Variant #0000328188 (NC_000002.11:g.234545928C>T, NM_000463.2:c.-123006C>T (UGT1A1))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.234545928C>T
DNA change (hg38) g.233637282C>T
Published as UGT1A10(NM_019075.2):c.760C>T (p.(Arg254Ter))
ISCN -
DB-ID UGT1A8_000001
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) 0.00035 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
UGT1A1 NM_000463.2 ?/. - c.-123006C>T - r.(?) p.(=)
DNAJB3 NM_001001394.3 ?/. - c.*106197G>A - r.(=) p.(=)
UGT1A6 NM_001072.3 ?/. - c.-55723C>T - r.(?) p.(=)
UGT1A4 NM_007120.2 ?/. - c.-81539C>T - r.(?) p.(=)
UGT1A10 NM_019075.2 ?/. - c.760C>T - r.(?) p.(Arg254Ter)
UGT1A8 NM_019076.4 ?/. - c.855+18720C>T - r.(=) p.(=)
UGT1A7 NM_019077.2 ?/. - c.-44656C>T - r.(?) p.(=)
UGT1A5 NM_019078.1 ?/. - c.-75710C>T - r.(?) p.(=)
UGT1A3 NM_019093.2 ?/. - c.-91845C>T - r.(?) p.(=)
UGT1A9 NM_021027.2 ?/. - c.-34653C>T - r.(?) p.(=)
UGT1A6 NM_205862.1 ?/. - c.-54546C>T - r.(?) p.(=)


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