ClinVar Miner

List of variants in gene ANKRD11 reported as uncertain significance

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 84
Download table as spreadsheet
HGVS dbSNP
NM_001256182.2(ANKRD11):c.226G>A (p.Glu76Lys) rs1555535454
NM_001256182.2(ANKRD11):c.4475_4498dup (p.1484_1491LLRHHRDE[3]) rs534329317
NM_001256182.2(ANKRD11):c.4616A>G (p.Glu1539Gly)
NM_001256182.2(ANKRD11):c.6232G>C (p.Asp2078His)
NM_001256182.2(ANKRD11):c.6254G>T (p.Cys2085Phe)
NM_001256182.2(ANKRD11):c.7519C>A (p.Gln2507Lys) rs572878194
NM_013275.6(ANKRD11):c.1133A>G (p.Asn378Ser) rs202203523
NM_013275.6(ANKRD11):c.116C>T (p.Thr39Ile)
NM_013275.6(ANKRD11):c.136G>A (p.Asp46Asn)
NM_013275.6(ANKRD11):c.1425G>T (p.Lys475Asn) rs1057523418
NM_013275.6(ANKRD11):c.149A>T (p.Glu50Val) rs1567614253
NM_013275.6(ANKRD11):c.1559C>T (p.Ala520Val) rs1415129056
NM_013275.6(ANKRD11):c.1763C>T (p.Ser588Leu)
NM_013275.6(ANKRD11):c.1994A>G (p.Lys665Arg)
NM_013275.6(ANKRD11):c.227-5C>G rs1303795065
NM_013275.6(ANKRD11):c.2518C>T (p.Arg840Trp)
NM_013275.6(ANKRD11):c.2535G>T (p.Leu845Phe) rs1555529022
NM_013275.6(ANKRD11):c.2684G>A (p.Arg895Gln) rs199800166
NM_013275.6(ANKRD11):c.2707C>T (p.Pro903Ser)
NM_013275.6(ANKRD11):c.2805G>A (p.Ser935=) rs149751840
NM_013275.6(ANKRD11):c.2942G>A (p.Cys981Tyr) rs1085307572
NM_013275.6(ANKRD11):c.295G>A (p.Gly99Ser) rs1567593338
NM_013275.6(ANKRD11):c.3005G>A (p.Arg1002Gln)
NM_013275.6(ANKRD11):c.3098G>T (p.Ser1033Ile) rs201522384
NM_013275.6(ANKRD11):c.3343A>G (p.Ile1115Val)
NM_013275.6(ANKRD11):c.3418G>A (p.Ala1140Thr) rs369869329
NM_013275.6(ANKRD11):c.3577G>A (p.Ala1193Thr)
NM_013275.6(ANKRD11):c.3625A>G (p.Lys1209Glu) rs866638426
NM_013275.6(ANKRD11):c.3736C>T (p.His1246Tyr) rs1170311302
NM_013275.6(ANKRD11):c.3889_3891dup (p.Asn1297dup) rs778998883
NM_013275.6(ANKRD11):c.4271C>A (p.Ser1424Tyr) rs1567569737
NM_013275.6(ANKRD11):c.4394A>G (p.His1465Arg)
NM_013275.6(ANKRD11):c.4401G>T (p.Glu1467Asp) rs1567569115
NM_013275.6(ANKRD11):c.4456C>T (p.Arg1486Trp)
NM_013275.6(ANKRD11):c.449C>T (p.Thr150Met)
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.4928C>A (p.Pro1643Gln)
NM_013275.6(ANKRD11):c.5296G>A (p.Val1766Met)
NM_013275.6(ANKRD11):c.5351C>T (p.Ser1784Phe)
NM_013275.6(ANKRD11):c.5552A>G (p.Tyr1851Cys) rs376366933
NM_013275.6(ANKRD11):c.5609C>T (p.Ala1870Val) rs864309571
NM_013275.6(ANKRD11):c.5651C>T (p.Ser1884Leu) rs1555526636
