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 | M272fs |
Impact List | frameshift |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | SMARCA4 M272fs results in a change in the amino acid sequence of the Smarca4 protein beginning at aa 272 of 1647, likely resulting in premature truncation of the functional protein (UniProt.org). Due to the loss of the Bromo domain (UniProt.org), M272fs is predicted to lead to a loss of Smarca4 protein function. |
Associated Drug Resistance | |
Category Variants Paths |
SMARCA4 mutant SMARCA4 inact mut SMARCA4 M272fs |
Transcript | NM_003072.5 |
gDNA | chr19:g.(10986957_10986958) |
cDNA | c.(814_813) |
Protein | p.M272fs |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_047439250.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
NM_003072.3 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_024451664.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_011528198.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
NM_001128847.4 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_047439243.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
NM_001128846 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_006722845 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_024451660.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
NM_001128846.2 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_024451658.2 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_006722845.2 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_024451667.2 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
NM_001128849.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_024451661.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
NM_001128845 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_024451663.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_017027166 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_047439251.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_017027160 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_017027167 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_017027162 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_017027161 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_017027164 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
NM_001128844.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_017027168 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_024451665.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
NM_001128849.3 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
NM_001128844 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
NM_001128847.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_047439244.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_017027163 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_047439248.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
NM_001128847 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
NM_001387283.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
NM_001411150.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
NM_001128848.2 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_011528198 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
NM_001128846.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
NM_001128848.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_024451662.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_024451667.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
NM_001128845.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
NM_001128849 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
NM_001128845.2 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_047439246.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_006722846 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
NM_003072.5 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_047439247.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_024451666.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_024451658.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_024451663.2 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
NM_001128844.3 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
NM_001374457.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_017027165 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_024451659.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_024451661.2 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_006722846.2 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
NM_003072 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_011528198.2 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_047439249.1 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
NM_001128848 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
XM_006722846.3 | chr19:g.(10986957_10986958) | c.(814_813) | p.M272fs | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
SMARCA4 M272fs | loss of function - predicted |