ClinVar Miner

List of variants reported as uncertain significance for Familial cancer of breast; Ovarian cancer

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Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_004360.5(CDH1):c.1996A>C (p.Asn666His) rs150427791 0.00009
NM_004360.5(CDH1):c.2644G>A (p.Asp882Asn) rs200104963 0.00009
NM_004360.5(CDH1):c.2017C>A (p.Gln673Lys) rs587781701 0.00003
NM_004360.5(CDH1):c.2074G>A (p.Ala692Thr) rs376854556 0.00003
NM_004360.5(CDH1):c.1930G>A (p.Asp644Asn) rs587781696 0.00002
NM_004360.5(CDH1):c.1008+4del rs746392709 0.00001
NM_004360.5(CDH1):c.125C>T (p.Pro42Leu) rs876659333 0.00001
NM_004360.5(CDH1):c.185G>T (p.Gly62Val) rs786203727 0.00001
NM_004360.5(CDH1):c.724G>A (p.Val242Ile) rs111662525 0.00001
NC_000016.9:g.(?_68771319)_(68849662_?)dup
NM_004360.5(CDH1):c.1008+8G>T rs990193541
NM_004360.5(CDH1):c.113C>T (p.Thr38Met) rs587778171
NM_004360.5(CDH1):c.1170CGT[1] (p.Val392del) rs1555515872
NM_004360.5(CDH1):c.1228G>C (p.Glu410Gln) rs187906987
NM_004360.5(CDH1):c.1296C>G (p.Asn432Lys) rs187862045
NM_004360.5(CDH1):c.1376T>C (p.Val459Ala) rs1555516109
NM_004360.5(CDH1):c.1526C>T (p.Thr509Ile) rs771551231
NM_004360.5(CDH1):c.1633C>G (p.Arg545Gly) rs863224727
NM_004360.5(CDH1):c.173A>T (p.Glu58Val) rs786202570
NM_004360.5(CDH1):c.1922A>G (p.Gln641Arg) rs876660113
NM_004360.5(CDH1):c.2076_2080delinsCGGCA (p.Val694Ile)
NM_004360.5(CDH1):c.2080G>A (p.Val694Ile) rs587780118
NM_004360.5(CDH1):c.2199G>C (p.Arg733Ser) rs1555517637
NM_004360.5(CDH1):c.2218C>T (p.Pro740Ser) rs773795943
NM_004360.5(CDH1):c.2324G>A (p.Gly775Asp) rs778581202
NM_004360.5(CDH1):c.2375T>C (p.Met792Thr) rs752349229
NM_004360.5(CDH1):c.2413_2414delinsAG (p.Asp805Ser) rs1961433417
NM_004360.5(CDH1):c.263C>G (p.Pro88Arg) rs1381409755
NM_004360.5(CDH1):c.272T>A (p.Phe91Tyr)
NM_004360.5(CDH1):c.36G>A (p.Leu12=)
NM_004360.5(CDH1):c.674T>C (p.Ile225Thr) rs786203207
NM_004360.5(CDH1):c.7C>A (p.Pro3Thr) rs1064793079
NM_004360.5(CDH1):c.871G>A (p.Asp291Asn) rs876660645

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