This report serves to describe the mutational landscape and properties of a given individual set, as well as rank genes and genesets according to mutational significance. MutSig 2CV v3.1 was used to generate the results found in this report.
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Working with individual set: BLCA-TP
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Number of patients in set: 130
The input for this pipeline is a set of individuals with the following files associated for each:
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An annotated .maf file describing the mutations called for the respective individual, and their properties.
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A .wig file that contains information about the coverage of the sample.
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MAF used for this analysis:BLCA-TP.final_analysis_set.maf
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Blacklist used for this analysis: pancan_mutation_blacklist.v14.hg19.txt
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Significantly mutated genes (q ≤ 0.1): 31
The mutation spectrum is depicted in the lego plots below in which the 96 possible mutation types are subdivided into six large blocks, color-coded to reflect the base substitution type. Each large block is further subdivided into the 16 possible pairs of 5' and 3' neighbors, as listed in the 4x4 trinucleotide context legend. The height of each block corresponds to the mutation frequency for that kind of mutation (counts of mutations normalized by the base coverage in a given bin). The shape of the spectrum is a signature for dominant mutational mechanisms in different tumor types.
Figure 1. Get High-res Image SNV Mutation rate lego plot for entire set. Each bin is normalized by base coverage for that bin. Colors represent the six SNV types on the upper right. The three-base context for each mutation is labeled in the 4x4 legend on the lower right. The fractional breakdown of SNV counts is shown in the pie chart on the upper left. If this figure is blank, not enough information was provided in the MAF to generate it.
![](BLCA-TP.final_analysis_set.maf.mutation_profile.png)
Figure 2. Get High-res Image SNV Mutation rate lego plots for 4 slices of mutation allele fraction (0<=AF<0.1, 0.1<=AF<0.25, 0.25<=AF<0.5, & 0.5<=AF) . The color code and three-base context legends are the same as the previous figure. If this figure is blank, not enough information was provided in the MAF to generate it.
![](BLCA-TP.final_analysis_set.maf.mutation_profile_AF.png)
Figure 3. Get High-res Image The matrix in the center of the figure represents individual mutations in patient samples, color-coded by type of mutation, for the significantly mutated genes. The rate of synonymous and non-synonymous mutations is displayed at the top of the matrix. The barplot on the left of the matrix shows the number of mutations in each gene. The percentages represent the fraction of tumors with at least one mutation in the specified gene. The barplot to the right of the matrix displays the q-values for the most significantly mutated genes. The purple boxplots below the matrix (only displayed if required columns are present in the provided MAF) represent the distributions of allelic fractions observed in each sample. The plot at the bottom represents the base substitution distribution of individual samples, using the same categories that were used to calculate significance.
![](BLCA-TP_coMut.png)
Column Descriptions:
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nnon = number of (nonsilent) mutations in this gene across the individual set
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npat = number of patients (individuals) with at least one nonsilent mutation
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nsite = number of unique sites having a non-silent mutation
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nsil = number of silent mutations in this gene across the individual set
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p = p-value (overall)
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q = q-value, False Discovery Rate (Benjamini-Hochberg procedure)
Table 1. Get Full Table A Ranked List of Significantly Mutated Genes. Number of significant genes found: 31. Number of genes displayed: 35. Click on a gene name to display its stick figure depicting the distribution of mutations and mutation types across the chosen gene (this feature may not be available for all significant genes).
rank | gene | longname | codelen | nnei | nncd | nsil | nmis | nstp | nspl | nind | nnon | npat | nsite | pCV | pCL | pFN | p | q |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1 | TP53 | tumor protein p53 | 1314 | 51 | 0 | 1 | 57 | 13 | 0 | 5 | 75 | 64 | 50 | 2.1e-16 | 1e-05 | 1e-05 | 1e-16 | 9.1e-13 |
2 | KDM6A | lysine (K)-specific demethylase 6A | 4318 | 120 | 0 | 2 | 4 | 16 | 1 | 11 | 32 | 31 | 26 | 1e-16 | 0.0074 | 0.068 | 1e-16 | 9.1e-13 |
3 | RB1 | retinoblastoma 1 (including osteosarcoma) | 2891 | 10 | 0 | 0 | 4 | 8 | 4 | 3 | 19 | 17 | 17 | 1e-16 | 0.12 | 0.55 | 5.6e-16 | 3.4e-12 |
4 | ARID1A | AT rich interactive domain 1A (SWI-like) | 6934 | 2 | 0 | 2 | 12 | 16 | 0 | 10 | 38 | 32 | 36 | 3.2e-16 | 0.27 | 0.84 | 4.7e-15 | 2.1e-11 |
5 | CDKN1A | cyclin-dependent kinase inhibitor 1A (p21, Cip1) | 503 | 334 | 0 | 0 | 3 | 3 | 0 | 12 | 18 | 18 | 17 | 3.3e-15 | 0.4 | 0.77 | 6e-14 | 2.2e-10 |
6 | MLL2 | myeloid/lymphoid or mixed-lineage leukemia 2 | 16826 | 1 | 0 | 5 | 15 | 14 | 2 | 9 | 40 | 36 | 40 | 1.6e-14 | 1 | 0.5 | 5.3e-13 | 1.6e-09 |
7 | ELF3 | E74-like factor 3 (ets domain transcription factor, epithelial-specific ) | 1148 | 44 | 0 | 0 | 6 | 1 | 0 | 8 | 15 | 11 | 14 | 7.1e-11 | 0.35 | 0.26 | 3.4e-10 | 8.8e-07 |
8 | FGFR3 | fibroblast growth factor receptor 3 (achondroplasia, thanatophoric dwarfism) | 2642 | 12 | 0 | 2 | 20 | 0 | 0 | 1 | 21 | 16 | 11 | 0.000017 | 2e-05 | 0.063 | 4e-09 | 9.2e-06 |
9 | CDKN2A | cyclin-dependent kinase inhibitor 2A (melanoma, p16, inhibits CDK4) | 1002 | 22 | 0 | 0 | 4 | 2 | 1 | 1 | 8 | 7 | 8 | 0.000036 | 1 | 1e-05 | 8.1e-09 | 0.000016 |
10 | STAG2 | stromal antigen 2 | 3939 | 8 | 0 | 3 | 2 | 5 | 2 | 5 | 14 | 14 | 13 | 3.3e-09 | 0.2 | 0.34 | 8.9e-09 | 0.000016 |
11 | NFE2L2 | nuclear factor (erythroid-derived 2)-like 2 | 1834 | 43 | 0 | 0 | 12 | 0 | 0 | 0 | 12 | 11 | 9 | 2.3e-06 | 0.00042 | 0.012 | 1.6e-08 | 0.000027 |
12 | ERCC2 | excision repair cross-complementing rodent repair deficiency, complementation group 2 (xeroderma pigmentosum D) | 2430 | 43 | 0 | 2 | 16 | 0 | 0 | 0 | 16 | 16 | 13 | 4.5e-07 | 0.004 | 0.12 | 1.8e-08 | 0.000027 |
13 | FBXW7 | F-box and WD repeat domain containing 7 | 2580 | 1 | 0 | 0 | 10 | 4 | 0 | 2 | 16 | 13 | 12 | 1e-05 | 0.0019 | 0.027 | 1.4e-07 | 0.0002 |
14 | RHOB | ras homolog gene family, member B | 591 | 20 | 0 | 1 | 7 | 0 | 0 | 0 | 7 | 7 | 6 | 1.8e-06 | 0.0097 | 0.41 | 1.5e-07 | 0.0002 |
15 | TSC1 | tuberous sclerosis 1 | 3579 | 6 | 0 | 0 | 3 | 5 | 2 | 1 | 11 | 11 | 11 | 1.9e-08 | 1 | 0.26 | 3.5e-07 | 0.00043 |
16 | FOXQ1 | forkhead box Q1 | 1212 | 6 | 0 | 1 | 3 | 1 | 0 | 3 | 7 | 7 | 4 | 1.7e-06 | 0.027 | 0.087 | 7.2e-07 | 0.00082 |
17 | PIK3CA | phosphoinositide-3-kinase, catalytic, alpha polypeptide | 3287 | 7 | 0 | 1 | 26 | 0 | 0 | 0 | 26 | 26 | 11 | 0.043 | 1e-05 | 0.00066 | 6.7e-06 | 0.0072 |
18 | RXRA | retinoid X receptor, alpha | 1425 | 3 | 0 | 2 | 12 | 0 | 0 | 0 | 12 | 12 | 6 | 0.0061 | 0.00012 | 0.052 | 7.6e-06 | 0.0077 |
19 | CREBBP | CREB binding protein (Rubinstein-Taybi syndrome) | 7449 | 30 | 0 | 3 | 12 | 5 | 0 | 1 | 18 | 17 | 17 | 4e-06 | 0.13 | 0.87 | 9.6e-06 | 0.0092 |
20 | ERBB3 | v-erb-b2 erythroblastic leukemia viral oncogene homolog 3 (avian) | 4266 | 3 | 0 | 1 | 14 | 0 | 0 | 0 | 14 | 14 | 10 | 0.11 | 1e-05 | 0.75 | 0.000016 | 0.014 |
21 | FAT1 | FAT tumor suppressor homolog 1 (Drosophila) | 13871 | 9 | 0 | 2 | 6 | 7 | 0 | 4 | 17 | 15 | 17 | 3.8e-06 | 1 | 0.31 | 0.000022 | 0.019 |
22 | MLL | myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila) | 12052 | 3 | 0 | 3 | 11 | 7 | 0 | 3 | 21 | 18 | 20 | 0.000014 | 0.15 | 0.38 | 0.000031 | 0.026 |
23 | HRAS | v-Ha-ras Harvey rat sarcoma viral oncogene homolog | 659 | 93 | 0 | 0 | 6 | 0 | 0 | 0 | 6 | 6 | 5 | 0.00018 | 0.12 | 0.047 | 0.000038 | 0.03 |
24 | ACRC | acidic repeat containing | 2124 | 10 | 0 | 0 | 4 | 1 | 0 | 0 | 5 | 4 | 4 | 0.022 | 0.0001 | 0.71 | 0.000042 | 0.032 |
25 | TXNIP | thioredoxin interacting protein | 1204 | 1 | 0 | 2 | 7 | 0 | 0 | 5 | 12 | 9 | 12 | 0.000034 | 1 | 0.057 | 0.000053 | 0.038 |
26 | ECM1 | extracellular matrix protein 1 | 1659 | 17 | 0 | 0 | 4 | 1 | 0 | 0 | 5 | 5 | 4 | 0.023 | 9e-05 | 0.85 | 0.000058 | 0.041 |
27 | KLF5 | Kruppel-like factor 5 (intestinal) | 1386 | 4 | 0 | 2 | 8 | 0 | 0 | 3 | 11 | 10 | 10 | 0.00016 | 0.22 | 0.046 | 0.000074 | 0.05 |
28 | RBM26 | RNA binding motif protein 26 | 3025 | 18 | 0 | 0 | 9 | 1 | 0 | 0 | 10 | 9 | 9 | 0.00015 | 0.081 | 0.45 | 0.000098 | 0.064 |
29 | RAD51C | RAD51 homolog C (S. cerevisiae) | 1167 | 103 | 0 | 1 | 5 | 0 | 0 | 0 | 5 | 4 | 3 | 0.096 | 0.00012 | 0.69 | 0.00011 | 0.067 |
30 | CEP192 | centrosomal protein 192kDa | 7790 | 15 | 0 | 2 | 2 | 2 | 1 | 0 | 5 | 5 | 4 | 0.016 | 0.0095 | 0.015 | 0.00011 | 0.067 |
31 | ASXL2 | additional sex combs like 2 (Drosophila) | 4352 | 8 | 0 | 0 | 7 | 4 | 0 | 0 | 11 | 9 | 11 | 0.00019 | 1 | 0.017 | 0.00012 | 0.071 |
32 | PSIP1 | PC4 and SFRS1 interacting protein 1 | 1678 | 13 | 0 | 0 | 3 | 1 | 2 | 1 | 7 | 7 | 7 | 0.000058 | 1 | 0.36 | 0.0003 | 0.17 |
33 | ZNF513 | zinc finger protein 513 | 1638 | 12 | 0 | 0 | 3 | 1 | 0 | 3 | 7 | 7 | 7 | 0.000027 | 1 | 0.54 | 0.00031 | 0.17 |
34 | FOXA1 | forkhead box A1 | 1423 | 114 | 0 | 1 | 2 | 0 | 0 | 5 | 7 | 7 | 7 | 0.000028 | 1 | 0.36 | 0.00032 | 0.17 |
35 | TRIP11 | thyroid hormone receptor interactor 11 | 6020 | 14 | 0 | 1 | 4 | 1 | 0 | 0 | 5 | 5 | 4 | 0.13 | 0.0066 | 0.028 | 0.00045 | 0.23 |
Figure S1. This figure depicts the distribution of mutations and mutation types across the TP53 significant gene.
![](TP53.stick_fig.png)
Figure S2. This figure depicts the distribution of mutations and mutation types across the KDM6A significant gene.
![](KDM6A.stick_fig.png)
Figure S3. This figure depicts the distribution of mutations and mutation types across the RB1 significant gene.
![](RB1.stick_fig.png)
Figure S4. This figure depicts the distribution of mutations and mutation types across the ARID1A significant gene.
![](ARID1A.stick_fig.png)
Figure S5. This figure depicts the distribution of mutations and mutation types across the CDKN1A significant gene.
![](CDKN1A.stick_fig.png)
Figure S6. This figure depicts the distribution of mutations and mutation types across the MLL2 significant gene.
![](MLL2.stick_fig.png)
Figure S7. This figure depicts the distribution of mutations and mutation types across the ELF3 significant gene.
![](ELF3.stick_fig.png)
Figure S8. This figure depicts the distribution of mutations and mutation types across the FGFR3 significant gene.
![](FGFR3.stick_fig.png)
Figure S9. This figure depicts the distribution of mutations and mutation types across the CDKN2A significant gene.
![](CDKN2A.stick_fig.png)
Figure S10. This figure depicts the distribution of mutations and mutation types across the STAG2 significant gene.
![](STAG2.stick_fig.png)
Figure S11. This figure depicts the distribution of mutations and mutation types across the NFE2L2 significant gene.
![](NFE2L2.stick_fig.png)
Figure S12. This figure depicts the distribution of mutations and mutation types across the ERCC2 significant gene.
![](ERCC2.stick_fig.png)
Figure S13. This figure depicts the distribution of mutations and mutation types across the FBXW7 significant gene.
![](FBXW7.stick_fig.png)
Figure S14. This figure depicts the distribution of mutations and mutation types across the RHOB significant gene.
![](RHOB.stick_fig.png)
Figure S15. This figure depicts the distribution of mutations and mutation types across the TSC1 significant gene.
![](TSC1.stick_fig.png)
Figure S16. This figure depicts the distribution of mutations and mutation types across the FOXQ1 significant gene.
![](FOXQ1.stick_fig.png)
Figure S17. This figure depicts the distribution of mutations and mutation types across the PIK3CA significant gene.
![](PIK3CA.stick_fig.png)
Figure S18. This figure depicts the distribution of mutations and mutation types across the RXRA significant gene.
![](RXRA.stick_fig.png)
Figure S19. This figure depicts the distribution of mutations and mutation types across the CREBBP significant gene.
![](CREBBP.stick_fig.png)
Figure S20. This figure depicts the distribution of mutations and mutation types across the ERBB3 significant gene.
![](ERBB3.stick_fig.png)
Figure S21. This figure depicts the distribution of mutations and mutation types across the FAT1 significant gene.
![](FAT1.stick_fig.png)
Figure S22. This figure depicts the distribution of mutations and mutation types across the MLL significant gene.
![](MLL.stick_fig.png)
Figure S23. This figure depicts the distribution of mutations and mutation types across the HRAS significant gene.
![](HRAS.stick_fig.png)
Figure S24. This figure depicts the distribution of mutations and mutation types across the ACRC significant gene.
![](ACRC.stick_fig.png)
Figure S25. This figure depicts the distribution of mutations and mutation types across the TXNIP significant gene.
![](TXNIP.stick_fig.png)
Figure S26. This figure depicts the distribution of mutations and mutation types across the ECM1 significant gene.
![](ECM1.stick_fig.png)
Figure S27. This figure depicts the distribution of mutations and mutation types across the KLF5 significant gene.
![](KLF5.stick_fig.png)
Figure S28. This figure depicts the distribution of mutations and mutation types across the RBM26 significant gene.
![](RBM26.stick_fig.png)
Figure S29. This figure depicts the distribution of mutations and mutation types across the RAD51C significant gene.
![](RAD51C.stick_fig.png)
Figure S30. This figure depicts the distribution of mutations and mutation types across the ASXL2 significant gene.
![](ASXL2.stick_fig.png)
In brief, we tabulate the number of mutations and the number of covered bases for each gene. The counts are broken down by mutation context category: four context categories that are discovered by MutSig, and one for indel and 'null' mutations, which include indels, nonsense mutations, splice-site mutations, and non-stop (read-through) mutations. For each gene, we calculate the probability of seeing the observed constellation of mutations, i.e. the product P1 x P2 x ... x Pm, or a more extreme one, given the background mutation rates calculated across the dataset. [1]
In addition to the links below, the full results of the analysis summarized in this report can also be downloaded programmatically using firehose_get, or interactively from either the Broad GDAC website or TCGA Data Coordination Center Portal.