ClinVar Miner

List of variants reported as likely pathogenic for Endometrial neoplasm

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Total variants: 13
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HGVS dbSNP
NM_000141.4(FGFR2):c.1115C>G (p.Ser372Cys) rs121913477
NM_000141.4(FGFR2):c.1121A>G (p.Asp374Gly) rs1057520028
NM_000141.4(FGFR2):c.1124A>G (p.Tyr375Cys) rs121913478
NM_000141.4(FGFR2):c.1141T>C (p.Tyr381His) rs387906678
NM_000141.4(FGFR2):c.1642A>C (p.Ile548Leu) rs1057519901
NM_000141.4(FGFR2):c.1914T>A (p.Asn638Lys) rs1057519854
NM_000141.4(FGFR2):c.1972A>G (p.Lys658Glu) rs1057520027
NM_000141.4(FGFR2):c.1974A>T (p.Lys658Asn) rs1057520029
NM_000141.4(FGFR2):c.755C>G (p.Ser252Trp) rs79184941
NM_000141.4(FGFR2):c.929A>G (p.Lys310Arg) rs121913475
NM_001904.4(CTNNB1):c.94G>A (p.Asp32Asn) rs28931588
NM_001904.4(CTNNB1):c.95A>T (p.Asp32Val) rs121913396
NM_001904.4(CTNNB1):c.98C>A (p.Ser33Tyr) rs121913400

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