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)
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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.529T>C UGT1A1*15 r.(?) p.(Cys177Arg)


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