ClinVar Miner

List of variants in gene ANKRD11 reported as pathogenic

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 120
Download table as spreadsheet
HGVS dbSNP
GRCh37/hg19 16q24.3(chr16:89296939-89420254)x1
GRCh37/hg19 16q24.3(chr16:89434509-89490401)x1
GRCh37/hg19 16q24.3(chr16:89539973-89570635)x1
NC_000016.10:g.89288654del
NC_000016.9:g.(?_89334866)_(89355098_?)del
NM_001256182.2(ANKRD11):c.1381_1382del (p.Glu461fs) rs1555529734
NM_001256182.2(ANKRD11):c.1389del (p.Gly464fs) rs1555529726
NM_001256182.2(ANKRD11):c.1623_1630del (p.His542fs) rs1555529572
NM_001256182.2(ANKRD11):c.2130G>A (p.Trp710Ter) rs1555529297
NM_001256182.2(ANKRD11):c.2494del (p.Ser832fs) rs1555529052
NM_001256182.2(ANKRD11):c.3334dup (p.Ser1112fs) rs1555528558
NM_001256182.2(ANKRD11):c.4114G>T (p.Glu1372Ter) rs146474985
NM_001256182.2(ANKRD11):c.4140C>G (p.Tyr1380Ter) rs1555528040
NM_001256182.2(ANKRD11):c.4205dup (p.Tyr1402Ter) rs1085307544
NM_001256182.2(ANKRD11):c.4902del (p.Leu1635fs) rs1555527497
NM_001256182.2(ANKRD11):c.5537del (p.Leu1846fs) rs1555526796
NM_001256182.2(ANKRD11):c.6792dup (p.Ala2265fs) rs878855327
NM_001256182.2(ANKRD11):c.6982dup (p.Arg2328fs) rs1555525088
NM_001256182.2(ANKRD11):c.7303del (p.Ala2435fs) rs1555524870
NM_001256182.2(ANKRD11):c.7327C>T (p.Gln2443Ter) rs1555524861
NM_001256182.2(ANKRD11):c.7825C>T (p.Gln2609Ter) rs797044900
NM_001256182:c.7545delG
NM_013275.6(ANKRD11):c.1124_1128del (p.Thr375fs) rs1555529864
NM_013275.6(ANKRD11):c.1197_1200AAAG[1] (p.Lys401fs) rs886042029
NM_013275.6(ANKRD11):c.1458_1459AG[2] (p.Ser488fs) rs1555529645
NM_013275.6(ANKRD11):c.160C>T (p.Arg54Ter) rs749607205
NM_013275.6(ANKRD11):c.1652G>A (p.Trp551Ter) rs886039713
NM_013275.6(ANKRD11):c.1679C>G (p.Ser560Ter) rs1555529551
NM_013275.6(ANKRD11):c.1801C>T (p.Arg601Ter) rs772229371
NM_013275.6(ANKRD11):c.1898_1902AAACA[1] (p.Lys635fs) rs886041125
NM_013275.6(ANKRD11):c.1948C>T (p.Gln650Ter) rs1567579525
NM_013275.6(ANKRD11):c.1970_1971del (p.Phe657fs) rs1555529364
NM_013275.6(ANKRD11):c.1977C>G (p.Tyr659Ter) rs749201074
NM_013275.6(ANKRD11):c.1996C>T (p.Gln666Ter) rs747922528
NM_013275.6(ANKRD11):c.2047_2048del (p.Lys683fs) rs1567579092
NM_013275.6(ANKRD11):c.2171_2174CAAA[1] (p.Asn725fs) rs886039734
NM_013275.6(ANKRD11):c.2197C>T (p.Arg733Ter) rs886041791
NM_013275.6(ANKRD11):c.2273_2274del (p.Leu758fs)
NM_013275.6(ANKRD11):c.2283C>G (p.Tyr761Ter) rs1567578243
NM_013275.6(ANKRD11):c.2305del (p.Ser769fs) rs863223320
NM_013275.6(ANKRD11):c.2329G>T (p.Glu777Ter) rs886041760
NM_013275.6(ANKRD11):c.2398_2401del (p.Glu800fs) rs797045027
NM_013275.6(ANKRD11):c.2404_2407del (p.Leu802fs) rs1555529181
NM_013275.6(ANKRD11):c.2408_2412del (p.Lys803fs) rs886039902
NM_013275.6(ANKRD11):c.2409_2412del (p.Glu805fs) rs886039902
NM_013275.6(ANKRD11):c.2454dup (p.Asn819Ter)
NM_013275.6(ANKRD11):c.2500del (p.Ser834fs) rs886041486
NM_013275.6(ANKRD11):c.2589dup (p.Asp864fs) rs886041724
NM_013275.6(ANKRD11):c.2647G>T (p.Glu883Ter) rs1135401804
NM_013275.6(ANKRD11):c.2692C>T (p.Arg898Ter) rs780011005
NM_013275.6(ANKRD11):c.2719_2730delinsT (p.Arg906_Lys907insTer) rs886041539
NM_013275.6(ANKRD11):c.2857del (p.Asp953fs) rs1064793599
NM_013275.6(ANKRD11):c.3084C>A (p.Tyr1028Ter) rs1064793539
NM_013275.6(ANKRD11):c.3084del (p.Arg1027_Tyr1028insTer) rs1555528719
NM_013275.6(ANKRD11):c.3096del (p.Ser1033fs) rs1555528717
NM_013275.6(ANKRD11):c.3122C>A (p.Ser1041Ter) rs1057518663
NM_013275.6(ANKRD11):c.3138T>A (p.Cys1046Ter) rs1567574466
NM_013275.6(ANKRD11):c.3198_3199del (p.His1066fs) rs1567574291
NM_013275.6(ANKRD11):c.3220_3223AAAG[1] (p.Glu1075fs) rs1064794330
NM_013275.6(ANKRD11):c.3309del (p.Asp1104fs) rs772267579
NM_013275.6(ANKRD11):c.3425_3431delinsTCCGTCCTG (p.Asp1142fs) rs1567573538
NM_013275.6(ANKRD11):c.3562C>T (p.Arg1188Ter) rs761848111
NM_013275.6(ANKRD11):c.3632_3633del (p.Lys1211fs) rs1555528400
NM_013275.6(ANKRD11):c.3702_3705del (p.Lys1235fs) rs1555528357
NM_013275.6(ANKRD11):c.3704_3707del (p.Lys1235fs) rs1555528354
NM_013275.6(ANKRD11):c.3708_3709del (p.Lys1237fs) rs1567572265
NM_013275.6(ANKRD11):c.3770_3771del (p.Lys1257fs) rs886039477
NM_013275.6(ANKRD11):c.3770_3773del (p.Lys1257fs) rs1567571990
NM_013275.6(ANKRD11):c.4087C>T (p.Arg1363Ter) rs1364690005
NM_013275.6(ANKRD11):c.4206C>G (p.Tyr1402Ter)
NM_013275.6(ANKRD11):c.424C>T (p.Gln142Ter) rs1567592494
NM_013275.6(ANKRD11):c.4372_4375del (p.Glu1458fs) rs886041829
NM_013275.6(ANKRD11):c.4384dup (p.Arg1462fs) rs886041521
NM_013275.6(ANKRD11):c.4875del (p.Lys1625fs) rs1555527511
NM_013275.6(ANKRD11):c.488_501del (p.Lys163fs) rs1555531390
NM_013275.6(ANKRD11):c.4933del (p.Leu1645fs) rs1064797050
NM_013275.6(ANKRD11):c.5065del (p.Leu1689fs) rs1567566026
NM_013275.6(ANKRD11):c.5317G>T (p.Glu1773Ter) rs1114167291
NM_013275.6(ANKRD11):c.5504del (p.Leu1835fs) rs1057519399
