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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
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Small Cell Lung Cancer
Table I : cell lines with wt p53
Cell line |
ATCC |
Reference |
SBC-3 |
|
1006 |
Lu24 |
|
1382 |
MS-18 |
|
1382 |
NCI-H209 |
HTB-172 |
1382 |
NCI-H128 |
HTB-120 |
2249 |
NCI-H1522 |
CRL-5874 |
2249 |
NCI-H2081 |
CRL-5920 |
2249 |
NCI-H446 |
HTB-171 |
2249 |
NCI-H711 |
CRL-5836 |
678 |
NCI-H748 |
CRL-5841 |
678 |
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)
Cell line |
ATCC |
Mutation |
reference |
NCI-H1694 |
CRL-5888 |
c.783-1G>T |
2249 |
NCI-H2227 |
CRL-5934 |
c.783-2A>C |
678 |
NCI-H526 |
CRL-5811 |
splice intron3 |
678 |
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)
Pos. |
WT |
Mut |
AA |
Mut |
Comp |
Name |
NB |
Ref |
Comments |
126 |
TAC |
TGC |
Tyr |
Cys |
SM |
ACC-LC-172 |
17 |
1976 |
Single report |
249 |
AGG |
AGT |
Arg |
Ser |
SM |
ACC-LC-48 |
389 |
1976 |
Single report |
110 |
CGT |
del1 |
Arg |
Fs. |
SM |
ACC-LC-49 |
3 |
1976 |
Single report |
152 |
CCG |
ins1 |
Pro |
Fs. |
SM |
ACC-LC-80 |
8 |
1976 |
Single report |
245 |
GGC |
TGC |
Gly |
Cys |
SM |
COLO-668 |
86 |
2249 |
Mutation in COSMIC database |
306 |
CGA |
TGA |
Arg |
Stop |
SM |
COR-L51 |
160 |
2249 |
Mutation in COSMIC database |
281 |
GAC |
CAC |
Asp |
His |
SM |
COR-L96CAR |
41 |
2249 |
Mutation in COSMIC database |
245 |
GGC |
GTC |
Gly |
Val |
SM |
CPC-N |
84 |
2249 |
Mutation in COSMIC database |
155 |
ACC |
CCC |
Thr |
Pro |
SM |
DMS-153 |
20 |
1953 |
wt in COSMIC |
245 |
GGC |
TGC |
Gly |
Cys |
SM |
DMS-273 |
86 |
2249 |
Mutation in COSMIC database |
241 |
TCC |
TTC |
Ser |
Phe |
SM |
DMS-53 |
101 |
2249 |
Mutation in COSMIC database |
278 |
CCT |
del2c |
Pro |
Fs. |
SM |
DMS-79 |
1 |
2249 |
Mutation in COSMIC database. del2 and ins 1 |
237 |
ATG |
ATA |
Met |
Ile |
SM |
DMS-92 |
123 |
16 |
Single report |
273 |
CGT |
CTT |
Arg |
Leu |
SM |
GLC14 |
147 |
1386 |
Single report |
282 |
CGG |
TGG |
Arg |
Trp |
SM |
GLC28 |
600 |
1386 |
Single report |
53 |
TGG |
TGA |
Trp |
Stop |
SM |
GLC3 |
7 |
1386 |
Single report |
146 |
TGG |
TAG |
Trp |
Stop |
DMU |
GLC35 |
46 |
1386 |
Single report |
175 |
CGC |
CAC |
Arg |
His |
DMU |
GLC35 |
1187 |
1386 |
Single report |
158 |
CGC |
CTC |
Arg |
Leu |
SM |
GLC36 |
92 |
1386 |
Single report |
132 |
AAG |
GAG |
Lys |
Glu |
SM |
GLC4 |
25 |
1386 |
Single report |
332 |
ATC |
del1c |
Ile |
Fs. |
SM |
GLC42 |
4 |
1386 |
Single report |
