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Variant : CV118051 (NC_000014.9:g.22148495C>A) Homo sapiens

Symbol: CV118051
Name: NC_000014.9:g.22148495C>A
Condition: Lung cancer [RCV000098571]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: TRA   TRAV27  
Variant Type: single nucleotide variant (SO:0001483)
Source: CLINVAR
Evidence: literature only|not provided
HGVS Name(s): NC_000014.9:g.22148495C>A
NC_000014.8:g.22616449C>A
Position
Human AssemblyChrPosition (strand)Source
GRCh381422,148,495 - 22,148,495CLINVAR
GRCh371422,616,449 - 22,616,449CLINVAR
Cytogenetic Map1414q11.2CLINVAR
Trait Synonyms: Lung cancer, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8583489
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2015-08-04
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.