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Mutations List

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41-60 of 160
EGFR Mutation

Exon19 (complex)

Exon

19

Description

Complex - Unknown

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Alternative Nomenclature

Exon19 (complex)

EGFR Mutation

Exon19DelIns

Exon

19

Description

Complex - Deletion/Insertion

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Alternative Nomenclature

Exon19DelIns, Delinsexon19, delins19

EGFR Mutation

Exon19Dup

Exon

19

Description

Complex - Duplication

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Alternative Nomenclature

Exon19Dup, Dupl exon 19

EGFR Mutation

Exon19Ins

Exon

19

Description

Complex - Insertion

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Alternative Nomenclature

Exon19Ins, Exon 19 insertion

EGFR Mutation

Exon19Mut

Exon

19

Description

Substitution - Missense

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Alternative Nomenclature

Exon19Mut, Point mutation in Exon 19

EGFR Mutation

Exon20Amp

Exon

20

Description

Amplification - Unknown

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Alternative Nomenclature

Exon20Amp, c.(2314_2319)

EGFR Mutation

Exon20Del

Exon

20

Description

Deletion - Unknown

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Alternative Nomenclature

Exon20Del, Deletion Exon 20, delexon20

EGFR Mutation

Exon20Dup

Exon

20

Description

Duplication - Unknown

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Alternative Nomenclature

Exon20Dup, Duplication in Exon 20

EGFR Mutation

Exon20Ins

Exon

20

Description

Complex - insertion inframe

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Alternative Nomenclature

Exon20Ins, Exon20, Insertion in Exon 20, Ins20

EGFR Mutation

Exon20Mut

Exon

20

Description

Substitution - Missense

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Alternative Nomenclature

Exon20Mut, Missense mutation in Exon20

EGFR Mutation

Exon21Del

Exon

21

Description

Deletion - Unknown

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Alternative Nomenclature

Exon21Del

EGFR Mutation

Exon21Ins

Exon

21

Description

Insertion - Unknown

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Alternative Nomenclature

Exon21Ins

EGFR Mutation

Exon21Mut

Exon

21

Description

Substitution - Missense

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Alternative Nomenclature

Exon21Mut, Missense mutation in Exon 21

EGFR Mutation

F723I

Exon

18

Description

Substitution - Missense

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Alternative Nomenclature

F723I, p.F723I, Phe723Ile, c.2167T>A

EGFR Mutation

G466R (BRAF)

Exon

11

Description

Substitution - Missense

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Alternative Nomenclature

G466R (BRAF), p.G466R (BRAF), Gly466Arg (BRAF), c.1396G>C (BRAF)

EGFR Mutation

G709T

Exon

18

Description

Substitution - Missense

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Alternative Nomenclature

G709T, p.G709T, Gly709Thr

EGFR Mutation

G716X

Exon

18

Description

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Alternative Nomenclature

G716X

EGFR Mutation

G719A

Exon

18

Description

Substitution - Missense

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Alternative Nomenclature

G719A, p.G719A, Gly719Ala, c.2156G>C, G719X, p.G719X, Gly719X

EGFR Mutation

G719C

Exon

18

Description

Substitution - Missense

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Alternative Nomenclature

G719C, p.G719C, Gly719Cys, c.2155G>T, G719X, p.G719X, Gly719X

EGFR Mutation

G719D

Exon

18

Description

Substitution - Missense

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Alternative Nomenclature

G719D, p.G719D, Gly719Asp, c.2156G>A, Gly719X, G719X, p.G719X

41-60 of 160