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Gene | FGFR1 |
Variant | K598N |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | FGFR1 K598N lies within the protein kinase domain of the Fgfr1 protein (UniProt.org). K598N has been identified in sequencing studies (PMID: 23525077), but has not been biochemically characterized and therefore, its effect on Fgfr1 protein function is unknown (PubMed, Oct 2024). |
Associated Drug Resistance | |
Category Variants Paths |
FGFR1 mutant FGFR1 K598N |
Transcript | NM_023110.3 |
gDNA | chr8:g.38415930C>G |
cDNA | c.1794G>C |
Protein | p.K598N |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_006716304 | chr8:g.38415930C>G | c.1794G>C | p.K598N | RefSeq | GRCh38/hg38 |
XM_047421576.1 | chr8:g.38413966C>G | c.1794G>C | p.K598N | RefSeq | GRCh38/hg38 |
XM_006716304.2 | chr8:g.38415930C>G | c.1794G>C | p.K598N | RefSeq | GRCh38/hg38 |
XM_011544450 | chr8:g.38414788C>G | c.1794G>C | p.K598N | RefSeq | GRCh38/hg38 |
XM_017013221.1 | chr8:g.38415930C>G | c.1794G>C | p.K598N | RefSeq | GRCh38/hg38 |
XM_011544450.3 | chr8:g.38414788C>G | c.1794G>C | p.K598N | RefSeq | GRCh38/hg38 |
NM_023110.3 | chr8:g.38415930C>G | c.1794G>C | p.K598N | RefSeq | GRCh38/hg38 |
XM_017013226 | chr8:g.38414788C>G | c.1794G>C | p.K598N | RefSeq | GRCh38/hg38 |
XM_006716303 | chr8:g.38415930C>G | c.1794G>C | p.K598N | RefSeq | GRCh38/hg38 |
XM_006716303.3 | chr8:g.38415930C>G | c.1794G>C | p.K598N | RefSeq | GRCh38/hg38 |
XM_011544450.2 | chr8:g.38414788C>G | c.1794G>C | p.K598N | RefSeq | GRCh38/hg38 |
XM_017013221 | chr8:g.38415930C>G | c.1794G>C | p.K598N | RefSeq | GRCh38/hg38 |
XM_006716304.1 | chr8:g.38415930C>G | c.1794G>C | p.K598N | RefSeq | GRCh38/hg38 |
XM_006716303.4 | chr8:g.38415930C>G | c.1794G>C | p.K598N | RefSeq | GRCh38/hg38 |
XM_011544449 | chr8:g.38414788C>G | c.1794G>C | p.K598N | RefSeq | GRCh38/hg38 |
XM_017013221.2 | chr8:g.38415930C>G | c.1794G>C | p.K598N | RefSeq | GRCh38/hg38 |
NM_023110.2 | chr8:g.38415930C>G | c.1794G>C | p.K598N | RefSeq | GRCh38/hg38 |
XM_017013226.2 | chr8:g.38414788C>G | c.1794G>C | p.K598N | RefSeq | GRCh38/hg38 |
XM_011544449.1 | chr8:g.38414788C>G | c.1794G>C | p.K598N | RefSeq | GRCh38/hg38 |
NM_023110 | chr8:g.38415930C>G | c.1794G>C | p.K598N | RefSeq | GRCh38/hg38 |
XM_011544449.2 | chr8:g.38414788C>G | c.1794G>C | p.K598N | RefSeq | GRCh38/hg38 |
XM_017013226.1 | chr8:g.38414788C>G | c.1794G>C | p.K598N | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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