List of variants reported as benign for colorectal cancer by Fulgent Genetics, Fulgent Genetics

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Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_000535.7(PMS2):c.780C>G (p.Ser260=)	rs1805319	0.82058
NM_000546.6(TP53):c.215C>G (p.Pro72Arg)	rs1042522	0.62654
NM_000038.6(APC):c.4479G>A (p.Thr1493=)	rs41115	0.59177
NM_004655.4(AXIN2):c.1386C>T (p.Pro462=)	rs1133683	0.52439
NM_000038.6(APC):c.1458T>C (p.Tyr486=)	rs2229992	0.46792
NM_000179.3(MSH6):c.3438+14A>T	rs2020911	0.32279
NM_000179.3(MSH6):c.540T>C (p.Asp180=)	rs1800935	0.23857
NM_000249.4(MLH1):c.-93G>A	rs1800734	0.22121
NM_002843.4(PTPRJ):c.827A>C (p.Gln276Pro)	rs1566734	0.14574
NM_000251.3(MSH2):c.2006-6T>C	rs2303428	0.08349
NM_000179.3(MSH6):c.642C>T (p.Tyr214=)	rs1800937	0.07457
NM_005215.4(DCC):c.91+7G>A	rs112558388	0.02064
NM_182643.3(DLC1):c.1530G>A (p.Ala510=)	rs1127606	0.01715
NM_004655.4(AXIN2):c.1615G>A (p.Val539Met)	rs9913621	0.01361
NM_000249.4(MLH1):c.588+11G>C	rs4647258	0.00993
NM_004333.6(BRAF):c.1315-18T>G	rs6959000	0.00840
NM_000038.6(APC):c.4326T>A (p.Pro1442=)	rs67622085	0.00705
NM_001429.4(EP300):c.631G>A (p.Gly211Ser)	rs142030651	0.00646
NM_000179.3(MSH6):c.2633T>C (p.Val878Ala)	rs2020912	0.00448
NM_182643.3(DLC1):c.2199C>T (p.Ser733=)	rs34941980	0.00252
NM_004655.4(AXIN2):c.1807G>C (p.Ala603Pro)	rs145353986	0.00128
NM_000546.6(TP53):c.139C>T (p.Pro47Ser)	rs1800371	0.00123
NM_000251.3(MSH2):c.1886A>G (p.Gln629Arg)	rs61756468	0.00042
NM_144997.7(FLCN):c.1538+10A>C	rs12451312	0.00010
NM_000142.5(FGFR3):c.1960-7C>T	rs779177992	0.00004
NM_144997.7(FLCN):c.75G>A (p.Leu25=)	rs200350612

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