326 |
GAA |
TAA |
Glu |
Stop |
SM |
GLC44 |
9 |
1386 |
Single report |
218 |
GTG |
GGG |
Val |
Gly |
SM |
GLC45 |
11 |
1386 |
Single report |
144 |
CAG |
CCG |
Gln |
Pro |
SM |
GLC7 |
10 |
1386 |
Single report |
280 |
AGA |
GGA |
Arg |
Gly |
SM |
GLC8 |
40 |
1386 |
Single report |
193 |
CAT |
CTT |
His |
Leu |
SM |
HOV |
55 |
1386 |
Single report |
294 |
GAG |
TAG |
Glu |
Stop |
SM |
IST-SL2 |
54 |
2249 |
Mutation in COSMIC database |
294 |
GAG |
del1a |
Glu |
Fs. |
SM |
LB647-SCLC |
1 |
2249 |
Mutation in COSMIC database |
278 |
CCT |
CTT |
Pro |
Leu |
SM |
LU-130 |
84 |
1382 |
Single report |
278 |
CCT |
CTT |
Pro |
Leu |
SM |
LU-134-A |
84 |
364 |
Single report |
244 |
GGC |
TGC |
Gly |
Cys |
SM |
LU-135 |
53 |
364 |
Single report |
248 |
CGG |
CTG |
Arg |
Leu |
SM |
LU-138 |
124 |
1382 |
Single report |
157 |
GTC |
TTC |
Val |
Phe |
SM |
LU-139 |
177 |
364 |
Single report |
342 |
CGA |
del1b |
Arg |
Fs. |
SM |
LU-140 |
1 |
1382 |
Single report |
179 |
CAT |
TAT |
His |
Tyr |
SM |
LU-141 |
128 |
1382 |
Single report |
156 |
CGC |
del13c |
Arg |
Fs. |
SM |
LU-165 |
1 |
2249 |
Mutation in COSMIC database |
244 |
GGC |
AGC |
Gly |
Ser |
SM |
MS-1 |
72 |
2242 |
Single report |
298 |
GAG |
TAG |
Glu |
Stop |
SM |
N230 |
71 |
1382 |
Single report |
298 |
GAG |
TAG |
Glu |
Stop |
SM |
N231 |
71 |
1382 |
Single report |
46 |
TCC |
del1b |
Ser |
Fs. |
DMU |
NCI-H1048 |
1 |
2249 |
Controversy with other publications |
273 |
CGT |
TGT |
Arg |
Cys |
SM |
NCI-H1048 |
687 |
22 |
Controversy with other publications |
273 |
CGT |
TGT |
Arg |
Cys |
DMU |
NCI-H1048 |
687 |
2249 |
Controversy with other publications |
249 |
AGG |
AGT |
Arg |
Ser |
SM |
NCI-H1105 |
389 |
2249 |
Mutation in COSMIC database |
334 |
GGG |
GTG |
Gly |
Val |
SM |
NCI-H1184 |
3 |
22 |
Single report |
175 |
CGC |
del1b |
Arg |
Fs. |
SM |
NCI-H1417 |
2 |
678 |
wt in COSMIC |
179 |
CAT |
CAG |
His |
Gln |
SM |
NCI-H1436 |
14 |
678 |
wt in COSMIC |
194 |
CTT |
CGT |
Leu |
Arg |
SM |
NCI-H1450 |
66 |
17 |
Single report |
318 |
CCA |
del19b |
Pro |
Fs. |
SM |
NCI-H146 |
1 |
2249 |
Mutation in COSMIC database |
68 |
GAG |
TAG |
Glu |
Stop |
SM |
NCI-H1514 |
5 |
22 |
Single report |
151 |
CCC |
CAC |
Pro |
His |
SM |
NCI-H1607 |
33 |
22 |
Single report |
248 |
CGG |
CTG |
Arg |
Leu |
SM |
NCI-H1618 |
124 |
22 |
wt in COSMIC |
266 |
GGA |
GTA |
Gly |
Val |
SM |
NCI-H1672 |
51 |
22 |
Single report |
241 |
TCC |
TGC |
Ser |
Cys |
SM |
NCI-H187 |
36 |
1712 |
Single report |
273 |
CGT |
CTT |
Arg |
Leu |
