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Gene | FGFR1 |
Variant | D128Y |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | FGFR1 D128Y lies within the extracellular domain of the Fgfr1 protein (UniProt.org). D128Y has not been characterized in the scientific literature and therefore, its effect on Fgfr1 protein function is unknown (PubMed, Apr 2024). |
Associated Drug Resistance | |
Category Variants Paths |
FGFR1 mutant FGFR1 D128Y |
Transcript | NM_023110.3 |
gDNA | chr8:g.38428412C>A |
cDNA | c.382G>T |
Protein | p.D128Y |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001174063.2 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_006716304 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_011544443.2 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_006716306 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_011544446.2 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_017013224 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_006716303 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
NM_001174067.1 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_017013219.1 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
NM_001174065 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_006716303.3 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_006716307.1 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
NM_001354367.2 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_011544444.2 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_006716307.2 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
NM_015850.4 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_011544452.2 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_047421570.1 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_017013221 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
NM_001174063.1 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_011544445.2 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_017013231.1 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_047421569.1 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_017013220 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
NM_001410922.1 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
NM_001354369.1 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_047421575.1 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
NM_015850 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
NM_001174065.1 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_011544446.3 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_011544444.1 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_017013222.2 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_017013219 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_017013225.2 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_011544452.3 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_011544447.2 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_017013225.3 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_017013222 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
NM_023110.3 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_011544443 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_011544444 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_017013221.2 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_017013219.2 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
NM_001174067.2 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_006716303.4 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_011544445.3 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_017013231 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
NM_015850.3 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_011544447 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_011544447.3 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
NM_001174063 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
NM_023110 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_006716304.2 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_011544452 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_011544446 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_017013224.2 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
NM_001174065.2 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_011544445 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_017013220.1 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
NM_001354367.1 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
NM_001174067 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_017013220.2 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_017013223 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
NM_001354369.2 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_017013221.1 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
NM_023110.2 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_017013225 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_006716304.1 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_006716307 | chr8:g.38428412C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
XM_017013231.2 | chr8:g.38429757C>A | c.382G>T | p.D128Y | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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