NM_013275.6(ANKRD11):c.5667del (p.Lys1889fs) rs886042016
NM_013275.6(ANKRD11):c.5682dup (p.Arg1895fs)
NM_013275.6(ANKRD11):c.5790C>G (p.Tyr1930Ter) rs886041574
NM_013275.6(ANKRD11):c.5951_5952CA[1] (p.Gln1985fs) rs863223321
NM_013275.6(ANKRD11):c.600_601dup (p.Gly201fs) rs1555531314
NM_013275.6(ANKRD11):c.6015dup (p.Gly2006fs) rs879253753
NM_013275.6(ANKRD11):c.6138del (p.Ala2047fs) rs1555526086
NM_013275.6(ANKRD11):c.6197_6198delinsAA (p.Phe2066Ter) rs1555525977
NM_013275.6(ANKRD11):c.6210_6211del (p.Lys2070fs) rs863225257
NM_013275.6(ANKRD11):c.6212C>G (p.Ser2071Ter) rs763407068
NM_013275.6(ANKRD11):c.6249del (p.Ala2084fs) rs1555525917
NM_013275.6(ANKRD11):c.6340C>T (p.Gln2114Ter) rs1555525792
NM_013275.6(ANKRD11):c.6430C>T (p.Gln2144Ter) rs1555525685
NM_013275.6(ANKRD11):c.6472G>T (p.Glu2158Ter) rs869312713
NM_013275.6(ANKRD11):c.6513del (p.Val2173fs) rs1555525603
NM_013275.6(ANKRD11):c.6624_6625del (p.Glu2210fs) rs1555525517
NM_013275.6(ANKRD11):c.6670G>T (p.Glu2224Ter) rs1381957912
NM_013275.6(ANKRD11):c.6677_6680delinsAGA (p.Val2226fs) rs1555525476
NM_013275.6(ANKRD11):c.6786_6787insA (p.Pro2263fs) rs1135401815
NM_013275.6(ANKRD11):c.6792del (p.Ala2265fs) rs878855327
NM_013275.6(ANKRD11):c.6834_6835TG[1] (p.Val2279fs) rs1555525296
NM_013275.6(ANKRD11):c.6847C>T (p.Gln2283Ter) rs1221781038
NM_013275.6(ANKRD11):c.6871G>T (p.Glu2291Ter) rs1064797012
NM_013275.6(ANKRD11):c.6968_6975del (p.Ala2323fs) rs1555525115
NM_013275.6(ANKRD11):c.7062del (p.Ser2355fs) rs886041942
NM_013275.6(ANKRD11):c.7083dup (p.Thr2362fs) rs886041822
NM_013275.6(ANKRD11):c.7138C>T (p.Gln2380Ter) rs1057520565
NM_013275.6(ANKRD11):c.7180C>T (p.Gln2394Ter) rs863225296
NM_013275.6(ANKRD11):c.7183C>T (p.Gln2395Ter) rs1250598768
NM_013275.6(ANKRD11):c.7234C>T (p.Gln2412Ter) rs886042019
NM_013275.6(ANKRD11):c.7354C>G (p.Arg2452Gly) rs1064795497
NM_013275.6(ANKRD11):c.7471-2A>G rs1555523580
NM_013275.6(ANKRD11):c.7552C>T (p.Gln2518Ter) rs886041889
NM_013275.6(ANKRD11):c.7569+1G>A rs797044890
NM_013275.6(ANKRD11):c.7570-1G>A rs863223319
NM_013275.6(ANKRD11):c.7570-1G>C rs863223319
NM_013275.6(ANKRD11):c.769G>T (p.Gly257Ter) rs1555530173
NM_013275.6(ANKRD11):c.7711C>T (p.Gln2571Ter) rs1567543920
NM_013275.6(ANKRD11):c.7714-2A>G rs886041976
NM_013275.6(ANKRD11):c.867C>A (p.Tyr289Ter)
NM_013275.6(ANKRD11):c.893-1G>C rs1567583835

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.