Variant #0000622423 (NC_000010.10:g.73579291G>A, NM_022124.5:c.*4256G>A (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.73579291G>A
DNA change (hg38) g.71819534G>A
Published as PSAP(NM_001042465.2):c.1290C>T (p.S430=)
ISCN -
DB-ID CDH23_000802
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) 0.00041 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-06-27 17:00:27 +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.-99913C>T r.(?) p.(=) -
PSAP NM_002778.2 -?/. - c.1281C>T r.(?) p.(Ser427=) -
CDH23 NM_022124.5 -?/. - c.*4256G>A r.(=) p.(=) -
C10orf54 NM_022153.1 -?/. - c.-46095C>T r.(?) p.(=) -


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