Genomic variant #0000576769

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.9107621G>A
Reference dbSNP
DB-ID A2M_000048
Frequency 0.009434
Allele Count 2
Allele Number 212
Depth 2707
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