ClinVar for Gene (Select 10481) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3369972	NM_006361.6(HOXB13):c.68G>A (p.Gly23Glu)	HOXB13 (G23E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3368270	NM_006361.6(HOXB13):c.454C>G (p.Leu152Val)	HOXB13 (L152V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3367965	NM_006361.6(HOXB13):c.700G>C (p.Glu234Gln)	HOXB13 (E234Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3361874	NM_006361.6(HOXB13):c.601+5del	HOXB13	Deletion (intron variant)	not provided	GUncertain significance
Select item 3284653	NM_006361.6(HOXB13):c.152T>C (p.Leu51Ser)	HOXB13 (L51S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3284652	NM_006361.6(HOXB13):c.301G>T (p.Ala101Ser)	HOXB13 (A101S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3284651	NM_006361.6(HOXB13):c.45C>A (p.Ile15=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3284650	NM_006361.6(HOXB13):c.345G>A (p.Thr115=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3284649	NM_006361.6(HOXB13):c.426T>C (p.Ser142=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3284648	NM_006361.6(HOXB13):c.424A>T (p.Ser142Cys)	HOXB13 (S142C)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3243177	NC_000017.10:g.(?_46805345)_(46805955_?)dup	HOXB13	Duplication	not provided	GUncertain significance
Select item 3242218	Single allele	KIF18B, LPO +196 more	Deletion	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 3242217	GRCh37/hg19 17q12-22(chr17:41196270-41277589)	SLC4A1, DCAKD +422 more	Copy number loss	Breast-ovarian cancer, familial, susceptibility to, 1	GPathogenic
Select item 3225548	NM_006361.6(HOXB13):c.812A>C (p.Glu271Ala)	HOXB13 (E271A)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3225547	NM_006361.6(HOXB13):c.791T>G (p.Phe264Cys)	HOXB13 (F264C)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3225546	NM_006361.6(HOXB13):c.721A>G (p.Ile241Val)	HOXB13 (I241V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3225545	NM_006361.6(HOXB13):c.714C>A (p.Asn238Lys)	HOXB13 (N238K)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3225544	NM_006361.6(HOXB13):c.609C>T (p.Ser203=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3225542	NM_006361.6(HOXB13):c.498G>A (p.Val166=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 3225541	NM_006361.6(HOXB13):c.483C>A (p.Asp161Glu)	HOXB13 (D161E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3225540	NM_006361.6(HOXB13):c.481G>A (p.Asp161Asn)	HOXB13 (D161N)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3225539	NM_006361.6(HOXB13):c.461C>G (p.Ala154Gly)	HOXB13 (A154G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3225538	NM_006361.6(HOXB13):c.37A>C (p.Lys13Gln)	HOXB13 (K13Q)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3225536	NM_006361.6(HOXB13):c.321C>G (p.Ala107=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 3225535	NM_006361.6(HOXB13):c.320C>G (p.Ala107Gly)	HOXB13 (A107G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3225534	NM_006361.6(HOXB13):c.266C>G (p.Ser89Cys)	HOXB13 (S89C)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3225533	NM_006361.6(HOXB13):c.220T>C (p.Ser74Pro)	HOXB13 (S74P)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3225532	NM_006361.6(HOXB13):c.16T>G (p.Tyr6Asp)	HOXB13 (Y6D)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3225531	NM_006361.6(HOXB13):c.10G>A (p.Gly4Ser)	HOXB13 (G4S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3033133	NM_006361.6(HOXB13):c.654G>T (p.Lys218Asn)	HOXB13 (K218N)	Single nucleotide variant (missense variant)	HOXB13-related disorder	GUncertain significance
