Subtype, tumor mutation burden (TMB), aneuploidy score (AS), and fraction genome altered (FGA) in colorectal cancers with or without APC and other WNT/β-catenin pathway alterations from the Cancer Genome Atlas (TCGA)

CharacteristicEntire cohort (n = 594)Quadruple altered (n = 95)APC only altered (n = 300)Triple altered (n = 44)Quadruple wild type (n = 95)P
Subtype
GS58 (12.7)11 (12.7)39 (13.8)2 (5)6 (12)GS versus CIN versus MSI: < 0.00001
CIN328 (71.4)46 (53.5)235 (83)14 (35)33 (66)
MSI63 (13.7)19 (22.1)9 (3.2)24 (60)11 (22)
POLE10 (2.2)10 (11.7)000-
NA135917445-
TMB
≤ 10 mutations/Mb451 (84.5)63 (66.3)288 (96)17 (38.6)83 (87.4)< 0.00001
> 10 mutations/Mb83 (15.5)32 (33.7)12 (4)27 (61.4)12 (12.6)
NA600000-
AS
< 4108 (18.4)30 (32.3)39 (13.1)29 (65.9)15 (15.8)< 0.00001
4–24427 (72.9)58 (62.4)226 (76.1)15 (34.1)70 (73.7)
> 2451 (8.7)5 (5.3)32 (10.8)010 (10.5)
NA82300-
FGA
< 0.075115 (19.7)28 (30.1)32 (10.9)24 (55.8)16 (17)< 0.00001
0.075–0.35319 (54.7)49 (52.7)179 (61.1)15 (34.9)54 (57.5)
> 0.35149 (25.6)16 (17.2)82 (28)4 (9.3)24 (25.5)
NA112711-

Percentages are shown in parentheses. GS: genomically stable; CIN: chromosomal instability, MSI: microsatellite instability; NA: not available; POLE: polymerase epsilon. -: no data