Genomic variant #0000434234

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.20739023G>A
Reference dbSNP
DB-ID ABCB5_000077
Frequency 0.788
Allele Count 167
Allele Number 212
Depth 2079
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_178559.5 ./.
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