Variant #0000949434 (NC_000010.10:g.73574873C>T, NM_022124.5:c.9903C>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.73574873C>T
DNA change (hg38) -
Published as CDH23(NM_022124.5):c.9903C>T (p.P3301=), CDH23(NM_022124.6):c.9903C>T (p.P3301=)
ISCN -
DB-ID CDH23_000179 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) 0.00179 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-11-27 17:35:39 +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.-95495G>A r.(?) p.(=) -
PSAP NM_002778.2 -?/. - c.*2325G>A r.(=) p.(=) -
CDH23 NM_022124.5 -?/. - c.9903C>T r.(?) p.(Pro3301=) -
C10orf54 NM_022153.1 -?/. - c.-41677G>A r.(?) p.(=) -


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