ClinVar Miner

Variants in gene AXIN2 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 70
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HGVS dbSNP gnomAD frequency
NM_004655.4(AXIN2):c.1615G>A (p.Val539Met) rs9913621 0.01361
NM_004655.4(AXIN2):c.1573C>G (p.Pro525Ala) rs73346297 0.00930
NM_004655.4(AXIN2):c.2282C>A (p.Ala761Asp) rs79732150 0.00649
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.1070G>A (p.Arg357His) rs8081536 0.00172
NM_004655.4(AXIN2):c.1713-18G>A rs147664289 0.00169
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.2439C>T (p.Ala813=) rs149533605 0.00157
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.2428G>A (p.Asp810Asn) rs140344858 0.00123
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.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.2213C>T (p.Ser738Phe) rs139209450 0.00031
NM_004655.4(AXIN2):c.1059+8C>T rs367595502 0.00025
NM_004655.4(AXIN2):c.815+7C>T rs142103235 0.00025
NM_004655.4(AXIN2):c.-33A>C rs190687283 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.1242G>A (p.Arg414=) rs200325634 0.00016
NM_004655.4(AXIN2):c.780T>C (p.Ser260=) rs147681058 0.00016
NM_004655.4(AXIN2):c.1305G>A (p.Pro435=) rs369221405 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.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.1907+17G>A rs201487132 0.00010
NM_004655.4(AXIN2):c.2142-20C>T rs764171738 0.00010
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.738C>T (p.Thr246=) rs201191083 0.00008
NM_004655.4(AXIN2):c.1267C>T (p.Leu423Phe) rs376630432 0.00006
NM_004655.4(AXIN2):c.2237+3G>A rs376584101 0.00006
NM_004655.4(AXIN2):c.623C>T (p.Ala208Val) rs201531372 0.00006
NM_004655.4(AXIN2):c.1092C>T (p.Pro364=) rs765518896 0.00004
NM_004655.4(AXIN2):c.2004G>A (p.Gly668=) rs144092307 0.00004
NM_004655.4(AXIN2):c.2083G>T (p.Ala695Ser) rs140510381 0.00004
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.645C>T (p.Leu215=) rs767834824 0.00003
NM_004655.4(AXIN2):c.1887G>A (p.Gln629=) rs140163819 0.00002
NM_004655.4(AXIN2):c.522G>T (p.Ala174=) rs780914406 0.00002
NM_004655.4(AXIN2):c.1200+8G>A rs776372607 0.00001
NM_004655.4(AXIN2):c.1251G>T (p.Ala417=) rs557397475 0.00001
NM_004655.4(AXIN2):c.1962C>A (p.Gly654=) rs377642903 0.00001
NM_004655.4(AXIN2):c.2499C>A (p.Gly833=) rs772461187 0.00001
NM_004655.4(AXIN2):c.815+4A>G rs565020131 0.00001
NM_004655.4(AXIN2):c.1235A>G (p.Asn412Ser) rs115931022
NM_004655.4(AXIN2):c.1338C>A (p.Val446=) rs369864600
NM_004655.4(AXIN2):c.1380T>C (p.Tyr460=) rs566313620
NM_004655.4(AXIN2):c.1404CCA[7] (p.His474dup) rs570443161
NM_004655.4(AXIN2):c.2124G>C (p.Ser708=) rs143243661
NM_004655.4(AXIN2):c.435C>G (p.Val145=) rs111470596
NM_004655.4(AXIN2):c.629T>C (p.Met210Thr) rs529954883

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