Genomic variant #0000581605

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.39646257_39646258insA
Reference dbSNP
DB-ID ABCD2_000032
Frequency 0.023
Allele Count 3
Allele Number 132
Depth 155
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