ClinVar for Gene (Select 100128811) - ClinVar

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Links from Gene

Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3282294	NM_020752.3(GPR158):c.755G>T (p.Arg252Leu)	GPR158, GPR158-AS1 (R252L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3282293	NM_020752.3(GPR158):c.301G>A (p.Gly101Ser)	GPR158, GPR158-AS1 (G101S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3282292	NM_020752.3(GPR158):c.368A>G (p.His123Arg)	GPR158, GPR158-AS1 (H123R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3282290	NM_020752.3(GPR158):c.107G>C (p.Arg36Pro)	GPR158, GPR158-AS1 (R36P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282286	NM_020752.3(GPR158):c.328G>T (p.Gly110Trp)	GPR158, GPR158-AS1 (G110W)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3101569	NM_020752.3(GPR158):c.800C>T (p.Pro267Leu)	GPR158, GPR158-AS1 (P267L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3101568	NM_020752.3(GPR158):c.412G>A (p.Val138Met)	GPR158, GPR158-AS1 (V138M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 3101567	NM_020752.3(GPR158):c.380A>T (p.Asp127Val)	GPR158, GPR158-AS1 (D127V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3101561	NM_020752.3(GPR158):c.269A>C (p.Asp90Ala)	GPR158, GPR158-AS1 (D90A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3101555	NM_020752.3(GPR158):c.146C>T (p.Pro49Leu)	GPR158, GPR158-AS1 (P49L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2640360	NM_020752.3(GPR158):c.849T>C (p.Val283=)	GPR158, GPR158-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
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)	not specified	GLikely benign
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)	not specified	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)	not specified	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)	not specified	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)	not specified	GUncertain significance
Select item 2330434	NM_020752.3(GPR158):c.328G>A (p.Gly110Arg)	GPR158, GPR158-AS1 (G110R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2298782	NM_020752.3(GPR158):c.556C>G (p.Pro186Ala)	GPR158, GPR158-AS1 (P186A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2276088	NM_020752.3(GPR158):c.410A>G (p.Asn137Ser)	GPR158, GPR158-AS1 (N137S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2267021	NM_020752.3(GPR158):c.712G>A (p.Gly238Ser)	GPR158, GPR158-AS1 (G238S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2255893	NM_020752.3(GPR158):c.116C>T (p.Thr39Ile)	GPR158, GPR158-AS1 (T39I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219199	NM_020752.3(GPR158):c.584C>T (p.Thr195Met)	GPR158, GPR158-AS1 (T195M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2209845	NM_020752.3(GPR158):c.170C>T (p.Ser57Phe)	GPR158, GPR158-AS1 (S57F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 152998	GRCh38/hg38 10p15.1-q11.22(chr10:4604734-48074662)x3	ABI1, ACBD5 +1221 more	Copy number gain	See cases	GBenign
Select item 150600	GRCh38/hg38 10p12.31-11.22(chr10:19088161-32732293)x3	ABI1, ACBD5 +376 more	Copy number gain	See cases	GLikely pathogenic
Select item 149407	GRCh38/hg38 10p15.3-12.1(chr10:90205-26339978)x3	ACBD7, ACBD7-DCLRE1CP1 +837 more	Copy number gain	See cases	GPathogenic
Select item 144415	GRCh38/hg38 10p12.2-12.1(chr10:24111341-25350640)x1	GPR158-AS1, KIAA1217 +35 more	Copy number loss	See cases	GPathogenic

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Links from Gene

Items: 27