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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
UGT1A1 NM_000463.2 +?/+? 1 c.115C>G UGT1A1*44 r.(?) p.(His39Asp)


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