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. 2005 Jul 26;93(3):355–363. doi: 10.1038/sj.bjc.6602707

Table 3. Types of EGFR gene mutations found in this study.

Exon Type of sequence Alteration Nucleotide alteration Amino-acid alteration No. of cases
18   Substitution 2156G>C G719A 1
    Substitution 2159C>T S720F 1
 
19 Type 1        
   1a Deletion 2235–2249delGGAATTAAGAGAAGC E746-A750del 14
   1b Deletion 2236–2250delGAATTAAGAGAAGCA E746-A750del 8
   1c Deletion+ 2235–2249delGGAATTAAGAGAAGC E746-A750del 1
    Substitution 2251A>G T751A  
   1d Deletion+ 2235–2236delGC E746-A750del 1
    Substitution 2242–2248delAGAGAAG ins I and P  
      2241A>C    
   1e Deletion 2235–2236delGC E746-T751del 2
      2239–2252delTAAGAGAAGCAAC ins I  
   1f Deletion+ 2235–2236delGC E746-T751del 1
    Substitution 2242–2251delAGAGAAGCAA ins I and P  
      2241A>C    
   1g Deletion+ 2237–2254delAATTAAGAGAAGCAACAT E746-S752del 1
    Substitution 2255C>T ins V  
  Type 2        
   2a Deletion+ 2240–2248delTAAGAGAAG L747-A750 1
    Substitution 2239T>C insP  
   2b Deletion+ 2240–2251delTAAGAGAAGCAA L747-T751del 2
    Substitution 2239T>C ins S  
   2c Deletion 2239–2253delTTAAGAGAAGCAACA L747-T751del 1
   2d Deletion 2239–2256delTTAAGAGAAGCAACATCT L747-S752del 1
   2e Deletion 2240–2257delTAAGAGAAGCAACATCTC L747-P753del 1
        ins S  
 
20   Insertion+ 2308ins/dup(CCAGCGTGG) ins779(ASV) 1
    Substitution 2310C>T, 2315C>G P782R  
    Insertion+ 2311ins/dup(GCGTGGACA) ins780(SVD) 1
    Substitution 2315C>G P782R  
 
21   Substitution 2573T>G L858R 20
    Substitution 2572–2573CT>AG L858R 1
    Substitution 2573–2574TG>GT L858R 1