Genomic variant #0000826642

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.75114581A>T
Reference dbSNP
DB-ID ABCB7_000018
Frequency 0.005495
Allele Count 1
Allele Number 182
Depth 322
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