Genomic variant #0000364062

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.88097476T>C
Reference dbSNP
DB-ID ABCG2_000015
Frequency 0.004717
Allele Count 1
Allele Number 212
Depth 3927
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