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Gene | TSC1 |
Variant | S575F |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | TSC1 S575F lies within the region of the Tsc1 protein that mediates interaction with WDR45B (UniProt.org). S575F has been identified in sequencing studies (PMID: 30348637), but has not been biochemically characterized and therefore, its effect on Tsc1 protein function is unknown (PubMed, Nov 2024). |
Associated Drug Resistance | |
Category Variants Paths |
TSC1 mutant TSC1 S575F |
Transcript | NM_000368.5 |
gDNA | chr9:g.132905854G>A |
cDNA | c.1724C>T |
Protein | p.S575F |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_017015097.1 | chr9:g.132905854G>A | c.1724C>T | p.S575F | RefSeq | GRCh38/hg38 |
NM_001406606.1 | chr9:g.132905854G>A | c.1724C>T | p.S575F | RefSeq | GRCh38/hg38 |
XM_005272211 | chr9:g.132905854G>A | c.1724C>T | p.S575F | RefSeq | GRCh38/hg38 |
XM_006717271 | chr9:g.132905854G>A | c.1724C>T | p.S575F | RefSeq | GRCh38/hg38 |
NM_000368.4 | chr9:g.132905854G>A | c.1724C>T | p.S575F | RefSeq | GRCh38/hg38 |
NM_001406605.1 | chr9:g.132905854G>A | c.1724C>T | p.S575F | RefSeq | GRCh38/hg38 |
XM_017015096.1 | chr9:g.132905854G>A | c.1724C>T | p.S575F | RefSeq | GRCh38/hg38 |
NM_001406595.1 | chr9:g.132905854G>A | c.1724C>T | p.S575F | RefSeq | GRCh38/hg38 |
NM_001406627.1 | chr9:g.132897558_132897559delAGinsTT | c.1723_1724delAGinsTT | p.S575F | RefSeq | GRCh38/hg38 |
NM_001406592.1 | chr9:g.132905854G>A | c.1724C>T | p.S575F | RefSeq | GRCh38/hg38 |
NM_000368 | chr9:g.132905854G>A | c.1724C>T | p.S575F | RefSeq | GRCh38/hg38 |
NM_001406628.1 | chr9:g.132897558_132897559delAGinsTT | c.1723_1724delAGinsTT | p.S575F | RefSeq | GRCh38/hg38 |
NM_000368.5 | chr9:g.132905854G>A | c.1724C>T | p.S575F | RefSeq | GRCh38/hg38 |
NM_001406594.1 | chr9:g.132905854G>A | c.1724C>T | p.S575F | RefSeq | GRCh38/hg38 |
XM_017015097 | chr9:g.132905854G>A | c.1724C>T | p.S575F | RefSeq | GRCh38/hg38 |
XM_011518979.3 | chr9:g.132905854G>A | c.1724C>T | p.S575F | RefSeq | GRCh38/hg38 |
XM_011518979 | chr9:g.132905854G>A | c.1724C>T | p.S575F | RefSeq | GRCh38/hg38 |
XM_011518979.2 | chr9:g.132905854G>A | c.1724C>T | p.S575F | RefSeq | GRCh38/hg38 |
NM_001406602.1 | chr9:g.132905854G>A | c.1724C>T | p.S575F | RefSeq | GRCh38/hg38 |
NM_001406607.1 | chr9:g.132905854G>A | c.1724C>T | p.S575F | RefSeq | GRCh38/hg38 |
NM_001406601.1 | chr9:g.132905854G>A | c.1724C>T | p.S575F | RefSeq | GRCh38/hg38 |
NM_001406593.1 | chr9:g.132905854G>A | c.1724C>T | p.S575F | RefSeq | GRCh38/hg38 |
XM_005272211.1 | chr9:g.132905854G>A | c.1724C>T | p.S575F | RefSeq | GRCh38/hg38 |
XM_017015096 | chr9:g.132905854G>A | c.1724C>T | p.S575F | RefSeq | GRCh38/hg38 |
NM_001406596.1 | chr9:g.132905854G>A | c.1724C>T | p.S575F | RefSeq | GRCh38/hg38 |
XM_006717271.1 | chr9:g.132905854G>A | c.1724C>T | p.S575F | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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