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 SMARCA4
Variant K586fs
Impact List frameshift
Protein Effect loss of function - predicted
Gene Variant Descriptions SMARCA4 K586fs results in a change in the amino acid sequence of the Smarca4 protein beginning at aa 586 of 1647, likely resulting in premature truncation of the functional protein (UniProt.org). Due to the loss of the Bromo domain (UniProt.org), K586fs is predicted to lead to a loss of Smarca4 protein function.
Associated Drug Resistance
Category Variants Paths

SMARCA4 mutant SMARCA4 inact mut SMARCA4 K586fs

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_003072.5
gDNA chr19:g.(10996374_10996375)
cDNA c.(1756_1755)
Protein p.K586fs
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_047439247.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_024451665.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_017027164 chr19:g.10996371delG c.1752delG p.K586fs*27 RefSeq GRCh38/hg38
XM_017027167 chr19:g.10996371delG c.1752delG p.K586fs*27 RefSeq GRCh38/hg38
XM_024451662.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
NM_003072.3 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
NM_001128847.4 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_011528198.2 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
NM_001128848 chr19:g.10996371delG c.1752delG p.K586fs*27 RefSeq GRCh38/hg38
XM_024451666.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_006722846.3 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
NM_001128849 chr19:g.10996371delG c.1752delG p.K586fs*27 RefSeq GRCh38/hg38
NM_001128846.2 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_024451667.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
NM_001128848.2 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
NM_001128845.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_024451660.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_006722846.2 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_047439251.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_017027166 chr19:g.10996371delG c.1752delG p.K586fs*27 RefSeq GRCh38/hg38
NM_003072.5 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
NM_001128844 chr19:g.10996371delG c.1752delG p.K586fs*27 RefSeq GRCh38/hg38
NM_001128844.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_006722845.2 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_047439249.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
NM_001128845.2 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
NM_001128846.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_011528198 chr19:g.10996371delG c.1752delG p.K586fs*27 RefSeq GRCh38/hg38
XM_047439248.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_017027160 chr19:g.10996371delG c.1752delG p.K586fs*27 RefSeq GRCh38/hg38
XM_017027163 chr19:g.10996371delG c.1752delG p.K586fs*27 RefSeq GRCh38/hg38
XM_024451659.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_006722845 chr19:g.10996371delG c.1752delG p.K586fs*27 RefSeq GRCh38/hg38
XM_024451658.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_006722846 chr19:g.10996371delG c.1752delG p.K586fs*27 RefSeq GRCh38/hg38
XM_024451661.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
NM_001411150.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_047439250.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_017027165 chr19:g.10996371delG c.1752delG p.K586fs*27 RefSeq GRCh38/hg38
XM_017027168 chr19:g.10996371delG c.1752delG p.K586fs*27 RefSeq GRCh38/hg38
NM_001128848.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
NM_001128844.3 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_024451667.2 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_017027162 chr19:g.10996371delG c.1752delG p.K586fs*27 RefSeq GRCh38/hg38
NM_001128845 chr19:g.10996371delG c.1752delG p.K586fs*27 RefSeq GRCh38/hg38
NM_001128849.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_024451661.2 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
NM_001128847 chr19:g.10996371delG c.1752delG p.K586fs*27 RefSeq GRCh38/hg38
XM_024451664.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
NM_001128849.3 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_024451658.2 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_047439244.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
NM_003072 chr19:g.10996371delG c.1752delG p.K586fs*27 RefSeq GRCh38/hg38
XM_011528198.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_024451663.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
NM_001387283.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_017027161 chr19:g.10996371delG c.1752delG p.K586fs*27 RefSeq GRCh38/hg38
NM_001128846 chr19:g.10996371delG c.1752delG p.K586fs*27 RefSeq GRCh38/hg38
NM_001128847.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_047439243.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_024451663.2 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
XM_047439246.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs RefSeq GRCh38/hg38
NM_001374457.1 chr19:g.(10996374_10996375) c.(1756_1755) p.K586fs 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