"Ambry Genetics"[submitter] AND "FBXL19"[gene] - ClinVar

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Items: 28

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2557720	NM_001382779.1(FBXL19):c.28G>A (p.Ala10Thr)	FBXL19 (A30T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2365452	NM_001382779.1(FBXL19):c.28G>T (p.Ala10Ser)	FBXL19 (A10S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3093522	NM_001382779.1(FBXL19):c.29C>T (p.Ala10Val)	FBXL19 (A32V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2294154	NM_001382779.1(FBXL19):c.191A>G (p.His64Arg)	FBXL19 (H64R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2289389	NM_001382779.1(FBXL19):c.241G>A (p.Glu81Lys)	FBXL19 (E103K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2407067	NM_001382779.1(FBXL19):c.415G>A (p.Gly139Ser)	FBXL19 (G159S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2596866	NM_001382779.1(FBXL19):c.526A>C (p.Lys176Gln)	FBXL19 (K196Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2285230	NM_001382779.1(FBXL19):c.547C>T (p.Pro183Ser)	FBXL19 (P183S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2588229	NM_001382779.1(FBXL19):c.551C>T (p.Pro184Leu)	FBXL19 (P206L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2385907	NM_001382779.1(FBXL19):c.607C>G (p.Pro203Ala)	FBXL19 (P203A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2602024	NM_001382779.1(FBXL19):c.664G>A (p.Gly222Ser)	FBXL19 (G222S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2555320	NM_001382779.1(FBXL19):c.707C>T (p.Pro236Leu)	FBXL19 (P236L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3093521	NM_001382779.1(FBXL19):c.800C>T (p.Pro267Leu)	FBXL19 (P287L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2369397	NM_001382779.1(FBXL19):c.827C>T (p.Ala276Val)	FBXL19 (A233V +3 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2379170	NM_001382779.1(FBXL19):c.982G>A (p.Gly328Ser)	FBXL19 (G307S +4 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3093516	NM_001382779.1(FBXL19):c.1048C>T (p.Arg350Trp)	FBXL19 (R307W +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612180	NM_001382779.1(FBXL19):c.1051C>T (p.Arg351Trp)	FBXL19 (R308W +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262435	NM_001382779.1(FBXL19):c.1124C>T (p.Pro375Leu)	FBXL19 (P354L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388894	NM_001382779.1(FBXL19):c.1136G>A (p.Arg379Gln)	FBXL19 (R358Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475652	NM_001382779.1(FBXL19):c.1201G>T (p.Asp401Tyr)	FBXL19 (D109Y +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330943	NM_001382779.1(FBXL19):c.1255C>T (p.Arg419Trp)	FBXL19 (R127W +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093517	NM_001382779.1(FBXL19):c.1363C>T (p.Pro455Ser)	FBXL19 (P412S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234089	NM_001382779.1(FBXL19):c.1576A>G (p.Lys526Glu)	FBXL19 (K546E +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093518	NM_001382779.1(FBXL19):c.1619C>G (p.Thr540Ser)	FBXL19 (T497S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259681	NM_001382779.1(FBXL19):c.1649G>A (p.Arg550Gln)	FBXL19 (R550Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483160	NM_001382779.1(FBXL19):c.1660G>T (p.Val554Leu)	FBXL19 (V262L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3093519	NM_001382779.1(FBXL19):c.1889G>A (p.Arg630His)	FBXL19 (R338H +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278051	NM_001382779.1(FBXL19):c.1904G>A (p.Arg635His)	FBXL19 (R343H +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 28