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Gene | RET |
Variant | Q986* |
Impact List | nonsense |
Protein Effect | unknown |
Gene Variant Descriptions | RET Q986* results in a premature truncation of the Ret protein at amino acid 986 of 1114 (UniProt.org). Q986* has been identified in sequencing studies (PMID: 27149842), 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 Q986* |
Transcript | NM_020975.6 |
gDNA | chr10:g.43124899C>T |
cDNA | c.2956C>T |
Protein | p.Q986* |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001406743.1 | chr10:g.43124899C>T | c.2956C>T | p.Q986* | RefSeq | GRCh38/hg38 |
NM_001406744.1 | chr10:g.43124899C>T | c.2956C>T | p.Q986* | RefSeq | GRCh38/hg38 |
NM_001406760.1 | chr10:g.43124899C>T | c.2956C>T | p.Q986* | RefSeq | GRCh38/hg38 |
NM_020975.5 | chr10:g.43124899C>T | c.2956C>T | p.Q986* | RefSeq | GRCh38/hg38 |
NM_001406759.1 | chr10:g.43124899C>T | c.2956C>T | p.Q986* | RefSeq | GRCh38/hg38 |
NM_020630.7 | chr10:g.43124899C>T | c.2956C>T | p.Q986* | RefSeq | GRCh38/hg38 |
NM_020630.5 | chr10:g.43124899C>T | c.2956C>T | p.Q986* | RefSeq | GRCh38/hg38 |
NM_020975.6 | chr10:g.43124899C>T | c.2956C>T | p.Q986* | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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