"PreventionGenetics, part of Exact Sciences"[submitter] AND "FOLR3"[ge - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3053790	NM_000804.4(FOLR3):c.-6-21_8del	FOLR3	Deletion (splice acceptor variant +1 more)	FOLR3-related disorder	GLikely benign
Select item 3035466	NM_000804.4(FOLR3):c.82C>A (p.Arg28=)	FOLR3	Single nucleotide variant (synonymous variant +1 more)	FOLR3-related disorder	GBenign
Select item 3049026	NM_000804.4(FOLR3):c.93G>A (p.Thr31=)	FOLR3	Single nucleotide variant (synonymous variant +1 more)	FOLR3-related disorder	GLikely benign
Select item 3053561	NM_000804.4(FOLR3):c.117C>T (p.Asn39=)	FOLR3	Single nucleotide variant (synonymous variant +1 more)	FOLR3-related disorder	GLikely benign
Select item 785366	NM_000804.4(FOLR3):c.153C>T (p.Asp51=)	FOLR3	Single nucleotide variant (synonymous variant +1 more)	FOLR3-related disorder +1 more	GBenign
Select item 3051814	NM_000804.4(FOLR3):c.201G>A (p.Thr67=)	FOLR3 (R110Q)	Single nucleotide variant (synonymous variant +2 more)	FOLR3-related disorder	GLikely benign
Select item 3048799	NM_000804.4(FOLR3):c.201G>C (p.Thr67=)	FOLR3 (R110P)	Single nucleotide variant (synonymous variant +2 more)	FOLR3-related disorder	GBenign
Select item 3048659	NM_000804.4(FOLR3):c.243G>A (p.Leu81=)	FOLR3 (C124Y)	Single nucleotide variant (synonymous variant +2 more)	FOLR3-related disorder	GLikely benign
Select item 3036822	NM_000804.4(FOLR3):c.259G>T (p.Asp87Tyr)	FOLR3 (D87Y)	Single nucleotide variant (missense variant +2 more)	FOLR3-related disorder	GLikely benign
Select item 3035503	NM_000804.4(FOLR3):c.292C>T (p.Arg98Cys)	FOLR3 (R7C +1 more)	Single nucleotide variant (missense variant +2 more)	FOLR3-related disorder	GBenign
Select item 3054790	NM_000804.4(FOLR3):c.309C>T (p.Asp103=)	FOLR3 (T146I)	Single nucleotide variant (synonymous variant +2 more)	FOLR3-related disorder	GLikely benign
Select item 3035533	NM_000804.4(FOLR3):c.320_321dup (p.Glu108fs)	FOLR3 (E108fs)	Duplication (frameshift variant +1 more)	FOLR3-related disorder	GBenign
Select item 3045094	NM_000804.4(FOLR3):c.322G>C (p.Glu108Gln)	FOLR3 (E108Q +2 more)	Single nucleotide variant (missense variant +1 more)	FOLR3-related disorder	GBenign
Select item 3048755	NM_000804.4(FOLR3):c.372G>A (p.Trp124Ter)	FOLR3 (W124* +2 more)	Single nucleotide variant (nonsense +1 more)	FOLR3-related disorder	GLikely benign
Select item 3053893	NM_000804.4(FOLR3):c.381G>A (p.Glu127=)	FOLR3	Single nucleotide variant (synonymous variant +1 more)	FOLR3-related disorder	GLikely benign
Select item 3053064	NM_000804.4(FOLR3):c.418G>A (p.Glu140Lys)	FOLR3 (E140K +2 more)	Single nucleotide variant (missense variant +1 more)	FOLR3-related disorder	GBenign
Select item 3035310	NM_000804.4(FOLR3):c.583C>T (p.His195Tyr)	FOLR3 (H104Y +2 more)	Single nucleotide variant (missense variant +1 more)	FOLR3-related disorder	GBenign
Select item 3055129	NM_000804.4(FOLR3):c.711C>T (p.Ala237=)	FOLR3	Single nucleotide variant (synonymous variant +1 more)	FOLR3-related disorder	GLikely benign