ClinVar Miner

List of variants in gene CDH1 reported as uncertain significance by PreventionGenetics, part of Exact Sciences

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Total variants: 41
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HGVS dbSNP gnomAD frequency
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.1996A>C (p.Asn666His) rs150427791 0.00009
NM_004360.5(CDH1):c.2644G>A (p.Asp882Asn) rs200104963 0.00009
NM_004360.5(CDH1):c.164T>G (p.Val55Gly) rs587778174 0.00008
NM_004360.5(CDH1):c.854C>T (p.Thr285Ile) rs587781634 0.00007
NM_004360.5(CDH1):c.214G>A (p.Asp72Asn) rs35606263 0.00006
NM_004360.5(CDH1):c.2336G>A (p.Arg779Gln) rs587781311 0.00004
NM_004360.5(CDH1):c.2450C>T (p.Ala817Val) rs587782024 0.00004
NM_004360.5(CDH1):c.377C>T (p.Pro126Leu) rs746703615 0.00004
NM_004360.5(CDH1):c.1318A>G (p.Lys440Glu) rs778212100 0.00003
NM_004360.5(CDH1):c.1585A>C (p.Thr529Pro) rs776890776 0.00003
NM_004360.5(CDH1):c.184G>A (p.Gly62Ser) rs587781898 0.00003
NM_004360.5(CDH1):c.1178T>A (p.Ile393Asn) rs34466743 0.00002
NM_004360.5(CDH1):c.1300G>C (p.Gly434Arg) rs587781783 0.00002
NM_004360.5(CDH1):c.1684A>G (p.Thr562Ala) rs587782061 0.00002
NM_004360.5(CDH1):c.371G>A (p.Arg124His) rs115418995 0.00002
NM_004360.5(CDH1):c.1070C>A (p.Thr357Lys) rs1260033180 0.00001
NM_004360.5(CDH1):c.1202C>A (p.Ala401Asp) rs150795245 0.00001
NM_004360.5(CDH1):c.1526C>A (p.Thr509Asn) rs771551231 0.00001
NM_004360.5(CDH1):c.1612G>T (p.Asp538Tyr) rs756154596 0.00001
NM_004360.5(CDH1):c.199G>A (p.Ala67Thr) rs1060501247 0.00001
NM_004360.5(CDH1):c.2077G>A (p.Gly693Ser) rs386833398 0.00001
NM_004360.5(CDH1):c.233G>A (p.Gly78Asp) rs587781404 0.00001
NM_004360.5(CDH1):c.2351G>A (p.Arg784His) rs763203357 0.00001
NM_004360.5(CDH1):c.365A>G (p.His122Arg) rs373668742 0.00001
NM_004360.5(CDH1):c.574A>G (p.Ile192Val) rs376102028 0.00001
NM_004360.5(CDH1):c.602C>G (p.Pro201Arg) rs146777134 0.00001
NM_004360.5(CDH1):c.687+92T>A rs1303357315 0.00001
NM_004360.5(CDH1):c.79C>T (p.Pro27Ser) rs878854696 0.00001
NM_004360.5(CDH1):c.1163_1171dup (p.Glu388_Asn390dup) rs772580163
NM_004360.5(CDH1):c.118A>C (p.Thr40Pro) rs876661278
NM_004360.5(CDH1):c.1204G>A (p.Asp402Asn)
NM_004360.5(CDH1):c.1277C>T (p.Thr426Ile) rs876658901
NM_004360.5(CDH1):c.1550T>A (p.Met517Lys) rs786203656
NM_004360.5(CDH1):c.177T>G (p.Asp59Glu) rs587780116
NM_004360.5(CDH1):c.2401C>G (p.Pro801Ala) rs876660704
NM_004360.5(CDH1):c.2641G>A (p.Asp881Asn) rs1198941336
NM_004360.5(CDH1):c.408A>G (p.Gln136=) rs1060501229
NM_004360.5(CDH1):c.719A>G (p.Asn240Ser) rs587780788
NM_004360.5(CDH1):c.761A>G (p.Asp254Gly)

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