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Variant : CV119132 (NM_002499.3(NEO1):c.2494+1282C>A) Homo sapiens

Symbol: CV119132
Name: NM_002499.3(NEO1):c.2494+1282C>A
Condition: Lung cancer [RCV000099652]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: NEO1  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron|intron variant
Evidence: literature only|not provided
HGVS Name(s): NM_002499.3:c.2494+1282C>A
NG_016965.1:g.220210C>A
NC_000015.10:g.73267693C>A
NC_000015.9:g.73560034C>A
Position
Human AssemblyChrPosition (strand)Source
GRCh381573,267,693 - 73,267,693CLINVAR
GRCh371573,560,034 - 73,560,034CLINVAR
Cytogenetic Map1515q24.1CLINVAR
Trait Synonyms: Lung cancer, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8584558
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.