"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "FEZF1-A - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 734305	NM_001024613.4(FEZF1):c.780C>T (p.Phe260=)	FEZF1, FEZF1-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1904434	NM_001024613.4(FEZF1):c.711G>T (p.Leu237=)	FEZF1, FEZF1-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 725249	NM_001024613.4(FEZF1):c.615G>A (p.Val205=)	FEZF1, FEZF1-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1940609	NM_001024613.4(FEZF1):c.590A>G (p.Tyr197Cys)	FEZF1, FEZF1-AS1 (Y197C +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 723308	NM_001024613.4(FEZF1):c.553T>C (p.Phe185Leu)	FEZF1, FEZF1-AS1 (F185L)	Single nucleotide variant (non-coding transcript variant +2 more)	not provided	GLikely benign
Select item 718873	NM_001024613.4(FEZF1):c.523G>C (p.Gly175Arg)	FEZF1-AS1, FEZF1 (G175R)	Single nucleotide variant (non-coding transcript variant +2 more)	not provided	GLikely benign
Select item 754082	NM_001024613.4(FEZF1):c.438G>A (p.Pro146=)	FEZF1, FEZF1-AS1	Single nucleotide variant (non-coding transcript variant +2 more)	not provided	GLikely benign
Select item 731510	NM_001024613.4(FEZF1):c.405G>A (p.Ala135=)	FEZF1, FEZF1-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 774664	NM_001024613.4(FEZF1):c.285G>C (p.Pro95=)	FEZF1-AS1, FEZF1	Single nucleotide variant (non-coding transcript variant +1 more)	not specified +1 more	GBenign/Likely benign
Select item 1938510	NM_001024613.4(FEZF1):c.266G>A (p.Gly89Glu)	FEZF1, FEZF1-AS1 (G89E)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 787587	NM_001024613.4(FEZF1):c.253A>G (p.Ser85Gly)	FEZF1, FEZF1-AS1 (S85G)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 721996	NM_001024613.4(FEZF1):c.252G>A (p.Thr84=)	FEZF1, FEZF1-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 788360	NM_001024613.4(FEZF1):c.213C>T (p.Ile71=)	FEZF1, FEZF1-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2118461	NM_001024613.4(FEZF1):c.197A>C (p.His66Pro)	FEZF1, FEZF1-AS1 (H66P)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 2103848	NM_001024613.4(FEZF1):c.188A>G (p.His63Arg)	FEZF1, FEZF1-AS1 (H63R)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 757582	NM_001024613.4(FEZF1):c.180A>G (p.Glu60=)	FEZF1, FEZF1-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 753625	NM_001024613.4(FEZF1):c.123A>T (p.Pro41=)	FEZF1, FEZF1-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1428079	NM_001024613.4(FEZF1):c.74C>A (p.Thr25Lys)	FEZF1, FEZF1-AS1 (T25K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance