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Variant : CV121592 (NM_001289922.2(C22orf34):c.-153-10835C>T) Homo sapiens

Symbol: CV121592
Name: NM_001289922.2(C22orf34):c.-153-10835C>T
Condition: Lung cancer [RCV000102112]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: C22orf34  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron|intron variant
Evidence: literature only|not provided
HGVS Name(s): NC_000022.11:g.49637882G>A
NC_000022.10:g.50031530G>A
NM_001289922.2:c.-153-10835C>T
Position
Human AssemblyChrPosition (strand)Source
GRCh382249,637,882 - 49,637,882CLINVAR
GRCh372250,031,530 - 50,031,530CLINVAR
Cytogenetic Map2222q13.33CLINVAR
Trait Synonyms: Lung cancer, somatic




Additional Information

 
CRRD Object Information
CRRD ID: 8586968
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.