Genomic variant #0000576559

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.8847367C>T
Reference dbSNP
DB-ID A2ML1_000048
Frequency 0.024
Allele Count 5
Allele Number 210
Depth 479
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
A2ML1 NM_001282424.1 ./.
A2ML1 NM_144670.4 ./.
A2ML1 XM_011520566.1 ./.
A2ML1 XM_011520567.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin