Genomic variant #0000624455

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.50878936G>A
Reference dbSNP
DB-ID ABHD12B_000042
Frequency 0.015
Allele Count 3
Allele Number 206
Depth 430
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_006720052.1 ./.
ABHD12B XM_011536472.1 ./.
ABHD12B XM_011536473.1 ./.
ABHD12B XM_011536474.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin