ClinVar Miner

List of variants in gene ANKRD11 reported as benign by Ambry Genetics

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Gene type:
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Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_013275.6(ANKRD11):c.2912C>T (p.Ala971Val) rs2279348 0.66687
NM_013275.6(ANKRD11):c.7128C>G (p.Asp2376Glu) rs4785560 0.09807
NM_013275.6(ANKRD11):c.6067G>C (p.Ala2023Pro) rs60520302 0.04744
NM_013275.6(ANKRD11):c.3822C>T (p.Ala1274=) rs61741725 0.04130
NM_013275.6(ANKRD11):c.4932G>A (p.Gly1644=) rs72821356 0.03413
NM_013275.6(ANKRD11):c.6787C>T (p.Pro2263Ser) rs76793093 0.03409
NM_013275.6(ANKRD11):c.4344T>C (p.Tyr1448=) rs61744778 0.02524
NM_013275.6(ANKRD11):c.6176C>A (p.Pro2059His) rs117997391 0.02470
NM_013275.6(ANKRD11):c.3162A>G (p.Lys1054=) rs61729371 0.02062
NM_013275.6(ANKRD11):c.6924C>T (p.Gly2308=) rs146575027 0.01595
NM_013275.6(ANKRD11):c.6084C>T (p.Pro2028=) rs189297725 0.01580
NM_013275.6(ANKRD11):c.1020G>A (p.Thr340=) rs142539117 0.01490
NM_013275.6(ANKRD11):c.2039C>G (p.Thr680Ser) rs145694621 0.01463
NM_013275.6(ANKRD11):c.372G>A (p.Thr124=) rs34016116 0.01190
NM_013275.6(ANKRD11):c.6497T>G (p.Met2166Arg) rs74033733 0.00879
NM_013275.6(ANKRD11):c.6106G>A (p.Asp2036Asn) rs201636725 0.00654
NM_013275.6(ANKRD11):c.1245C>T (p.Asp415=) rs79499872 0.00490
NM_013275.6(ANKRD11):c.5338G>A (p.Ala1780Thr) rs75362060 0.00424
NM_013275.6(ANKRD11):c.5509C>T (p.Pro1837Ser) rs145906515 0.00377
NM_013275.6(ANKRD11):c.3578C>T (p.Ala1193Val) rs61744864 0.00143
NM_013275.6(ANKRD11):c.6868C>T (p.Pro2290Ser) rs374668457 0.00140
NM_013275.6(ANKRD11):c.890C>T (p.Thr297Met) rs140998225 0.00131
NM_013275.6(ANKRD11):c.6745C>T (p.Arg2249Cys) rs202081612 0.00121
NM_013275.6(ANKRD11):c.4884C>T (p.Asp1628=) rs144721281 0.00076
NM_013275.6(ANKRD11):c.2240C>T (p.Ser747Leu) rs138898373 0.00057
NM_013275.6(ANKRD11):c.5665A>G (p.Lys1889Glu) rs202034147 0.00050
NM_013275.6(ANKRD11):c.5766C>T (p.Ala1922=) rs373393326 0.00034
NM_013275.6(ANKRD11):c.280G>C (p.Ala94Pro) rs190143218 0.00019
NM_013275.6(ANKRD11):c.6375C>T (p.Ala2125=) rs75629150 0.00014
NM_013275.6(ANKRD11):c.6781G>A (p.Glu2261Lys) rs770262960 0.00004
NM_013275.6(ANKRD11):c.1296G>C (p.Thr432=) rs74033734
NM_013275.6(ANKRD11):c.1844C>G (p.Ala615Gly) rs115797011
NM_013275.6(ANKRD11):c.3431C>T (p.Pro1144Leu) rs137894790
NM_013275.6(ANKRD11):c.3573C>G (p.Ala1191=) rs62000377
NM_013275.6(ANKRD11):c.4912C>G (p.Pro1638Ala) rs113527563
NM_013275.6(ANKRD11):c.6484C>T (p.Pro2162Ser)
NM_013275.6(ANKRD11):c.6489A>G (p.Pro2163=)

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