Select item 3019076	NM_006361.6(HOXB13):c.640C>T (p.Arg214Cys)	HOXB13 (R214C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3014739	NM_006361.6(HOXB13):c.819G>C (p.Lys273Asn)	HOXB13 (K273N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3009857	NM_006361.6(HOXB13):c.118C>T (p.Pro40Ser)	HOXB13 (P40S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3006064	NM_006361.6(HOXB13):c.679C>A (p.Gln227Lys)	HOXB13 (Q227K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2998390	NM_006361.6(HOXB13):c.843C>G (p.Ser281Arg)	HOXB13 (S281R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2995246	NM_006361.6(HOXB13):c.541dup (p.Gln181fs)	HOXB13 (Q181fs)	Duplication (frameshift variant)	not provided	GUncertain significance
Select item 2992132	NM_006361.6(HOXB13):c.602-5C>G	HOXB13	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2991057	NM_006361.6(HOXB13):c.671_672delinsAA (p.Ser224Lys)	HOXB13 (S224K)	Indel (missense variant)	not provided	GUncertain significance
Select item 2982079	NM_006361.6(HOXB13):c.110C>G (p.Pro37Arg)	HOXB13 (P37R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2982078	NM_006361.6(HOXB13):c.210C>G (p.Pro70=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2978641	NM_006361.6(HOXB13):c.369C>T (p.Arg123=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2975306	NM_006361.6(HOXB13):c.462T>C (p.Ala154=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2959152	NM_006361.6(HOXB13):c.25T>C (p.Leu9=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2957810	NM_006361.6(HOXB13):c.601+14C>T	HOXB13	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2906216	NM_006361.6(HOXB13):c.422C>T (p.Ala141Val)	HOXB13 (A141V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2902765	NM_006361.6(HOXB13):c.460G>C (p.Ala154Pro)	HOXB13 (A154P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2899606	NM_006361.6(HOXB13):c.708G>T (p.Ala236=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2897529	NM_006361.6(HOXB13):c.231C>G (p.Pro77=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2897289	NM_006361.6(HOXB13):c.362C>T (p.Pro121Leu)	HOXB13 (P121L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2891600	NM_006361.6(HOXB13):c.647_650dup (p.Lys218fs)	HOXB13 (K218fs)	Duplication (frameshift variant)	not provided	GUncertain significance
Select item 2886763	NM_006361.6(HOXB13):c.659G>A (p.Arg220His)	HOXB13 (R220H)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2886174	NM_006361.6(HOXB13):c.851C>G (p.Pro284Arg)	HOXB13 (P284R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2885170	NM_006361.6(HOXB13):c.6G>T (p.Glu2Asp)	HOXB13 (E2D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2876078	NM_006361.6(HOXB13):c.512C>A (p.Ser171Tyr)	HOXB13 (S171Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2870494	NM_006361.6(HOXB13):c.495T>C (p.Pro165=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2866046	NM_006361.6(HOXB13):c.325T>A (p.Tyr109Asn)	HOXB13 (Y109N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2863362	NM_006361.6(HOXB13):c.171G>A (p.Ala57=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2860004	NM_006361.6(HOXB13):c.617A>G (p.His206Arg)	HOXB13 (H206R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2855306	NM_006361.6(HOXB13):c.561A>G (p.Glu187=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2851945	NM_006361.6(HOXB13):c.640C>G (p.Arg214Gly)	HOXB13 (R214G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2848589	NM_006361.6(HOXB13):c.346G>A (p.Ala116Thr)	HOXB13 (A116T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2848346	NM_006361.6(HOXB13):c.848C>A (p.Thr283Asn)	HOXB13 (T283N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2840201	NM_006361.6(HOXB13):c.247T>A (p.Phe83Ile)	HOXB13 (F83I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2837343	NM_006361.6(HOXB13):c.760A>G (p.Ser254Gly)	HOXB13 (S254G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2836030	NM_006361.6(HOXB13):c.124C>T (p.Leu42=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2832380	NM_006361.6(HOXB13):c.625G>C (p.Asp209His)	HOXB13 (D209H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2827927	NM_006361.6(HOXB13):c.478C>T (p.His160Tyr)	HOXB13 (H160Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2823746	NM_006361.6(HOXB13):c.579C>G (p.Pro193=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 2817267	NM_006361.6(HOXB13):c.798C>A (p.Asn266Lys)	HOXB13 (N266K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2814866	NM_006361.6(HOXB13):c.154G>A (p.Asp52Asn)	HOXB13 (D52N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2814393	NM_006361.6(HOXB13):c.150C>A (p.Pro50=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2810482	NM_006361.6(HOXB13):c.800_801delinsAA (p.Arg267Gln)	HOXB13 (R267Q)	Indel (missense variant)	not provided	GUncertain significance
