ClinVar Miner

List of variants in gene AXIN2 reported as uncertain significance for not specified

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Gene type:
ClinVar version:
Total variants: 87
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HGVS dbSNP gnomAD frequency
NM_004655.4(AXIN2):c.2272G>A (p.Ala758Thr) rs145007501 0.00179
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.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.1712G>A (p.Gly571Asp) rs146744662 0.00013
NM_004655.4(AXIN2):c.1882C>T (p.Arg628Trp) rs200201811 0.00011
NM_004655.4(AXIN2):c.475G>T (p.Asp159Tyr) rs753036084 0.00008
NM_004655.4(AXIN2):c.2182G>A (p.Ala728Thr) rs141260153 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.242C>T (p.Ser81Phe) rs146238336 0.00006
NM_004655.4(AXIN2):c.623C>T (p.Ala208Val) rs201531372 0.00006
NM_004655.4(AXIN2):c.1450G>A (p.Gly484Ser) rs371446806 0.00005
NM_004655.4(AXIN2):c.1481C>T (p.Pro494Leu) rs730881396 0.00005
NM_004655.4(AXIN2):c.2140C>T (p.Arg714Trp) rs148765149 0.00005
NM_004655.4(AXIN2):c.2249C>T (p.Pro750Leu) rs772888193 0.00005
NM_004655.4(AXIN2):c.563A>G (p.Gln188Arg) rs149000772 0.00005
NM_004655.4(AXIN2):c.1553A>G (p.Tyr518Cys) rs368289818 0.00004
NM_004655.4(AXIN2):c.2083G>T (p.Ala695Ser) rs140510381 0.00004
NM_004655.4(AXIN2):c.2021C>T (p.Pro674Leu) rs1341498392 0.00003
NM_004655.4(AXIN2):c.2123C>T (p.Ser708Leu) rs587780123 0.00003
NM_004655.4(AXIN2):c.2405+4A>G rs377423720 0.00003
NM_004655.4(AXIN2):c.1384C>T (p.Pro462Ser) rs1060502156 0.00002
NM_004655.4(AXIN2):c.1557C>G (p.Ile519Met) rs374444786 0.00002
NM_004655.4(AXIN2):c.1976G>A (p.Arg659Gln) rs730881400 0.00002
NM_004655.4(AXIN2):c.2447C>T (p.Ala816Val) rs755508971 0.00002
NM_004655.4(AXIN2):c.1103C>T (p.Ala368Val) rs1480983759 0.00001
NM_004655.4(AXIN2):c.13A>G (p.Met5Val) rs148691166 0.00001
NM_004655.4(AXIN2):c.1582A>G (p.Lys528Glu) rs756551019 0.00001
NM_004655.4(AXIN2):c.1748G>A (p.Gly583Glu) rs777186938 0.00001
NM_004655.4(AXIN2):c.1931A>G (p.Tyr644Cys) rs1025003994 0.00001
NM_004655.4(AXIN2):c.1969G>A (p.Ala657Thr) rs1254934681 0.00001
NM_004655.4(AXIN2):c.2141+5G>A rs769868369 0.00001
NM_004655.4(AXIN2):c.2405+7G>A rs373593841 0.00001
NM_004655.4(AXIN2):c.2420A>T (p.Lys807Ile) rs780367025 0.00001
NM_004655.4(AXIN2):c.370G>A (p.Asp124Asn) rs755990979 0.00001
NM_004655.4(AXIN2):c.564G>C (p.Gln188His) rs753137017 0.00001
NM_004655.4(AXIN2):c.592G>C (p.Glu198Gln) rs772550463 0.00001
NM_004655.4(AXIN2):c.808G>A (p.Gly270Arg) rs2044291330 0.00001
NM_004655.4(AXIN2):c.893A>G (p.Asn298Ser) rs139274803 0.00001
NM_004655.4(AXIN2):c.940A>G (p.Met314Val) rs778252248 0.00001
GRCh37/hg19 17q24.1(chr17:63481404-63618180)x3
NM_004655.4(AXIN2):c.1079A>T (p.Lys360Met) rs146249973
NM_004655.4(AXIN2):c.1103C>G (p.Ala368Gly)
NM_004655.4(AXIN2):c.1200+38G>A rs202063197
NM_004655.4(AXIN2):c.1210A>G (p.Arg404Gly)
NM_004655.4(AXIN2):c.1216G>C (p.Gly406Arg)
NM_004655.4(AXIN2):c.1235A>C (p.Asn412Thr) rs115931022
NM_004655.4(AXIN2):c.1300G>T (p.Asp434Tyr)
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.1429T>A (p.Tyr477Asn) rs1555577851
NM_004655.4(AXIN2):c.1504G>T (p.Gly502Cys) rs978541876
NM_004655.4(AXIN2):c.1531A>G (p.Thr511Ala) rs376936740
NM_004655.4(AXIN2):c.1540G>A (p.Val514Ile)
NM_004655.4(AXIN2):c.1561C>T (p.His521Tyr) rs2144459300
NM_004655.4(AXIN2):c.1786G>A (p.Glu596Lys) rs2043935287
NM_004655.4(AXIN2):c.1801G>C (p.Gly601Arg) rs750354919
NM_004655.4(AXIN2):c.1829G>C (p.Arg610Pro) rs376248072
NM_004655.4(AXIN2):c.1883G>A (p.Arg628Gln) rs2043931823
NM_004655.4(AXIN2):c.1890C>A (p.Ser630Arg)
NM_004655.4(AXIN2):c.1927G>T (p.Ala643Ser) rs748005374
NM_004655.4(AXIN2):c.1933C>G (p.Pro645Ala) rs1405864888
NM_004655.4(AXIN2):c.1954T>C (p.Ser652Pro) rs917901663
NM_004655.4(AXIN2):c.1975C>G (p.Arg659Gly) rs142670753
NM_004655.4(AXIN2):c.2017A>C (p.Thr673Pro)
NM_004655.4(AXIN2):c.2047C>T (p.Pro683Ser) rs1598096797
NM_004655.4(AXIN2):c.2048C>T (p.Pro683Leu) rs1555577092
NM_004655.4(AXIN2):c.2062C>A (p.Leu688Met) rs35415678
NM_004655.4(AXIN2):c.2117A>G (p.Glu706Gly) rs1598096605
NM_004655.4(AXIN2):c.2121G>A (p.Val707=) rs2144439332
NM_004655.4(AXIN2):c.2206C>A (p.Pro736Thr) rs951676348
NM_004655.4(AXIN2):c.2324T>C (p.Ile775Thr) rs1555576382
NM_004655.4(AXIN2):c.2406-49A>G
NM_004655.4(AXIN2):c.2420A>C (p.Lys807Thr) rs780367025
NM_004655.4(AXIN2):c.249C>G (p.His83Gln) rs763904249
NM_004655.4(AXIN2):c.607G>C (p.Gly203Arg) rs62640027
NM_004655.4(AXIN2):c.661G>T (p.Val221Leu) rs1402235122
NM_004655.4(AXIN2):c.750G>T (p.Leu250Phe) rs1060502149
NM_004655.4(AXIN2):c.754_755delinsCC (p.Ser252Pro) rs1064796197
NM_004655.4(AXIN2):c.830G>A (p.Ser277Asn) rs763027598
NM_004655.4(AXIN2):c.958G>C (p.Asp320His) rs1060502136

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