(Q28532458)

English

ASXL1 EXON 12 MUTATION

genetic variant

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Statements

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/557

human chromosome 20

genomic assembly

Genome assembly GRCh37

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/557

31021087

genomic assembly

Genome assembly GRCh37

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/557

31021720

genomic assembly

Genome assembly GRCh37

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/557

biological variant of

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/557

negative prognostic predictor for

acute myeloid leukemia

determination method

CIViC evidence level B

CIViC 4-star trust rating

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/evidence/1379

ASXL1 exon 12 mutations are frequent in AML with intermediate risk karyotype and are independently associated with an adverse outcome

Identifiers

CIViC variant ID

1 reference

28 March 2022

https://civic.genome.wustl.edu/links/variants/557

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