Genomic variant #0000364091

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.88139757T>C
Reference dbSNP
DB-ID ABCG2_000030
Frequency 0.09
Allele Count 19
Allele Number 212
Depth 1222
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