Genomic variant #0000715321

Individual ID 00000003
Chromosome 17
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.69214917T>A
Reference dbSNP
DB-ID ABCA10_000066
Frequency 0.57
Allele Count 57
Allele Number 100
Depth 156
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCA10 NM_080282.3 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin