"Revvity Omics, Revvity"[submitter] AND "EGFR"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 848579	NM_005228.5(EGFR):c.61G>A (p.Ala21Thr)	EGFR (A21T)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1123013	NM_005228.5(EGFR):c.769G>A (p.Glu257Lys)	EGFR (E204K +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 2441190	NM_005228.5(EGFR):c.1337C>T (p.Thr446Ile)	EGFR (T179I +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 134025	NM_005228.5(EGFR):c.2024G>A (p.Arg675Gln)	EGFR (R675Q +3 more)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 1923090	NM_005228.5(EGFR):c.2618G>A (p.Gly873Glu)	EGFR (G606E +3 more)	Single nucleotide variant (missense variant)	EGFR-related lung cancer +1 more	GUncertain significance
Select item 730373	NM_005228.5(EGFR):c.3143C>T (p.Ala1048Val)	EGFR (A1048V +3 more)	Single nucleotide variant (missense variant)	EGFR-related lung cancer +1 more	GConflicting classifications of pathogenicity
Select item 584702	NM_005228.5(EGFR):c.3352G>A (p.Ala1118Thr)	EGFR (A1118T +3 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity

ClinVar