"Ambry Genetics"[submitter] AND "GPR158"[gene] - ClinVar

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Items: 42

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2255893	NM_020752.3(GPR158):c.116C>T (p.Thr39Ile)	GPR158-AS1, GPR158 (T39I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2209845	NM_020752.3(GPR158):c.170C>T (p.Ser57Phe)	GPR158-AS1, GPR158 (S57F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2518643	NM_020752.3(GPR158):c.287G>A (p.Arg96Gln)	GPR158, GPR158-AS1 (R96Q)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2330434	NM_020752.3(GPR158):c.328G>A (p.Gly110Arg)	GPR158-AS1, GPR158 (G110R)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2395119	NM_020752.3(GPR158):c.341C>T (p.Ala114Val)	GPR158, GPR158-AS1 (A114V)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2494122	NM_020752.3(GPR158):c.385C>A (p.Leu129Met)	GPR158, GPR158-AS1 (L129M)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2276088	NM_020752.3(GPR158):c.410A>G (p.Asn137Ser)	GPR158-AS1, GPR158 (N137S)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2616115	NM_020752.3(GPR158):c.484T>C (p.Trp162Arg)	GPR158, GPR158-AS1 (W162R)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2298782	NM_020752.3(GPR158):c.556C>G (p.Pro186Ala)	GPR158-AS1, GPR158 (P186A)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2354969	NM_020752.3(GPR158):c.566A>T (p.Gln189Leu)	GPR158, GPR158-AS1 (Q189L)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2219199	NM_020752.3(GPR158):c.584C>T (p.Thr195Met)	GPR158-AS1, GPR158 (T195M)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2267021	NM_020752.3(GPR158):c.712G>A (p.Gly238Ser)	GPR158-AS1, GPR158 (G238S)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2245860	NM_020752.3(GPR158):c.860C>T (p.Ser287Phe)	GPR158 (S287F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2387143	NM_020752.3(GPR158):c.962A>G (p.Asp321Gly)	GPR158 (D321G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2398013	NM_020752.3(GPR158):c.1036G>A (p.Val346Ile)	GPR158 (V346I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2380794	NM_020752.3(GPR158):c.1342C>T (p.Arg448Trp)	GPR158 (R448W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2207617	NM_020752.3(GPR158):c.1480A>G (p.Thr494Ala)	GPR158 (T494A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2309278	NM_020752.3(GPR158):c.1510C>T (p.His504Tyr)	GPR158 (H504Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2552348	NM_020752.3(GPR158):c.1627G>A (p.Gly543Ser)	GPR158 (G543S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2515781	NM_020752.3(GPR158):c.1679G>A (p.Gly560Asp)	GPR158 (G560D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2232689	NM_020752.3(GPR158):c.1699C>T (p.His567Tyr)	GPR158 (H567Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2527345	NM_020752.3(GPR158):c.1712A>G (p.Asn571Ser)	GPR158 (N571S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2491035	NM_020752.3(GPR158):c.1724T>C (p.Ile575Thr)	GPR158 (I575T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2258914	NM_020752.3(GPR158):c.1940A>G (p.Tyr647Cys)	GPR158 (Y647C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2402791	NM_020752.3(GPR158):c.1976T>C (p.Ile659Thr)	GPR158 (I659T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2457857	NM_020752.3(GPR158):c.2299C>T (p.Arg767Trp)	GPR158 (R767W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2255240	NM_020752.3(GPR158):c.2429G>A (p.Arg810Gln)	GPR158 (R810Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2290140	NM_020752.3(GPR158):c.2483C>G (p.Thr828Arg)	GPR158 (T828R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2285005	NM_020752.3(GPR158):c.2489A>C (p.Glu830Ala)	GPR158 (E830A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2599846	NM_020752.3(GPR158):c.2558C>T (p.Ser853Leu)	GPR158 (S853L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2261571	NM_020752.3(GPR158):c.2716A>G (p.Ile906Val)	GPR158 (I906V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2226024	NM_020752.3(GPR158):c.2782C>T (p.Arg928Cys)	GPR158 (R928C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2542942	NM_020752.3(GPR158):c.2783G>A (p.Arg928His)	GPR158 (R928H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2314963	NM_020752.3(GPR158):c.2795A>G (p.Gln932Arg)	GPR158 (Q932R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2460042	NM_020752.3(GPR158):c.3103G>A (p.Glu1035Lys)	GPR158 (E1035K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2292369	NM_020752.3(GPR158):c.3239C>T (p.Ser1080Phe)	GPR158 (S1080F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2492431	NM_020752.3(GPR158):c.3386C>T (p.Thr1129Ile)	GPR158 (T1129I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2623845	NM_020752.3(GPR158):c.3408A>C (p.Gln1136His)	GPR158 (Q1136H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2412322	NM_020752.3(GPR158):c.3410T>C (p.Ile1137Thr)	GPR158 (I1137T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2454838	NM_020752.3(GPR158):c.3458G>A (p.Gly1153Asp)	GPR158 (G1153D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2209776	NM_020752.3(GPR158):c.3538G>C (p.Ala1180Pro)	GPR158 (A1180P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2281671	NM_020752.3(GPR158):c.3577T>A (p.Ser1193Thr)	GPR158 (S1193T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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Items: 42