Genomic variant #0000581604

Individual ID 00000003
Chromosome 12
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.39643925A>G
Reference dbSNP
DB-ID ABCD2_000031
Frequency 0.825
Allele Count 175
Allele Number 212
Depth 1087
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
C12orf40 NM_001031748.2 ./.
C12orf40 XM_005268806.2 ./.
C12orf40 XM_006719358.2 ./.
ABCD2 XM_011538027.1 ./.
C12orf40 XM_011538231.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin