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Variant : CV55214 (NM_022124.5(CDH23):c.8499C>T (p.Arg2833=)) Homo sapiens

Symbol: CV55214
Name: NM_022124.5(CDH23):c.8499C>T (p.Arg2833=)
Condition: AllHighlyPenetrant [RCV000039285]|not specified [RCV000039285]
Clinical Significance: likely benign
Last Evaluated: 01/09/2013
Review Status: classified by single submitter|criteria provided, single submitter
Related Genes: CDH23  
Variant Type: single nucleotide variant (SO:0001819)
Source: CLINVAR
Molecular Consequence: synonymous variant
Evidence: clinical testing
HGVS Name(s): NM_022124.5:c.8499C>T
NG_008835.1:g.415760C>T
NC_000010.11:g.71807706C>T
NC_000010.10:g.73567463C>T
NP_071407.4:p.Arg2833=
c.8499C>T
p.Arg2833Arg
Position
Human AssemblyChrPosition (strand)Source
GRCh381071,807,706 - 71,807,706CLINVAR
GRCh371073,567,463 - 73,567,463CLINVAR
Cytogenetic Map1010q22.1CLINVAR
Trait Synonyms: AllHighlyPenetrant



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 8608911
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2019-07-16
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.