ClinVar Miner

List of variants in gene ANKRD11 reported by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 174
Download table as spreadsheet
HGVS dbSNP
NM_001256182.1(ANKRD11):c.1020G>A (p.Thr340=)
NM_001256182.1(ANKRD11):c.1296G>C (p.Thr432=) rs74033734
NM_001256182.1(ANKRD11):c.136G>A (p.Asp46Asn)
NM_001256182.1(ANKRD11):c.1844C>G (p.Ala615Gly)
NM_001256182.1(ANKRD11):c.2039C>G (p.Thr680Ser)
NM_001256182.1(ANKRD11):c.3045C>G (p.Pro1015=)
NM_001256182.1(ANKRD11):c.306G>C (p.Leu102=)
NM_001256182.1(ANKRD11):c.3660G>A (p.Arg1220=)
NM_001256182.1(ANKRD11):c.372G>A (p.Thr124=)
NM_001256182.1(ANKRD11):c.375C>T (p.Ala125=)
NM_001256182.1(ANKRD11):c.4344T>C (p.Tyr1448=)
NM_001256182.1(ANKRD11):c.4872G>A (p.Ala1624=) rs143426579
NM_001256182.1(ANKRD11):c.5250C>T (p.Thr1750=)
NM_001256182.1(ANKRD11):c.5629C>T (p.Pro1877Ser)
NM_001256182.1(ANKRD11):c.6084C>T (p.Pro2028=)
NM_001256182.1(ANKRD11):c.6140C>G (p.Ala2047Gly)
NM_001256182.1(ANKRD11):c.6323G>A (p.Gly2108Asp) rs201509886
NM_001256182.1(ANKRD11):c.6580C>G (p.Gln2194Glu)
NM_001256182.1(ANKRD11):c.6712A>G (p.Ser2238Gly)
NM_001256182.1(ANKRD11):c.6725C>T (p.Ala2242Val)
NM_001256182.1(ANKRD11):c.6746G>A (p.Arg2249His)
NM_001256182.1(ANKRD11):c.6919C>T (p.Pro2307Ser) rs575642464
NM_013275.5(ANKRD11):c.1027G>A (p.Val343Ile)
NM_013275.5(ANKRD11):c.1035C>T (p.Asp345=)
NM_013275.5(ANKRD11):c.1245C>T (p.Asp415=)
NM_013275.5(ANKRD11):c.1381_1382delGA (p.Glu461Asnfs) rs1555529734
NM_013275.5(ANKRD11):c.1389delA (p.Gly464Alafs) rs1555529726
NM_013275.5(ANKRD11):c.1413G>A (p.Lys471=)
NM_013275.5(ANKRD11):c.1462_1463delAG (p.Ser488Trpfs) rs1555529645
NM_013275.5(ANKRD11):c.1623_1630delGCACACCA (p.His542Alafs) rs1555529572
NM_013275.5(ANKRD11):c.1725C>T (p.Ser575=)
NM_013275.5(ANKRD11):c.1763C>T (p.Ser588Leu)
NM_013275.5(ANKRD11):c.1842C>T (p.Ser614=)
NM_013275.5(ANKRD11):c.1851C>T (p.Gly617=)
NM_013275.5(ANKRD11):c.1852G>A (p.Ala618Thr)
NM_013275.5(ANKRD11):c.1857C>T (p.Val619=)
NM_013275.5(ANKRD11):c.1903_1907delAAACA (p.Lys635Glnfs) rs886041125
NM_013275.5(ANKRD11):c.195C>T (p.Gly65=)
NM_013275.5(ANKRD11):c.207G>A (p.Glu69=)
NM_013275.5(ANKRD11):c.2130G>A (p.Trp710Ter) rs1555529297
NM_013275.5(ANKRD11):c.2184C>G (p.Ile728Met)
