List of variants reported as not provided for adenocarcinoma

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Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_024529.5(CDC73):c.-11G>A	rs80356643	0.00056
NM_004360.5(CDH1):c.808T>G (p.Ser270Ala)	rs587776399	0.00038
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.1223C>T (p.Ala408Val)	rs138135866	0.00011
NM_024529.5(CDC73):c.1066+8T>C	rs80356647	0.00006
NM_000245.4(MET):c.4007G>A (p.Arg1336Gln)	rs369312680	0.00005
NM_004360.5(CDH1):c.2074G>A (p.Ala692Thr)	rs376854556	0.00003
NM_020975.6(RET):c.1998G>T (p.Lys666Asn)	rs146646971	0.00003
NM_004360.5(CDH1):c.1493A>C (p.Asp498Ala)	rs876661065	0.00001
NM_004360.5(CDH1):c.2398C>T (p.Arg800Cys)	rs587782162	0.00001
NM_004360.5(CDH1):c.370C>T (p.Arg124Cys)	rs748086082	0.00001
NM_020975.6(RET):c.1826G>A (p.Cys609Tyr)	rs77939446	0.00001
NM_000245.4(MET):c.1357G>A (p.Ala453Thr)	rs1793019219
NM_000245.4(MET):c.2432T>A (p.Leu811Gln)	rs1554396554
NM_004333.6(BRAF):c.1799T>A (p.Val600Glu)	rs113488022
NM_004360.5(CDH1):c.1009_1010del (p.Ser337Phefs)	rs786201045
NM_004360.5(CDH1):c.1015C>G (p.Pro339Ala)	rs1555515709
NM_004360.5(CDH1):c.1137G>A (p.Thr379=)	rs587783050
NM_004360.5(CDH1):c.1202C>T (p.Ala401Val)	rs150795245
NM_004360.5(CDH1):c.1454T>C (p.Ile485Thr)	rs587783049
NM_004360.5(CDH1):c.1488_1494del (p.Glu497fs)	rs876658261
NM_004360.5(CDH1):c.1565+1G>A	rs587780113
NM_004360.5(CDH1):c.1942G>T (p.Glu648Ter)	rs971882211
NM_004360.5(CDH1):c.2064_2065del (p.Cys688_Glu689delinsTer)	rs587781276
NM_004360.5(CDH1):c.504del (p.Gly169fs)	rs864622655
NM_004985.5(KRAS):c.35G>C (p.Gly12Ala)	rs121913529
NM_006218.4(PIK3CA):c.1412C>T (p.Pro471Leu)	rs1057519872
NM_020975.6(RET):c.1998G>C (p.Lys666Asn)	rs146646971
NM_024529.5(CDC73):c.131+1G>A	rs587776558
NM_024529.5(CDC73):c.1418-17C>G	rs11583414
NM_024529.5(CDC73):c.679_680insAG (p.Arg227fs)	rs80356649
NM_024529.5(CDC73):c.766_767del (p.Val256fs)	rs80356650

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