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Gene | TSC2 |
Variant | M280T |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | TSC2 M280T lies within the TSC1-interacting region of the Tsc2 protein (UniProt.org). M280T results in disruption of the Tsc complex function as indicated by reduced inhibition of S6k phosphorylation and leads to decreased interaction with Tsc1 in cultured cells (PMID: 31799751). |
Associated Drug Resistance | |
Category Variants Paths |
TSC2 mutant TSC2 inact mut TSC2 M280T |
Transcript | NM_000548.5 |
gDNA | chr16:g.2057169T>C |
cDNA | c.839T>C |
Protein | p.M280T |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_017023616.1 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
NM_001370405.1 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
XM_017023615.1 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
XM_005255529.4 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
NM_001077183.2 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
NM_001406665.1 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
XM_005255531.4 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
XM_011522636.3 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
XM_024450413.1 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
NM_001077183.3 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
NM_001406664.1 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
XM_011522640.2 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
NM_001114382.2 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
XM_011522636.2 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
XM_011522637.3 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
NM_001370404.1 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
XM_011522637.2 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
XM_011522639.2 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
NM_001406663.1 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
XM_011522639.3 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
NM_001114382.3 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
NM_000548.4 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
NM_021055.3 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
NM_001363528.2 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
NM_000548.5 | chr16:g.2057169T>C | c.839T>C | p.M280T | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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