ClinVar for Gene (Select 123497940) - ClinVar - NCBI

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Links from Gene

Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 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 155679	GRCh38/hg38 5q14.3-31.1(chr5:91411708-131319563)x1	LOC129994229, LOC129994230 +688 more	Copy number loss	See cases	GPathogenic
Select item 155182	GRCh38/hg38 5q15-22.2(chr5:93193104-113287795)x1	LOC129994289, LOC129994290 +342 more	Copy number loss	See cases	GPathogenic
Select item 152734	GRCh38/hg38 5q14.3-23.1(chr5:92899734-119614119)x1	LOC129994369, LOC129994370 +495 more	Copy number loss	See cases	GPathogenic
Select item 151143	GRCh38/hg38 5q14.3-23.3(chr5:90374606-128076423)x1	ADGRV1, ALDH7A1 +682 more	Copy number loss	See cases	GPathogenic
Select item 150860	GRCh38/hg38 5q14.3-22.1(chr5:84603580-111435081)x1	ADGRV1, ARB2A +435 more	Copy number loss	See cases	GPathogenic
Select item 150147	GRCh38/hg38 5q15(chr5:94902711-95930059)x3	ARSK, ELL2 +41 more	Copy number gain	See cases	GLikely benign
Select item 59667	GRCh38/hg38 5q14.3-15(chr5:91386552-98365880)x1	ARB2A, ARRDC3-AS1 +146 more	Copy number loss	See cases	GPathogenic
Select item 59664	GRCh38/hg38 5q14.3-21.2(chr5:89081352-104687248)x1	ADGRV1, ARB2A +274 more	Copy number loss	See cases	GPathogenic
Select item 59443	GRCh38/hg38 5q15(chr5:93405010-97716265)x3	ARB2A, ARSK +119 more	Copy number gain	See cases	GUncertain significance
Select item 58096	GRCh38/hg38 5q13.3-22.1(chr5:74163186-110809453)x3	ENC1, ERAP1 +690 more	Copy number gain	See cases	GPathogenic
Select item 57272	GRCh38/hg38 5q14.3-21.1(chr5:87376883-101524443)x1	ADGRV1, ARB2A +276 more	Copy number loss	See cases	GPathogenic