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 KIT
Variant K623M
Impact List missense
Protein Effect loss of function
Gene Variant Descriptions KIT K623M lies within the protein kinase domain of the Kit protein (UniProt.org). K623M results in a loss of Kit autophosphorylation, reduced phosphorylation upon ligand stimulation as compared to wild-type Kit, and decreased downstream signaling, as demonstrated by reduced phosphorylation of Erk1/2 in cell culture (PMID: 20824047).
Associated Drug Resistance
Category Variants Paths

KIT mutant KIT K623M

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_000222.3
gDNA chr4:g.54727916A>T
cDNA c.1868A>T
Protein p.K623M
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_017008178 chr4:g.54727916A>T c.1868A>T p.K623M RefSeq GRCh38/hg38
NM_000222.3 chr4:g.54727916A>T c.1868A>T p.K623M RefSeq GRCh38/hg38
NM_000222 chr4:g.54727916A>T c.1868A>T p.K623M RefSeq GRCh38/hg38
XM_005265742 chr4:g.54727925A>T c.1868A>T p.K623M RefSeq GRCh38/hg38
XM_017008179 chr4:g.54727925A>T c.1868A>T p.K623M RefSeq GRCh38/hg38
NM_001385288.1 chr4:g.54727925A>T c.1868A>T p.K623M RefSeq GRCh38/hg38
NM_000222.2 chr4:g.54727916A>T c.1868A>T p.K623M RefSeq GRCh38/hg38
XM_005265742.3 chr4:g.54727925A>T c.1868A>T p.K623M RefSeq GRCh38/hg38
XM_017008178.1 chr4:g.54727916A>T c.1868A>T p.K623M RefSeq GRCh38/hg38
NM_001385292.1 chr4:g.54727925A>T c.1868A>T p.K623M RefSeq GRCh38/hg38
XM_017008179.1 chr4:g.54727925A>T c.1868A>T p.K623M RefSeq GRCh38/hg38
NM_001385285.1 chr4:g.54727916A>T c.1868A>T p.K623M 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