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Gene | TSC1 |
Variant | M18Cfs*8 |
Impact List | frameshift |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | TSC1 M18Cfs*8 indicates a shift in the reading frame starting at amino acid 18 and terminating 8 residues downstream causing a premature truncation of the 1164 amino acid Tsc1 protein (UniProt.org). M18Cfs*8 has not been characterized however, due to the effects of other truncation mutations downstream of M18 (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 M18fs TSC1 M18Cfs*8 |
Transcript | NM_000368.5 |
gDNA | chr9:g.132928821delT |
cDNA | c.52delA |
Protein | p.M18Cfs*8 |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_006717271.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406618.1 | chr9:g.132923441_132923442insTTGGGGGGGCA | c.51_52insTGCCCCCCCAA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406619.1 | chr9:g.132923441_132923442insTTGGGGGGGCA | c.51_52insTGCCCCCCCAA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_000368.4 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406623.1 | chr9:g.132923441_132923442insTTGGGGGGGCA | c.51_52insTGCCCCCCCAA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
XM_017015097.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406613.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406621.1 | chr9:g.132923441_132923442insTTGGGGGGGCA | c.51_52insTGCCCCCCCAA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
XM_017015101 | chr9:g.132923443_132923444insGGGGGGGCAAG | c.50_51insTTGCCCCCCCC | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001162427.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
XM_017015099.1 | chr9:g.132923441_132923442insTTGGGGGGGCA | c.51_52insTGCCCCCCCAA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001162427.2 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_000368.5 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406610.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406611.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
XM_017015096.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406614.1 | chr9:g.132923441_132923442insTTGGGGGGGCA | c.51_52insTGCCCCCCCAA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406608.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406607.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406597.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406616.1 | chr9:g.132923441_132923442insTTGGGGGGGCA | c.51_52insTGCCCCCCCAA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
XM_011518979 | chr9:g.132928826delG | c.51delC | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
XM_017015096 | chr9:g.132928826delG | c.51delC | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
XM_017015098.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406612.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406598.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406595.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
XM_011518979.3 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001162426.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406594.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
XM_017015100 | chr9:g.132923443_132923444insGGGGGGGCAAG | c.50_51insTTGCCCCCCCC | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406596.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
XM_011518979.2 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406592.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001362177.2 | chr9:g.132923441_132923442insTTGGGGGGGCA | c.51_52insTGCCCCCCCAA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001162427 | chr9:g.132928826delG | c.51delC | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406605.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406599.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
XM_017015100.1 | chr9:g.132923441_132923442insTTGGGGGGGCA | c.51_52insTGCCCCCCCAA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406620.1 | chr9:g.132923441_132923442insTTGGGGGGGCA | c.51_52insTGCCCCCCCAA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406615.1 | chr9:g.132923441_132923442insTTGGGGGGGCA | c.51_52insTGCCCCCCCAA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406625.1 | chr9:g.132923441_132923442insTTGGGGGGGCA | c.51_52insTGCCCCCCCAA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
XM_017015099 | chr9:g.132923443_132923444insGGGGGGGCAAG | c.50_51insTTGCCCCCCCC | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
XM_017015097 | chr9:g.132928826delG | c.51delC | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
XM_017015098 | chr9:g.132928826delG | c.51delC | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406617.1 | chr9:g.132923441_132923442insTTGGGGGGGCA | c.51_52insTGCCCCCCCAA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
XM_006717271 | chr9:g.132928826delG | c.51delC | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
XM_005272211 | chr9:g.132928826delG | c.51delC | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
XM_017015101.1 | chr9:g.132923441_132923442insTTGGGGGGGCA | c.51_52insTGCCCCCCCAA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406606.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406593.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406603.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406600.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406622.1 | chr9:g.132923441_132923442insTTGGGGGGGCA | c.51_52insTGCCCCCCCAA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001162426 | chr9:g.132928826delG | c.51delC | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_000368 | chr9:g.132928826delG | c.51delC | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406609.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406602.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001162426.2 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406604.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
XM_005272211.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406601.1 | chr9:g.132928821delT | c.52delA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
NM_001406624.1 | chr9:g.132923441_132923442insTTGGGGGGGCA | c.51_52insTGCCCCCCCAA | p.M18Cfs*8 | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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