Variant #0000319331 (NC_000001.10:g.45478988G>T, NM_000374.4:c.238G>T (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.45478988G>T
DNA change (hg38) g.45013316G>T
Published as UROD(NM_000374.5):c.238G>T (p.A80S)
ISCN -
DB-ID UROD_000002 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) 1.0E-5 View details
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UROD NM_000374.4 +/. - c.238G>T r.(?) p.(Ala80Ser)
ZSWIM5 NM_020883.1 +/. - c.*5138C>A r.(=) p.(=)
HECTD3 NM_024602.5 +/. - c.-2059C>A r.(?) p.(=)


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