List of variants reported as likely benign for adenocarcinoma by Mendelics

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Total variants: 38

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HGVS	dbSNP	gnomAD frequency
NM_000245.4(MET):c.504G>T (p.Glu168Asp)	rs55985569	0.00420
NM_000245.4(MET):c.2908C>T (p.Arg970Cys)	rs34589476	0.00327
NM_004360.5(CDH1):c.1774G>A (p.Ala592Thr)	rs35187787	0.00311
NM_000245.4(MET):c.2365-21G>C	rs140853140	0.00242
NM_000245.4(MET):c.1715G>A (p.Ser572Asn)	rs199771406	0.00188
NM_004360.5(CDH1):c.2292C>T (p.Asp764=)	rs61747636	0.00159
NM_004360.5(CDH1):c.164-45T>C	rs189978842	0.00155
NM_004360.5(CDH1):c.2440-6C>G	rs139757930	0.00145
NM_004360.5(CDH1):c.88C>A (p.Pro30Thr)	rs139866691	0.00129
NM_001904.4(CTNNB1):c.860A>G (p.Asn287Ser)	rs35288908	0.00086
NM_004360.5(CDH1):c.2520C>T (p.Ser840=)	rs140328601	0.00064
NM_004360.5(CDH1):c.2439+10C>T	rs35236080	0.00057
NM_000245.4(MET):c.71G>A (p.Gly24Glu)	rs180985111	0.00055
NM_000245.4(MET):c.2715C>T (p.Ser905=)	rs45572835	0.00039
NM_004360.5(CDH1):c.892G>A (p.Ala298Thr)	rs142822590	0.00028
NM_000245.4(MET):c.3632+42C>G	rs376183825	0.00021
NM_004360.5(CDH1):c.670C>T (p.Arg224Cys)	rs200310662	0.00021
NM_000245.4(MET):c.4087G>A (p.Ala1363Thr)	rs45578433	0.00016
NM_004360.5(CDH1):c.393C>T (p.Ser131=)	rs145430811	0.00006
NM_004958.4(MTOR):c.889G>A (p.Asp297Asn)	rs141936187	0.00006
NM_004360.5(CDH1):c.375C>A (p.Pro125=)	rs773044699	0.00004
NM_004360.5(CDH1):c.1138-44G>A	rs374676556	0.00003
NM_004360.5(CDH1):c.1273G>A (p.Val425Ile)	rs570930882	0.00002
NM_000245.4(MET):c.1306G>A (p.Glu436Lys)	rs200740468	0.00001
NM_004360.5(CDH1):c.2358C>T (p.Asp786=)	rs760701558	0.00001
NM_000245.4(MET):c.1393-2A>T	rs1584921898
NM_000245.4(MET):c.1973T>C (p.Val658Ala)	rs1584941533
NM_000245.4(MET):c.2103-1G>T	rs1336351205
NM_000245.4(MET):c.2103-2A>T	rs1470403316
NM_000245.4(MET):c.252C>T (p.Tyr84=)	rs1584876265
NM_000245.4(MET):c.2584-1G>T	rs1240673121
NM_000245.4(MET):c.2584-3C>T	rs1337305891
NM_000245.4(MET):c.850A>G (p.Ile284Val)	rs776014448
NM_004360.5(CDH1):c.*179G>T	rs1596977076
NM_004360.5(CDH1):c.-57C>T	rs981792194
NM_004360.5(CDH1):c.1416C>T (p.Thr472=)	rs139937234
NM_004360.5(CDH1):c.32TGC[4] (p.Leu15del)	rs587782476
NM_004360.5(CDH1):c.687+56del	rs771109236

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