Genomic variant #0000372295

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.170089661C>T
Reference dbSNP
DB-ID AADAT_000029
Frequency 0.004717
Allele Count 1
Allele Number 212
Depth 3796
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