ClinVar Miner

List of variants reported as likely 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: 91
Download table as spreadsheet
HGVS dbSNP
NM_013275.6(ANKRD11):c.1027G>A (p.Val343Ile) rs147744268
NM_013275.6(ANKRD11):c.1035C>T (p.Asp345=) rs376386664
NM_013275.6(ANKRD11):c.136G>A (p.Asp46Asn) rs144947610
NM_013275.6(ANKRD11):c.1413G>A (p.Lys471=) rs145731868
NM_013275.6(ANKRD11):c.1725C>T (p.Ser575=) rs151124308
NM_013275.6(ANKRD11):c.1763C>T (p.Ser588Leu) rs202142344
NM_013275.6(ANKRD11):c.1842C>T (p.Ser614=) rs764479350
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.1857C>T (p.Val619=) rs780814224
NM_013275.6(ANKRD11):c.195C>T (p.Gly65=) rs368375632
NM_013275.6(ANKRD11):c.207G>A (p.Glu69=) rs549000119
NM_013275.6(ANKRD11):c.2184C>G (p.Ile728Met) rs150810048
NM_013275.6(ANKRD11):c.2216C>T (p.Ser739Leu) rs146294483
NM_013275.6(ANKRD11):c.2217G>A (p.Ser739=) rs781423571
NM_013275.6(ANKRD11):c.2373G>A (p.Lys791=) rs138267414
NM_013275.6(ANKRD11):c.2610C>T (p.Ser870=) rs142560514
NM_013275.6(ANKRD11):c.2684G>A (p.Arg895Gln) rs199800166
NM_013275.6(ANKRD11):c.282C>G (p.Ala94=) rs139469151
NM_013275.6(ANKRD11):c.2841C>T (p.Ala947=) rs558841836
NM_013275.6(ANKRD11):c.2888_2896del (p.Asp963_Arg965del) rs769651265
NM_013275.6(ANKRD11):c.2889C>T (p.Asp963=) rs139955323
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.3197A>G (p.His1066Arg) rs747326096
NM_013275.6(ANKRD11):c.3437C>T (p.Thr1146Met) rs150325340
NM_013275.6(ANKRD11):c.3483C>T (p.Ser1161=) rs150642594
NM_013275.6(ANKRD11):c.3584G>A (p.Arg1195Lys) rs144199827
NM_013275.6(ANKRD11):c.3660G>A (p.Arg1220=) rs150015583
NM_013275.6(ANKRD11):c.375C>T (p.Ala125=) rs768468182
NM_013275.6(ANKRD11):c.3826G>A (p.Ala1276Thr) rs139239852
NM_013275.6(ANKRD11):c.389A>G (p.Asn130Ser) rs745320027
NM_013275.6(ANKRD11):c.3969C>T (p.Val1323=) rs201938879
NM_013275.6(ANKRD11):c.3973T>C (p.Phe1325Leu) rs138543822
NM_013275.6(ANKRD11):c.3977C>T (p.Thr1326Met) rs144673419
NM_013275.6(ANKRD11):c.4149C>T (p.Gly1383=) rs146025366
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=) rs61743619
NM_013275.6(ANKRD11):c.4382A>G (p.Lys1461Arg) rs769926682
NM_013275.6(ANKRD11):c.4440T>C (p.His1480=) rs139429949
NM_013275.6(ANKRD11):c.4443G>A (p.Ala1481=) rs377279757
NM_013275.6(ANKRD11):c.4533C>T (p.Pro1511=) rs769180959
NM_013275.6(ANKRD11):c.4568C>T (p.Pro1523Leu) rs942199653
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=) rs946642356
NM_013275.6(ANKRD11):c.5112C>A (p.Pro1704=) rs141292414
NM_013275.6(ANKRD11):c.5178C>T (p.Ser1726=) rs200783129
NM_013275.6(ANKRD11):c.5241C>T (p.Pro1747=) rs772552969
NM_013275.6(ANKRD11):c.5250C>T (p.Thr1750=) rs202126162
NM_013275.6(ANKRD11):c.543C>T (p.Ala181=) rs367937349
NM_013275.6(ANKRD11):c.5484G>A (p.Ser1828=) rs140164595
NM_013275.6(ANKRD11):c.5578C>T (p.Pro1860Ser) rs144516367
NM_013275.6(ANKRD11):c.5625C>T (p.Val1875=) rs201082380
NM_013275.6(ANKRD11):c.5629C>T (p.Pro1877Ser) rs142527333
NM_013275.6(ANKRD11):c.5632T>C (p.Ser1878Pro) rs143743958
NM_013275.6(ANKRD11):c.5889C>T (p.Ile1963=) rs748114867
NM_013275.6(ANKRD11):c.5916C>T (p.Ser1972=) rs1025761111
NM_013275.6(ANKRD11):c.5998C>T (p.Leu2000Phe) rs777086823
NM_013275.6(ANKRD11):c.6020C>T (p.Pro2007Leu) rs200531141
NM_013275.6(ANKRD11):c.6065C>T (p.Pro2022Leu) rs373218212
NM_013275.6(ANKRD11):c.6125A>G (p.Asp2042Gly) rs534182728
NM_013275.6(ANKRD11):c.6140C>G (p.Ala2047Gly) rs199691161
NM_013275.6(ANKRD11):c.6153A>G (p.Ser2051=) rs553002021
NM_013275.6(ANKRD11):c.6193TTC[1] (p.Phe2066del) rs781573469
NM_013275.6(ANKRD11):c.6283C>G (p.Leu2095Val) rs772144411
NM_013275.6(ANKRD11):c.6312C>T (p.Asp2104=) rs777466601
NM_013275.6(ANKRD11):c.6323G>A (p.Gly2108Asp) rs201509886
NM_013275.6(ANKRD11):c.6366C>T (p.Asp2122=) rs202049186
NM_013275.6(ANKRD11):c.6580C>G (p.Gln2194Glu) rs201589586
NM_013275.6(ANKRD11):c.6597C>T (p.Leu2199=) rs762643863
NM_013275.6(ANKRD11):c.6628G>C (p.Glu2210Gln) rs1350625482
NM_013275.6(ANKRD11):c.6698G>A (p.Gly2233Glu) rs570265865
NM_013275.6(ANKRD11):c.6712A>G (p.Ser2238Gly) rs770209899
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.6826C>T (p.Pro2276Ser) rs201957371
NM_013275.6(ANKRD11):c.6919C>T (p.Pro2307Ser) rs575642464
NM_013275.6(ANKRD11):c.7090G>A (p.Ala2364Thr) rs999130123
NM_013275.6(ANKRD11):c.7296C>T (p.Ser2432=) rs146648782
NM_013275.6(ANKRD11):c.7324C>T (p.Leu2442=) rs373934412
NM_013275.6(ANKRD11):c.7519C>A (p.Gln2507Lys) rs572878194
NM_013275.6(ANKRD11):c.7677G>A (p.Leu2559=) rs143429968
NM_013275.6(ANKRD11):c.7731A>C (p.Ser2577=) rs564437715
NM_013275.6(ANKRD11):c.7839C>G (p.Ala2613=) rs143287644
NM_013275.6(ANKRD11):c.843C>T (p.Asn281=) rs912859980
NM_013275.6(ANKRD11):c.868A>G (p.Thr290Ala) rs776494318
NM_013275.6(ANKRD11):c.888G>A (p.Ser296=) rs763790556

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.