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 BRAF
Variant E695K
Impact List missense
Protein Effect unknown
Gene Variant Descriptions BRAF E695K lies within the protein kinase domain of the Braf protein (UniProt.org). E695K results in increased transformation ability compared to wild-type Braf in one of two different cell lines in culture (PMID: 29533785), but has not been fully biochemically characterized and therefore, its effect on Braf protein function is unknown.
Associated Drug Resistance
Category Variants Paths

BRAF mutant BRAF E695K

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_004333.6
gDNA chr7:g.140739856C>T
cDNA c.2083G>A
Protein p.E695K
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001378468.1 chr7:g.140739856C>T c.2083G>A p.E695K RefSeq GRCh38/hg38
NM_004333.5 chr7:g.140739856C>T c.2083G>A p.E695K RefSeq GRCh38/hg38
NM_001378474.1 chr7:g.140739856C>T c.2083G>A p.E695K RefSeq GRCh38/hg38
NM_004333 chr7:g.140739856C>T c.2083G>A p.E695K RefSeq GRCh38/hg38
NM_004333.6 chr7:g.140739856C>T c.2083G>A p.E695K RefSeq GRCh38/hg38
NM_001354609.2 chr7:g.140739856C>T c.2083G>A p.E695K RefSeq GRCh38/hg38
XM_005250045 chr7:g.140739856C>T c.2083G>A p.E695K RefSeq GRCh38/hg38
NM_001354609.1 chr7:g.140739856C>T c.2083G>A p.E695K 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