Genomic variant #0000581598

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.39618495C>T
Reference dbSNP
DB-ID ABCD2_000025
Frequency 0.185
Allele Count 37
Allele Number 200
Depth 520
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