Supplementary Figure 1: Identification of MYOD1 L122R in RMS. | Nature Genetics

Supplementary Figure 1: Identification of MYOD1 L122R in RMS.

From: A recurrent neomorphic mutation in MYOD1 defines a clinically aggressive subset of embryonal rhabdomyosarcoma associated with PI3K-AKT pathway mutations

Supplementary Figure 1

IGV views of exome and RNA-seq reads at MYOD1 L122 in embryonal RMS case RMS1. A mutation (c.365T>G) was seen in the tumor exome and tumor transcriptome but not in the normal exome; the read counts for the reference and variant alleles in these three sequencing runs were, respectively, 35T:40G, 284T:389G and 143T:0G.

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