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Gene | CSF3R |
Variant | L723V |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | CSF3R L723V lies within the cytoplasmic domain of the Csf3r protein (UniProt.org). L723V has been identified in the scientific literature (Blood (2021), 131 (Supplement 1): 3677), but has not been biochemically characterized and therefore, its effect on Csf3r protein function is unknown (PubMed, Aug 2024). |
Associated Drug Resistance | |
Category Variants Paths |
CSF3R mutant CSF3R L723V |
Transcript | NM_000760.4 |
gDNA | chr1:g.36466701G>C |
cDNA | c.2167C>G |
Protein | p.L723V |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_047446753.1 | chr1:g.36466782G>C | c.2167C>G | p.L723V | RefSeq | GRCh38/hg38 |
NM_000760.4 | chr1:g.36466701G>C | c.2167C>G | p.L723V | RefSeq | GRCh38/hg38 |
NM_172313.2 | chr1:g.36466701G>C | c.2167C>G | p.L723V | RefSeq | GRCh38/hg38 |
NM_172313.3 | chr1:g.36466701G>C | c.2167C>G | p.L723V | RefSeq | GRCh38/hg38 |
NM_156039.3 | chr1:g.36466782G>C | c.2167C>G | p.L723V | RefSeq | GRCh38/hg38 |
NM_000760.3 | chr1:g.36466701G>C | c.2167C>G | p.L723V | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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