SM |
NCI-H1881 |
147 |
22 |
Single report |
273 |
CGT |
CTT |
Arg |
Leu |
SM |
NCI-H1882 |
147 |
678 |
wt in COSMIC |
213 |
CGA |
TGA |
Arg |
Stop |
SM |
NCI-H1926 |
306 |
22 |
wt in COSMIC |
245 |
GGC |
CGC |
Gly |
Arg |
SM |
NCI-H1930 |
20 |
2249 |
Mutation in COSMIC database |
147 |
GTT |
GAT |
Val |
Asp |
DMU |
NCI-H1963 |
7 |
22 |
wt in COSMIC |
214 |
CAT |
CGT |
His |
Arg |
DMU |
NCI-H1963 |
69 |
22 |
wt in COSMIC |
220 |
TAT |
GAT |
Tyr |
Asp |
SM |
NCI-H2029 |
5 |
2249 |
Mutation in COSMIC database |
248 |
CGG |
CAG |
Arg |
Gln |
SM |
NCI-H211 |
883 |
22 |
Single report |
209 |
AGA |
TGA |
Arg |
Stop |
SM |
NCI-H2141 |
14 |
22 |
Single report |
144 |
CAG |
TAG |
Gln |
Stop |
SM |
NCI-H2171 |
53 |
2249 |
Mutation in COSMIC database |
157 |
GTC |
TTC |
Val |
Phe |
SM |
NCI-H2196 |
177 |
2249 |
Mutation in COSMIC database |
134 |
TTT |
TTA |
Phe |
Leu |
SM |
NCI-H231 |
4 |
9 |
Single report |
65 |
AGA |
TGA |
Arg |
Stop |
SM |
NCI-H2330 |
9 |
2249 |
Mutation in COSMIC database |
277 |
TGT |
TTT |
Cys |
Phe |
SM |
NCI-H250 |
48 |
2249 |
Mutation in COSMIC database |
236 |
TAC |
TGC |
Tyr |
Cys |
SM |
NCI-H345 |
75 |
2249 |
Mutation in COSMIC database |
282 |
CGG |
GGG |
Arg |
Gly |
SM |
NCI-H510 |
48 |
22 |
wt in COSMIC |
283 |
CGC |
CCC |
Arg |
Pro |
SM |
NCI-H64 |
35 |
2249 |
Mutation in COSMIC database |
171 |
GAG |
TAG |
Glu |
Stop |
SM |
NCI-H69 |
25 |
47 |
Confirmed in three other publications |
248 |
CGG |
CAG |
Arg |
Gln |
SM |
NCI-H719 |
883 |
2249 |
Mutation in COSMIC database |
342 |
CGA |
TGA |
Arg |
Stop |
SM |
NCI-H774 |
74 |
22 |
Confirmed in another publication |
242 |
TGC |
TCC |
Cys |
Ser |
SM |
NCI-H841 |
19 |
1382 |
Single report |
242 |
TGC |
TCC |
Cys |
Ser |
SM |
NCI-H889 |
19 |
17 |
Confirmed in another publication |
298 |
GAG |
TAG |
Glu |
Stop |
SM |
NCI-N417 |
71 |
106 |
Single report |
298 |
GAG |
TAG |
Glu |
Stop |
SM |
RERF-LCMA |
71 |
364 |
Confirmed in another publication |
120 |
AAG |
TAG |
Lys |
Stop |
SM |
SBC-1 |
2 |
2249 |
Mutation in COSMIC database |
248 |
CGG |
CTG |
Arg |
Leu |
SM |
SBC-5 |
124 |
364 |
Confirmed in another publication. wt in COSMIC |
278 |
CCT |
CGT |
Pro |
Arg |
SM |
SCLC-21H |
39 |
2249 |
Mutation in COSMIC database |
85 |
CCT |
del1 |
Pro |
Fs. |
SM |
SK-LC-2 |
1 |
1976 |
Single report |
259 |
GAC |
GTC |
Asp |
Val |
SM |
U-1690 |
21 |
2021 |
Single report |
248 |
CGG |
CTG |
Arg |
Leu |
SM |
U-1906 |
124 |
2021 |
Single report |
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