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Gene | FGFR2 |
Variant | V169_K176delinsE |
Impact List | indel |
Protein Effect | unknown |
Gene Variant Descriptions | FGFR2 V169_K176delinsE results in a deletion of eight amino acids from aa 169 to aa 176 within Ig-like C2-type domain 2 of the Fgfr2 protein, combined with the insertion of a glutamic acid (E) at the same site (UniProt.org). V169_K176delinsE has not been characterized in the scientific literature and therefore, its effect on Fgfr2 protein function is unknown (PubMed, Feb 2025). |
Associated Drug Resistance | |
Category Variants Paths |
FGFR2 mutant FGFR2 exon5 FGFR2 exon 5 del FGFR2 V169_K176delinsE |
Transcript | NM_000141.5 |
gDNA | chr10:g.121551388_121551408del21 |
cDNA | c.506_526del21 |
Protein | p.V169_K176delinsE |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001144917.2 | chr10:g.121551388_121551408del21 | c.506_526del21 | p.V169_K176delinsE | RefSeq | GRCh38/hg38 |
NM_000141.5 | chr10:g.121551388_121551408del21 | c.506_526del21 | p.V169_K176delinsE | RefSeq | GRCh38/hg38 |
NM_001144914.1 | chr10:g.121551388_121551408del21 | c.506_526del21 | p.V169_K176delinsE | RefSeq | GRCh38/hg38 |
NM_001144913.1 | chr10:g.121551388_121551408del21 | c.506_526del21 | p.V169_K176delinsE | RefSeq | GRCh38/hg38 |
NM_022970.4 | chr10:g.121551388_121551408del21 | c.506_526del21 | p.V169_K176delinsE | RefSeq | GRCh38/hg38 |
NM_001320658.2 | chr10:g.121551388_121551408del21 | c.506_526del21 | p.V169_K176delinsE | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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