"Ambry Genetics"[submitter] AND "GPR150"[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 34

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2309538	NM_199243.3(GPR150):c.9T>G (p.Asp3Glu)	GPR150 (D3E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101473	NM_199243.3(GPR150):c.41C>T (p.Pro14Leu)	GPR150 (P14L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101475	NM_199243.3(GPR150):c.46A>G (p.Ile16Val)	GPR150 (I16V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300583	NM_199243.3(GPR150):c.98G>A (p.Gly33Glu)	GPR150 (G33E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282244	NM_199243.3(GPR150):c.151G>C (p.Val51Leu)	GPR150 (V51L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101471	NM_199243.3(GPR150):c.151G>A (p.Val51Ile)	GPR150 (V51I)	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 2356016	NM_199243.3(GPR150):c.383T>C (p.Leu128Pro)	GPR150, LOC129994226 (L128P)	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 2281909	NM_199243.3(GPR150):c.478C>T (p.Pro160Ser)	GPR150, LOC129994226 (P160S)	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 3282245	NM_199243.3(GPR150):c.491T>G (p.Leu164Arg)	GPR150, LOC129994226 (L164R)	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 3101476	NM_199243.3(GPR150):c.526G>A (p.Ala176Thr)	GPR150, LOC129994226 (A176T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382849	NM_199243.3(GPR150):c.584C>T (p.Pro195Leu)	GPR150 (P195L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299374	NM_199243.3(GPR150):c.587C>T (p.Pro196Leu)	GPR150 (P196L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101477	NM_199243.3(GPR150):c.622G>T (p.Ala208Ser)	GPR150 (A208S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282247	NM_199243.3(GPR150):c.628G>C (p.Ala210Pro)	GPR150 (A210P)	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 2512397	NM_199243.3(GPR150):c.805G>A (p.Ala269Thr)	GPR150, LOC123497940 (A269T)	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 2551595	NM_199243.3(GPR150):c.994G>A (p.Gly332Ser)	GPR150, LOC123497940 (G332S)	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 2537123	NM_199243.3(GPR150):c.1111G>T (p.Gly371Cys)	GPR150, LOC123497940 (G371C)	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 2223668	NM_199243.3(GPR150):c.1169A>C (p.His390Pro)	GPR150 (H390P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101470	NM_199243.3(GPR150):c.1183C>T (p.Arg395Cys)	GPR150 (R395C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282246	NM_199243.3(GPR150):c.1236C>G (p.Asp412Glu)	GPR150 (D412E)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2308089	NM_199243.3(GPR150):c.1244G>A (p.Gly415Asp)	GPR150 (G415D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347786	NM_199243.3(GPR150):c.1282T>G (p.Cys428Gly)	GPR150 (C428G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402654	NM_199243.3(GPR150):c.1290C>G (p.Cys430Trp)	GPR150 (C430W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 34