Genomic variant #0000783598

Individual ID 00000003
Chromosome 20
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.25294875del
Reference -
DB-ID PYGB_000094
Frequency 0.014
Allele Count 3
Allele Number 212
Depth 920
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
PYGB NM_002862.3 ./.
ABHD12 NM_015600.4 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin