Variant #0000319253 (NC_000002.11:g.234676504C>T, NM_000463.2:c.1006C>T (UGT1A1))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.234676504C>T
DNA change (hg38) g.233767858C>T
Published as UGT1A1(NM_000463.2):c.1006C>T (p.R336W)
ISCN -
DB-ID UGT1A1_000034 See all 7 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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
UGT1A1 NM_000463.2 +/. - c.1006C>T - r.(?) p.(Arg336Trp)
DNAJB3 NM_001001394.3 +/. - c.-23942G>A - r.(?) p.(=)
UGT1A6 NM_001072.3 +/. - c.1003C>T - r.(?) p.(Arg335Trp)
UGT1A4 NM_007120.2 +/. - c.1009C>T - r.(?) p.(Arg337Trp)
UGT1A10 NM_019075.2 +/. - c.997C>T - r.(?) p.(Arg333Trp)
UGT1A8 NM_019076.4 +/. - c.997C>T - r.(?) p.(Arg333Trp)
UGT1A7 NM_019077.2 +/. - c.997C>T - r.(?) p.(Arg333Trp)
UGT1A5 NM_019078.1 +/. - c.1009C>T - r.(?) p.(Arg337Trp)
UGT1A3 NM_019093.2 +/. - c.1009C>T - r.(?) p.(Arg337Trp)
UGT1A9 NM_021027.2 +/. - c.997C>T - r.(?) p.(Arg333Trp)
UGT1A6 NM_205862.1 +/. - c.202C>T - r.(?) p.(Arg68Trp)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.