"Ambry Genetics"[submitter] AND "RBM14-RBM4"[gene] - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2208158	NM_006328.4(RBM14):c.520G>A (p.Ala174Thr)	RBM14, RBM14-RBM4 (A174T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2269051	NM_006328.4(RBM14):c.622C>T (p.Pro208Ser)	RBM14, RBM14-RBM4 (P208S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3152191	NM_006328.4(RBM14):c.623C>A (p.Pro208His)	RBM14, RBM14-RBM4 (P208H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2337621	NM_006328.4(RBM14):c.647C>G (p.Pro216Arg)	RBM14, RBM14-RBM4 (P216R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2470234	NM_006328.4(RBM14):c.653G>A (p.Arg218His)	RBM14, RBM14-RBM4 (R218H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2354806	NM_006328.4(RBM14):c.727G>A (p.Val243Met)	RBM14, RBM14-RBM4 (V243M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3152192	NM_006328.4(RBM14):c.782A>G (p.Tyr261Cys)	RBM14, RBM14-RBM4 (Y261C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2335176	NM_006328.4(RBM14):c.800C>T (p.Thr267Ile)	RBM14, RBM14-RBM4 (T267I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2530794	NM_006328.4(RBM14):c.893C>G (p.Ala298Gly)	RBM14, RBM14-RBM4 (A298G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2225757	NM_006328.4(RBM14):c.896C>T (p.Ala299Val)	RBM14, RBM14-RBM4 (A299V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2495375	NM_006328.4(RBM14):c.919G>A (p.Gly307Arg)	RBM14, RBM14-RBM4 (G307R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2570245	NM_006328.4(RBM14):c.950C>G (p.Ser317Cys)	RBM14, RBM14-RBM4 (S317C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2622935	NM_006328.4(RBM14):c.958G>A (p.Gly320Ser)	RBM14, RBM14-RBM4 (G320S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2317063	NM_006328.4(RBM14):c.980C>T (p.Ser327Leu)	RBM14, RBM14-RBM4 (S327L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2325478	NM_006328.4(RBM14):c.1058C>T (p.Ala353Val)	RBM14, RBM14-RBM4 (A353V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2494883	NM_006328.4(RBM14):c.1267G>A (p.Ala423Thr)	RBM14, RBM14-RBM4 (A423T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3152190	NM_006328.4(RBM14):c.1364C>G (p.Thr455Ser)	RBM14, RBM14-RBM4 (T455S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2221359	NM_006328.4(RBM14):c.1394C>T (p.Pro465Leu)	RBM14, RBM14-RBM4 (P465L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2617512	NM_006328.4(RBM14):c.1445T>C (p.Leu482Pro)	RBM14, RBM14-RBM4 (L482P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2305713	NM_006328.4(RBM14):c.1682T>C (p.Met561Thr)	RBM14, RBM14-RBM4 (M561T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2206292	NM_006328.4(RBM14):c.1721C>T (p.Pro574Leu)	RBM14, RBM14-RBM4 (P574L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2494884	NM_006328.4(RBM14):c.1754G>A (p.Arg585Gln)	RBM14, RBM14-RBM4 (R585Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2282688	NM_006328.4(RBM14):c.1880C>T (p.Ser627Leu)	RBM14, RBM14-RBM4 (S627L)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2211929	NM_002896.4(RBM4):c.712G>A (p.Ala238Thr)	RBM14-RBM4, RBM4 (A213T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 24