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Gene | FGFR1 |
Variant | A431S |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | FGFR1 A431S lies within the cytoplasmic domain of the Fgfr1 protein (UniProt.org). A431S has been identified in sequencing studies (PMID: 12738854), 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 A431S |
Transcript | NM_023110.3 |
gDNA | chr8:g.38418367C>A |
cDNA | c.1291G>T |
Protein | p.A431S |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_023110 | chr8:g.38418367C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_006716303.3 | chr8:g.38418367C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
NM_001354369.2 | chr8:g.38418355C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
NM_001410922.1 | chr8:g.38418355C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_006716303 | chr8:g.38418367C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_017013225.2 | chr8:g.38418355C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
NM_023110.3 | chr8:g.38418367C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_006716311 | chr8:g.38417411C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_006716303.4 | chr8:g.38418367C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_017013221.2 | chr8:g.38418367C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_017013225.3 | chr8:g.38418355C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_006716310 | chr8:g.38417411C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_006716304.1 | chr8:g.38418367C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_006716311.1 | chr8:g.38417411C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_006716310.4 | chr8:g.38417411C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_017013224 | chr8:g.38418355C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
NM_023105.3 | chr8:g.38417411C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
NM_001174066.2 | chr8:g.38417411C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_006716312.2 | chr8:g.38417411C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_017013225 | chr8:g.38418355C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_017013221.1 | chr8:g.38418367C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
NM_001174066.1 | chr8:g.38417411C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_047421569.1 | chr8:g.38418355C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
NM_023110.2 | chr8:g.38418367C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
NM_023105 | chr8:g.38417411C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_017013221 | chr8:g.38418367C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_006716311.1 | chr8:g.38417411C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_006716312.2 | chr8:g.38417411C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_017013224.2 | chr8:g.38418355C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
NM_001174066 | chr8:g.38417411C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_006716310.3 | chr8:g.38417411C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_006716304.2 | chr8:g.38418367C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_017013223 | chr8:g.38418355C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_006716312 | chr8:g.38417411C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
NM_001354369.1 | chr8:g.38418355C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
NM_023105.2 | chr8:g.38417411C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
XM_006716304 | chr8:g.38418367C>A | c.1291G>T | p.A431S | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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