"Ambry Genetics"[submitter] AND "RNF186"[gene] - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2318635	NM_019062.2(RNF186):c.679G>A (p.Ala227Thr)	RNF186, RNF186-AS1 (A227T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2327476	NM_019062.2(RNF186):c.653A>G (p.Gln218Arg)	RNF186, RNF186-AS1 (Q218R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2282387	NM_019062.2(RNF186):c.644G>T (p.Cys215Phe)	RNF186, RNF186-AS1 (C215F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2394638	NM_019062.2(RNF186):c.608G>A (p.Arg203Gln)	RNF186, RNF186-AS1 (R203Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2520112	NM_019062.2(RNF186):c.607C>T (p.Arg203Trp)	RNF186, RNF186-AS1 (R203W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2614169	NM_019062.2(RNF186):c.560C>T (p.Ala187Val)	RNF186, RNF186-AS1 (A187V)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2371713	NM_019062.2(RNF186):c.536G>A (p.Arg179Gln)	RNF186, RNF186-AS1 (R179Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2355226	NM_019062.2(RNF186):c.524C>T (p.Pro175Leu)	RNF186, RNF186-AS1 (P175L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2557389	NM_019062.2(RNF186):c.515T>A (p.Phe172Tyr)	RNF186, RNF186-AS1 (F172Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2349039	NM_019062.2(RNF186):c.470C>T (p.Ala157Val)	RNF186, RNF186-AS1 (A157V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2460659	NM_019062.2(RNF186):c.469G>A (p.Ala157Thr)	RNF186, RNF186-AS1 (A157T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2274375	NM_019062.2(RNF186):c.457C>T (p.Arg153Trp)	RNF186, RNF186-AS1 (R153W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2321546	NM_019062.2(RNF186):c.445C>A (p.His149Asn)	RNF186, RNF186-AS1 (H149N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2324855	NM_019062.2(RNF186):c.399C>A (p.His133Gln)	RNF186, RNF186-AS1 (H133Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2271750	NM_019062.2(RNF186):c.370G>A (p.Val124Met)	RNF186, RNF186-AS1 (V124M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2461949	NM_019062.2(RNF186):c.338G>A (p.Cys113Tyr)	RNF186, RNF186-AS1 (C113Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2595545	NM_019062.2(RNF186):c.298C>T (p.Arg100Cys)	RNF186, RNF186-AS1 (R100C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2614168	NM_019062.2(RNF186):c.195C>G (p.Ile65Met)	RNF186, RNF186-AS1 (I65M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2222110	NM_019062.2(RNF186):c.152G>A (p.Arg51Gln)	RNF186, RNF186-AS1 (R51Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2352442	NM_019062.2(RNF186):c.98C>G (p.Ser33Cys)	RNF186, RNF186-AS1 (S33C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2495742	NM_019062.2(RNF186):c.40T>G (p.Ser14Ala)	RNF186, RNF186-AS1 (S14A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2397129	NM_019062.2(RNF186):c.39C>G (p.Ile13Met)	RNF186, RNF186-AS1 (I13M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2331402	NM_019062.2(RNF186):c.20T>C (p.Leu7Pro)	RNF186, RNF186-AS1 (L7P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign

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Items: 23