ClinVar Miner

List of variants in gene BARD1 reported as pathogenic for Gastric cancer

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_000465.4(BARD1):c.1921C>T (p.Arg641Ter) rs587781948 0.00003
NM_000465.4(BARD1):c.448C>T (p.Arg150Ter) rs730881411 0.00001
NM_000465.4(BARD1):c.886dup (p.Glu296fs) rs1694984038 0.00001
NM_000465.4(BARD1):c.1029del (p.Ser344fs) rs2469504845
NM_000465.4(BARD1):c.1156G>T (p.Glu386Ter) rs1553622218
NM_000465.4(BARD1):c.1345C>T (p.Gln449Ter) rs1553619721
NM_000465.4(BARD1):c.1568+1G>A rs2106076135
NM_000465.4(BARD1):c.159-2A>C rs1424761304
NM_000465.4(BARD1):c.1641_1645dup (p.Asn549fs) rs1553616361
NM_000465.4(BARD1):c.1810+1G>T rs876659894
NM_000465.4(BARD1):c.1843C>T (p.Gln615Ter) rs751710099
NM_000465.4(BARD1):c.1903+1G>C rs876660237
NM_000465.4(BARD1):c.1903+1del rs2469337523
NM_000465.4(BARD1):c.1904-2_1904-1del rs771472958
NM_000465.4(BARD1):c.1935_1954del (p.Cys645_Glu652delinsTer) rs587780024
NM_000465.4(BARD1):c.417_427del (p.Lys139fs) rs2469513748
NM_000465.4(BARD1):c.629del (p.Thr210fs) rs2469510863
NM_000465.4(BARD1):c.735del (p.Gln245fs) rs2469509131
NM_000465.4(BARD1):c.829_833dup (p.Ser279fs) rs2469507728

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