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Gene | TSC1 |
Variant | K477* |
Impact List | nonsense |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | TSC1 K477* results in a premature truncation of the Tsc1 protein at amino acid 477 of 1164 (UniProt.org). K477* has not been characterized however, due to the effects of other truncation mutations downstream of K477 (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 K477* |
Transcript | NM_000368.5 |
gDNA | chr9:g.132906740T>A |
cDNA | c.1429A>T |
Protein | p.K477* |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_006717271 | chr9:g.132906740T>A | c.1429A>T | p.K477* | RefSeq | GRCh38/hg38 |
NM_001406606.1 | chr9:g.132906740T>A | c.1429A>T | p.K477* | RefSeq | GRCh38/hg38 |
NM_000368 | chr9:g.132906740T>A | c.1429A>T | p.K477* | RefSeq | GRCh38/hg38 |
XM_017015097 | chr9:g.132906740T>A | c.1429A>T | p.K477* | RefSeq | GRCh38/hg38 |
XM_005272211 | chr9:g.132906740T>A | c.1429A>T | p.K477* | RefSeq | GRCh38/hg38 |
NM_000368.4 | chr9:g.132906740T>A | c.1429A>T | p.K477* | RefSeq | GRCh38/hg38 |
NM_001406601.1 | chr9:g.132906740T>A | c.1429A>T | p.K477* | RefSeq | GRCh38/hg38 |
XM_017015097.1 | chr9:g.132906740T>A | c.1429A>T | p.K477* | RefSeq | GRCh38/hg38 |
NM_001406595.1 | chr9:g.132906740T>A | c.1429A>T | p.K477* | RefSeq | GRCh38/hg38 |
NM_001406596.1 | chr9:g.132906740T>A | c.1429A>T | p.K477* | RefSeq | GRCh38/hg38 |
XM_005272211.1 | chr9:g.132906740T>A | c.1429A>T | p.K477* | RefSeq | GRCh38/hg38 |
XM_017015096.1 | chr9:g.132906740T>A | c.1429A>T | p.K477* | RefSeq | GRCh38/hg38 |
NM_001406592.1 | chr9:g.132906740T>A | c.1429A>T | p.K477* | RefSeq | GRCh38/hg38 |
NM_001406602.1 | chr9:g.132906740T>A | c.1429A>T | p.K477* | RefSeq | GRCh38/hg38 |
XM_006717271.1 | chr9:g.132906740T>A | c.1429A>T | p.K477* | RefSeq | GRCh38/hg38 |
XM_011518979.3 | chr9:g.132906740T>A | c.1429A>T | p.K477* | RefSeq | GRCh38/hg38 |
XM_017015096 | chr9:g.132906740T>A | c.1429A>T | p.K477* | RefSeq | GRCh38/hg38 |
NM_001406607.1 | chr9:g.132906740T>A | c.1429A>T | p.K477* | RefSeq | GRCh38/hg38 |
XM_011518979 | chr9:g.132906740T>A | c.1429A>T | p.K477* | RefSeq | GRCh38/hg38 |
NM_001406605.1 | chr9:g.132906740T>A | c.1429A>T | p.K477* | RefSeq | GRCh38/hg38 |
NM_000368.5 | chr9:g.132906740T>A | c.1429A>T | p.K477* | RefSeq | GRCh38/hg38 |
NM_001406593.1 | chr9:g.132906740T>A | c.1429A>T | p.K477* | RefSeq | GRCh38/hg38 |
XM_011518979.2 | chr9:g.132906740T>A | c.1429A>T | p.K477* | RefSeq | GRCh38/hg38 |
NM_001406594.1 | chr9:g.132906740T>A | c.1429A>T | p.K477* | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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