Genomic variant #0000342688

Individual ID 00000003
Chromosome 3
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.151880081T>C
Reference dbSNP
DB-ID AADACL2-AS1_000018
Frequency 0.165
Allele Count 35
Allele Number 212
Depth 1921
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
SUCNR1 NM_033050.4 ./.
AADACL2-AS1 NR_110203.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin