POLR3G

RNA polymerase III subunit G O15318 RPC7_HUMAN
Protein Coding Chr 5 5q14.3 Swiss-Prot reviewed Entrez 10622
Mutations
217
CL 39 · Tissue 177
Samples
99
CL 22 · Tissue 76
Peptides
76
unique mutant peptides
Transcripts
5
isoforms mutated

Stats by Source

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

How the counts split by source
Stats by Source

Total = all mutations for this gene across every source.

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

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

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

TotalCell lineTissue
Mutations21739177
Samples992276
Peptides761857

Function

POLR3G · RNA polymerase III subunit G

Enables chromatin binding activity. Involved in positive regulation of innate immune response; positive regulation of interferon-beta production; and transcription by RNA polymerase III. Acts upstream of or within cell population proliferation. Located in cytosol and nuclear body. Part of RNA polymerase III complex. [provided by Alliance of Genome Resources, Apr 2022]

Isoforms & Proteins

5 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
ENST00000504930 O15318 87 64
ENST00000651687 O15318 56 43
ENST00000399107 A0A7I2R591* 42 29
ENST00000514483 D6RJH6* 31 23
ENST00000505345 D6RIT0* 1 1

Gene Properties

Type
Protein Coding
Chromosome
5
Cytoband
5q14.3
Entrez ID
Aliases
C31RPC32RPC7

Recurrent Mutations

All 64 amino-acid changes on canonical ENST00000504930 · needle height = samples · drag the mini-map to zoom

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 frequency across cancer types

% of samples with a missense/complex mutation in POLR3G · cell line vs tissue

How this frequency is counted
Cancer-type mutation frequency

For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in POLR3G – counted as distinct samples (a sample counts once no matter how many mutations it has).

Split into cell line and tissue; each cell shows mutated / total and the percentage. Cohorts with <20 samples are omitted. Ordered by combined frequency.

Cancer typeCell linesTissue samples
T-Lymphoblastic Leukemia
2/40 5%
0/0 0%
Glioblastoma
3/98 3%
0/0 0%
Osteosarcoma
2/45 4%
0/166 0%
Bladder Carcinoma
0/58 0%
9/956 1%
Endometrial Carcinoma
1/42 2%
4/612 1%
Ewings Sarcoma
0/63 0%
2/262 1%
Squamous Cell Lung Carcinoma
0/57 0%
4/810 0%
Cervical Carcinoma
0/35 0%
2/422 0%
Non-Small Cell Lung Carcinoma
1/304 0%
6/1390 0%
Melanoma
3/210 1%
5/1899 0%
Gastric Carcinoma
0/74 0%
6/1809 0%
Colorectal Carcinoma
3/143 2%
7/3239 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Esophageal Squamous Cell Carcinoma
0/51 0%
6/2550 0%
Biliary Tract Carcinoma
2/54 4%
0/950 0%
Other Solid Cancers
0/94 0%
3/1515 0%
Breast Carcinoma
1/144 1%
5/3264 0%
Glioma
0/52 0%
4/2127 0%
Pancreatic Carcinoma
2/89 2%
1/1611 0%
Kidney Carcinoma
0/85 0%
3/1862 0%
Head and Neck Carcinoma
0/85 0%
2/1574 0%
Non-Cancerous
0/104 0%
1/830 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
1/2534 0%
Ovarian Carcinoma
0/109 0%
1/998 0%
Hepatocellular Carcinoma
0/46 0%
2/2210 0%

Mutation Distribution

Where POLR3G is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in POLR3G 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 217 mutations in POLR3G

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 CDSTypeSourceMutant PeptideWild-type Peptide