Genomic variant #0000452036

Individual ID 00000003
Chromosome 7
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.122092724_122092725insA
Reference dbSNP
DB-ID AASS_000014
Frequency 0.082
Allele Count 15
Allele Number 184
Depth 349
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
AASS NM_005763.3 ./.
AASS XM_011515725.1 ./.
AASS XM_011515726.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin