Genomic variant #0000795455

Individual ID 00000003
Chromosome 21
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.14299523G>A
Reference dbSNP
DB-ID ABCC13_000022
Frequency 0.156
Allele Count 33
Allele Number 212
Depth 3881
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCC13 NR_003087.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin