SMARCA2 SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 P51531 SMCA2_HUMAN
Protein Coding Chr 9 9p24.3 Swiss-Prot reviewed Entrez 6595
Mutations
4,975
CL 427 · Tissue 4,495
Samples
770
CL 135 · Tissue 627
Peptides
652
unique mutant peptides
Transcripts
17
isoforms mutated

Stats by Source

Global, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)

How the counts split by source
Stats by Source

Global = all mutations for this gene across every source.

Cell line = COSMIC Cell Lines Project + DepMap + PubMed.

Tissue = COSMIC primary-tissue (patient tumour) samples.

Global can exceed cell line + tissue: COSMIC tissue-derived models sit only in global, and a peptide can be shared across both.

GlobalCell lineTissue
Mutations4,9754274,495
Samples770135627
Peptides652102570

Function

SMARCA2 · SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2

The protein encoded by this gene is a member of the SWI/SNF family of proteins and is highly similar to the brahma protein of Drosophila. Members of this family have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI, which is required for transcriptional activation of genes normally repressed by chromatin. Alternatively spliced transcript variants encoding different isoforms have been found for this gene, which contains a trinucleotide repeat (CAG) length polymorphism. [provided by RefSeq, Jan 2014].

Isoforms & Proteins

17 transcripts · UniProt mapping is sequence-verified (AA-safe)

About the isoform mapping
Isoforms & Proteins

Each Ensembl transcript (ENST) this gene is mutated on, with its matched UniProt accession.

The mapping is sequence-verified: the UniProt sequence is identical to the transcript translation, so amino-acid positions line up exactly. A * marks an unreviewed (TrEMBL) entry.

Counts are mutations and unique mutant peptides on each transcript.

TranscriptUniProtMutationsPeptides
ENST00000349721 P51531 829 601
ENST00000382203 P51531 734 566
ENST00000357248 P51531-2 728 559
ENST00000382194 P51531-2 727 559
ENST00000450198 F6VDE0* 703 539
ENST00000636559 A0A1B0GWA8* 116 95
ENST00000637806 A0A1B0GWA8* 116 95
ENST00000636903 A0A1B0GU54* 107 90
ENST00000637103 A0A1B0GU54* 107 90
ENST00000302401 B1ALF6* 106 79
ENST00000382185 B4DNT1* 106 79
ENST00000417599 B4DNT1* 106 79
ENST00000382186 B1ALG2* 100 75
ENST00000634931 B1ALG2* 100 75
ENST00000634781 A0A0U1RR26* 99 72
ENST00000324954 F6T8Q0* 98 71
ENST00000382183 B1ALG1* 93 68

Gene Properties

Type
Protein Coding
Chromosome
9
Cytoband
9p24.3
Entrez ID
Aliases
BAF190BISBRMNCBRSSAMRCA2SNF2

Recurrent Mutations

Top recurrent amino-acid changes along the protein · needle height = number of mutations

What this lollipop shows
Recurrent Mutations

A lollipop / needle plot – the standard way to show recurrent mutations along a protein (as used by cBioPortal and MutationMapper).

X-axis = amino-acid position in the protein.

Needle height & head size = how often that exact amino-acid change was observed (its recurrence). Tall/large heads are mutational hotspots.

The most recurrent changes are labelled; hover any needle for the change, position and counts.

Mutation Distribution

Where SMARCA2 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in SMARCA2 were found in each tissue, across the whole database.

Each bar is a tissue (cell-line and tissue names are merged to the standard tissue), split into cell line and tissue (patient tumour) contributions.

This shows the cancer-context where this gene is recurrently altered.

GTEx Expression

Median TPM across 54 healthy tissues

GTEx Portal ↗
About the expression data
GTEx Expression

Median gene expression (TPM) in normal, non-cancer human tissues from the GTEx project.

Useful for judging tumour specificity – a strong neoantigen target ideally comes from a gene with low expression in healthy tissues.

Scroll or drag the mini-axis below the chart to browse all tissues.

Mutations

All 4,975 mutations in SMARCA2

About the mutation list
Mutations

Every mutation record for this gene, across all samples and sources.

The Sample column links to the cell line (cell-line samples) or the tissue type (tissue samples).

Use the Type / Source filters, the search box, and column sorting to explore; each CAN-IMMUNE ID opens the full mutation & peptide view.

IDSampleTranscriptAA Change CDSTypeSourcePeptide