Genomic variant #0000477032

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.116942766C>T
Reference dbSNP
DB-ID AARD_000012
Frequency 0.232
Allele Count 44
Allele Number 190
Depth 428
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