ClinVar Miner

List of variants in gene ANKRD11 reported as likely pathogenic by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
Download table as spreadsheet
HGVS dbSNP
NM_013275.6(ANKRD11):c.1977C>G (p.Tyr659Ter) rs749201074
NM_013275.6(ANKRD11):c.2684G>A (p.Arg895Gln) rs199800166
NM_013275.6(ANKRD11):c.5030_5031del (p.Lys1677fs) rs1057518578
NM_013275.6(ANKRD11):c.5974A>T (p.Lys1992Ter) rs763207005
NM_013275.6(ANKRD11):c.6436A>C (p.Lys2146Gln) rs1283976400
NM_013275.6(ANKRD11):c.6580C>T (p.Gln2194Ter) rs201589586
NM_013275.6(ANKRD11):c.674C>T (p.Ala225Val) rs746852311
NM_013275.6(ANKRD11):c.7354C>T (p.Arg2452Cys) rs1064795497
NM_013275.6(ANKRD11):c.7480C>A (p.Pro2494Thr) rs1064794992
NM_013275.6(ANKRD11):c.7788_7804del (p.Asp2596fs) rs1555521779
NM_013275.6(ANKRD11):c.7814T>G (p.Leu2605Arg) rs1131691512

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.