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Add VEP annotations to the somatic SNVs #30

Description

@NagaComBio

Feature Requirements:

  • Add VEP annotations to the SNV calls.
  • Parse transcripts with "HIGH" or "MODERATE" VEP consequences impact from the INFO column and add them to a new column with Gene, Consequences, Exon/Intron counts, HGVSc and HGVSp information.
  • Still to be decided:
    • Should this be done for all variants?
    • Should the VEP annotation be removed from the INFO column once it is parsed?

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