Mutations List
View amino acid codes here.
Mutations List
Please return to Search Results/Clinical Outcomes page to search for individual patient results.
201-210 of 210
EGFR Mutation
V769_D770insGVV
Exon
20
Description
Insertion - In frame
Alternative Nomenclature
V769_D770insGVV, p.V769_D770insGVV, c.2308_2309insGGGTCGTGG
EGFR Mutation
V769_D770insV
Exon
20
Description
Insertion - Unknown
Alternative Nomenclature
V769_D770insV
EGFR Mutation
V769delinsDGQL
Exon
20
Description
Insertion - In frame
Alternative Nomenclature
V769delinsDGQL, p.V769delinsDGQL, Val769delinsAspGlyGlnLeu, c.2305_2306insATGGACAGC
EGFR Mutation
V769I
Exon
20
Description
Substitution - Missense
Alternative Nomenclature
V769I, p.V769I, Val769Ile
EGFR Mutation
V769L
Exon
20
Description
Substitution - Missense
Alternative Nomenclature
V769L, p.V769L, Val769Leu, c.2305G>T
EGFR Mutation
V769M
Exon
20
Description
Substitution - Missense
Alternative Nomenclature
V769M, p.V769M, Val769Met, c.2305G>A
EGFR Mutation
V774M
Exon
20
Description
Substitution - Missense
Alternative Nomenclature
V774M, p.V774M, Val774Met, c.2320G>A
EGFR Mutation
V786M
Exon
20
Description
Substitution - Missense
Alternative Nomenclature
V786M, p.V786M, Val786Met, c.2356G>A
EGFR Mutation
V834L
Exon
21
Description
Substitution - Missense
Alternative Nomenclature
V834L, p.V834L, Val834Leu, c.2500G>T
EGFR Mutation
Y891D
Exon
22
Description
Substitution - Missense
Alternative Nomenclature
Y891D, p.Y891D, Tyr891Asp, c.2671Y>D
