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 | P20L |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | CSF3R P20L lies within the signal peptide region of the Csf3r protein (UniProt.org). P20L 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 P20L |
Transcript | NM_000760.4 |
gDNA | chr1:g.36479438G>A |
cDNA | c.59C>T |
Protein | p.P20L |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_172313.2 | chr1:g.36479438G>A | c.59C>T | p.P20L | RefSeq | GRCh38/hg38 |
XM_011540748.3 | chr1:g.36479438G>A | c.59C>T | p.P20L | RefSeq | GRCh38/hg38 |
XM_017000370.1 | chr1:g.36479438G>A | c.59C>T | p.P20L | RefSeq | GRCh38/hg38 |
NM_156039 | chr1:g.36479438G>A | c.59C>T | p.P20L | RefSeq | GRCh38/hg38 |
NM_000760.3 | chr1:g.36479438G>A | c.59C>T | p.P20L | RefSeq | GRCh38/hg38 |
NM_172313 | chr1:g.36479438G>A | c.59C>T | p.P20L | RefSeq | GRCh38/hg38 |
XM_017000370 | chr1:g.36479438G>A | c.59C>T | p.P20L | RefSeq | GRCh38/hg38 |
XM_011540750.1 | chr1:g.36472629G>A | c.59C>T | p.P20L | RefSeq | GRCh38/hg38 |
XM_005270493.1 | chr1:g.36479438G>A | c.59C>T | p.P20L | RefSeq | GRCh38/hg38 |
XM_047446753.1 | chr1:g.36479438G>A | c.59C>T | p.P20L | RefSeq | GRCh38/hg38 |
XM_011540748 | chr1:g.36479438G>A | c.59C>T | p.P20L | RefSeq | GRCh38/hg38 |
XM_011540749 | chr1:g.36479438G>A | c.59C>T | p.P20L | RefSeq | GRCh38/hg38 |
NM_000760.4 | chr1:g.36479438G>A | c.59C>T | p.P20L | RefSeq | GRCh38/hg38 |
NM_156039.3 | chr1:g.36479438G>A | c.59C>T | p.P20L | RefSeq | GRCh38/hg38 |
XM_011540750 | chr1:g.36472629G>A | c.59C>T | p.P20L | RefSeq | GRCh38/hg38 |
XM_011540749.1 | chr1:g.36479438G>A | c.59C>T | p.P20L | RefSeq | GRCh38/hg38 |
NM_156039.3 | chr1:g.36479438G>A | c.59C>T | p.P20L | RefSeq | GRCh38/hg38 |
XM_005270493 | chr1:g.36479438G>A | c.59C>T | p.P20L | RefSeq | GRCh38/hg38 |
NM_172313.3 | chr1:g.36479438G>A | c.59C>T | p.P20L | RefSeq | GRCh38/hg38 |
XM_005270493.1 | chr1:g.36479438G>A | c.59C>T | p.P20L | RefSeq | GRCh38/hg38 |
NM_000760 | chr1:g.36479438G>A | c.59C>T | p.P20L | RefSeq | GRCh38/hg38 |
XM_011540749.1 | chr1:g.36479438G>A | c.59C>T | p.P20L | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
---|