ClinVar Miner

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

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 30
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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.144C>T (p.Pro48=) rs144099816
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.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.2213C>T (p.Ser738Phe) rs139209450
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.270C>T (p.Asp90=) rs141655687
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

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