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 E667fs
Impact List frameshift
Protein Effect loss of function - predicted
Gene Variant Descriptions SMARCA4 E667fs results in a change in the amino acid sequence of the Smarca4 protein beginning at aa 667 of 1647, likely resulting in premature truncation of the functional protein (UniProt.org). Due to the loss of the Bromo domain (UniProt.org), E667fs is predicted to lead to a loss of Smarca4 protein function.
Associated Drug Resistance
Category Variants Paths

SMARCA4 mutant SMARCA4 inact mut SMARCA4 E667fs

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.(11003394_11003395)
cDNA c.(1999_1998)
Protein p.E667fs
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001128844.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
NM_001411150.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
NM_001128848 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_011528198.2 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
NM_001387283.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
NM_001128849.3 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_024451658.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_047439251.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_006722845 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
NM_003072 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
NM_001128846.2 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_047439243.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_006722845.2 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
NM_003072.3 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
NM_001128846.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
NM_001128845 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_024451659.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
NM_001128844.3 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_047439250.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_024451665.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
NM_001128844 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_024451662.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
NM_001374457.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_024451658.2 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_017027167 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_017027163 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_017027164 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
NM_003072.5 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_024451663.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
NM_001128847.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_017027168 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_047439244.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
NM_001128846 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_024451667.2 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_011528198 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
NM_001128848.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_006722846.2 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
NM_001128845.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_024451660.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_047439246.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_017027166 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_024451661.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_047439247.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_011528198.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_017027162 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_017027161 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
NM_001128849.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_024451664.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
NM_001128848.2 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
NM_001128849 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_024451661.2 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_024451663.2 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
NM_001128847.4 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
NM_001128847 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_006722846 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_006722846.3 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_047439248.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_024451667.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_017027160 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_017027165 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_047439249.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
XM_024451666.1 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs RefSeq GRCh38/hg38
NM_001128845.2 chr19:g.(11003394_11003395) c.(1999_1998) p.E667fs 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
SMARCA4 E667fs loss of function - predicted