Variant #0000055892 (NC_000002.11:g.234669558C>T, NM_000463.2:c.625C>T (UGT1A1))

Chromosome 2
Allele Both (homozygous)
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.234669558C>T
DNA change (hg38) g.233760912C>T
Published as -
ISCN -
DB-ID UGT1A1_000012 See all 14 reported entries
Variant remarks Crigler Najjar Syndrome type II
Reference -
ClinVar ID -
dbSNP ID rs72551343
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner Giulia Canu
Database submission license No license selected
Created by Giulia Canu
Date created 2015-02-04 09:57:33 +01:00 (CET)
Date last edited 2023-01-18 13:41:28 +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.625C>T UGT1A1*8 r.(?) p.(Arg209Trp)


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