ClinVar Miner

List of variants in gene AXIN2 reported by PreventionGenetics, part of Exact Sciences

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Gene type:
ClinVar version:
Total variants: 86
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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.148C>T (p.Pro50Ser) rs2240308 0.39067
NM_004655.4(AXIN2):c.1712+19G>T rs7219582 0.14767
NM_004655.4(AXIN2):c.2062C>T (p.Leu688=) rs35415678 0.11118
NM_004655.4(AXIN2):c.1907+39T>A rs9906513 0.10671
NM_004655.4(AXIN2):c.956+16A>G rs35285779 0.08430
NM_004655.4(AXIN2):c.432T>C (p.Ile144=) rs2240307 0.04207
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.2272G>A (p.Ala758Thr) rs145007501 0.00179
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.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.2285G>A (p.Ser762Asn) rs117688560 0.00064
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.815+7C>T rs142103235 0.00025
NM_004655.4(AXIN2):c.879A>G (p.Pro293=) rs374479599 0.00024
NM_004655.4(AXIN2):c.203G>A (p.Arg68Gln) rs138056036 0.00020
NM_004655.4(AXIN2):c.780T>C (p.Ser260=) rs147681058 0.00016
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.1327C>T (p.Leu443=) rs371691797 0.00013
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.1376G>A (p.Arg459His) rs368525111 0.00010
NM_004655.4(AXIN2):c.2406-8C>G rs143905290 0.00009
NM_004655.4(AXIN2):c.894C>T (p.Asn298=) rs368689290 0.00007
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.2140C>T (p.Arg714Trp) rs148765149 0.00005
NM_004655.4(AXIN2):c.1127C>G (p.Ser376Trp) rs772908702 0.00004
NM_004655.4(AXIN2):c.1222G>A (p.Glu408Lys) rs749846538 0.00004
NM_004655.4(AXIN2):c.2083G>T (p.Ala695Ser) rs140510381 0.00004
NM_004655.4(AXIN2):c.2216A>G (p.Asn739Ser) rs547630327 0.00004
NM_004655.4(AXIN2):c.719A>G (p.Lys240Arg) rs746819327 0.00004
NM_004655.4(AXIN2):c.1171C>T (p.Leu391=) rs372767920 0.00003
NM_004655.4(AXIN2):c.1284C>T (p.Ser428=) rs750126379 0.00003
NM_004655.4(AXIN2):c.2184C>T (p.Ala728=) rs146547133 0.00003
NM_004655.4(AXIN2):c.2405+4A>G rs377423720 0.00003
NM_004655.4(AXIN2):c.923C>T (p.Thr308Met) rs779083840 0.00003
NM_004655.4(AXIN2):c.2010C>G (p.Pro670=) rs781484593 0.00002
NM_004655.4(AXIN2):c.2053A>G (p.Met685Val) rs111650787 0.00002
NM_004655.4(AXIN2):c.1251G>T (p.Ala417=) rs557397475 0.00001
NM_004655.4(AXIN2):c.1284C>A (p.Ser428=) rs750126379 0.00001
NM_004655.4(AXIN2):c.1293C>T (p.Tyr431=) rs552141978 0.00001
NM_004655.4(AXIN2):c.1651T>C (p.Cys551Arg) rs730881398 0.00001
NM_004655.4(AXIN2):c.1889G>A (p.Ser630Asn) rs578156841 0.00001
NM_004655.4(AXIN2):c.1900C>T (p.Pro634Ser) rs141699123 0.00001
NM_004655.4(AXIN2):c.1914A>G (p.Gln638=) rs1282533521 0.00001
NM_004655.4(AXIN2):c.1929C>T (p.Ala643=) rs780233103 0.00001
NM_004655.4(AXIN2):c.2141+4A>G rs376613525 0.00001
NM_004655.4(AXIN2):c.2219C>G (p.Pro740Arg) rs747903181 0.00001
NM_004655.4(AXIN2):c.2274G>A (p.Ala758=) rs756178538 0.00001
NM_004655.4(AXIN2):c.2347G>T (p.Ala783Ser) rs760217787 0.00001
NM_004655.4(AXIN2):c.2499C>A (p.Gly833=) rs772461187 0.00001
NM_004655.4(AXIN2):c.2521C>T (p.Arg841Trp) rs527766429 0.00001
NM_004655.4(AXIN2):c.252C>T (p.Ser84=) rs1172662195 0.00001
NM_004655.4(AXIN2):c.598G>A (p.Val200Met) rs752081909 0.00001
NM_004655.4(AXIN2):c.660C>T (p.Val220=) rs1416113967 0.00001
NM_004655.4(AXIN2):c.1207_1209del (p.Glu403del) rs1064793048
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.1344G>C (p.Lys448Asn) rs2144465376
NM_004655.4(AXIN2):c.1397C>T (p.Ser466Phe) rs1064793954
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.1630C>T (p.Pro544Ser) rs778153491
NM_004655.4(AXIN2):c.1712+10G>A rs374250367
NM_004655.4(AXIN2):c.1932C>A (p.Tyr644Ter)
NM_004655.4(AXIN2):c.2013_2024del (p.Thr672_Arg675del) rs151279728
NM_004655.4(AXIN2):c.2278C>T (p.Gln760Ter)
NM_004655.4(AXIN2):c.2338A>G (p.Met780Val) rs2043866117
NM_004655.4(AXIN2):c.2406-8C>T
NM_004655.4(AXIN2):c.339C>T (p.Ala113=) rs1598119867
NM_004655.4(AXIN2):c.435C>G (p.Val145=) rs111470596
NM_004655.4(AXIN2):c.505A>G (p.Ile169Val) rs1060502155
NM_004655.4(AXIN2):c.6T>G (p.Ser2Arg) rs1475337539
NM_004655.4(AXIN2):c.815+3dup rs745726935

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