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Gene RET
Variant C611F
Impact List missense
Protein Effect unknown
Gene Variant Descriptions RET C611F lies within the extracellular domain of the Ret protein (UniProt.org). C611F has been identified in the scientific literature (PMID: 11331212, PMID: 9950371, PMID: 33827484), but has not been biochemically characterized and therefore, its effect on Ret protein function is unknown (PubMed, Feb 2024).
Associated Drug Resistance
Category Variants Paths

RET mutant RET C611X RET C611F

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Transcript NM_020975.6
gDNA chr10:g.43113628G>T
cDNA c.1832G>T
Protein p.C611F
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_020630 chr10:g.43113628G>T c.1832G>T p.C611F RefSeq GRCh38/hg38
NM_001406743.1 chr10:g.43113628G>T c.1832G>T p.C611F RefSeq GRCh38/hg38
NM_020975.5 chr10:g.43113628G>T c.1832G>T p.C611F RefSeq GRCh38/hg38
NM_020630.7 chr10:g.43113628G>T c.1832G>T p.C611F RefSeq GRCh38/hg38
NM_001406744.1 chr10:g.43113628G>T c.1832G>T p.C611F RefSeq GRCh38/hg38
NM_001406765.1 chr10:g.43113628G>T c.1832G>T p.C611F RefSeq GRCh38/hg38
NM_020630.5 chr10:g.43113628G>T c.1832G>T p.C611F RefSeq GRCh38/hg38
NM_001406763.1 chr10:g.43113628G>T c.1832G>T p.C611F RefSeq GRCh38/hg38
NM_001406760.1 chr10:g.43113628G>T c.1832G>T p.C611F RefSeq GRCh38/hg38
NM_020975 chr10:g.43113628G>T c.1832G>T p.C611F RefSeq GRCh38/hg38
NM_020975.6 chr10:g.43113628G>T c.1832G>T p.C611F RefSeq GRCh38/hg38
NM_001406759.1 chr10:g.43113628G>T c.1832G>T p.C611F RefSeq GRCh38/hg38

Filtering

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  • 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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Sorting

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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References