Genomic variant #0000783601

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.25294985T>C
Reference dbSNP
DB-ID PYGB_000097
Frequency 0.061
Allele Count 13
Allele Number 212
Depth 3790
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