Genomic variant #0000278821
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.43874290_43874291del |
Reference |
- |
DB-ID |
ABCG8_000012 |
Frequency |
0.005263 |
Allele Count |
1 |
Allele Number |
190 |
Depth |
334 |
Average frequency (large NGS studies) |
Variant not found in online data sets |
Owner |
Admin |
Variant on transcripts
Screenings
|
|