ClinVar Miner

List of variants in gene CDH1 reported as uncertain significance for Malignant tumor of breast

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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_004360.5(CDH1):c.2635G>A (p.Gly879Ser) rs200911775 0.00013
NM_004360.5(CDH1):c.846G>A (p.Met282Ile) rs200932258 0.00006
NM_004360.5(CDH1):c.1019C>T (p.Thr340Met) rs61747631 0.00005
NM_004360.5(CDH1):c.1988A>G (p.Tyr663Cys) rs372182377 0.00005
NM_004360.5(CDH1):c.1225T>C (p.Trp409Arg) rs587778176 0.00003
NM_004360.5(CDH1):c.304G>A (p.Ala102Thr) rs368492235 0.00003
NM_004360.5(CDH1):c.2131C>G (p.Leu711Val) rs121964871 0.00002
NM_004360.5(CDH1):c.2359G>A (p.Val787Ile) rs766270336 0.00002
NM_004360.5(CDH1):c.371G>A (p.Arg124His) rs115418995 0.00002
NM_004360.5(CDH1):c.1009-13G>A rs557444760 0.00001
NM_004360.5(CDH1):c.200C>A (p.Ala67Asp) rs730881660 0.00001
NM_004360.5(CDH1):c.2046G>A (p.Glu682=) rs753209043 0.00001
NM_004360.5(CDH1):c.2380G>A (p.Val794Ile) rs587782466 0.00001
NM_004360.5(CDH1):c.2414A>G (p.Asp805Gly) rs1481419710 0.00001
NM_004360.5(CDH1):c.2638G>A (p.Glu880Lys) rs34507583 0.00001
NM_004360.5(CDH1):c.322A>G (p.Arg108Gly) rs587778172 0.00001
NM_004360.5(CDH1):c.369C>G (p.His123Gln) rs778954591 0.00001
NM_004360.5(CDH1):c.546A>C (p.Lys182Asn) rs201141645 0.00001
NM_004360.5(CDH1):c.574A>G (p.Ile192Val) rs376102028 0.00001
NM_004360.5(CDH1):c.1170CGT[1] (p.Val392del) rs1555515872
NM_004360.5(CDH1):c.1585A>G (p.Thr529Ala) rs776890776
NM_004360.5(CDH1):c.2052C>A (p.Ser684Arg) rs764379691
NM_004360.5(CDH1):c.2165-12C>G rs760834250
NM_004360.5(CDH1):c.2245C>T (p.Arg749Trp) rs776975632
NM_004360.5(CDH1):c.2584T>G (p.Leu862Val) rs2152144131
NM_004360.5(CDH1):c.900C>G (p.Ile300Met) rs775452740

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