Variant #0000540775 (NC_000010.10:g.73570333C>T, NC_000010.10(NM_022124.5):c.9077+7C>T (CDH23))

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.73570333C>T
DNA change (hg38) g.71810576C>T
Published as CDH23(NM_022124.5):c.9077+7C>T, CDH23(NM_022124.6):c.9077+7C>T
ISCN -
DB-ID CDH23_000571 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) 0.00148 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +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.-90955G>A r.(?) p.(=) -
CDH23 NM_022124.5 -/. - c.9077+7C>T r.(=) p.(=) -
C10orf54 NM_022153.1 -/. - c.-37137G>A r.(?) p.(=) -


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