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Variant : CV306474 (NM_005228.5(EGFR):c.-21C>A) Homo sapiens

Symbol: CV306474
Name: NM_005228.5(EGFR):c.-21C>A
Condition: Lung cancer [RCV000315983]
Clinical Significance: uncertain significance
Last Evaluated: 06/14/2016
Review Status: criteria provided, single submitter
Related Genes: EGFR  
Variant Type: single nucleotide variant (SO:0001623)
Source: CLINVAR
Molecular Consequence: 5 prime utr variant
Evidence: clinical testing
HGVS Name(s): NM_001346898.2:c.-21C>A
NM_001346897.2:c.-21C>A
LRG_304:g.5226C>A
NG_007726.3:g.5226C>A
NC_000007.14:g.55019257C>A
NC_000007.13:g.55086950C>A
NM_005228.3:c.-21C>A
NM_201282.2:c.-21C>A
NM_201283.1:c.-21C>A
NM_201284.2:c.-21C>A
LRG_304t1:c.-21C>A
NM_001346899.1:c.-21C>A
NM_001346941.2:c.-21C>A
NM_005228.5:c.-21C>A
Position
Human AssemblyChrPosition (strand)Source
GRCh38755,019,257 - 55,019,257CLINVAR
GRCh37755,086,950 - 55,086,950CLINVAR
Cytogenetic Map77p11.2CLINVAR
Trait Synonyms: Lung cancer, somatic



Disease Annotations

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11605114
Created: 2017-01-11
Species: Homo sapiens
Last Modified: 2019-12-03
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.