Variant #0000319332 (NC_000001.10:g.45479388_45479390delinsCCA, NM_000374.4:c.399_401delinsCCA (UROD))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.45479388_45479390delinsCCA
DNA change (hg38) g.45013716_45013718delinsCCA
Published as UROD(NM_000374.5):c.399_401delTGTinsCCA (p.V134Q)
ISCN -
DB-ID UROD_000004 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) 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.399_401delinsCCA r.(?) p.(Val134Gln)
ZSWIM5 NM_020883.1 +?/. - c.*4736_*4738delinsTGG r.(=) p.(=)
HECTD3 NM_024602.5 +?/. - c.-2461_-2459delinsTGG r.(?) p.(=)


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