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@jax.org

Gene BRAF
Variant V226L
Impact List missense
Protein Effect unknown
Gene Variant Descriptions BRAF V226L lies within the RBD domain of the Braf protein (UniProt.org). V226L has been identified in sequencing studies (PMID: 34449929), but has not been biochemically characterized and therefore, its effect on Braf protein function is unknown (PubMed, Dec 2023).
Associated Drug Resistance
Category Variants Paths

BRAF mutant BRAF V226L

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.140807995C>G
cDNA c.676G>C
Protein p.V226L
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001354609.2 chr7:g.140807995C>G c.676G>C p.V226L RefSeq GRCh38/hg38
XM_047420767.1 chr7:g.140807995C>G c.676G>C p.V226L RefSeq GRCh38/hg38
XM_017012558.1 chr7:g.140807995C>G c.676G>C p.V226L RefSeq GRCh38/hg38
NM_001374258.1 chr7:g.140807995C>G c.676G>C p.V226L RefSeq GRCh38/hg38
XM_017012559.1 chr7:g.140807995C>G c.676G>C p.V226L RefSeq GRCh38/hg38
XM_017012559 chr7:g.140807995C>G c.676G>C p.V226L RefSeq GRCh38/hg38
NM_001354609.1 chr7:g.140807995C>G c.676G>C p.V226L RefSeq GRCh38/hg38
NM_001378471.1 chr7:g.140807995C>G c.676G>C p.V226L RefSeq GRCh38/hg38
NM_004333.6 chr7:g.140807995C>G c.676G>C p.V226L RefSeq GRCh38/hg38
XM_005250045 chr7:g.140807995C>G c.676G>C p.V226L RefSeq GRCh38/hg38
XM_017012558 chr7:g.140807995C>G c.676G>C p.V226L RefSeq GRCh38/hg38
XM_047420768.1 chr7:g.140807995C>G c.676G>C p.V226L RefSeq GRCh38/hg38
NM_004333 chr7:g.140807995C>G c.676G>C p.V226L RefSeq GRCh38/hg38
XM_017012559.2 chr7:g.140807995C>G c.676G>C p.V226L RefSeq GRCh38/hg38
NM_001374244.1 chr7:g.140807995C>G c.676G>C p.V226L RefSeq GRCh38/hg38
NM_001378469.1 chr7:g.140807995C>G c.676G>C p.V226L RefSeq GRCh38/hg38
NM_004333.5 chr7:g.140807995C>G c.676G>C p.V226L RefSeq GRCh38/hg38
XM_047420769.1 chr7:g.140807995C>G c.676G>C p.V226L RefSeq GRCh38/hg38
NM_001378468.1 chr7:g.140807995C>G c.676G>C p.V226L RefSeq GRCh38/hg38
NM_001378474.1 chr7:g.140807995C>G c.676G>C p.V226L 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 Protein Effect Treatment Approaches
BRAF V226L unknown