(Q32965999)

English

VHL V166F (c.496G>T)

genetic variant

V166F (c.496G>T)
C.496G>T
VAL166PHE
RS104893825

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No description defined

Statements

missense mutation

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1825

human chromosome 3

genomic assembly

Genome assembly GRCh37

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1825

10191503

genomic assembly

Genome assembly GRCh37

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1825

10191503

genomic assembly

Genome assembly GRCh37

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1825

biological variant of

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1825

Identifiers

CIViC variant ID

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1825

dbSNP Reference SNP number

1 reference

HGVS nomenclature

NM_000551.3:c.496G>T

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1825

NP_000542.1:p.Val166Phe

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1825

NC_000003.11:g.10191503G>T

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1825

ENST00000256474.2:c.496G>T

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/1825

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