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Mutations List

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1-20 of 132
EGFR Mutation

A127del

Exon

3

Description

Deletion - Unknown

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Alternative Nomenclature

A127del, p.A127del, Ala127del, 3pDel127

EGFR Mutation

A289V

Exon

7

Description

Substitution - Missense

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Alternative Nomenclature

A289V, p.A289V, Ala289Val, c.866C>T

EGFR Mutation

A702S

Exon

18

Description

Substitution - Missense

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Alternative Nomenclature

A702S, p.A702S, Ala702Ser, c.2104G>T

EGFR Mutation

A750V

Exon

18

Description

Substitution - Missense

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Alternative Nomenclature

A750V, p.A750V, Ala750Val, c.2249C>T

EGFR Mutation

A763_V765dup

Exon

20

Description

Duplication - Unknown

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Alternative Nomenclature

A763_V765dup, p.A763_V765dup, Ala763_Val765dup, A763-V765 duplication in EGFR Exon 20

EGFR Mutation

A763_Y764insFQEA

Exon

20

Description

Insertion - In frame

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Alternative Nomenclature

A763_Y764insFQEA, Ala763_Tyr764dup

EGFR Mutation

A767_S768insSVA

Exon

20

Description

Insertion - In frame

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Alternative Nomenclature

A767_S768insSVA, p.A767_S768insSVA, Ala767_Ser768insSerValAla

EGFR Mutation

A767insASVD

Exon

20

Description

Complex - insertion inframe

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Alternative Nomenclature

A767insASVD, p.A767insASVD, Ala767insAlaSerValAsp

EGFR Mutation

A864T

Exon

21

Description

Substitution - Missense

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Alternative Nomenclature

A864T, p.A864T, Ala864Thr, c.2590G>A

EGFR Mutation

activating mutation in KRAS Exon 9

Exon

9

Description

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Alternative Nomenclature

activating mutation in KRAS Exon 9

EGFR Mutation

CDK4 amplification

Exon

Description

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Alternative Nomenclature

CDK4 amplification

EGFR Mutation

D770_N771

Exon

20

Description

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Alternative Nomenclature

D770_N771

EGFR Mutation

D770_N771insGL

Exon

20

Description

Insertion - In frame

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Alternative Nomenclature

D770_N771insGL, p.D770_N771insGL, c.2310_2311insGGGTTA

EGFR Mutation

D770ins

Exon

20

Description

Insertion - Unknown

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Alternative Nomenclature

D770ins, p.D770Ins, Asp770Ins

EGFR Mutation

Del19

Exon

19

Description

Deletion - In frame

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Alternative Nomenclature

Del19, c.(2185_2283)del?, c.2238_2248>GC, c.2235_2249del15, p.(729_761)del?, p.L747_A750>P, p.E746_A750delELREA, p.T751_I759del

EGFR Mutation

delE709_T710insD

Exon

18

Description

Complex - deletion inframe

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Alternative Nomenclature

delE709_T710insD, p.E709_T710>D, Glu709_Thr710>Asp, c.2127_2129delAAC, E709_T710>D

EGFR Mutation

E709_710del

Exon

18

Description

Deletion - In frame

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Alternative Nomenclature

E709_710del, p.E709_710del, Glu709_710del, Exon 18 2127-2130 deletion

EGFR Mutation

E709A

Exon

18

Description

Substitution - Missense

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Alternative Nomenclature

E709A, p.E709A, Glu709Ala, c.2126A>C

EGFR Mutation

E709A

Exon

18

Description

Substitution - Missense

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Alternative Nomenclature

E709A, p.E709A, Glu709Ala, c.2126A>C

EGFR Mutation

E709F

Exon

18

Description

Substitution - Missense

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Alternative Nomenclature

E709F, p.E709F, Glu709Phe, c.2126F>C

1-20 of 132