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Gene | FGFR1 |
Variant | W4C |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | FGFR1 W4C does not lie within any known functional domains of the Fgfr1 protein (UniProt.org). W4C has been identified in the scientific literature (PMID: 34593528), but has not been biochemically characterized and therefore, its effect on Fgfr1 protein function is unknown (PubMed, Mar 2024). |
Associated Drug Resistance | |
Category Variants Paths |
FGFR1 mutant FGFR1 W4C |
Transcript | NM_023110.3 |
gDNA | chr8:g.38457435C>A |
cDNA | c.12G>T |
Protein | p.W4C |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_047421573.1 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
XM_006716314.2 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
XM_006716304.1 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
XM_047421570.1 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
NM_001410922.1 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
XM_047421574.1 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
XM_006716310.4 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
NM_001174066.2 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
XM_017013221.1 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
NM_001174066.1 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
XM_006716307.1 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
NM_001354370.1 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
NM_001354367.2 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
NM_023110.2 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
NM_001354369.1 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
NM_023106.2 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
NM_023105.3 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
XM_006716311.1 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
XM_017013222.2 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
NM_001354368.1 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
NM_015850.3 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
XM_017013224.2 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
XM_006716303.3 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
XM_017013225.3 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
NM_001174065.1 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
XM_017013221.2 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
NM_023105.2 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
NM_001174063.2 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
XM_006716312.2 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
NM_001174063.1 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
XM_047421569.1 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
NM_015850.4 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
NM_001354368.2 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
XM_006716312.2 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
XM_006716314.3 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
XM_006716303.4 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
XM_006716304.2 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
NM_023106.3 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
NM_001354367.1 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
NM_001354370.2 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
XM_006716311.1 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
NM_001354369.2 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
NM_001174065.2 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
XM_017013225.2 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
NM_023110.3 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
XM_006716310.3 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
XM_006716307.2 | chr8:g.38457435C>A | c.12G>T | p.W4C | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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