Genomic variant #0000778234

Individual ID 00000003
Chromosome 19
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.58353124C>T
Reference dbSNP
DB-ID A1BG_000027
Frequency 0.004717
Allele Count 1
Allele Number 212
Depth 4296
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
A1BG NM_130786.3 ./.
A1BG-AS1 NR_015380.2 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin