Genomic variant #0000434172

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.20645885T>G
Reference dbSNP
DB-ID ABCB5_000022
Frequency 0.316
Allele Count 67
Allele Number 212
Depth 2870
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