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

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2380555	NM_004494.3(HDGF):c.709C>T (p.His237Tyr)	HDGF (H205Y +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3104681	NM_004494.3(HDGF):c.646G>A (p.Glu216Lys)	HDGF (E184K +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3104680	NM_004494.3(HDGF):c.635A>G (p.Gln212Arg)	HDGF (Q205R +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2510891	NM_004494.3(HDGF):c.623G>A (p.Arg208Gln)	HDGF (R176Q +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2210382	NM_004494.3(HDGF):c.622C>T (p.Arg208Trp)	HDGF (R176W +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3104679	NM_004494.3(HDGF):c.571C>T (p.Leu191Phe)	HDGF (L159F +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2590669	NM_004494.3(HDGF):c.569C>G (p.Pro190Arg)	HDGF (P190R +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3283722	NM_004494.3(HDGF):c.484C>A (p.Leu162Met)	HDGF (L155M +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2396518	NM_004494.3(HDGF):c.418G>T (p.Val140Phe)	HDGF (V108F +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3283724	NM_004494.3(HDGF):c.367G>C (p.Gly123Arg)	HDGF (G146R +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3104678	NM_004494.3(HDGF):c.323G>C (p.Cys108Ser)	HDGF (C108S +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3283723	NM_004494.3(HDGF):c.313A>C (p.Lys105Gln)	HDGF (K98Q +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2236793	NM_004494.3(HDGF):c.299A>G (p.Tyr100Cys)	HDGF (Y100C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3104677	NM_004494.3(HDGF):c.250G>A (p.Glu84Lys)	HDGF (E100K +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2241039	NM_004494.3(HDGF):c.129C>A (p.Asn43Lys)	HDGF (N43K +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2252744	NM_001126050.2(HDGF):c.132T>A (p.His44Gln)	HDGF (H44Q)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign