Variant #0000540670 (NC_000010.10:g.73453966C>T, NM_022124.5:c.2239C>T (CDH23))

Chromosome 10
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.73453966C>T
DNA change (hg38) g.71694209C>T
Published as CDH23(NM_022124.5):c.2239C>T (p.R747C)
ISCN -
DB-ID CDH23_000077 See all 2 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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
C10orf105 NM_001164375.2 ?/. - c.*21727G>A r.(=) p.(=) -
CDH23 NM_022124.5 ?/. - c.2239C>T r.(?) p.(Arg747Cys) -
C10orf54 NM_022153.1 ?/. - c.*57044G>A r.(=) p.(=) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.