Variant #0000319336 (NC_000001.10:g.45479772G>T, NC_000001.10(NM_000374.4):c.636+30G>T (UROD))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.45479772G>T
DNA change (hg38) g.45014100G>T
Published as UROD(NM_000374.5):c.636+30G>T
ISCN -
DB-ID UROD_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) 0.26325 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.636+30G>T r.(=) p.(=)
ZSWIM5 NM_020883.1 -/. - c.*4354C>A r.(=) p.(=)
HECTD3 NM_024602.5 -/. - c.-2843C>A r.(?) p.(=)


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