SEMA4G[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 708988	NM_017893.4(SEMA4G):c.39C>T (p.Leu13=)	SEMA4G	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2558787	NM_017893.4(SEMA4G):c.50C>A (p.Ala17Glu)	SEMA4G (A17E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2458041	NM_017893.4(SEMA4G):c.115C>T (p.Pro39Ser)	SEMA4G (P39S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2238460	NM_017893.4(SEMA4G):c.151G>A (p.Gly51Ser)	SEMA4G (G51S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2274365	NM_017893.4(SEMA4G):c.158C>T (p.Ala53Val)	SEMA4G (A53V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2608997	NM_017893.4(SEMA4G):c.205C>A (p.Leu69Met)	SEMA4G (L69M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3159840	NM_017893.4(SEMA4G):c.214G>A (p.Ala72Thr)	SEMA4G (A72T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3159841	NM_017893.4(SEMA4G):c.218G>A (p.Arg73Gln)	SEMA4G (R73Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2265315	NM_017893.4(SEMA4G):c.247G>T (p.Asp83Tyr)	SEMA4G (D83Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2568911	NM_017893.4(SEMA4G):c.266A>G (p.His89Arg)	SEMA4G (H89R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2368357	NM_017893.4(SEMA4G):c.318A>C (p.Gln106His)	SEMA4G (Q106H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2319957	NM_017893.4(SEMA4G):c.352C>T (p.His118Tyr)	SEMA4G (H118Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2338440	NM_017893.4(SEMA4G):c.358C>T (p.Arg120Trp)	SEMA4G (R120W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3159844	NM_017893.4(SEMA4G):c.371G>A (p.Arg124Gln)	SEMA4G (R124Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3159845	NM_017893.4(SEMA4G):c.382A>G (p.Thr128Ala)	SEMA4G (T128A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2485794	NM_017893.4(SEMA4G):c.406C>G (p.His136Asp)	SEMA4G (H136D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3159846	NM_017893.4(SEMA4G):c.434T>C (p.Ile145Thr)	SEMA4G (I145T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance