Genomic variant #0000783603

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.25295207C>T
Reference dbSNP
DB-ID PYGB_000099
Frequency 0.373
Allele Count 79
Allele Number 212
Depth 1460
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_011529214.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin