Variant #0000543814 (NC_000011.9:g.32451994_32451995insGG, NC_000011.9(NM_024426.4):c.647-1829_647-1828insCC (WT1))

Chromosome 11
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.32451994_32451995insGG
DNA change (hg38) g.32430448_32430449insGG
Published as WT1(NM_024426.3):c.647-1829_647-1828insCC
ISCN -
DB-ID WT1_000157
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 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     
WT1 NM_024426.4 -/. - c.647-1829_647-1828insCC r.(=) p.(=)


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