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Gene SMARCA4
Variant D779G
Impact List missense
Protein Effect unknown
Gene Variant Descriptions SMARCA4 D779G lies within the ATP-binding helicase domain of the Smarca4 protein (UniProt.org). D779G has not been characterized in the scientific literature and therefore, its effect on Smarca4 protein function is unknown (PubMed, Jun 2024).
Associated Drug Resistance
Category Variants Paths

SMARCA4 mutant SMARCA4 D779G

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Transcript NM_003072.5
gDNA chr19:g.11013010A>G
cDNA c.2336A>G
Protein p.D779G
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_006722846.2 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_024451667.2 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
NM_001128848.2 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_024451664.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_024451661.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_017027166 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
NM_001128847 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
NM_003072 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_024451658.2 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
NM_001128844 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_017027168 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
NM_001128847.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_017027162 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_047439244.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
NM_001128849.3 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_011528198.2 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_024451665.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_011528198.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_017027167 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
NM_001128844.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_047439249.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_017027165 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
NM_001411150.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_006722846.3 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
NM_001128848 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_006722846 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
NM_001128846 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_024451660.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_017027161 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
NM_001128846.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_047439251.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_017027164 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_047439247.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
NM_001128848.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_047439250.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_011528198 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_024451658.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_024451661.2 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
NM_001387283.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_047439243.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
NM_003072.5 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_024451659.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_024451663.2 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
NM_001128847.4 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_006722845 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_024451666.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_006722845.2 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
NM_001128846.2 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
NM_001128845.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
NM_003072.3 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_024451667.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
NM_001374457.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
NM_001128849.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
NM_001128844.3 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
NM_001128845.2 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
NM_001128849 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_024451663.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
NM_001128845 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_047439246.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_047439248.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_024451662.1 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_017027160 chr19:g.11013010A>G c.2336A>G p.D779G RefSeq GRCh38/hg38
XM_017027163 chr19:g.11013010A>G c.2336A>G p.D779G 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