ClinVar Miner

List of variants in gene ANKRD11 reported as uncertain significance by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 179
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_013275.6(ANKRD11):c.6193T>C (p.Phe2065Leu) rs200351209 0.00083
NM_013275.6(ANKRD11):c.3274C>T (p.Pro1092Ser) rs773172347 0.00011
NM_013275.6(ANKRD11):c.7087C>G (p.Pro2363Ala) rs769501453 0.00010
NM_013275.6(ANKRD11):c.3005G>A (p.Arg1002Gln) rs757870881 0.00009
NM_013275.6(ANKRD11):c.6113A>C (p.Lys2038Thr) rs370006772 0.00008
NM_013275.6(ANKRD11):c.6910G>A (p.Glu2304Lys) rs905177395 0.00007
NM_013275.6(ANKRD11):c.6760G>A (p.Gly2254Arg) rs1003478010 0.00005
NM_013275.6(ANKRD11):c.7167T>G (p.Phe2389Leu) rs927582667 0.00005
NM_013275.6(ANKRD11):c.3978G>A (p.Thr1326=) rs200351769 0.00004
NM_013275.6(ANKRD11):c.4456C>T (p.Arg1486Trp) rs189656772 0.00004
NM_013275.6(ANKRD11):c.5552A>G (p.Tyr1851Cys) rs376366933 0.00004
NM_013275.6(ANKRD11):c.5726C>T (p.Pro1909Leu) rs780224924 0.00004
NM_013275.6(ANKRD11):c.6436A>G (p.Lys2146Glu) rs1283976400 0.00004
NM_013275.6(ANKRD11):c.7103G>A (p.Arg2368Lys) rs1018954790 0.00004
NM_013275.6(ANKRD11):c.1432T>C (p.Ser478Pro) rs372688828 0.00003
NM_013275.6(ANKRD11):c.449C>T (p.Thr150Met) rs777070083 0.00003
NM_013275.6(ANKRD11):c.5216G>A (p.Cys1739Tyr) rs757264535 0.00003
NM_013275.6(ANKRD11):c.2518C>T (p.Arg840Trp) rs761259443 0.00002
NM_013275.6(ANKRD11):c.301G>A (p.Gly101Arg) rs1373571533 0.00002
NM_013275.6(ANKRD11):c.4001C>T (p.Pro1334Leu) rs765151001 0.00002
NM_013275.6(ANKRD11):c.7111G>T (p.Ala2371Ser) rs747911603 0.00002
NM_013275.6(ANKRD11):c.1875G>C (p.Glu625Asp) rs1267173254 0.00001
NM_013275.6(ANKRD11):c.2695G>A (p.Asp899Asn) rs1423885373 0.00001
NM_013275.6(ANKRD11):c.295G>A (p.Gly99Ser) rs1567593338 0.00001
NM_013275.6(ANKRD11):c.3418G>A (p.Ala1140Thr) rs369869329 0.00001
NM_013275.6(ANKRD11):c.3577G>A (p.Ala1193Thr) rs111737495 0.00001
NM_013275.6(ANKRD11):c.3736C>T (p.His1246Tyr) rs1170311302 0.00001
NM_013275.6(ANKRD11):c.4271C>A (p.Ser1424Tyr) rs1567569737 0.00001
NM_013275.6(ANKRD11):c.4669C>G (p.Pro1557Ala) rs374295517 0.00001
NM_013275.6(ANKRD11):c.5351C>T (p.Ser1784Phe) rs751323481 0.00001
NM_013275.6(ANKRD11):c.5716G>A (p.Ala1906Thr) rs1428749185 0.00001
NM_013275.6(ANKRD11):c.6622T>G (p.Ser2208Ala) rs778171762 0.00001
NM_013275.6(ANKRD11):c.7799G>A (p.Arg2600His) rs1354874973 0.00001
