ClinVar Miner

List of variants in gene AXIN2 reported by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 117
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_004655.4(AXIN2):c.1365A>G (p.Pro455=) rs9915936 0.90382
NM_004655.4(AXIN2):c.1386C>T (p.Pro462=) rs1133683 0.52439
NM_004655.4(AXIN2):c.*1012T>A rs7591 0.48929
NM_004655.4(AXIN2):c.148C>T (p.Pro50Ser) rs2240308 0.39067
NM_004655.4(AXIN2):c.2062C>T (p.Leu688=) rs35415678 0.11118
NM_004655.4(AXIN2):c.432T>C (p.Ile144=) rs2240307 0.04207
NM_004655.4(AXIN2):c.*957T>G rs112415132 0.03202
NM_004655.4(AXIN2):c.1383C>T (p.Ser461=) rs9914661 0.01367
NM_004655.4(AXIN2):c.1615G>A (p.Val539Met) rs9913621 0.01361
NM_004655.4(AXIN2):c.*846G>A rs75257056 0.01027
NM_004655.4(AXIN2):c.*309C>A rs192185171 0.00463
NM_004655.4(AXIN2):c.2109G>A (p.Arg703=) rs116525755 0.00396
NM_004655.4(AXIN2):c.1410C>T (p.His470=) rs149483825 0.00394
NM_004655.4(AXIN2):c.1530G>A (p.Thr510=) rs141014640 0.00299
NM_004655.4(AXIN2):c.2272G>A (p.Ala758Thr) rs145007501 0.00179
NM_004655.4(AXIN2):c.1807G>C (p.Ala603Pro) rs145353986 0.00128
NM_004655.4(AXIN2):c.2051C>T (p.Ala684Val) rs138287857 0.00112
NM_004655.4(AXIN2):c.1532C>T (p.Thr511Met) rs200883019 0.00109
NM_004655.4(AXIN2):c.1101C>T (p.Pro367=) rs141697521 0.00094
NM_004655.4(AXIN2):c.*469T>C rs567413750 0.00089
NM_004655.4(AXIN2):c.1985T>C (p.Leu662Pro) rs142476324 0.00084
NM_004655.4(AXIN2):c.*147C>T rs150336911 0.00076
NM_004655.4(AXIN2):c.270C>T (p.Asp90=) rs141655687 0.00076
NM_004655.4(AXIN2):c.1168A>G (p.Ser390Gly) rs139871607 0.00075
NM_004655.4(AXIN2):c.*500T>G rs187274855 0.00073
NM_004655.4(AXIN2):c.1545C>T (p.His515=) rs139316692 0.00070
NM_004655.4(AXIN2):c.1250C>T (p.Ala417Val) rs201460658 0.00064
NM_004655.4(AXIN2):c.2285G>A (p.Ser762Asn) rs117688560 0.00064
NM_004655.4(AXIN2):c.*1016C>T rs746778698 0.00048
NM_004655.4(AXIN2):c.2052G>A (p.Ala684=) rs200573256 0.00046
NM_004655.4(AXIN2):c.733C>T (p.Pro245Ser) rs62640028 0.00043
NM_004655.4(AXIN2):c.*1209T>C rs758283240 0.00041
NM_004655.4(AXIN2):c.1685C>T (p.Pro562Leu) rs149764887 0.00031
NM_004655.4(AXIN2):c.2213C>T (p.Ser738Phe) rs139209450 0.00031
NM_004655.4(AXIN2):c.-181T>G rs886053285 0.00027
NM_004655.4(AXIN2):c.1059+8C>T rs367595502 0.00025
NM_004655.4(AXIN2):c.-33A>C rs190687283 0.00024
NM_004655.4(AXIN2):c.*71T>C rs201239861 0.00021
NM_004655.4(AXIN2):c.*220A>G rs556547077 0.00017
NM_004655.4(AXIN2):c.1242G>A (p.Arg414=) rs200325634 0.00016
NM_004655.4(AXIN2):c.780T>C (p.Ser260=) rs147681058 0.00016
NM_004655.4(AXIN2):c.1975C>T (p.Arg659Trp) rs142670753 0.00014
NM_004655.4(AXIN2):c.1327C>T (p.Leu443=) rs371691797 0.00013
NM_004655.4(AXIN2):c.144C>T (p.Pro48=) rs144099816 0.00013
NM_004655.4(AXIN2):c.*1136T>G rs561447577 0.00011
NM_004655.4(AXIN2):c.*489C>T rs763712300 0.00011
NM_004655.4(AXIN2):c.1882C>T (p.Arg628Trp) rs200201811 0.00011
NM_004655.4(AXIN2):c.*74G>A rs62063439 0.00010
NM_004655.4(AXIN2):c.-281C>T rs886053288 0.00010
NM_004655.4(AXIN2):c.1376G>A (p.Arg459His) rs368525111 0.00010
NM_004655.4(AXIN2):c.2195C>T (p.Thr732Met) rs373911689 0.00009
NM_004655.4(AXIN2):c.2406-8C>G rs143905290 0.00009
NM_004655.4(AXIN2):c.1623C>T (p.Cys541=) rs199931425 0.00008
NM_004655.4(AXIN2):c.2239C>T (p.His747Tyr) rs143571197 0.00008
NM_004655.4(AXIN2):c.-165C>T rs886053284 0.00007
NM_004655.4(AXIN2):c.-273T>C rs1035215819 0.00006
NM_004655.4(AXIN2):c.1267C>T (p.Leu423Phe) rs376630432 0.00006
NM_004655.4(AXIN2):c.242C>T (p.Ser81Phe) rs146238336 0.00006
NM_004655.4(AXIN2):c.623C>T (p.Ala208Val) rs201531372 0.00006
NM_004655.4(AXIN2):c.*326A>G rs533959126 0.00004
NM_004655.4(AXIN2):c.2004G>A (p.Gly668=) rs144092307 0.00004
NM_004655.4(AXIN2):c.*320A>C rs886053269 0.00003
NM_004655.4(AXIN2):c.*376A>G rs562795435 0.00003
NM_004655.4(AXIN2):c.-117+11A>T rs886053283 0.00003
NM_004655.4(AXIN2):c.1485C>T (p.Gly495=) rs770556906 0.00003
NM_004655.4(AXIN2):c.2196G>A (p.Thr732=) rs878854725 0.00003
NM_004655.4(AXIN2):c.645C>T (p.Leu215=) rs767834824 0.00003
NM_004655.4(AXIN2):c.*1180G>A rs1015586349 0.00002
NM_004655.4(AXIN2):c.1744A>C (p.Asn582His) rs567511335 0.00002
NM_004655.4(AXIN2):c.1887G>A (p.Gln629=) rs140163819 0.00002
NM_004655.4(AXIN2):c.897C>T (p.Asp299=) rs748143308 0.00002
NM_004655.4(AXIN2):c.*561T>C rs147057034 0.00001
NM_004655.4(AXIN2):c.*88A>G rs886053271 0.00001
NM_004655.4(AXIN2):c.-266G>A rs2044377857 0.00001
NM_004655.4(AXIN2):c.1000C>G (p.Gln334Glu) rs770254456 0.00001
NM_004655.4(AXIN2):c.1200+8G>A rs776372607 0.00001
NM_004655.4(AXIN2):c.1529C>T (p.Thr510Met) rs367938045 0.00001
NM_004655.4(AXIN2):c.1531A>T (p.Thr511Ser) rs376936740 0.00001
NM_004655.4(AXIN2):c.1597G>A (p.Ala533Thr) rs1376819064 0.00001
NM_004655.4(AXIN2):c.1713C>T (p.Gly571=) rs761978806 0.00001
NM_004655.4(AXIN2):c.1962C>A (p.Gly654=) rs377642903 0.00001
NM_004655.4(AXIN2):c.1978C>G (p.His660Asp) rs1598097035 0.00001
NM_004655.4(AXIN2):c.2100C>T (p.Ala700=) rs1057522521 0.00001
NM_004655.4(AXIN2):c.598G>A (p.Val200Met) rs752081909 0.00001
NM_004655.4(AXIN2):c.776C>T (p.Ala259Val) rs1239640498 0.00001
NM_004655.4(AXIN2):c.815+4A>G rs565020131 0.00001
NM_004655.4(AXIN2):c.*1153C>T rs1239200867
NM_004655.4(AXIN2):c.*156G>A rs886053270
NM_004655.4(AXIN2):c.*293A>T rs944038906
NM_004655.4(AXIN2):c.*345T>C rs1433448292
NM_004655.4(AXIN2):c.*400C>G rs2043782215
NM_004655.4(AXIN2):c.*631dup rs796431470
NM_004655.4(AXIN2):c.*703G>C rs989239047
NM_004655.4(AXIN2):c.*737G>A rs576136173
NM_004655.4(AXIN2):c.*794C>A rs10438779
NM_004655.4(AXIN2):c.*987T>G rs1049925344
NM_004655.4(AXIN2):c.-116-13del rs530658215
NM_004655.4(AXIN2):c.-117+14C>T rs886053282
NM_004655.4(AXIN2):c.-237G>C rs886053286
NM_004655.4(AXIN2):c.-260T>G rs886053287
NM_004655.4(AXIN2):c.-262A>T rs1048485136
NM_004655.4(AXIN2):c.1162C>T (p.Arg388Cys) rs886053273
NM_004655.4(AXIN2):c.1235A>C (p.Asn412Thr) rs115931022
NM_004655.4(AXIN2):c.1235A>G (p.Asn412Ser) rs115931022
NM_004655.4(AXIN2):c.1347C>T (p.Thr449=) rs762279806
NM_004655.4(AXIN2):c.1404CCA[7] (p.His474dup) rs570443161
NM_004655.4(AXIN2):c.1443C>T (p.Leu481=) rs886053272
NM_004655.4(AXIN2):c.1531A>G (p.Thr511Ala) rs376936740
NM_004655.4(AXIN2):c.1713-3C>T rs2043937671
NM_004655.4(AXIN2):c.174C>T (p.Asn58=) rs763012548
NM_004655.4(AXIN2):c.2124G>A (p.Ser708=) rs143243661
NM_004655.4(AXIN2):c.2124G>C (p.Ser708=) rs143243661
NM_004655.4(AXIN2):c.212C>T (p.Pro71Leu) rs1060502145
NM_004655.4(AXIN2):c.2405+4A>C rs377423720
NM_004655.4(AXIN2):c.517C>A (p.Gln173Lys) rs886053281
NM_004655.4(AXIN2):c.629T>C (p.Met210Thr) rs529954883
NM_004655.4(AXIN2):c.667G>C (p.Gly223Arg) rs878854733

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.