Genomic variant #0000576746

Individual ID 00000003
Chromosome 12
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.9093581_9093585del
Reference dbSNP
DB-ID A2M_000051
Frequency 0.118
Allele Count 25
Allele Number 212
Depth 2895
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
A2M NM_000014.4 ./.
A2M XM_006719056.2 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin