Variant #0000951098 (NC_000018.9:g.25568523_25568524insGT, NM_001792.3:c.1706_1707insCA (CDH2))

Chromosome 18
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.25568523_25568524insGT
DNA change (hg38) -
Published as CDH2(NM_001792.5):c.1706_1707insCA (p.N572Ifs*15)
ISCN -
DB-ID CDH2_000082
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDH2 NM_001792.3 ?/. - c.1706_1707insCA r.(?) p.(Asn572Ilefs*15)


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