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 | TET2 |
Variant | Q1389* |
Impact List | nonsense |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | TET2 Q1389* results in a premature truncation of the Tet2 protein at amino acid 1389 of 2002 (UniProt.org). Q1389* has not been characterized however, due to the effects of other truncation mutations downstream of Q1389 (PMID: 24994606), is predicted to lead to a loss of Tet2 protein function. |
Associated Drug Resistance | |
Category Variants Paths |
TET2 mutant TET2 inact mut TET2 Q1389* |
Transcript | NM_001127208.3 |
gDNA | chr4:g.105269730C>T |
cDNA | c.4165C>T |
Protein | p.Q1389* |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_005263082.3 | chr4:g.105269730C>T | c.4165C>T | p.Q1389* | RefSeq | GRCh38/hg38 |
XM_024454102.1 | chr4:g.105269730C>T | c.4165C>T | p.Q1389* | RefSeq | GRCh38/hg38 |
XM_024454103.2 | chr4:g.105269730C>T | c.4165C>T | p.Q1389* | RefSeq | GRCh38/hg38 |
NM_001127208.2 | chr4:g.105269730C>T | c.4165C>T | p.Q1389* | RefSeq | GRCh38/hg38 |
XM_024454102.2 | chr4:g.105269730C>T | c.4165C>T | p.Q1389* | RefSeq | GRCh38/hg38 |
NM_001127208.3 | chr4:g.105269730C>T | c.4165C>T | p.Q1389* | RefSeq | GRCh38/hg38 |
XM_024454103.1 | chr4:g.105269730C>T | c.4165C>T | p.Q1389* | RefSeq | GRCh38/hg38 |
XM_005263082 | chr4:g.105269730C>T | c.4165C>T | p.Q1389* | RefSeq | GRCh38/hg38 |
XM_005263082.4 | chr4:g.105269730C>T | c.4165C>T | p.Q1389* | RefSeq | GRCh38/hg38 |
NM_001127208 | chr4:g.105269730C>T | c.4165C>T | p.Q1389* | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
---|