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Gene | SMARCA4 |
Variant | G1232S |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | SMARCA4 G1232S lies within the C-terminal helicase domain of the Smarca4 protein (UniProt.org). G1232S results in cell growth similar to wild-type Smarca4, 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 G1232S |
Transcript | NM_003072.5 |
gDNA | chr19:g.11033437G>A |
cDNA | c.3694G>A |
Protein | p.G1232S |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001128847.4 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
NM_001128844.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_024451660.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_017027166 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_017027167 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
NM_001128848.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_047439247.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_006722846.2 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
NM_001128848.2 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_024451659.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_024451664.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
NM_001128844.3 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_047439249.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_017027168 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_024451661.2 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
NM_001128849 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_017027161 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
NM_001411150.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_006722845.2 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
NM_001128845 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_024451666.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_024451665.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
NM_001128846.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_006722846.3 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
NM_003072.3 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
NM_001128849.3 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
NM_003072.5 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
NM_001128849.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
NM_001128846 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_024451667.2 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
NM_001128845.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
NM_001387283.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
NM_001128848 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_047439243.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_017027164 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_047439246.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_017027160 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_006722845 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_011528198.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
NM_001128846.2 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_024451658.2 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_047439250.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_024451661.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_047439244.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_017027162 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
NM_001128847.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_047439248.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_024451662.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_017027165 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_024451667.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
NM_001128847 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_011528198 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
NM_003072 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_006722846 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_017027163 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_024451658.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_024451663.2 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
NM_001374457.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
NM_001128844 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_024451663.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_011528198.2 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
XM_047439251.1 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
NM_001128845.2 | chr19:g.11033437G>A | c.3694G>A | p.G1232S | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
SMARCA4 G1232S | loss of function |