SPDI normalization with refseq files #76
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Need to run the Flask server in a background thread so the seqfetcher endpoint is available for the hgvs library to call. Details here: https://stackoverflow.com/questions/77676757/run-a-full-flask-server-under-pytest-to-handle-http-requests-on-a-given-port Also need to pick the relevat transcript in `process_NC_HGVS()` in such a way that we select the one with the most up to date version so we don't end up unable to find the RefSeq data because it looks like we don't have all the RNA transcripts that UTA knows about.
This is a workaround for some liftover failures: biocommons/hgvs#717
Also remove them from the variants
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Description
Follow-up to #69.
How Has This Been Tested?