Genomic variant #0000826645

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.75114852T>C
Reference dbSNP
DB-ID ABCB7_000021
Frequency 0.137
Allele Count 29
Allele Number 212
Depth 3213
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