Variant #0001059769 (NC_000016.9:g.68771416_68771428dup, NC_000016.9(NM_004360.3):c.48+50_48+62dup (CDH1))

Chromosome 16
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.68771416_68771428dup
DNA change (hg38) -
Published as -
ISCN -
DB-ID CDH1_000174
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1962430034
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-11-20 18:46:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDH1 NM_004360.3 -?/. - c.48+50_48+62dup r.(?) p.(?)


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