Genomic variant #0000342691

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.151881605C>T
Reference dbSNP
DB-ID AADACL2-AS1_000021
Frequency 0.434
Allele Count 92
Allele Number 212
Depth 1077
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