Related gene-specific medical variations for Gene (Select 2850) - ClinVar - NCBI

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Links from Gene

Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3282366	NM_018971.3(GPR27):c.20C>T (p.Pro7Leu)	EIF4E3, GPR27 (P7L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3282364	NM_018971.3(GPR27):c.232G>A (p.Ala78Thr)	EIF4E3, GPR27 (A78T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3101697	NM_018971.3(GPR27):c.250G>T (p.Ala84Ser)	EIF4E3, GPR27 (A84S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2619983	NM_018971.3(GPR27):c.202G>A (p.Ala68Thr)	EIF4E3, GPR27 (A68T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2614316	NM_018971.3(GPR27):c.268C>G (p.Pro90Ala)	EIF4E3, GPR27 (P90A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2606421	NM_018971.3(GPR27):c.718G>A (p.Ala240Thr)	EIF4E3, GPR27 (A240T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2555393	NM_018971.3(GPR27):c.495C>G (p.Asp165Glu)	EIF4E3, GPR27 (D165E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517350	NM_018971.3(GPR27):c.530C>A (p.Pro177His)	EIF4E3, GPR27 (P177H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2471634	NM_018971.3(GPR27):c.691G>A (p.Gly231Ser)	EIF4E3, GPR27 (G231S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2383384	NM_018971.3(GPR27):c.136G>A (p.Glu46Lys)	EIF4E3, GPR27 (E46K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2260301	NM_018971.3(GPR27):c.656T>C (p.Leu219Pro)	EIF4E3, GPR27 (L219P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2248818	NM_018971.3(GPR27):c.18G>T (p.Glu6Asp)	EIF4E3, GPR27 (E6D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance