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 L1198M
Impact List missense
Protein Effect unknown
Gene Variant Descriptions TSC2 L1198M does not lie within any known functional domains of the Tsc2 protein (UniProt.org). L1198M has been identified in sequencing studies (PMID: 27149842), but has not been biochemically characterized and therefore, its effect on Tsc2 protein function is unknown (PubMed, Nov 2024).
Associated Drug Resistance
Category Variants Paths

TSC2 mutant TSC2 L1198M

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_000548.5
gDNA chr16:g.2080359C>A
cDNA c.3592C>A
Protein p.L1198M
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001406680.1 chr16:g.2084414_2084416delCTCinsATG c.3592_3594delCTCinsATG p.L1198M RefSeq GRCh38/hg38
XM_011522638.3 chr16:g.2081687_2081689delCTCinsATG c.3592_3594delCTCinsATG p.L1198M RefSeq GRCh38/hg38
XM_011522636.2 chr16:g.2080359C>A c.3592C>A p.L1198M RefSeq GRCh38/hg38
NM_001114382.3 chr16:g.2080359C>A c.3592C>A p.L1198M RefSeq GRCh38/hg38
NM_001114382.2 chr16:g.2080359C>A c.3592C>A p.L1198M RefSeq GRCh38/hg38
XM_011522636.3 chr16:g.2080359C>A c.3592C>A p.L1198M RefSeq GRCh38/hg38
NM_000548.4 chr16:g.2080359C>A c.3592C>A p.L1198M RefSeq GRCh38/hg38
NM_000548.5 chr16:g.2080359C>A c.3592C>A p.L1198M RefSeq GRCh38/hg38
NM_001318832.2 chr16:g.2081675C>A c.3592C>A p.L1198M RefSeq GRCh38/hg38
NM_001406668.1 chr16:g.2081618C>A c.3592C>A p.L1198M RefSeq GRCh38/hg38
NM_001406670.1 chr16:g.2081687_2081689delCTCinsATG c.3592_3594delCTCinsATG p.L1198M 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