Variant #0000622422 (NC_000010.10:g.73572354dup, NM_022124.5:c.9498dup (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.73572354dup
DNA change (hg38) g.71812597dup
Published as CDH23(NM_022124.5):c.9498dupC (p.T3167Hfs*10)
ISCN -
DB-ID CDH23_000800
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) Retrieve
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 16:52:46 +02:00 (CEST)
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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.-92973dup r.(?) p.(=) -
PSAP NM_002778.2 +/. - c.*4847dup r.(?) p.(=) -
CDH23 NM_022124.5 +/. - c.9498dup r.(?) p.(Thr3167HisfsTer10) -
C10orf54 NM_022153.1 +/. - c.-39155dup r.(?) p.(=) -


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