"GeneDx"[submitter] AND "HOXB13"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1196252	NM_006361.6(HOXB13):c.*57G>A	HOXB13	Single nucleotide variant (3 prime UTR variant)	not provided	GLikely benign
Select item 182506	NM_006361.6(HOXB13):c.853del (p.Ter285LysextTer?)	HOXB13	Deletion (frameshift variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity; association
Select item 2325388	NM_006361.6(HOXB13):c.850C>A (p.Pro284Thr)	HOXB13 (P284T)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 483493	NM_006361.6(HOXB13):c.849C>T (p.Thr283=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 128038	NM_006361.6(HOXB13):c.832G>T (p.Val278Leu)	HOXB13 (V278L)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 9 +3 more	GConflicting classifications of pathogenicity
Select item 827545	NM_006361.6(HOXB13):c.826G>A (p.Ala276Thr)	HOXB13 (A276T)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1305649	NM_006361.6(HOXB13):c.814AAG[1] (p.Lys273del)	HOXB13 (K273del)	Microsatellite (inframe_deletion)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 691214	NM_006361.6(HOXB13):c.811G>A (p.Glu271Lys)	HOXB13 (E271K)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 827418	NM_006361.6(HOXB13):c.804G>T (p.Arg268=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 483500	NM_006361.6(HOXB13):c.803G>A (p.Arg268Gln)	HOXB13 (R268Q)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 827375	NM_006361.6(HOXB13):c.799C>G (p.Arg267Gly)	HOXB13 (R267G)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 483529	NM_006361.6(HOXB13):c.773G>A (p.Arg258His)	HOXB13 (R258H)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 858844	NM_006361.6(HOXB13):c.772C>A (p.Arg258Ser)	HOXB13 (R258S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 827155	NM_006361.6(HOXB13):c.761G>C (p.Ser254Thr)	HOXB13 (S254T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 962132	NM_006361.6(HOXB13):c.752C>T (p.Ala251Val)	HOXB13 (A251V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 827025	NM_006361.6(HOXB13):c.740G>A (p.Arg247His)	HOXB13 (R247H)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 827017	NM_006361.6(HOXB13):c.739C>T (p.Arg247Cys)	HOXB13 (R247C)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 182504	NM_006361.6(HOXB13):c.735G>A (p.Lys245=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 483495	NM_006361.6(HOXB13):c.730G>A (p.Asp244Asn)	HOXB13 (D244N)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 483524	NM_006361.6(HOXB13):c.728A>G (p.Lys243Arg)	HOXB13 (K243R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 999436	NM_006361.6(HOXB13):c.725C>T (p.Thr242Ile)	HOXB13 (T242I)	Single nucleotide variant (missense variant)	not provided +1 more	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 826676	NM_006361.6(HOXB13):c.686G>A (p.Arg229Gln)	HOXB13 (R229Q)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 963681	NM_006361.6(HOXB13):c.685C>G (p.Arg229Gly)	HOXB13 (R229G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 826616	NM_006361.6(HOXB13):c.677G>A (p.Gly226Glu)	HOXB13 (G226E)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 826533	NM_006361.6(HOXB13):c.664C>A (p.Pro222Thr)	HOXB13 (P222T)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3371111	NM_006361.6(HOXB13):c.650_659dup (p.Ile221fs)	HOXB13 (I221fs)	Duplication (frameshift variant)	not provided	GUncertain significance
Select item 483510	NM_006361.6(HOXB13):c.650G>T (p.Arg217Leu)	HOXB13 (R217L)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 483512	NM_006361.6(HOXB13):c.649C>G (p.Arg217Gly)	HOXB13 (R217G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 483473	NM_006361.6(HOXB13):c.649C>T (p.Arg217Cys)	HOXB13 (R217C)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1018707	NM_006361.6(HOXB13):c.644G>A (p.Arg215His)	HOXB13 (R215H)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 826392	NM_006361.6(HOXB13):c.641G>T (p.Arg214Leu)	HOXB13 (R214L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 691129	NM_006361.6(HOXB13):c.640C>A (p.Arg214Ser)	