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| Gene | B2M |
| Variant | E64* |
| Impact List | nonsense |
| Protein Effect | unknown |
| Gene Variant Descriptions | B2M E64* results in a premature truncation of the B2m protein at amino acid 64 of 119 (UniProt.org). E64* has been identified in the scientific literature (PMID: 31008436), but has not been biochemically characterized and therefore, its effect on B2m protein function is unknown (PubMed, Jun 2025). |
| Associated Drug Resistance | |
| Category Variants Paths |
B2M mutant B2M E64* |
| Transcript | NM_004048.4 |
| gDNA | chr15:g.44715545G>T |
| cDNA | c.190G>T |
| Protein | p.E64* |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| XM_005254549.4 | chr15:g.44715545G>T | c.190G>T | p.E64* | RefSeq | GRCh38/hg38 |
| NM_004048.4 | chr15:g.44715545G>T | c.190G>T | p.E64* | RefSeq | GRCh38/hg38 |
| NM_004048 | chr15:g.44715545G>T | c.190G>T | p.E64* | RefSeq | GRCh38/hg38 |
| XM_005254549 | chr15:g.44715545G>T | c.190G>T | p.E64* | RefSeq | GRCh38/hg38 |
| NM_004048.2 | chr15:g.44715545G>T | c.190G>T | p.E64* | RefSeq | GRCh38/hg38 |
| XM_005254549.3 | chr15:g.44715545G>T | c.190G>T | p.E64* | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
|---|---|---|---|---|---|---|---|
| B2M mutant | colorectal cancer | predicted - sensitive | unspecified PD-1 antibody | Clinical Study - Cohort | Actionable | In a clinical study, a cohort of colorectal cancer patients harboring B2M mutations demonstrated a clinical benefit of either a partial response or stable disease in 85% (11/13) when treated with a PD-1 or PD-L1 inhibitor (PMID: 31008436). | 31008436 |
| B2M mutant | colorectal cancer | predicted - sensitive | unspecified PD-L1 antibody | Clinical Study - Cohort | Actionable | In a clinical study, a cohort of colorectal cancer patients harboring B2M mutations demonstrated a clinical benefit of either a partial response or stable disease in 85% (11/13) when treated with a PD-1 or PD-L1 inhibitor (PMID: 31008436). | 31008436 |