Genomic variant #0000581593

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.39607788T>C
Reference dbSNP
DB-ID ABCD2_000020
Frequency 0.005952
Allele Count 1
Allele Number 168
Depth 250
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCD2 NM_005164.3 ./.
ABCD2 XM_011538027.1 ./.
ABCD2 XM_011538028.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin