Variant allele fraction for a genotype
This annotation describes the proportion of the sample's reads that support the variant allele(s). It uses only reads that are actually considered informative by HaplotypeCaller (HC) or Mutect2, using pre-read likelihoods that are produced internally by HC/Mutect2.
In this context, an informative read is defined as one that allows the allele it carries to be easily distinguished. In contrast, a read might be considered uninformative if, for example, it only partially overlaps a short tandem repeat and it is not clear whether the read contains the reference allele or an extra repeat.
See the method documentation on using coverage information for important interpretation details.
GATK version 220.127.116.11 built at Wed, 9 Oct 2019 15:19:59 -0400.