Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV121623 (NM_017416.1(IL1RAPL2):c.82+189344T>C) Homo sapiens

Symbol: CV121623
Name: NM_017416.1(IL1RAPL2):c.82+189344T>C
Condition: Lung cancer [RCV000102143]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: IL1RAPL2  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron|intron variant
Evidence: literature only|not provided
HGVS Name(s): NM_017416.1:c.82+189344T>C
NG_012566.2:g.287025T>C
NC_000023.11:g.104848340T>C
NC_000023.10:g.104093020T>C
Position
Human AssemblyChrPosition (strand)Source
GRCh38X104,848,340 - 104,848,340CLINVAR
GRCh37X104,093,020 - 104,093,020CLINVAR
Cytogenetic MapXXq22.3CLINVAR
Trait Synonyms: Lung cancer, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8586997
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2015-08-04
Status: ACTIVE



NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.