ClinVar Miner

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

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 14
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HGVS dbSNP
NM_004655.4(AXIN2):c.1347C>T (p.Thr449=) rs762279806
NM_004655.4(AXIN2):c.1443C>T (p.Leu481=) rs886053272
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.174C>T (p.Asn58=) rs763012548
NM_004655.4(AXIN2):c.1985T>C (p.Leu662Pro) rs142476324
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.2239C>T (p.His747Tyr) rs143571197
NM_004655.4(AXIN2):c.2272G>A (p.Ala758Thr) rs145007501
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.897C>T (p.Asp299=) rs748143308

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