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Mutations List
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View amino acid codes here.

Mutations List

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181-200 of 210
EGFR Mutation

T710_714Ins

Exon

18

Description

Insertion - In frame

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Alternative Nomenclature

T710_714Ins, p.T710_714ins, Thr710_714ins, Exon 18 2130-2141 insertion, T710_714

EGFR Mutation

T710S

Exon

Description

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Alternative Nomenclature

T710S

EGFR Mutation

T719X

Exon

18

Description

Substitution - Missense

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Alternative Nomenclature

T719X, p.T719X, Thr719X

EGFR Mutation

T725M

Exon

18

Description

Substitution - Missense

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Alternative Nomenclature

T725M, p.T725M, Thr725Met, c.2174C>T

EGFR Mutation

T751_I759delinsS

Exon

19

Description

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Alternative Nomenclature

T751_I759delinsS, p.T751_I759delinsS, Thr751_Ile759delinsSer

EGFR Mutation

T785A

Exon

20

Description

Substitution - Missense

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Alternative Nomenclature

T785A, p.T785A, Thr785Ala, c.2353A>G

EGFR Mutation

T790M

Exon

20

Description

Substitution - Missense

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Alternative Nomenclature

T790M, p.T790M, Thr790Met, c.2369C>T

EGFR Mutation

T854A

Exon

21

Description

Substitution - Missense

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Alternative Nomenclature

T854A, p.T854A, Thr854Ala, c.2560A>G

EGFR Mutation

tp53

Exon

Description

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Alternative Nomenclature

tp53

EGFR Mutation

V1010M

Exon

Description

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Alternative Nomenclature

V1010M, p.V1010M, Val1010Met

EGFR Mutation

V600E

Exon

Description

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Alternative Nomenclature

V600E, p.V600E, Val600Glu

EGFR Mutation

V659D

Exon

Description

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Alternative Nomenclature

V659D

EGFR Mutation

V717A

Exon

18

Description

Substitution - Missense

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Alternative Nomenclature

V717A, p.V717A, Val717Ala, c.2150T>C

EGFR Mutation

V726M

Exon

18

Description

Substitution - Missense

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Alternative Nomenclature

V726M, p.V726M, Val726Met, c.2176G>A

EGFR Mutation

V765L

Exon

20

Description

Substitution - Missense

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Alternative Nomenclature

V765L, p.V765L, Ser695Ile, c.2293G>T

EGFR Mutation

V765M

Exon

20

Description

Substitution - Missense

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Alternative Nomenclature

V765M, p.V765M, Val765Met, c.2293G>A

EGFR Mutation

V769_D770

Exon

20

Description

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Alternative Nomenclature

V769_D770

EGFR Mutation

V769_D770ins

Exon

20

Description

Insertion - Unknown

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Alternative Nomenclature

V769_D770ins

EGFR Mutation

V769_D770insASV

Exon

20

Description

Insertion - In frame

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Alternative Nomenclature

V769_D770insASV, p.V769_D770insASV, Val769_Asp770insAlaSerVal, c.2296_2297insTGGCCAGCG, c.2303_2304insTGTGGCCAG, c.2307_2308insGCCAGCGTG, c.2308_2309insCCAGCGTGG, c.2309_2310AC>CCAGCGTGGAT

EGFR Mutation

V769_D770insGSV

Exon

20

Description

Insertion - In frame

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Alternative Nomenclature

V769_D770insGSV, p.V769_D770insGSV, Val769_Asp770insGlySerVal, c.2308_2309insGCAGCGTGG

181-200 of 210