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Variant : CV115553 (NM_138453.2(RAB3C):c.372-48549A>G) Homo sapiens

Symbol: CV115553
Name: NM_138453.2(RAB3C):c.372-48549A>G
Condition: Lung cancer [RCV000096076]
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.58776489A>G
NC_000005.9:g.58072316A>G
NM_138453.2:c.372-48549A>G
Position
Human AssemblyChrPosition (strand)Source
GRCh38558,776,489 - 58,776,489CLINVAR
GRCh37558,072,316 - 58,072,316CLINVAR
Cytogenetic Map55q11.2CLINVAR
Trait Synonyms: Lung cancer, somatic



References - curated

Additional Information

 
CRRD Object Information
CRRD ID: 8581116
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.