ClinVar Miner

List of variants studied for Thrombocytopenia 2 by St. Jude Molecular Pathology, St. Jude Children's Research Hospital

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 35
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_014915.3(ANKRD26):c.425C>T (p.Ala142Val) rs768779673 0.00041
NM_014915.3(ANKRD26):c.679C>T (p.Pro227Ser) rs201638257 0.00035
NM_014915.3(ANKRD26):c.3761A>G (p.Asp1254Gly) rs368705077 0.00024
NM_014915.3(ANKRD26):c.153C>G (p.His51Gln) rs139049098 0.00021
NM_014915.3(ANKRD26):c.3G>A (p.Met1Ile) rs199683454 0.00020
NM_014915.3(ANKRD26):c.2053G>A (p.Asp685Asn) rs368408857 0.00017
NM_014915.3(ANKRD26):c.2005A>G (p.Asn669Asp) rs368602859 0.00010
NM_014915.3(ANKRD26):c.4391A>C (p.His1464Pro) rs762858115 0.00008
NM_014915.3(ANKRD26):c.1756A>G (p.Lys586Glu) rs377530499 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.4725-10A>G rs369868995 0.00004
NM_014915.3(ANKRD26):c.3044C>T (p.Ala1015Val) rs758480659 0.00003
NM_014915.3(ANKRD26):c.4684G>A (p.Glu1562Lys) rs200392387 0.00003
NM_014915.3(ANKRD26):c.1035_1036insT (p.Lys346Ter) rs780613456 0.00002
NM_014915.3(ANKRD26):c.1858A>G (p.Lys620Glu) rs112661579 0.00002
NM_014915.3(ANKRD26):c.1210A>G (p.Met404Val) rs751538106 0.00001
NM_014915.3(ANKRD26):c.1495A>G (p.Thr499Ala) rs370398342 0.00001
NM_014915.3(ANKRD26):c.1636-8del rs2054556291 0.00001
NM_014915.3(ANKRD26):c.3439C>T (p.Arg1147Ter) rs151033255 0.00001
NM_014915.3(ANKRD26):c.4006A>G (p.Met1336Val) rs777101648 0.00001
NM_014915.3(ANKRD26):c.1364-5C>A rs1049457907
NM_014915.3(ANKRD26):c.1501G>A (p.Glu501Lys) rs1397484113
NM_014915.3(ANKRD26):c.2125A>T (p.Met709Leu)
NM_014915.3(ANKRD26):c.2405_2409del (p.Arg802fs) rs755734556
NM_014915.3(ANKRD26):c.2555A>G (p.Asn852Ser)
NM_014915.3(ANKRD26):c.320A>G (p.Asn107Ser) rs756157730
NM_014915.3(ANKRD26):c.3692C>G (p.Thr1231Ser) rs751964173
NM_014915.3(ANKRD26):c.3841G>A (p.Val1281Ile) rs2538699975
NM_014915.3(ANKRD26):c.3965C>A (p.Ala1322Glu)
NM_014915.3(ANKRD26):c.418A>G (p.Asn140Asp)
NM_014915.3(ANKRD26):c.475A>T (p.Ile159Leu) rs201548038
NM_014915.3(ANKRD26):c.5107G>A (p.Val1703Ile) rs1330485324
NM_014915.3(ANKRD26):c.556G>T (p.Ala186Ser) rs767744358
NM_014915.3(ANKRD26):c.821C>G (p.Pro274Arg) rs1589347239

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.