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Variant : CV27637 (PDGFB, 135-BP DEL, IVS5) Homo sapiens

Symbol: CV27637
Name: PDGFB, 135-BP DEL, IVS5
Condition: Meningioma [RCV000013429]
Clinical Significance: pathogenic
Last Evaluated: 10/25/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: PDGFB  
Variant Type: deletion (SO:0000159)
Source: CLINVAR
Nucleotide Change: 135-bp del, ivs5
Evidence: literature only
Position
Human AssemblyChrPosition (strand)Source
Cytogenetic Map2222q12.3-q13.1CLINVAR
Trait Synonyms: Meligioma; Mengioma; Mengiomia; Menigiom; Menigioma; Meningioma, somatic



Disease Annotations
References - curated
References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 8563221
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2020-10-20
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.