How to get the number of RNA reads for mutations of exome-seq?

Question

[agicict]

Hi.

I am studying how do mutations have influence on protein quantification in mass spectrometry.

I called variants from exome-seq data and made it vcf format.

In addition, I have RNA-seq data and would like to get two kinds of information.

One is the number of RNA reads supporting the identified mutation based on exome-seq. The other is the number of RNA reads that don't provide evidence for the mutation.

Does GATK provide these kinds of information?