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Variant : CV117231 (NR_120392.1(LINC00403):n.84+14312G>T) Homo sapiens

Symbol: CV117231
Name: NR_120392.1(LINC00403):n.84+14312G>T
Condition: Lung cancer [RCV000097752]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: SOX1-OT  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron variant
Evidence: literature only|not provided
HGVS Name(s): NC_000013.11:g.111986705G>T
NC_000013.10:g.112641019G>T
NR_120392.1:n.84+14312G>T
Position
Human AssemblyChrPosition (strand)Source
GRCh3813111,986,705 - 111,986,705CLINVAR
GRCh3713112,641,019 - 112,641,019CLINVAR
Cytogenetic Map1313q34CLINVAR
Trait Synonyms: Lung cancer, somatic




Additional Information

 
CRRD Object Information
CRRD ID: 8582678
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.