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Gene CSF3R
Variant G147_P148insR
Impact List insertion
Protein Effect unknown
Gene Variant Descriptions CSF3R G147_P148insR results in the insertion of an arginine (R) in fibronectin type-III domain 1 of the Csf3r protein between amino acids 147 and 148 (UniProt.org). G147_P148insR has not been characterized in the scientific literature and therefore, its effect on Csf3r protein function is unknown (PubMed, Aug 2024).
Associated Drug Resistance
Category Variants Paths

CSF3R mutant CSF3R G147_P148insR

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Transcript NM_000760.4
gDNA chr1:g.36473807_36473808insCCT
cDNA c.441_442insAGG
Protein p.G147_P148insR
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_172313.3 chr1:g.36473807_36473808insCCT c.441_442insAGG p.G147_P148insR RefSeq GRCh38/hg38
NM_172313 chr1:g.36473807_36473808insCCT c.441_442insAGG p.G147_P148insR RefSeq GRCh38/hg38
NM_172313.2 chr1:g.36473807_36473808insCCT c.441_442insAGG p.G147_P148insR RefSeq GRCh38/hg38
NM_156039.3 chr1:g.36473807_36473808insCCT c.441_442insAGG p.G147_P148insR RefSeq GRCh38/hg38
XM_005270493 chr1:g.36473807_36473808insCCT c.441_442insAGG p.G147_P148insR RefSeq GRCh38/hg38
XM_011540748.3 chr1:g.36473807_36473808insCCT c.441_442insAGG p.G147_P148insR RefSeq GRCh38/hg38
NM_000760 chr1:g.36473807_36473808insCCT c.441_442insAGG p.G147_P148insR RefSeq GRCh38/hg38
XM_005270493.1 chr1:g.36473807_36473808insCCT c.441_442insAGG p.G147_P148insR RefSeq GRCh38/hg38
XM_011540748 chr1:g.36473807_36473808insCCT c.441_442insAGG p.G147_P148insR RefSeq GRCh38/hg38
XM_011540749.1 chr1:g.36473807_36473808insCCT c.441_442insAGG p.G147_P148insR RefSeq GRCh38/hg38
XM_047446753.1 chr1:g.36473807_36473808insCCT c.441_442insAGG p.G147_P148insR RefSeq GRCh38/hg38
XM_017000370 chr1:g.36473807_36473808insCCT c.441_442insAGG p.G147_P148insR RefSeq GRCh38/hg38
XM_011540749 chr1:g.36473807_36473808insCCT c.441_442insAGG p.G147_P148insR RefSeq GRCh38/hg38
XM_011540749.1 chr1:g.36473807_36473808insCCT c.441_442insAGG p.G147_P148insR RefSeq GRCh38/hg38
XM_005270493.1 chr1:g.36473807_36473808insCCT c.441_442insAGG p.G147_P148insR RefSeq GRCh38/hg38
NM_000760.3 chr1:g.36473807_36473808insCCT c.441_442insAGG p.G147_P148insR RefSeq GRCh38/hg38
NM_156039.3 chr1:g.36473807_36473808insCCT c.441_442insAGG p.G147_P148insR RefSeq GRCh38/hg38
XM_017000370.1 chr1:g.36473807_36473808insCCT c.441_442insAGG p.G147_P148insR RefSeq GRCh38/hg38
NM_156039 chr1:g.36473807_36473808insCCT c.441_442insAGG p.G147_P148insR RefSeq GRCh38/hg38
NM_000760.4 chr1:g.36473807_36473808insCCT c.441_442insAGG p.G147_P148insR RefSeq GRCh38/hg38

Filtering

  • Case insensitive filtering will display rows if any text in any cell matches the filter term
  • 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
CSF3R mutant bone marrow cancer not applicable N/A Clinical Study Emerging In clinical studies, high frequency of CSF3R mutations was identified in patients with chronic neutrophilic leukemia (PMID: 23656643, PMID: 24081659), suggesting that this may serve as a future diagnostic biomarker (PMID: 24441292). 24081659 23656643 24441292