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Variant : CV55123 (NM_022124.5(CDH23):c.4953C>T (p.Asn1651=)) Homo sapiens

Symbol: CV55123
Name: NM_022124.5(CDH23):c.4953C>T (p.Asn1651=)
Condition: AllHighlyPenetrant [RCV000039192]|not specified [RCV000039192]
Clinical Significance: likely benign
Last Evaluated: 04/17/2012
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.4953C>T
NG_008835.1:g.385841C>T
NC_000010.11:g.71777787C>T
NC_000010.10:g.73537544C>T
NP_071407.4:p.Asn1651=
c.4953C>T
p.Asn1651Asn
Position
Human AssemblyChrPosition (strand)Source
GRCh381071,777,787 - 71,777,787CLINVAR
GRCh371073,537,544 - 73,537,544CLINVAR
Cytogenetic Map1010q22.1CLINVAR
Trait Synonyms: AllHighlyPenetrant



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 8608820
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.