Variant #0001013689 (NC_000002.11:g.234680952G>A, NM_000463.2:c.1349G>A (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.234680952G>A
DNA change (hg38) -
Published as UGT1A4(NM_007120.3):c.1352G>A (p.R451H)
ISCN -
DB-ID UGT1A1_000193
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) 5.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-10-29 20:49:11 +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.1349G>A - r.(?) p.(Arg450His)
DNAJB3 NM_001001394.3 ?/. - c.-28390C>T - r.(?) p.(=)
UGT1A6 NM_001072.3 ?/. - c.1346G>A - r.(?) p.(Arg449His)
UGT1A4 NM_007120.2 ?/. - c.1352G>A - r.(?) p.(Arg451His)
UGT1A10 NM_019075.2 ?/. - c.1340G>A - r.(?) p.(Arg447His)
UGT1A8 NM_019076.4 ?/. - c.1340G>A - r.(?) p.(Arg447His)
UGT1A7 NM_019077.2 ?/. - c.1340G>A - r.(?) p.(Arg447His)
UGT1A5 NM_019078.1 ?/. - c.1352G>A - r.(?) p.(Arg451His)
UGT1A3 NM_019093.2 ?/. - c.1352G>A - r.(?) p.(Arg451His)
UGT1A9 NM_021027.2 ?/. - c.1340G>A - r.(?) p.(Arg447His)
UGT1A6 NM_205862.1 ?/. - c.545G>A - r.(?) p.(Arg182His)
MROH2A XM_291007.11 ?/. - c.-3466G>A - r.(?) p.(=)


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