(Q44847114)

English

EGFR V774M

genetic variant

V774M
VAL774MET

In more languages

default for all languages

No label defined

No description defined

Statements

missense mutation

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1894

human chromosome 7

genomic assembly

Genome assembly GRCh37

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1894

55249022

genomic assembly

Genome assembly GRCh37

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1894

55249022

genomic assembly

Genome assembly GRCh37

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1894

biological variant of

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1894

positive therapeutic predictor for

medical condition treated

non-small-cell lung carcinoma

statement disputed by

Effectiveness of tyrosine kinase inhibitors on "uncommon" epidermal growth factor receptor mutations of unknown clinical significance in non-small cell lung cancer.

determination method or standard

CIViC evidence level C

CIViC 2-star trust rating

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/evidence/4231

Effectiveness of tyrosine kinase inhibitors on "uncommon" epidermal growth factor receptor mutations of unknown clinical significance in non-small cell lung cancer.

Identifiers

CIViC variant ID

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1894

dbSNP Reference SNP number

1 reference

HGVS nomenclature

ENST00000275493.2:c.2320G>A

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1894

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