ClinVar Miner

List of variants reported as likely pathogenic for Hereditary diffuse gastric cancer

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Total variants: 41
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HGVS dbSNP
NC_000016.10:g.(?_68801664)_(68801899_?)dup
NC_000016.10:g.(?_68819274)_(68829803_?)dup
NC_000016.10:g.(?_68821995)_(68823632_?)del
NC_000016.9:g.(?_68835567)_(68847404_?)dup
NM_004360.3(CDH1):c.2430delT (p.Phe810Leufs) rs786203752
NM_004360.3(CDH1):c.382delC (p.His128Ilefs) rs1555514492
NM_004360.3(CDH1):c.832+1G>A rs878854697
NM_004360.4(CDH1):c.1008+2T>C rs1060501237
NM_004360.4(CDH1):c.12G>A (p.Trp4Ter) rs1555509636
NM_004360.4(CDH1):c.1565+2_1565+3insTT rs1555516200
NM_004360.4(CDH1):c.1566-1G>C rs113583899
NM_004360.4(CDH1):c.1566-2A>G rs1555516520
NM_004360.4(CDH1):c.1711+1G>A rs886041161
NM_004360.4(CDH1):c.1895_1896delAC (p.His632Argfs) rs1060501224
NM_004360.4(CDH1):c.1901C>T (p.Ala634Val) rs121964878
NM_004360.4(CDH1):c.1921C>T (p.Gln641Ter) rs587782750
NM_004360.4(CDH1):c.1942G>T (p.Glu648Ter) rs971882211
NM_004360.4(CDH1):c.1A>G (p.Met1Val) rs1555509622
NM_004360.4(CDH1):c.2165-1G>C rs1385720097
NM_004360.4(CDH1):c.2287G>T (p.Glu763Ter) rs587780787
NM_004360.4(CDH1):c.2439+1G>T
NM_004360.4(CDH1):c.2446A>T (p.Lys816Ter) rs1555518211
NM_004360.4(CDH1):c.2T>C (p.Met1Thr) rs1555509623
NM_004360.4(CDH1):c.2T>G (p.Met1Arg) rs1555509623
NM_004360.4(CDH1):c.531+1G>A rs1131690808
NM_004360.4(CDH1):c.532-1G>C rs771085839
NM_004360.4(CDH1):c.655delC (p.Pro219Leufs) rs1555515284
NM_004360.4(CDH1):c.687+2T>C rs1555515297
NM_004360.4(CDH1):c.715G>A (p.Gly239Arg) rs587780537
NM_004360.4(CDH1):c.720delT (p.Asn240Lysfs) rs1131690819
NM_004360.4(CDH1):c.833-8_836del
NM_004360.5(CDH1):c.1008G>A (p.Glu336=) rs267606712
NM_004360.5(CDH1):c.1008G>T (p.Glu336Asp) rs267606712
NM_004360.5(CDH1):c.1137G>A (p.Thr379=) rs587783050
NM_004360.5(CDH1):c.1137G>T (p.Thr379=)
NM_004360.5(CDH1):c.1679C>G (p.Thr560Arg) rs746481984
NM_004360.5(CDH1):c.2195G>A (p.Arg732Gln) rs1060501244
NM_004360.5(CDH1):c.2296-1G>A rs1057517542
NM_004360.5(CDH1):c.2296-2A>G rs876660393
NM_004360.5(CDH1):c.2494G>A (p.Val832Met) rs35572355
NM_004360.5(CDH1):c.3G>A (p.Met1Ile) rs878854691

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