Genomic variant #0000649944

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.67209639C>T
Reference dbSNP
DB-ID AAGAB_000004
Frequency 0.199
Allele Count 37
Allele Number 186
Depth 350
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_005254664.2 ./.
AAGAB XM_006720683.2 ./.
AAGAB XM_011522020.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin