Variant #0000975095 (NC_000002.11:g.234669329_234669334del, NM_000463.2:c.396_401del (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.234669329_234669334del
DNA change (hg38) -
Published as UGT1A1(NM_000463.3):c.396_401del (p.(His132_Lys134delinsGln))
ISCN -
DB-ID UGT1A1_000150 See all 2 reported entries
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:20:39 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
UGT1A1 NM_000463.2 ?/. - c.396_401del - r.(?) p.(His132_Lys134delinsGln)
DNAJB3 NM_001001394.3 ?/. - c.-16771_-16766del - r.(?) p.(=)
UGT1A6 NM_001072.3 ?/. - c.862-6351_862-6346del - r.(=) p.(=)
UGT1A4 NM_007120.2 ?/. - c.868-6351_868-6346del - r.(=) p.(=)
UGT1A10 NM_019075.2 ?/. - c.856-6351_856-6346del - r.(=) p.(=)
UGT1A8 NM_019076.4 ?/. - c.856-6351_856-6346del - r.(=) p.(=)
UGT1A7 NM_019077.2 ?/. - c.856-6351_856-6346del - r.(=) p.(=)
UGT1A5 NM_019078.1 ?/. - c.868-6351_868-6346del - r.(=) p.(=)
UGT1A3 NM_019093.2 ?/. - c.868-6351_868-6346del - r.(=) p.(=)
UGT1A9 NM_021027.2 ?/. - c.856-6351_856-6346del - r.(=) p.(=)
UGT1A6 NM_205862.1 ?/. - c.61-6351_61-6346del - r.(=) p.(=)


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