Genomic variant #0000278839

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.43877472_43877473del
Reference dbSNP
DB-ID ABCG8_000064
Frequency 0.114
Allele Count 19
Allele Number 166
Depth 255
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