Variant : CV119131 (NM_002499.3(NEO1):c.1292-13787C>T) Homo sapiens

Symbol: CV119131
Name: NM_002499.3(NEO1):c.1292-13787C>T
Condition: Lung cancer [RCV000099651]
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.1292-13787C>T
NG_016965.1:g.175077C>T
NC_000015.10:g.73222560C>T
NC_000015.9:g.73514901C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh381573,222,560 - 73,222,560CLINVAR
GRCh371573,514,901 - 73,514,901CLINVAR
Cytogenetic Map1515q24.1CLINVAR
Trait Synonyms: Lung cancer, somatic



References - curated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 8584557
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.