Mutation Assessor
Sarcoma (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/C1PZ583G
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: 720

  • Medium Functional Impact Missense Mutations: 3817

  • Low Functional Impact Missense Mutations: 3915

  • Neutral Functional Impact Mutations: 2767

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 46 3 0 3.0200 medium medium
RB1 3 0 1 1 0 1.8825 low medium/low
EOMES 6 0 0 1 0 1.0400 low low
PKD2 7 0 1 1 0 1.5525 low medium/low
WNK1 10 0 0 1 0 0.8950 low low
PTEN 12 5 1 0 0 3.7950 high high
KRTAP5-5 13 0 3 0 0 3.1450 medium medium
TRAF7 14 0 0 2 0 1.2650 low low
COL18A1 18 0 2 0 1 1.9050 medium medium
LHCGR 19 0 0 1 0 1.7600 low low
Methods & Data
Input
  1. SARC-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 SARC-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)