"Genome-Nilou Lab"[submitter] AND "EGFR"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 259680	NM_005228.5(EGFR):c.474C>T (p.Asn158=)	EGFR	Single nucleotide variant (synonymous variant +1 more)	Inflammatory skin and bowel disease, neonatal, 2 +4 more	GBenign
Select item 1255377	NM_005228.5(EGFR):c.1498+22A>T	EGFR	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 134021	NM_005228.5(EGFR):c.1562G>A (p.Arg521Lys)	EGFR (R521K +3 more)	Single nucleotide variant (missense variant)	not specified +4 more	GBenign
Select item 259677	NM_005228.5(EGFR):c.1887T>A (p.Thr629=)	EGFR	Single nucleotide variant (synonymous variant)	not provided +4 more	GBenign
Select item 45271	NM_005228.5(EGFR):c.2361G>A (p.Gln787=)	EGFR, EGFR-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary cancer-predisposing syndrome +6 more	GBenign
Select item 1166017	NM_005228.5(EGFR):c.2709T>C (p.Thr903=)	EGFR	Single nucleotide variant (synonymous variant)	Inflammatory skin and bowel disease, neonatal, 2 +2 more	GBenign

ClinVar