Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV115554 (NM_138453.2(RAB3C):c.497-3537C>G) Homo sapiens

Symbol: CV115554
Name: NM_138453.2(RAB3C):c.497-3537C>G
Condition: Lung cancer [RCV000096077]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: RAB3C  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron|intron variant
Evidence: literature only|not provided
HGVS Name(s): NC_000005.10:g.58847627C>G
NC_000005.9:g.58143454C>G
NM_138453.2:c.497-3537C>G
Position
Human AssemblyChrPosition (strand)Source
GRCh38558,847,627 - 58,847,627CLINVAR
GRCh37558,143,454 - 58,143,454CLINVAR
Cytogenetic Map55q11.2CLINVAR
Trait Synonyms: Lung cancer, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8581117
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2015-08-04
Status: ACTIVE



NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.