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Gene | TSC2 |
Variant | V1547I |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | TSC2 V1547I lies within the Rap-GAP domain of the Tsc2 protein (UniProt.org). V1547I results in decreased GAP activity of Tsc2 and increased phosphorylation of S6K in cell culture (PMID: 28215400). |
Associated Drug Resistance | |
Category Variants Paths |
TSC2 mutant TSC2 inact mut TSC2 V1547I |
Transcript | NM_000548.5 |
gDNA | chr16:g.2085299G>A |
cDNA | c.4639G>A |
Protein | p.V1547I |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_011522638 | chr16:g.2084645G>A | c.4639G>A | p.V1547I | RefSeq | GRCh38/hg38 |
XM_011522638.2 | chr16:g.2084645G>A | c.4639G>A | p.V1547I | RefSeq | GRCh38/hg38 |
NM_001406673.1 | chr16:g.2086734G>A | c.4639G>A | p.V1547I | RefSeq | GRCh38/hg38 |
NM_000548 | chr16:g.2085299G>A | c.4639G>A | p.V1547I | RefSeq | GRCh38/hg38 |
NM_000548.4 | chr16:g.2085299G>A | c.4639G>A | p.V1547I | RefSeq | GRCh38/hg38 |
NM_000548.5 | chr16:g.2085299G>A | c.4639G>A | p.V1547I | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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