Genomic variant #0000508822

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.137009341A>C
Reference -
DB-ID ABCA2_000023
Frequency 0.006329
Allele Count 1
Allele Number 158
Depth 671
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