Genomic variant #0000434202

Individual ID 00000003
Chromosome 7
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.20659128C>G
Reference dbSNP
DB-ID ABCB5_000031
Frequency 0.004717
Allele Count 1
Allele Number 212
Depth 1835
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCB5 NM_001163941.1 ./.
ABCB5 NM_001163942.1 ./.
ABCB5 NM_001163993.2 ./.
ABCB5 NM_178559.5 ./.
ABCB5 XM_006715722.2 ./.
ABCB5 XM_011515367.1 ./.
ABCB5 XM_011515368.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin