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Gene TSC1
Variant Q413Rfs*27
Impact List frameshift
Protein Effect loss of function - predicted
Gene Variant Descriptions TSC1 Q413Rfs*27 indicates a shift in the reading frame starting at amino acid 413 and terminating 27 residues downstream causing a premature truncation of the 1164 amino acid Tsc1 protein (UniProt.org). Q413Rfs*27 has not been characterized however, due to the effects of other truncation mutations downstream of Q413 (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 Q413Rfs*27

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Transcript NM_000368.5
gDNA chr9:g.132910596delT
cDNA c.1238delA
Protein p.Q413Rfs*27
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001406607.1 chr9:g.132910596delT c.1238delA p.Q413Rfs*27 RefSeq GRCh38/hg38
NM_001406596.1 chr9:g.132910596delT c.1238delA p.Q413Rfs*27 RefSeq GRCh38/hg38
NM_001406593.1 chr9:g.132910596delT c.1238delA p.Q413Rfs*27 RefSeq GRCh38/hg38
XM_006717271.1 chr9:g.132910596delT c.1238delA p.Q413Rfs*27 RefSeq GRCh38/hg38
NM_001406605.1 chr9:g.132910596delT c.1238delA p.Q413Rfs*27 RefSeq GRCh38/hg38
XM_011518979.2 chr9:g.132910596delT c.1238delA p.Q413Rfs*27 RefSeq GRCh38/hg38
NM_001406592.1 chr9:g.132910596delT c.1238delA p.Q413Rfs*27 RefSeq GRCh38/hg38
XM_011518979.3 chr9:g.132910596delT c.1238delA p.Q413Rfs*27 RefSeq GRCh38/hg38
NM_000368.4 chr9:g.132910596delT c.1238delA p.Q413Rfs*27 RefSeq GRCh38/hg38
XM_017015097.1 chr9:g.132910596delT c.1238delA p.Q413Rfs*27 RefSeq GRCh38/hg38
XM_005272211.1 chr9:g.132910596delT c.1238delA p.Q413Rfs*27 RefSeq GRCh38/hg38
XM_017015096.1 chr9:g.132910596delT c.1238delA p.Q413Rfs*27 RefSeq GRCh38/hg38
NM_001406595.1 chr9:g.132910596delT c.1238delA p.Q413Rfs*27 RefSeq GRCh38/hg38
NM_001406594.1 chr9:g.132910596delT c.1238delA p.Q413Rfs*27 RefSeq GRCh38/hg38
NM_001406606.1 chr9:g.132910596delT c.1238delA p.Q413Rfs*27 RefSeq GRCh38/hg38
NM_000368.5 chr9:g.132910596delT c.1238delA p.Q413Rfs*27 RefSeq GRCh38/hg38
NM_001406602.1 chr9:g.132910596delT c.1238delA p.Q413Rfs*27 RefSeq GRCh38/hg38
NM_001406601.1 chr9:g.132910596delT c.1238delA p.Q413Rfs*27 RefSeq GRCh38/hg38

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  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References