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Variant : CV306502 (NM_005228.5(EGFR):c.*137G>A) Homo sapiens

Symbol: CV306502
Name: NM_005228.5(EGFR):c.*137G>A
Condition: Lung cancer [RCV000278048]
Clinical Significance: uncertain significance
Last Evaluated: 06/14/2016
Review Status: criteria provided, single submitter
Related Genes: EGFR  
Variant Type: single nucleotide variant (SO:0001624)
Source: CLINVAR
Molecular Consequence: 3 prime utr variant
Evidence: clinical testing
HGVS Name(s): LRG_304:g.191723G>A
NG_007726.3:g.191723G>A
NC_000007.14:g.55205754G>A
NC_000007.13:g.55273447G>A
NM_005228.3:c.*137G>A
NM_001346941.2:c.*137G>A
LRG_304t1:c.*137G>A
NM_001346899.1:c.*137G>A
NM_001346900.2:c.*137G>A
NM_005228.5:c.*137G>A
Position
Human AssemblyChrPosition (strand)Source
GRCh38755,205,754 - 55,205,754CLINVAR
GRCh37755,273,447 - 55,273,447CLINVAR
Cytogenetic Map77p11.2CLINVAR
Trait Synonyms: Lung cancer, somatic



Disease Annotations

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11600901
Created: 2017-01-11
Species: Homo sapiens
Last Modified: 2019-11-12
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.