Genomic variant #0000778233

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.58353113T>C
Reference dbSNP
DB-ID A1BG_000026
Frequency 0.91
Allele Count 193
Allele Number 212
Depth 4935
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