Genomic variant #0000826621

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.75065161T>C
Reference dbSNP
DB-ID ABCB7_000026
Frequency 0.057
Allele Count 12
Allele Number 212
Depth 2295
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