All variants in the EGFR gene

Information The variants shown are described using the NM_005228.3 transcript reference sequence.

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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
?/. - c.2885G>A r.(?) p.(Arg962His) - VUS g.55268045G>A g.55200352G>A - - EGFR_000032 3 heterozygous, no homozygous; Clinindb (India) Faruq 2020, submtted - rs144496976 Germline - 3/2795 individuals - 0 - Mohammed Faruq
?/. - c.2885G>A r.(?) p.(Arg962His) - VUS g.55268045G>A g.55200352G>A EGFR(NM_001346899.1):c.2750G>A (p.R917H) - EGFR_000032 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
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