANKRD26):c.4284A>C (p.Gln1428His) rs771059446 0.00001
NM_014915.3(ANKRD26):c.*1029G>A rs1045894805
NM_014915.3(ANKRD26):c.*1169C>T rs1589194013
NM_014915.3(ANKRD26):c.*1170G>A rs886046939
NM_014915.3(ANKRD26):c.*1174C>G rs886046938
NM_014915.3(ANKRD26):c.*142G>A rs886046942
NM_014915.3(ANKRD26):c.*170G>A rs377417678
NM_014915.3(ANKRD26):c.*566G>T rs149300287
NM_014915.3(ANKRD26):c.*595G>A rs374615840
NM_014915.3(ANKRD26):c.-138C>A rs886046950
NM_014915.3(ANKRD26):c.1269+7T>A rs201014646
NM_014915.3(ANKRD26):c.1269+8_1269+12del rs199920305
NM_014915.3(ANKRD26):c.1364-17_1364-15del rs150168938
NM_014915.3(ANKRD26):c.1727del (p.Asp576fs) rs886046946
NM_014915.3(ANKRD26):c.1787C>T (p.Pro596Leu) rs2054550014
NM_014915.3(ANKRD26):c.1986-3dup rs113123391
NM_014915.3(ANKRD26):c.3053A>G (p.His1018Arg) rs2054011229
NM_014915.3(ANKRD26):c.319A>G (p.Asn107Asp) rs777897967
NM_014915.3(ANKRD26):c.3216A>G (p.Lys1072=) rs1010361619
NM_014915.3(ANKRD26):c.3218T>C (p.Leu1073Pro) rs2054004758
NM_014915.3(ANKRD26):c.3896C>A (p.Ala1299Asp) rs1429452589
NM_014915.3(ANKRD26):c.3940G>A (p.Glu1314Lys) rs886046945
NM_014915.3(ANKRD26):c.4595A>G (p.Asp1532Gly) rs2053228815
NM_014915.3(ANKRD26):c.4808C>G (p.Thr1603Ser) rs886046944
NM_014915.3(ANKRD26):c.565G>A (p.Gly189Arg) rs2056331522
NM_014915.3(ANKRD26):c.789C>G (p.Asp263Glu) rs777702991
NM_014915.3(ANKRD26):c.983_986del (p.Ile328fs) rs749858810

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.