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Gene RET
Variant F893L
Impact List missense
Protein Effect loss of function
Gene Variant Descriptions RET F893L lies within the protein kinase domain of the Ret protein (UniProt.org). F893L results in a loss of ligand-dependent phosphorylation of Ret and downstream signaling molecules including Erk, Akt, and PLCgamma, is not transforming in culture, and abolishes the activity of a concurrent activating IDH1 mutation (C634R) in culture (PMID: 11438491, PMID: 22837065).
Associated Drug Resistance
Category Variants Paths

RET mutant RET inact mut RET F893L

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Transcript NM_020975.6
gDNA chr10:g.43120150T>C
cDNA c.2677T>C
Protein p.F893L
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001406760.1 chr10:g.43120150T>C c.2677T>C p.F893L RefSeq GRCh38/hg38
NM_020975 chr10:g.43120150T>C c.2677T>C p.F893L RefSeq GRCh38/hg38
NM_020630 chr10:g.43120150T>C c.2677T>C p.F893L RefSeq GRCh38/hg38
NM_020975.5 chr10:g.43120150T>C c.2677T>C p.F893L RefSeq GRCh38/hg38
NM_020630.7 chr10:g.43120150T>C c.2677T>C p.F893L RefSeq GRCh38/hg38
NM_001406759.1 chr10:g.43120150T>C c.2677T>C p.F893L RefSeq GRCh38/hg38
NM_001406744.1 chr10:g.43120150T>C c.2677T>C p.F893L RefSeq GRCh38/hg38
NM_020630.5 chr10:g.43120150T>C c.2677T>C p.F893L RefSeq GRCh38/hg38
NM_020975.6 chr10:g.43120150T>C c.2677T>C p.F893L RefSeq GRCh38/hg38
NM_001406743.1 chr10:g.43120150T>C c.2677T>C p.F893L RefSeq GRCh38/hg38

Filtering

  • Case insensitive filtering will display rows if any text in any cell matches the filter term
  • Use simple literal full or partial string matches
  • Separate multiple filter terms with a space. Any order may be used (i. e. a b c and c b a are equivalent )
  • Filtering will only apply to rows that are already loaded on the page. Filtering has no impact on query parameters.
  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

Sorting

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Clinical Trial Phase Therapies Title Recruitment Status Covered Countries Other Countries