RET C609F
Gene Variant Detail

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Gene RET
Variant C609F
Impact List missense
Protein Effect unknown
Gene Variant Descriptions RET C609F lies within the extracellular domain of the Ret protein (UniProt.org). C609F has been identified in the scientific literature (PMID: 9068588, PMID: 24699901, PMID: 38339246), but has not been biochemically characterized and therefore, its effect on Ret protein function is unknown (PubMed, Aug 2025).
Associated Drug Resistance
Category Variants Paths

RET mutant RET C609X RET C609F

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Transcript NM_020975.6
gDNA chr10:g.43113622G>T
cDNA c.1826G>T
Protein p.C609F
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_020975.5 chr10:g.43113622G>T c.1826G>T p.C609F RefSeq GRCh38/hg38
NM_020975.6 chr10:g.43113622G>T c.1826G>T p.C609F RefSeq GRCh38/hg38
NM_020630.7 chr10:g.43113622G>T c.1826G>T p.C609F RefSeq GRCh38/hg38
NM_001406763.1 chr10:g.43113622G>T c.1826G>T p.C609F RefSeq GRCh38/hg38
NM_020630.5 chr10:g.43113622G>T c.1826G>T p.C609F RefSeq GRCh38/hg38
NM_020975 chr10:g.43113622G>T c.1826G>T p.C609F RefSeq GRCh38/hg38
NM_001406760.1 chr10:g.43113622G>T c.1826G>T p.C609F RefSeq GRCh38/hg38
NM_001406759.1 chr10:g.43113622G>T c.1826G>T p.C609F RefSeq GRCh38/hg38
NM_001406744.1 chr10:g.43113622G>T c.1826G>T p.C609F RefSeq GRCh38/hg38
NM_001406743.1 chr10:g.43113622G>T c.1826G>T p.C609F RefSeq GRCh38/hg38
NM_001406765.1 chr10:g.43113622G>T c.1826G>T p.C609F RefSeq GRCh38/hg38
NM_020630 chr10:g.43113622G>T c.1826G>T p.C609F 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 )
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  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

Sorting

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Molecular Profile Protein Effect Treatment Approaches
RET C609F unknown