Variant #0000507636 (NC_000001.10:g.45480232T>A, NM_000374.4:c.758T>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.45480232T>A
DNA change (hg38) g.45014560T>A
Published as UROD(NM_000374.5):c.758T>A (p.L253Q)
ISCN -
DB-ID HECTD3_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) 0.00592 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-06 12:43:26 +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.758T>A r.(?) p.(Leu253Gln)
ZSWIM5 NM_020883.1 ?/. - c.*3894A>T r.(=) p.(=)
HECTD3 NM_024602.5 ?/. - c.-3303A>T r.(?) p.(=)


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