Variant #0000505673 (NC_000001.10:g.22447646_22447647dup, NC_000001.10(NM_030761.4):c.588+57_588+58dup (WNT4))

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.22447646_22447647dup
DNA change (hg38) g.22121153_22121154dup
Published as WNT4(NM_030761.5):c.588+57_588+58dupCA
ISCN -
DB-ID WNT4_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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
WNT4 NM_030761.4 -/. - c.588+57_588+58dup r.(=) p.(=)


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