"Ambry Genetics"[submitter] AND "HOXB-AS1"[gene] - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2248996	NM_002145.4(HOXB2):c.335C>T (p.Thr112Met)	HOXB-AS1, HOXB2 (T112M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2273752	NM_002145.4(HOXB2):c.263C>T (p.Ala88Val)	HOXB2, HOXB-AS1 (A88V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2540810	NM_002145.4(HOXB2):c.181T>C (p.Ser61Pro)	HOXB-AS1, HOXB2 (S61P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2231213	NM_002145.4(HOXB2):c.178G>A (p.Ala60Thr)	HOXB2, HOXB-AS1 (A60T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2364443	NM_002145.4(HOXB2):c.155C>A (p.Thr52Asn)	HOXB-AS1, HOXB2 (T52N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2350893	NM_002145.4(HOXB2):c.46C>T (p.Pro16Ser)	HOXB-AS1, HOXB2 (P16S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2321651	NM_001384749.1(HOXB3):c.1205A>C (p.Glu402Ala)	HOXB3, HOXB-AS1 (E329A +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2220169	NM_001384749.1(HOXB3):c.1198C>T (p.Pro400Ser)	HOXB-AS1, HOXB3 (P268S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2515163	NM_001384749.1(HOXB3):c.1148A>G (p.Asn383Ser)	HOXB-AS1, HOXB3 (N310S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2262855	NM_001384749.1(HOXB3):c.1134T>A (p.His378Gln)	HOXB-AS1, HOXB3 (H305Q +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2276061	NM_001384749.1(HOXB3):c.1072T>G (p.Tyr358Asp)	HOXB3, HOXB-AS1 (Y226D +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2335201	NM_001384749.1(HOXB3):c.1066G>A (p.Gly356Ser)	HOXB-AS1, HOXB3 (G224S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2216195	NM_001384749.1(HOXB3):c.1031C>G (p.Pro344Arg)	HOXB-AS1, HOXB3 (P344R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2227123	NM_001384749.1(HOXB3):c.1012G>A (p.Gly338Arg)	HOXB-AS1, HOXB3 (G338R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2412424	NM_001384749.1(HOXB3):c.1006G>A (p.Ala336Thr)	HOXB-AS1, HOXB3 (A204T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2233999	NM_001384749.1(HOXB3):c.968C>T (p.Pro323Leu)	HOXB-AS1, HOXB3 (P323L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2542603	NM_001384749.1(HOXB3):c.894C>G (p.His298Gln)	HOXB-AS1, HOXB3 (H298Q +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2270550	NM_001384749.1(HOXB3):c.854G>A (p.Ser285Asn)	HOXB-AS1, HOXB3 (S153N +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2615868	NM_001384749.1(HOXB3):c.817G>A (p.Ala273Thr)	HOXB3, HOXB-AS1 (A141T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2609549	NM_001384749.1(HOXB3):c.776C>T (p.Pro259Leu)	HOXB-AS1, HOXB3 (P259L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2404561	NM_001384749.1(HOXB3):c.769G>T (p.Gly257Trp)	HOXB-AS1, HOXB3 (G257W +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2550373	NM_001384749.1(HOXB3):c.524G>A (p.Gly175Asp)	HOXB-AS1, HOXB3 (G175D +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2319078	NM_001384749.1(HOXB3):c.487G>C (p.Gly163Arg)	HOXB-AS1, HOXB3 (G163R +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2319077	NM_001384749.1(HOXB3):c.458G>A (p.Cys153Tyr)	HOXB-AS1, HOXB3 (C153Y +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance

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Items: 24