Variant #0000055826 (NC_000002.11:g.234669048C>G, NM_000463.2:c.115C>G (UGT1A1))
| Chromosome |
2 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
- |
| Clinical classification |
likely pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.234669048C>G |
| DNA change (hg38) |
g.233760402C>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
UGT1A1_000005 See all 8 reported entries |
| Variant remarks |
Crigler Najjar Syndrome type I |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs7255339 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Giulia Canu |
| Database submission license |
No license selected |
| Created by |
Giulia Canu |
| Date created |
2015-02-03 10:57:14 +01:00 (CET) |
| Date last edited |
2023-01-18 13:34:34 +01:00 (CET) |

Variant on transcripts
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