Genomic variant #0000452052

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.122129167G>A
Reference dbSNP
DB-ID AASS_000019
Frequency 0.006944
Allele Count 1
Allele Number 144
Depth 148
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