Genomic variant #0000452050

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.122126584A>T
Reference dbSNP
DB-ID AASS_000015
Frequency 0.103
Allele Count 18
Allele Number 174
Depth 283
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