HOXD4[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 729793	NM_014621.3(HOXD4):c.64G>A (p.Glu22Lys)	HOXD4 (E22K)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3106750	NM_014621.3(HOXD4):c.91G>C (p.Glu31Gln)	HOXD4 (E31Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300158	NM_014621.3(HOXD4):c.98G>A (p.Gly33Asp)	HOXD4 (G33D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342113	NM_014621.3(HOXD4):c.113G>A (p.Gly38Asp)	HOXD4 (G38D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 775792	NM_014621.3(HOXD4):c.135C>T (p.Asp45=)	HOXD4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2397817	NM_014621.3(HOXD4):c.143C>A (p.Pro48His)	HOXD4 (P48H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346108	NM_014621.3(HOXD4):c.160C>T (p.Arg54Trp)	HOXD4 (R54W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293045	NM_014621.3(HOXD4):c.175G>A (p.Glu59Lys)	HOXD4 (E59K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 14888	NM_014621.3(HOXD4):c.242A>T (p.Glu81Val)	HOXD4 (E81V)	Single nucleotide variant (missense variant)	Leukemia, acute lymphoblastic, susceptibility to	GUncertain significance
Select item 2373823	NM_014621.3(HOXD4):c.274C>A (p.Pro92Thr)	HOXD4 (P92T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601646	NM_014621.3(HOXD4):c.311C>A (p.Pro104Gln)	HOXD4 (P104Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106747	NM_014621.3(HOXD4):c.349G>C (p.Asp117His)	HOXD4 (D117H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106748	NM_014621.3(HOXD4):c.400T>C (p.Tyr134His)	HOXD4 (Y134H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 791157	NM_014621.3(HOXD4):c.433+6G>T	HOXD4	Single nucleotide variant (intron variant)	not provided	GBenign