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Gene | SMARCB1 |
Variant | T72Qfs*13 |
Impact List | frameshift |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | SMARCB1 T72Qfs*13 indicates a shift in the reading frame starting at amino acid 72 and terminating 13 residues downstream causing a premature truncation of the 385 amino acid Smarcb1 protein (UniProt.org). Due to the loss of the MYC-binding and tandem repeat regions (UniProt.org), T72Qfs*13 is predicted to lead to a loss of Smarcb1 protein function. |
Associated Drug Resistance | |
Category Variants Paths |
SMARCB1 mutant SMARCB1 inact mut SMARCB1 T72Qfs*13 |
Transcript | NM_003073.5 |
gDNA | chr22:g.23791876delA |
cDNA | c.214delA |
Protein | p.T72Qfs*13 |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_011530345.2 | chr22:g.23791876delA | c.214delA | p.T72Qfs*13 | RefSeq | GRCh38/hg38 |
NM_003073 | chr22:g.23791876delA | c.214delA | p.T72Qfs*13 | RefSeq | GRCh38/hg38 |
NM_003073.4 | chr22:g.23791876delA | c.214delA | p.T72Qfs*13 | RefSeq | GRCh38/hg38 |
NM_001362877.2 | chr22:g.23791876delA | c.214delA | p.T72Qfs*13 | RefSeq | GRCh38/hg38 |
NM_003073.5 | chr22:g.23791876delA | c.214delA | p.T72Qfs*13 | RefSeq | GRCh38/hg38 |
XM_011530345 | chr22:g.23791876delA | c.214delA | p.T72Qfs*13 | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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