Genomic variant #0000508877

Individual ID 00000003
Chromosome 9
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.137017531T>G
Reference dbSNP
DB-ID ABCA2_000041
Frequency 0.113
Allele Count 24
Allele Number 212
Depth 3415
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCA2 NM_001606.4 ./.
ABCA2 NM_212533.2 ./.
ABCA2 XM_006716996.2 ./.
ABCA2 XM_011518346.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin