Genomic variant #0000342684

Individual ID 00000003
Chromosome 3
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.151827813G>A
Reference dbSNP
DB-ID AADACL2-AS1_000014
Frequency 0.769
Allele Count 163
Allele Number 212
Depth 3034
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
AADAC NM_001086.2 ./.
AADACL2-AS1 NR_110203.1 ./.
AADAC XM_005247104.3 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin