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Items: 3

1.

Modified penetrance of coding variants by cis-regulatory variation contributes to disease risk

(Submitter supplied) Edited mendelian disease SNP rs199643834 responsible for Birt-Hogg-Dubé Syndrome into 293T cells using CRISPR/Cas9
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
13 Samples
Download data: TXT
Series
Accession:
GSE116061
ID:
200116061
2.

Illumina NovaSeq 6000 (Homo sapiens)

Platform
Accession:
GPL24676
ID:
100024676
3.

HEK293T_rs199643834_EDIT_HET [15_36]

Organism:
Homo sapiens
Source name:
HEK293T_rs199643834_EDIT_HET
Platform:
GPL24676
Series:
GSE116061
Download data
Sample
Accession:
GSM3208203
ID:
303208203
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Supplemental Content

db=gds|term=GSM3208203[Accession]|query=1|qty=2|blobid=MCID_674c4ce996d9ad040624a138|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
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