Variant #0000321604 (NC_000010.10:g.73573037C>T, NM_022124.5:c.9670C>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.73573037C>T
DNA change (hg38) g.71813280C>T
Published as CDH23(NM_001171933.1):c.2950C>T (p.(Arg984Trp)), CDH23(NM_022124.5):c.9670C>T (p.R3224W)
ISCN -
DB-ID CDH23_000583 See all 3 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) 0.00084 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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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.-93659G>A r.(?) p.(=) -
PSAP NM_002778.2 ?/. - c.*4161G>A r.(=) p.(=) -
CDH23 NM_022124.5 ?/. - c.9670C>T r.(?) p.(Arg3224Trp) -
C10orf54 NM_022153.1 ?/. - c.-39841G>A r.(?) p.(=) -


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