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Gene | FGFR2 |
Variant | R165W |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | FGFR2 R165W lies within Ig-like C2-type domain 2 of the Fgfr2 protein (UniProt.org). R165W has been identified in sequencing studies (PMID: 27147599), 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 exon5 FGFR2 R165W |
Transcript | NM_000141.5 |
gDNA | chr10:g.121551421G>A |
cDNA | c.493C>T |
Protein | p.R165W |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001320658.1 | chr10:g.121551421G>A | c.493C>T | p.R165W | RefSeq | GRCh38/hg38 |
NM_001144913.1 | chr10:g.121551421G>A | c.493C>T | p.R165W | RefSeq | GRCh38/hg38 |
NM_022970.4 | chr10:g.121551421G>A | c.493C>T | p.R165W | RefSeq | GRCh38/hg38 |
NM_000141 | chr10:g.121551421G>A | c.493C>T | p.R165W | RefSeq | GRCh38/hg38 |
NM_022970 | chr10:g.121551421G>A | c.493C>T | p.R165W | RefSeq | GRCh38/hg38 |
NM_000141.4 | chr10:g.121551421G>A | c.493C>T | p.R165W | RefSeq | GRCh38/hg38 |
NM_001144917 | chr10:g.121551421G>A | c.493C>T | p.R165W | RefSeq | GRCh38/hg38 |
NM_001144914 | chr10:g.121551421G>A | c.493C>T | p.R165W | RefSeq | GRCh38/hg38 |
NM_001144917.2 | chr10:g.121551421G>A | c.493C>T | p.R165W | RefSeq | GRCh38/hg38 |
NM_001144913.1 | chr10:g.121551421G>A | c.493C>T | p.R165W | RefSeq | GRCh38/hg38 |
NM_001144914.1 | chr10:g.121551421G>A | c.493C>T | p.R165W | RefSeq | GRCh38/hg38 |
NM_000141.5 | chr10:g.121551421G>A | c.493C>T | p.R165W | RefSeq | GRCh38/hg38 |
NM_022970.3 | chr10:g.121551421G>A | c.493C>T | p.R165W | RefSeq | GRCh38/hg38 |
NM_001144914.1 | chr10:g.121551421G>A | c.493C>T | p.R165W | RefSeq | GRCh38/hg38 |
NM_001144917.1 | chr10:g.121551421G>A | c.493C>T | p.R165W | RefSeq | GRCh38/hg38 |
NM_001320658 | chr10:g.121551421G>A | c.493C>T | p.R165W | RefSeq | GRCh38/hg38 |
NM_001144913 | chr10:g.121551421G>A | c.493C>T | p.R165W | RefSeq | GRCh38/hg38 |
NM_001320658.2 | chr10:g.121551421G>A | c.493C>T | p.R165W | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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