Variant #0000319335 (NC_000001.10:g.45479660C>T, NM_000374.4:c.554C>T (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.45479660C>T
DNA change (hg38) g.45013988C>T
Published as UROD(NM_000374.5):c.554C>T (p.P185L)
ISCN -
DB-ID UROD_000006
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 2020-03-23 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.554C>T r.(?) p.(Pro185Leu)
ZSWIM5 NM_020883.1 ?/. - c.*4466G>A r.(=) p.(=)
HECTD3 NM_024602.5 ?/. - c.-2731G>A r.(?) p.(=)


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