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 | E821K |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | SMARCA4 E821K lies within the ATP-binding helicase domain of the Smarca4 protein (UniProt.org). E821K results in cell growth similar to wild-type Smarca4 in culture, but leads to decreased nucleosomal remodeling in an 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 E821K |
Transcript | NM_003072.5 |
gDNA | chr19:g.11018979G>A |
cDNA | c.2461G>A |
Protein | p.E821K |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_006722845.2 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_047439243.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_006722846.2 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_006722846 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_017027160 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_006722845 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_017027167 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_017027166 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
NM_001128844.3 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_024451664.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_024451663.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
NM_001128846.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
NM_001128847 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
NM_001128845 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
NM_001411150.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_047439246.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_047439247.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
NM_001128848.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
NM_003072 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
NM_001128845.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_006722846.3 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_024451661.2 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_024451659.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
NM_001128846 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_017027162 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_024451667.2 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_017027164 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_024451667.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_024451658.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_017027163 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_017027168 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
NM_001128849.3 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_024451660.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
NM_001128849 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_024451662.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
NM_003072.5 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_024451661.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
NM_003072.3 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_047439244.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_047439251.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
NM_001128845.2 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_011528198.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_024451665.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_011528198.2 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
NM_001128844 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_024451658.2 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_047439248.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
NM_001128846.2 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_024451666.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
NM_001128844.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
NM_001128849.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_017027165 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_047439249.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
NM_001128848 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
NM_001128847.4 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
NM_001128848.2 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
NM_001387283.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_047439250.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_024451663.2 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_011528198 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
NM_001128847.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
NM_001374457.1 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
XM_017027161 | chr19:g.11018979G>A | c.2461G>A | p.E821K | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
---|