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Table 1 Mutation status in CRC critical genes. Cell lines were examined by Sanger sequencing, targeted sequencing or by both methods

From: Multi-omics of 34 colorectal cancer cell lines - a resource for biomedical studies

 

TP53

KRAS

BRAF

PIK3CA

PTEN

MSI

CIMP

CaCo2

p.E204X

wt

wt

wt

wt

MSS

CIMP-

CL-11a

p.S215N

p.V14I; p.Q61H

wt

wt

wt

MSS

CIMP+

CL-34a

p.S127P; p.K382fs

wt

p.V600E

wt

wt

MSI

CIMP+

CL-40a

p.R248Q

p.G12D

wt

wt

wt

MSS

CIMP+

Co115

wt

wt

p.V600E

wt

p.E157fs; p.R233X

MSI

CIMP+

Colo205b

p.Y107fs; p.Y103fs

wt

p.V600E

wt

wt

MSS

CIMP+

Colo320

p.R248W

wt

wt

wt

wt

MSS

CIMP-

Colo678a

wt

p.G12D

wt

wt

wt

MSS

CIMP+

DLD-1

p.S241F

p.G13D

wt

p.E545K; p.D549N

wt

MSI

CIMP+

EB

wt

p.G12D

wt

p.E545K

wt

MSS

CIMP+

FRI

p.C277F

p.G13D

wt

p.E545K

wt

MSS

CIMP-

HCC2998b

p.R213X

p.A146T

wt

wt

p.Y46C; p.R130Q; p.F341V

MSS

CIMP-

HCT116

wt

p.G13D

wt

p.H1047R

wt

MSI

CIMP+

HCT15

p.S241F

p.G13D

wt

p.E545K; p.D549N

wt

MSI

CIMP+

HT29

p.R273H

wt

p.V600E; p.T119Sc

wt

wt

MSS

CIMP+

IS1

p.Y163H

p.G12D

wt

wt

wt

MSS

CIMP-

IS3

p.Y163H

p.G12D

wt

wt

wt

MSS

CIMP-

KM12b

p.P72fs; p.H179R

wt

p.P403fs

wt

p.G129X; p.K267fs

MSI

CIMP+

LoVo

wt

p.G13D; p.V14A

wt

wt

wt

MSI

CIMP-

LS1034

p.G245S

p.A146T

wt

wt

wt

MSS

CIMP-

LS174T

wt

p.G12D

p.D211Gc

p.H1047R

wt

MSI

CIMP-

NCI-H508

p.R273H

wt

p.G596R

p.E545K

wt

MSS

CIMP-

RKO

wt

wt

p.V600E

p.H1047R

wt

MSI

CIMP+

SW1116

p.A159D

p.G12A

wt

wt

wt

MSS

CIMP-

SW1463a

p.R248Q

p.G12C

wt

wt

wt

MSS

CIMP-

SW403a

p.E51X

p.G12V

wt

wt

wt

MSS

CIMP-

SW48

wt

wt

p.R347Xc

p.G914Rc

wt

MSI

CIMP+

SW480

p.R273H; p.P309S

p.G12V

wt

wt

wt

MSS

CIMP-

SW620

p.R273H; p.P309S

p.G12V

wt

wt

wt

MSS

CIMP-

SW837a

p.R248W

p.G12C

wt

wt

wt

MSS

CIMP+

SW948

p.G117fs

p.Q61L

wt

p.E542K

wt

MSS

CIMP-

TC71

p.C176Y; p.R213X

p.G12D

wt

p.R88Qc

p.R233X

MSI

CIMP-

V9P

p.G245D

wt

wt

wt

wt

MSS

CIMP-

WiDr

p.R273H

wt

p.V600E; p.T119Sc

wt

wt

MSS

CIMP+

  1. All variants found with targeted sequencing and not observed in Sanger sequencing data were found in regions outside codons targeted by Sanger. HT29/WiDr had two variants each in BRAF, where one was verified by Sanger, and the other was outside of codons assessed. Only non-synonymous mutations were reported from targeted sequencing data
  2. aMutation data were available from Sanger sequencing only
  3. bMutation data were available from targeted sequencing only
  4. cMutations found with targeted sequencing only, but outside of regions assessed by Sanger sequencing