Related gene-specific medical variations for Gene (Select 5281) - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3314226	NM_012249.4(RHOQ):c.614C>T (p.Thr205Met)	PIGF, RHOQ (T205M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3212785	NM_002643.4(PIGF):c.656A>G (p.Asn219Ser)	PIGF, RHOQ (N219S)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3154090	NM_012249.4(RHOQ):c.563A>T (p.His188Leu)	PIGF, RHOQ (H188L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2510910	NM_002643.4(PIGF):c.619A>T (p.Ile207Leu)	PIGF, RHOQ (I207L)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2510909	NM_002643.4(PIGF):c.618G>T (p.Trp206Cys)	PIGF, RHOQ (W206C)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2307426	NM_002643.4(PIGF):c.589G>A (p.Val197Met)	PIGF, RHOQ (V197M)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2298975	NM_012249.4(RHOQ):c.560A>G (p.Lys187Arg)	PIGF, RHOQ (K187R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2245826	NM_012249.4(RHOQ):c.482T>C (p.Val161Ala)	PIGF, RHOQ (V161A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2209631	NM_002643.4(PIGF):c.654C>A (p.Asn218Lys)	PIGF, RHOQ (N218K)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance