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| Gene | TSC1 |
| Variant | R420Gfs*20 |
| Impact List | frameshift |
| Protein Effect | loss of function - predicted |
| Gene Variant Descriptions | TSC1 R420Gfs*20 indicates a shift in the reading frame starting at amino acid 420 and terminating 20 residues downstream causing a premature truncation of the 1164 amino acid Tsc1 protein (UniProt.org). R420Gfs*20 has not been characterized however, due to the effects of other truncation mutations downstream of R420 (PMID: 11875047, PMID: 20547222), is predicted to lead to a loss of Tsc1 protein function. |
| Associated Drug Resistance | |
| Category Variants Paths |
TSC1 mutant TSC1 inact mut TSC1 R420Gfs*20 |
| Transcript | NM_000368.5 |
| gDNA | chr9:g.132910576delT |
| cDNA | c.1258delA |
| Protein | p.R420Gfs*20 |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| XM_017015097.1 | chr9:g.132910576delT | c.1258delA | p.R420Gfs*20 | RefSeq | GRCh38/hg38 |
| NM_000368.5 | chr9:g.132910576delT | c.1258delA | p.R420Gfs*20 | RefSeq | GRCh38/hg38 |
| NM_000368.4 | chr9:g.132910576delT | c.1258delA | p.R420Gfs*20 | RefSeq | GRCh38/hg38 |
| NM_001406607.1 | chr9:g.132910576delT | c.1258delA | p.R420Gfs*20 | RefSeq | GRCh38/hg38 |
| NM_001406592.1 | chr9:g.132910576delT | c.1258delA | p.R420Gfs*20 | RefSeq | GRCh38/hg38 |
| XM_017015096.1 | chr9:g.132910576delT | c.1258delA | p.R420Gfs*20 | RefSeq | GRCh38/hg38 |
| NM_001406606.1 | chr9:g.132910576delT | c.1258delA | p.R420Gfs*20 | RefSeq | GRCh38/hg38 |
| XM_006717271.1 | chr9:g.132910576delT | c.1258delA | p.R420Gfs*20 | RefSeq | GRCh38/hg38 |
| NM_001406593.1 | chr9:g.132910576delT | c.1258delA | p.R420Gfs*20 | RefSeq | GRCh38/hg38 |
| NM_001406605.1 | chr9:g.132910576delT | c.1258delA | p.R420Gfs*20 | RefSeq | GRCh38/hg38 |
| XM_011518979.2 | chr9:g.132910576delT | c.1258delA | p.R420Gfs*20 | RefSeq | GRCh38/hg38 |
| XM_005272211.1 | chr9:g.132910576delT | c.1258delA | p.R420Gfs*20 | RefSeq | GRCh38/hg38 |
| XM_011518979.3 | chr9:g.132910576delT | c.1258delA | p.R420Gfs*20 | RefSeq | GRCh38/hg38 |
| NM_001406595.1 | chr9:g.132910576delT | c.1258delA | p.R420Gfs*20 | RefSeq | GRCh38/hg38 |
| NM_001406601.1 | chr9:g.132910576delT | c.1258delA | p.R420Gfs*20 | RefSeq | GRCh38/hg38 |
| NM_001406596.1 | chr9:g.132910576delT | c.1258delA | p.R420Gfs*20 | RefSeq | GRCh38/hg38 |
| NM_001406594.1 | chr9:g.132910576delT | c.1258delA | p.R420Gfs*20 | RefSeq | GRCh38/hg38 |
| NM_001406602.1 | chr9:g.132910576delT | c.1258delA | p.R420Gfs*20 | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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