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Variant : CV430627 (NM_178151.2(DCX):c.809-3C>T) Homo sapiens

Symbol: CV430627
Name: NM_178151.2(DCX):c.809-3C>T
Condition: not specified [RCV000500261]
Clinical Significance: uncertain significance
Last Evaluated: 04/03/2017
Review Status: criteria provided, single submitter
Related Genes: DCX  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron variant
Evidence: clinical testing
HGVS Name(s): NM_178151.2:c.809-3C>T
NM_178152.2:c.809-3C>T
NG_011750.1:g.86135C>T
NC_000023.11:g.111331044G>A
NC_000023.10:g.110574272G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh38X111,331,044 - 111,331,044CLINVAR
GRCh37X110,574,272 - 110,574,272CLINVAR
Cytogenetic MapXXq23CLINVAR
Trait Synonyms: AllHighlyPenetrant



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13213639
Created: 2017-09-12
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.