NM_013275.5(ANKRD11):c.2197C>T (p.Arg733Ter) rs886041791
NM_013275.5(ANKRD11):c.2216C>T (p.Ser739Leu) rs146294483
NM_013275.5(ANKRD11):c.2217G>A (p.Ser739=)
NM_013275.5(ANKRD11):c.226G>A (p.Glu76Lys) rs1555535454
NM_013275.5(ANKRD11):c.2373G>A (p.Lys791=) rs138267414
NM_013275.5(ANKRD11):c.2494delA (p.Ser832Alafs) rs1555529052
NM_013275.5(ANKRD11):c.2518C>T (p.Arg840Trp)
NM_013275.5(ANKRD11):c.2610C>T (p.Ser870=)
NM_013275.5(ANKRD11):c.2684G>A (p.Arg895Gln) rs199800166
NM_013275.5(ANKRD11):c.280G>C (p.Ala94Pro)
NM_013275.5(ANKRD11):c.282C>G (p.Ala94=)
NM_013275.5(ANKRD11):c.2841C>T (p.Ala947=)
NM_013275.5(ANKRD11):c.2888_2896del (p.Asp963_Arg965del)
NM_013275.5(ANKRD11):c.2889C>T (p.Asp963=)
NM_013275.5(ANKRD11):c.2912C>T (p.Ala971Val)
NM_013275.5(ANKRD11):c.295G>A (p.Gly99Ser)
NM_013275.5(ANKRD11):c.3005G>A (p.Arg1002Gln)
NM_013275.5(ANKRD11):c.3138T>A (p.Cys1046Ter)
NM_013275.5(ANKRD11):c.3162A>G (p.Lys1054=) rs61729371
NM_013275.5(ANKRD11):c.3197A>G (p.His1066Arg)
NM_013275.5(ANKRD11):c.3334dup (p.Ser1112Lysfs) rs1555528558
NM_013275.5(ANKRD11):c.3437C>T (p.Thr1146Met)
NM_013275.5(ANKRD11):c.3483C>T (p.Ser1161=)
NM_013275.5(ANKRD11):c.3573C>G (p.Ala1191=) rs62000377
NM_013275.5(ANKRD11):c.3577G>A (p.Ala1193Thr)
NM_013275.5(ANKRD11):c.3578C>T (p.Ala1193Val)
NM_013275.5(ANKRD11):c.3584G>A (p.Arg1195Lys)
NM_013275.5(ANKRD11):c.3702_3705delTAAA (p.Lys1235Argfs) rs1555528357
NM_013275.5(ANKRD11):c.3736C>T (p.His1246Tyr)
NM_013275.5(ANKRD11):c.3770_3771delAA (p.Lys1257Argfs) rs886039477
NM_013275.5(ANKRD11):c.3822C>T (p.Ala1274=) rs61741725
NM_013275.5(ANKRD11):c.3826G>A (p.Ala1276Thr)
NM_013275.5(ANKRD11):c.3889_3891dup (p.Asn1297_Asp1298insAsn)
NM_013275.5(ANKRD11):c.389A>G (p.Asn130Ser)
NM_013275.5(ANKRD11):c.3969C>T (p.Val1323=)
NM_013275.5(ANKRD11):c.3973T>C (p.Phe1325Leu)
NM_013275.5(ANKRD11):c.3977C>T (p.Thr1326Met) rs144673419
NM_013275.5(ANKRD11):c.4114G>T (p.Glu1372Ter) rs146474985
NM_013275.5(ANKRD11):c.4140C>G (p.Tyr1380Ter) rs1555528040
NM_013275.5(ANKRD11):c.4149C>T (p.Gly1383=)
NM_013275.5(ANKRD11):c.4237G>A (p.Glu1413Lys) rs140373729
NM_013275.5(ANKRD11):c.4271C>A (p.Ser1424Tyr)
NM_013275.5(ANKRD11):c.4297T>C (p.Ser1433Pro)
