ClinVar Miner

List of variants in gene ANKRD11 reported as likely benign for Autism spectrum disorder

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 90
Download table as spreadsheet
HGVS dbSNP
NM_001256182.2(ANKRD11):c.2216C>T (p.Ser739Leu) rs146294483
NM_001256182.2(ANKRD11):c.6283C>G (p.Leu2095Val)
NM_001256182.2(ANKRD11):c.7090G>A (p.Ala2364Thr)
NM_013275.6(ANKRD11):c.1027G>A (p.Val343Ile)
NM_013275.6(ANKRD11):c.1035C>T (p.Asp345=)
NM_013275.6(ANKRD11):c.1413G>A (p.Lys471=)
NM_013275.6(ANKRD11):c.1725C>T (p.Ser575=)
NM_013275.6(ANKRD11):c.1842C>T (p.Ser614=)
NM_013275.6(ANKRD11):c.1851C>T (p.Gly617=)
NM_013275.6(ANKRD11):c.1852G>A (p.Ala618Thr)
NM_013275.6(ANKRD11):c.1857C>T (p.Val619=)
NM_013275.6(ANKRD11):c.195C>T (p.Gly65=)
NM_013275.6(ANKRD11):c.207G>A (p.Glu69=)
NM_013275.6(ANKRD11):c.2184C>G (p.Ile728Met)
NM_013275.6(ANKRD11):c.2217G>A (p.Ser739=)
NM_013275.6(ANKRD11):c.2373G>A (p.Lys791=) rs138267414
NM_013275.6(ANKRD11):c.2610C>T (p.Ser870=)
NM_013275.6(ANKRD11):c.2684G>A (p.Arg895Gln) rs199800166
NM_013275.6(ANKRD11):c.282C>G (p.Ala94=)
NM_013275.6(ANKRD11):c.2841C>T (p.Ala947=)
NM_013275.6(ANKRD11):c.2888_2896del (p.Asp963_Arg965del) rs769651265
NM_013275.6(ANKRD11):c.2889C>T (p.Asp963=)
NM_013275.6(ANKRD11):c.3045C>G (p.Pro1015=)
NM_013275.6(ANKRD11):c.306G>C (p.Leu102=)
NM_013275.6(ANKRD11):c.3197A>G (p.His1066Arg)
NM_013275.6(ANKRD11):c.3437C>T (p.Thr1146Met)
NM_013275.6(ANKRD11):c.3483C>T (p.Ser1161=)
NM_013275.6(ANKRD11):c.3578C>T (p.Ala1193Val)
NM_013275.6(ANKRD11):c.3584G>A (p.Arg1195Lys)
NM_013275.6(ANKRD11):c.3660G>A (p.Arg1220=)
NM_013275.6(ANKRD11):c.375C>T (p.Ala125=)
NM_013275.6(ANKRD11):c.3826G>A (p.Ala1276Thr)
NM_013275.6(ANKRD11):c.389A>G (p.Asn130Ser)
NM_013275.6(ANKRD11):c.3969C>T (p.Val1323=)
NM_013275.6(ANKRD11):c.3973T>C (p.Phe1325Leu)
NM_013275.6(ANKRD11):c.3977C>T (p.Thr1326Met) rs144673419
NM_013275.6(ANKRD11):c.4149C>T (p.Gly1383=)
NM_013275.6(ANKRD11):c.4237G>A (p.Glu1413Lys) rs140373729
NM_013275.6(ANKRD11):c.4297T>C (p.Ser1433Pro) rs1567569593
NM_013275.6(ANKRD11):c.4317G>A (p.Lys1439=)
NM_013275.6(ANKRD11):c.4382A>G (p.Lys1461Arg)
NM_013275.6(ANKRD11):c.4440T>C (p.His1480=)
NM_013275.6(ANKRD11):c.4443G>A (p.Ala1481=)
NM_013275.6(ANKRD11):c.4533C>T (p.Pro1511=)
