Genomic variant #0000649937

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.67203948A>T
Reference dbSNP
DB-ID AAGAB_000021
Frequency 0.004808
Allele Count 1
Allele Number 208
Depth 610
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