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Variant : CV121934 (NM_198270.3(NHS):c.566-6583C>G) Homo sapiens

Symbol: CV121934
Name: NM_198270.3(NHS):c.566-6583C>G
Condition: Lung cancer [RCV000102454]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: NHS  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron|intron variant
Evidence: literature only|not provided
HGVS Name(s): NM_198270.3:c.566-6583C>G
NC_000023.11:g.17681159C>G
NC_000023.10:g.17699279C>G
NG_011553.2:g.310740C>G
NG_011553.1:g.310737C>G
Position
Human AssemblyChrPosition (strand)Source
GRCh38X17,681,159 - 17,681,159CLINVAR
GRCh37X17,699,279 - 17,699,279CLINVAR
Cytogenetic MapXXp22.13CLINVAR
Trait Synonyms: Lung cancer, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8587307
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.