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Variant : CV118966 (NM_018145.2(RMDN3):c.525-9C>T) Homo sapiens

Symbol: CV118966
Name: NM_018145.2(RMDN3):c.525-9C>T
Condition: Lung cancer [RCV000099486]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: RMDN3  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron|intron variant
Evidence: literature only|not provided
HGVS Name(s): NC_000015.10:g.40745268G>A
NC_000015.9:g.41037466G>A
NM_018145.2:c.525-9C>T
NM_018145.1:c.525-9C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh381540,745,268 - 40,745,268CLINVAR
GRCh371541,037,466 - 41,037,466CLINVAR
Cytogenetic Map1515q15.1CLINVAR
Trait Synonyms: Lung cancer, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8584393
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.