"Ambry Genetics"[submitter] AND "GPR75"[gene] - ClinVar

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Items: 44

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3101838	NM_006794.4(GPR75):c.1618G>A (p.Val540Ile)	GPR75, GPR75-ASB3 (V540I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2473651	NM_006794.4(GPR75):c.1615T>C (p.Ser539Pro)	GPR75, GPR75-ASB3 (S539P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2366335	NM_006794.4(GPR75):c.1457A>G (p.Tyr486Cys)	GPR75, GPR75-ASB3 (Y486C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2609442	NM_006794.4(GPR75):c.1435A>C (p.Ile479Leu)	GPR75, GPR75-ASB3 (I479L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101837	NM_006794.4(GPR75):c.1433G>A (p.Arg478Gln)	GPR75, GPR75-ASB3 (R478Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2469404	NM_006794.4(GPR75):c.1427A>G (p.Asn476Ser)	GPR75, GPR75-ASB3 (N476S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101836	NM_006794.4(GPR75):c.1405C>G (p.Gln469Glu)	GPR75, GPR75-ASB3 (Q469E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101835	NM_006794.4(GPR75):c.1399T>A (p.Cys467Ser)	GPR75, GPR75-ASB3 (C467S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101834	NM_006794.4(GPR75):c.1370G>A (p.Ser457Asn)	GPR75, GPR75-ASB3 (S457N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2532761	NM_006794.4(GPR75):c.1322T>C (p.Phe441Ser)	GPR75, GPR75-ASB3 (F441S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2527843	NM_006794.4(GPR75):c.1291T>G (p.Tyr431Asp)	GPR75, GPR75-ASB3 (Y431D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2330142	NM_006794.4(GPR75):c.1265C>A (p.Ser422Tyr)	GPR75, GPR75-ASB3 (S422Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101833	NM_006794.4(GPR75):c.1223G>A (p.Arg408Gln)	GPR75, GPR75-ASB3 (R408Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2244108	NM_006794.4(GPR75):c.1214C>G (p.Thr405Ser)	GPR75, GPR75-ASB3 (T405S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2304201	NM_006794.4(GPR75):c.1094T>C (p.Ile365Thr)	GPR75, GPR75-ASB3 (I365T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2618258	NM_006794.4(GPR75):c.1093A>G (p.Ile365Val)	GPR75, GPR75-ASB3 (I365V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101832	NM_006794.4(GPR75):c.1001G>T (p.Cys334Phe)	GPR75, GPR75-ASB3 (C334F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101831	NM_006794.4(GPR75):c.1001G>A (p.Cys334Tyr)	GPR75, GPR75-ASB3 (C334Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101851	NM_006794.4(GPR75):c.977T>C (p.Ile326Thr)	GPR75, GPR75-ASB3 (I326T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101850	NM_006794.4(GPR75):c.905G>A (p.Arg302Gln)	GPR75, GPR75-ASB3 (R302Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101848	NM_006794.4(GPR75):c.670A>G (p.Met224Val)	GPR75, GPR75-ASB3 (M224V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2527144	NM_006794.4(GPR75):c.667A>C (p.Ile223Leu)	GPR75, GPR75-ASB3 (I223L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2290894	NM_006794.4(GPR75):c.665A>C (p.Tyr222Ser)	GPR75, GPR75-ASB3 (Y222S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2530863	NM_006794.4(GPR75):c.614C>A (p.Ser205Tyr)	GPR75, GPR75-ASB3 (S205Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2299093	NM_006794.4(GPR75):c.604G>A (p.Ala202Thr)	GPR75, GPR75-ASB3 (A202T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101847	NM_006794.4(GPR75):c.499C>T (p.Leu167Phe)	GPR75, GPR75-ASB3 (L167F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2337874	NM_006794.4(GPR75):c.470C>T (p.Ser157Phe)	GPR75, GPR75-ASB3 (S157F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101846	NM_006794.4(GPR75):c.461G>T (p.Arg154Leu)	GPR75, GPR75-ASB3 (R154L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2602838	NM_006794.4(GPR75):c.460C>T (p.Arg154Cys)	GPR75, GPR75-ASB3 (R154C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2391637	NM_006794.4(GPR75):c.459T>A (p.Asn153Lys)	GPR75, GPR75-ASB3 (N153K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101844	NM_006794.4(GPR75):c.433C>T (p.Arg145Trp)	GPR75, GPR75-ASB3 (R145W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101842	NM_006794.4(GPR75):c.359C>G (p.Thr120Ser)	GPR75, GPR75-ASB3 (T120S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101841	NM_006794.4(GPR75):c.276C>G (p.Phe92Leu)	GPR75, GPR75-ASB3 (F92L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101840	NM_006794.4(GPR75):c.274T>C (p.Phe92Leu)	GPR75, GPR75-ASB3 (F92L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101839	NM_006794.4(GPR75):c.226A>G (p.Arg76Gly)	GPR75, GPR75-ASB3 (R76G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2295517	NM_006794.4(GPR75):c.127G>A (p.Val43Met)	GPR75, GPR75-ASB3 (V43M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2298622	NM_006794.4(GPR75):c.67G>A (p.Glu23Lys)	GPR75, GPR75-ASB3 (E23K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101843	NM_006794.4(GPR75):c.41C>G (p.Thr14Ser)	GPR75, GPR75-ASB3 (T14S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2324137	NM_006794.4(GPR75):c.-117C>T	GPR75, GPR75-ASB3 (P32S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101853	NM_006794.4(GPR75):c.-123C>T	GPR75, GPR75-ASB3 (R30W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2403330	NM_006794.4(GPR75):c.-159G>A	GPR75, GPR75-ASB3 (G18R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2296991	NM_006794.4(GPR75):c.-167C>T	GPR75, GPR75-ASB3 (A15V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2379041	NM_006794.4(GPR75):c.-173G>A	GPR75, GPR75-ASB3 (R13Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101852	NM_006794.4(GPR75):c.-199G>A	GPR75, GPR75-ASB3 (M4I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 44