Tuesday, 27 June 2017

Small Cell Lung Cancer

Small Cell Lung Cancer

Table I : cell lines with wt p53
Cell lineATCCReference
SBC-3 1006
Lu24 1382
MS-18 1382
NCI-H209HTB-1721382
NCI-H128HTB-1202249
NCI-H1522CRL-58742249
NCI-H2081CRL-59202249
NCI-H446HTB-1712249
NCI-H711CRL-5836678
NCI-H748CRL-5841678
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 lineATCCMutationreference
NCI-H1694CRL-5888c.783-1G>T2249
NCI-H2227CRL-5934c.783-2A>C678
NCI-H526CRL-5811splice intron3678
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
126TACTGCTyrCysSMACC-LC-172171976Single report
249AGGAGTArgSerSMACC-LC-483891976Single report
110CGTdel1ArgFs.SMACC-LC-4931976Single report
152CCGins1ProFs.SMACC-LC-8081976Single report
245GGCTGCGlyCysSMCOLO-668862249Mutation in COSMIC database
306CGATGAArgStopSMCOR-L511602249Mutation in COSMIC database
281GACCACAspHisSMCOR-L96CAR412249Mutation in COSMIC database
245GGCGTCGlyValSMCPC-N842249Mutation in COSMIC database
155ACCCCCThrProSMDMS-153201953wt in COSMIC
245GGCTGCGlyCysSMDMS-273862249Mutation in COSMIC database
241TCCTTCSerPheSMDMS-531012249Mutation in COSMIC database
278CCTdel2cProFs.SMDMS-7912249Mutation in COSMIC database. del2 and ins 1
237ATGATAMetIleSMDMS-9212316Single report
273CGTCTTArgLeuSMGLC141471386Single report
282CGGTGGArgTrpSMGLC286001386Single report
53TGGTGATrpStopSMGLC371386Single report
146TGGTAGTrpStopDMUGLC35461386Single report
175CGCCACArgHisDMUGLC3511871386Single report
158CGCCTCArgLeuSMGLC36921386Single report
132AAGGAGLysGluSMGLC4251386Single report
332ATCdel1cIleFs.SMGLC4241386Single report
326GAATAAGluStopSMGLC4491386Single report
218GTGGGGValGlySMGLC45111386Single report
144CAGCCGGlnProSMGLC7101386Single report
280AGAGGAArgGlySMGLC8401386Single report
193CATCTTHisLeuSMHOV551386Single report
294GAGTAGGluStopSMIST-SL2542249Mutation in COSMIC database
294GAGdel1aGluFs.SMLB647-SCLC12249Mutation in COSMIC database
278CCTCTTProLeuSMLU-130841382Single report
278CCTCTTProLeuSMLU-134-A84364Single report
244GGCTGCGlyCysSMLU-13553364Single report
248CGGCTGArgLeuSMLU-1381241382Single report
157GTCTTCValPheSMLU-139177364Single report
342CGAdel1bArgFs.SMLU-14011382Single report
179CATTATHisTyrSMLU-1411281382Single report
156CGCdel13cArgFs.SMLU-16512249Mutation in COSMIC database
244GGCAGCGlySerSMMS-1722242Single report
298GAGTAGGluStopSMN230711382Single report
298GAGTAGGluStopSMN231711382Single report
46TCCdel1bSerFs.DMUNCI-H104812249Controversy with other publications
273CGTTGTArgCysSMNCI-H104868722Controversy with other publications
273CGTTGTArgCysDMUNCI-H10486872249Controversy with other publications
249AGGAGTArgSerSMNCI-H11053892249Mutation in COSMIC database
334GGGGTGGlyValSMNCI-H1184322Single report
175CGCdel1bArgFs.SMNCI-H14172678wt in COSMIC
179CATCAGHisGlnSMNCI-H143614678wt in COSMIC
194CTTCGTLeuArgSMNCI-H14506617Single report
318CCAdel19bProFs.SMNCI-H14612249Mutation in COSMIC database
68GAGTAGGluStopSMNCI-H1514522Single report
151CCCCACProHisSMNCI-H16073322Single report
248CGGCTGArgLeuSMNCI-H161812422wt in COSMIC
266GGAGTAGlyValSMNCI-H16725122Single report
241TCCTGCSerCysSMNCI-H187361712Single report
273CGTCTTArgLeuSMNCI-H188114722Single report
273CGTCTTArgLeuSMNCI-H1882147678wt in COSMIC
213CGATGAArgStopSMNCI-H192630622wt in COSMIC
245GGCCGCGlyArgSMNCI-H1930202249Mutation in COSMIC database
147GTTGATValAspDMUNCI-H1963722wt in COSMIC
214CATCGTHisArgDMUNCI-H19636922wt in COSMIC
220TATGATTyrAspSMNCI-H202952249Mutation in COSMIC database
248CGGCAGArgGlnSMNCI-H21188322Single report
209AGATGAArgStopSMNCI-H21411422Single report
144CAGTAGGlnStopSMNCI-H2171532249Mutation in COSMIC database
157GTCTTCValPheSMNCI-H21961772249Mutation in COSMIC database
134TTTTTAPheLeuSMNCI-H23149Single report
65AGATGAArgStopSMNCI-H233092249Mutation in COSMIC database
277TGTTTTCysPheSMNCI-H250482249Mutation in COSMIC database
236TACTGCTyrCysSMNCI-H345752249Mutation in COSMIC database
282CGGGGGArgGlySMNCI-H5104822wt in COSMIC
283CGCCCCArgProSMNCI-H64352249Mutation in COSMIC database
171GAGTAGGluStopSMNCI-H692547Confirmed in three other publications
248CGGCAGArgGlnSMNCI-H7198832249Mutation in COSMIC database
342CGATGAArgStopSMNCI-H7747422Confirmed in another publication
242TGCTCCCysSerSMNCI-H841191382Single report
242TGCTCCCysSerSMNCI-H8891917Confirmed in another publication
298GAGTAGGluStopSMNCI-N41771106Single report
298GAGTAGGluStopSMRERF-LCMA71364Confirmed in another publication
120AAGTAGLysStopSMSBC-122249Mutation in COSMIC database
248CGGCTGArgLeuSMSBC-5124364Confirmed in another publication. wt in COSMIC
278CCTCGTProArgSMSCLC-21H392249Mutation in COSMIC database
85CCTdel1ProFs.SMSK-LC-211976Single report
259GACGTCAspValSMU-1690212021Single report
248CGGCTGArgLeuSMU-19061242021Single report


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