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C22orf39 has not been detected as a mutational cancer driver

C22orf39
Ensembl id ENSG00000242259
Mutated samples
Coding Sequence 78 (1.1%)
Protein Affecting 9 (0.1%)
Mode of action Unclassified
Known driver No
Cancer type Signals (Biases)
Clust Clustered Mutations FM Functional Mutations Rec Recurrent Mutations
This plot shows the most recurrently mutated cancer types in all C22orf39 gene mutations. Each bar of the histogram indicates the amount of samples with PAMs.

Cancer type Driver Mutated samples (CS) Mutated samples (PAM) % Mutated samples (PAM)
Bladder carcinoma No 3 2 2.04
Lung adenocarcinoma No 5 1 0.26
Lung squamous cell carcinoma No 4 1 0.57
Non small cell lung carcinoma No 1 1 3.23
Chronic lymphocytic leukemia No 2 1 0.34
Stomach adenocarcinoma No 9 1 0.62
Head and neck squamous cell carcinoma No 8 1 0.27
Acute lymphocytic leukemia No 1 1 0.82
Prostate adenocarcinoma No 1 0 0.00
Breast carcinoma No 7 0 0.00
Cutaneous melanoma No 20 0 0.00
Neuroblastoma No 2 0 0.00
Uterine corpus endometrioid carcinoma No 6 0 0.00
Serous ovarian adenocarcinoma No 2 0 0.00
Pylocytic astrocytoma No 2 0 0.00
Small cell lung carcinoma No 2 0 0.00
Colorectal adenocarcinoma No 1 0 0.00
Glioblastoma multiforme No 1 0 0.00
Esophageal carcinoma No 1 0 0.00
The mutations needle plot shows the distribution of the observed cancer mutations along the protein sequence and it's possible mutational clusters and hotspots. The needles' height and head size represent mutational recurrence. Needles of different categories that fall in the same amino acid residues are stacked.

Variant Locus Samples AA pos AA change Consequence