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BRINP3
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BRINP3 any mutation
GeneBRINP3
Variantany
Transcript ID (GRCh37/hg19)ENST00000367462
Germline/Somatic?Somatic
Pertinent Negative In
Tumor TypePrimary Site
See All Pertinent Negatives

Interpretations

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BRINP3
Variants
BRINP3 any mutation
Primary Sites
Blood
Bone Marrow
Tumor Types
Acute Myeloid Leukemia
Acute Leukemia of Unspecified Cell Type
Anemia, Unspecified
Cytopenia
Leukocytosis
Leukopenia
Monocytosis
Other Acute Leukemia
Thrombocytopenia, Unspecified
Interpretation

BRINP3(FAM5C) has been reported to be mutated in <10% of some types of AML.

Last updated: 2018-11-12 20:40:58 UTC
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Disclaimer: You assume full responsibility for all risks associated with using this PMKB website. The Englander Institute for Precision Medicine at Weill Cornell Medicine makes no guarantee of the comprehensiveness, reliability or accuracy of the information on this website and assumes no responsibility for errors in the information associated with this web site. Healthcare providers and patients must integrate all clinical and laboratory findings as well as information from a variety of sources before deciding on appropriate clinical care options.

When using PMKB, please cite: Huang et al., JAMIA 2017

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