(Q32965809)

English

VHL W117C (c.351G>T)

genetic variant

W117C (c.351G>T)
C.351G>T
TRP117CYS
RS727504215

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No label defined

No description defined

Statements

missense mutation

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1767

human chromosome 3

genomic assembly

Genome assembly GRCh37

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1767

10188208

genomic assembly

Genome assembly GRCh37

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1767

10188208

genomic assembly

Genome assembly GRCh37

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1767

biological variant of

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1767

Identifiers

CIViC variant ID

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1767

dbSNP Reference SNP number

1 reference

HGVS nomenclature

NM_000551.3:c.351G>T

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1767

NP_000542.1:p.Trp117Cys

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1767

NC_000003.11:g.10188208G>T

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1767

ENST00000256474.2:c.351G>T

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1767

Sitelinks

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