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. 1999 Jun 22;96(13):7382–7387. doi: 10.1073/pnas.96.13.7382

Table 2.

p53 gene mutations detected by the GeneChip p53 assay and not detected by dideoxynucleotide sequencing

Sample p53 gene mutation* p53 GeneChip score Confirmed
Mutation missed on first sequencing (gel-reader error)
 778 g → t, intron 8 14 ND
 901 GAG  → TAG at 294 23 Yes
 938 CAG  → TAG at 165 14 ND
 971 a → g, intron 6 32 Yes
 1,105 CGA  → TGA at 213 15 Yes
 1,133 TGT  → TTT at 277 17 ND
Mutation not visible on first sequencing gel but present on repeat gel
 847 ATC  → TTC at 195 24/20 Yes
 1174 GCC  → CCC at 159 17/17 Yes
Mutation not visible on first or on repeat sequencing gels
 864 CCT  → CTT at 190 26/24 Yes
 1,049 ACC  → ATC at 253 15/12 Yes
 1,052 TAT  → TGT at 220 13/17 Yes
 1,113 GAC  → GTC at 208 14/13 Yes
Mutation outside of conserved regions evaluated (not by  dideoxynucleotide sequencing)
 1,011 GAG  → TAG at 339 15 Yes
 1,102 GGG  → TGG at 334 32 Yes
Mutation present in intron 8 and not included on sequencing gel
 1,023 a → t, intron 8 31 ND
Mutation not present on sequencing gel or on repeat GeneChip  analysis
 1,318 GGC  → GGT at 154 13/0 ND
*

p53 mutation gene mutation at given codon determined by the GeneChip p53 assay. 

Samples 847, 864, 1,049, 1,052, 1,113, 1,174, and 1,318 were analyzed twice from two different PCR amplifications. 

Mutation confirmed by hybridization of mutant specific oligonucleotide probe to tumor DNA and not to normal DNA. ND, not done.