Genomic variant #0000826637

Individual ID 00000003
Chromosome X
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.75112761_75112762del
Reference -
DB-ID ABCB7_000013
Frequency 0.02
Allele Count 4
Allele Number 196
Depth 385
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCB7 NM_001271696.1 ./.
ABCB7 NM_001271697.1 ./.
ABCB7 NM_001271698.1 ./.
ABCB7 NM_001271699.1 ./.
ABCB7 NM_004299.4 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin