Related gene-specific medical variations for Gene (Select 100534589) - ClinVar

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Links from Gene

Items: 72

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3106608	NM_152739.4(HOXA9):c.772A>T (p.Arg258Trp)	HOXA10-HOXA9, HOXA9 +1 more (R258W)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3106607	NM_152739.4(HOXA9):c.72G>C (p.Glu24Asp)	HOXA10-HOXA9, HOXA9 +1 more (E24D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106606	NM_152739.4(HOXA9):c.640A>C (p.Thr214Pro)	HOXA10-HOXA9, HOXA9 +1 more (T214P)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3106605	NM_152739.4(HOXA9):c.551G>C (p.Ser184Thr)	HOXA10-HOXA9, HOXA9 +1 more (S184T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3106604	NM_152739.4(HOXA9):c.521C>T (p.Ala174Val)	HOXA10-HOXA9, HOXA9 +1 more (A174V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3106603	NM_152739.4(HOXA9):c.328T>C (p.Ser110Pro)	HOXA10-HOXA9, HOXA9 +1 more (S110P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106602	NM_152739.4(HOXA9):c.170A>G (p.Gln57Arg)	HOXA10-HOXA9, HOXA9 +1 more (Q57R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106601	NM_152739.4(HOXA9):c.142C>A (p.His48Asn)	HOXA10-HOXA9, HOXA9 +1 more (H48N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106548	NM_018951.4(HOXA10):c.737C>T (p.Pro246Leu)	HOXA10, HOXA10-HOXA9 (P246L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3106547	NM_018951.4(HOXA10):c.686G>A (p.Gly229Asp)	HOXA10, HOXA10-HOXA9 (G229D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3106546	NM_018951.4(HOXA10):c.670A>G (p.Lys224Glu)	HOXA10, HOXA10-HOXA9 (K224E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3106545	NM_018951.4(HOXA10):c.526G>A (p.Asp176Asn)	HOXA10, HOXA10-HOXA9 (D176N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3106544	NM_018951.4(HOXA10):c.16G>A (p.Gly6Ser)	HOXA10, HOXA10-HOXA9 (G6S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3106543	NM_018951.4(HOXA10):c.154G>T (p.Gly52Cys)	HOXA10, HOXA10-HOXA9 (G52C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3106542	NM_018951.4(HOXA10):c.1167G>A (p.Met389Ile)	HOXA10, HOXA10-HOXA9 (M389I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3056353	NM_018951.4(HOXA10):c.1203G>A (p.Arg401=)	HOXA10, HOXA10-HOXA9	Single nucleotide variant (synonymous variant +1 more)	HOXA10-related condition	GBenign
Select item 3052831	NM_018951.4(HOXA10):c.669C>T (p.Ala223=)	HOXA10, HOXA10-HOXA9	Single nucleotide variant (synonymous variant)	HOXA10-related condition	GLikely benign
Select item 3049459	NM_018951.4(HOXA10):c.738G>T (p.Pro246=)	HOXA10, HOXA10-HOXA9	Single nucleotide variant (synonymous variant)	HOXA10-related condition	GBenign
Select item 3047584	NM_018951.4(HOXA10):c.210C>T (p.Asp70=)	HOXA10, HOXA10-HOXA9	Single nucleotide variant (synonymous variant)	HOXA10-related condition	GLikely benign
Select item 3047042	NM_018951.4(HOXA10):c.135_155del (p.42AGGGGGG[1])	HOXA10, HOXA10-HOXA9	Deletion (inframe deletion)	HOXA10-related condition	GLikely benign
Select item 3044896	NM_018951.4(HOXA10):c.546G>T (p.Ser182=)	HOXA10, HOXA10-HOXA9	Single nucleotide variant (synonymous variant)	HOXA10-related condition	GLikely benign
Select item 3043254	NM_018951.4(HOXA10):c.99G>T (p.Ser33=)	HOXA10, HOXA10-HOXA9	Single nucleotide variant (synonymous variant)	HOXA10-related condition	GLikely benign
Select item 3042964	NM_018951.4(HOXA10):c.825C>G (p.Pro275=)	HOXA10, HOXA10-HOXA9	Single nucleotide variant (synonymous variant)	HOXA10-related condition	GLikely benign
Select item 3039306	NM_018951.4(HOXA10):c.699G>T (p.Ala233=)	HOXA10, HOXA10-HOXA9	Single nucleotide variant (synonymous variant)	HOXA10-related condition	GBenign
Select item 3035569	NM_018951.4(HOXA10):c.958+9G>T	HOXA10, HOXA10-HOXA9	Single nucleotide variant (intron variant)	HOXA10-related condition	GBenign
Select item 2609863	NM_018951.4(HOXA10):c.803G>A (p.Arg268Gln)	HOXA10, HOXA10-HOXA9 (R268Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2603300	NM_018951.4(HOXA10):c.592G>A (p.Asp198Asn)	HOXA10, HOXA10-HOXA9 (D198N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2601723	NM_018951.4(HOXA10):c.281C>A (p.Pro94Gln)	HOXA10, HOXA10-HOXA9 (P94Q)	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)	not specified	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)	not specified	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)	not specified	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)	not specified	GUncertain significance
Select item 2522395	NM_018951.4(HOXA10):c.455C>A (p.Pro152Gln)	HOXA10, HOXA10-HOXA9 (P152Q)	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)	not specified	GUncertain significance
Select item 2508455	NM_018951.4(HOXA10):c.20A>G (p.Tyr7Cys)	HOXA10, HOXA10-HOXA9 (Y7C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2477004	NM_018951.4(HOXA10):c.601G>T (p.Ala201Ser)	HOXA10, HOXA10-HOXA9 (A201S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2460596	NM_018951.4(HOXA10):c.913G>A (p.Ala305Thr)	HOXA10, HOXA10-HOXA9 (A305T)	Single nucleotide variant (missense variant)	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)	not specified	GUncertain significance
Select item 2459077	NM_018951.4(HOXA10):c.938C>T (p.Ser313Leu)	HOXA10, HOXA10-HOXA9 (S313L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2410892	NM_018951.4(HOXA10):c.661G>C (p.Gly221Arg)	HOXA10, HOXA10-HOXA9 (G221R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2410821	NM_018951.4(HOXA10):c.784G>A (p.Asp262Asn)	HOXA10, HOXA10-HOXA9 (D262N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2408736	NM_152739.4(HOXA9):c.565C>A (p.Pro189Thr)	HOXA10-HOXA9, HOXA9 +1 more (P189T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2407929	NM_152739.4(HOXA9):c.193G>A (p.Ala65Thr)	HOXA10-HOXA9, HOXA9 +1 more (A65T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387791	NM_018951.4(HOXA10):c.149G>A (p.Gly50Glu)	HOXA10, HOXA10-HOXA9 (G50E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2385577	NM_152739.4(HOXA9):c.346C>A (p.Pro116Thr)	HOXA10-HOXA9, HOXA9 +1 more (P116T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384475	NM_018951.4(HOXA10):c.413A>C (p.Gln138Pro)	HOXA10, HOXA10-HOXA9 (Q138P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2374529	NM_018951.4(HOXA10):c.793C>G (p.Arg265Gly)	HOXA10, HOXA10-HOXA9 (R265G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2372050	NM_018951.4(HOXA10):c.619G>T (p.Gly207Trp)	HOXA10, HOXA10-HOXA9 (G207W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2366336	NM_018951.4(HOXA10):c.805G>T (p.Ala269Ser)	HOXA10, HOXA10-HOXA9 (A269S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2366041	NM_152739.4(HOXA9):c.722G>T (p.Arg241Leu)	HOXA10-HOXA9, HOXA9 +1 more (R241L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2357940	NM_018951.4(HOXA10):c.803G>C (p.Arg268Pro)	HOXA10, HOXA10-HOXA9 (R268P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2345683	NM_152739.4(HOXA9):c.470A>G (p.Tyr157Cys)	HOXA10-HOXA9, HOXA9 +1 more (Y157C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342277	NM_018951.4(HOXA10):c.847G>T (p.Gly283Cys)	HOXA10, HOXA10-HOXA9 (G283C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2339677	NM_018951.4(HOXA10):c.910C>T (p.Pro304Ser)	HOXA10, HOXA10-HOXA9 (P304S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2319586	NM_152739.4(HOXA9):c.582T>A (p.Asn194Lys)	HOXA10-HOXA9, HOXA9 +1 more (N194K)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2313180	NM_018951.4(HOXA10):c.581G>A (p.Gly194Asp)	HOXA10, HOXA10-HOXA9 (G194D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2312250	NM_018951.4(HOXA10):c.742C>A (p.Arg248Ser)	HOXA10, HOXA10-HOXA9 (R248S)	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)	not specified	GUncertain significance
Select item 2281910	NM_152739.4(HOXA9):c.101C>T (p.Thr34Ile)	HOXA10-HOXA9, HOXA9 +1 more (T34I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272368	NM_152739.4(HOXA9):c.296C>T (p.Ala99Val)	HOXA10-HOXA9, HOXA9 +1 more (A99V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268963	NM_018951.4(HOXA10):c.1135C>G (p.Gln379Glu)	HOXA10, HOXA10-HOXA9 (Q379E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2255958	NM_152739.4(HOXA9):c.786G>C (p.Lys262Asn)	HOXA10-HOXA9, HOXA9 +1 more (K262N)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2250459	NM_018951.4(HOXA10):c.419A>C (p.Gln140Pro)	HOXA10-HOXA9, HOXA10 (Q140P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2240286	NM_152739.4(HOXA9):c.79G>A (p.Val27Ile)	HOXA10-HOXA9, HOXA9 +1 more (V27I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235254	NM_152739.4(HOXA9):c.713A>C (p.Glu238Ala)	HOXA10-HOXA9, HOXA9 +1 more (E238A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2220785	NM_152739.4(HOXA9):c.97G>T (p.Gly33Trp)	HOXA10-HOXA9, HOXA9 +1 more (G33W)	Single nucleotide variant (missense variant)	not specified	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)	not specified	GUncertain significance
Select item 1801486	NM_152739.4(HOXA9):c.304G>C (p.Ala102Pro)	HOXA9, HOXA10-HOXA9 +1 more (A102P)	Single nucleotide variant (missense variant)	Hand-foot-genital syndrome	GUncertain significance
Select item 1684802	NM_018951.4(HOXA10):c.170A>G (p.Tyr57Cys)	HOXA10, HOXA10-HOXA9 (Y57C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 787701	NM_152739.4(HOXA9):c.627G>A (p.Lys209=)	HOXA10-HOXA9, HOXA9 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 714346	NM_018951.4(HOXA10):c.364C>T (p.Pro122Ser)	HOXA10, HOXA10-HOXA9 (P122S)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 425408	NM_152739.4(HOXA9):c.668A>C (p.Lys223Thr)	HOXA10-HOXA9, HOXA9 +1 more (K223T)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance

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Items: 72