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Gene JAK2
Variant G417P
Impact List missense
Protein Effect gain of function - predicted
Gene Variant Descriptions JAK2 G417P lies within the atypical SH2 domain of the Jak2 protein (PMID: 26419724). G417P results in transformation of cells in culture (PMID: 26419724), and therefore, is predicted to lead to a gain of Jak2 protein function.
Associated Drug Resistance
Category Variants Paths

JAK2 mutant JAK2 act mut JAK2 G417P

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Transcript NM_004972.4
gDNA chr9:g.5066712_5066713delGGinsCC
cDNA c.1249_1250delGGinsCC
Protein p.G417P
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_004972 chr9:g.5066712_5066713delGGinsCC c.1249_1250delGGinsCC p.G417P RefSeq GRCh38/hg38
NM_004972.3 chr9:g.5066712_5066713delGGinsCC c.1249_1250delGGinsCC p.G417P RefSeq GRCh38/hg38
NM_001322194 chr9:g.5066712_5066713delGGinsCC c.1249_1250delGGinsCC p.G417P RefSeq GRCh38/hg38
NM_001322196 chr9:g.5066712_5066713delGGinsCC c.1249_1250delGGinsCC p.G417P RefSeq GRCh38/hg38
NM_001322195 chr9:g.5066712_5066713delGGinsCC c.1249_1250delGGinsCC p.G417P RefSeq GRCh38/hg38
NM_001322194.1 chr9:g.5066712_5066713delGGinsCC c.1249_1250delGGinsCC p.G417P RefSeq GRCh38/hg38
NM_004972.4 chr9:g.5066712_5066713delGGinsCC c.1249_1250delGGinsCC p.G417P RefSeq GRCh38/hg38
NM_001322194.2 chr9:g.5066712_5066713delGGinsCC c.1249_1250delGGinsCC p.G417P RefSeq GRCh38/hg38
NM_001322196.2 chr9:g.5066712_5066713delGGinsCC c.1249_1250delGGinsCC p.G417P RefSeq GRCh38/hg38
NM_001322195.1 chr9:g.5066712_5066713delGGinsCC c.1249_1250delGGinsCC p.G417P RefSeq GRCh38/hg38
NM_001322196.1 chr9:g.5066712_5066713delGGinsCC c.1249_1250delGGinsCC p.G417P RefSeq GRCh38/hg38
NM_001322195.2 chr9:g.5066712_5066713delGGinsCC c.1249_1250delGGinsCC p.G417P RefSeq GRCh38/hg38

Filtering

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  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

Sorting

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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References