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Gene | RET |
Variant | A919V |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | RET A919V lies within the protein kinase domain of the Ret protein (UniProt.org). A919V is predicted to result in decreased Ret protein stability in computational models (PMID: 16928683, PMID: 19186126), but has not been biochemically characterized and therefore, its effect on Ret protein function is unknown (PubMed, Jun 2024). |
Associated Drug Resistance | |
Category Variants Paths |
RET mutant RET A919V |
Transcript | NM_020975.6 |
gDNA | chr10:g.43121971C>T |
cDNA | c.2756C>T |
Protein | p.A919V |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_020975.6 | chr10:g.43121971C>T | c.2756C>T | p.A919V | RefSeq | GRCh38/hg38 |
NM_001406769.1 | chr10:g.43126687C>T | c.2756C>T | p.A919V | RefSeq | GRCh38/hg38 |
NM_020630.5 | chr10:g.43121971C>T | c.2756C>T | p.A919V | RefSeq | GRCh38/hg38 |
NM_020630.7 | chr10:g.43121971C>T | c.2756C>T | p.A919V | RefSeq | GRCh38/hg38 |
NM_001406759.1 | chr10:g.43121971C>T | c.2756C>T | p.A919V | RefSeq | GRCh38/hg38 |
NM_020975 | chr10:g.43121971C>T | c.2756C>T | p.A919V | RefSeq | GRCh38/hg38 |
NM_001406760.1 | chr10:g.43121971C>T | c.2756C>T | p.A919V | RefSeq | GRCh38/hg38 |
NM_001406743.1 | chr10:g.43121971C>T | c.2756C>T | p.A919V | RefSeq | GRCh38/hg38 |
NM_001406744.1 | chr10:g.43121971C>T | c.2756C>T | p.A919V | RefSeq | GRCh38/hg38 |
NM_020630 | chr10:g.43121971C>T | c.2756C>T | p.A919V | RefSeq | GRCh38/hg38 |
NM_020975.5 | chr10:g.43121971C>T | c.2756C>T | p.A919V | RefSeq | GRCh38/hg38 |
NM_001406772.1 | chr10:g.43126687C>T | c.2756C>T | p.A919V | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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