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Gene JAK2
Variant V563I
Impact List missense
Protein Effect unknown
Gene Variant Descriptions JAK2 V563I lies within protein kinase domain 1 of the Jak2 protein (UniProt.org). V563I has not been characterized and therefore, its effect on Jak2 protein function is unknown (PubMed, Jun 2024).
Associated Drug Resistance
Category Variants Paths

JAK2 mutant JAK2 V563I

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Transcript NM_004972.4
gDNA chr9:g.5072537G>A
cDNA c.1687G>A
Protein p.V563I
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001322196.1 chr9:g.5072537G>A c.1687G>A p.V563I RefSeq GRCh38/hg38
NM_004972.4 chr9:g.5072537G>A c.1687G>A p.V563I RefSeq GRCh38/hg38
NM_001322195 chr9:g.5072537G>A c.1687G>A p.V563I RefSeq GRCh38/hg38
NM_001322195.2 chr9:g.5072537G>A c.1687G>A p.V563I RefSeq GRCh38/hg38
NM_001322195.1 chr9:g.5072537G>A c.1687G>A p.V563I RefSeq GRCh38/hg38
NM_001322194.1 chr9:g.5072537G>A c.1687G>A p.V563I RefSeq GRCh38/hg38
NM_001322194 chr9:g.5072537G>A c.1687G>A p.V563I RefSeq GRCh38/hg38
NM_001322196 chr9:g.5072537G>A c.1687G>A p.V563I RefSeq GRCh38/hg38
NM_004972.3 chr9:g.5072537G>A c.1687G>A p.V563I RefSeq GRCh38/hg38
NM_001322196.2 chr9:g.5072537G>A c.1687G>A p.V563I RefSeq GRCh38/hg38
NM_004972 chr9:g.5072537G>A c.1687G>A p.V563I RefSeq GRCh38/hg38
NM_001322194.2 chr9:g.5072537G>A c.1687G>A p.V563I RefSeq GRCh38/hg38

Filtering

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  • Separate multiple filter terms with a space. Any order may be used (i. e. a b c and c b a are equivalent )
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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References
JAK2 mutant B-cell acute lymphoblastic leukemia not applicable N/A Guideline Prognostic JAK2 mutations are associated with a poor prognosis in patients with B-cell acute lymphoblastic leukemia (NCCN.org). detail...
JAK2 mutant childhood B-cell acute lymphoblastic leukemia not applicable N/A Guideline Prognostic JAK2 mutations are associated with a poor prognosis in pediatric patients with B-cell acute lymphoblastic leukemia (NCCN.org). detail...
JAK2 mutant essential thrombocythemia not applicable N/A Guideline Diagnostic JAK2 mutations aid in the diagnosis of essential thrombocythemia (NCCN.org). detail...
JAK2 mutant myelofibrosis not applicable N/A Guideline Diagnostic JAK2 mutations aid in the diagnosis of primary myelofibrosis (NCCN.org). detail...