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| Gene | CTNNB1 |
| Variant | T41_P52del |
| Impact List | deletion |
| Protein Effect | unknown |
| Gene Variant Descriptions | CTNNB1 T41_P52del results in the deletion of 12 amino acids of the Ctnnb1 protein from amino acids 41 to 52 (UniProt.org). T41_P52del has not been characterized in the scientific literature and therefore, its effect on Ctnnb1 protein function is unknown (PubMed, Jan 2026). |
| Associated Drug Resistance | |
| Category Variants Paths |
CTNNB1 mutant CTNNB1 T41_P52del |
| Transcript | NM_001904.4 |
| gDNA | chr3:g.41224633_41224668del36 |
| cDNA | c.121_156del36 |
| Protein | p.T41_P52del12 |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| XM_017005738 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| XM_006712985.2 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| NM_001098209.2 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| NM_001098209.1 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| XM_005264886 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| NM_001330729.2 | chr3:g.41224654_41224689del36 | c.121_156del36 | p.G41_T52del12 | RefSeq | GRCh38/hg38 |
| XM_047447482.1 | chr3:g.41224654_41224689del36 | c.121_156del36 | p.G41_T52del12 | RefSeq | GRCh38/hg38 |
| XM_017005738.2 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| NM_001330729.1 | chr3:g.41224654_41224689del36 | c.121_156del36 | p.G41_T52del12 | RefSeq | GRCh38/hg38 |
| XM_024453356.2 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| XM_024453356.1 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| XM_024453359.1 | chr3:g.41224654_41224689del36 | c.121_156del36 | p.G41_T52del12 | RefSeq | GRCh38/hg38 |
| NM_001904.3 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| NM_001904.4 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| XM_047447480.1 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| NM_001098209 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| NM_001098210 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| XM_047447477.1 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| XM_024453358.1 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| XM_006712985.1 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| XM_017005738.1 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| XM_024453360.1 | chr3:g.41224654_41224689del36 | c.121_156del36 | p.G41_T52del12 | RefSeq | GRCh38/hg38 |
| NM_001098210.1 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del | RefSeq | GRCh38/hg38 |
| XM_006712983 | chr3:g.41224654_41224689del36 | c.121_156del36 | p.G41_T52del12 | RefSeq | GRCh38/hg38 |
| XM_047447481.1 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| XM_047447483.1 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| XM_047447479.1 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| XM_006712984 | chr3:g.41224654_41224689del36 | c.121_156del36 | p.G41_T52del12 | RefSeq | GRCh38/hg38 |
| NM_001098210.2 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| XM_047447478.1 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| XM_024453357.1 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| NM_001904 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| XM_006712985 | chr3:g.41224633_41224668del36 | c.121_156del36 | p.T41_P52del12 | RefSeq | GRCh38/hg38 |
| XM_006712983.2 | chr3:g.41224654_41224689del36 | c.121_156del36 | p.G41_T52del12 | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
|---|