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Gene | TSC2 |
Variant | G294E |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | TSC2 G294E lies within the TSC1-interacting region of the Tsc2 protein (UniProt.org). G294E results in increased expression of Mcp-1 compared to wild-type Tsc2 in cell culture (PMID: 16129702) and failure to bind TSC1 in vitro (PMID: 11741833, PMID: 23955302). |
Associated Drug Resistance | |
Category Variants Paths |
TSC2 mutant TSC2 inact mut TSC2 G294E |
Transcript | NM_000548.5 |
gDNA | chr16:g.2058779G>A |
cDNA | c.881G>A |
Protein | p.G294E |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_011522637.3 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
XM_005255531 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
NM_001077183.2 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
NM_001406663.1 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
NM_001114382 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
NM_001406664.1 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
XM_011522636 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
NM_001077183 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
NM_001077183.3 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
XM_005255529 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
XM_017023615.1 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
XM_005255529.4 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
XM_011522639.2 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
XM_005255531.4 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
XM_024450413.1 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
XM_011522639.3 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
NM_000548 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
XM_017023616 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
NM_001406665.1 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
XM_011522637 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
NM_001114382.3 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
XM_011522640 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
NM_001114382.2 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
XM_011522636.2 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
XM_017023616.1 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
XM_011522636.3 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
XM_011522640.2 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
NM_000548.5 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
NM_001363528.2 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
XM_017023615 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
XM_011522637.2 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
NM_021055.3 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
NM_001370405.1 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
XM_011522639 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
NM_000548.4 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
NM_001370404.1 | chr16:g.2058779G>A | c.881G>A | p.G294E | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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