Genomic variant #0000278782

Individual ID 00000003
Chromosome 2
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.43844486C>A
Reference dbSNP
DB-ID ABCG8_000032
Frequency 0.392
Allele Count 83
Allele Number 212
Depth 4108
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCG8 NM_022437.2 ./.
ABCG8 XM_005264483.2 ./.
ABCG8 XM_011533029.1 ./.
ABCG8 XM_011533030.1 ./.
ABCG8 XM_011533031.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin