Genomic variant #0000718660

Individual ID 00000003
Chromosome 17
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.76469834C>T
Reference dbSNP
DB-ID AANAT_000002
Frequency 0.009434
Allele Count 2
Allele Number 212
Depth 3489
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
AANAT NM_001166579.1 ./.
AANAT XM_011524415.1 ./.
AANAT XM_011524416.1 ./.
AANAT XM_011524417.1 ./.
AANAT XM_011524418.1 ./.
AANAT XM_011524419.1 ./.
AANAT XM_011524420.1 ./.
AANAT XM_011524421.1 ./.
AANAT XM_011524422.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin