Variant #0000961972 (NC_000002.11:g.234669048C>G, NM_000463.2:c.115C>G (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.234669048C>G
DNA change (hg38) -
Published as UGT1A1(NM_000463.3):c.115C>G (p.H39D)
ISCN -
DB-ID UGT1A1_000005 See all 8 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-02-26 20:06:56 +01:00 (CET)
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.115C>G - r.(?) p.(His39Asp)
DNAJB3 NM_001001394.3 +/. - c.-16486G>C - r.(?) p.(=)
UGT1A6 NM_001072.3 +/. - c.862-6632C>G - r.(=) p.(=)
UGT1A4 NM_007120.2 +/. - c.868-6632C>G - r.(=) p.(=)
UGT1A10 NM_019075.2 +/. - c.856-6632C>G - r.(=) p.(=)
UGT1A8 NM_019076.4 +/. - c.856-6632C>G - r.(=) p.(=)
UGT1A7 NM_019077.2 +/. - c.856-6632C>G - r.(=) p.(=)
UGT1A5 NM_019078.1 +/. - c.868-6632C>G - r.(=) p.(=)
UGT1A3 NM_019093.2 +/. - c.868-6632C>G - r.(=) p.(=)
UGT1A9 NM_021027.2 +/. - c.856-6632C>G - r.(=) p.(=)
UGT1A6 NM_205862.1 +/. - c.61-6632C>G - r.(=) p.(=)


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