Variant #0000799390 (NC_000001.10:g.45478808A>G, NM_000374.4:c.134A>G (UROD))

Chromosome 1
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.45478808A>G
DNA change (hg38) -
Published as UROD(NM_000374.5):c.134A>G (p.E45G)
ISCN -
DB-ID HECTD3_000011
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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UROD NM_000374.4 ?/. - c.134A>G r.(?) p.(Glu45Gly)
ZSWIM5 NM_020883.1 ?/. - c.*5318T>C r.(=) p.(=)
HECTD3 NM_024602.5 ?/. - c.-1879T>C r.(?) p.(=)


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