Missing content? – Request curation!
Request curation for specific Genes, Variants, or PubMed publications.
Have questions, comments, or suggestions? - Let us know!
Email us at : ckbsupport@genomenon.com
Gene | RET |
Variant | M1009T |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | RET M1009T lies within the protein kinase domain of the Ret protein (UniProt.org). M1009T has been identified in sequencing studies (PMID: 27149458, PMID: 24429398, PMID: 35181378), 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 M1009T |
Transcript | NM_020975.6 |
gDNA | chr10:g.43124969T>C |
cDNA | c.3026T>C |
Protein | p.M1009T |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_020975 | chr10:g.43124969T>C | c.3026T>C | p.M1009T | RefSeq | GRCh38/hg38 |
NM_001406759.1 | chr10:g.43124969T>C | c.3026T>C | p.M1009T | RefSeq | GRCh38/hg38 |
NM_020975.6 | chr10:g.43124969T>C | c.3026T>C | p.M1009T | RefSeq | GRCh38/hg38 |
NM_001406760.1 | chr10:g.43124969T>C | c.3026T>C | p.M1009T | RefSeq | GRCh38/hg38 |
NM_001406743.1 | chr10:g.43124969T>C | c.3026T>C | p.M1009T | RefSeq | GRCh38/hg38 |
NM_020630.7 | chr10:g.43124969T>C | c.3026T>C | p.M1009T | RefSeq | GRCh38/hg38 |
NM_001406744.1 | chr10:g.43124969T>C | c.3026T>C | p.M1009T | RefSeq | GRCh38/hg38 |
NM_020975.5 | chr10:g.43124969T>C | c.3026T>C | p.M1009T | RefSeq | GRCh38/hg38 |
NM_020630.5 | chr10:g.43124969T>C | c.3026T>C | p.M1009T | RefSeq | GRCh38/hg38 |
NM_020630 | chr10:g.43124969T>C | c.3026T>C | p.M1009T | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
---|