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Gene TSC2
Variant S1036F
Impact List missense
Protein Effect unknown
Gene Variant Descriptions TSC2 S1036F does not lie within any known functional domains of the Tsc2 protein (UniProt.org). S1036F has not been characterized in the scientific literature and therefore, its effect on Tsc2 protein function is unknown (PubMed, Sep 2024).
Associated Drug Resistance
Category Variants Paths

TSC2 mutant TSC2 S1036F

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Transcript NM_000548.5
gDNA chr16:g.2079172C>T
cDNA c.3107C>T
Protein p.S1036F
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_011522636 chr16:g.2079172C>T c.3107C>T p.S1036F RefSeq GRCh38/hg38
XM_005255531.4 chr16:g.2079380_2079381delCGinsTT c.3107_3108delCGinsTT p.S1036F RefSeq GRCh38/hg38
NM_000548 chr16:g.2079172C>T c.3107C>T p.S1036F RefSeq GRCh38/hg38
NM_001114382 chr16:g.2079172C>T c.3107C>T p.S1036F RefSeq GRCh38/hg38
XM_011522639.2 chr16:g.2079380_2079381delCGinsTT c.3107_3108delCGinsTT p.S1036F RefSeq GRCh38/hg38
NM_000548.5 chr16:g.2079172C>T c.3107C>T p.S1036F RefSeq GRCh38/hg38
XM_011522639.3 chr16:g.2079380_2079381delCGinsTT c.3107_3108delCGinsTT p.S1036F RefSeq GRCh38/hg38
NM_000548.4 chr16:g.2079172C>T c.3107C>T p.S1036F RefSeq GRCh38/hg38
XM_005255529.4 chr16:g.2079380_2079381delCGinsTT c.3107_3108delCGinsTT p.S1036F RefSeq GRCh38/hg38
NM_001370405.1 chr16:g.2079380_2079381delCGinsTT c.3107_3108delCGinsTT p.S1036F RefSeq GRCh38/hg38
XM_011522636.3 chr16:g.2079172C>T c.3107C>T p.S1036F RefSeq GRCh38/hg38
NM_001114382.2 chr16:g.2079172C>T c.3107C>T p.S1036F RefSeq GRCh38/hg38
NM_001363528.2 chr16:g.2079380_2079381delCGinsTT c.3107_3108delCGinsTT p.S1036F RefSeq GRCh38/hg38
NM_001114382.3 chr16:g.2079172C>T c.3107C>T p.S1036F RefSeq GRCh38/hg38
NM_001406675.1 chr16:g.2079398_2079399delCGinsTT c.3107_3108delCGinsTT p.S1036F RefSeq GRCh38/hg38
XM_011522639 chr16:g.2079380_2079381delCGinsTT c.3107_3108delCGinsTT p.S1036F RefSeq GRCh38/hg38
NM_021055.3 chr16:g.2079380_2079381delCGinsTT c.3107_3108delCGinsTT p.S1036F RefSeq GRCh38/hg38
XM_017023618.1 chr16:g.2084619_2084620delCGinsTT c.3107_3108delCGinsTT p.S1036F RefSeq GRCh38/hg38
XM_017023618 chr16:g.2084619_2084620delCGinsTT c.3107_3108delCGinsTT p.S1036F RefSeq GRCh38/hg38
XM_005255529 chr16:g.2079380_2079381delCGinsTT c.3107_3108delCGinsTT p.S1036F RefSeq GRCh38/hg38
XM_005255531 chr16:g.2079380_2079381delCGinsTT c.3107_3108delCGinsTT p.S1036F RefSeq GRCh38/hg38
NM_001406689.1 chr16:g.2084977C>T c.3107C>T p.S1036F RefSeq GRCh38/hg38
XM_011522636.2 chr16:g.2079172C>T c.3107C>T p.S1036F RefSeq GRCh38/hg38

Filtering

  • Case insensitive filtering will display rows if any text in any cell matches the filter term
  • 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

  • Generally, the default sort order for tables is set to be first column ascending; however, specific tables may set a different default sort order.
  • Click on any column header arrows to sort by that column
  • Hold down the Shift key and click multiple columns to sort by more than one column. Be sure to set ascending or descending order for a given column before moving on to the next column.

Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References