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Gene RET
Variant G601W
Impact List missense
Protein Effect unknown
Gene Variant Descriptions RET G601W lies within the extracellular domain of the Ret protein (UniProt.org). G601W has been identified in sequencing studies (PMID: 22980975), 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 G601W

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Transcript NM_020975.6
gDNA chr10:g.43113597G>T
cDNA c.1801G>T
Protein p.G601W
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_020975.6 chr10:g.43113597G>T c.1801G>T p.G601W RefSeq GRCh38/hg38
NM_001406769.1 chr10:g.43116644_43116646delGGCinsTGG c.1801_1803delGGCinsTGG p.G601W RefSeq GRCh38/hg38
NM_020630.7 chr10:g.43113597G>T c.1801G>T p.G601W RefSeq GRCh38/hg38
NM_020630 chr10:g.43113597G>T c.1801G>T p.G601W RefSeq GRCh38/hg38
NM_020630.5 chr10:g.43113597G>T c.1801G>T p.G601W RefSeq GRCh38/hg38
NM_001406763.1 chr10:g.43113597G>T c.1801G>T p.G601W RefSeq GRCh38/hg38
NM_020975 chr10:g.43113597G>T c.1801G>T p.G601W RefSeq GRCh38/hg38
NM_020975.5 chr10:g.43113597G>T c.1801G>T p.G601W RefSeq GRCh38/hg38
NM_001406772.1 chr10:g.43116644_43116646delGGCinsTGG c.1801_1803delGGCinsTGG p.G601W RefSeq GRCh38/hg38
NM_001406759.1 chr10:g.43113597G>T c.1801G>T p.G601W RefSeq GRCh38/hg38
NM_001406744.1 chr10:g.43113597G>T c.1801G>T p.G601W RefSeq GRCh38/hg38
NM_001406765.1 chr10:g.43113597G>T c.1801G>T p.G601W RefSeq GRCh38/hg38
NM_001406743.1 chr10:g.43113597G>T c.1801G>T p.G601W RefSeq GRCh38/hg38
NM_001406760.1 chr10:g.43113597G>T c.1801G>T p.G601W RefSeq GRCh38/hg38

Filtering

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  • 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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  • Click on any column header arrows to sort by that column
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Clinical Trial Phase Therapies Title Recruitment Status Covered Countries Other Countries