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CHRNG has not been detected as a mutational cancer driver

CHRNG
Ensembl id ENSG00000196811
Mutated samples
Coding Sequence 46 (0.7%)
Protein Affecting 21 (0.3%)
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 CHRNG 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)
Head and neck squamous cell carcinoma No 6 5 1.33
Lung squamous cell carcinoma No 5 3 1.72
Cutaneous melanoma No 10 3 0.81
Stomach adenocarcinoma No 3 3 1.86
Breast carcinoma No 3 2 0.17
Esophageal carcinoma No 2 2 1.37
Lung adenocarcinoma No 3 1 0.26
Non small cell lung carcinoma No 1 1 3.23
Colorectal adenocarcinoma No 2 1 0.44
Hepatocarcinoma No 3 0 0.00
Bladder carcinoma No 1 0 0.00
Medulloblastoma No 1 0 0.00
Uterine corpus endometrioid carcinoma No 3 0 0.00
Multiple myeloma No 1 0 0.00
Small cell lung carcinoma No 1 0 0.00
Glioblastoma multiforme 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