Variant #0000558805 (NC_000016.9:g.68714912G>T, NM_001793.4:c.909G>T (CDH3))

Chromosome 16
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.68714912G>T
DNA change (hg38) g.68681009G>T
Published as CDH3(NM_001793.4):c.909G>T (p.(Met303Ile)), CDH3(NM_001793.5):c.909G>T (p.M303I), CDH3(NM_001793.6):c.909G>T (p.M303I)
ISCN -
DB-ID CDH3_000028 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) 0.00107 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDH3 NM_001793.4 ?/. - c.909G>T r.(?) p.(Met303Ile)


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