Select item 2809739	NM_006361.6(HOXB13):c.562C>T (p.Gln188Ter)	HOXB13 (Q188*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2809671	NM_006361.6(HOXB13):c.733A>G (p.Lys245Glu)	HOXB13 (K245E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2807059	NM_006361.6(HOXB13):c.108C>A (p.His36Gln)	HOXB13 (H36Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2802383	NM_006361.6(HOXB13):c.840C>T (p.Asn280=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2801622	NM_006361.6(HOXB13):c.65G>T (p.Gly22Val)	HOXB13 (G22V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2792705	NM_006361.6(HOXB13):c.46G>T (p.Glu16Ter)	HOXB13 (E16*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2792615	NM_006361.6(HOXB13):c.602A>C (p.Asp201Ala)	HOXB13 (D201A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2780088	NM_006361.6(HOXB13):c.164G>C (p.Gly55Ala)	HOXB13 (G55A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2773124	NM_006361.6(HOXB13):c.504T>A (p.Ser168Arg)	HOXB13 (S168R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2772851	NM_006361.6(HOXB13):c.284G>C (p.Ser95Thr)	HOXB13 (S95T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2771706	NM_006361.6(HOXB13):c.507C>G (p.Tyr169Ter)	HOXB13 (Y169*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2771698	NM_006361.6(HOXB13):c.258G>T (p.Gly86=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2770892	NM_006361.6(HOXB13):c.214G>C (p.Gly72Arg)	HOXB13 (G72R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2770235	NM_006361.6(HOXB13):c.463C>T (p.Pro155Ser)	HOXB13 (P155S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2767377	NM_006361.6(HOXB13):c.789G>C (p.Trp263Cys)	HOXB13 (W263C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2766812	NM_006361.6(HOXB13):c.443_444del (p.Val148fs)	HOXB13 (V148fs)	Microsatellite (frameshift variant)	not provided	GUncertain significance
Select item 2763229	NM_006361.6(HOXB13):c.212A>T (p.Gln71Leu)	HOXB13 (Q71L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2753666	NM_006361.6(HOXB13):c.442GTG[1] (p.Val149del)	HOXB13 (V149del)	Microsatellite (inframe_deletion)	not provided	GUncertain significance
Select item 2752332	NM_006361.6(HOXB13):c.316_330del (p.Leu106_Pro110del)	HOXB13	Deletion (inframe_deletion)	not provided	GUncertain significance
Select item 2747061	NM_006361.6(HOXB13):c.364A>G (p.Ser122Gly)	HOXB13 (S122G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2746950	NM_006361.6(HOXB13):c.559G>C (p.Glu187Gln)	HOXB13 (E187Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2744297	NM_006361.6(HOXB13):c.467G>C (p.Gly156Ala)	HOXB13 (G156A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2736613	NM_006361.6(HOXB13):c.720C>A (p.Phe240Leu)	HOXB13 (F240L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2730577	NM_006361.6(HOXB13):c.432G>A (p.Leu144=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2719979	NM_006361.6(HOXB13):c.123G>C (p.Thr41=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2717376	NM_006361.6(HOXB13):c.749_750delinsTC (p.Ser250Phe)	HOXB13 (S250F)	Indel (missense variant)	not provided	GUncertain significance
Select item 2714663	NM_006361.6(HOXB13):c.675G>C (p.Lys225Asn)	HOXB13 (K225N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2707318	NM_006361.6(HOXB13):c.601+5C>A	HOXB13	Single nucleotide variant (intron variant)	not provided	GUncertain significance

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