"Ambry Genetics"[submitter] AND "FBXL6"[gene] - ClinVar

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Items: 51

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2265603	NM_012162.4(FBXL6):c.1613C>G (p.Pro538Arg)	FBXL6 (P532R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382846	NM_012162.4(FBXL6):c.1558C>T (p.Arg520Trp)	FBXL6 (R514W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220442	NM_012162.4(FBXL6):c.1556A>G (p.Tyr519Cys)	FBXL6 (Y519C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291472	NM_012162.4(FBXL6):c.1553C>T (p.Ala518Val)	FBXL6 (A512V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596782	NM_012162.4(FBXL6):c.1516G>A (p.Glu506Lys)	FBXL6 (E506K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093550	NM_012162.4(FBXL6):c.1505A>G (p.Tyr502Cys)	FBXL6 (Y496C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093549	NM_012162.4(FBXL6):c.1499T>G (p.Leu500Arg)	FBXL6 (L500R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379925	NM_012162.4(FBXL6):c.1453G>A (p.Val485Ile)	FBXL6 (V479I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588970	NM_012162.4(FBXL6):c.1451G>A (p.Arg484Gln)	FBXL6 (R484Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264942	NM_012162.4(FBXL6):c.1450C>T (p.Arg484Trp)	FBXL6 (R484W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390098	NM_012162.4(FBXL6):c.1396A>G (p.Ser466Gly)	FBXL6 (S460G +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2510351	NM_012162.4(FBXL6):c.1345G>A (p.Gly449Ser)	FBXL6 (G443S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285082	NM_012162.4(FBXL6):c.1343G>A (p.Ser448Asn)	FBXL6 (S442N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386312	NM_012162.4(FBXL6):c.1292G>A (p.Ser431Asn)	FBXL6 (S425N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557300	NM_012162.4(FBXL6):c.1287G>C (p.Glu429Asp)	FBXL6 (E423D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368001	NM_012162.4(FBXL6):c.1267C>T (p.Arg423Trp)	FBXL6 (R417W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356346	NM_012162.4(FBXL6):c.1259C>T (p.Thr420Met)	FBXL6 (T420M +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2205425	NM_012162.4(FBXL6):c.1235A>G (p.Gln412Arg)	FBXL6 (Q412R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348313	NM_012162.4(FBXL6):c.1222C>T (p.Arg408Trp)	FBXL6 (R402W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222181	NM_012162.4(FBXL6):c.1186C>T (p.Arg396Cys)	FBXL6 (R396C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290477	NM_012162.4(FBXL6):c.1184C>T (p.Ala395Val)	FBXL6 (A389V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613535	NM_012162.4(FBXL6):c.1175G>A (p.Arg392His)	FBXL6 (R386H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377914	NM_012162.4(FBXL6):c.1034C>T (p.Pro345Leu)	FBXL6 (P339L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2363071	NM_012162.4(FBXL6):c.1034C>A (p.Pro345Gln)	FBXL6 (P339Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409159	NM_012162.4(FBXL6):c.1001G>A (p.Arg334Gln)	FBXL6 (R328Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093547	NM_012162.4(FBXL6):c.1000C>T (p.Arg334Trp)	FBXL6 (R328W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282299	NM_012162.4(FBXL6):c.952C>G (p.Leu318Val)	FBXL6 (L312V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536954	NM_012162.4(FBXL6):c.922G>A (p.Gly308Ser)	FBXL6 (G302S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093562	NM_012162.4(FBXL6):c.824G>A (p.Arg275His)	FBXL6 (R269H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268954	NM_012162.4(FBXL6):c.824G>T (p.Arg275Leu)	FBXL6 (R269L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406000	NM_012162.4(FBXL6):c.818G>A (p.Arg273Gln)	FBXL6 (R267Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093561	NM_012162.4(FBXL6):c.718A>G (p.Met240Val)	FBXL6 (M234V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093560	NM_012162.4(FBXL6):c.694G>A (p.Gly232Ser)	FBXL6 (G226S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093559	NM_012162.4(FBXL6):c.628C>T (p.Pro210Ser)	FBXL6 (P210S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2330273	NM_012162.4(FBXL6):c.610T>C (p.Trp204Arg)	FBXL6 (W204R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093557	NM_012162.4(FBXL6):c.521G>C (p.Gly174Ala)	FBXL6 (G174A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093556	NM_012162.4(FBXL6):c.464C>T (p.Ala155Val)	FBXL6 (A155V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093555	NM_012162.4(FBXL6):c.389C>T (p.Ala130Val)	FBXL6 (A130V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559235	NM_012162.4(FBXL6):c.361G>A (p.Val121Met)	FBXL6 (V121M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360466	NM_012162.4(FBXL6):c.308C>T (p.Pro103Leu)	FBXL6 (P103L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093554	NM_012162.4(FBXL6):c.298A>G (p.Thr100Ala)	FBXL6 (T100A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548422	NM_012162.4(FBXL6):c.284C>A (p.Pro95His)	FBXL6 (P95H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405324	NM_012162.4(FBXL6):c.277C>T (p.Pro93Ser)	FBXL6 (P93S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335696	NM_012162.4(FBXL6):c.250G>A (p.Gly84Arg)	FBXL6, LOC130001388 (G84R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3093553	NM_012162.4(FBXL6):c.239A>C (p.Lys80Thr)	FBXL6, LOC130001388 (K80T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093552	NM_012162.4(FBXL6):c.203C>T (p.Pro68Leu)	FBXL6, LOC130001388 (P68L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409056	NM_012162.4(FBXL6):c.193C>T (p.Arg65Cys)	FBXL6, LOC130001388 (R65C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093551	NM_012162.4(FBXL6):c.166C>T (p.Arg56Trp)	FBXL6, LOC130001388 (R56W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244209	NM_012162.4(FBXL6):c.110A>G (p.Tyr37Cys)	FBXL6, LOC130001388 (Y37C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343292	NM_012162.4(FBXL6):c.40C>T (p.Arg14Trp)	FBXL6, LOC130001388 (R14W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613871	NM_012162.4(FBXL6):c.25G>A (p.Val9Ile)	FBXL6 (V9I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 51