Variant #0000297410 (NC_000010.10:g.73580002T>A, NM_022124.5:c.*4967T>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.73580002T>A
DNA change (hg38) g.71820245T>A
Published as PSAP(NM_001042465.3):c.1009A>T (p.T337S)
ISCN -
DB-ID PSAP_000013
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) 3.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.-100624A>T r.(?) p.(=) -
PSAP NM_002778.2 -?/. - c.1000A>T r.(?) p.(Thr334Ser) -
CDH23 NM_022124.5 -?/. - c.*4967T>A r.(=) p.(=) -
C10orf54 NM_022153.1 -?/. - c.-46806A>T r.(?) p.(=) -


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