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Feature #539
opencall synonymous amino acids that match pathogenic reference alleles (e.g. F5 R534R)
Status:
New
Priority:
Normal
Assigned To:
-
Target version:
-
Start date:
03/08/2011
Due date:
% Done:
0%
Estimated time:
Billable:
Estimatedhours:
Hours:
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Resolution:
Story points:
-
Description
The easiest example is F5 Leiden -- an amino acid "change" that happens to be reference. We want the nonsynonymous caller to (optionally) check the GET-Evidence flat file for instances of interesting/pathogenic gene + synonymous change, then check that position in the gene and call it as a "variant" rather than ignore it.
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