Variant #0000719905 (NC_000004.11:g.39205292C>G, WDR19(NM_025132.3):c.553C>G)

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.39205292C>G
DNA change (hg38) -
Published as WDR19(NM_025132.3):c.553C>G (p.Q185E), WDR19(NM_025132.4):c.553C>G (p.Q185E)
ISCN -
DB-ID WDR19_000074 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) 0 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WDR19 NM_025132.3 -?/. - c.553C>G r.(?) p.(Gln185Glu)