Genomic variant #0000649936

Individual ID 00000003
Chromosome 15
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.67203475T>A
Reference dbSNP
DB-ID AAGAB_000020
Frequency 0.009434
Allele Count 2
Allele Number 212
Depth 776
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
AAGAB NM_001271885.1 ./.
AAGAB NM_001271886.1 ./.
AAGAB NM_024666.4 ./.
AAGAB XM_011522020.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin