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

Variant : CV306490 (NM_005228.5(EGFR):c.3162+7A>G) Homo sapiens

Symbol: CV306490
Name: NM_005228.5(EGFR):c.3162+7A>G
Condition: Lung cancer [RCV000389736]
Clinical Significance: uncertain significance
Last Evaluated: 06/14/2016
Review Status: criteria provided, single submitter
Related Genes: EGFR  
Variant Type: single nucleotide variant (SO:0001627)
Source: CLINVAR
Molecular Consequence: intron variant
Evidence: clinical testing
HGVS Name(s): LRG_304:g.187758A>G
NG_007726.3:g.187758A>G
NC_000007.14:g.55201789A>G
NC_000007.13:g.55269482A>G
NM_005228.3:c.3162+7A>G
LRG_304t1:c.3162+7A>G
NM_001346900.2:c.3003+7A>G
NM_001346897.2:c.3027+7A>G
NM_001346899.1:c.3027+7A>G
NM_001346898.2:c.3162+7A>G
NM_005228.5:c.3162+7A>G
NM_001346941.2:c.2361+7A>G
Position
Human AssemblyChrPosition (strand)Source
GRCh38755,201,789 - 55,201,789CLINVAR
GRCh37755,269,482 - 55,269,482CLINVAR
Cytogenetic Map77p11.2CLINVAR
Trait Synonyms: Lung cancer, somatic



Disease Annotations

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11611029
Created: 2017-01-11
Species: Homo sapiens
Last Modified: 2019-12-03
Status: ACTIVE



NHLBI Logo

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