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Gene | TSC1 |
Variant | Q55Sfs*7 |
Impact List | frameshift |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | TSC1 Q55Sfs*7 indicates a shift in the reading frame starting at amino acid 55 and terminating 7 residues downstream causing a premature truncation of the 1164 amino acid Tsc1 protein (UniProt.org). Q55Sfs*7 has not been characterized however, due to the effects of other truncation mutations downstream of Q55 (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 Q55Sfs*7 |
Transcript | NM_000368.5 |
gDNA | chr9:g.132927248delG |
cDNA | c.163delC |
Protein | p.Q55Sfs*7 |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_005272211 | chr9:g.132927249delA | c.162delT | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001406595.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
XM_017015098 | chr9:g.132927249delA | c.162delT | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001162427.2 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_000368 | chr9:g.132927249delA | c.162delT | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
XM_017015097 | chr9:g.132927249delA | c.162delT | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_000368.4 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001406593.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001162426.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001406603.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001162426.2 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001406599.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001162427 | chr9:g.132927249delA | c.162delT | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001406604.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001162427.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
XM_017015096.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
XM_011518979.3 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001406596.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
XM_011518979.2 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001406597.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001406607.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001406606.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001406609.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
XM_017015096 | chr9:g.132927249delA | c.162delT | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001406610.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001406598.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
XM_017015098.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001406608.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
XM_005272211.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001406601.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_000368.5 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001162426 | chr9:g.132927249delA | c.162delT | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001406611.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001406602.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001406594.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001406600.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001406592.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
XM_017015097.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001406613.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001406612.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
XM_011518979 | chr9:g.132927249delA | c.162delT | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
XM_006717271.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
NM_001406605.1 | chr9:g.132927248delG | c.163delC | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
XM_006717271 | chr9:g.132927249delA | c.162delT | p.Q55Sfs*7 | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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