Variant #0000654049 (NC_000001.10:g.45479447G>A, NM_000374.4:c.458G>A (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.45479447G>A
DNA change (hg38) g.45013775G>A
Published as UROD(NM_000374.5):c.458G>A (p.G153D)
ISCN -
DB-ID HECTD3_000008
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 2020-03-23 16:13:27 +01:00 (CET)
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.458G>A r.(?) p.(Gly153Asp)
ZSWIM5 NM_020883.1 ?/. - c.*4679C>T r.(=) p.(=)
HECTD3 NM_024602.5 ?/. - c.-2518C>T r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.