"Ambry Genetics"[submitter] AND "ADGRG3"[gene] - ClinVar

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Items: 35

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2205966	NM_170776.5(ADGRG3):c.50C>T (p.Pro17Leu)	ADGRG3 (P17L)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2380433	NM_170776.5(ADGRG3):c.118G>A (p.Asp40Asn)	ADGRG3 (D40N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2330409	NM_170776.5(ADGRG3):c.137A>G (p.Asp46Gly)	ADGRG3 (D46G)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2339793	NM_170776.5(ADGRG3):c.138C>G (p.Asp46Glu)	ADGRG3 (D46E)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2557751	NM_170776.5(ADGRG3):c.154A>G (p.Thr52Ala)	ADGRG3 (T52A)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2378836	NM_170776.5(ADGRG3):c.163A>G (p.Arg55Gly)	ADGRG3 (R55G)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2473957	NM_170776.5(ADGRG3):c.178G>A (p.Asp60Asn)	ADGRG3 (D60N)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2227659	NM_170776.5(ADGRG3):c.314A>G (p.Glu105Gly)	ADGRG3 (E105G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2286324	NM_170776.5(ADGRG3):c.350C>T (p.Pro117Leu)	ADGRG3 (P117L)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2459823	NM_170776.5(ADGRG3):c.370G>A (p.Glu124Lys)	ADGRG3 (E124K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2257314	NM_170776.5(ADGRG3):c.406A>T (p.Ser136Cys)	ADGRG3 (S16C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2338405	NM_170776.5(ADGRG3):c.424C>T (p.Pro142Ser)	ADGRG3 (P22S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2341757	NM_170776.5(ADGRG3):c.446G>A (p.Arg149His)	ADGRG3 (R29H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2281031	NM_170776.5(ADGRG3):c.500G>A (p.Arg167Gln)	ADGRG3 (R167Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2477100	NM_170776.5(ADGRG3):c.506G>T (p.Gly169Val)	ADGRG3 (G169V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2527040	NM_170776.5(ADGRG3):c.523G>A (p.Gly175Ser)	ADGRG3 (G55S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2388257	NM_170776.5(ADGRG3):c.539G>A (p.Arg180His)	ADGRG3 (R60H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2568524	NM_170776.5(ADGRG3):c.554G>A (p.Ser185Asn)	ADGRG3 (S65N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2463090	NM_170776.5(ADGRG3):c.704C>A (p.Thr235Lys)	ADGRG3 (T235K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2456482	NM_170776.5(ADGRG3):c.724A>T (p.Thr242Ser)	ADGRG3 (T122S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2219178	NM_170776.5(ADGRG3):c.757G>A (p.Ala253Thr)	ADGRG3 (A133T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2368533	NM_170776.5(ADGRG3):c.760C>A (p.Leu254Met)	ADGRG3 (L134M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2311372	NM_170776.5(ADGRG3):c.832G>A (p.Val278Ile)	ADGRG3 (V158I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2240067	NM_170776.5(ADGRG3):c.839T>C (p.Met280Thr)	ADGRG3 (M160T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2238303	NM_170776.5(ADGRG3):c.992C>T (p.Ser331Leu)	ADGRG3 (S331L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2294924	NM_170776.5(ADGRG3):c.1021C>T (p.Arg341Trp)	ADGRG3 (R341W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2383968	NM_170776.5(ADGRG3):c.1022G>C (p.Arg341Pro)	ADGRG3 (R221P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2330408	NM_170776.5(ADGRG3):c.1153G>A (p.Val385Met)	ADGRG3 (V265M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2591729	NM_170776.5(ADGRG3):c.1303G>A (p.Val435Ile)	ADGRG3 (V315I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2291628	NM_170776.5(ADGRG3):c.1312T>C (p.Tyr438His)	ADGRG3 (Y318H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2595581	NM_170776.5(ADGRG3):c.1406G>A (p.Arg469Gln)	ADGRG3 (R349Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2365159	NM_170776.5(ADGRG3):c.1448C>T (p.Ser483Leu)	ADGRG3 (S483L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2617586	NM_170776.5(ADGRG3):c.1507G>A (p.Val503Ile)	ADGRG3 (V503I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2207146	NM_170776.5(ADGRG3):c.1582A>G (p.Ser528Gly)	ADGRG3 (S528G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2460611	NM_170776.5(ADGRG3):c.1636G>A (p.Ala546Thr)	ADGRG3 (A426T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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Items: 35