FGFR2 R178C
Gene Variant Detail

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Gene FGFR2
Variant R178C
Impact List missense
Protein Effect unknown
Gene Variant Descriptions FGFR2 R178C lies within Ig-like C2-type domain 2 of the Fgfr2 protein (UniProt.org). R178C has not been characterized in the scientific literature and therefore, its effect on Fgfr2 protein function is unknown (PubMed, Oct 2025).
Associated Drug Resistance
Category Variants Paths

FGFR2 mutant FGFR2 exon5 FGFR2 R178C

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Transcript NM_000141.5
gDNA chr10:g.121551382G>A
cDNA c.532C>T
Protein p.R178C
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001144914.1 chr10:g.121551382G>A c.532C>T p.R178C RefSeq GRCh38/hg38
NM_001144913.1 chr10:g.121551382G>A c.532C>T p.R178C RefSeq GRCh38/hg38
NM_001144917.1 chr10:g.121551382G>A c.532C>T p.R178C RefSeq GRCh38/hg38
NM_000141.4 chr10:g.121551382G>A c.532C>T p.R178C RefSeq GRCh38/hg38
NM_001144913.1 chr10:g.121551382G>A c.532C>T p.R178C RefSeq GRCh38/hg38
NM_000141.5 chr10:g.121551382G>A c.532C>T p.R178C RefSeq GRCh38/hg38
NM_022970.3 chr10:g.121551382G>A c.532C>T p.R178C RefSeq GRCh38/hg38
NM_001144917.2 chr10:g.121551382G>A c.532C>T p.R178C RefSeq GRCh38/hg38
NM_022970.4 chr10:g.121551382G>A c.532C>T p.R178C RefSeq GRCh38/hg38
NM_001144914.1 chr10:g.121551382G>A c.532C>T p.R178C RefSeq GRCh38/hg38
NM_001320658.2 chr10:g.121551382G>A c.532C>T p.R178C RefSeq GRCh38/hg38
NM_001320658.1 chr10:g.121551382G>A c.532C>T p.R178C RefSeq GRCh38/hg38

Filtering

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Clinical Trial Phase Therapies Title Recruitment Status Covered Countries Other Countries