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 per condition Variants with at least 2 submissions on the same condition 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 conflict
1359 61 0 30 16 0 0 43

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.

uncertain significance likely benign benign
uncertain significance 0 14 3
likely benign 14 0 30
benign 3 30 0

All variants with conflicting interpretations #

Total variants: 43
Download table as spreadsheet
HGVS dbSNP
NM_004655.4(AXIN2):c.1059+8C>T rs367595502
NM_004655.4(AXIN2):c.1101C>T (p.Pro367=) rs141697521
NM_004655.4(AXIN2):c.1168A>G (p.Ser390Gly) rs139871607
NM_004655.4(AXIN2):c.1200+8G>A rs776372607
NM_004655.4(AXIN2):c.1267C>T (p.Leu423Phe) rs376630432
NM_004655.4(AXIN2):c.1327C>T (p.Leu443=) rs371691797
NM_004655.4(AXIN2):c.1347C>T (p.Thr449=) rs762279806
NM_004655.4(AXIN2):c.1376G>A (p.Arg459His) rs368525111
NM_004655.4(AXIN2):c.1443C>T (p.Leu481=) rs886053272
NM_004655.4(AXIN2):c.144C>T (p.Pro48=) rs144099816
NM_004655.4(AXIN2):c.1485C>T (p.Gly495=) rs770556906
NM_004655.4(AXIN2):c.1531A>T (p.Thr511Ser) rs376936740
NM_004655.4(AXIN2):c.1545C>T (p.His515=) rs139316692
NM_004655.4(AXIN2):c.1573C>G (p.Pro525Ala) rs73346297
NM_004655.4(AXIN2):c.1615G>A (p.Val539Met) rs9913621
NM_004655.4(AXIN2):c.1623C>T (p.Cys541=) rs199931425
NM_004655.4(AXIN2):c.1685C>T (p.Pro562Leu) rs149764887
NM_004655.4(AXIN2):c.1713-18G>A rs147664289
NM_004655.4(AXIN2):c.174C>T (p.Asn58=) rs763012548
NM_004655.4(AXIN2):c.1882C>T (p.Arg628Trp) rs200201811
NM_004655.4(AXIN2):c.1887G>A (p.Gln629=) rs140163819
NM_004655.4(AXIN2):c.1952C>T (p.Ser651Leu) rs74006838
NM_004655.4(AXIN2):c.1985T>C (p.Leu662Pro) rs142476324
NM_004655.4(AXIN2):c.2004G>A (p.Gly668=) rs144092307
NM_004655.4(AXIN2):c.2051C>T (p.Ala684Val) rs138287857
NM_004655.4(AXIN2):c.2052G>A (p.Ala684=) rs200573256
NM_004655.4(AXIN2):c.2083G>T (p.Ala695Ser) rs140510381
NM_004655.4(AXIN2):c.2124G>A (p.Ser708=) rs143243661
NM_004655.4(AXIN2):c.2196G>A (p.Thr732=) rs878854725
NM_004655.4(AXIN2):c.2213C>T (p.Ser738Phe) rs139209450
NM_004655.4(AXIN2):c.2239C>T (p.His747Tyr) rs143571197
NM_004655.4(AXIN2):c.2272G>A (p.Ala758Thr) rs145007501
NM_004655.4(AXIN2):c.2282C>A (p.Ala761Asp) rs79732150
NM_004655.4(AXIN2):c.2285G>A (p.Ser762Asn) rs117688560
NM_004655.4(AXIN2):c.270C>T (p.Asp90=) rs141655687
NM_004655.4(AXIN2):c.598G>A (p.Val200Met) rs752081909
NM_004655.4(AXIN2):c.623C>T (p.Ala208Val) rs201531372
NM_004655.4(AXIN2):c.629T>C (p.Met210Thr) rs529954883
NM_004655.4(AXIN2):c.645C>T (p.Leu215=) rs767834824
NM_004655.4(AXIN2):c.733C>T (p.Pro245Ser) rs62640028
NM_004655.4(AXIN2):c.780T>C (p.Ser260=) rs147681058
NM_004655.4(AXIN2):c.815+4A>G rs565020131
NM_004655.4(AXIN2):c.897C>T (p.Asp299=) rs748143308

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