Variant #0000791286 (NC_000002.11:g.(?_43991388)_(44102695_?)del, NM_022436.2:c.-140_*644{0} (ABCG5))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(?_43991388)_(44102695_?)del |
| DNA change (hg38) |
- |
| Published as |
g.43991388_44102695del |
| ISCN |
- |
| DB-ID |
ABCG5_000258 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Wenjuan Qiu |
| Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
| Created by |
Wenjuan Qiu |
| Date created |
2021-07-21 04:33:22 +02:00 (CEST) |
| Date last edited |
2022-07-22 10:58:53 +02:00 (CEST) |

Variant on transcripts
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