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| Gene | TSC2 |
| Variant | R905Q |
| Impact List | missense |
| Protein Effect | loss of function |
| Gene Variant Descriptions | TSC2 R905Q does not lie within any known functional domains of the Tsc2 protein (UniProt.org). R905Q results in 14-3-3 binding (PMID: 12176984), chaperone function, Tsc2 phosphorylation, Tsc1 binding, and Tsc1 subcellular localization similar to wild-type Tsc2 (PMID: 11741832) but results in decreased suppression of S6k phosphorylation (PMID: 15483652, PMID: 21309039, PMID: 17120248), decreased Rheb GTPase activity (PMID: 15483652, PMID: 17120248), and decreased Tsc2 stability in culture (PMID: 16464865, PMID: 21309039). |
| Associated Drug Resistance | |
| Category Variants Paths |
TSC2 mutant TSC2 inact mut TSC2 R905Q |
| Transcript | NM_000548.5 |
| gDNA | chr16:g.2076142G>A |
| cDNA | c.2714G>A |
| Protein | p.R905Q |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_001114382.3 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| XM_005255529.4 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| NM_001370404.1 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| XM_011522639.3 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| XM_005255531.4 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| XM_024450413.1 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| NM_001406664.1 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| XM_011522636.2 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| XM_017023615.1 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| XM_017023616.1 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| NM_001406665.1 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| NM_000548.4 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| NM_001363528.2 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| XM_011522636.3 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| NM_001406663.1 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| NM_001370405.1 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| NM_001077183.2 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| XM_011522640.2 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| NM_001077183.3 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| NM_001114382.2 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| XM_011522637.3 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| NM_021055.3 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| XM_011522639.2 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| NM_000548.5 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| XM_011522637.2 | chr16:g.2076142G>A | c.2714G>A | p.R905Q | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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