Variant #0000609362 (NC_000005.9:g.11111142_11111143del, NM_001332.2:c.2296_2297del (CTNND2))

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.11111142_11111143del
DNA change (hg38) g.11111030_11111031del
Published as CTNND2(NM_001332.4):c.2296_2297delTG (p.C766Hfs*38)
ISCN -
DB-ID CTNND2_000029
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +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     
CTNND2 NM_001332.2 +/. - c.2296_2297del r.(?) p.(Cys766HisfsTer38)


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