ClinVar Miner

List of variants in gene AXIN2 reported as pathogenic for Hereditary cancer-predisposing syndrome

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Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_004655.4(AXIN2):c.1159del (p.Ser387fs)
NM_004655.4(AXIN2):c.1195del (p.Arg399fs) rs2144475594
NM_004655.4(AXIN2):c.1274dup (p.Leu426fs)
NM_004655.4(AXIN2):c.1306C>T (p.Gln436Ter)
NM_004655.4(AXIN2):c.1466_1478del (p.Pro489fs)
NM_004655.4(AXIN2):c.1565dup (p.His522fs)
NM_004655.4(AXIN2):c.1637del (p.Gly546fs) rs1555577625
NM_004655.4(AXIN2):c.1642G>T (p.Glu548Ter) rs367624903
NM_004655.4(AXIN2):c.1705C>T (p.Gln569Ter) rs2144455707
NM_004655.4(AXIN2):c.1722dup (p.Gly575fs)
NM_004655.4(AXIN2):c.1724dup (p.Ser576fs)
NM_004655.4(AXIN2):c.1822del (p.Leu608fs) rs1567754914
NM_004655.4(AXIN2):c.1831G>T (p.Glu611Ter) rs2043933208
NM_004655.4(AXIN2):c.1838_1848dup (p.Gln617fs)
NM_004655.4(AXIN2):c.1873G>T (p.Glu625Ter)
NM_004655.4(AXIN2):c.1879G>T (p.Glu627Ter)
NM_004655.4(AXIN2):c.1912C>T (p.Gln638Ter) rs1598097196
NM_004655.4(AXIN2):c.1925del (p.Lys642fs)
NM_004655.4(AXIN2):c.1966C>T (p.Arg656Ter) rs121908568
NM_004655.4(AXIN2):c.1993_1994delinsT (p.Gly665fs)
NM_004655.4(AXIN2):c.1994del (p.Gly665fs) rs267606674
NM_004655.4(AXIN2):c.1994dup (p.Asn666fs) rs267606674
NM_004655.4(AXIN2):c.2018_2025dup (p.Ala676fs)
NM_004655.4(AXIN2):c.2023del (p.Arg675fs)
NM_004655.4(AXIN2):c.2023dup (p.Arg675fs) rs1555577121
NM_004655.4(AXIN2):c.2052del (p.Met685fs) rs2144440894
NM_004655.4(AXIN2):c.2137C>T (p.Gln713Ter) rs2043913790
NM_004655.4(AXIN2):c.2202del (p.Thr735fs)
NM_004655.4(AXIN2):c.254del (p.Leu85fs)
NM_004655.4(AXIN2):c.323dup (p.Leu108fs)
NM_004655.4(AXIN2):c.332G>A (p.Trp111Ter)
NM_004655.4(AXIN2):c.355C>T (p.Gln119Ter) rs1598119841
NM_004655.4(AXIN2):c.479del (p.Gly160fs)
NM_004655.4(AXIN2):c.490C>T (p.Gln164Ter)
NM_004655.4(AXIN2):c.611del (p.Gly204fs)
NM_004655.4(AXIN2):c.702G>A (p.Trp234Ter)
NM_004655.4(AXIN2):c.763_764del (p.Leu255fs) rs1598118962
NM_004655.4(AXIN2):c.801dup (p.Asp268Ter) rs2144581824

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