"PreventionGenetics, part of Exact Sciences"[submitter] AND "HOXB13"[g - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 182506	NM_006361.6(HOXB13):c.853del (p.Ter285LysextTer?)	HOXB13	Deletion (frameshift variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity; association
Select item 483493	NM_006361.6(HOXB13):c.849C>T (p.Thr283=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 128038	NM_006361.6(HOXB13):c.832G>T (p.Val278Leu)	HOXB13 (V278L)	Single nucleotide variant (missense variant)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 483498	NM_006361.6(HOXB13):c.825C>T (p.Leu275=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 827281	NM_006361.6(HOXB13):c.783C>A (p.Thr261=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 182504	NM_006361.6(HOXB13):c.735G>A (p.Lys245=)	HOXB13	Single nucleotide variant (synonymous variant)	not specified +4 more	GBenign/Likely benign
Select item 826880	NM_006361.6(HOXB13):c.716A>G (p.Lys239Arg)	HOXB13 (K239R)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1667961	NM_006361.6(HOXB13):c.682T>C (p.Leu228=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 483518	NM_006361.6(HOXB13):c.666G>A (p.Pro222=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 3033133	NM_006361.6(HOXB13):c.654G>T (p.Lys218Asn)	HOXB13 (K218N)	Single nucleotide variant (missense variant)	HOXB13-related condition	GUncertain significance
Select item 1038652	NM_006361.6(HOXB13):c.635C>T (p.Ala212Val)	HOXB13 (A212V)	Single nucleotide variant (missense variant)	HOXB13-related condition +2 more	GUncertain significance
Select item 483477	NM_006361.6(HOXB13):c.610G>A (p.Gly204Arg)	HOXB13 (G204R)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 182503	NM_006361.6(HOXB13):c.602-9G>A	HOXB13	Single nucleotide variant (intron variant)	HOXB13-related condition +4 more	GBenign/Likely benign
Select item 825581	NM_006361.6(HOXB13):c.523G>T (p.Ala175Ser)	HOXB13 (A175S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 128035	NM_006361.6(HOXB13):c.499G>A (p.Asp167Asn)	HOXB13 (D167N)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 483479	NM_006361.6(HOXB13):c.474G>A (p.Pro158=)	HOXB13	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 483476	NM_006361.6(HOXB13):c.411C>T (p.Tyr137=)	HOXB13	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 824296	NM_006361.6(HOXB13):c.384C>T (p.Ala128=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 483490	NM_006361.6(HOXB13):c.361C>G (p.Pro121Ala)	HOXB13 (P121A)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 966226	NM_006361.6(HOXB13):c.352del (p.Glu118fs)	HOXB13 (E118fs)	Deletion (frameshift variant)	not provided +2 more	GUncertain significance
Select item 822690	NM_006361.6(HOXB13):c.303C>G (p.Ala101=)	HOXB13	Single nucleotide variant (synonymous variant)	HOXB13-related condition +2 more	GLikely benign
Select item 937563	NM_006361.6(HOXB13):c.290T>A (p.Leu97Gln)	HOXB13 (L97Q)	Single nucleotide variant (missense variant)	HOXB13-related condition +1 more	GUncertain significance
Select item 483507	NM_006361.6(HOXB13):c.258G>C (p.Gly86=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 483481	NM_006361.6(HOXB13):c.215G>T (p.Gly72Val)	HOXB13 (G72V)	Single nucleotide variant (missense variant)	not specified +3 more	GUncertain significance
Select item 820713	NM_006361.6(HOXB13):c.209C>T (p.Pro70Leu)	HOXB13 (P70L)	Single nucleotide variant (missense variant)	HOXB13-related condition +2 more	GUncertain significance
Select item 2629787	NM_006361.6(HOXB13):c.202G>A (p.Gly68Arg)	HOXB13 (G68R)	Single nucleotide variant (missense variant)	HOXB13-related condition	GUncertain significance
Select item 483487	NM_006361.6(HOXB13):c.140A>G (p.Asn47Ser)	HOXB13 (N47S)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 9 +3 more	GUncertain significance
Select item 690532	NM_006361.6(HOXB13):c.116C>T (p.Ala39Val)	HOXB13 (A39V)	Single nucleotide variant (missense variant)	HOXB13-related condition +2 more	GUncertain significance
Select item 690971	NM_006361.6(HOXB13):c.81G>T (p.Leu27=)	HOXB13	Single nucleotide variant (synonymous variant)	HOXB13-related condition +2 more	GLikely benign
Select item 826379	NM_006361.6(HOXB13):c.63G>C (p.Ala21=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 483494	NM_006361.6(HOXB13):c.33A>T (p.Gly11=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 2629997	NM_006361.6(HOXB13):c.23C>A (p.Thr8Asn)	HOXB13 (T8N)	Single nucleotide variant (missense variant)	HOXB13-related condition	GUncertain significance

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Items: 32