Genomic variant #0000702211

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.29562560T>C
Reference dbSNP
DB-ID ABHD15_000012
Frequency 0.613
Allele Count 130
Allele Number 212
Depth 3751
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABHD15 NM_198147.2 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin