(Q28423327)

English

CDKN2A RS3814960

genetic variant

RS3814960

In more languages

Statements

5 Prime UTR Exon Variant

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/641

human chromosome 9

genomic assembly

Genome assembly GRCh37

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/641

21975017

genomic assembly

Genome assembly GRCh37

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/641

21975017

genomic assembly

Genome assembly GRCh37

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/641

biological variant of

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/641

negative prognostic predictor for

esophagus squamous cell carcinoma

determination method

CIViC evidence level B

CIViC 3-star trust rating

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/evidence/1635

Genetic Variants in the p14ARF/MDM2/TP53 Pathway Are Associated with the Prognosis of Esophageal Squamous Cell Carcinoma Patients Treated with Radical Resection

Identifiers

CIViC variant ID

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/641

dbSNP Reference SNP number

1 reference

HGVS nomenclature

NC_000009.11:g.21975017C>T

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/641

NM_000077.4:c.-191G>A

1 reference

23 May 2022

https://civic.genome.wustl.edu/links/variants/641

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