Variant #0000622421 (NC_000010.10:g.73571731C>T, NM_022124.5:c.9339C>T (CDH23))

Chromosome 10
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.73571731C>T
DNA change (hg38) g.71811974C>T
Published as CDH23(NM_022124.5):c.9339C>T (p.D3113=)
ISCN -
DB-ID CDH23_000799
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) 1.0E-5 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-06-27 16:50:11 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
C10orf105 NM_001164375.2 -?/. - c.-92353G>A r.(?) p.(=) -
PSAP NM_002778.2 -?/. - c.*5467G>A r.(=) p.(=) -
CDH23 NM_022124.5 -?/. - c.9339C>T r.(?) p.(Asp3113=) -
C10orf54 NM_022153.1 -?/. - c.-38535G>A r.(?) p.(=) -


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