ClinVar Miner

List of variants in gene ANKRD11 reported as benign by Invitae

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Gene type:
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Total variants: 60
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HGVS dbSNP
NM_013275.6(ANKRD11):c.1027G>A (p.Val343Ile) rs147744268
NM_013275.6(ANKRD11):c.1245C>T (p.Asp415=) rs79499872
NM_013275.6(ANKRD11):c.1296G>C (p.Thr432=) rs74033734
NM_013275.6(ANKRD11):c.1725C>T (p.Ser575=) rs151124308
NM_013275.6(ANKRD11):c.172C>A (p.Arg58=) rs144364610
NM_013275.6(ANKRD11):c.1842C>T (p.Ser614=) rs764479350
NM_013275.6(ANKRD11):c.1844C>G (p.Ala615Gly) rs115797011
NM_013275.6(ANKRD11):c.1851C>T (p.Gly617=) rs144309427
NM_013275.6(ANKRD11):c.1852G>A (p.Ala618Thr) rs140370885
NM_013275.6(ANKRD11):c.2240C>T (p.Ser747Leu) rs138898373
NM_013275.6(ANKRD11):c.227-10C>T rs201226457
NM_013275.6(ANKRD11):c.2292G>A (p.Glu764=) rs149626938
NM_013275.6(ANKRD11):c.2505C>T (p.Asp835=) rs544199816
NM_013275.6(ANKRD11):c.2610C>T (p.Ser870=) rs142560514
NM_013275.6(ANKRD11):c.275G>A (p.Arg92Gln) rs143894223
NM_013275.6(ANKRD11):c.280G>C (p.Ala94Pro) rs190143218
NM_013275.6(ANKRD11):c.3045C>G (p.Pro1015=) rs150652124
NM_013275.6(ANKRD11):c.306G>C (p.Leu102=) rs150497848
NM_013275.6(ANKRD11):c.3162A>G (p.Lys1054=) rs61729371
NM_013275.6(ANKRD11):c.3423C>T (p.Ser1141=) rs142005632
NM_013275.6(ANKRD11):c.3431C>T (p.Pro1144Leu) rs137894790
NM_013275.6(ANKRD11):c.3483C>T (p.Ser1161=) rs150642594
NM_013275.6(ANKRD11):c.3578C>T (p.Ala1193Val) rs61744864
NM_013275.6(ANKRD11):c.3660G>A (p.Arg1220=) rs150015583
NM_013275.6(ANKRD11):c.372G>A (p.Thr124=) rs34016116
NM_013275.6(ANKRD11):c.3869A>G (p.His1290Arg) rs764356904
NM_013275.6(ANKRD11):c.3927G>A (p.Thr1309=) rs143428884
NM_013275.6(ANKRD11):c.4149C>T (p.Gly1383=) rs146025366
NM_013275.6(ANKRD11):c.4317G>A (p.Lys1439=) rs61743619
NM_013275.6(ANKRD11):c.4391A>G (p.Lys1464Arg) rs147285830
NM_013275.6(ANKRD11):c.4440T>C (p.His1480=) rs139429949
NM_013275.6(ANKRD11):c.4619A>G (p.Lys1540Arg) rs145415643
NM_013275.6(ANKRD11):c.4872G>A (p.Ala1624=) rs143426579
NM_013275.6(ANKRD11):c.4884C>T (p.Asp1628=) rs144721281
NM_013275.6(ANKRD11):c.5167A>C (p.Arg1723=) rs200482809
NM_013275.6(ANKRD11):c.5198C>T (p.Ala1733Val) rs148243995
NM_013275.6(ANKRD11):c.5237C>T (p.Thr1746Met) rs561668093
NM_013275.6(ANKRD11):c.5338G>A (p.Ala1780Thr) rs75362060
NM_013275.6(ANKRD11):c.5509C>T (p.Pro1837Ser) rs145906515
NM_013275.6(ANKRD11):c.5586C>T (p.Val1862=) rs772818159
NM_013275.6(ANKRD11):c.5625C>T (p.Val1875=) rs201082380
NM_013275.6(ANKRD11):c.5661A>G (p.Gln1887=) rs147726863
NM_013275.6(ANKRD11):c.5665A>G (p.Lys1889Glu) rs202034147
NM_013275.6(ANKRD11):c.601+7A>G rs202074713
NM_013275.6(ANKRD11):c.6020C>T (p.Pro2007Leu) rs200531141
NM_013275.6(ANKRD11):c.6084C>T (p.Pro2028=) rs189297725
NM_013275.6(ANKRD11):c.6085G>A (p.Val2029Ile) rs199785661
NM_013275.6(ANKRD11):c.6106G>A (p.Asp2036Asn) rs201636725
NM_013275.6(ANKRD11):c.6111C>G (p.Val2037=) rs376468392
NM_013275.6(ANKRD11):c.6323G>A (p.Gly2108Asp) rs201509886
NM_013275.6(ANKRD11):c.6497T>G (p.Met2166Arg) rs74033733
NM_013275.6(ANKRD11):c.6622T>G (p.Ser2208Ala)
NM_013275.6(ANKRD11):c.6725C>T (p.Ala2242Val) rs372632879
NM_013275.6(ANKRD11):c.6746G>A (p.Arg2249His) rs201043388
NM_013275.6(ANKRD11):c.6760G>A (p.Gly2254Arg) rs1003478010
NM_013275.6(ANKRD11):c.6826C>T (p.Pro2276Ser) rs201957371
NM_013275.6(ANKRD11):c.6827C>T (p.Pro2276Leu) rs573355746
NM_013275.6(ANKRD11):c.69G>A (p.Glu23=) rs533051571
NM_013275.6(ANKRD11):c.7623G>A (p.Ala2541=) rs190789698
NM_013275.6(ANKRD11):c.7839C>G (p.Ala2613=) rs143287644

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