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| Gene | TET2 |
| Variant | G1814* |
| Impact List | nonsense |
| Protein Effect | unknown |
| Gene Variant Descriptions | TET2 G1814* results in a premature truncation of the Tet2 protein at amino acid 1814 of 2002 (UniProt.org). G1814* has been identified in sequencing studies (PMID: 32107212), but has not been biochemically characterized and therefore, its effect on Tet2 protein function is unknown (PubMed, Jul 2025). |
| Associated Drug Resistance | |
| Category Variants Paths |
TET2 mutant TET2 G1814* |
| Transcript | NM_001127208.3 |
| gDNA | chr4:g.105275950G>T |
| cDNA | c.5440G>T |
| Protein | p.G1814* |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| XM_024454103.1 | chr4:g.105275950G>T | c.5440G>T | p.G1814* | RefSeq | GRCh38/hg38 |
| XM_024454102.2 | chr4:g.105275950G>T | c.5440G>T | p.G1814* | RefSeq | GRCh38/hg38 |
| NM_001127208.2 | chr4:g.105275950G>T | c.5440G>T | p.G1814* | RefSeq | GRCh38/hg38 |
| XM_024454102.1 | chr4:g.105275950G>T | c.5440G>T | p.G1814* | RefSeq | GRCh38/hg38 |
| XM_005263082.3 | chr4:g.105275950G>T | c.5440G>T | p.G1814* | RefSeq | GRCh38/hg38 |
| XM_005263082.4 | chr4:g.105275950G>T | c.5440G>T | p.G1814* | RefSeq | GRCh38/hg38 |
| XM_024454103.2 | chr4:g.105275950G>T | c.5440G>T | p.G1814* | RefSeq | GRCh38/hg38 |
| NM_001127208.3 | chr4:g.105275950G>T | c.5440G>T | p.G1814* | RefSeq | GRCh38/hg38 |
| Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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