TP53 Tumor protein p53 P04637 P53_HUMAN
Protein Coding Chr 17 17p13.1 Swiss-Prot reviewed Entrez 7157
Mutations
196,874
CL 9,547 · Tissue 182,210
Samples
12,354
CL 1,303 · Tissue 10,753
Peptides
970
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
Mutations196,8749,547182,210
Samples12,3541,30310,753
Peptides970350923

Function

TP53 · Tumor protein p53

This gene encodes a tumor suppressor protein containing transcriptional activation, DNA binding, and oligomerization domains. The encoded protein responds to diverse cellular stresses to regulate expression of target genes, thereby inducing cell cycle arrest, apoptosis, senescence, DNA repair, or changes in metabolism. Mutations in this gene are associated with a variety of human cancers, including hereditary cancers such as Li-Fraumeni syndrome. Alternative splicing of this gene and the use of alternate promoters result in multiple transcript variants and isoforms. Additional isoforms have also been shown to result from the use of alternate translation initiation codons from identical transcript variants (PMIDs: 12032546, 20937277). [provided by RefSeq, Dec 2016].

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
ENST00000269305 P04637 13,847 765
ENST00000610292 P04637-4 12,772 741
ENST00000445888 P04637 12,357 733
ENST00000619485 P04637-4 12,305 708
ENST00000620739 P04637-4 12,305 708
ENST00000455263 P04637-3 12,130 689
ENST00000420246 P04637-2 12,098 681
ENST00000359597 J3KP33* 12,095 680
ENST00000610538 P04637-6 12,065 662
ENST00000622645 P04637-5 12,047 657
ENST00000504937 P04637-7 11,409 592
ENST00000504290 P04637-9 11,168 546
ENST00000510385 P04637-8 11,151 541
ENST00000619186 A0A087X1Q1* 10,239 502
ENST00000610623 A0A087WT22* 9,998 456
ENST00000618944 A0A087WXZ1* 9,981 451
ENST00000413465 E7EQX7* 8,907 550

Gene Properties

Type
Protein Coding
Chromosome
17
Cytoband
17p13.1
Entrez ID
Aliases
BCC7BMFS5LFS1P53TRP53

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 TP53 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in TP53 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 196,874 mutations in TP53

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