RAD51C

RAD51 paralog C O43502 RA51C_HUMAN
Protein Coding Chr 17 17q22 Swiss-Prot reviewed Entrez 5889
Mutations
317
CL 50 · Tissue 262
Samples
148
CL 32 · Tissue 113
Peptides
123
unique mutant peptides
Transcripts
3
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
Mutations31750262
Samples14832113
Peptides12322103

Function

RAD51C · RAD51 paralog C

This gene is a member of the RAD51 family. RAD51 family members are highly similar to bacterial RecA and Saccharomyces cerevisiae Rad51 and are known to be involved in the homologous recombination and repair of DNA. This protein can interact with other RAD51 paralogs and is reported to be important for Holliday junction resolution. Mutations in this gene are associated with Fanconi anemia-like syndrome. This gene is one of four localized to a region of chromosome 17q23 where amplification occurs frequently in breast tumors. Overexpression of the four genes during amplification has been observed and suggests a possible role in tumor progression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013].

Isoforms & Proteins

3 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
ENST00000337432 O43502 153 115
ENST00000583539 J3QKK3* 117 95
ENST00000421782 O43502-2 47 40

Gene Properties

Type
Protein Coding
Chromosome
17
Cytoband
17q22
Entrez ID
Aliases
BROVCA3FANCOR51H3RAD51L2

Recurrent Mutations

All 115 amino-acid changes on canonical ENST00000337432 · 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 RAD51C · 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 RAD51C – 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
Chordoma
3/7 43%
0/13 0%
T-Lymphoblastic Leukemia
4/40 10%
0/0 0%
Endometrial Carcinoma
4/42 10%
9/612 1%
Hodgkins Lymphoma
2/16 12%
0/122 0%
Cervical Carcinoma
0/35 0%
5/422 1%
Germ Cell Tumour
2/25 8%
0/169 0%
Glioblastoma
1/98 1%
0/0 0%
Bladder Carcinoma
2/58 3%
7/956 1%
Gastrointestinal Stromal Tumour
0/0 0%
1/133 1%
Neuroendocrine Tumour
2/154 1%
3/577 1%
Melanoma
0/210 0%
14/1899 1%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Squamous Cell Lung Carcinoma
0/57 0%
4/810 0%
Mesothelioma
1/62 2%
0/165 0%
Non-Cancerous
1/104 1%
3/830 0%
Non-Small Cell Lung Carcinoma
2/304 1%
5/1390 0%
Hepatocellular Carcinoma
0/46 0%
9/2210 0%
Colorectal Carcinoma
0/143 0%
13/3239 0%
Head and Neck Carcinoma
0/85 0%
5/1574 0%
Ovarian Carcinoma
2/109 2%
1/998 0%
Other Sarcomas
0/69 0%
2/699 0%
Breast Carcinoma
0/144 0%
9/3264 0%
Other Solid Cancers
0/94 0%
4/1515 0%
Thyroid Gland Carcinoma
0/45 0%
4/1592 0%
Medulloblastoma
0/0 0%
1/450 0%
Gastric Carcinoma
1/74 1%
3/1809 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%
B-Cell Non-Hodgkins Lymphoma
4/88 5%
1/2534 0%
Glioma
0/52 0%
4/2127 0%
Esophageal Carcinoma
0/23 0%
1/769 0%

Mutation Distribution

Where RAD51C is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in RAD51C 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 317 mutations in RAD51C

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