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

Variant : CV111301 (NM_001277372.1(LOC100652824):c.685+750G>A) Homo sapiens

Symbol: CV111301
Name: NM_001277372.1(LOC100652824):c.685+750G>A
Condition: Lung cancer [RCV000091824]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: KIAA2012  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron|intron variant
Evidence: literature only|not provided
HGVS Name(s): NC_000002.12:g.202093935G>A
NC_000002.11:g.202958658G>A
NM_001277372.1:c.685+750G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh382202,093,935 - 202,093,935CLINVAR
GRCh372202,958,658 - 202,958,658CLINVAR
Cytogenetic Map22q33.1CLINVAR
Trait Synonyms: Lung cancer, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8576932
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.