Gene Variant Detail

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Gene FGFR1
Variant R189H
Impact List missense
Protein Effect unknown
Gene Variant Descriptions FGFR1 R189H lies within Ig-like C2-type domain 2 of the Fgfr1 protein (UniProt.org). R189H has been identified in sequencing studies (PMID: 29106415, PMID: 30885352), but has not been biochemically characterized and therefore, its effect on Fgfr1 protein function is unknown (PubMed, Oct 2023).
Associated Drug Resistance
Category Variants Paths

FGFR1 mutant FGFR1 R189H

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Transcript NM_023110.3
gDNA chr8:g.38427976C>T
cDNA c.566G>A
Protein p.R189H
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_017013222 chr8:g.38427976C>T c.566G>A p.R189H RefSeq GRCh38/hg38
XM_017013221.1 chr8:g.38427976C>T c.566G>A p.R189H RefSeq GRCh38/hg38
XM_006716303.4 chr8:g.38427976C>T c.566G>A p.R189H RefSeq GRCh38/hg38
NM_001174063.2 chr8:g.38427976C>T c.566G>A p.R189H RefSeq GRCh38/hg38
NM_023110.3 chr8:g.38427976C>T c.566G>A p.R189H RefSeq GRCh38/hg38
XM_006716304.2 chr8:g.38427976C>T c.566G>A p.R189H RefSeq GRCh38/hg38
XM_006716304.1 chr8:g.38427976C>T c.566G>A p.R189H RefSeq GRCh38/hg38
NM_001174063 chr8:g.38427976C>T c.566G>A p.R189H RefSeq GRCh38/hg38
NM_023110.2 chr8:g.38427976C>T c.566G>A p.R189H RefSeq GRCh38/hg38
XM_006716303.3 chr8:g.38427976C>T c.566G>A p.R189H RefSeq GRCh38/hg38
XM_006716303 chr8:g.38427976C>T c.566G>A p.R189H RefSeq GRCh38/hg38
XM_006716304 chr8:g.38427976C>T c.566G>A p.R189H RefSeq GRCh38/hg38
XM_047421570.1 chr8:g.38427976C>T c.566G>A p.R189H RefSeq GRCh38/hg38
XM_017013221.2 chr8:g.38427976C>T c.566G>A p.R189H RefSeq GRCh38/hg38
XM_017013221 chr8:g.38427976C>T c.566G>A p.R189H RefSeq GRCh38/hg38
NM_001174063.1 chr8:g.38427976C>T c.566G>A p.R189H RefSeq GRCh38/hg38
XM_017013222.2 chr8:g.38427976C>T c.566G>A p.R189H RefSeq GRCh38/hg38
NM_023110 chr8:g.38427976C>T c.566G>A p.R189H RefSeq GRCh38/hg38

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