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Gene | FGFR2 |
Variant | L262_A266delinsD |
Impact List | indel |
Protein Effect | unknown |
Gene Variant Descriptions | FGFR2 L262_A266delinsD results in a deletion of five amino acids from aa 262 to aa 266 within Ig-like C2-type domain 3 of the Fgfr2 protein, combined with the insertion of an aspartic acid (D) at the same site (UniProt.org). L262_A266delinsD has been identified in the scientific literature (PMID: 39706336), but has not been biochemically characterized and therefore, its effect on Fgfr2 protein function is unknown (PubMed, Jan 2025). |
Associated Drug Resistance | |
Category Variants Paths |
FGFR2 mutant FGFR2 exon7 FGFR2 exon 7 del FGFR2 L262_A266delinsD |
Transcript | NM_000141.5 |
gDNA | chr10:g.121520120_121520134delinsGTC |
cDNA | c.784_798delinsGAC |
Protein | p.L262_A266delinsD |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001144917.2 | chr10:g.121520120_121520134delinsGTC | c.784_798delinsGAC | p.L262_A266delinsD | RefSeq | GRCh38/hg38 |
NM_001320658.2 | chr10:g.121520120_121520134delinsGTC | c.784_798delinsGAC | p.L262_A266delinsD | RefSeq | GRCh38/hg38 |
NM_022970.4 | chr10:g.121520120_121520134delinsGTC | c.784_798delinsGAC | p.L262_A266delinsD | RefSeq | GRCh38/hg38 |
NM_001144913.1 | chr10:g.121520120_121520134delinsGTC | c.784_798delinsGAC | p.L262_A266delinsD | RefSeq | GRCh38/hg38 |
NM_000141.5 | chr10:g.121520120_121520134delinsGTC | c.784_798delinsGAC | p.L262_A266delinsD | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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