Variant #0000656542 (NC_000010.10:g.73570263C>T, NM_022124.5:c.9014C>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.73570263C>T
DNA change (hg38) g.71810506C>T
Published as CDH23(NM_001171933.1):c.2294C>T (p.(Ala765Val))
ISCN -
DB-ID CDH23_000270 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) 1.0E-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 2020-03-23 16:13:27 +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.-90885G>A r.(?) p.(=) -
CDH23 NM_022124.5 ?/. - c.9014C>T r.(?) p.(Ala3005Val) -
C10orf54 NM_022153.1 ?/. - c.-37067G>A r.(?) p.(=) -


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