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Gene | TSC1 |
Variant | P141S |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | TSC1 P141S does not lie within any known functional domains of the Tsc1 protein (UniProt.org). P141S has not been characterized and therefore, its effect on Tsc1 protein function is unknown (PubMed, Nov 2024). |
Associated Drug Resistance | |
Category Variants Paths |
TSC1 mutant TSC1 P141S |
Transcript | NM_000368.5 |
gDNA | chr9:g.132923435G>A |
cDNA | c.421C>T |
Protein | p.P141S |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001406593.1 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
XM_006717271.1 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
XM_017015097.1 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
NM_001406602.1 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
XM_005272211 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
XM_017015098 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
NM_001406594.1 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
NM_001406603.1 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
NM_001406600.1 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
XM_011518979.2 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
NM_001162426.2 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
NM_001406609.1 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
NM_001406595.1 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
XM_017015098.1 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
NM_001406608.1 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
NM_000368 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
NM_001406598.1 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
NM_001406599.1 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
NM_001162426 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
NM_001406601.1 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
XM_006717271 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
NM_001406605.1 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
XM_005272211.1 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
XM_017015097 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
XM_011518979.3 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
XM_017015096 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
NM_001406604.1 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
NM_000368.4 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
NM_000368.5 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
NM_001162426.1 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
NM_001406607.1 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
NM_001406596.1 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
NM_001406606.1 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
XM_011518979 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
XM_017015096.1 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
NM_001406592.1 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
NM_001406597.1 | chr9:g.132923435G>A | c.421C>T | p.P141S | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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