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

Variant : CV119273 (NM_001102612.2(PGPEP1L):c.21+3403G>C) Homo sapiens

Symbol: CV119273
Name: NM_001102612.2(PGPEP1L):c.21+3403G>C
Condition: Lung cancer [RCV000099793]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: PGPEP1L  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron|intron variant
Evidence: literature only|not provided
HGVS Name(s): NC_000015.10:g.98997784C>G
NC_000015.9:g.99541013C>G
NM_001102612.2:c.21+3403G>C
Position
Human AssemblyChrPosition (strand)Source
GRCh381598,997,784 - 98,997,784CLINVAR
GRCh371599,541,013 - 99,541,013CLINVAR
Cytogenetic Map1515q26.3CLINVAR
Trait Synonyms: Lung cancer, somatic



References - curated

Additional Information

 
RGD Object Information
RGD ID: 8584697
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.