Genomic variant #0000226013

Individual ID 00000003
Chromosome 1
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.33312462G>A
Reference dbSNP
DB-ID A3GALT2_000002
Frequency 0.047
Allele Count 10
Allele Number 212
Depth 2013
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
A3GALT2 NM_001080438.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin