Variant #0000861979 (NC_000010.10:g.73570263C>G, NM_022124.5:c.9014C>G (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.73570263C>G
DNA change (hg38) -
Published as CDH23(NM_001171933.1):c.2294C>G (p.(Ala765Gly)), CDH23(NM_022124.5):c.9014C>G (p.A3005G), CDH23(NM_022124.6):c.9014C>G (p.A3005G)
ISCN -
DB-ID CDH23_000567 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) 0.00131 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +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.-90885G>C r.(?) p.(=) -
CDH23 NM_022124.5 -?/. - c.9014C>G r.(?) p.(Ala3005Gly) -
C10orf54 NM_022153.1 -?/. - c.-37067G>C r.(?) p.(=) -


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