Missing content? – Request curation!
Request curation for specific Genes, Variants, or PubMed publications.
Have questions, comments, or suggestions? - Let us know!
Email us at : ckbsupport@genomenon.com
Gene | JAK2 |
Variant | G614fs |
Impact List | frameshift |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | JAK2 G614fs results in a change in the amino acid sequence of the Jak2 protein beginning at aa 614 of 1132, likely resulting in premature truncation of the functional protein (UniProt.org). Due to the loss of most of protein kinase domain 1 and all of protein kinase domain 2 (UniProt.org), G614fs is predicted to lead to a loss of Jak2 protein function. |
Associated Drug Resistance | |
Category Variants Paths |
JAK2 mutant JAK2 inact mut JAK2 G614fs |
Transcript | NM_004972.4 |
gDNA | chr9:g.(5073760_5073761) |
cDNA | c.(1840_1839) |
Protein | p.G614fs |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_004972.3 | chr9:g.(5073760_5073761) | c.(1840_1839) | p.G614fs | RefSeq | GRCh38/hg38 |
NM_001322195 | chr9:g.(5073760_5073761) | c.(1840_1839) | p.G614fs | RefSeq | GRCh38/hg38 |
NM_001322194 | chr9:g.(5073760_5073761) | c.(1840_1839) | p.G614fs | RefSeq | GRCh38/hg38 |
NM_001322194.2 | chr9:g.(5073760_5073761) | c.(1840_1839) | p.G614fs | RefSeq | GRCh38/hg38 |
NM_001322196.2 | chr9:g.(5073760_5073761) | c.(1840_1839) | p.G614fs | RefSeq | GRCh38/hg38 |
NM_004972.4 | chr9:g.(5073760_5073761) | c.(1840_1839) | p.G614fs | RefSeq | GRCh38/hg38 |
NM_004972 | chr9:g.(5073760_5073761) | c.(1840_1839) | p.G614fs | RefSeq | GRCh38/hg38 |
NM_001322194.1 | chr9:g.(5073760_5073761) | c.(1840_1839) | p.G614fs | RefSeq | GRCh38/hg38 |
NM_001322195.1 | chr9:g.(5073760_5073761) | c.(1840_1839) | p.G614fs | RefSeq | GRCh38/hg38 |
NM_001322196.1 | chr9:g.(5073760_5073761) | c.(1840_1839) | p.G614fs | RefSeq | GRCh38/hg38 |
NM_001322196 | chr9:g.(5073760_5073761) | c.(1840_1839) | p.G614fs | RefSeq | GRCh38/hg38 |
NM_001322195.2 | chr9:g.(5073760_5073761) | c.(1840_1839) | p.G614fs | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
---|