(Q29938353)

English

ATM T2666A

genetic variant

T2666A

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No label defined

No description defined

Statements

missense mutation

1 reference

22 January 2022

https://civic.genome.wustl.edu/links/variants/901

human chromosome 11

genomic assembly

Genome assembly GRCh37

1 reference

22 January 2022

https://civic.genome.wustl.edu/links/variants/901

108204681

genomic assembly

Genome assembly GRCh37

1 reference

22 January 2022

https://civic.genome.wustl.edu/links/variants/901

108204681

genomic assembly

Genome assembly GRCh37

1 reference

22 January 2022

https://civic.genome.wustl.edu/links/variants/901

biological variant of

1 reference

22 January 2022

https://civic.genome.wustl.edu/links/variants/901

negative therapeutic predictor for

determination method or standard

CIViC evidence level D

CIViC 3-star trust rating

medical condition treated

chronic lymphocytic leukemia

1 reference

22 January 2022

https://civic.genome.wustl.edu/links/evidence/2221

ATM mutations uniformly lead to ATM dysfunction in chronic lymphocytic leukemia: application of functional test using doxorubicin.

Identifiers

CIViC variant ID

1 reference

22 January 2022

https://civic.genome.wustl.edu/links/variants/901

dbSNP Reference SNP number

1 reference

HGVS nomenclature

NC_000011.9:g.108204681A>G

1 reference

22 January 2022

https://civic.genome.wustl.edu/links/variants/901

Sitelinks

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