Genomic variant #0000783619

Individual ID 00000003
Chromosome 20
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.25302331C>T
Reference dbSNP
DB-ID ABHD12_000008
Frequency 0.047
Allele Count 10
Allele Number 212
Depth 2845
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABHD12 NM_001042472.2 ./.
ABHD12 NM_015600.4 ./.
ABHD12 XM_005260698.1 ./.
ABHD12 XM_005260699.3 ./.
ABHD12 XM_005260700.1 ./.
ABHD12 XM_011529214.1 ./.
ABHD12 XM_011529215.1 ./.
ABHD12 XM_011529216.1 ./.
ABHD12 XM_011529217.1 ./.
ABHD12 XM_011529218.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin