Genomic variant #0000603955

Individual ID 00000003
Chromosome 12
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.125118606C>T
Reference dbSNP
DB-ID AACS_000031
Frequency 0.142
Allele Count 30
Allele Number 212
Depth 5282
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
AACS NM_023928.3 ./.
AACS XM_005253609.2 ./.
AACS XM_005253610.2 ./.
AACS XM_005253611.2 ./.
AACS XM_011538692.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin