(Q29938265)

English

VHL N7D (c.19A>G)

genetic variant

N7D (c.19A>G)
ASN7ASP
C.19A>G
RS1311403806

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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/849

human chromosome 3

genomic assembly

Genome assembly GRCh37

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/849

10183550

genomic assembly

Genome assembly GRCh37

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/849

10183550

genomic assembly

Genome assembly GRCh37

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/849

biological variant of

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/849

Identifiers

CIViC variant ID

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/849

dbSNP Reference SNP number

1 reference

HGVS nomenclature

NC_000003.11:g.10183550A>G

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/849

NM_000551.3:c.19A>G

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/849

ENST00000256474.2:c.19A>G

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/849

NP_000542.1:c.Asn7Asp

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/849

Sitelinks

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