SACGF / SACGF/variantgrid

Flag Alleles in pseudoautosomal (PAR) regions

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#518 2 comments 0 reactions 1 assignee Claimed by @TheMadBug View on GitHub
Dominant language
Python
Stars
30
Forks
3
Avg merge
9h 28m
Merged PRs (30d)
42

Description

* Create a new flag type / images etc
* When variant is matched against a transcript with data that contains ```{"other_chroms":["NC_000024.9"]}``` then raise that flag
* Have it turn up in the right places on HGVS issues etc

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