Genomic variant #0000342686

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.151828170T>C
Reference dbSNP
DB-ID AADACL2-AS1_000016
Frequency 0.014
Allele Count 3
Allele Number 212
Depth 1058
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