"Ambry Genetics"[submitter] AND "RNF128"[gene] - ClinVar

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Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3155014	NM_194463.2(RNF128):c.17G>C (p.Gly6Ala)	RNF128 (G6A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2621139	NM_194463.2(RNF128):c.20C>A (p.Ala7Asp)	RNF128 (A7D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2477539	NM_194463.2(RNF128):c.23G>A (p.Gly8Glu)	RNF128 (G8E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2475874	NM_194463.2(RNF128):c.64G>A (p.Ala22Thr)	RNF128 (A22T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3155013	NM_194463.2(RNF128):c.154C>T (p.Arg52Trp)	RNF128 (R52W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2489658	NM_194463.2(RNF128):c.292C>A (p.Pro98Thr)	RNF128 (P98T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2393884	NM_194463.2(RNF128):c.411G>C (p.Glu137Asp)	RNF128 (E137D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2509102	NM_194463.2(RNF128):c.457A>G (p.Asn153Asp)	RNF128 (N153D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3155016	NM_194463.2(RNF128):c.481C>T (p.Pro161Ser)	RNF128 (P161S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3155017	NM_194463.2(RNF128):c.502G>A (p.Ala168Thr)	RNF128 (A142T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330180	NM_194463.2(RNF128):c.514G>T (p.Gly172Cys)	RNF128 (G172C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612509	NM_194463.2(RNF128):c.612T>A (p.Asn204Lys)	RNF128 (N178K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155018	NM_194463.2(RNF128):c.623T>C (p.Ile208Thr)	RNF128 (I182T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402308	NM_194463.2(RNF128):c.656C>T (p.Thr219Met)	RNF128 (T219M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460055	NM_194463.2(RNF128):c.871C>T (p.Arg291Cys)	RNF128 (R265C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466535	NM_194463.2(RNF128):c.881C>G (p.Thr294Arg)	RNF128 (T268R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272440	NM_194463.2(RNF128):c.1001G>T (p.Gly334Val)	RNF128 (G334V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468953	NM_194463.2(RNF128):c.1124C>T (p.Pro375Leu)	RNF128 (P375L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510365	NM_194463.2(RNF128):c.1135G>C (p.Glu379Gln)	RNF128 (E353Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309216	NM_194463.2(RNF128):c.1190C>T (p.Ser397Phe)	RNF128 (S397F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352219	NM_194463.2(RNF128):c.1258G>A (p.Glu420Lys)	RNF128 (E394K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411860	NM_194463.2(RNF128):c.1259A>T (p.Glu420Val)	RNF128 (E394V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 22