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 CHEK2
Variant L226F
Impact List missense
Protein Effect unknown
Gene Variant Descriptions CHEK2 L226F lies within the protein kinase domain of the Chek2 protein (UniProt.org). L226F has been identified in sequencing studies (PMID: 27442865), but has not been biochemically characterized and therefore, its effect on Chek2 protein function is unknown (PubMed, Sep 2024).
Associated Drug Resistance
Category Variants Paths

CHEK2 mutant CHEK2 L226F

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_007194.4
gDNA chr22:g.28719402G>A
cDNA c.676C>T
Protein p.L226F
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_007194.3 chr22:g.28719402G>A c.676C>T p.L226F RefSeq GRCh38/hg38
XM_024452149.2 chr22:g.28719430T>A c.678A>T p.L226F RefSeq GRCh38/hg38
NM_001005735 chr22:g.28725020C>A c.678G>T p.L226F RefSeq GRCh38/hg38
XM_024452148.1 chr22:g.28719430T>A c.678A>T p.L226F RefSeq GRCh38/hg38
NM_001005735.1 chr22:g.28725020C>A c.678G>T p.L226F RefSeq GRCh38/hg38
XM_006724114.3 chr22:g.28695844C>A c.678G>T p.L226F RefSeq GRCh38/hg38
NM_001005735.2 chr22:g.28725020C>A c.678G>T p.L226F RefSeq GRCh38/hg38
XM_024452148.2 chr22:g.28719430T>A c.678A>T p.L226F RefSeq GRCh38/hg38
XM_006724114 chr22:g.28695844C>A c.678G>T p.L226F RefSeq GRCh38/hg38
XM_047441105.1 chr22:g.28725020C>A c.678G>T p.L226F RefSeq GRCh38/hg38
NM_145862.2 chr22:g.28719402G>A c.676C>T p.L226F RefSeq GRCh38/hg38
XM_024452149.1 chr22:g.28719430T>A c.678A>T p.L226F RefSeq GRCh38/hg38
NM_145862.2 chr22:g.28719402G>A c.676C>T p.L226F RefSeq GRCh38/hg38
NM_145862 chr22:g.28719402G>A c.676C>T p.L226F RefSeq GRCh38/hg38
NM_007194.4 chr22:g.28719402G>A c.676C>T p.L226F RefSeq GRCh38/hg38
NM_007194 chr22:g.28719402G>A c.676C>T p.L226F 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