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Gene JAK2
Variant S797C
Impact List missense
Protein Effect unknown
Gene Variant Descriptions JAK2 S797C lies within protein kinase domain 1 of the Jak2 protein (UniProt.org). S797C has been identified in sequencing studies (PMID: 30811597, PMID: 30337359), but has not been biochemically characterized and therefore, its effect on Jak2 protein function is unknown (PubMed, Mar 2024).
Associated Drug Resistance
Category Variants Paths

JAK2 mutant JAK2 S797C

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Transcript NM_004972.4
gDNA chr9:g.5080639C>G
cDNA c.2390C>G
Protein p.S797C
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001322196 chr9:g.5080639C>G c.2390C>G p.S797C RefSeq GRCh38/hg38
NM_001322195.2 chr9:g.5080639C>G c.2390C>G p.S797C RefSeq GRCh38/hg38
NM_001322196.2 chr9:g.5080639C>G c.2390C>G p.S797C RefSeq GRCh38/hg38
NM_004972.4 chr9:g.5080639C>G c.2390C>G p.S797C RefSeq GRCh38/hg38
NM_001322194.1 chr9:g.5080639C>G c.2390C>G p.S797C RefSeq GRCh38/hg38
NM_001322195.1 chr9:g.5080639C>G c.2390C>G p.S797C RefSeq GRCh38/hg38
NM_001322196.1 chr9:g.5080639C>G c.2390C>G p.S797C RefSeq GRCh38/hg38
NM_001322195 chr9:g.5080639C>G c.2390C>G p.S797C RefSeq GRCh38/hg38
NM_001322194.2 chr9:g.5080639C>G c.2390C>G p.S797C RefSeq GRCh38/hg38
NM_004972.3 chr9:g.5080639C>G c.2390C>G p.S797C RefSeq GRCh38/hg38
NM_001322194 chr9:g.5080639C>G c.2390C>G p.S797C RefSeq GRCh38/hg38
NM_004972 chr9:g.5080639C>G c.2390C>G p.S797C RefSeq GRCh38/hg38

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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References
JAK2 mutant essential thrombocythemia not applicable N/A Guideline Diagnostic JAK2 mutations aid in the diagnosis of essential thrombocythemia (NCCN.org). detail...
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 myelofibrosis not applicable N/A Guideline Diagnostic JAK2 mutations aid in the diagnosis of primary myelofibrosis (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...