Genomic variant #0000477029

Individual ID 00000003
Chromosome 8
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.116938596C>T
Reference -
DB-ID AARD_000009
Frequency 0.004717
Allele Count 1
Allele Number 212
Depth 1725
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
AARD NM_001025357.2 ./.
AARD XM_011517043.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin