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Gene TSC2
Variant R751*
Impact List nonsense
Protein Effect loss of function - predicted
Gene Variant Descriptions TSC2 R751* results in a premature truncation of the Tsc2 protein at amino acid 751 of 1807 (UniProt.org). R751* has not been characterized however, due to the effects of other truncation mutations downstream of R751 (PMID: 22903760, PMID: 31454656), is predicted to lead to a loss of Tsc2 protein function.
Associated Drug Resistance
Category Variants Paths

TSC2 mutant TSC2 inact mut TSC2 R751*

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Transcript NM_000548.5
gDNA chr16:g.2072879C>T
cDNA c.2251C>T
Protein p.R751*
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_011522639.2 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38
XM_017023616.1 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38
XM_011522636.2 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38
NM_001406665.1 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38
NM_001406663.1 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38
XM_005255529.4 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38
NM_001077183.2 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38
NM_001406680.1 chr16:g.2077611A>T c.2251A>T p.R751* RefSeq GRCh38/hg38
XM_011522639.3 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38
XM_017023615.1 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38
NM_000548.5 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38
NM_000548.4 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38
NM_001406664.1 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38
NM_001363528.2 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38
NM_001406681.1 chr16:g.2076141_2076142delCGinsTA c.2251_2252delCGinsTA p.R751* RefSeq GRCh38/hg38
NM_021055.3 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38
NM_001406683.1 chr16:g.2077611A>T c.2251A>T p.R751* RefSeq GRCh38/hg38
XM_011522640.2 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38
NM_001406682.1 chr16:g.2077611A>T c.2251A>T p.R751* RefSeq GRCh38/hg38
XM_024450413.1 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38
XM_005255531.4 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38
NM_001114382.2 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38
NM_001370404.1 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38
NM_001370405.1 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38
XM_011522637.2 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38
XM_011522636.3 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38
NM_001114382.3 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38
XM_011522637.3 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38
NM_001406684.1 chr16:g.2077611A>T c.2251A>T p.R751* RefSeq GRCh38/hg38
NM_001077183.3 chr16:g.2072879C>T c.2251C>T p.R751* RefSeq GRCh38/hg38

Filtering

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  • Use simple literal full or partial string matches
  • Separate multiple filter terms with a space. Any order may be used (i. e. a b c and c b a are equivalent )
  • Filtering will only apply to rows that are already loaded on the page. Filtering has no impact on query parameters.
  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

Sorting

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  • Click on any column header arrows to sort by that column
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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References