Genomic variant #0000372284

Individual ID 00000003
Chromosome 4
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.170073404del
Reference dbSNP
DB-ID AADAT_000018
Frequency 0.411
Allele Count 74
Allele Number 180
Depth 668
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
AADAT NM_001286682.1 ./.
AADAT NM_001286683.1 ./.
AADAT NM_016228.3 ./.
AADAT NM_182662.1 ./.
AADAT XM_006714231.2 ./.
AADAT XM_011532020.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin