Variant #0000780197 (NC_000010.10:g.73466716G>A, NM_022124.5:c.3016G>A (CDH23))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.73466716G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID CDH23_000327 See all 10 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs745571683
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-05-04 15:14:01 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
CDH23 NM_022124.5 +?/. - c.3016G>A r.(?) p.(Glu1006Lys) -


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