NM_013275.6(ANKRD11):c.5716G>A (p.Ala1906Thr) rs1428749185
NM_013275.6(ANKRD11):c.5726C>T (p.Pro1909Leu)
NM_013275.6(ANKRD11):c.5786G>A (p.Ser1929Asn)
NM_013275.6(ANKRD11):c.5875G>A (p.Ala1959Thr)
NM_013275.6(ANKRD11):c.5962C>T (p.Pro1988Ser)
NM_013275.6(ANKRD11):c.6046C>T (p.Pro2016Ser) rs1449729767
NM_013275.6(ANKRD11):c.6052_6060del (p.Pro2018_Ala2020del) rs775221712
NM_013275.6(ANKRD11):c.6060_6061delinsGC (p.Ser2021Pro) rs1567559902
NM_013275.6(ANKRD11):c.6063_6071del (p.Pro2022_Pro2024del) rs771037147
NM_013275.6(ANKRD11):c.6083C>T (p.Pro2028Leu)
NM_013275.6(ANKRD11):c.6112_6132del (p.Lys2038_Val2044del) rs748553966
NM_013275.6(ANKRD11):c.6127G>A (p.Ala2043Thr) rs1322632964
NM_013275.6(ANKRD11):c.6193_6195TTC[1] (p.Phe2066del) rs781573469
NM_013275.6(ANKRD11):c.6377G>A (p.Gly2126Asp)
NM_013275.6(ANKRD11):c.6415C>T (p.Pro2139Ser) rs1567557350
NM_013275.6(ANKRD11):c.6436A>G (p.Lys2146Glu)
NM_013275.6(ANKRD11):c.6448G>A (p.Asp2150Asn) rs1567557144
NM_013275.6(ANKRD11):c.6580C>G (p.Gln2194Glu)
NM_013275.6(ANKRD11):c.6704C>T (p.Pro2235Leu) rs1394383095
NM_013275.6(ANKRD11):c.6712A>G (p.Ser2238Gly)
NM_013275.6(ANKRD11):c.6893G>T (p.Arg2298Leu) rs1304326484
NM_013275.6(ANKRD11):c.6919C>T (p.Pro2307Ser) rs575642464
NM_013275.6(ANKRD11):c.6923G>T (p.Gly2308Val) rs1057522245
NM_013275.6(ANKRD11):c.6982C>G (p.Arg2328Gly) rs1567553783
NM_013275.6(ANKRD11):c.6985G>C (p.Val2329Leu)
NM_013275.6(ANKRD11):c.7087C>G (p.Pro2363Ala)
NM_013275.6(ANKRD11):c.7095G>A (p.Pro2365=) rs1343429737
NM_013275.6(ANKRD11):c.7167T>G (p.Phe2389Leu)
NM_013275.6(ANKRD11):c.7198_7200dup (p.Leu2400dup) rs1371024836
NM_013275.6(ANKRD11):c.7418C>T (p.Thr2473Met) rs765378650
NM_013275.6(ANKRD11):c.7436A>G (p.Asp2479Gly) rs1555524796
NM_013275.6(ANKRD11):c.7470+5G>T rs1555524784
NM_013275.6(ANKRD11):c.7618C>T (p.Arg2540Trp) rs1555523386
NM_013275.6(ANKRD11):c.7671G>A (p.Met2557Ile) rs1567544079
NM_013275.6(ANKRD11):c.7735C>T (p.Arg2579Cys) rs1567537413
NM_013275.6(ANKRD11):c.7753C>T (p.Arg2585Cys) rs1567537304
NM_013275.6(ANKRD11):c.7799G>A (p.Arg2600His) rs1354874973
NM_013275.6(ANKRD11):c.7847T>C (p.Leu2616Pro) rs1567533174
NM_013275.6(ANKRD11):c.7927G>A (p.Glu2643Lys) rs1064796264
NM_013275.6(ANKRD11):c.868A>G (p.Thr290Ala)
NM_013275.6(ANKRD11):c.988A>G (p.Lys330Glu) rs1555529962

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.