Variant #0000688704 (NC_000002.11:g.234680925T>C, NM_000463.2:c.1322T>C (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.234680925T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID UGT1A1_000071
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) 9.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2020-09-15 15:50:26 +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.1322T>C - r.(?) p.(Met441Thr)
DNAJB3 NM_001001394.3 ?/. - c.-28363A>G - r.(?) p.(=)
UGT1A6 NM_001072.3 ?/. - c.1319T>C - r.(?) p.(Met440Thr)
UGT1A4 NM_007120.2 ?/. - c.1325T>C - r.(?) p.(Met442Thr)
UGT1A10 NM_019075.2 ?/. - c.1313T>C - r.(?) p.(Met438Thr)
UGT1A8 NM_019076.4 ?/. - c.1313T>C - r.(?) p.(Met438Thr)
UGT1A7 NM_019077.2 ?/. - c.1313T>C - r.(?) p.(Met438Thr)
UGT1A5 NM_019078.1 ?/. - c.1325T>C - r.(?) p.(Met442Thr)
UGT1A3 NM_019093.2 ?/. - c.1325T>C - r.(?) p.(Met442Thr)
UGT1A9 NM_021027.2 ?/. - c.1313T>C - r.(?) p.(Met438Thr)
UGT1A6 NM_205862.1 ?/. - c.518T>C - r.(?) p.(Met173Thr)
MROH2A XM_291007.11 ?/. - c.-3493T>C - r.(?) p.(=)


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