NM_013275.6(ANKRD11):c.4568C>T (p.Pro1523Leu)
NM_013275.6(ANKRD11):c.4609G>A (p.Gly1537Ser) rs1347006212
NM_013275.6(ANKRD11):c.4667C>G (p.Ala1556Gly) rs781186923
NM_013275.6(ANKRD11):c.4831C>T (p.Leu1611=) rs1567567396
NM_013275.6(ANKRD11):c.4872G>A (p.Ala1624=) rs143426579
NM_013275.6(ANKRD11):c.5061G>A (p.Glu1687=)
NM_013275.6(ANKRD11):c.5112C>A (p.Pro1704=)
NM_013275.6(ANKRD11):c.5178C>T (p.Ser1726=)
NM_013275.6(ANKRD11):c.5241C>T (p.Pro1747=)
NM_013275.6(ANKRD11):c.5250C>T (p.Thr1750=)
NM_013275.6(ANKRD11):c.543C>T (p.Ala181=)
NM_013275.6(ANKRD11):c.5484G>A (p.Ser1828=)
NM_013275.6(ANKRD11):c.5509C>T (p.Pro1837Ser)
NM_013275.6(ANKRD11):c.5578C>T (p.Pro1860Ser)
NM_013275.6(ANKRD11):c.5625C>T (p.Val1875=)
NM_013275.6(ANKRD11):c.5629C>T (p.Pro1877Ser)
NM_013275.6(ANKRD11):c.5632T>C (p.Ser1878Pro)
NM_013275.6(ANKRD11):c.5889C>T (p.Ile1963=)
NM_013275.6(ANKRD11):c.5916C>T (p.Ser1972=)
NM_013275.6(ANKRD11):c.5998C>T (p.Leu2000Phe)
NM_013275.6(ANKRD11):c.6020C>T (p.Pro2007Leu) rs200531141
NM_013275.6(ANKRD11):c.6065C>T (p.Pro2022Leu)
NM_013275.6(ANKRD11):c.6125A>G (p.Asp2042Gly)
NM_013275.6(ANKRD11):c.6140C>G (p.Ala2047Gly)
NM_013275.6(ANKRD11):c.6153A>G (p.Ser2051=)
NM_013275.6(ANKRD11):c.6312C>T (p.Asp2104=)
NM_013275.6(ANKRD11):c.6323G>A (p.Gly2108Asp) rs201509886
NM_013275.6(ANKRD11):c.6366C>T (p.Asp2122=)
NM_013275.6(ANKRD11):c.6580C>G (p.Gln2194Glu)
NM_013275.6(ANKRD11):c.6597C>T (p.Leu2199=)
NM_013275.6(ANKRD11):c.6628G>C (p.Glu2210Gln) rs1350625482
NM_013275.6(ANKRD11):c.6698G>A (p.Gly2233Glu)
NM_013275.6(ANKRD11):c.6712A>G (p.Ser2238Gly)
NM_013275.6(ANKRD11):c.6725C>T (p.Ala2242Val)
NM_013275.6(ANKRD11):c.6745C>T (p.Arg2249Cys) rs202081612
NM_013275.6(ANKRD11):c.6746G>A (p.Arg2249His)
NM_013275.6(ANKRD11):c.6826C>T (p.Pro2276Ser)
NM_013275.6(ANKRD11):c.6919C>T (p.Pro2307Ser) rs575642464
NM_013275.6(ANKRD11):c.7296C>T (p.Ser2432=)
NM_013275.6(ANKRD11):c.7324C>T (p.Leu2442=)
NM_013275.6(ANKRD11):c.7677G>A (p.Leu2559=)
NM_013275.6(ANKRD11):c.7731A>C (p.Ser2577=)
NM_013275.6(ANKRD11):c.7839C>G (p.Ala2613=)
NM_013275.6(ANKRD11):c.843C>T (p.Asn281=)
NM_013275.6(ANKRD11):c.888G>A (p.Ser296=)
NM_013275.6(ANKRD11):c.890C>T (p.Thr297Met)

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.