Genomic variant #0000783631

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.25315118C>T
Reference dbSNP
DB-ID ABHD12_000020
Frequency 0.004762
Allele Count 1
Allele Number 210
Depth 610
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