Gene Variant Detail

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Gene FGFR1
Variant P150S
Impact List missense
Protein Effect unknown
Gene Variant Descriptions FGFR1 P150S lies within the extracellular domain of the Fgfr1 protein (UniProt.org). P150S results in altered proliferation relative to wild-type Fgfr1 in a competition assay, but results in transformation activity similar to wild-type Fgfr1 in cultured cells (PMID: 34272467), and therefore, its effect on Fgfr1 protein function is unknown.
Associated Drug Resistance
Category Variants Paths

FGFR1 mutant FGFR1 P150S

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Transcript NM_023110.3
gDNA chr8:g.38428346G>A
cDNA c.448C>T
Protein p.P150S
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_017013221 chr8:g.38428346G>A c.448C>T p.P150S RefSeq GRCh38/hg38
NM_001174063.1 chr8:g.38428346G>A c.448C>T p.P150S RefSeq GRCh38/hg38
XM_017013221.2 chr8:g.38428346G>A c.448C>T p.P150S RefSeq GRCh38/hg38
XM_006716304 chr8:g.38428346G>A c.448C>T p.P150S RefSeq GRCh38/hg38
XM_017013230 chr8:g.38418238G>A c.448C>T p.P150S RefSeq GRCh38/hg38
XM_006716303.4 chr8:g.38428346G>A c.448C>T p.P150S RefSeq GRCh38/hg38
XM_006716303.3 chr8:g.38428346G>A c.448C>T p.P150S RefSeq GRCh38/hg38
NM_023110 chr8:g.38428346G>A c.448C>T p.P150S RefSeq GRCh38/hg38
XM_017013230.1 chr8:g.38418238G>A c.448C>T p.P150S RefSeq GRCh38/hg38
XM_017013229.2 chr8:g.38418238G>A c.448C>T p.P150S RefSeq GRCh38/hg38
XM_024447097.1 chr8:g.38428070G>A c.448C>T p.P150S RefSeq GRCh38/hg38
XM_017013222 chr8:g.38428346G>A c.448C>T p.P150S RefSeq GRCh38/hg38
XM_006716304.2 chr8:g.38428346G>A c.448C>T p.P150S RefSeq GRCh38/hg38
XM_047421570.1 chr8:g.38428346G>A c.448C>T p.P150S RefSeq GRCh38/hg38
NM_001174063.2 chr8:g.38428346G>A c.448C>T p.P150S RefSeq GRCh38/hg38
XM_006716303 chr8:g.38428346G>A c.448C>T p.P150S RefSeq GRCh38/hg38
NM_001174064.1 chr8:g.38428070G>A c.448C>T p.P150S RefSeq GRCh38/hg38
XM_017013222.2 chr8:g.38428346G>A c.448C>T p.P150S RefSeq GRCh38/hg38
XM_006716304.1 chr8:g.38428346G>A c.448C>T p.P150S RefSeq GRCh38/hg38
XM_017013229 chr8:g.38418238G>A c.448C>T p.P150S RefSeq GRCh38/hg38
NM_001174064 chr8:g.38428070G>A c.448C>T p.P150S RefSeq GRCh38/hg38
XM_024447097.1 chr8:g.38428070G>A c.448C>T p.P150S RefSeq GRCh38/hg38
NM_023110.2 chr8:g.38428346G>A c.448C>T p.P150S RefSeq GRCh38/hg38
NM_001174063 chr8:g.38428346G>A c.448C>T p.P150S RefSeq GRCh38/hg38
NM_001174064.2 chr8:g.38428070G>A c.448C>T p.P150S RefSeq GRCh38/hg38
XM_006716309 chr8:g.38428070G>A c.448C>T p.P150S RefSeq GRCh38/hg38
XM_017013221.1 chr8:g.38428346G>A c.448C>T p.P150S RefSeq GRCh38/hg38
NM_023110.3 chr8:g.38428346G>A c.448C>T p.P150S RefSeq GRCh38/hg38

Filtering

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  • Use simple literal full or partial string matches
  • Separate multiple filter terms with a space. Any order may be used (i. e. a b c and c b a are equivalent )
  • Filtering will only apply to rows that are already loaded on the page. Filtering has no impact on query parameters.
  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

Sorting

  • Generally, the default sort order for tables is set to be first column ascending; however, specific tables may set a different default sort order.
  • Click on any column header arrows to sort by that column
  • Hold down the Shift key and click multiple columns to sort by more than one column. Be sure to set ascending or descending order for a given column before moving on to the next column.

Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References
FGFR1 mutant Advanced Solid Tumor predicted - sensitive Debio 1347 Phase I Actionable In a Phase I trial, Debio 1347 treatment resulted in partial response in 10.5% (6/57) and stable disease in 28.1% (16/57) of patients with advanced solid tumors harboring genomic alterations of FGFR1/2/3, including amplifications, fusions, and mutations (PMID: 30745300; NCT01948297). 30745300
FGFR1 mutant Advanced Solid Tumor sensitive Pemigatinib Preclinical - Cell line xenograft Actionable In a preclinical study, a variety of cancer cell lines harboring mutations in FGFR1, FGFR2, and/or FGFR3 demonstrated sensitivity to Pemazyre (pemigatinib) in culture and in cell line xenograft models, resulting in inhibition of tumor growth (Cancer Res 2015;75(15 Suppl):Abstract nr 771). detail...
FGFR1 mutant Advanced Solid Tumor predicted - sensitive ICP-192 Phase I Actionable In a Phase I trial, ICP-192 (gunagratinib) was well-tolerated, and resulted in an overall response rate or 33.3% (4/12, 1 complete response, 3 partial response) and a disease control rate of 91.7% (11/12) in patients with advanced solid tumors harboring FGF/FGFR gene aberrations (J Clin Oncol 39, 2021 (suppl 15; abstr 4092); NCT03758664). detail...
FGFR1 mutant transitional cell carcinoma predicted - sensitive Erdafitinib Phase II Actionable In a Phase II trial, Balversa (erdafitinib) treatment resulted in an objective response rate of 42% (40/96, 3 complete response, 37 partial response) and a disease control rate of 80% in patients with metastatic or unresectable urothelial carcinoma harboring FGFR alterations (J Clin Oncol 36, 2018 (suppl; abstr 4503); NCT02365597). detail...