GPR89B[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3101898	NM_016334.5(GPR89B):c.104T>C (p.Ile35Thr)	GPR89B (I10T +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2360005	NM_016334.5(GPR89B):c.107G>A (p.Arg36His)	GPR89B (R36H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2213626	NM_016334.5(GPR89B):c.121C>G (p.Gln41Glu)	GPR89B (Q41E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2411788	NM_016334.5(GPR89B):c.140C>T (p.Thr47Met)	GPR89B (T22M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2472789	NM_016334.5(GPR89B):c.246T>G (p.Ile82Met)	GPR89B (I57M +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2249249	NM_016334.5(GPR89B):c.266T>C (p.Met89Thr)	GPR89B (M64T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2553532	NM_016334.5(GPR89B):c.301A>G (p.Asn101Asp)	GPR89B (N101D +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2295121	NM_016334.5(GPR89B):c.326G>A (p.Arg109Gln)	GPR89B (R84Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2237209	NM_016334.5(GPR89B):c.337T>C (p.Ser113Pro)	GPR89B (S113P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 394965	GRCh37/hg19 1q21.2(chr1:147394188-147424808)x3	GPR89B	Copy number gain	See cases	GBenign