ClinVar Miner

List of variants in gene CDH1 reported as likely benign by Quest Diagnostics Nichols Institute San Juan Capistrano

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Gene type:
ClinVar version:
Total variants: 65
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HGVS dbSNP gnomAD frequency
NM_004360.5(CDH1):c.808T>G (p.Ser270Ala) rs587776399 0.00038
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.1568A>G (p.Tyr523Cys) rs553907248 0.00016
NM_004360.5(CDH1):c.394G>A (p.Val132Ile) rs142498771 0.00015
NM_004360.5(CDH1):c.2635G>A (p.Gly879Ser) rs200911775 0.00013
NM_004360.5(CDH1):c.1143G>C (p.Lys381Asn) rs143727462 0.00012
NM_004360.5(CDH1):c.*8G>A rs201223411 0.00011
NM_004360.5(CDH1):c.2512A>G (p.Ser838Gly) rs121964872 0.00011
NM_004360.5(CDH1):c.1996A>C (p.Asn666His) rs150427791 0.00009
NM_004360.5(CDH1):c.1297G>A (p.Asp433Asn) rs199886166 0.00007
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.214G>A (p.Asp72Asn) rs35606263 0.00006
NM_004360.5(CDH1):c.846G>A (p.Met282Ile) rs200932258 0.00006
NM_004360.5(CDH1):c.1174G>A (p.Val392Ile) rs141864044 0.00004
NM_004360.5(CDH1):c.1392C>T (p.Val464=) rs373811706 0.00004
NM_004360.5(CDH1):c.1793G>A (p.Arg598Gln) rs780759537 0.00004
NM_004360.5(CDH1):c.1865A>G (p.Asn622Ser) rs147925149 0.00004
NM_004360.5(CDH1):c.213C>T (p.Leu71=) rs376667778 0.00004
NM_004360.5(CDH1):c.375C>A (p.Pro125=) rs773044699 0.00004
NM_004360.5(CDH1):c.780C>T (p.Pro260=) rs765090311 0.00004
NM_004360.5(CDH1):c.1417G>A (p.Val473Ile) rs36087757 0.00003
NM_004360.5(CDH1):c.1689C>T (p.Ala563=) rs587780786 0.00003
NM_004360.5(CDH1):c.759C>T (p.Thr253=) rs372934565 0.00003
NM_004360.5(CDH1):c.833-3C>T rs587782839 0.00003
NM_004360.5(CDH1):c.1017T>C (p.Pro339=) rs746639322 0.00002
NM_004360.5(CDH1):c.1273G>A (p.Val425Ile) rs570930882 0.00002
NM_004360.5(CDH1):c.1977G>A (p.Glu659=) rs368243190 0.00002
NM_004360.5(CDH1):c.2079C>T (p.Gly693=) rs771993728 0.00002
NM_004360.5(CDH1):c.2157T>G (p.Ala719=) rs762224244 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.957T>A (p.Ile319=) rs549252135 0.00002
NM_004360.5(CDH1):c.1132A>C (p.Thr378Pro) rs587781432 0.00001
NM_004360.5(CDH1):c.114G>C (p.Thr38=) rs786201492 0.00001
NM_004360.5(CDH1):c.1164G>A (p.Glu388=) rs774875972 0.00001
NM_004360.5(CDH1):c.1266A>G (p.Gln422=) rs776805501 0.00001
NM_004360.5(CDH1):c.1503G>A (p.Val501=) rs775290153 0.00001
NM_004360.5(CDH1):c.1929C>T (p.Asn643=) rs374152504 0.00001
NM_004360.5(CDH1):c.2322G>A (p.Arg774=) rs150734856 0.00001
NM_004360.5(CDH1):c.2515G>A (p.Gly839Ser) rs587780121 0.00001
NM_004360.5(CDH1):c.387+6T>C rs764434962 0.00001
NM_004360.5(CDH1):c.48+7C>T rs587782380 0.00001
NM_004360.5(CDH1):c.532-7T>C rs1432324307 0.00001
NM_004360.5(CDH1):c.561G>A (p.Lys187=) rs765426607 0.00001
NM_004360.5(CDH1):c.832+9A>T rs1057521268 0.00001
NM_004360.5(CDH1):c.1026C>T (p.Thr342=) rs2152132512
NM_004360.5(CDH1):c.1170C>T (p.Asn390=) rs766505270
NM_004360.5(CDH1):c.1230G>A (p.Glu410=) rs876659952
NM_004360.5(CDH1):c.1242C>T (p.Thr414=) rs779601817
NM_004360.5(CDH1):c.1368G>A (p.Val456=) rs1555516103
NM_004360.5(CDH1):c.163+4_163+6dup rs1205684749
NM_004360.5(CDH1):c.1680G>A (p.Thr560=) rs35741240
NM_004360.5(CDH1):c.1711+9G>C rs368770384
NM_004360.5(CDH1):c.2124T>A (p.Pro708=) rs786201660
NM_004360.5(CDH1):c.2205G>A (p.Ala735=) rs138493551
NM_004360.5(CDH1):c.2229C>T (p.Pro743=) rs786203083
NM_004360.5(CDH1):c.2406C>T (p.Ala802=) rs1555517903
NM_004360.5(CDH1):c.2454T>C (p.Ala818=) rs761471987
NM_004360.5(CDH1):c.2475G>A (p.Pro825=) rs755658014
NM_004360.5(CDH1):c.45G>A (p.Leu15=) rs746331438
NM_004360.5(CDH1):c.612C>T (p.Val204=) rs1555515273
NM_004360.5(CDH1):c.651A>G (p.Thr217=) rs2152130262
NM_004360.5(CDH1):c.924T>C (p.Asp308=) rs1555515629

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