A tibble of the annotation results from ANNOVAR. It was joined with the sample information. Get more information on the returned values from the ANNOVAR documentation
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a tibble (411 x 19)
file ID
chromosome
start of variant
end of variant
reference allele
alternate allele
where the alteration is
gene name
type of mutation
amino acid change
more usable amino acid change
name of the file
category of data (are all "Sequencing Reads")
type of data (are all "Aligned Reads")
ID of the source project (TCGA-COAD or -READ)
case ID
sample ID
from where the sample was taken
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