C0242379[trait identifier] AND "KCCC/NGS Laboratory, Kuwait Cancer Con - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1246877	NM_005228.5(EGFR):c.-216G>T	EGFR	Single nucleotide variant (5 prime UTR variant)	Lung cancer +1 more	GBenign/Likely benign
Select item 1232163	NM_005228.5(EGFR):c.-191A>C	EGFR	Single nucleotide variant (5 prime UTR variant)	Lung cancer +1 more	GBenign/Likely benign
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 360455	NM_005228.5(EGFR):c.531G>A (p.Ser177=)	EGFR	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GBenign/Likely benign
Select item 259681	NM_005228.5(EGFR):c.559+10G>A	EGFR	Single nucleotide variant (intron variant)	EGFR-related lung cancer +3 more	GBenign
Select item 360458	NM_005228.5(EGFR):c.1299-7A>G	EGFR	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign
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 360460	NM_005228.5(EGFR):c.1830C>T (p.Tyr610=)	EGFR	Single nucleotide variant (synonymous variant)	EGFR-related lung cancer +2 more	GBenign/Likely benign
Select item 360461	NM_005228.5(EGFR):c.1839C>T (p.Ala613=)	EGFR	Single nucleotide variant (synonymous variant)	not specified +3 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 45270	NM_005228.5(EGFR):c.2355C>T (p.Thr785=)	EGFR, EGFR-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +3 more	GLikely benign
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 259678	NM_005228.5(EGFR):c.2487G>A (p.Glu829=)	EGFR	Single nucleotide variant (synonymous variant)	Lung cancer +4 more	GBenign
Select item 45281	NM_005228.5(EGFR):c.2508C>T (p.Arg836=)	EGFR	Single nucleotide variant (synonymous variant)	EGFR-related lung cancer +3 more	GBenign
Select item 45296	NM_005228.5(EGFR):c.2748C>T (p.Asp916=)	EGFR	Single nucleotide variant (synonymous variant)	Lung cancer +3 more	GBenign/Likely benign
Select item 134029	NM_005228.5(EGFR):c.2963A>C (p.His988Pro)	EGFR (H988P +3 more)	Single nucleotide variant (missense variant)	Lung cancer +3 more	GBenign/Likely benign
Select item 259679	NM_005228.5(EGFR):c.2982C>T (p.Asp994=)	EGFR	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign
Select item 55601	NM_007294.4(BRCA1):c.5503C>T (p.Arg1835Ter)	BRCA1 (R1835* +80 more)	Single nucleotide variant (nonsense +2 more)	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic