Variant #0000913318 (NC_000010.10:g.73578882T>C, NM_022124.5:c.*3847T>C (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.73578882T>C
DNA change (hg38) -
Published as PSAP(NM_001042465.3):c.1360-14A>G
ISCN -
DB-ID CDH23_000978
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) 0.34012 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-01-11 15:44:22 +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.-99504A>G r.(?) p.(=) -
PSAP NM_002778.2 -/. - c.1351-14A>G r.(=) p.(=) -
CDH23 NM_022124.5 -/. - c.*3847T>C r.(=) p.(=) -
C10orf54 NM_022153.1 -/. - c.-45686A>G r.(?) p.(=) -


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