Variant #0000612625 (NC_000010.10:g.73572093C>A, NC_000010.10(NM_022124.5):c.9381-144C>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.73572093C>A
DNA change (hg38) g.71812336C>A
Published as CDH23(NM_001171935.1):c.45C>A (p.T15=)
ISCN -
DB-ID CDH23_000768 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) 0.00032 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 2019-12-04 15:24:38 +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.-92715G>T r.(?) p.(=) -
PSAP NM_002778.2 -?/. - c.*5105G>T r.(=) p.(=) -
CDH23 NM_022124.5 -?/. - c.9381-144C>A r.(=) p.(=) -
C10orf54 NM_022153.1 -?/. - c.-38897G>T r.(?) p.(=) -


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