(Q32965787)

English

VHL W88R (c.262T>A)

genetic variant

W88R (c.262T>A)
TRP88ARG
C.262T>A
RS1553619431

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No label defined

No description defined

Statements

missense mutation

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/1761

human chromosome 3

genomic assembly

Genome assembly GRCh37

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/1761

10183793

genomic assembly

Genome assembly GRCh37

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/1761

10183793

genomic assembly

Genome assembly GRCh37

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/1761

biological variant of

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/1761

Identifiers

CIViC variant ID

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/1761

dbSNP Reference SNP number

1 reference

HGVS nomenclature

ENST00000256474.2:c.262T>A

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/1761

NP_000542.1:p.Trp88Arg

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/1761

NC_000003.11:g.10183793T>A

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/1761

NM_000551.3:c.262T>A

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/1761

Sitelinks

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