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Gene | TSC1 |
Variant | R509Q |
Impact List | missense |
Protein Effect | no effect |
Gene Variant Descriptions | TSC1 R509Q lies within the region of the Tsc1 protein that mediates interaction with WDR45B (UniProt.org). R509Q demonstrates protein stability and mTOR pathway inhibition similar to wild-type Tsc1 in cell culture (PMID: 18830229). |
Associated Drug Resistance | |
Category Variants Paths |
TSC1 mutant TSC1 R509Q |
Transcript | NM_000368.5 |
gDNA | chr9:g.132906052C>T |
cDNA | c.1526G>A |
Protein | p.R509Q |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_000368 | chr9:g.132906052C>T | c.1526G>A | p.R509Q | RefSeq | GRCh38/hg38 |
XM_011518979 | chr9:g.132906052C>T | c.1526G>A | p.R509Q | RefSeq | GRCh38/hg38 |
NM_001406602.1 | chr9:g.132906052C>T | c.1526G>A | p.R509Q | RefSeq | GRCh38/hg38 |
XM_017015097 | chr9:g.132906052C>T | c.1526G>A | p.R509Q | RefSeq | GRCh38/hg38 |
NM_001406605.1 | chr9:g.132906052C>T | c.1526G>A | p.R509Q | RefSeq | GRCh38/hg38 |
XM_017015096 | chr9:g.132906052C>T | c.1526G>A | p.R509Q | RefSeq | GRCh38/hg38 |
NM_001406595.1 | chr9:g.132906052C>T | c.1526G>A | p.R509Q | RefSeq | GRCh38/hg38 |
XM_017015097.1 | chr9:g.132906052C>T | c.1526G>A | p.R509Q | RefSeq | GRCh38/hg38 |
XM_005272211.1 | chr9:g.132906052C>T | c.1526G>A | p.R509Q | RefSeq | GRCh38/hg38 |
NM_001406607.1 | chr9:g.132906052C>T | c.1526G>A | p.R509Q | RefSeq | GRCh38/hg38 |
NM_000368.4 | chr9:g.132906052C>T | c.1526G>A | p.R509Q | RefSeq | GRCh38/hg38 |
XM_011518979.3 | chr9:g.132906052C>T | c.1526G>A | p.R509Q | RefSeq | GRCh38/hg38 |
NM_001406594.1 | chr9:g.132906052C>T | c.1526G>A | p.R509Q | RefSeq | GRCh38/hg38 |
XM_006717271 | chr9:g.132906052C>T | c.1526G>A | p.R509Q | RefSeq | GRCh38/hg38 |
NM_001406606.1 | chr9:g.132906052C>T | c.1526G>A | p.R509Q | RefSeq | GRCh38/hg38 |
XM_017015096.1 | chr9:g.132906052C>T | c.1526G>A | p.R509Q | RefSeq | GRCh38/hg38 |
NM_001406593.1 | chr9:g.132906052C>T | c.1526G>A | p.R509Q | RefSeq | GRCh38/hg38 |
NM_001406601.1 | chr9:g.132906052C>T | c.1526G>A | p.R509Q | RefSeq | GRCh38/hg38 |
NM_000368.5 | chr9:g.132906052C>T | c.1526G>A | p.R509Q | RefSeq | GRCh38/hg38 |
XM_006717271.1 | chr9:g.132906052C>T | c.1526G>A | p.R509Q | RefSeq | GRCh38/hg38 |
NM_001406592.1 | chr9:g.132906052C>T | c.1526G>A | p.R509Q | RefSeq | GRCh38/hg38 |
XM_005272211 | chr9:g.132906052C>T | c.1526G>A | p.R509Q | RefSeq | GRCh38/hg38 |
XM_011518979.2 | chr9:g.132906052C>T | c.1526G>A | p.R509Q | RefSeq | GRCh38/hg38 |
NM_001406596.1 | chr9:g.132906052C>T | c.1526G>A | p.R509Q | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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