Gene Variant Detail

Contact

Missing content? – Request curation!

Request curation for specific Genes, Variants, or PubMed publications.

Have questions, comments, or suggestions? - Let us know!

Email us at : ckbsupport@genomenon.com

Gene TSC2
Variant S1410L
Impact List missense
Protein Effect no effect - predicted
Gene Variant Descriptions TSC2 S1410L (corresponds to S1433L in the canonical isoform) does not lie within any known functional domains of the Tsc2 protein (UniProt.org). S1410L results in Tsc1, Tsc2, and S6k expression (PMID: 21309039) and inhibition of S6k phosphorylation similar to wild-type Tsc2 in cell culture (PMID: 18854862), and therefore, is predicted to have no effect on Tsc2 protein function.
Associated Drug Resistance
Category Variants Paths

TSC2 mutant TSC2 S1410L

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.

Transcript NM_001114382.3
gDNA chr16:g.2084520C>T
cDNA c.4229C>T
Protein p.S1410L
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001406663.1 chr16:g.2084453_2084454delAGinsCT c.4228_4229delAGinsCT p.S1410L RefSeq GRCh38/hg38
NM_001406678.1 chr16:g.2084998C>T c.4229C>T p.S1410L RefSeq GRCh38/hg38
NM_001406668.1 chr16:g.2084561_2084562delTCinsCT c.4228_4229delTCinsCT p.S1410L RefSeq GRCh38/hg38
NM_001114382.3 chr16:g.2084520C>T c.4229C>T p.S1410L RefSeq GRCh38/hg38
NM_001318832.2 chr16:g.2084619C>T c.4229C>T p.S1410L RefSeq GRCh38/hg38
NM_001406675.1 chr16:g.2084666_2084667delAGinsCT c.4228_4229delAGinsCT p.S1410L RefSeq GRCh38/hg38
NM_001114382.2 chr16:g.2084520C>T c.4229C>T p.S1410L RefSeq GRCh38/hg38
NM_001370404.1 chr16:g.2084582_2084583delAGinsCT c.4228_4229delAGinsCT p.S1410L RefSeq GRCh38/hg38
NM_001406679.1 chr16:g.2085236_2085237delTCinsCT c.4228_4229delTCinsCT p.S1410L 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