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| Gene | B2M |
| Variant | T93Hfs*2 |
| Impact List | frameshift |
| Protein Effect | unknown |
| Gene Variant Descriptions | B2M T93Hfs*2 indicates a shift in the reading frame starting at amino acid 93 and terminating 2 residues downstream causing a premature truncation of the 119 amino acid B2m protein (UniProt.org). T93Hfs*2 has been identified in sequencing studies (PMID: 31008436, PMID: 36724040), but has not been biochemically characterized and therefore, its effect on B2m protein function is unknown (PubMed, Jul 2025). |
| Associated Drug Resistance | |
| Category Variants Paths |
B2M mutant B2M T93fs B2M T93Hfs*2 |
| Transcript | NM_004048.4 |
| gDNA | chr15:g.44715631dupC |
| cDNA | c.276dupC |
| Protein | p.T93Hfs*2 |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_004048 | chr15:g.44715631dupC | c.276dupC | p.T93Hfs*2 | RefSeq | GRCh38/hg38 |
| NM_004048.2 | chr15:g.44715631dupC | c.276dupC | p.T93Hfs*2 | RefSeq | GRCh38/hg38 |
| NM_004048.4 | chr15:g.44715631dupC | c.276dupC | p.T93Hfs*2 | RefSeq | GRCh38/hg38 |
| XM_005254549.3 | chr15:g.44715631dupC | c.276dupC | p.T93Hfs*2 | RefSeq | GRCh38/hg38 |
| XM_005254549.4 | chr15:g.44715631dupC | c.276dupC | p.T93Hfs*2 | RefSeq | GRCh38/hg38 |
| XM_005254549 | chr15:g.44715631dupC | c.276dupC | p.T93Hfs*2 | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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