ClinVar Miner

List of variants reported as likely benign for Malignant tumor of prostate

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Total variants: 13
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HGVS dbSNP gnomAD frequency
NM_004360.5(CDH1):c.-84G>A rs374268061 0.00369
NM_007294.4(BRCA1):c.2167A>G (p.Asn723Asp) rs4986845 0.00209
NM_004360.5(CDH1):c.670C>T (p.Arg224Cys) rs200310662 0.00021
NM_002485.5(NBN):c.1036G>A (p.Val346Met) rs200297914 0.00011
NM_004360.5(CDH1):c.1371G>A (p.Thr457=) rs370368644 0.00003
NM_004360.5(CDH1):c.759C>T (p.Thr253=) rs372934565 0.00003
NM_004360.5(CDH1):c.2046G>A (p.Glu682=) rs753209043 0.00001
NM_004360.5(CDH1):c.1020G>T (p.Thr340=) rs61747632
NM_004360.5(CDH1):c.1680G>A (p.Thr560=) rs35741240
NM_004360.5(CDH1):c.1937-4C>T rs1057523153
NM_004360.5(CDH1):c.2493C>T (p.Leu831=) rs779267700
NM_004360.5(CDH1):c.2640G>A (p.Glu880=) rs864622218
NM_020529.3(NFKBIA):c.560T>C (p.Leu187Pro) rs2138831226

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