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Gene | FGFR2 |
Variant | L770V |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | FGFR2 L770V lies within the protein kinase domain of the Fgfr2 protein (UniProt.org). L770V is predicted to decrease phospholipase C-gamma activation by Fgfr2 based on structural modeling (PMID: 19147536), but has not been biochemically characterized and therefore, its effect on Fgfr2 protein function is unknown (PubMed, Nov 2024). |
Associated Drug Resistance | |
Category Variants Paths |
FGFR2 mutant FGFR2 L770V |
Transcript | NM_000141.5 |
gDNA | chr10:g.121480015A>C |
cDNA | c.2308T>G |
Protein | p.L770V |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_017015921.2 | chr10:g.121483742A>C | c.2308T>G | p.L770V | RefSeq | GRCh38/hg38 |
NM_001320658.2 | chr10:g.121480009G>C | c.2308C>G | p.L770V | RefSeq | GRCh38/hg38 |
XM_017015921 | chr10:g.121483742A>C | c.2308T>G | p.L770V | RefSeq | GRCh38/hg38 |
NM_001320658.1 | chr10:g.121480009G>C | c.2308C>G | p.L770V | RefSeq | GRCh38/hg38 |
XM_017015921.3 | chr10:g.121483742A>C | c.2308T>G | p.L770V | RefSeq | GRCh38/hg38 |
NM_000141.5 | chr10:g.121480015A>C | c.2308T>G | p.L770V | RefSeq | GRCh38/hg38 |
NM_000141.4 | chr10:g.121480015A>C | c.2308T>G | p.L770V | RefSeq | GRCh38/hg38 |
NM_001320658 | chr10:g.121480009G>C | c.2308C>G | p.L770V | RefSeq | GRCh38/hg38 |
NM_000141 | chr10:g.121480015A>C | c.2308T>G | p.L770V | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
FGFR2 L770V | unknown |