Genomic variant #0000576729

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.9077976G>T
Reference dbSNP
DB-ID A2M_000001
Frequency 0.319
Allele Count 67
Allele Number 210
Depth 1326
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