ClinVar Miner

List of variants in gene AXIN2 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 143
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HGVS dbSNP gnomAD frequency
NM_004655.4(AXIN2):c.2406-284C>T rs4074948 0.02451
NM_004655.4(AXIN2):c.1908-75A>G rs72856668 0.01484
NM_004655.4(AXIN2):c.2238-292G>A rs9903837 0.01370
NM_004655.4(AXIN2):c.1201-105C>T rs9915188 0.01363
NM_004655.4(AXIN2):c.1200+146G>A rs74006840 0.01361
NM_004655.4(AXIN2):c.956+311T>A rs114048502 0.01244
NM_004655.4(AXIN2):c.957-206T>C rs116173676 0.01092
NM_004655.4(AXIN2):c.1907+133C>T rs78211272 0.00688
NM_004655.4(AXIN2):c.1060-41T>C rs149089442 0.00575
NM_004655.4(AXIN2):c.1410C>T (p.His470=) rs149483825 0.00394
NM_004655.4(AXIN2):c.1060-94G>A rs78028780 0.00366
NM_004655.4(AXIN2):c.1530G>A (p.Thr510=) rs141014640 0.00299
NM_004655.4(AXIN2):c.2405+180C>T rs559720236 0.00234
NM_004655.4(AXIN2):c.2272G>A (p.Ala758Thr) rs145007501 0.00179
NM_004655.4(AXIN2):c.1070G>A (p.Arg357His) rs8081536 0.00172
NM_004655.4(AXIN2):c.1200+19T>C rs116931989 0.00165
NM_004655.4(AXIN2):c.1200+18T>G rs117258157 0.00163
NM_004655.4(AXIN2):c.1807G>C (p.Ala603Pro) rs145353986 0.00128
NM_004655.4(AXIN2):c.1952C>T (p.Ser651Leu) rs74006838 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.1985T>C (p.Leu662Pro) rs142476324 0.00084
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.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.1908-21C>G rs190627728 0.00051
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.1685C>T (p.Pro562Leu) rs149764887 0.00031
NM_004655.4(AXIN2):c.1059+8C>T rs367595502 0.00025
NM_004655.4(AXIN2):c.1491C>T (p.Cys497=) rs150292240 0.00024
NM_004655.4(AXIN2):c.879A>G (p.Pro293=) rs374479599 0.00024
NM_004655.4(AXIN2):c.1368C>T (p.Gly456=) rs372841853 0.00021
NM_004655.4(AXIN2):c.1829G>A (p.Arg610Gln) rs376248072 0.00018
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.344A>G (p.Asn115Ser) rs370257532 0.00015
NM_004655.4(AXIN2):c.1176G>A (p.Glu392=) rs376052287 0.00014
NM_004655.4(AXIN2):c.1305G>A (p.Pro435=) rs369221405 0.00014
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.435C>A (p.Val145=) rs111470596 0.00013
NM_004655.4(AXIN2):c.1882C>T (p.Arg628Trp) rs200201811 0.00011
NM_004655.4(AXIN2):c.2433G>A (p.Glu811=) rs147134295 0.00011
NM_004655.4(AXIN2):c.1181G>A (p.Arg394His) rs200899695 0.00010
NM_004655.4(AXIN2):c.2239C>T (p.His747Tyr) rs143571197 0.00008
NM_004655.4(AXIN2):c.475G>T (p.Asp159Tyr) rs753036084 0.00008
NM_004655.4(AXIN2):c.738C>T (p.Thr246=) rs201191083 0.00008
NM_004655.4(AXIN2):c.894C>T (p.Asn298=) rs368689290 0.00007
NM_004655.4(AXIN2):c.1201-7C>T rs760667639 0.00006
NM_004655.4(AXIN2):c.1267C>T (p.Leu423Phe) rs376630432 0.00006
NM_004655.4(AXIN2):c.2478G>T (p.Thr826=) rs148159432 0.00006
NM_004655.4(AXIN2):c.623C>T (p.Ala208Val) rs201531372 0.00006
NM_004655.4(AXIN2):c.1060-10C>T rs376505336 0.00004
NM_004655.4(AXIN2):c.1092C>T (p.Pro364=) rs765518896 0.00004
NM_004655.4(AXIN2):c.1222G>A (p.Glu408Lys) rs749846538 0.00004
NM_004655.4(AXIN2):c.2004G>A (p.Gly668=) rs144092307 0.00004
NM_004655.4(AXIN2):c.2130C>A (p.Pro710=) rs760740780 0.00004
NM_004655.4(AXIN2):c.549G>A (p.Glu183=) rs370765600 0.00004
NM_004655.4(AXIN2):c.888C>T (p.Ser296=) rs755968982 0.00004
NM_004655.4(AXIN2):c.1089C>A (p.Thr363=) rs748698260 0.00003
NM_004655.4(AXIN2):c.1171C>T (p.Leu391=) rs372767920 0.00003
NM_004655.4(AXIN2):c.1273C>T (p.Leu425=) rs746718165 0.00003
NM_004655.4(AXIN2):c.1485C>T (p.Gly495=) rs770556906 0.00003
NM_004655.4(AXIN2):c.1635G>A (p.Gly545=) rs778710067 0.00003
NM_004655.4(AXIN2):c.2184C>T (p.Ala728=) rs146547133 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.1191G>A (p.Gln397=) rs1360433499 0.00002
NM_004655.4(AXIN2):c.1272C>G (p.Ser424=) rs768259872 0.00002
NM_004655.4(AXIN2):c.135C>T (p.Val45=) rs376726966 0.00002
NM_004655.4(AXIN2):c.1758G>A (p.Thr586=) rs542864768 0.00002
NM_004655.4(AXIN2):c.1887G>A (p.Gln629=) rs140163819 0.00002
NM_004655.4(AXIN2):c.2238-7T>C rs759875493 0.00002
NM_004655.4(AXIN2):c.1020T>C (p.Ser340=) rs768986730 0.00001
NM_004655.4(AXIN2):c.1149G>C (p.Leu383=) rs371063358 0.00001
NM_004655.4(AXIN2):c.1188G>A (p.Gln396=) rs1060504488 0.00001
NM_004655.4(AXIN2):c.1251G>T (p.Ala417=) rs557397475 0.00001
NM_004655.4(AXIN2):c.1293C>T (p.Tyr431=) rs552141978 0.00001
NM_004655.4(AXIN2):c.1320C>T (p.Asp440=) rs376935084 0.00001
NM_004655.4(AXIN2):c.13A>G (p.Met5Val) rs148691166 0.00001
NM_004655.4(AXIN2):c.1422T>C (p.His474=) rs748049932 0.00001
NM_004655.4(AXIN2):c.1473C>T (p.Ala491=) rs1048751630 0.00001
NM_004655.4(AXIN2):c.1482G>T (p.Pro494=) rs1057522677 0.00001
NM_004655.4(AXIN2):c.1569C>T (p.Ala523=) rs745968863 0.00001
NM_004655.4(AXIN2):c.1785G>A (p.Arg595=) rs1313383874 0.00001
NM_004655.4(AXIN2):c.1962C>A (p.Gly654=) rs377642903 0.00001
NM_004655.4(AXIN2):c.2079G>A (p.Thr693=) rs551098654 0.00001
NM_004655.4(AXIN2):c.2262A>C (p.Ala754=) rs1060504485 0.00001
NM_004655.4(AXIN2):c.2271C>T (p.His757=) rs772041910 0.00001
NM_004655.4(AXIN2):c.2343G>A (p.Leu781=) rs1057522118 0.00001
NM_004655.4(AXIN2):c.2403T>C (p.Tyr801=) rs745869388 0.00001
NM_004655.4(AXIN2):c.2405+7G>A rs373593841 0.00001
NM_004655.4(AXIN2):c.2487G>A (p.Pro829=) rs768793839 0.00001
NM_004655.4(AXIN2):c.2499C>A (p.Gly833=) rs772461187 0.00001
NM_004655.4(AXIN2):c.295C>T (p.Leu99=) rs761972319 0.00001
NM_004655.4(AXIN2):c.30C>A (p.Leu10=) rs761670939 0.00001
NM_004655.4(AXIN2):c.390A>G (p.Val130=) rs1266454647 0.00001
NM_004655.4(AXIN2):c.39C>T (p.Pro13=) rs1060504478 0.00001
NM_004655.4(AXIN2):c.405C>T (p.Tyr135=) rs141608578 0.00001
NM_004655.4(AXIN2):c.6T>C (p.Ser2=) rs1475337539 0.00001
NM_004655.4(AXIN2):c.721T>G (p.Cys241Gly) rs370549410 0.00001
NM_004655.4(AXIN2):c.831C>T (p.Ser277=) rs186951572 0.00001
NM_004655.4(AXIN2):c.924G>A (p.Thr308=) rs376829389 0.00001
NM_004655.4(AXIN2):c.*476_*487del
NM_004655.4(AXIN2):c.-116-8C>T rs1598120733
NM_004655.4(AXIN2):c.1060-6del rs1060504487
NM_004655.4(AXIN2):c.1200+109_1200+129dup rs753361517
NM_004655.4(AXIN2):c.1200+121G>C rs116306590
NM_004655.4(AXIN2):c.1200+148del rs150405491
NM_004655.4(AXIN2):c.1235A>G (p.Asn412Ser) rs115931022
NM_004655.4(AXIN2):c.1275A>G (p.Leu425=) rs758219268
NM_004655.4(AXIN2):c.1317G>A (p.Leu439=) rs763400320
NM_004655.4(AXIN2):c.1338C>A (p.Val446=) rs369864600
NM_004655.4(AXIN2):c.1338C>T (p.Val446=) rs369864600
NM_004655.4(AXIN2):c.1365A>T (p.Pro455=) rs9915936
NM_004655.4(AXIN2):c.1380T>C (p.Tyr460=) rs566313620
NM_004655.4(AXIN2):c.1398C>G (p.Ser466=) rs760282693
NM_004655.4(AXIN2):c.1404CCA[5] (p.His474del) rs570443161
NM_004655.4(AXIN2):c.1404CCA[7] (p.His474dup) rs570443161
NM_004655.4(AXIN2):c.1470G>A (p.Ala490=) rs1060502143
NM_004655.4(AXIN2):c.1479G>T (p.Ser493=)
NM_004655.4(AXIN2):c.1500C>A (p.Leu500=) rs745903369
NM_004655.4(AXIN2):c.1554C>T (p.Tyr518=) rs2043949599
NM_004655.4(AXIN2):c.166A>C (p.Arg56=) rs1431601772
NM_004655.4(AXIN2):c.1908-102C>G rs549052961
NM_004655.4(AXIN2):c.1953G>A (p.Ser651=) rs372086777
NM_004655.4(AXIN2):c.2012G>C (p.Arg671Pro) rs765845684
NM_004655.4(AXIN2):c.2124G>C (p.Ser708=) rs143243661
NM_004655.4(AXIN2):c.2142-10G>C rs550146601
NM_004655.4(AXIN2):c.2405+4A>C rs377423720
NM_004655.4(AXIN2):c.384A>G (p.Leu128=) rs200699935
NM_004655.4(AXIN2):c.426C>T (p.Asn142=) rs1322519354
NM_004655.4(AXIN2):c.528C>T (p.Thr176=) rs781572220
NM_004655.4(AXIN2):c.629T>C (p.Met210Thr) rs529954883
NM_004655.4(AXIN2):c.672T>C (p.Tyr224=) rs375671211
NM_004655.4(AXIN2):c.815+3dup rs745726935
NM_004655.4(AXIN2):c.815+73_815+80del rs574040746
NM_004655.4(AXIN2):c.876A>G (p.Ala292=) rs755685014
NM_004655.4(AXIN2):c.957-5C>T rs1060504482

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