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 | FGFR2 |
Variant | M584V |
Impact List | missense |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | FGFR2 M584V lies within the protein kinase domain of the Fgfr2 protein (UniProt.org). M584V results in decreased Erk phosphorylation in cell culture (PMID: 38561822), and therefore is predicted to lead to a loss of Fgfr2 protein function. |
Associated Drug Resistance | |
Category Variants Paths |
FGFR2 mutant FGFR2 inact mut FGFR2 M584V |
Transcript | NM_000141.5 |
gDNA | chr10:g.121496645T>C |
cDNA | c.1750A>G |
Protein | p.M584V |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_000141 | chr10:g.121496645T>C | c.1750A>G | p.M584V | RefSeq | GRCh38/hg38 |
NM_000141.5 | chr10:g.121496645T>C | c.1750A>G | p.M584V | RefSeq | GRCh38/hg38 |
NM_000141.4 | chr10:g.121496645T>C | c.1750A>G | p.M584V | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
---|