Variant #0000515163 (NC_000002.11:g.234676395_234676396insGT, NC_000002.11(NM_000463.2):c.997-100_997-99insGT (UGT1A1))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.234676395_234676396insGT
DNA change (hg38) g.233767749_233767750insGT
Published as UGT1A1(NM_000463.2):c.997-100_997-99insGT
ISCN -
DB-ID UGT1A1_000060
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.997-100_997-99insGT - r.(=) p.(=)
DNAJB3 NM_001001394.3 -/. - c.-23834_-23833insAC - r.(?) p.(=)
UGT1A6 NM_001072.3 -/. - c.994-100_994-99insGT - r.(=) p.(=)
UGT1A4 NM_007120.2 -/. - c.1000-100_1000-99insGT - r.(=) p.(=)
UGT1A10 NM_019075.2 -/. - c.988-100_988-99insGT - r.(=) p.(=)
UGT1A8 NM_019076.4 -/. - c.988-100_988-99insGT - r.(=) p.(=)
UGT1A7 NM_019077.2 -/. - c.988-100_988-99insGT - r.(=) p.(=)
UGT1A5 NM_019078.1 -/. - c.1000-100_1000-99insGT - r.(=) p.(=)
UGT1A3 NM_019093.2 -/. - c.1000-100_1000-99insGT - r.(=) p.(=)
UGT1A9 NM_021027.2 -/. - c.988-100_988-99insGT - r.(=) p.(=)
UGT1A6 NM_205862.1 -/. - c.193-100_193-99insGT - r.(=) p.(=)


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