Genomic variant #0000624489

Individual ID 00000003
Chromosome 14
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.50903821A>G
Reference dbSNP
DB-ID ABHD12B_000036
Frequency 0.119
Allele Count 20
Allele Number 168
Depth 256
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABHD12B NM_001206673.1 ./.
ABHD12B NM_181814.1 ./.
ABHD12B XM_005267356.2 ./.
ABHD12B XM_011536474.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin