Variant #0000248855 (NC_000010.10:g.73492079A>G, NM_022124.5:c.4051A>G (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.73492079A>G
DNA change (hg38) g.71732322A>G
Published as C10orf105(NM_001168390.2):c.-6+5406T>C, CDH23(NM_022124.6):c.4051A>G (p.N1351D)
ISCN -
DB-ID CDH23_000031 See all 30 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) 0.8059 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.-12701T>C r.(?) p.(=) -
CDH23 NM_022124.5 -/. - c.4051A>G r.(?) p.(Asn1351Asp) -
C10orf54 NM_022153.1 -/. - c.*18931T>C r.(=) p.(=) -


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