Variant #0001053587 (NC_000010.10:g.73550880G>A, NC_000010.10(NM_022124.5):c.6050-9G>A (CDH23))

Chromosome 10
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.73550880G>A
DNA change (hg38) -
Published as CDH23(NM_022124.5):c.6050-9G>A, CDH23(NM_022124.6):c.6050-9G>A
ISCN -
DB-ID CDH23_000007 See all 87 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) 5.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
C10orf105 NM_001164375.2 +/. - c.-71502C>T r.(?) p.(=) -
CDH23 NM_022124.5 +/. - c.6050-9G>A r.(=) p.(=) -
C10orf54 NM_022153.1 +/. - c.-17684C>T r.(?) p.(=) -


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