Variant #0000540771 (NC_000010.10:g.73569662C>T, NM_022124.5:c.8808C>T (CDH23))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.73569662C>T
DNA change (hg38) g.71809905C>T
Published as CDH23(NM_022124.5):c.8808C>T (p.D2936=)
ISCN -
DB-ID CDH23_000758
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) 0.00061 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-27 16:43:10 +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.-90284G>A r.(?) p.(=) -
CDH23 NM_022124.5 -?/. - c.8808C>T r.(?) p.(Asp2936=) -
C10orf54 NM_022153.1 -?/. - c.-36466G>A r.(?) p.(=) -


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