(Q50092413)

English

BRAF N581S

genetic variant

N581S
N189S
N9S
RS121913370

In more languages

default values for all languages

No label defined

No description defined

Statements

missense mutation

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1186

human chromosome 7

genomic assembly

Genome assembly GRCh37

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1186

140453193

genomic assembly

Genome assembly GRCh37

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1186

140453193

genomic assembly

Genome assembly GRCh37

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1186

biological variant of

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1186

positive therapeutic predictor for

medical condition treated

statement disputed by

Targeted Therapy for Advanced Solid Tumors on the Basis of Molecular Profiles: Results From MyPathway, an Open-Label, Phase IIa Multiple Basket Study

determination method

CIViC evidence level C

CIViC 2-star trust rating

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/evidence/5967

Targeted Therapy for Advanced Solid Tumors on the Basis of Molecular Profiles: Results From MyPathway, an Open-Label, Phase IIa Multiple Basket Study

Identifiers

CIViC variant ID

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1186

dbSNP Reference SNP number

1 reference

Sitelinks

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Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

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Multilingual sites(0 entries)

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