"Ambry Genetics"[submitter] AND "FN3K"[gene] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2334712	NM_022158.4(FN3K):c.7C>G (p.Gln3Glu)	FN3K (Q3E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339672	NM_022158.4(FN3K):c.38C>T (p.Thr13Ile)	FN3K (T13I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279378	NM_022158.4(FN3K):c.49T>G (p.Phe17Val)	FN3K (F17V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095963	NM_022158.4(FN3K):c.239C>T (p.Pro80Leu)	FN3K (P80L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225077	NM_022158.4(FN3K):c.245G>A (p.Gly82Asp)	FN3K (G82D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513984	NM_022158.4(FN3K):c.358A>G (p.Lys120Glu)	FN3K (K120E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365568	NM_022158.4(FN3K):c.400G>T (p.Gly134Cys)	FN3K (G134C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279380	NM_022158.4(FN3K):c.430G>T (p.Gly144Cys)	FN3K (G144C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535729	NM_022158.4(FN3K):c.433T>C (p.Phe145Leu)	FN3K (F145L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279379	NM_022158.4(FN3K):c.440C>T (p.Thr147Met)	FN3K (T147M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380852	NM_022158.4(FN3K):c.454G>A (p.Gly152Ser)	FN3K (G152S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617553	NM_022158.4(FN3K):c.506C>T (p.Ala169Val)	FN3K (A169V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405487	NM_022158.4(FN3K):c.508C>T (p.Arg170Trp)	FN3K (R170W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402608	NM_022158.4(FN3K):c.524C>T (p.Ala175Val)	FN3K (A175V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279377	NM_022158.4(FN3K):c.602C>T (p.Pro201Leu)	FN3K (P201L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095964	NM_022158.4(FN3K):c.727G>A (p.Glu243Lys)	FN3K (E243K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095965	NM_022158.4(FN3K):c.761G>C (p.Gly254Ala)	FN3K (G254A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216146	NM_022158.4(FN3K):c.770G>A (p.Arg257Lys)	FN3K (R257K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362583	NM_022158.4(FN3K):c.792C>A (p.His264Gln)	FN3K (H264Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274108	NM_022158.4(FN3K):c.794G>A (p.Arg265Gln)	FN3K (R265Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600387	NM_022158.4(FN3K):c.823C>G (p.Gln275Glu)	FN3K (Q275E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411066	NM_022158.4(FN3K):c.826C>G (p.Arg276Gly)	FN3K (R276G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237119	NM_022158.4(FN3K):c.847T>C (p.Phe283Leu)	FN3K (F283L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095967	NM_022158.4(FN3K):c.854A>C (p.Tyr285Ser)	FN3K (Y285S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593999	NM_022158.4(FN3K):c.905G>C (p.Gly302Ala)	FN3K (G302A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 25