ClinVar Miner

List of variants reported as likely pathogenic for Neoplasm of stomach

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Total variants: 8
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HGVS dbSNP
NM_000546.5(TP53):c.847C>T (p.Arg283Cys) rs149633775
NM_001904.4(CTNNB1):c.109T>C (p.Ser37Pro) rs121913228
NM_001904.4(CTNNB1):c.110C>A (p.Ser37Tyr) rs121913403
NM_001904.4(CTNNB1):c.118A>G (p.Thr40Ala) rs1057519836
NM_001982.3(ERBB3):c.850G>A (p.Gly284Arg) rs1057519803
NM_002524.5(NRAS):c.37G>A (p.Gly13Ser) rs121434595
NM_004360.5(CDH1):c.1296C>G (p.Asn432Lys) rs187862045
NM_004360.5(CDH1):c.2494G>A (p.Val832Met) rs35572355

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