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 V909Cfs*6
Impact List frameshift
Protein Effect loss of function - predicted
Gene Variant Descriptions TSC2 V909Cfs*6 indicates a shift in the reading frame starting at amino acid 909 and terminating 6 residues downstream causing a premature truncation of the 1807 amino acid Tsc2 protein (UniProt.org). V909Cfs*6 results in increased phosphorylation of S6k1 and Stat3 in cultured cells (PMID: 31454656), and therefore, is predicted to lead to a loss of Tsc2 protein function.
Associated Drug Resistance
Category Variants Paths

TSC2 mutant TSC2 inact mut TSC2 V909Cfs*6

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.2076152dupT
cDNA c.2724dupT
Protein p.V909Cfs*6
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001370405.1 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
NM_000548 chr16:g.2076148_2076149insC c.2720_2721insC p.V909Cfs*6 RefSeq GRCh38/hg38
XM_005255529.4 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
XM_017023616.1 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
XM_005255531.4 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
XM_017023615 chr16:g.2076148_2076149insC c.2720_2721insC p.V909Cfs*6 RefSeq GRCh38/hg38
NM_001363528.2 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
XM_011522636 chr16:g.2076148_2076149insC c.2720_2721insC p.V909Cfs*6 RefSeq GRCh38/hg38
XM_005255531 chr16:g.2076148_2076149insC c.2720_2721insC p.V909Cfs*6 RefSeq GRCh38/hg38
XM_011522636.2 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
XM_017023618.1 chr16:g.2084236_2084237insTGCCCCCCCCCCCCCTA c.2724_2725insTGCCCCCCCCCCCCCTA p.V909Cfs*6 RefSeq GRCh38/hg38
NM_001406663.1 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
XM_011522640 chr16:g.2076148_2076149insC c.2720_2721insC p.V909Cfs*6 RefSeq GRCh38/hg38
NM_001114382.2 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
NM_001370404.1 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
NM_001077183.2 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
XM_017023615.1 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
NM_000548.5 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
XM_011522639.2 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
XM_011522637 chr16:g.2076148_2076149insC c.2720_2721insC p.V909Cfs*6 RefSeq GRCh38/hg38
XM_011522639 chr16:g.2076148_2076149insC c.2720_2721insC p.V909Cfs*6 RefSeq GRCh38/hg38
NM_001114382 chr16:g.2076148_2076149insC c.2720_2721insC p.V909Cfs*6 RefSeq GRCh38/hg38
XM_011522636.3 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
NM_001406665.1 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
XM_011522637.2 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
XM_011522640.2 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
NM_000548.4 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
XM_024450413.1 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
NM_001114382.3 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
XM_011522639.3 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
NM_001077183 chr16:g.2076148_2076149insC c.2720_2721insC p.V909Cfs*6 RefSeq GRCh38/hg38
XM_017023616 chr16:g.2076148_2076149insC c.2720_2721insC p.V909Cfs*6 RefSeq GRCh38/hg38
XM_005255529 chr16:g.2076148_2076149insC c.2720_2721insC p.V909Cfs*6 RefSeq GRCh38/hg38
NM_021055.3 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
NM_001077183.3 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
XM_011522637.3 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
NM_001406664.1 chr16:g.2076152dupT c.2724dupT p.V909Cfs*6 RefSeq GRCh38/hg38
XM_017023618 chr16:g.2084235_2084236insCTGCCCCCCCCCCCCCT c.2723_2724insCTGCCCCCCCCCCCCCT p.V909Cfs*6 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.

Clinical Trial Phase Therapies Title Recruitment Status Covered Countries Other Countries