ClinVar for Gene (Select 53831) - ClinVar

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Links from Gene

Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3282458	NM_020370.3(GPR84):c.724G>C (p.Asp242His)	GPR84, GPR84-AS1 (D242H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282457	NM_020370.3(GPR84):c.944G>A (p.Gly315Glu)	GPR84, GPR84-AS1 (G315E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282455	NM_020370.3(GPR84):c.514C>T (p.Arg172Cys)	GPR84, GPR84-AS1 (R172C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101883	NM_020370.3(GPR84):c.709C>T (p.Arg237Cys)	GPR84, GPR84-AS1 (R237C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101881	NM_020370.3(GPR84):c.623C>T (p.Ala208Val)	GPR84, GPR84-AS1 (A208V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101880	NM_020370.3(GPR84):c.526C>T (p.Arg176Trp)	GPR84, GPR84-AS1 (R176W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101879	NM_020370.3(GPR84):c.496T>C (p.Cys166Arg)	GPR84, GPR84-AS1 (C166R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101878	NM_020370.3(GPR84):c.172C>T (p.Leu58Phe)	GPR84, GPR84-AS1 (L58F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101877	NM_020370.3(GPR84):c.1010T>C (p.Leu337Pro)	GPR84, GPR84-AS1 (L337P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2684674	GRCh37/hg19 12q13.13(chr12:54429002-54898430)x3	CBX5, COPZ1 +11 more	Copy number gain	not provided	GUncertain significance
Select item 2607919	NM_020370.3(GPR84):c.914G>C (p.Arg305Thr)	GPR84, GPR84-AS1 (R305T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549451	NM_020370.3(GPR84):c.25T>C (p.Phe9Leu)	GPR84, GPR84-AS1 (F9L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525561	NM_020370.3(GPR84):c.608G>A (p.Arg203His)	GPR84, GPR84-AS1 (R203H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493775	NM_020370.3(GPR84):c.646A>C (p.Lys216Gln)	GPR84, GPR84-AS1 (K216Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376358	NM_020370.3(GPR84):c.761T>C (p.Ile254Thr)	GPR84, GPR84-AS1 (I254T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345836	NM_020370.3(GPR84):c.653G>A (p.Arg218Gln)	GPR84, GPR84-AS1 (R218Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286378	NM_020370.3(GPR84):c.1042C>T (p.Pro348Ser)	GPR84, GPR84-AS1 (P348S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256145	NM_020370.3(GPR84):c.1045C>T (p.Arg349Trp)	GPR84, GPR84-AS1 (R349W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231543	NM_020370.3(GPR84):c.568G>C (p.Gly190Arg)	GPR84, GPR84-AS1 (G190R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222483	NM_020370.3(GPR84):c.490G>A (p.Val164Ile)	GPR84, GPR84-AS1 (V164I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213148	NM_020370.3(GPR84):c.83T>G (p.Val28Gly)	GPR84, GPR84-AS1 (V28G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 441984	GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)	SLC15A5, SLC16A7 +1006 more	Copy number gain	See cases	GPathogenic
Select item 441983	GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)x3	A2M, A2ML1 +1006 more	Copy number gain	See cases	GPathogenic
Select item 268075	GRCh37/hg19 12p13.33-q24.33(chr12:1-133851895)x3	GALNT8, H2AJ +1007 more	Copy number gain	See cases	GPathogenic
Select item 152934	GRCh38/hg38 12q13.13-13.3(chr12:53420606-56202942)x3	PMEL, PPP1R1A +219 more	Copy number gain	See cases	GPathogenic
Select item 150740	GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3	FERRY3, FGD4 +4837 more	Copy number gain	See cases	GPathogenic

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Links from Gene

Items: 26