Variant #0000690755 (NC_000010.10:g.73406294C>T, NM_022124.5:c.1369C>T (CDH23))

Chromosome 10
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.73406294C>T
DNA change (hg38) -
Published as CDH23(NM_022124.5):c.1369C>T (p.R457W)
ISCN -
DB-ID CDH23_000288 See all 2 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 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 2020-09-15 15:50:26 +02:00 (CEST)
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.*69399G>A r.(=) p.(=) -
CDH23 NM_022124.5 ?/. - c.1369C>T r.(?) p.(Arg457Trp) -
C10orf54 NM_022153.1 ?/. - c.*104716G>A r.(=) p.(=) -


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