(Q32966075)

English

VHL P86R (c.257C>G)

genetic variant

P86R (c.257C>G)
PRO86ARG
C.257C>G
RS730882034

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No description defined

Statements

missense mutation

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1849

human chromosome 3

genomic assembly

Genome assembly GRCh37

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1849

10183788

genomic assembly

Genome assembly GRCh37

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1849

10183788

genomic assembly

Genome assembly GRCh37

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1849

biological variant of

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1849

Identifiers

CIViC variant ID

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1849

dbSNP Reference SNP number

1 reference

HGVS nomenclature

NM_000551.3:c.257C>G

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1849

NP_000542.1:p.Pro86Arg

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1849

NC_000003.11:g.10183788C>G

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1849

ENST00000256474.2:c.257C>G

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1849

Sitelinks

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