"Ambry Genetics"[submitter] AND "HOXB13"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 822543	NM_006361.6(HOXB13):c.853T>C (p.Ter285Gln)	HOXB13	Single nucleotide variant (stop lost)	not provided +1 more	GUncertain significance
Select item 483515	NM_006361.6(HOXB13):c.853T>G (p.Ter285Glu)	HOXB13	Single nucleotide variant (stop lost)	Hereditary cancer-predisposing syndrome	GUncertain significance
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 2325388	NM_006361.6(HOXB13):c.850C>A (p.Pro284Thr)	HOXB13 (P284T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 822523	NM_006361.6(HOXB13):c.850C>T (p.Pro284Ser)	HOXB13 (P284S)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1763591	NM_006361.6(HOXB13):c.849C>A (p.Thr283=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
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 822505	NM_006361.6(HOXB13):c.848C>T (p.Thr283Ile)	HOXB13 (T283I)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 822484	NM_006361.6(HOXB13):c.847A>G (p.Thr283Ala)	HOXB13 (T283A)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1514664	NM_006361.6(HOXB13):c.845C>T (p.Ala282Val)	HOXB13 (A282V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1039167	NM_006361.6(HOXB13):c.844G>T (p.Ala282Ser)	HOXB13 (A282S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1907540	NM_006361.6(HOXB13):c.843C>A (p.Ser281Arg)	HOXB13 (S281R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1650295	NM_006361.6(HOXB13):c.843C>T (p.Ser281=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 822415	NM_006361.6(HOXB13):c.842G>C (p.Ser281Thr)	HOXB13 (S281T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 861623	NM_006361.6(HOXB13):c.841A>G (p.Ser281Gly)	HOXB13 (S281G)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 822362	NM_006361.6(HOXB13):c.838A>G (p.Asn280Asp)	HOXB13 (N280D)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
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 1762920	NM_006361.6(HOXB13):c.831G>C (p.Lys277Asn)	HOXB13 (K277N)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1762917	NM_006361.6(HOXB13):c.831G>A (p.Lys277=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2448423	NM_006361.6(HOXB13):c.829A>G (p.Lys277Glu)	HOXB13 (K277E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 827553	NM_006361.6(HOXB13):c.827C>G (p.Ala276Gly)	HOXB13 (A276G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 827545	NM_006361.6(HOXB13):c.826G>A (p.Ala276Thr)	HOXB13 (A276T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
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 1482770	NM_006361.6(HOXB13):c.820G>A (p.Val274Ile)	HOXB13 (V274I)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1561262	NM_006361.6(HOXB13):c.819G>A (p.Lys273=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1305649	NM_006361.6(HOXB13):c.814AAG[1] (p.Lys273del)	HOXB13 (K273del)	Microsatellite (inframe_deletion)	not provided +1 more	GUncertain significance
Select item 1762339	NM_006361.6(HOXB13):c.818A>G (p.Lys273Arg)	HOXB13 (K273R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 691219	NM_006361.6(HOXB13):c.816G>T (p.Lys272Asn)	HOXB13 (K272N)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 691218	NM_006361.6(HOXB13):c.816G>A (p.Lys272=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
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 2563732	NM_006361.6(HOXB13):c.812A>G (p.Glu271Gly)	HOXB13 (E271G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	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 1555739	NM_006361.6(HOXB13):c.810A>G (p.Lys270=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 827447	NM_006361.6(HOXB13):c.809A>G (p.Lys270Arg)	HOXB13 (K270R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 959177	NM_006361.6(HOXB13):c.808A>G (p.Lys270Glu)	HOXB13 (K270E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1668926	NM_006361.6(HOXB13):c.807C>T (p.Val269=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2010012	NM_006361.6(HOXB13):c.805G>A (p.Val269Ile)	HOXB13 (V269I)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +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	GLikely benign
Select item 1001068	NM_006361.6(HOXB13):c.803G>C (p.Arg268Pro)	HOXB13 (R268P)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 483500	NM_006361.6(HOXB13):c.803G>A (p.Arg268Gln)	HOXB13 (R268Q)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1380509	NM_006361.6(HOXB13):c.802C>T (p.Arg268Trp)	HOXB13 (R268W)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 940825	NM_006361.6(HOXB13):c.802C>A (p.Arg268=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 827407	NM_006361.6(HOXB13):c.802C>G (p.Arg268Gly)	HOXB13 (R268G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1153361	NM_006361.6(HOXB13):c.801C>T (p.Arg267=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 827390	NM_006361.6(HOXB13):c.800G>T (p.Arg267Leu)	HOXB13 (R267L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 834616	NM_006361.6(HOXB13):c.799C>T (p.Arg267Cys)	HOXB13 (R267C)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 827375	NM_006361.6(HOXB13):c.799C>G (p.Arg267Gly)	HOXB13 (R267G)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1099823	NM_006361.6(HOXB13):c.798C>T (p.Asn266=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2563739	NM_006361.6(HOXB13):c.797A>G (p.Asn266Ser)	HOXB13 (N266S)	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 485701	NM_006361.6(HOXB13):c.791T>C (p.Phe264Ser)	HOXB13 (F264S)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1761045	NM_006361.6(HOXB13):c.788G>C (p.Trp263Ser)	HOXB13 (W263S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1760946	NM_006361.6(HOXB13):c.786C>G (p.Ile262Met)	HOXB13 (I262M)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1116595	NM_006361.6(HOXB13):c.786C>A (p.Ile262=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided +1 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 966330	NM_006361.6(HOXB13):c.779T>G (p.Ile260Ser)	HOXB13 (I260S)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 827259	NM_006361.6(HOXB13):c.779T>A (p.Ile260Asn)	HOXB13 (I260N)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 955197	NM_006361.6(HOXB13):c.778A>G (p.Ile260Val)	HOXB13 (I260V)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2625787	NM_006361.6(HOXB13):c.777G>C (p.Gln259His)	HOXB13 (Q259H)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1034876	NM_006361.6(HOXB13):c.776A>G (p.Gln259Arg)	HOXB13 (Q259R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 827233	NM_006361.6(HOXB13):c.773G>T (p.Arg258Leu)	HOXB13 (R258L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +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 827225	NM_006361.6(HOXB13):c.772C>T (p.Arg258Cys)	HOXB13 (R258C)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1760182	NM_006361.6(HOXB13):c.769G>A (p.Glu257Lys)	HOXB13 (E257K)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 827204	NM_006361.6(HOXB13):c.769G>C (p.Glu257Gln)	HOXB13 (E257Q)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 827195	NM_006361.6(HOXB13):c.768G>A (p.Ser256=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 483519	NM_006361.6(HOXB13):c.767C>T (p.Ser256Leu)	HOXB13 (S256L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1008259	NM_006361.6(HOXB13):c.766T>C (p.Ser256Pro)	HOXB13 (S256P)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 691192	NM_006361.6(HOXB13):c.765C>T (p.Leu255=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 827166	NM_006361.6(HOXB13):c.763C>T (p.Leu255Phe)	HOXB13 (L255F)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1404913	NM_006361.6(HOXB13):c.762C>G (p.Ser254Arg)	HOXB13 (S254R)	Single nucleotide variant (missense variant)	not provided +1 more	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 1759692	NM_006361.6(HOXB13):c.759C>T (p.Thr253=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1430895	NM_006361.6(HOXB13):c.758C>G (p.Thr253Ser)	HOXB13 (T253S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2563733	NM_006361.6(HOXB13):c.757A>G (p.Thr253Ala)	HOXB13 (T253A)	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)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2563737	NM_006361.6(HOXB13):c.751G>A (p.Ala251Thr)	HOXB13 (A251T)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 691181	NM_006361.6(HOXB13):c.751del (p.Ala251fs)	HOXB13 (A251fs)	Deletion (frameshift variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1153722	NM_006361.6(HOXB13):c.750G>A (p.Ser250=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 691180	NM_006361.6(HOXB13):c.750G>C (p.Ser250=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1759187	NM_006361.6(HOXB13):c.749C>T (p.Ser250Leu)	HOXB13 (S250L)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1759094	NM_006361.6(HOXB13):c.747C>G (p.Ile249Met)	HOXB13 (I249M)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 691178	NM_006361.6(HOXB13):c.747C>T (p.Ile249=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 1758784	NM_006361.6(HOXB13):c.740G>T (p.Arg247Leu)	HOXB13 (R247L)	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 808288	NM_006361.6(HOXB13):c.738G>A (p.Arg246=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 827002	NM_006361.6(HOXB13):c.737G>A (p.Arg246Lys)	HOXB13 (R246K)	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)	not specified +4 more	GBenign/Likely benign
Select item 1758437	NM_006361.6(HOXB13):c.734A>G (p.Lys245Arg)	HOXB13 (K245R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 826964	NM_006361.6(HOXB13):c.731A>T (p.Asp244Val)	HOXB13 (D244V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
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)	not provided +1 more	GUncertain significance
Select item 483530	NM_006361.6(HOXB13):c.726del (p.Lys243fs)	HOXB13 (K243fs)	Deletion (frameshift variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 999436	NM_006361.6(HOXB13):c.725C>T (p.Thr242Ile)	HOXB13 (T242I)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	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 691162	NM_006361.6(HOXB13):c.720C>T (p.Phe240=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1590515	NM_006361.6(HOXB13):c.717G>A (p.Lys239=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 826890	NM_006361.6(HOXB13):c.717G>T (p.Lys239Asn)	HOXB13 (K239N)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
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

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