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Variant : CV121629 (NM_017416.1(IL1RAPL2):c.697+51327C>T) Homo sapiens

Symbol: CV121629
Name: NM_017416.1(IL1RAPL2):c.697+51327C>T
Condition: Lung cancer [RCV000102149]
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.697+51327C>T
NG_012566.2:g.757554C>T
NC_000023.11:g.105318866C>T
NC_000023.10:g.104563551C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh38X105,318,866 - 105,318,866CLINVAR
GRCh37X104,563,551 - 104,563,551CLINVAR
Cytogenetic MapXXq22.3CLINVAR
Trait Synonyms: Lung cancer, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8587003
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.