Genomic variant #0000783611

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.25296483C>T
Reference dbSNP
DB-ID PYGB_000107
Frequency 0.004717
Allele Count 1
Allele Number 212
Depth 2731
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