Genomic variant #0000783608

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.25295888G>A
Reference dbSNP
DB-ID PYGB_000104
Frequency 0.009434
Allele Count 2
Allele Number 212
Depth 1386
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABHD12 NM_001042472.2 ./.
PYGB NM_002862.3 ./.
ABHD12 NM_015600.4 ./.
ABHD12 XM_005260699.3 ./.
ABHD12 XM_011529214.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin