Variant #0000055830 (NC_000002.11:g.234669462T>C, NM_000463.2:c.529T>C (UGT1A1))
| Chromosome |
2 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.234669462T>C |
| DNA change (hg38) |
g.233760816T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
UGT1A1_000009 See all 2 reported entries |
| Variant remarks |
Crigler Najjar Syndrome type I. |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs7255342 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0 View details |
| Owner |
Giulia Canu |
| Database submission license |
No license selected |
| Created by |
Giulia Canu |
| Date created |
2015-02-03 12:05:49 +01:00 (CET) |
| Date last edited |
2023-01-18 13:40:36 +01:00 (CET) |

Variant on transcripts
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