NM_013275.6(ANKRD11):c.-2C>T
NM_013275.6(ANKRD11):c.1024C>G (p.Pro342Ala)
NM_013275.6(ANKRD11):c.1024C>T (p.Pro342Ser)
NM_013275.6(ANKRD11):c.1229C>T (p.Thr410Met)
NM_013275.6(ANKRD11):c.1232C>T (p.Ser411Leu)
NM_013275.6(ANKRD11):c.1318C>G (p.Arg440Gly)
NM_013275.6(ANKRD11):c.1408G>A (p.Gly470Arg)
NM_013275.6(ANKRD11):c.1508A>G (p.Lys503Arg)
NM_013275.6(ANKRD11):c.1561T>G (p.Ser521Ala)
NM_013275.6(ANKRD11):c.1618G>A (p.Asp540Asn)
NM_013275.6(ANKRD11):c.1649A>G (p.Asn550Ser)
NM_013275.6(ANKRD11):c.164C>G (p.Ala55Gly)
NM_013275.6(ANKRD11):c.1700A>G (p.Asp567Gly)
NM_013275.6(ANKRD11):c.1720A>T (p.Thr574Ser)
NM_013275.6(ANKRD11):c.1805C>T (p.Ala602Val)
NM_013275.6(ANKRD11):c.1829C>T (p.Pro610Leu)
NM_013275.6(ANKRD11):c.1871A>G (p.Lys624Arg)
NM_013275.6(ANKRD11):c.1894C>T (p.His632Tyr)
NM_013275.6(ANKRD11):c.2078A>C (p.His693Pro)
NM_013275.6(ANKRD11):c.2124A>T (p.Lys708Asn)
NM_013275.6(ANKRD11):c.2156A>G (p.Lys719Arg)
NM_013275.6(ANKRD11):c.216C>A (p.Asp72Glu)
NM_013275.6(ANKRD11):c.2315G>A (p.Arg772Gln)
NM_013275.6(ANKRD11):c.2437G>A (p.Ala813Thr)
NM_013275.6(ANKRD11):c.2506G>A (p.Asp836Asn)
NM_013275.6(ANKRD11):c.2576A>G (p.Asp859Gly)
NM_013275.6(ANKRD11):c.2597G>A (p.Arg866Lys)
NM_013275.6(ANKRD11):c.2677C>T (p.Arg893Trp)
NM_013275.6(ANKRD11):c.2717G>A (p.Arg906Gln)
NM_013275.6(ANKRD11):c.2727C>G (p.Asp909Glu)
NM_013275.6(ANKRD11):c.2814C>G (p.Asp938Glu)
NM_013275.6(ANKRD11):c.2882G>T (p.Arg961Leu)
NM_013275.6(ANKRD11):c.2971G>A (p.Gly991Ser)
NM_013275.6(ANKRD11):c.2992G>C (p.Glu998Gln)
NM_013275.6(ANKRD11):c.3034A>G (p.Lys1012Glu)
NM_013275.6(ANKRD11):c.3241G>A (p.Asp1081Asn)
NM_013275.6(ANKRD11):c.3263A>G (p.Glu1088Gly)
NM_013275.6(ANKRD11):c.3442G>C (p.Gly1148Arg)
NM_013275.6(ANKRD11):c.3754G>T (p.Ala1252Ser)
NM_013275.6(ANKRD11):c.3769A>C (p.Lys1257Gln)
NM_013275.6(ANKRD11):c.3781G>C (p.Asp1261His)
NM_013275.6(ANKRD11):c.3889_3891dup (p.Asn1297dup) rs778998883
NM_013275.6(ANKRD11):c.3911C>T (p.Ser1304Phe)
NM_013275.6(ANKRD11):c.3944C>T (p.Pro1315Leu) rs186068075
NM_013275.6(ANKRD11):c.4030C>G (p.Leu1344Val)
NM_013275.6(ANKRD11):c.4051A>G (p.Arg1351Gly)
NM_013275.6(ANKRD11):c.4064C>G (p.Ser1355Cys)
NM_013275.6(ANKRD11):c.4139A>T (p.Tyr1380Phe)
NM_013275.6(ANKRD11):c.4207G>A (p.Gly1403Arg)
NM_013275.6(ANKRD11):c.4236AGA[1] (p.Glu1413del) rs778347369
NM_013275.6(ANKRD11):c.4268T>G (p.Phe1423Cys)
NM_013275.6(ANKRD11):c.4401G>T (p.Glu1467Asp) rs1567569115
NM_013275.6(ANKRD11):c.4418A>G (p.Lys1473Arg)
NM_013275.6(ANKRD11):c.4453C>G (p.Leu1485Val)
NM_013275.6(ANKRD11):c.455A>T (p.Asn152Ile)
NM_013275.6(ANKRD11):c.4616A>G (p.Glu1539Gly) rs751369171
NM_013275.6(ANKRD11):c.4853C>T (p.Pro1618Leu)
NM_013275.6(ANKRD11):c.4891C>T (p.Arg1631Trp)
NM_013275.6(ANKRD11):c.4892G>A (p.Arg1631Gln)
NM_013275.6(ANKRD11):c.4928C>A (p.Pro1643Gln) rs147690079
NM_013275.6(ANKRD11):c.4959G>T (p.Lys1653Asn)
NM_013275.6(ANKRD11):c.4964A>G (p.Lys1655Arg)
NM_013275.6(ANKRD11):c.5069C>T (p.Pro1690Leu) rs376034086
NM_013275.6(ANKRD11):c.5075C>T (p.Ser1692Phe)
NM_013275.6(ANKRD11):c.5102C>G (p.Thr1701Ser)
NM_013275.6(ANKRD11):c.5114C>G (p.Thr1705Ser)
NM_013275.6(ANKRD11):c.5123C>T (p.Ser1708Leu)
NM_013275.6(ANKRD11):c.5146G>A (p.Glu1716Lys)
NM_013275.6(ANKRD11):c.5174C>T (p.Pro1725Leu)
NM_013275.6(ANKRD11):c.5184C>G (p.Ser1728Arg)
NM_013275.6(ANKRD11):c.5188G>A (p.Asp1730Asn)
NM_013275.6(ANKRD11):c.5296G>A (p.Val1766Met) rs751326964
NM_013275.6(ANKRD11):c.5399A>G (p.Glu1800Gly)
NM_013275.6(ANKRD11):c.5483C>G (p.Ser1828Trp)
NM_013275.6(ANKRD11):c.5498C>T (p.Ala1833Val)
NM_013275.6(ANKRD11):c.5500C>T (p.Pro1834Ser)
NM_013275.6(ANKRD11):c.5507C>T (p.Pro1836Leu)
NM_013275.6(ANKRD11):c.5560G>A (p.Asp1854Asn)
NM_013275.6(ANKRD11):c.5581A>G (p.Lys1861Glu)
NM_013275.6(ANKRD11):c.5609C>T (p.Ala1870Val) rs864309571
NM_013275.6(ANKRD11):c.5611G>A (p.Ala1871Thr)
NM_013275.6(ANKRD11):c.5614G>T (p.Val1872Phe)
NM_013275.6(ANKRD11):c.5681C>T (p.Pro1894Leu)
NM_013275.6(ANKRD11):c.5684G>C (p.Arg1895Thr)
NM_013275.6(ANKRD11):c.5738C>T (p.Thr1913Ile)
NM_013275.6(ANKRD11):c.5773C>A (p.Pro1925Thr) rs199914958
NM_013275.6(ANKRD11):c.5810G>A (p.Gly1937Asp)
NM_013275.6(ANKRD11):c.5875G>A (p.Ala1959Thr) rs372148958
NM_013275.6(ANKRD11):c.5909C>T (p.Pro1970Leu)
NM_013275.6(ANKRD11):c.5935C>T (p.Leu1979Phe)
NM_013275.6(ANKRD11):c.5938CTG[1] (p.Leu1981del)
NM_013275.6(ANKRD11):c.5962C>T (p.Pro1988Ser) rs534220503
NM_013275.6(ANKRD11):c.5981T>C (p.Phe1994Ser)
NM_013275.6(ANKRD11):c.6005C>T (p.Ser2002Phe)
NM_013275.6(ANKRD11):c.6060_6061delinsGC (p.Ser2021Pro) rs1567559902
NM_013275.6(ANKRD11):c.6061_6069dup (p.Ala2023_Pro2024insSerProAla)
NM_013275.6(ANKRD11):c.6063_6071del (p.Pro2022_Pro2024del) rs771037147
NM_013275.6(ANKRD11):c.6070C>A (p.Pro2024Thr)
NM_013275.6(ANKRD11):c.6071C>T (p.Pro2024Leu)
NM_013275.6(ANKRD11):c.6109G>A (p.Val2037Ile)
NM_013275.6(ANKRD11):c.6119G>A (p.Gly2040Glu)
NM_013275.6(ANKRD11):c.6139G>T (p.Ala2047Ser)
NM_013275.6(ANKRD11):c.6157G>A (p.Ala2053Thr) rs2034097605
NM_013275.6(ANKRD11):c.6232G>A (p.Asp2078Asn)
NM_013275.6(ANKRD11):c.6232G>C (p.Asp2078His) rs1038750030
NM_013275.6(ANKRD11):c.6238G>T (p.Ala2080Ser)
NM_013275.6(ANKRD11):c.6254G>T (p.Cys2085Phe) rs755786402
NM_013275.6(ANKRD11):c.630C>G (p.Asn210Lys) rs2034818361
NM_013275.6(ANKRD11):c.6377G>C (p.Gly2126Ala)
NM_013275.6(ANKRD11):c.6394_6395delinsAT (p.Asp2132Ile) rs2151736540
NM_013275.6(ANKRD11):c.6415C>T (p.Pro2139Ser) rs1567557350
NM_013275.6(ANKRD11):c.6425C>G (p.Pro2142Arg)
NM_013275.6(ANKRD11):c.6448G>A (p.Asp2150Asn) rs1567557144
NM_013275.6(ANKRD11):c.6517G>T (p.Val2173Phe)
NM_013275.6(ANKRD11):c.6559C>G (p.Pro2187Ala)
NM_013275.6(ANKRD11):c.6562C>A (p.Pro2188Thr)
NM_013275.6(ANKRD11):c.6620C>T (p.Pro2207Leu)
NM_013275.6(ANKRD11):c.6659C>T (p.Ala2220Val)
NM_013275.6(ANKRD11):c.6674C>T (p.Thr2225Met)
NM_013275.6(ANKRD11):c.6734C>G (p.Pro2245Arg) rs2151733996
NM_013275.6(ANKRD11):c.6772G>A (p.Ala2258Thr)
NM_013275.6(ANKRD11):c.6824C>T (p.Ala2275Val)
NM_013275.6(ANKRD11):c.6845C>G (p.Ala2282Gly)
NM_013275.6(ANKRD11):c.6890C>T (p.Ser2297Phe)
NM_013275.6(ANKRD11):c.6952A>G (p.Lys2318Glu)
NM_013275.6(ANKRD11):c.6985G>C (p.Val2329Leu) rs760933701
NM_013275.6(ANKRD11):c.7055C>A (p.Pro2352Gln)
NM_013275.6(ANKRD11):c.7058C>T (p.Pro2353Leu)
NM_013275.6(ANKRD11):c.7061C>A (p.Pro2354His) rs749176560
NM_013275.6(ANKRD11):c.7073A>G (p.Glu2358Gly)
NM_013275.6(ANKRD11):c.7091C>G (p.Ala2364Gly)
NM_013275.6(ANKRD11):c.7162C>T (p.Arg2388Cys)
NM_013275.6(ANKRD11):c.7198_7200dup (p.Leu2400dup) rs1371024836
NM_013275.6(ANKRD11):c.7207T>A (p.Ser2403Thr)
NM_013275.6(ANKRD11):c.731A>G (p.Asn244Ser)
NM_013275.6(ANKRD11):c.7370G>T (p.Cys2457Phe)
NM_013275.6(ANKRD11):c.7671G>A (p.Met2557Ile) rs1567544079
NM_013275.6(ANKRD11):c.7736G>A (p.Arg2579His)
NM_013275.6(ANKRD11):c.7847T>C (p.Leu2616Pro) rs1567533174
NM_013275.6(ANKRD11):c.7873C>T (p.Gln2625Ter) rs2032836923
NM_013275.6(ANKRD11):c.7929G>C (p.Glu2643Asp)
NM_013275.6(ANKRD11):c.859G>C (p.Gly287Arg)
NM_013275.6(ANKRD11):c.88-5T>C
NM_013275.6(ANKRD11):c.967T>C (p.Phe323Leu)
NM_013275.6(ANKRD11):c.969C>G (p.Phe323Leu)
NM_013275.6(ANKRD11):c.970G>A (p.Glu324Lys)

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.