Genomic variant #0000364096

Individual ID 00000003
Chromosome 4
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.88159119_88159125del
Reference dbSNP
DB-ID ABCG2_000040
Frequency 0.057
Allele Count 12
Allele Number 212
Depth 3072
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCG2 NM_001257386.1 ./.
ABCG2 NM_004827.2 ./.
ABCG2 XM_005263354.2 ./.
ABCG2 XM_005263355.2 ./.
ABCG2 XM_005263356.2 ./.
ABCG2 XM_011532420.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin