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In some cases for variants with low counts or high dropout rates, a synonymous variant gets a score when there is no score for a corresponding nucleotide variant. Two examples from the BRCA1 example dataset are p.Val10Asp and p.Ile20Ter.
There should be an option to automatically filter these variants out of the default /main/synonymous/scores table (and consequently shown as missing in sequence-function maps).
Thanks to Adebola Adeniran for raising this issue via email.
The text was updated successfully, but these errors were encountered:
In some cases for variants with low counts or high dropout rates, a synonymous variant gets a score when there is no score for a corresponding nucleotide variant. Two examples from the BRCA1 example dataset are
p.Val10Asp
andp.Ile20Ter
.There should be an option to automatically filter these variants out of the default
/main/synonymous/scores
table (and consequently shown as missing in sequence-function maps).Thanks to Adebola Adeniran for raising this issue via email.
The text was updated successfully, but these errors were encountered: