ClinVar Miner

List of variants in gene CDH1 reported as likely benign by Sema4, Sema4

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Gene type:
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Total variants: 67
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HGVS dbSNP gnomAD frequency
NM_004360.5(CDH1):c.1138-3C>T rs36103202 0.00042
NM_004360.5(CDH1):c.303C>T (p.Tyr101=) rs150789339 0.00027
NM_004360.5(CDH1):c.2413G>A (p.Asp805Asn) rs200894246 0.00026
NM_004360.5(CDH1):c.8C>G (p.Pro3Arg) rs587782484 0.00023
NM_004360.5(CDH1):c.670C>T (p.Arg224Cys) rs200310662 0.00021
NM_004360.5(CDH1):c.1296C>T (p.Asn432=) rs187862045 0.00019
NM_004360.5(CDH1):c.2329G>A (p.Asp777Asn) rs372989292 0.00015
NM_004360.5(CDH1):c.394G>A (p.Val132Ile) rs142498771 0.00015
NM_004360.5(CDH1):c.1353T>C (p.Ile451=) rs114192597 0.00014
NM_004360.5(CDH1):c.2635G>A (p.Gly879Ser) rs200911775 0.00013
NM_004360.5(CDH1):c.1409C>T (p.Thr470Ile) rs370864592 0.00012
NM_004360.5(CDH1):c.1223C>T (p.Ala408Val) rs138135866 0.00011
NM_004360.5(CDH1):c.2512A>G (p.Ser838Gly) rs121964872 0.00011
NM_004360.5(CDH1):c.1298A>G (p.Asp433Gly) rs376097289 0.00007
NM_004360.5(CDH1):c.1710T>C (p.Asn570=) rs202115589 0.00007
NM_004360.5(CDH1):c.2136G>T (p.Gly712=) rs763402728 0.00006
NM_004360.5(CDH1):c.214G>A (p.Asp72Asn) rs35606263 0.00006
NM_004360.5(CDH1):c.49-3C>T rs587782366 0.00006
NM_004360.5(CDH1):c.699C>T (p.His233=) rs115494727 0.00005
NM_004360.5(CDH1):c.1174G>A (p.Val392Ile) rs141864044 0.00004
NM_004360.5(CDH1):c.2020A>T (p.Asn674Tyr) rs201637081 0.00004
NM_004360.5(CDH1):c.2165-15C>A rs552874184 0.00004
NM_004360.5(CDH1):c.2280C>T (p.Gly760=) rs768547540 0.00004
NM_004360.5(CDH1):c.2494G>A (p.Val832Met) rs35572355 0.00004
NM_004360.5(CDH1):c.712A>C (p.Asn238His) rs730881664 0.00004
NM_004360.5(CDH1):c.1173C>T (p.Val391=) rs148080550 0.00003
NM_004360.5(CDH1):c.1417G>A (p.Val473Ile) rs36087757 0.00003
NM_004360.5(CDH1):c.2204C>T (p.Ala735Val) rs587782464 0.00003
NM_004360.5(CDH1):c.2331C>T (p.Asp777=) rs114265540 0.00003
NM_004360.5(CDH1):c.2514C>T (p.Ser838=) rs770974998 0.00003
NM_004360.5(CDH1):c.671G>A (p.Arg224His) rs201511530 0.00003
NM_004360.5(CDH1):c.759C>T (p.Thr253=) rs372934565 0.00003
NM_004360.5(CDH1):c.1017T>C (p.Pro339=) rs746639322 0.00002
NM_004360.5(CDH1):c.1119G>A (p.Pro373=) rs758258272 0.00002
NM_004360.5(CDH1):c.1488C>T (p.Ser496=) rs751346548 0.00002
NM_004360.5(CDH1):c.1684A>G (p.Thr562Ala) rs587782061 0.00002
NM_004360.5(CDH1):c.1824G>A (p.Lys608=) rs373987896 0.00002
NM_004360.5(CDH1):c.2103C>T (p.Val701=) rs730881656 0.00002
NM_004360.5(CDH1):c.2399G>A (p.Arg800His) rs370345996 0.00002
NM_004360.5(CDH1):c.510A>G (p.Pro170=) rs774962542 0.00002
NM_004360.5(CDH1):c.906C>T (p.Tyr302=) rs370197479 0.00002
NM_004360.5(CDH1):c.1383T>A (p.Pro461=) rs1238176229 0.00001
NM_004360.5(CDH1):c.1569T>C (p.Tyr523=) rs876659716 0.00001
NM_004360.5(CDH1):c.1842C>T (p.Ile614=) rs773368593 0.00001
NM_004360.5(CDH1):c.2077G>A (p.Gly693Ser) rs386833398 0.00001
NM_004360.5(CDH1):c.2322G>A (p.Arg774=) rs150734856 0.00001
NM_004360.5(CDH1):c.2638G>A (p.Glu880Lys) rs34507583 0.00001
NM_004360.5(CDH1):c.561G>A (p.Lys187=) rs765426607 0.00001
NM_004360.5(CDH1):c.570C>T (p.Tyr190=) rs761753486 0.00001
NM_004360.5(CDH1):c.867G>A (p.Ala289=) rs754143182 0.00001
NM_004360.5(CDH1):c.879G>A (p.Val293=) rs778959722 0.00001
NM_004360.5(CDH1):c.1160A>G (p.Asn387Ser) rs779426744
NM_004360.5(CDH1):c.1572G>C (p.Arg524=) rs771419468
NM_004360.5(CDH1):c.1572G>T (p.Arg524=) rs771419468
NM_004360.5(CDH1):c.1779C>T (p.Pro593=) rs1596963500
NM_004360.5(CDH1):c.2205G>A (p.Ala735=) rs138493551
NM_004360.5(CDH1):c.2205G>C (p.Ala735=) rs138493551
NM_004360.5(CDH1):c.2217G>A (p.Glu739=) rs1596970771
NM_004360.5(CDH1):c.2370C>A (p.Thr790=) rs1596972620
NM_004360.5(CDH1):c.2454T>C (p.Ala818=) rs761471987
NM_004360.5(CDH1):c.2493C>T (p.Leu831=) rs779267700
NM_004360.5(CDH1):c.2553A>G (p.Ser851=) rs1555518253
NM_004360.5(CDH1):c.2556G>A (p.Glu852=) rs760315494
NM_004360.5(CDH1):c.2628C>T (p.Tyr876=) rs778681919
NM_004360.5(CDH1):c.270G>A (p.Arg90=) rs777822181
NM_004360.5(CDH1):c.510A>C (p.Pro170=) rs774962542
NM_004360.5(CDH1):c.90T>C (p.Pro30=) rs1555509766

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