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 R905fs
Impact List frameshift
Protein Effect loss of function
Gene Variant Descriptions TSC2 R905fs results in a change in the amino acid sequence of the Tsc2 protein beginning at aa 905 of 1807, likely resulting in premature truncation of the functional protein (UniProt.org). R905fs confers a loss of function to the Tsc2 protein as indicated by increased p62 expression associated with decreased autophagy, and reduced ciliogenesis in patient samples (PMID: 29937275).
Associated Drug Resistance
Category Variants Paths

TSC2 mutant TSC2 inact mut TSC2 R905fs

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.(2076140_2076141)
cDNA c.(2713_2712)
Protein p.R905fs
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_017023618.1 chr16:g.(2083813_2083814) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
NM_001406664.1 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
XM_017023616.1 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
XM_017023616 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
NM_021055.3 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
NM_001370405.1 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
XM_024450413.1 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
NM_001077183 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
XM_011522637.2 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
NM_001406663.1 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
NM_001370404.1 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
XM_005255529 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
XM_011522640.2 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
NM_001077183.2 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
XM_005255529.4 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
NM_001114382.3 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
XM_011522639.3 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
XM_011522637 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
NM_001077183.3 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
NM_001406665.1 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
NM_000548.5 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
XM_011522636.3 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
XM_011522636.2 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
NM_001363528.2 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
XM_011522639.2 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
XM_011522637.3 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
NM_000548.4 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
NM_001114382 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
XM_011522640 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
NM_000548 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
NM_001114382.2 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
XM_017023615 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
XM_011522636 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
XM_017023615.1 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
XM_005255531 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
XM_011522639 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs RefSeq GRCh38/hg38
XM_005255531.4 chr16:g.(2076140_2076141) c.(2713_2712) p.R905fs 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