Variant #0000055893 (NC_000002.11:g.234669576A>G, NM_000463.2:c.643A>G (UGT1A1))

Chromosome 2
Allele Parent #1
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.234669576A>G
DNA change (hg38) g.233760930A>G
Published as -
ISCN -
DB-ID UGT1A1_000013 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs144398951
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 6.0E-5 View details
Owner Giulia Canu
Database submission license No license selected
Created by Giulia Canu
Date created 2015-02-04 10:08:06 +01:00 (CET)
Date last edited 2023-01-18 13:42:07 +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.643A>G - r.(?) p.(Ile215Val)


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