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Gene | FGFR1 |
Variant | G70R |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | FGFR1 G70R lies within Ig-like C2-type domain 1 of the Fgfr1 protein (UniProt.org). G70R has been identified in the scientific literature (PMID: 27581340), but has not been biochemically characterized and therefore, its effect on Fgfr1 protein function is unknown (PubMed, Apr 2024). |
Associated Drug Resistance | |
Category Variants Paths |
FGFR1 mutant FGFR1 G70R |
Transcript | NM_023110.3 |
gDNA | chr8:g.38429832C>T |
cDNA | c.208G>A |
Protein | p.G70R |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_017013221.2 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
NM_015850.4 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
NM_001174063.2 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_006716307 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
NM_001354369.2 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
NM_023110.2 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_017013225.2 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_017013221 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_006716303.3 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
NM_001174065.2 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_017013230.1 | chr8:g.38419643C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_047421570.1 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_047421569.1 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
NM_015850.3 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_006716304.1 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
NM_001174063 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
NM_001174065.1 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_017013229.2 | chr8:g.38419643C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_017013223 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_017013230 | chr8:g.38419643C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
NM_015850 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_006716303.4 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_006716307.2 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_017013222 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_006716303 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
NM_001174063.1 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_017013229 | chr8:g.38419643C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_017013224 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
NM_001174065 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
NM_001354367.2 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_017013221.1 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_006716304 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
NM_001354369.1 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_017013225.3 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
NM_023110 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
NM_001354367.1 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
NM_023110.3 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_017013222.2 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_006716304.2 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_006716306 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_017013224.2 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_017013225 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
XM_006716307.1 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
NM_001410922.1 | chr8:g.38429832C>T | c.208G>A | p.G70R | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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