NM_013275.5(ANKRD11):c.4317G>A (p.Lys1439=)
NM_013275.5(ANKRD11):c.4382A>G (p.Lys1461Arg)
NM_013275.5(ANKRD11):c.4401G>T (p.Glu1467Asp)
NM_013275.5(ANKRD11):c.4440T>C (p.His1480=)
NM_013275.5(ANKRD11):c.4443G>A (p.Ala1481=)
NM_013275.5(ANKRD11):c.4456C>T (p.Arg1486Trp)
NM_013275.5(ANKRD11):c.449C>T (p.Thr150Met)
NM_013275.5(ANKRD11):c.4533C>T (p.Pro1511=)
NM_013275.5(ANKRD11):c.4568C>T (p.Pro1523Leu)
NM_013275.5(ANKRD11):c.4609G>A (p.Gly1537Ser) rs1347006212
NM_013275.5(ANKRD11):c.4616A>G (p.Glu1539Gly)
NM_013275.5(ANKRD11):c.4667C>G (p.Ala1556Gly) rs781186923
NM_013275.5(ANKRD11):c.4831C>T (p.Leu1611=)
NM_013275.5(ANKRD11):c.4902delT (p.Leu1635Trpfs) rs1555527497
NM_013275.5(ANKRD11):c.4912C>G (p.Pro1638Ala)
NM_013275.5(ANKRD11):c.4928C>A (p.Pro1643Gln)
NM_013275.5(ANKRD11):c.4932G>A (p.Gly1644=) rs72821356
NM_013275.5(ANKRD11):c.5061G>A (p.Glu1687=)
NM_013275.5(ANKRD11):c.5112C>A (p.Pro1704=)
NM_013275.5(ANKRD11):c.5178C>T (p.Ser1726=)
NM_013275.5(ANKRD11):c.5241C>T (p.Pro1747=)
NM_013275.5(ANKRD11):c.5296G>A (p.Val1766Met)
NM_013275.5(ANKRD11):c.5338G>A (p.Ala1780Thr) rs75362060
NM_013275.5(ANKRD11):c.543C>T (p.Ala181=)
NM_013275.5(ANKRD11):c.5484G>A (p.Ser1828=)
NM_013275.5(ANKRD11):c.5509C>T (p.Pro1837Ser)
NM_013275.5(ANKRD11):c.5537delT (p.Leu1846Cysfs) rs1555526796
NM_013275.5(ANKRD11):c.5578C>T (p.Pro1860Ser)
NM_013275.5(ANKRD11):c.5625C>T (p.Val1875=)
NM_013275.5(ANKRD11):c.5632T>C (p.Ser1878Pro)
NM_013275.5(ANKRD11):c.5665A>G (p.Lys1889Glu)
NM_013275.5(ANKRD11):c.5716G>A (p.Ala1906Thr)
NM_013275.5(ANKRD11):c.5726C>T (p.Pro1909Leu)
NM_013275.5(ANKRD11):c.5875G>A (p.Ala1959Thr)
NM_013275.5(ANKRD11):c.5889C>T (p.Ile1963=)
NM_013275.5(ANKRD11):c.5916C>T (p.Ser1972=)
NM_013275.5(ANKRD11):c.5962C>T (p.Pro1988Ser)
NM_013275.5(ANKRD11):c.5998C>T (p.Leu2000Phe)
NM_013275.5(ANKRD11):c.6020C>T (p.Pro2007Leu) rs200531141
NM_013275.5(ANKRD11):c.6060_6061delCTinsGC (p.Ser2021Pro)
NM_013275.5(ANKRD11):c.6063_6071del (p.Pro2022_Pro2024del)
NM_013275.5(ANKRD11):c.6065C>T (p.Pro2022Leu)
NM_013275.5(ANKRD11):c.6067G>C (p.Ala2023Pro) rs60520302
NM_013275.5(ANKRD11):c.6106G>A (p.Asp2036Asn) rs201636725
NM_013275.5(ANKRD11):c.6125A>G (p.Asp2042Gly)