HOXB13 (R214S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1038652	NM_006361.6(HOXB13):c.635C>T (p.Ala212Val)	HOXB13 (A212V)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 128036	NM_006361.6(HOXB13):c.634G>A (p.Ala212Thr)	HOXB13 (A212T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 826307	NM_006361.6(HOXB13):c.629C>T (p.Ala210Val)	HOXB13 (A210V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 483477	NM_006361.6(HOXB13):c.610G>A (p.Gly204Arg)	HOXB13 (G204R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1711997	NM_006361.6(HOXB13):c.609C>A (p.Ser203Arg)	HOXB13 (S203R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 826167	NM_006361.6(HOXB13):c.606C>T (p.Ser202=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 861092	NM_006361.6(HOXB13):c.602-7C>A	HOXB13	Single nucleotide variant (intron variant)	not provided	GConflicting classifications of pathogenicity
Select item 182503	NM_006361.6(HOXB13):c.602-9G>A	HOXB13	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 9 +3 more	GBenign/Likely benign
Select item 1196696	NM_006361.6(HOXB13):c.602-10C>G	HOXB13	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1281224	NM_006361.6(HOXB13):c.602-335G>A	HOXB13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 676480	NM_006361.6(HOXB13):c.601+134G>A	HOXB13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 826134	NM_006361.6(HOXB13):c.601+1G>T	HOXB13	Single nucleotide variant (splice donor variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 483525	NM_006361.6(HOXB13):c.590C>T (p.Ala197Val)	HOXB13 (A197V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 965074	NM_006361.6(HOXB13):c.589G>A (p.Ala197Thr)	HOXB13 (A197T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 825988	NM_006361.6(HOXB13):c.580T>A (p.Phe194Ile)	HOXB13 (F194I)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 483492	NM_006361.6(HOXB13):c.567C>T (p.Asn189=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 956348	NM_006361.6(HOXB13):c.563A>G (p.Gln188Arg)	HOXB13 (Q188R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 825801	NM_006361.6(HOXB13):c.551G>T (p.Cys184Phe)	HOXB13 (C184F)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 483504	NM_006361.6(HOXB13):c.545T>C (p.Met182Thr)	HOXB13 (M182T)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 825581	NM_006361.6(HOXB13):c.523G>T (p.Ala175Ser)	HOXB13 (A175S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 825549	NM_006361.6(HOXB13):c.520C>G (p.Leu174Val)	HOXB13 (L174V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 480871	NM_006361.6(HOXB13):c.513T>C (p.Ser171=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign
Select item 128035	NM_006361.6(HOXB13):c.499G>A (p.Asp167Asn)	HOXB13 (D167N)	Single nucleotide variant (missense variant)	HOXB13-related disorder +2 more	GUncertain significance
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 953309	NM_006361.6(HOXB13):c.484_485insAGGG (p.Ser162Ter)	HOXB13 (S162*)	Insertion (nonsense)	not provided	GUncertain significance
Select item 483479	NM_006361.6(HOXB13):c.474G>A (p.Pro158=)	HOXB13	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 825135	NM_006361.6(HOXB13):c.473C>G (p.Pro158Arg)	HOXB13 (P158R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 690785	NM_006361.6(HOXB13):c.472C>T (p.Pro158Ser)	HOXB13 (P158S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 825090	NM_006361.6(HOXB13):c.467G>A (p.Gly156Glu)	HOXB13 (G156E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 128034	NM_006361.6(HOXB13):c.461C>T (p.Ala154Val)	HOXB13 (A154V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 1001052	NM_006361.6(HOXB13):c.457G>T (p.Gly153Cys)	HOXB13 (G153C)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 514908	NM_006361.6(HOXB13):c.456G>C (p.Leu152=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
