List of variants reported as likely benign for Colorectal cancer

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Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_006231.4(POLE):c.16G>C (p.Gly6Arg)	rs202220778	0.00293
NM_182643.3(DLC1):c.3856-6G>A	rs200102232	0.00179
NM_182643.3(DLC1):c.167A>G (p.Glu56Gly)	rs143324598	0.00168
NM_182643.3(DLC1):c.2147T>C (p.Ile716Thr)	rs114637912	0.00117
NM_004655.4(AXIN2):c.2051C>T (p.Ala684Val)	rs138287857	0.00112
NM_001211.6(BUB1B):c.1371A>G (p.Gln457=)	rs141013408	0.00033
NM_182643.3(DLC1):c.2265G>C (p.Thr755=)	rs138749997	0.00018
NM_182643.3(DLC1):c.3609C>A (p.Thr1203=)	rs145989730	0.00008
NM_001211.6(BUB1B):c.255A>G (p.Thr85=)	rs140273483	0.00005
NM_000546.6(TP53):c.459C>T (p.Pro153=)	rs72661116	0.00003
NM_182643.3(DLC1):c.1348+9A>C	rs200908536	0.00002
NM_182643.3(DLC1):c.3327+8C>T	rs559854315	0.00001
NM_182643.3(DLC1):c.1697C>A (p.Ser566Tyr)
NM_182643.3(DLC1):c.2348A>G (p.Asn783Ser)
NM_182643.3(DLC1):c.3968A>T (p.His1323Leu)
NM_182643.3(DLC1):c.4067A>G (p.Tyr1356Cys)
NM_182643.3(DLC1):c.4466+4T>A
NM_182643.3(DLC1):c.769T>A (p.Phe257Ile)

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