Genomic variant #0000372291

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.170089355C>T
Reference dbSNP
DB-ID AADAT_000025
Frequency 0.071
Allele Count 15
Allele Number 212
Depth 1354
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