List of variants reported as likely benign for diffuse type adenocarcinoma by Illumina Laboratory Services, Illumina

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Total variants: 23

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HGVS	dbSNP	gnomAD frequency
NM_004360.5(CDH1):c.1849G>A (p.Ala617Thr)	rs33935154	0.01412
NM_004360.5(CDH1):c.-71C>G	rs34033771	0.00927
NM_004360.4(CDH1):c.*2050T>A	rs181705992	0.00746
NM_004360.5(CDH1):c.1774G>A (p.Ala592Thr)	rs35187787	0.00311
NM_004360.5(CDH1):c.-54G>C	rs5030874	0.00208
NM_004360.5(CDH1):c.2440-6C>G	rs139757930	0.00145
NM_004360.5(CDH1):c.88C>A (p.Pro30Thr)	rs139866691	0.00129
NM_004360.5(CDH1):c.808T>G (p.Ser270Ala)	rs587776399	0.00038
NM_004360.5(CDH1):c.892G>A (p.Ala298Thr)	rs142822590	0.00028
NM_004360.5(CDH1):c.2413G>A (p.Asp805Asn)	rs200894246	0.00026
NM_004360.5(CDH1):c.1018A>G (p.Thr340Ala)	rs116093741	0.00022
NM_004360.5(CDH1):c.2589C>T (p.Asn863=)	rs115817750	0.00022
NM_004360.5(CDH1):c.393C>T (p.Ser131=)	rs145430811	0.00006
NM_004360.5(CDH1):c.1023T>C (p.Tyr341=)	rs587776398	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.1689C>T (p.Ala563=)	rs587780786	0.00003
NM_004360.5(CDH1):c.184G>A (p.Gly62Ser)	rs587781898	0.00003
NM_004360.5(CDH1):c.2331C>T (p.Asp777=)	rs114265540	0.00003
NM_004360.5(CDH1):c.671G>A (p.Arg224His)	rs201511530	0.00003
NM_004360.5(CDH1):c.1936A>G (p.Thr646Ala)	rs771064558	0.00001
NM_004360.5(CDH1):c.604G>A (p.Val202Ile)	rs546716073	0.00001
NM_004360.5(CDH1):c.1974_1978del	rs557163298

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