"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "HOXB13" - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1578605	NM_006361.6(HOXB13):c.855A>G (p.Ter285=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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 182506	NM_006361.6(HOXB13):c.853del (p.Ter285LysextTer?)	HOXB13	Deletion (frameshift variant +1 more)	not specified +3 more	GConflicting classifications of pathogenicity; association
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 822523	NM_006361.6(HOXB13):c.850C>T (p.Pro284Ser)	HOXB13 (P284S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2107164	NM_006361.6(HOXB13):c.849C>G (p.Thr283=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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 2848346	NM_006361.6(HOXB13):c.848C>A (p.Thr283Asn)	HOXB13 (T283N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
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)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 2190080	NM_006361.6(HOXB13):c.846T>C (p.Ala282=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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 943647	NM_006361.6(HOXB13):c.844G>A (p.Ala282Thr)	HOXB13 (A282T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 691225	NM_006361.6(HOXB13):c.844G>C (p.Ala282Pro)	HOXB13 (A282P)	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 1907540	NM_006361.6(HOXB13):c.843C>A (p.Ser281Arg)	HOXB13 (S281R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1650295	NM_006361.6(HOXB13):c.843C>T (p.Ser281=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +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 1402401	NM_006361.6(HOXB13):c.841A>C (p.Ser281Arg)	HOXB13 (S281R)	Single nucleotide variant (missense variant)	not provided	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 2802383	NM_006361.6(HOXB13):c.840C>T (p.Asn280=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 691247	NM_006361.6(HOXB13):c.840C>A (p.Asn280Lys)	HOXB13 (N280K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1423625	NM_006361.6(HOXB13):c.837G>C (p.Lys279Asn)	HOXB13 (K279N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1060719	NM_006361.6(HOXB13):c.832G>A (p.Val278Met)	HOXB13 (V278M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
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 1762917	NM_006361.6(HOXB13):c.831G>A (p.Lys277=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1978231	NM_006361.6(HOXB13):c.830A>G (p.Lys277Arg)	HOXB13 (K277R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1149575	NM_006361.6(HOXB13):c.828C>T (p.Ala276=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 827553	NM_006361.6(HOXB13):c.827C>G (p.Ala276Gly)	HOXB13 (A276G)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1486102	NM_006361.6(HOXB13):c.826G>T (p.Ala276Ser)	HOXB13 (A276S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1416476	NM_006361.6(HOXB13):c.826G>C (p.Ala276Pro)	HOXB13 (A276P)	Single nucleotide variant (missense variant)	not provided	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)	not provided +1 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 960241	NM_006361.6(HOXB13):c.820G>T (p.Val274Phe)	HOXB13 (V274F)	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 1561262	NM_006361.6(HOXB13):c.819G>A (p.Lys273=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
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 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 1468863	NM_006361.6(HOXB13):c.817A>T (p.Lys273Ter)	HOXB13 (K273*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 1714156	NM_006361.6(HOXB13):c.815A>G (p.Lys272Arg)	HOXB13 (K272R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1002606	NM_006361.6(HOXB13):c.813_814dup (p.Lys272fs)	HOXB13 (K272fs)	Microsatellite (frameshift variant)	not provided	GUncertain significance
Select item 691216	NM_006361.6(HOXB13):c.813G>T (p.Glu271Asp)	HOXB13 (E271D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2123749	NM_006361.6(HOXB13):c.811G>C (p.Glu271Gln)	HOXB13 (E271Q)	Single nucleotide variant (missense variant)	not provided	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)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 827447	NM_006361.6(HOXB13):c.809A>G (p.Lys270Arg)	HOXB13 (K270R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +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)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 2010012	NM_006361.6(HOXB13):c.805G>A (p.Val269Ile)	HOXB13 (V269I)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1721533	NM_006361.6(HOXB13):c.805G>C (p.Val269Leu)	HOXB13 (V269L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 827418	NM_006361.6(HOXB13):c.804G>T (p.Arg268=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
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)	not provided +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 2810482	NM_006361.6(HOXB13):c.800_801delinsAA (p.Arg267Gln)	HOXB13 (R267Q)	Indel (missense variant)	not provided	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)	not provided +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)	not provided +1 more	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 1099823	NM_006361.6(HOXB13):c.798C>T (p.Asn266=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1105825	NM_006361.6(HOXB13):c.795G>A (p.Gln265=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 691205	NM_006361.6(HOXB13):c.795G>T (p.Gln265His)	HOXB13 (Q265H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1406491	NM_006361.6(HOXB13):c.792T>G (p.Phe264Leu)	HOXB13 (F264L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 485701	NM_006361.6(HOXB13):c.791T>C (p.Phe264Ser)	HOXB13 (F264S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	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 1407357	NM_006361.6(HOXB13):c.788G>A (p.Trp263Ter)	HOXB13 (W263*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 1926872	NM_006361.6(HOXB13):c.787T>C (p.Trp263Arg)	HOXB13 (W263R)	Single nucleotide variant (missense variant)	not provided	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 1383323	NM_006361.6(HOXB13):c.785T>C (p.Ile262Thr)	HOXB13 (I262T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1064220	NM_006361.6(HOXB13):c.784A>G (p.Ile262Val)	HOXB13 (I262V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 691201	NM_006361.6(HOXB13):c.784del (p.Ile262fs)	HOXB13 (I262fs)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 2023532	NM_006361.6(HOXB13):c.783C>T (p.Thr261=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 827281	NM_006361.6(HOXB13):c.783C>A (p.Thr261=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1473268	NM_006361.6(HOXB13):c.782C>G (p.Thr261Ser)	HOXB13 (T261S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1099567	NM_006361.6(HOXB13):c.780T>A (p.Ile260=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 966330	NM_006361.6(HOXB13):c.779T>G (p.Ile260Ser)	HOXB13 (I260S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 827259	NM_006361.6(HOXB13):c.779T>A (p.Ile260Asn)	HOXB13 (I260N)	Single nucleotide variant (missense variant)	not provided +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 1034876	NM_006361.6(HOXB13):c.776A>G (p.Gln259Arg)	HOXB13 (Q259R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 2025471	NM_006361.6(HOXB13):c.775C>T (p.Gln259Ter)	HOXB13 (Q259*)	Single nucleotide variant (nonsense)	not provided	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)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 1436641	NM_006361.6(HOXB13):c.772C>G (p.Arg258Gly)	HOXB13 (R258G)	Single nucleotide variant (missense variant)	not provided	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 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 1003485	NM_006361.6(HOXB13):c.769del (p.Glu257fs)	HOXB13 (E257fs)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 827204	NM_006361.6(HOXB13):c.769G>C (p.Glu257Gln)	HOXB13 (E257Q)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1133862	NM_006361.6(HOXB13):c.768G>T (p.Ser256=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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)	not provided +1 more	GUncertain significance
Select item 1008259	NM_006361.6(HOXB13):c.766T>C (p.Ser256Pro)	HOXB13 (S256P)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2026428	NM_006361.6(HOXB13):c.765C>G (p.Leu255=)	HOXB13	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 955099	NM_006361.6(HOXB13):c.764_765delinsAA (p.Leu255Gln)	HOXB13 (L255Q)	Indel (missense variant)	not provided	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

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