Variant #0000979126 (NC_000010.10:g.73579217C>G, NM_022124.5:c.*4182C>G (CDH23))

Chromosome 10
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.73579217C>G
DNA change (hg38) -
Published as PSAP(NM_002778.4):c.1350+5G>C
ISCN -
DB-ID CDH23_001010
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
C10orf105 NM_001164375.2 ?/. - c.-99839G>C r.(?) p.(=) -
PSAP NM_002778.2 ?/. - c.1350+5G>C r.spl? p.? -
CDH23 NM_022124.5 ?/. - c.*4182C>G r.(=) p.(=) -
C10orf54 NM_022153.1 ?/. - c.-46021G>C r.(?) p.(=) -


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