Variant #0000861980 (NC_000010.10:g.73571307G>A, NM_022124.5:c.9238G>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.73571307G>A
DNA change (hg38) -
Published as CDH23(NM_001171933.1):c.2518G>A (p.(Ala840Thr)), CDH23(NM_022124.5):c.9238G>A (p.A3080T), CDH23(NM_022124.6):c.9238G>A (p.A3080T)
ISCN -
DB-ID CDH23_000231 See all 3 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) 0.00139 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +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.-91929C>T r.(?) p.(=) -
PSAP NM_002778.2 -?/. - c.*5891C>T r.(=) p.(=) -
CDH23 NM_022124.5 -?/. - c.9238G>A r.(?) p.(Ala3080Thr) -
C10orf54 NM_022153.1 -?/. - c.-38111C>T r.(?) p.(=) -


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