10.1.1 Mutación detectada en EGFR
G
E
M
EN
XÓN
UTACIÓN
EGFR
Deleción 21
Deleción 24
20
T790M
S768I
InsG
InsASV(9)
InsASV(11)
InsSVD
InsH
21
L858R
L861Q
C
AMBIO PROTEICO
p.Glu746_Ser752delinsAla
p.Glu746_Ser752delinsAsp
p.Glu746_Pro753delinsValSer
p.Glu746_Ser752delinsIle
p.Glu746_Ser752delinsVal
p.Leu747_Pro753del
p.Glu746_Ser752del
p.Ser752_Ile759del
p.Thr790Met
p.Ser768Ile
p.Asp770_Asn771insGly
p.Val769_Asp770insAlaSerVal
p.Val769_Asp770insAlaSerVal
p.Asp770_Asn771insSerValAsp c.2311_2312insGCGTGGACA
p.His773_Val774insHis
p.Leu858Arg
p.Leu861Gln
-22-
C
AMBIO NUCLEOTÍDICO
c.2237_2254del
c.2238_2255del
c.2237_2257delinsTCT
c.2236_2255delinsAT
c.2236_2256delinsATC
c.2237_2256delinsTT
c.2237_2256delinsTC
c.2235_2255delinsGGT
c.2238_2258del
c.2236_2256del
c.2253_2276del
c.2369C>T
c.2303G>T
c.2310_2311insGGT
c.2307_2308insGCCAGCGTG
c.2309_2310delinsCCAGCGTGGAT
c.2319_2320insCAC
c.2573T>G
c.2573_2574delinsGT
c.2573_2574delinsGA
c.2582T>A
EGFR
L
LAMADA
GENÉTICA
T790M
S768I
Inserción
de exón
20
L858R
L861Q