ClinVar Miner

List of variants in gene CDH1 reported as uncertain significance by St. Jude Molecular Pathology, St. Jude Children's Research Hospital

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Gene type:
ClinVar version:
Total variants: 12
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HGVS dbSNP gnomAD frequency
NM_004360.5(CDH1):c.1568A>G (p.Tyr523Cys) rs553907248 0.00016
NM_004360.5(CDH1):c.1241C>A (p.Thr414Asn) rs755571454 0.00006
NM_004360.5(CDH1):c.846G>A (p.Met282Ile) rs200932258 0.00006
NM_004360.5(CDH1):c.1988A>G (p.Tyr663Cys) rs372182377 0.00005
NM_004360.5(CDH1):c.1865A>G (p.Asn622Ser) rs147925149 0.00004
NM_004360.5(CDH1):c.1351A>C (p.Ile451Leu) rs377416092 0.00001
NM_004360.5(CDH1):c.1018A>T (p.Thr340Ser) rs116093741
NM_004360.5(CDH1):c.1181C>A (p.Thr394Asn) rs1332444039
NM_004360.5(CDH1):c.1566-8C>G rs587780114
NM_004360.5(CDH1):c.1928A>G (p.Asn643Ser) rs1567512606
NM_004360.5(CDH1):c.1955T>G (p.Leu652Trp) rs1567513174
NM_004360.5(CDH1):c.2351G>C (p.Arg784Pro) rs763203357

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