MLH1 R497Gfs*11
Gene Variant Detail

Request Content

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 MLH1
Variant R497Gfs*11
Impact List frameshift
Protein Effect loss of function - predicted
Gene Variant Descriptions MLH1 R497Gfs*11 indicates a shift in the reading frame starting at amino acid 497 and terminating 11 residues downstream causing a premature truncation of the 756 amino acid Mlh1 protein (UniProt.org). Due to the loss of the C-terminal domain (PMID: 16338176), R497Gfs*11 is predicted to lead to a loss of Mlh1 protein function.
Associated Drug Resistance
Category Variants Paths

MLH1 mutant MLH1 inact mut MLH1 R497Gfs*11

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_000249.4
gDNA chr3:g.37028863delC
cDNA c.1489delC
Protein p.R497Gfs*11
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_000249 chr3:g.37028863delC c.1489delC p.R497Gfs*11 RefSeq GRCh38/hg38
NM_001258271.2 chr3:g.37028863delC c.1489delC p.R497Gfs*11 RefSeq GRCh38/hg38
NM_001354628.1 chr3:g.37028863delC c.1489delC p.R497Gfs*11 RefSeq GRCh38/hg38
NM_001258271.1 chr3:g.37028863delC c.1489delC p.R497Gfs*11 RefSeq GRCh38/hg38
NM_001354630.1 chr3:g.37028863delC c.1489delC p.R497Gfs*11 RefSeq GRCh38/hg38
NM_001354628.2 chr3:g.37028863delC c.1489delC p.R497Gfs*11 RefSeq GRCh38/hg38
NM_001354630.2 chr3:g.37028863delC c.1489delC p.R497Gfs*11 RefSeq GRCh38/hg38
NM_000249.4 chr3:g.37028863delC c.1489delC p.R497Gfs*11 RefSeq GRCh38/hg38
NM_001258271 chr3:g.37028863delC c.1489delC p.R497Gfs*11 RefSeq GRCh38/hg38
NM_000249.3 chr3:g.37028863delC c.1489delC p.R497Gfs*11 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