"Ambry Genetics"[submitter] AND "RNF151"[gene] - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2615146	NM_174903.6(RNF151):c.5G>T (p.Gly2Val)	RNF151 (G2V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489164	NM_174903.6(RNF151):c.51C>G (p.Asn17Lys)	RNF151 (N17K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338593	NM_174903.6(RNF151):c.74G>C (p.Gly25Ala)	RNF151 (G25A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155117	NM_174903.6(RNF151):c.76G>T (p.Val26Phe)	RNF151 (V26F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516717	NM_174903.6(RNF151):c.146C>T (p.Ala49Val)	RNF151 (A49V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308035	NM_174903.6(RNF151):c.178G>C (p.Glu60Gln)	RNF151 (E60Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2404269	NM_174903.6(RNF151):c.218G>A (p.Arg73Gln)	RNF151 (R73Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3155108	NM_174903.6(RNF151):c.232C>T (p.Arg78Cys)	RNF151 (R78C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3155109	NM_174903.6(RNF151):c.256G>A (p.Ala86Thr)	RNF151 (A86T)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3155110	NM_174903.6(RNF151):c.271A>T (p.Ile91Leu)	RNF151 (I91L)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 3155111	NM_174903.6(RNF151):c.391C>T (p.Arg131Trp)	RNF151 (R131W)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3155112	NM_174903.6(RNF151):c.422G>A (p.Arg141His)	RNF151 (R141H)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3155113	NM_174903.6(RNF151):c.434G>T (p.Gly145Val)	RNF151 (G145V)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2555284	NM_174903.6(RNF151):c.439G>C (p.Gly147Arg)	RNF151 (G147R)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3155114	NM_174903.6(RNF151):c.463C>T (p.Arg155Cys)	RNF151 (R155C)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2253328	NM_174903.6(RNF151):c.517G>A (p.Glu173Lys)	RNF151 (E173K)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3155115	NM_174903.6(RNF151):c.520C>T (p.Arg174Cys)	RNF151 (R174C)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2328807	NM_174903.6(RNF151):c.524G>A (p.Arg175His)	RNF151 (R175H)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2378359	NM_174903.6(RNF151):c.556G>A (p.Val186Met)	RNF151 (V186M)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2475326	NM_174903.6(RNF151):c.560G>A (p.Arg187His)	RNF151 (R187H)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2258522	NM_174903.6(RNF151):c.589C>T (p.Arg197Cys)	RNF151 (R197C)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2315226	NM_174903.6(RNF151):c.658G>A (p.Glu220Lys)	RNF151 (E220K)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2230079	NM_174903.6(RNF151):c.688G>A (p.Val230Ile)	RNF151 (V230I)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2411495	NM_174903.6(RNF151):c.694G>A (p.Ala232Thr)	RNF151 (A232T)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance

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Items: 24