Gene Variant Detail

Contact

Missing content? – Request curation!

Request curation for specific Genes, Variants, or PubMed publications.

Have questions, comments, or suggestions? - Let us know!

Email us at : ckbsupport@genomenon.com

Gene CSF3R
Variant L595V
Impact List missense
Protein Effect unknown
Gene Variant Descriptions CSF3R L595V lies within fibronectin type-III domain 5 of the Csf3r protein (UniProt.org). L595V 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 L595V

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.

Transcript NM_000760.4
gDNA chr1:g.36467903G>C
cDNA c.1783C>G
Protein p.L595V
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_017000370.1 chr1:g.36467903G>C c.1783C>G p.L595V RefSeq GRCh38/hg38
NM_000760 chr1:g.36467903G>C c.1783C>G p.L595V RefSeq GRCh38/hg38
NM_172313.2 chr1:g.36467903G>C c.1783C>G p.L595V RefSeq GRCh38/hg38
XM_011540749.1 chr1:g.36467903G>C c.1783C>G p.L595V RefSeq GRCh38/hg38
XM_005270493.1 chr1:g.36467903G>C c.1783C>G p.L595V RefSeq GRCh38/hg38
XM_011540748.3 chr1:g.36467903G>C c.1783C>G p.L595V RefSeq GRCh38/hg38
XM_047446753.1 chr1:g.36467903G>C c.1783C>G p.L595V RefSeq GRCh38/hg38
NM_000760.3 chr1:g.36467903G>C c.1783C>G p.L595V RefSeq GRCh38/hg38
XM_011540749.1 chr1:g.36467903G>C c.1783C>G p.L595V RefSeq GRCh38/hg38
XM_011540749 chr1:g.36467903G>C c.1783C>G p.L595V RefSeq GRCh38/hg38
NM_000760.4 chr1:g.36467903G>C c.1783C>G p.L595V RefSeq GRCh38/hg38
NM_172313 chr1:g.36467903G>C c.1783C>G p.L595V RefSeq GRCh38/hg38
XM_005270493 chr1:g.36467903G>C c.1783C>G p.L595V RefSeq GRCh38/hg38
NM_156039.3 chr1:g.36467903G>C c.1783C>G p.L595V RefSeq GRCh38/hg38
XM_011540748 chr1:g.36467903G>C c.1783C>G p.L595V RefSeq GRCh38/hg38
XM_005270493.1 chr1:g.36467903G>C c.1783C>G p.L595V RefSeq GRCh38/hg38
NM_156039.3 chr1:g.36467903G>C c.1783C>G p.L595V RefSeq GRCh38/hg38
NM_156039 chr1:g.36467903G>C c.1783C>G p.L595V RefSeq GRCh38/hg38
NM_172313.3 chr1:g.36467903G>C c.1783C>G p.L595V RefSeq GRCh38/hg38
XM_017000370 chr1:g.36467903G>C c.1783C>G p.L595V 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 Protein Effect Treatment Approaches
CSF3R L595V unknown