Variant #0001033121 (NC_000002.11:g.234637905C>T, NM_000463.2:c.-31029C>T (UGT1A1))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.234637905C>T
DNA change (hg38) -
Published as UGT1A3(NM_019093.4):c.133C>T (p.(Arg45Trp))
ISCN -
DB-ID UGT1A3_000004 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00428 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
UGT1A1 NM_000463.2 -?/. - c.-31029C>T - r.(?) p.(=)
DNAJB3 NM_001001394.3 -?/. - c.*14220G>A - r.(=) p.(=)
UGT1A6 NM_001072.3 -?/. - c.861+35394C>T - r.(=) p.(=)
UGT1A4 NM_007120.2 -?/. - c.867+9572C>T - r.(=) p.(=)
UGT1A10 NM_019075.2 -?/. - c.856-37775C>T - r.(=) p.(=)
UGT1A8 NM_019076.4 -?/. - c.856-37775C>T - r.(=) p.(=)
UGT1A7 NM_019077.2 -?/. - c.856-37775C>T - r.(=) p.(=)
UGT1A5 NM_019078.1 -?/. - c.867+15401C>T - r.(=) p.(=)
UGT1A3 NM_019093.2 -?/. - c.133C>T - r.(?) p.(Arg45Trp)
UGT1A9 NM_021027.2 -?/. - c.856-37775C>T - r.(=) p.(=)
UGT1A6 NM_205862.1 -?/. - c.60+35394C>T - r.(=) p.(=)


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