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Variant : CV55188 (NM_022124.5(CDH23):c.6968delC (p.Pro2323Leufs)) Homo sapiens

Symbol: CV55188
Name: NM_022124.5(CDH23):c.6968delC (p.Pro2323Leufs)
Condition: Retinitis pigmentosa-deafness syndrome [RCV000039259]|Usher syndrome, type 1D [RCV000039259]|Usher syndrome, type 1D [RCV000150314]
Clinical Significance: pathogenic
Last Evaluated: 01/07/2013
Review Status: classified by single submitter|criteria provided, single submitter
Related Genes: CDH23  
Variant Type: deletion (SO:0001589)
Source: CLINVAR
Molecular Consequence: frameshift variant
Evidence: clinical testing
HGVS Name(s): NM_022124.5:c.6968delC
NC_000010.11:g.71798492delC
NC_000010.10:g.73558249delC
NP_071407.4:p.Pro2323Leufs
c.6968delC
p.Pro2323fs
Position
Human AssemblyChrPosition (strand)Source
GRCh381071,798,492 - 71,798,492CLINVAR
GRCh371073,558,249 - 73,558,249CLINVAR
Cytogenetic Map1010q22.1CLINVAR
Trait Synonyms: USHER SYNDROME, TYPE ID
Age Of Onset: neonatal/infancy
Prevalence: 1-9 / 100 000



Disease Annotations
References - curated
References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 8608885
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2019-07-09
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.