Cell lines database

p53 database

p53 mutations in cell lines

The hanbook of p53 mutation in cell lines

Cell lines with a controversial p53 status

The NCI 60 panel

Bladder cancer cell lines

Brain cancer cell lines

Breast cancer cell lines

Cervical carcinoma

Colorectal cancer cell lines

Esophageal cancer cell lines

Gastric cancer cell lines

Head and Neck cancer cell lines

Leukemia / Lymphoma cell lines

NSCLC cancer cell lines

Ovarian cancer cell lines

Pancreatic cancer cell lines

Sarcoma cell lines

SCLC cancer cell lines

Melanoma cell lines

Hepatocellular carcinoma

References

Colorectal carcinoma

Table I : cell lines with wt p53

Cell line ATCC
Reference
C32  
2051
C99  
2051
COLO678  
2051
Gp2D  
2051
HCT116 CCL-247
2051
LOVO CCL-229
2051
LS180 CL-187
2051
LS174T CL-188
2051
LS513 CRL-2134
2051
NCI-747  
2051
RKO CRL-2577
2051
SKCO-1 HTB-39
2051
Col15  
2251
TC7  
2251
EB  
2251

Table II : cell lines with p53 gene deletion or rearrangement

No data

Table III : cell lines with p53 splice mutation
(exonic mutations that modify splice are listed in table IV)

no data

Table IV: cell lines with p53 mutations (missense or frameshift)
More information is available in the handbook

Pos: Codon position (1 to 393);
WT: Normal base sequence of the codon in which the mutation occurred;
Mut Sequence of the mutated codon. If the mutation is a deletion or an insertion, it is indicated by "del" or "ins" followed by the number of deleted or inserted bases. The position in the codon is indicated by “a”, “b”, or “c” for the first, second or third base of the codon respectively. Example: "del66b" is a deletion of 66 bases including the second base of the codon; "ins4a" is an insertion of 4 bases occurring between the first and the second base of the codon. Label a, b, or c is omitted if the boundary of the deletion or insertion is unknown
AA: Wild type amino acid;
Mut: Mutant amino acid. Stop: nonsense mutation: Fs.: Frameshift mutation: InF: In-frame insertion or deletion;
Comp: complexity of the mutation: SM: Single mutational event in the tumor; DMU (Double Mutation Unknown): Two p53 mutations in the same tumor but their allelique distribution is unknown; DMD (Double Mutation Different allele): Two p53 mutations in the same tumor on two different p53 alleles; DMS (Double Mutation Same allele): Two p53 mutations in the same tumor on the same p53 allele: MM (Multiple Mutation): More than two p53 mutations in the same tumor;
NB: Number of tumors with this particular mutant in the database;
Ref: reference number;
Comments: information;

 

Table of references (available also in the handbook)

Colorectal adenoma

Pos.
WT
Mut
      AA
Mut
Comp
Name
NB
Ref
Comments
282 CGG TGG Arg Trp SM RG 600 1 Single report
248 CGG TGG Arg Trp SM VACO330 728 1 Single report