NM_013275.5(ANKRD11):c.6153A>G (p.Ser2051=)
NM_013275.5(ANKRD11):c.6176C>A (p.Pro2059His)
NM_013275.5(ANKRD11):c.6196_6198del (p.Phe2066del)
NM_013275.5(ANKRD11):c.6232G>C (p.Asp2078His)
NM_013275.5(ANKRD11):c.6254G>T (p.Cys2085Phe)
NM_013275.5(ANKRD11):c.6283C>G (p.Leu2095Val)
NM_013275.5(ANKRD11):c.6312C>T (p.Asp2104=)
NM_013275.5(ANKRD11):c.6366C>T (p.Asp2122=)
NM_013275.5(ANKRD11):c.6415C>T (p.Pro2139Ser)
NM_013275.5(ANKRD11):c.6448G>A (p.Asp2150Asn)
NM_013275.5(ANKRD11):c.6497T>G (p.Met2166Arg)
NM_013275.5(ANKRD11):c.6597C>T (p.Leu2199=)
NM_013275.5(ANKRD11):c.6628G>C (p.Glu2210Gln)
NM_013275.5(ANKRD11):c.6698G>A (p.Gly2233Glu)
NM_013275.5(ANKRD11):c.6745C>T (p.Arg2249Cys) rs202081612
NM_013275.5(ANKRD11):c.6781G>A (p.Glu2261Lys)
NM_013275.5(ANKRD11):c.6787C>T (p.Pro2263Ser) rs76793093
NM_013275.5(ANKRD11):c.6792dup (p.Ala2265Argfs) rs878855327
NM_013275.5(ANKRD11):c.6826C>T (p.Pro2276Ser)
NM_013275.5(ANKRD11):c.6847C>T (p.Gln2283Ter) rs1221781038
NM_013275.5(ANKRD11):c.6868C>T (p.Pro2290Ser)
NM_013275.5(ANKRD11):c.6924C>T (p.Gly2308=)
NM_013275.5(ANKRD11):c.6985G>C (p.Val2329Leu)
NM_013275.5(ANKRD11):c.7087C>G (p.Pro2363Ala)
NM_013275.5(ANKRD11):c.7090G>A (p.Ala2364Thr)
NM_013275.5(ANKRD11):c.7128C>G (p.Asp2376Glu)
NM_013275.5(ANKRD11):c.7167T>G (p.Phe2389Leu)
NM_013275.5(ANKRD11):c.7198_7200dup (p.Leu2400_Asn2401insLeu)
NM_013275.5(ANKRD11):c.7296C>T (p.Ser2432=)
NM_013275.5(ANKRD11):c.7303delG (p.Ala2435Profs) rs1555524870
NM_013275.5(ANKRD11):c.7324C>T (p.Leu2442=)
NM_013275.5(ANKRD11):c.7327C>T (p.Gln2443Ter) rs1555524861
NM_013275.5(ANKRD11):c.7519C>A (p.Gln2507Lys) rs572878194
NM_013275.5(ANKRD11):c.7569+1G>A rs797044890
NM_013275.5(ANKRD11):c.7671G>A (p.Met2557Ile)
NM_013275.5(ANKRD11):c.7677G>A (p.Leu2559=)
NM_013275.5(ANKRD11):c.7731A>C (p.Ser2577=)
NM_013275.5(ANKRD11):c.7799G>A (p.Arg2600His)
NM_013275.5(ANKRD11):c.7825C>T (p.Gln2609Ter) rs797044900
NM_013275.5(ANKRD11):c.7839C>G (p.Ala2613=)
NM_013275.5(ANKRD11):c.7847T>C (p.Leu2616Pro)
NM_013275.5(ANKRD11):c.843C>T (p.Asn281=)
NM_013275.5(ANKRD11):c.868A>G (p.Thr290Ala)
NM_013275.5(ANKRD11):c.888G>A (p.Ser296=)
NM_013275.5(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.