Genomic variant #0000624474

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.50886775T>C
Reference dbSNP
DB-ID ABHD12B_000014
Frequency 0.967
Allele Count 205
Allele Number 212
Depth 3907
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