Colorectal carcinoma

Pos.
WT
Mut
      AA
Mut
Comp
Name
NB
Ref
Comments
301
CCA
del1a
Pro
Fs.
SM
ala
6
724
 Single report
245
GGC
AGC
Gly
Ser
SM
C10
440
2051
Single report
125
ACG
ATG
Thr
Met
SM
C106
12
2051
Single report
196
CGA
TGA
Arg
Stop
SM
C125-PM
241
2051
Single report
249
AGG
AGC
Arg
Ser
SM
C75
34
2051
Single report
52
CAA
TAA
Gln
Stop
SM
C80
6
2051
Single report
342
CGA
TGA
Arg
Stop
SM
C84
74
2051
Single report
204
GAG
TAG
Glu
Stop
SM
CACO2
46
2051
Single report
234
TAC
TGC
Tyr
Cys
SM
CaR-1
133
1006
Controversy with other publications. wt in COSMIC
272
GTG
ATG
Val
Met
SM
CaR-1
105
2051
Controversy with other publications. wt in COSMIC
245
GGC
AGC
Gly
Ser
SM
CBS
440
724
Single report
245
GGC
AGC
Gly
Ser
SM
CC07
440
2051
Single report
126
TAC
TAG
Tyr
Stop
SM
CC20
14
2051
Single report
278
CCT
CAT
Pro
His
SM
CCK-81
13
2051
Single report
241
TCC
TTC
Ser
Phe
SM
CLONE A
101
492
Single report
241
TCC
TTC
Ser
Phe
SM
CLONE D
101
492
Single report
134
TTT
TTG
Phe
Leu
SM
Co74
6
2258
193
CAT
CGT
His
Arg
SM
Co82
86
2258
144
CAG
TAG
Gln
Stop
SM
Co84
53
2258
273
CGT
TGT
Arg
Cys
SM
Co92
687
2258
196
CGA
TGA
Arg
Stop
SM
CoCM-1
241
2051
Single report
103
TAC
del27
Tyr
InF
SM
COLO-205
1
492
Controversy with other publications
266
GGA
GAA
Gly
Glu
SM
COLO-205
74
1018
Controversy with other publications
248
CGG
TGG
Arg
Trp
SM
COLO-320
728
38
Confirmed in two other publications
321
AAA
ins2a
Lys
Fs.
SM
COLO-741
1
2051
Single report
273
CGT
CAT
Arg
His
SM
CX-1
780
492
Single report
248
CGG
CAG
Arg
Gln
SM
CX27
883
1
Single report
241
TCC
TTC
Ser
Phe
SM
DLD-1
101
27
Confirmed in three other publications
176
TGC
TTC
Cys
Phe
SM
FET
191
724
Single report
277
TGT
TTT
Cys
Phe
SM
FRI
48
724
Single report
245
GGC
GAC
Gly
Asp
SM
GLY
171
724
Single report
273
CGT
CAT
Arg
His
SM
H-110
780
1689
Single report
306
CGA
TGA
Arg
Stop
SM
H-173
160
1689
Single report
272
GTG
del2b
Val
Fs.
SM
HCA46
1
2051
Single report
300
CCC
del1a
Pro
Fs.
SM
HCA7
8
2051
Single report
213
CGA
TGA
Arg
Stop
SM
HCC-2998
306
1018
Confirmed in COSMIC database
153
CCC
GCC
Pro
Ala
SM
HCT-15
5
1018
Controversy with other publications
241
TCC
TTC
Ser
Phe
SM
HCT-15
101
2251
Controversy with other publications
273
CGT
CAT
Arg
His
SM
HRA19
780
2051
Single report
273
CGT
CAT
Arg
His
SM
HT-29
780
492
Confirmed in two other publications
213
CGA
CTA
Arg
Leu
SM
HT55
33
2051
wt in COSMIC
163
TAC
CAC
Tyr
His
SM
ISRECO1
26
724
Single report
72
CCC
del1b
Pro
Fs.
SM
KM12
1
2249
Controversy with other publications
179
CAT
CGT
His
Arg
SM
KM12
146
1018
Controversy with other publications
234
TAC
CAC
Tyr
His
SM
LIM1863
25
2051
Single report
245
GGC
GAC
Gly
Asp
SM
LS-1034
171
724
Single report
175
CGC
CAC
Arg
His
SM
LS-123
1187
2051
Single report
126
TAC
TAA
Tyr
Stop
SM
LS-411
11
2051
Single report
241
TCC
TTC
Ser
Phe
SM
MIP 101
101
492
Single report
161
GCC
ACC
Ala
Thr
SM
MOSER
75
492
Single report
273
CGT
CAT
Arg
His
SM
NCI-H508
780
2249
Mutation in COSMIC database
342
CGA
TGA
Arg
Stop
SM
NCI-H630
74
2249
Mutation in COSMIC database
224
GAG
GAT
Glu
Asp
SM
NCI-H716
6
2051
wt in COSMIC
158
CGC
CTC
Arg
Leu
SM
NCI-H747
92
219
Single report
272
GTG
ATG
Val
Met
SM
P-6
105
1006
Single report
306
CGA
TGA
Arg
Stop
SM
RCM-1
160
2051
Single report
190
CCT
CTT
Pro
Leu
SM
SNU-1033
52
1204
Single report
248
CGG
TGG
Arg
Trp
SM
SNU-1040
728
1204
Single report
254
ATC
ACC
Ile
Thr
SM
SNU-1047
11
1204
Single report
175
CGC
CAC
Arg
His
SM
SNU-1097
1187
1204
Single report
273
CGT
CTT
Arg
Leu
SM
SNU-503
147
1204
Single report
175
CGC
CAC
Arg
His
SM
SNU-61
1187
1204
Single report
166
TCA
TGA
Ser
Stop
SM
SNU-C1
18
2249
Mutation in COSMIC database
273
CGT
TGT
Arg
Cys
DMD
SNU-C2B
687
2051
Single report
273
CGT
CAT
Arg
His
DMD
SNU-C2B
780
2051
Single report
218
GTG
TTG
Val
Leu
DMD
SNU-C5
3
1038
Single report
248
CGG
TGG
Arg
Trp
DMD
SNU-C5
728
1038
Single report
159
GCC
GAC
Ala
Asp
SM
SW1116
8
219
Confirmed in two other publications. wt in COSMIC
237
ATG
del14
Met
Fs.
SM
SW1417
1
492
wt in COSMIC
248
CGG
CAG
Arg
Gln
SM
SW1463
883
2249
Mutation in COSMIC database
51
GAA
TAA
Glu
Stop
SM
SW403
6
2051
Single report
248
CGG
TGG
Arg
Trp
SM
SW48
728
492
Confirmed in another publication. wt in COSMIC
273
CGT
CAT
Arg
His
DMU
SW480
780
9
Single report
309
CCC
TCC
Pro
Ser
DMU
SW480
6
9
Single report
248
CGG
TGG
Arg
Trp
SM
SW837
728
9
Confirmed in two other publications
117
GGG
del1a
Gly
Fs.
SM
SW948
3
2051
wt in COSMIC
245
GGC
GAC
Gly
Asp
SM
V9P
171
724
Single report
175
CGC
CAC
Arg
His
SM
VACO10MS
1187
2051
Single report
306
CGA
TGA
Arg
Stop
SM
VACO429
160
2051
Single report
154
GGC
AGC
Gly
Ser
SM
VACO457
14
996
Single report
135
TGC
TGG
Cys
Trp
SM
VACO489
25
996
Single report
329
ACC
ins1a
Thr
Fs.
SM
VACO4A
1
2051
Single report
282
CGG
TGG
Arg
Trp
SM
VACO5
600
996
Single report
273
CGT
TGT
Arg
Cys
SM
VACO576
687
996
Single report
181
CGC
TGC
Arg
Cys
SM
VACO670
28
996
Single report
190
CCT
CTT
Pro
Leu
SM
VACO8
52
996
Single report
273
CGT
CAT
Arg
His
SM
WIDR
780
27
Confirmed in another publication

 

 

 

 
 
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