Variant #0000515164 (NC_000002.11:g.234676505_234676508dup, NM_000463.2:c.1007_1010dup (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.234676505_234676508dup
DNA change (hg38) g.233767859_233767862dup
Published as UGT1A1(NM_000463.2):c.1007_1010dupGGTA (p.Y337*)
ISCN -
DB-ID UGT1A1_000061
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.1007_1010dup - r.(?) p.(Tyr337Ter)
DNAJB3 NM_001001394.3 +/. - c.-23946_-23943dup - r.(?) p.(=)
UGT1A6 NM_001072.3 +/. - c.1004_1007dup - r.(?) p.(Tyr336Ter)
UGT1A4 NM_007120.2 +/. - c.1010_1013dup - r.(?) p.(Tyr338Ter)
UGT1A10 NM_019075.2 +/. - c.998_1001dup - r.(?) p.(Tyr334Ter)
UGT1A8 NM_019076.4 +/. - c.998_1001dup - r.(?) p.(Tyr334Ter)
UGT1A7 NM_019077.2 +/. - c.998_1001dup - r.(?) p.(Tyr334Ter)
UGT1A5 NM_019078.1 +/. - c.1010_1013dup - r.(?) p.(Tyr338Ter)
UGT1A3 NM_019093.2 +/. - c.1010_1013dup - r.(?) p.(Tyr338Ter)
UGT1A9 NM_021027.2 +/. - c.998_1001dup - r.(?) p.(Tyr334Ter)
UGT1A6 NM_205862.1 +/. - c.203_206dup - r.(?) p.(Tyr69Ter)


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