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Gene | FGFR1 |
Variant | P123S |
Impact List | missense |
Protein Effect | no effect - predicted |
Gene Variant Descriptions | FGFR1 P123S lies within the extracellular domain of the Fgfr1 protein (UniProt.org). P123S has not been biochemically characterized, but results in similar cell proliferation and viability levels as wild-type Fgfr1 in cultured cells (PMID: 29533785), and therefore, is predicted to have no effect on Fgfr1 protein function. |
Associated Drug Resistance | |
Category Variants Paths |
FGFR1 mutant FGFR1 P123S |
Transcript | NM_023110.3 |
gDNA | chr8:g.38428427G>A |
cDNA | c.367C>T |
Protein | p.P123S |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_047421569.1 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
NM_001174065 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_017013222 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
NM_023110 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_006716304 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
NM_001174063.2 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_017013226.2 | chr8:g.38428007G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
NM_015850.3 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_017013221 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_017013221.1 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_017013221.2 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_017013223 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
NM_001354367.2 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
NM_001174065.2 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
NM_023110.2 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_017013226.1 | chr8:g.38428007G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_006716303 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_017013226 | chr8:g.38428007G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_006716306 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_011544448.1 | chr8:g.38428007G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_006716307 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_017013225 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_006716304.2 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
NM_001354367.1 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_017013225.3 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
NM_001354369.1 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
NM_001174063 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_017013224 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
NM_001410922.1 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
NM_001174065.1 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_006716304.1 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_017013222.2 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_006716303.3 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_006716307.1 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_017013224.2 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_006716307.2 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
NM_001174063.1 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_006716303.4 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_011544448 | chr8:g.38428007G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
NM_023110.3 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
NM_015850 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_017013225.2 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
NM_015850.4 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_047421570.1 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
NM_001354369.2 | chr8:g.38428427G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
XM_011544448.2 | chr8:g.38428007G>A | c.367C>T | p.P123S | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
FGFR1 P123S | no effect - predicted |