"Ambry Genetics"[submitter] AND "GPR142"[gene] - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2483922	NM_001331076.1(GPR142):c.-263G>A	GPR142 (E34K)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2338591	NM_001331076.1(GPR142):c.-162C>A	GPR142 (D67E)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2604663	NM_001331076.1(GPR142):c.-4G>A	GPR142 (G105S)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2358064	NM_001331076.1(GPR142):c.21G>A (p.Gly7=)	GPR142 (G113R)	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2374578	NM_001331076.1(GPR142):c.140G>A (p.Gly47Glu)	GPR142 (G47E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2367862	NM_001331076.1(GPR142):c.178G>A (p.Ala60Thr)	GPR142 (A148T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2553327	NM_001331076.1(GPR142):c.245G>A (p.Gly82Glu)	GPR142 (G82E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2371689	NM_001331076.1(GPR142):c.268G>A (p.Ala90Thr)	GPR142 (A90T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2393735	NM_001331076.1(GPR142):c.308C>T (p.Pro103Leu)	GPR142 (P191L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2315262	NM_001331076.1(GPR142):c.354C>G (p.Ile118Met)	GPR142 (I206M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2272964	NM_001331076.1(GPR142):c.367G>A (p.Val123Met)	GPR142 (V123M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2389725	NM_001331076.1(GPR142):c.431G>A (p.Arg144His)	GPR142 (R144H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2392373	NM_001331076.1(GPR142):c.433A>G (p.Thr145Ala)	GPR142 (T145A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2589002	NM_001331076.1(GPR142):c.439A>G (p.Asn147Asp)	GPR142 (N235D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2350607	NM_001331076.1(GPR142):c.466G>A (p.Ala156Thr)	GPR142 (A156T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2372774	NM_001331076.1(GPR142):c.481G>A (p.Ala161Thr)	GPR142 (A161T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2556365	NM_001331076.1(GPR142):c.536G>A (p.Arg179Gln)	GPR142 (R267Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2411982	NM_001331076.1(GPR142):c.541G>A (p.Ala181Thr)	GPR142 (A269T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2259892	NM_001331076.1(GPR142):c.563G>A (p.Arg188His)	GPR142 (R188H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2454373	NM_001331076.1(GPR142):c.646G>A (p.Asp216Asn)	GPR142 (D304N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2376199	NM_001331076.1(GPR142):c.752G>A (p.Arg251Gln)	GPR142 (R251Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2455130	NM_001331076.1(GPR142):c.788G>A (p.Arg263Gln)	GPR142 (R351Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2400411	NM_001331076.1(GPR142):c.956C>T (p.Thr319Met)	GPR142 (T319M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2322698	NM_001331076.1(GPR142):c.965A>G (p.Asn322Ser)	GPR142 (N322S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2276605	NM_001331076.1(GPR142):c.970G>T (p.Gly324Cys)	GPR142 (G412C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2460604	NM_001331076.1(GPR142):c.1013G>A (p.Arg338Gln)	GPR142 (R338Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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Items: 26