ClinVar Miner

Variants in gene AXIN2 with conflicting interpretations

Y axis minimum submission review status: Y axis collection method:
X axis minimum submission review status: X axis collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than two submissions, it may have multiple conflicts and therefore be counted in more than one conflict column. If this is the case, the "Variants with any kind of conflict" cell will be less than the sum of the conflicted variants cells to its left.

Variants with only 1 submission Variants with at least 2 submissions and no conflicts Variants with a synonymous conflict
(e.g. benign vs non-pathogenic)
Variants with a confidence conflict
(e.g. benign vs likely benign)
Variants with a benign or likely benign vs uncertain conflict Variants with a category conflict
(e.g. benign vs affects)
Variants with a clinically significant conflict
(e.g. benign vs pathogenic)
Variants with any kind of conflict
671 146 0 27 32 0 1 59

Significance breakdown #

In the table below, cells that correspond to a term paired with itself represent synonymous conflicts, i.e. variants that have been annotated with different terms that map to the same standard term. To compare the terms that were actually submitted, check the box in the filters section at the top of this page.

likely pathogenic uncertain significance likely benign benign
likely pathogenic 0 0 1 1
uncertain significance 0 0 27 5
likely benign 1 27 0 27
benign 1 5 27 0

All variants with conflicting interpretations #

Total variants: 59
Download table as spreadsheet
HGVS dbSNP
NM_004655.3(AXIN2):c.-116-13delC rs530658215
NM_004655.3(AXIN2):c.1059+8C>T rs367595502
NM_004655.3(AXIN2):c.1070G>A (p.Arg357His) rs8081536
NM_004655.3(AXIN2):c.1101C>T (p.Pro367=) rs141697521
NM_004655.3(AXIN2):c.1168A>G (p.Ser390Gly) rs139871607
NM_004655.3(AXIN2):c.1176G>A (p.Glu392=) rs376052287
NM_004655.3(AXIN2):c.1181G>A (p.Arg394His) rs200899695
NM_004655.3(AXIN2):c.1242G>A (p.Arg414=) rs200325634
NM_004655.3(AXIN2):c.1250C>T (p.Ala417Val) rs201460658
NM_004655.3(AXIN2):c.129C>T (p.Gly43=) rs878854720
NM_004655.3(AXIN2):c.1305G>A (p.Pro435=) rs369221405
NM_004655.3(AXIN2):c.1347C>T (p.Thr449=) rs762279806
NM_004655.3(AXIN2):c.1383C>T (p.Ser461=) rs9914661
NM_004655.3(AXIN2):c.13A>G (p.Met5Val) rs148691166
NM_004655.3(AXIN2):c.1410C>T (p.His470=) rs149483825
NM_004655.3(AXIN2):c.1443C>T (p.Leu481=) rs886053272
NM_004655.3(AXIN2):c.144C>T (p.Pro48=) rs144099816
NM_004655.3(AXIN2):c.1470G>A (p.Ala490=) rs1060502143
NM_004655.3(AXIN2):c.1485C>T (p.Gly495=) rs770556906
NM_004655.3(AXIN2):c.1530G>A (p.Thr510=) rs141014640
NM_004655.3(AXIN2):c.1532C>T (p.Thr511Met) rs200883019
NM_004655.3(AXIN2):c.1545C>T (p.His515=) rs139316692
NM_004655.3(AXIN2):c.1573C>G (p.Pro525Ala) rs73346297
NM_004655.3(AXIN2):c.1615G>A (p.Val539Met) rs9913621
NM_004655.3(AXIN2):c.1637G>T (p.Gly546Val) rs145717795
NM_004655.3(AXIN2):c.1685C>T (p.Pro562Leu) rs149764887
NM_004655.3(AXIN2):c.1713-18G>A rs147664289
NM_004655.3(AXIN2):c.1713C>T (p.Gly571=) rs761978806
NM_004655.3(AXIN2):c.1807G>C (p.Ala603Pro) rs145353986
NM_004655.3(AXIN2):c.1882C>T (p.Arg628Trp) rs200201811
NM_004655.3(AXIN2):c.1952C>T (p.Ser651Leu) rs74006838
NM_004655.3(AXIN2):c.1962C>A (p.Gly654=) rs377642903
NM_004655.3(AXIN2):c.1975C>T (p.Arg659Trp) rs142670753
NM_004655.3(AXIN2):c.1985T>C (p.Leu662Pro) rs142476324
NM_004655.3(AXIN2):c.2034G>T (p.Leu678=) rs748632114
NM_004655.3(AXIN2):c.2052G>A (p.Ala684=) rs200573256
NM_004655.3(AXIN2):c.2083G>T (p.Ala695Ser) rs140510381
NM_004655.3(AXIN2):c.2109G>A (p.Arg703=) rs116525755
NM_004655.3(AXIN2):c.2124G>A (p.Ser708=) rs143243661
NM_004655.3(AXIN2):c.2124G>C (p.Ser708=) rs143243661
NM_004655.3(AXIN2):c.2140C>T (p.Arg714Trp) rs148765149
NM_004655.3(AXIN2):c.2213C>T (p.Ser738Phe) rs139209450
NM_004655.3(AXIN2):c.2239C>T (p.His747Tyr) rs143571197
NM_004655.3(AXIN2):c.2272G>A (p.Ala758Thr) rs145007501
NM_004655.3(AXIN2):c.2285G>A (p.Ser762Asn) rs117688560
NM_004655.3(AXIN2):c.2428G>A (p.Asp810Asn) rs140344858
NM_004655.3(AXIN2):c.270C>T (p.Asp90=) rs141655687
NM_004655.3(AXIN2):c.435C>G (p.Val145=) rs111470596
NM_004655.3(AXIN2):c.623C>T (p.Ala208Val) rs201531372
NM_004655.3(AXIN2):c.629T>C (p.Met210Thr) rs529954883
NM_004655.3(AXIN2):c.815+5G>A rs1057520237
NM_004655.3(AXIN2):c.828G>A (p.Arg276=) rs730881404
NM_004655.3(AXIN2):c.897C>T (p.Asp299=) rs748143308
NM_004655.4(AXIN2):c.1419_1421dup (p.His474_Ser475insHis) rs570443161
NM_004655.4(AXIN2):c.2051C>T (p.Ala684Val) rs138287857
NM_004655.4(AXIN2):c.2237+3G>A rs376584101
NM_004655.4(AXIN2):c.2282C>A (p.Ala761Asp) rs79732150
NM_004655.4(AXIN2):c.2433G>A (p.Glu811=) rs147134295
NM_004655.4(AXIN2):c.815+4dup rs745726935

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