ClinVar Miner

List of variants reported as benign for autism spectrum disorder by Ambry Genetics

Included ClinVar conditions (38):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 30
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HGVS dbSNP
NM_013275.6(ANKRD11):c.1020G>A (p.Thr340=) rs142539117
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.1844C>G (p.Ala615Gly) rs115797011
NM_013275.6(ANKRD11):c.2039C>G (p.Thr680Ser) rs145694621
NM_013275.6(ANKRD11):c.280G>C (p.Ala94Pro) rs190143218
NM_013275.6(ANKRD11):c.2912C>T (p.Ala971Val) rs2279348
NM_013275.6(ANKRD11):c.3162A>G (p.Lys1054=) rs61729371
NM_013275.6(ANKRD11):c.3573C>G (p.Ala1191=) rs62000377
NM_013275.6(ANKRD11):c.3578C>T (p.Ala1193Val) rs61744864
NM_013275.6(ANKRD11):c.372G>A (p.Thr124=) rs34016116
NM_013275.6(ANKRD11):c.3822C>T (p.Ala1274=) rs61741725
NM_013275.6(ANKRD11):c.4344T>C (p.Tyr1448=) rs61744778
NM_013275.6(ANKRD11):c.4912C>G (p.Pro1638Ala) rs113527563
NM_013275.6(ANKRD11):c.4932G>A (p.Gly1644=) rs72821356
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.5665A>G (p.Lys1889Glu) rs202034147
NM_013275.6(ANKRD11):c.6067G>C (p.Ala2023Pro) rs60520302
NM_013275.6(ANKRD11):c.6084C>T (p.Pro2028=) rs189297725
NM_013275.6(ANKRD11):c.6106G>A (p.Asp2036Asn) rs201636725
NM_013275.6(ANKRD11):c.6176C>A (p.Pro2059His) rs117997391
NM_013275.6(ANKRD11):c.6497T>G (p.Met2166Arg) rs74033733
NM_013275.6(ANKRD11):c.6745C>T (p.Arg2249Cys) rs202081612
NM_013275.6(ANKRD11):c.6781G>A (p.Glu2261Lys) rs770262960
NM_013275.6(ANKRD11):c.6787C>T (p.Pro2263Ser) rs76793093
NM_013275.6(ANKRD11):c.6868C>T (p.Pro2290Ser) rs374668457
NM_013275.6(ANKRD11):c.6924C>T (p.Gly2308=) rs146575027
NM_013275.6(ANKRD11):c.7128C>G (p.Asp2376Glu) rs4785560
NM_013275.6(ANKRD11):c.890C>T (p.Thr297Met) rs140998225

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