https://t.co/LjpdlHa0C7 is getting a good face-lift.
Samples now have variant tables with annotation on their impact to the gene.
There is also an IGV integration. You need IGV installed locally but the Start|Jump links will open up you BAM file in IGV.

You must have IGV open and then click the start link.
The sample's BAM will show up for viewing in IGV.
Once open, you can use the jump link to move swiftly around to each variant. This is a variant in THCAS.

You can jump to other variants in the same gene. In this case we have one non-synonymous variant in phase with a synonymous variant in THCAS.

Cannabinoid synthase genes are cute but some folks can answer those questions with HPLC.
How about flowering genes?

This sample has a disruptive in frame deletion on a late flowering gene. And it's very rare in the population.

Looks to be heterozygous....
But its never this simple in cannabis.

Let's look at what other damaging variations it has.