Variant #0000998484 (NC_000010.10:g.73406232G>A, NM_022124.5:c.1307G>A (CDH23))

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.73406232G>A
DNA change (hg38) -
Published as CDH23(NM_022124.5):c.1307G>A (p.S436N), CDH23(NM_022124.6):c.1307G>A (p.S436N)
ISCN -
DB-ID CDH23_000234 See all 7 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) 0.00279 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
C10orf105 NM_001164375.2 -/. - c.*69461C>T r.(=) p.(=) -
CDH23 NM_022124.5 -/. - c.1307G>A r.(?) p.(Ser436Asn) -
C10orf54 NM_022153.1 -/. - c.*104778C>T r.(=) p.(=) -


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