"Ambry Genetics"[submitter] AND "HOXA9"[gene] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2255958	NM_152739.4(HOXA9):c.786G>C (p.Lys262Asn)	LOC107197952, HOXA9 +1 more (K262N)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2366041	NM_152739.4(HOXA9):c.722G>T (p.Arg241Leu)	LOC107197952, HOXA10-HOXA9 +1 more (R241L)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2235254	NM_152739.4(HOXA9):c.713A>C (p.Glu238Ala)	HOXA10-HOXA9, LOC107197952 +1 more (E238A)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2459550	NM_152739.4(HOXA9):c.601C>T (p.Leu201Phe)	HOXA10-HOXA9, HOXA9 +1 more (L201F)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2319586	NM_152739.4(HOXA9):c.582T>A (p.Asn194Lys)	HOXA10-HOXA9, LOC107197952 +1 more (N194K)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2408736	NM_152739.4(HOXA9):c.565C>A (p.Pro189Thr)	HOXA10-HOXA9, LOC107197952 +1 more (P189T)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2554163	NM_152739.4(HOXA9):c.551G>A (p.Ser184Asn)	HOXA10-HOXA9, HOXA9 +1 more (S184N)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2345683	NM_152739.4(HOXA9):c.470A>G (p.Tyr157Cys)	LOC107197952, HOXA10-HOXA9 +1 more (Y157C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2517390	NM_152739.4(HOXA9):c.413C>T (p.Ser138Leu)	HOXA10-HOXA9, HOXA9 +1 more (S138L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2555835	NM_152739.4(HOXA9):c.359C>A (p.Ser120Tyr)	HOXA10-HOXA9, HOXA9 +1 more (S120Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2385577	NM_152739.4(HOXA9):c.346C>A (p.Pro116Thr)	HOXA10-HOXA9, LOC107197952 +1 more (P116T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2272368	NM_152739.4(HOXA9):c.296C>T (p.Ala99Val)	HOXA9, LOC107197952 +1 more (A99V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2208523	NM_152739.4(HOXA9):c.289C>T (p.Pro97Ser)	HOXA10-HOXA9, HOXA9 +1 more (P97S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2407929	NM_152739.4(HOXA9):c.193G>A (p.Ala65Thr)	HOXA10-HOXA9, LOC107197952 +1 more (A65T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2556609	NM_152739.4(HOXA9):c.185T>G (p.Val62Gly)	HOXA10-HOXA9, HOXA9 +1 more (V62G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2557021	NM_152739.4(HOXA9):c.125C>G (p.Ala42Gly)	HOXA10-HOXA9, HOXA9 +1 more (A42G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2298559	NM_152739.4(HOXA9):c.118C>G (p.Arg40Gly)	HOXA10-HOXA9, HOXA9 +1 more (R40G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2281910	NM_152739.4(HOXA9):c.101C>T (p.Thr34Ile)	LOC107197952, HOXA10-HOXA9 +1 more (T34I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2220785	NM_152739.4(HOXA9):c.97G>T (p.Gly33Trp)	LOC107197952, HOXA9 +1 more (G33W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2240286	NM_152739.4(HOXA9):c.79G>A (p.Val27Ile)	HOXA9, HOXA10-HOXA9 +1 more (V27I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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Items: 20