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Variant : CV121621 (NM_017416.1(IL1RAPL2):c.-20+1221C>A) Homo sapiens

Symbol: CV121621
Name: NM_017416.1(IL1RAPL2):c.-20+1221C>A
Condition: Lung cancer [RCV000102141]
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.-20+1221C>A
NG_012566.2:g.6958C>A
NC_000023.11:g.104568272C>A
NC_000023.10:g.103812953C>A
Position
Human AssemblyChrPosition (strand)Source
GRCh38X104,568,272 - 104,568,272CLINVAR
GRCh37X103,812,953 - 103,812,953CLINVAR
Cytogenetic MapXXq22.3CLINVAR
Trait Synonyms: Lung cancer, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8586995
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.