List of variants reported as pathogenic for attenuated familial adenomatous polyposis by Fulgent Genetics, Fulgent Genetics

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Total variants: 29

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HGVS	dbSNP	gnomAD frequency
NM_001048174.2(MUTYH):c.1103G>A (p.Gly368Asp)	rs36053993	0.00341
NM_001048174.2(MUTYH):c.452A>G (p.Tyr151Cys)	rs34612342	0.00168
NM_001048174.2(MUTYH):c.650G>A (p.Arg217His)	rs140342925	0.00009
NM_001048174.2(MUTYH):c.305-1G>C	rs372267274	0.00004
NM_001048174.2(MUTYH):c.928C>T (p.Gln310Ter)	rs587780082	0.00004
NM_000038.6(APC):c.70C>T (p.Arg24Ter)	rs145945630	0.00003
NM_001048174.2(MUTYH):c.1130C>T (p.Pro377Leu)	rs529008617	0.00003
NM_001048174.2(MUTYH):c.383G>A (p.Trp128Ter)	rs762307622	0.00002
NM_001048174.2(MUTYH):c.649C>T (p.Arg217Cys)	rs200495564	0.00002
NM_000038.6(APC):c.646C>T (p.Arg216Ter)	rs62619935	0.00001
NM_001048174.2(MUTYH):c.1103-2A>G	rs587781628	0.00001
NM_000038.6(APC):c.1660C>T (p.Arg554Ter)	rs137854573
NM_000038.6(APC):c.2805C>A (p.Tyr935Ter)	rs137854575
NM_000038.6(APC):c.3867T>A (p.Cys1289Ter)	rs1554085355
NM_000038.6(APC):c.3901dup (p.Thr1301fs)	rs1554085382
NM_000038.6(APC):c.637C>T (p.Arg213Ter)	rs587781392
NM_000038.6(APC):c.643C>T (p.Gln215Ter)	rs137854577
NM_000038.6(APC):c.694C>T (p.Arg232Ter)	rs397515734
NM_000038.6(APC):c.74_75del (p.Gln25fs)	rs1554067124
NM_000038.6(APC):c.835-17A>G	rs1580511131
NM_000038.6(APC):c.847C>T (p.Arg283Ter)	rs786201856
NM_000038.6(APC):c.933+1G>A	rs876660765
NM_000038.6(APC):c.994C>T (p.Arg332Ter)	rs775126020
NM_001048174.2(MUTYH):c.1350GGA[1] (p.Glu452del)	rs587778541
NM_001048174.2(MUTYH):c.1354G>T (p.Glu452Ter)	rs121908381
NM_001048174.2(MUTYH):c.13C>T (p.Arg5Ter)	rs587780088
NM_001048174.2(MUTYH):c.228C>A (p.Tyr76Ter)	rs121908380
NM_001048174.2(MUTYH):c.461G>A (p.Arg154His)	rs143353451
NM_006231.4(POLE):c.1270C>G (p.Leu424Val)	rs483352909

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