ClinVar Miner

List of variants in gene ANKRD11 reported by Genetic Services Laboratory, University of Chicago

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 30
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_013275.6(ANKRD11):c.6106G>A (p.Asp2036Asn) rs201636725 0.00654
NM_013275.6(ANKRD11):c.5509C>T (p.Pro1837Ser) rs145906515 0.00377
NM_013275.6(ANKRD11):c.4149C>T (p.Gly1383=) rs146025366 0.00285
NM_013275.6(ANKRD11):c.5661A>G (p.Gln1887=) rs147726863 0.00185
NM_013275.6(ANKRD11):c.6745C>T (p.Arg2249Cys) rs202081612 0.00121
NM_013275.6(ANKRD11):c.2519G>A (p.Arg840Gln) rs149776253 0.00070
NM_013275.6(ANKRD11):c.2240C>T (p.Ser747Leu) rs138898373 0.00057
NM_013275.6(ANKRD11):c.5481C>G (p.Pro1827=) rs142469039 0.00041
NM_013275.6(ANKRD11):c.6797C>T (p.Ala2266Val) rs748996527 0.00035
NM_013275.6(ANKRD11):c.2373G>A (p.Lys791=) rs138267414 0.00024
NM_013275.6(ANKRD11):c.116C>T (p.Thr39Ile) rs149152296 0.00022
NM_013275.6(ANKRD11):c.5178C>T (p.Ser1726=) rs200783129 0.00020
NM_013275.6(ANKRD11):c.1577A>T (p.His526Leu) rs374369335 0.00012
NM_013275.6(ANKRD11):c.2505C>T (p.Asp835=) rs544199816 0.00008
NM_013275.6(ANKRD11):c.6024C>T (p.Phe2008=) rs375589721 0.00006
NM_013275.6(ANKRD11):c.2805G>A (p.Ser935=) rs149751840 0.00005
NM_013275.6(ANKRD11):c.5898C>T (p.Thr1966=) rs140586593 0.00002
NM_013275.6(ANKRD11):c.3418G>A (p.Ala1140Thr) rs369869329 0.00001
NM_013275.6(ANKRD11):c.4970C>T (p.Ser1657Leu) rs749114664 0.00001
NM_013275.6(ANKRD11):c.7750G>A (p.Ala2584Thr) rs150393722 0.00001
NM_013275.6(ANKRD11):c.2464C>T (p.Gln822Ter) rs2151759808
NM_013275.6(ANKRD11):c.2716C>T (p.Arg906Ter) rs929007085
NM_013275.6(ANKRD11):c.3632_3633del (p.Lys1211fs) rs1555528400
NM_013275.6(ANKRD11):c.4244A>G (p.Glu1415Gly) rs756014125
NM_013275.6(ANKRD11):c.6072G>C (p.Pro2024=) rs542077760
NM_013275.6(ANKRD11):c.6218C>T (p.Pro2073Leu) rs770387752
NM_013275.6(ANKRD11):c.6670G>T (p.Glu2224Ter) rs1381957912
NM_013275.6(ANKRD11):c.6893G>T (p.Arg2298Leu) rs1304326484
NM_013275.6(ANKRD11):c.6982dup (p.Arg2328fs) rs1555525088
NM_013275.6(ANKRD11):c.988A>G (p.Lys330Glu) rs1555529962

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.