Variant #0000950703 (NC_000016.9:g.68719119T>C, NM_001793.4:c.1436T>C (CDH3))

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.68719119T>C
DNA change (hg38) -
Published as CDH3(NM_001317195.1):c.1436T>C (p.L479P, p.(Leu479Pro)), CDH3(NM_001793.6):c.1436T>C (p.L479P)
ISCN -
DB-ID CDH3_000010 See all 4 reported entries
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) 0.0014 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-11-27 17:35:39 +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     
CDH3 NM_001793.4 -?/. - c.1436T>C r.(?) p.(Leu479Pro)


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