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 | E636K |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | FGFR2 E636K lies within the protein kinase domain of the Fgfr2 protein (UniProt.org). E636K is predicted to affect the kinase activity of Fgfr2 by structural modeling (PMID: 19147536), but has not been biochemically characterized and therefore, its effect on Fgfr2 protein function is unknown (PubMed, Nov 2024). |
Associated Drug Resistance | |
Category Variants Paths |
FGFR2 mutant FGFR2 E636K |
Transcript | NM_000141.5 |
gDNA | chr10:g.121488071C>T |
cDNA | c.1906G>A |
Protein | p.E636K |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_000141 | chr10:g.121488071C>T | c.1906G>A | p.E636K | RefSeq | GRCh38/hg38 |
NM_000141.4 | chr10:g.121488071C>T | c.1906G>A | p.E636K | RefSeq | GRCh38/hg38 |
NM_000141.5 | chr10:g.121488071C>T | c.1906G>A | p.E636K | RefSeq | GRCh38/hg38 |
XM_024447891.2 | chr10:g.121485399C>T | c.1906G>A | p.E636K | RefSeq | GRCh38/hg38 |
XM_024447891.1 | chr10:g.121485399C>T | c.1906G>A | p.E636K | RefSeq | GRCh38/hg38 |
XM_006717712 | chr10:g.121485399C>T | c.1906G>A | p.E636K | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
---|