Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2018 Feb 26;8:3623. doi: 10.1038/s41598-018-21844-6

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© The Author(s) 2018

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

PMC Copyright notice

mtDNA variants in DLBCL. Graphs from periphery to center: (1) Map of the mitochondrial genome (2) Average sequence depth for each position among the samples carrying variants, ranging from 0 to 4000 reads. (3) SNVs found in DLBCL, with the height of each bar depicting the VAF. tRNA and rRNA variants are green, stop-gains are red, non-synonymous variants are blue, synonymous and non-coding variants are grey. (4) The MutPred pathogenicity score for each non-synonymous variant. (5) The log GenBank frequency of each variant, represented as 5 + log10(x/30589), where x is the number of genomes in GenBank that carry that variant. (a) Somatic Mutations in 29 samples. (b) Private constitutional variants in 34 samples.