Genomic variant #0000434224

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.20722986T>C
Reference dbSNP
DB-ID ABCB5_000076
Frequency 0.228
Allele Count 46
Allele Number 202
Depth 487
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