Variant #0000319337 (NC_000001.10:g.45480170del, NM_000374.4:c.696del (UROD))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.45480170del
DNA change (hg38) g.45014498del
Published as UROD(NM_000374.5):c.696delT (p.F232Lfs*13)
ISCN -
DB-ID UROD_000009
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UROD NM_000374.4 +/. - c.696del r.(?) p.(Phe232LeufsTer13)
ZSWIM5 NM_020883.1 +/. - c.*3958del r.(?) p.(=)
HECTD3 NM_024602.5 +/. - c.-3239del r.(?) p.(=)


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