Variant #0000312939 (NC_000002.11:g.234676903T>C, NM_000463.2:c.1122T>C (UGT1A1))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.234676903T>C
DNA change (hg38) g.233768257T>C
Published as UGT1A1(NM_000463.3):c.1122T>C (p.G374=)
ISCN -
DB-ID UGT1A1_000037
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) 0.00099 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 2018-01-15 20:58:59 +01:00 (CET)
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.1122T>C - r.(?) p.(Gly374=)
DNAJB3 NM_001001394.3 -?/. - c.-24341A>G - r.(?) p.(=)
UGT1A6 NM_001072.3 -?/. - c.1119T>C - r.(?) p.(Gly373=)
UGT1A4 NM_007120.2 -?/. - c.1125T>C - r.(?) p.(Gly375=)
UGT1A10 NM_019075.2 -?/. - c.1113T>C - r.(?) p.(Gly371=)
UGT1A8 NM_019076.4 -?/. - c.1113T>C - r.(?) p.(Gly371=)
UGT1A7 NM_019077.2 -?/. - c.1113T>C - r.(?) p.(Gly371=)
UGT1A5 NM_019078.1 -?/. - c.1125T>C - r.(?) p.(Gly375=)
UGT1A3 NM_019093.2 -?/. - c.1125T>C - r.(?) p.(Gly375=)
UGT1A9 NM_021027.2 -?/. - c.1113T>C - r.(?) p.(Gly371=)
UGT1A6 NM_205862.1 -?/. - c.318T>C - r.(?) p.(Gly106=)


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