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Variant : CV117371 (NR_047500.1(LINC00571):n.313-10607G>C) Homo sapiens

Symbol: CV117371
Name: NR_047500.1(LINC00571):n.313-10607G>C
Condition: Lung cancer [RCV000097892]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LINC00571  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron|intron variant
Evidence: literature only|not provided
HGVS Name(s): NC_000013.11:g.38072841C>G
NC_000013.10:g.38646978C>G
NR_047500.1:n.313-10607G>C
Position
Human AssemblyChrPosition (strand)Source
GRCh381338,072,841 - 38,072,841CLINVAR
GRCh371338,646,978 - 38,646,978CLINVAR
Cytogenetic Map1313q13.3CLINVAR
Trait Synonyms: Lung cancer, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8582815
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.