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FAM168B has not been detected as a mutational cancer driver

FAM168B
Ensembl id ENSG00000152102
Mutated samples
Coding Sequence 28 (0.4%)
Protein Affecting 10 (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 FAM168B 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)
Lung adenocarcinoma No 3 2 0.51
Bladder carcinoma No 2 2 2.04
Cutaneous melanoma No 5 2 0.54
Breast carcinoma No 1 1 0.09
Uterine corpus endometrioid carcinoma No 2 1 0.43
Stomach adenocarcinoma No 4 1 0.62
Esophageal carcinoma No 1 1 0.68
Hepatocarcinoma No 1 0 0.00
Lung squamous cell carcinoma No 1 0 0.00
Neuroblastoma No 1 0 0.00
Lower grade glioma No 2 0 0.00
Serous ovarian adenocarcinoma No 2 0 0.00
Pylocytic astrocytoma No 2 0 0.00
Head and neck squamous cell 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