ClinVar Miner

List of variants in gene ANKRD26 reported as uncertain significance for blood platelet disease

Included ClinVar conditions (105):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 87
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HGVS dbSNP gnomAD frequency
NM_014915.3(ANKRD26):c.3007G>A (p.Glu1003Lys) rs41304587 0.00141
NM_014915.3(ANKRD26):c.2170A>C (p.Ser724Arg) rs141748831 0.00136
NM_014915.3(ANKRD26):c.425C>T (p.Ala142Val) rs768779673 0.00041
NM_014915.3(ANKRD26):c.679C>T (p.Pro227Ser) rs201638257 0.00039
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.1970A>T (p.Asp657Val) rs193178384 0.00027
NM_014915.3(ANKRD26):c.3761A>G (p.Asp1254Gly) rs368705077 0.00024
NM_014915.3(ANKRD26):c.1327G>A (p.Gly443Arg) rs199787000 0.00017
NM_014915.3(ANKRD26):c.2005A>G (p.Asn669Asp) rs368602859 0.00010
NM_014915.3(ANKRD26):c.*482A>C rs760890734 0.00009
NM_014915.3(ANKRD26):c.4391A>C (p.His1464Pro) rs762858115 0.00008
NM_014915.2(ANKRD26):c.-172A>T rs886046951 0.00006
NM_014915.3(ANKRD26):c.2260A>T (p.Lys754Ter) rs767240266 0.00006
NM_014915.3(ANKRD26):c.4636G>C (p.Asp1546His) rs753924410 0.00006
NM_014915.3(ANKRD26):c.4725-15C>T rs373529426 0.00006
NM_014915.3(ANKRD26):c.1166A>G (p.Asn389Ser) rs372397062 0.00005
NM_014915.3(ANKRD26):c.4249G>C (p.Gly1417Arg) rs764763153 0.00005
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.1035_1036insT (p.Lys346Ter) rs780613456 0.00002
NM_014915.3(ANKRD26):c.1537A>G (p.Met513Val) rs770459954 0.00002
NM_014915.3(ANKRD26):c.1858A>G (p.Lys620Glu) rs112661579 0.00002
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.244A>G (p.Thr82Ala) rs2056378213 0.00001
NM_014915.3(ANKRD26):c.4006A>G (p.Met1336Val) rs777101648 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.-116C>T rs1589393739
NM_014915.3(ANKRD26):c.-125T>G
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.1495A>G (p.Thr499Ala)
NM_014915.3(ANKRD26):c.1636-8del
NM_014915.3(ANKRD26):c.1727del (p.Asp576fs) rs886046946
NM_014915.3(ANKRD26):c.1756A>G (p.Lys586Glu)
NM_014915.3(ANKRD26):c.1787C>T (p.Pro596Leu) rs2054550014
NM_014915.3(ANKRD26):c.1986-3dup rs113123391
NM_014915.3(ANKRD26):c.2053G>A (p.Asp685Asn)
NM_014915.3(ANKRD26):c.2405_2409del (p.Arg802fs)
NM_014915.3(ANKRD26):c.245C>T (p.Thr82Met)
NM_014915.3(ANKRD26):c.3053A>G (p.His1018Arg) rs2054011229
NM_014915.3(ANKRD26):c.317T>G (p.Leu106Arg)
NM_014915.3(ANKRD26):c.319A>G (p.Asn107Asp) rs777897967
NM_014915.3(ANKRD26):c.320A>G (p.Asn107Ser) rs756157730
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.3589A>C (p.Ile1197Leu)
NM_014915.3(ANKRD26):c.3686C>T (p.Ala1229Val) rs1386447841
NM_014915.3(ANKRD26):c.3692C>G (p.Thr1231Ser) rs751964173
NM_014915.3(ANKRD26):c.371A>T (p.Gln124Leu) rs200100926
NM_014915.3(ANKRD26):c.3841G>A (p.Val1281Ile)
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.4155T>A (p.His1385Gln)
NM_014915.3(ANKRD26):c.4595A>G (p.Asp1532Gly) rs2053228815
NM_014915.3(ANKRD26):c.4684G>A (p.Glu1562Lys)
NM_014915.3(ANKRD26):c.4725-10A>G
NM_014915.3(ANKRD26):c.475A>T (p.Ile159Leu)
NM_014915.3(ANKRD26):c.4808C>G (p.Thr1603Ser) rs886046944
NM_014915.3(ANKRD26):c.5102_5106del (p.Val1701fs) rs2052846280
NM_014915.3(ANKRD26):c.5107G>A (p.Val1703Ile)
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.821C>G (p.Pro274Arg)
NM_014915.3(ANKRD26):c.983_986del (p.Ile328fs) rs749858810

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