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Variant : CV122336 (NM_000390.2(CHM):c.1167-282T>G) Homo sapiens

Symbol: CV122336
Name: NM_000390.2(CHM):c.1167-282T>G
Condition: Lung cancer [RCV000102856]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CHM  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron|intron variant
Evidence: literature only|not provided
HGVS Name(s): NM_000390.2:c.1167-282T>G
NC_000023.11:g.85911620A>C
NC_000023.10:g.85166625A>C
NG_009874.2:g.140943T>G
NG_009874.1:g.140942T>G
Position
Human AssemblyChrPosition (strand)Source
GRCh38X85,911,620 - 85,911,620CLINVAR
GRCh37X85,166,625 - 85,166,625CLINVAR
Cytogenetic MapXXq21.2CLINVAR
Trait Synonyms: Lung cancer, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8587705
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.