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Variant : CV169858 (NM_178151.2(DCX):c.740_742del (p.Asp247del)) Homo sapiens

Symbol: CV169858
Name: NM_178151.2(DCX):c.740_742del (p.Asp247del)
Condition: Heterotopia [RCV000145886]
Clinical Significance: pathogenic
Last Evaluated: 02/08/2013
Review Status: classified by single submitter|criteria provided, single submitter
Related Genes: DCX  
Variant Type: deletion (SO:0000159)
Source: CLINVAR
Molecular Consequence: inframe_variant
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.111333117_111333119delCAT
NC_000023.10:g.110576345_110576347delCAT
NP_835365.1:p.Asp247del
NP_835364.1:p.Asp247del
NM_178151.2:c.740_742del
Position
Human AssemblyChrPosition (strand)Source
GRCh38X111,333,117 - 111,333,119CLINVAR
GRCh37X110,576,345 - 110,576,347CLINVAR
Cytogenetic MapXXq23CLINVAR
Trait Synonyms: Abnormality of neuronal migration; Heterotopias



References - curated
References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9682409
Created: 2014-12-09
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.