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 824965	NM_006361.6(HOXB13):c.451A>C (p.Thr151Pro)	HOXB13 (T151P)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2013082	NM_006361.6(HOXB13):c.437T>C (p.Val146Ala)	HOXB13 (V146A)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 128033	NM_006361.6(HOXB13):c.436G>A (p.Val146Met)	HOXB13 (V146M)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 483476	NM_006361.6(HOXB13):c.411C>T (p.Tyr137=)	HOXB13	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 824284	NM_006361.6(HOXB13):c.383C>A (p.Ala128Asp)	HOXB13 (A128D)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 480873	NM_006361.6(HOXB13):c.366C>T (p.Ser122=)	HOXB13	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign
Select item 128032	NM_006361.6(HOXB13):c.366C>A (p.Ser122Arg)	HOXB13 (S122R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 483490	NM_006361.6(HOXB13):c.361C>G (p.Pro121Ala)	HOXB13 (P121A)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 514907	NM_006361.6(HOXB13):c.360C>T (p.Tyr120=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 823942	NM_006361.6(HOXB13):c.356A>T (p.Glu119Val)	HOXB13 (E119V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 823867	NM_006361.6(HOXB13):c.350G>A (p.Gly117Glu)	HOXB13 (G117E)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1510045	NM_006361.6(HOXB13):c.344C>A (p.Thr115Lys)	HOXB13 (T115K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 690715	NM_006361.6(HOXB13):c.338C>A (p.Thr113Asn)	HOXB13 (T113N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 933797	NM_006361.6(HOXB13):c.332C>A (p.Ala111Glu)	HOXB13 (A111E)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 823611	NM_006361.6(HOXB13):c.332C>T (p.Ala111Val)	HOXB13 (A111V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 480872	NM_006361.6(HOXB13):c.330C>A (p.Pro110=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign/Likely benign
Select item 483480	NM_006361.6(HOXB13):c.328C>G (p.Pro110Ala)	HOXB13 (P110A)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 823391	NM_006361.6(HOXB13):c.327C>G (p.Tyr109Ter)	HOXB13 (Y109*)	Single nucleotide variant (nonsense)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 485697	NM_006361.6(HOXB13):c.322G>A (p.Ala108Thr)	HOXB13 (A108T)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1005967	NM_006361.6(HOXB13):c.320C>T (p.Ala107Val)	HOXB13 (A107V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 823100	NM_006361.6(HOXB13):c.317T>G (p.Leu106Arg)	HOXB13 (L106R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1488867	NM_006361.6(HOXB13):c.314C>G (p.Thr105Ser)	HOXB13 (T105S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 822995	NM_006361.6(HOXB13):c.314C>T (p.Thr105Ile)	HOXB13 (T105I)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 483511	NM_006361.6(HOXB13):c.309_311del (p.Ala104del)	HOXB13 (A104del)	Deletion (inframe_deletion)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1799130	NM_006361.6(HOXB13):c.303C>T (p.Ala101=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 483482	NM_006361.6(HOXB13):c.302C>T (p.Ala101Val)	HOXB13 (A101V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 937563	NM_006361.6(HOXB13):c.290T>A (p.Leu97Gln)	HOXB13 (L97Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 821851	NM_006361.6(HOXB13):c.281G>A (p.Arg94Gln)	HOXB13 (R94Q)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 483499	NM_006361.6(HOXB13):c.277T>G (p.Ser93Ala)	HOXB13 (S93A)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 821687	NM_006361.6(HOXB13):c.269G>A (p.Cys90Tyr)	HOXB13 (C90Y)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 483522	NM_006361.6(HOXB13):c.253G>A (p.Gly85Ser)	HOXB13 (G85S)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 128031	NM_006361.6(HOXB13):c.251G>A (p.Gly84Glu)	HOXB13 (G84E)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 9 +7 more	GPathogenic/Likely pathogenic; association
Select item 821262	NM_006361.6(HOXB13):c.242G>A (p.Gly81Asp)	HOXB13 (G81D)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 485690	NM_006361.6(HOXB13):c.232G>A (p.Val78Met)	HOXB13 (V78M)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance

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