Related gene-specific medical variations for Gene (Select 285601) - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3282245	NM_199243.3(GPR150):c.491T>G (p.Leu164Arg)	GPR150, LOC129994226 (L164R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101479	NM_199243.3(GPR150):c.863G>A (p.Arg288His)	GPR150, LOC123497940 (R288H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101478	NM_199243.3(GPR150):c.692T>G (p.Val231Gly)	GPR150, LOC129994227 (V231G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101476	NM_199243.3(GPR150):c.526G>A (p.Ala176Thr)	GPR150, LOC129994226 (A176T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101474	NM_199243.3(GPR150):c.442C>T (p.Arg148Trp)	GPR150, LOC129994226 (R148W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101472	NM_199243.3(GPR150):c.374T>G (p.Leu125Arg)	GPR150, LOC129994226 (L125R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101469	NM_199243.3(GPR150):c.1150G>C (p.Glu384Gln)	GPR150, LOC123497940 (E384Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101468	NM_199243.3(GPR150):c.1026G>A (p.Met342Ile)	GPR150, LOC123497940 (M342I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592241	NM_199243.3(GPR150):c.1082G>A (p.Arg361Gln)	GPR150, LOC123497940 (R361Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2552891	NM_199243.3(GPR150):c.1109T>G (p.Leu370Arg)	GPR150, LOC123497940 (L370R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551595	NM_199243.3(GPR150):c.994G>A (p.Gly332Ser)	GPR150, LOC123497940 (G332S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537123	NM_199243.3(GPR150):c.1111G>T (p.Gly371Cys)	GPR150, LOC123497940 (G371C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512397	NM_199243.3(GPR150):c.805G>A (p.Ala269Thr)	GPR150, LOC123497940 (A269T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494730	NM_199243.3(GPR150):c.503G>A (p.Gly168Asp)	GPR150, LOC129994226 (G168D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356016	NM_199243.3(GPR150):c.383T>C (p.Leu128Pro)	GPR150, LOC129994226 (L128P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326644	NM_199243.3(GPR150):c.485G>A (p.Arg162His)	GPR150, LOC129994226 (R162H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311106	NM_199243.3(GPR150):c.488C>A (p.Ala163Asp)	GPR150, LOC129994226 (A163D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281909	NM_199243.3(GPR150):c.478C>T (p.Pro160Ser)	GPR150, LOC129994226 (P160S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance