Related gene-specific medical variations for Gene (Select 9248) - ClinVar - NCBI

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

Links from Gene

Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3522078	NM_004224.3(GPR50):c.133G>C (p.Gly45Arg)	GPR50, GPR50-AS1 (G45R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3522070	NM_004224.3(GPR50):c.116T>C (p.Ile39Thr)	GPR50, GPR50-AS1 (I39T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3282408	NM_004224.3(GPR50):c.145G>T (p.Val49Phe)	GPR50, GPR50-AS1 (V49F)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3101784	NM_004224.3(GPR50):c.61C>G (p.Pro21Ala)	GPR50, GPR50-AS1 (P21A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603759	NM_004224.3(GPR50):c.17C>T (p.Ala6Val)	GPR50, GPR50-AS1 (A6V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594921	NM_004224.3(GPR50):c.98G>C (p.Cys33Ser)	GPR50, GPR50-AS1 (C33S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2527796	NM_004224.3(GPR50):c.168C>G (p.Asn56Lys)	GPR50, GPR50-AS1 (N56K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507601	NM_004224.3(GPR50):c.179G>A (p.Arg60Gln)	GPR50, GPR50-AS1 (R60Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457416	NM_004224.3(GPR50):c.92T>C (p.Met31Thr)	GPR50, GPR50-AS1 (M31T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2250136	NM_004224.3(GPR50):c.55C>T (p.Pro19Ser)	GPR50, GPR50-AS1 (P19S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1206241	NM_004224.3(GPR50):c.178C>T (p.Arg60Trp)	GPR50-AS1, GPR50 (R60W)	Single nucleotide variant (missense variant)	not provided	GLikely benign