List of variants in gene ANKRD11 reported by Institute Of Human Genetics Munich, Klinikum Rechts Der Isar, Tu München

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_013275.6(ANKRD11):c.2175_2178del (p.Asn725fs)	rs886039734
NM_013275.6(ANKRD11):c.2273_2274del (p.Leu758fs)	rs1597461334
NM_013275.6(ANKRD11):c.2704G>T (p.Glu902Ter)	rs1597459649
NM_013275.6(ANKRD11):c.2716C>T (p.Arg906Ter)	rs929007085
NM_013275.6(ANKRD11):c.2826_2829del (p.Arg942fs)	rs1597459077
NM_013275.6(ANKRD11):c.3228_3232del (p.Arg1076fs)
NM_013275.6(ANKRD11):c.4206C>G (p.Tyr1402Ter)	rs749632782
NM_013275.6(ANKRD11):c.6807_6808del (p.Ala2270fs)	rs1597435393

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.