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Variant : CV121933 (NM_198270.3(NHS):c.565+123559G>C) Homo sapiens

Symbol: CV121933
Name: NM_198270.3(NHS):c.565+123559G>C
Condition: Lung cancer [RCV000102453]
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.565+123559G>C
NC_000023.11:g.17499881G>C
NC_000023.10:g.17518004G>C
NG_011553.2:g.129462G>C
NG_011553.1:g.129462G>C
Position
Human AssemblyChrPosition (strand)Source
GRCh38X17,499,881 - 17,499,881CLINVAR
GRCh37X17,518,004 - 17,518,004CLINVAR
Cytogenetic MapXXp22.13CLINVAR
Trait Synonyms: Lung cancer, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8587306
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.