(Q32965724)

English

VHL F119L (c.357C>G)

genetic variant

F119L (c.357C>G)
C.357C>G
PHE119LEU
RS1559428077

In more languages

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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/1743

human chromosome 3

genomic assembly

Genome assembly GRCh37

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/1743

10188214

genomic assembly

Genome assembly GRCh37

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/1743

10188214

genomic assembly

Genome assembly GRCh37

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/1743

biological variant of

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/1743

Identifiers

CIViC variant ID

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/1743

dbSNP Reference SNP number

1 reference

HGVS nomenclature

ENST00000256474.2:c.357C>G

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/1743

NC_000003.11:g.10188214C>G

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/1743

NM_000551.3:c.357C>G

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/1743

NP_000542.1:p.Phe119Leu

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/1743

Sitelinks

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