Variant #0000620990 (NC_000002.11:g.234680946A>G, NM_000463.2:c.1343A>G (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.234680946A>G
DNA change (hg38) g.233772300A>G
Published as UGT1A1(NM_000463.2):c.1343A>G (p.K448R)
ISCN -
DB-ID UGT1A1_000062
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 2019-12-06 12:43:26 +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.1343A>G - r.(?) p.(Lys448Arg)
DNAJB3 NM_001001394.3 -?/. - c.-28384T>C - r.(?) p.(=)
UGT1A6 NM_001072.3 -?/. - c.1340A>G - r.(?) p.(Lys447Arg)
UGT1A4 NM_007120.2 -?/. - c.1346A>G - r.(?) p.(Lys449Arg)
UGT1A10 NM_019075.2 -?/. - c.1334A>G - r.(?) p.(Lys445Arg)
UGT1A8 NM_019076.4 -?/. - c.1334A>G - r.(?) p.(Lys445Arg)
UGT1A7 NM_019077.2 -?/. - c.1334A>G - r.(?) p.(Lys445Arg)
UGT1A5 NM_019078.1 -?/. - c.1346A>G - r.(?) p.(Lys449Arg)
UGT1A3 NM_019093.2 -?/. - c.1346A>G - r.(?) p.(Lys449Arg)
UGT1A9 NM_021027.2 -?/. - c.1334A>G - r.(?) p.(Lys445Arg)
UGT1A6 NM_205862.1 -?/. - c.539A>G - r.(?) p.(Lys180Arg)
MROH2A XM_291007.11 -?/. - c.-3472A>G - r.(?) p.(=)


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