(Q28370983)

English

ERBB2 R896C

genetic variant

R896C
ARG896CYS
R866C
R881C
RS758222990

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/43

human chromosome 17

genomic assembly

Genome assembly GRCh37

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/43

37881616

genomic assembly

Genome assembly GRCh37

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/43

37881616

genomic assembly

Genome assembly GRCh37

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/43

biological variant of

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/43

positive therapeutic predictor for

medical condition treated

determination method

CIViC evidence level D

CIViC 5-star trust rating

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/evidence/287

Activating HER2 mutations in HER2 gene amplification negative breast cancer

Identifiers

CIViC variant ID

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/43

dbSNP Reference SNP number

1 reference

HGVS nomenclature

NC_000017.10:g.37881616C>T

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/43

ENST00000269571.5:c.2686C>T

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/43

NM_004448.3:c.2686C>T

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/43

NP_004439.2:p.Arg896Cys

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/43

Sitelinks

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