Genomic variant #0000508865

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.137014828G>A
Reference dbSNP
DB-ID ABCA2_000079
Frequency 0.004717
Allele Count 1
Allele Number 212
Depth 3734
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