Variant #0000678899 (NC_000010.10:g.73571179T>C, NM_022124.5:c.9185T>C (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.73571179T>C
DNA change (hg38) -
Published as CDH23(NM_022124.5):c.9185T>C (p.M3062T), CDH23(NM_022124.6):c.9185T>C (p.(Met3062Thr))
ISCN -
DB-ID CDH23_000822 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 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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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.-91801A>G r.(?) p.(=) -
PSAP NM_002778.2 ?/. - c.*6019A>G r.(=) p.(=) -
CDH23 NM_022124.5 ?/. - c.9185T>C r.(?) p.(Met3062Thr) -
C10orf54 NM_022153.1 ?/. - c.-37983A>G r.(?) p.(=) -


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