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Gene | FGFR2 |
Variant | E636* |
Impact List | nonsense |
Protein Effect | unknown |
Gene Variant Descriptions | FGFR2 E636* results in the premature truncation of the Fgfr2 protein at amino acid 636 of 821 (UniProt.org). E636* has not been characterized in the scientific literature and therefore, its effect on Fgfr2 protein function is unknown (PubMed, Nov 2024). |
Associated Drug Resistance | |
Category Variants Paths |
FGFR2 mutant FGFR2 E636* |
Transcript | NM_000141.5 |
gDNA | chr10:g.121488071C>A |
cDNA | c.1906G>T |
Protein | p.E636* |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_024447891.1 | chr10:g.121485399C>A | c.1906G>T | p.E636* | RefSeq | GRCh38/hg38 |
NM_000141.5 | chr10:g.121488071C>A | c.1906G>T | p.E636* | RefSeq | GRCh38/hg38 |
NM_000141 | chr10:g.121488071C>A | c.1906G>T | p.E636* | RefSeq | GRCh38/hg38 |
XM_006717712 | chr10:g.121485399C>A | c.1906G>T | p.E636* | RefSeq | GRCh38/hg38 |
NM_000141.4 | chr10:g.121488071C>A | c.1906G>T | p.E636* | RefSeq | GRCh38/hg38 |
XM_024447891.2 | chr10:g.121485399C>A | c.1906G>T | p.E636* | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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