Genomic variant #0000278773

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.43837951G>A
Reference dbSNP
DB-ID ABCG5_000005
Frequency 0.057
Allele Count 12
Allele Number 212
Depth 1881
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCG5 NM_022436.2 ./.
ABCG8 NM_022437.2 ./.
ABCG5 XM_005264480.2 ./.
ABCG8 XM_005264483.2 ./.
ABCG5 XM_006712073.2 ./.
ABCG5 XM_006712074.2 ./.
ABCG5 XM_011533024.1 ./.
ABCG5 XM_011533025.1 ./.
ABCG5 XM_011533026.1 ./.
ABCG5 XM_011533027.1 ./.
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