"Ambry Genetics"[submitter] AND "GFOD1"[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2296859	NM_018988.4(GFOD1):c.1166A>G (p.Tyr389Cys)	GFOD1 (Y389C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301023	NM_018988.4(GFOD1):c.1147C>T (p.Arg383Cys)	GFOD1 (R280C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233655	NM_018988.4(GFOD1):c.788C>T (p.Thr263Ile)	GFOD1 (T160I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207049	NM_018988.4(GFOD1):c.701C>G (p.Thr234Ser)	GFOD1 (T131S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099467	NM_018988.4(GFOD1):c.619G>C (p.Asp207His)	GFOD1 (D104H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554201	NM_018988.4(GFOD1):c.577G>A (p.Val193Ile)	GFOD1 (V90I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099466	NM_018988.4(GFOD1):c.424G>A (p.Glu142Lys)	GFOD1 (E142K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099465	NM_018988.4(GFOD1):c.406G>A (p.Glu136Lys)	GFOD1 (E136K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222817	NM_018988.4(GFOD1):c.308G>A (p.Arg103His)	GFOD1 (R103H)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3099464	NM_018988.4(GFOD1):c.161G>A (p.Arg54His)	GFOD1, GFOD1-AS1 (R54H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2369336	NM_018988.4(GFOD1):c.80C>A (p.Ala27Glu)	GFOD1 (A27E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance