Mutation Assessor
Ovarian Serous Cystadenocarcinoma (Primary solid tumor)
21 August 2015  |  analyses__2015_08_21
Maintainer Information
Citation Information
Maintained by David Heiman (Broad Institute)
Cite as Broad Institute TCGA Genome Data Analysis Center (2015): Mutation Assessor. Broad Institute of MIT and Harvard. doi:10.7908/C1TT4Q74
Overview
Introduction

This report serves to summarize the functional impact of missense mutations in each gene as determined by Mutation Assessor[1].

Summary
  • High Functional Impact Missense Mutations: 1017

  • Medium Functional Impact Missense Mutations: 5406

  • Low Functional Impact Missense Mutations: 5358

  • Neutral Functional Impact Mutations: 3823

Results
Functional Impact by Gene

Table 1.  Get Full Table A gene-level breakdown of missense mutation functional impact, ordered by MutSig rank. Includes missense mutation counts broken down by level of functional impact (high, medium, low, neutral), median functional impact score and level, and most common level(s) of functional impact (mode) per gene.

Gene MutSig
Rank
High
Functional Impact
Count
Medium
Functional Impact
Count
Low
Functional Impact
Count
Neutral
Functional Impact
Count
Median
Functional Impact
Score
Median
Functional Impact
Level
Mode
Functional Impact
Level
TP53 1 0 248 6 1 3.1050 medium medium
RB1 2 0 2 1 2 1.0850 low medium/neutral
BRCA1 3 1 0 0 0 4.3700 high high
NF1 4 1 5 1 0 2.2500 medium medium
CDK12 5 1 2 3 0 1.6500 low low
KRAS 6 0 5 0 0 3.1350 medium medium
HNF1B 7 0 2 1 0 2.3600 medium medium
PTEN 8 1 0 1 0 2.8325 medium high/low
BRCA2 10 0 0 2 2 1.1800 low low/neutral
EFEMP1 11 1 1 0 2 1.1100 low neutral
Methods & Data
Input
  1. OV-TP.maf.annotated

  2. sig_genes.txt

  3. Mutation Assessor Scores Release 2:

A lookup is done against the relevant Mutation Assessor Scores table for each missense mutation in a given MAF file, and available functional impact score and level are appended as two new columns to generate OV-TP.maf.annotated. These are summarized in Table 1, sorted by MutSig rank.

Download Results

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.

References
[1] Boris Reva, Yevgeniy Antipin, and Chris Sander, Predicting the functional impact of protein mutations: application to cancer genomics, Nucl. Acids Res. 39(17):e118 (2011)