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 G1162C
Impact List missense
Protein Effect loss of function
Gene Variant Descriptions SMARCA4 G1162C lies within the C-terminal helicase domain of the Smarca4 protein (UniProt.org). G1162C results in cell growth similar to wild-type Smarca4 in culture, but leads to decreased nucleosomal remodeling activity in an in vitro assay, reduced chromatin accessibility, decreased ability to activate target genes, and impaired ability to rescue cell growth of SMARCA2-deficient cells in culture (PMID: 33144586).
Associated Drug Resistance
Category Variants Paths

SMARCA4 mutant SMARCA4 inact mut SMARCA4 G1162C

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.11030831G>T
cDNA c.3484G>T
Protein p.G1162C
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001128848.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_047439251.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_006722845.2 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_047439244.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_024451666.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_047439247.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
NM_001128847.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
NM_001128846.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
NM_001128849.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_024451667.2 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_024451659.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
NM_001128845.2 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
NM_001128847.4 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_024451665.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
NM_001128849.3 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
NM_001128845.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_047439243.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
NM_001128849 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_011528198 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_017027161 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_017027167 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_047439248.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_006722846 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
NM_001128848 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
NM_001374457.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
NM_001128848.2 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_011528198.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_017027165 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_017027162 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_017027166 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_047439249.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_024451661.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_024451658.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
NM_001128845 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_024451660.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_024451663.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_006722846.2 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
NM_001128844.3 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
NM_001128847 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
NM_001128844 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
NM_001411150.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_017027160 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_024451661.2 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_024451667.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_024451662.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
NM_001128846 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_024451664.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_011528198.2 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_024451658.2 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
NM_003072 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
NM_003072.3 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
NM_001387283.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_006722845 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_017027163 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_047439246.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
NM_001128846.2 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_017027164 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_024451663.2 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
NM_003072.5 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_006722846.3 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_017027168 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
XM_047439250.1 chr19:g.11030831G>T c.3484G>T p.G1162C RefSeq GRCh38/hg38
NM_001128844.1 chr19:g.11030831G>T c.3484G>T p.G1162C 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.

Clinical Trial Phase Therapies Title Recruitment Status Covered Countries Other Countries