Related gene-specific medical variations for Gene (Select 10481) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3361874	NM_006361.6(HOXB13):c.601+5del	HOXB13	Deletion (intron variant)	not provided	GUncertain significance
Select item 3243177	NC_000017.10:g.(?_46805345)_(46805955_?)dup	HOXB13	Duplication	not provided	GUncertain significance
Select item 2689221	NM_006361.6(HOXB13):c.95C>A (p.Pro32His)	HOXB13 (P32H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1330134	NM_006361.6(HOXB13):c.843del (p.Ser281fs)	HOXB13 (S281fs)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 691248	NM_006361.6(HOXB13):c.852T>C (p.Pro284=)	HOXB13	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691246	NM_006361.6(HOXB13):c.833del (p.Val278fs)	HOXB13 (V278fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691245	NM_006361.6(HOXB13):c.829A>C (p.Lys277Gln)	HOXB13 (K277Q)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691244	NM_006361.6(HOXB13):c.822del (p.Leu275fs)	HOXB13 (L275fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691243	NM_006361.6(HOXB13):c.811del (p.Glu271fs)	HOXB13 (E271fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691242	NM_006361.6(HOXB13):c.807del (p.Glu271fs)	HOXB13 (E271fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691241	NM_006361.6(HOXB13):c.805G>T (p.Val269Phe)	HOXB13 (V269F)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691240	NM_006361.6(HOXB13):c.784A>C (p.Ile262Leu)	HOXB13 (I262L)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691239	NM_006361.6(HOXB13):c.768G>C (p.Ser256=)	HOXB13	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691237	NM_006361.6(HOXB13):c.704A>T (p.Tyr235Phe)	HOXB13 (Y235F)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691236	NM_006361.6(HOXB13):c.671G>T (p.Ser224Ile)	HOXB13 (S224I)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691235	NM_006361.6(HOXB13):c.602-81_602-80insC	HOXB13	Insertion (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691234	NM_006361.6(HOXB13):c.602-113A>G	HOXB13	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691233	NM_006361.6(HOXB13):c.602-105C>T	HOXB13	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691232	NM_006361.6(HOXB13):c.602-103G>T	HOXB13	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691231	NM_006361.6(HOXB13):c.*88del	HOXB13	Deletion (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691230	NM_006361.6(HOXB13):c.*143del	HOXB13	Deletion (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691229	NM_006361.6(HOXB13):c.*136G>C	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691228	NM_006361.6(HOXB13):c.853_854insTA (p.Ter285LeuextTer?)	HOXB13	Insertion (frameshift variant +1 more)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691227	NM_006361.6(HOXB13):c.851dup (p.Ter285LeuextTer?)	HOXB13	Duplication (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691226	NM_006361.6(HOXB13):c.846del (p.Thr283fs)	HOXB13 (T283fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691224	NM_006361.6(HOXB13):c.842del (p.Ser281fs)	HOXB13 (S281fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691223	NM_006361.6(HOXB13):c.837G>A (p.Lys279=)	HOXB13	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691222	NM_006361.6(HOXB13):c.832del (p.Lys277_Val278insTer)	HOXB13	Deletion (nonsense)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691221	NM_006361.6(HOXB13):c.830del (p.Lys277fs)	HOXB13 (K277fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691220	NM_006361.6(HOXB13):c.821T>G (p.Val274Gly)	HOXB13 (V274G)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691217	NM_006361.6(HOXB13):c.815del (p.Lys272fs)	HOXB13 (K272fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691215	NM_006361.6(HOXB13):c.813G>A (p.Glu271=)	HOXB13	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691213	NM_006361.6(HOXB13):c.812dup (p.Lys272fs)	HOXB13 (K272fs)	Duplication (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691212	NM_006361.6(HOXB13):c.807C>G (p.Val269=)	HOXB13	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691211	NM_006361.6(HOXB13):c.800G>C (p.Arg267Pro)	HOXB13 (R267P)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691210	NM_006361.6(HOXB13):c.800del (p.Arg267fs)	HOXB13 (R267fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691209	NM_006361.6(HOXB13):c.802dup (p.Arg268fs)	HOXB13 (R268fs)	Duplication (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691208	NM_006361.6(HOXB13):c.799dup (p.Arg267fs)	HOXB13 (R267fs)	Duplication (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691207	NM_006361.6(HOXB13):c.797A>C (p.Asn266Thr)	HOXB13 (N266T)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691206	NM_006361.6(HOXB13):c.796A>C (p.Asn266His)	HOXB13 (N266H)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691204	NM_006361.6(HOXB13):c.795del (p.Asn266fs)	HOXB13 (N266fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691203	NM_006361.6(HOXB13):c.790T>G (p.Phe264Val)	HOXB13 (F264V)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691202	NM_006361.6(HOXB13):c.789dup (p.Phe264fs)	HOXB13 (F264fs)	Duplication (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691200	NM_006361.6(HOXB13):c.776del (p.Gln259fs)	HOXB13 (Q259fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691199	NM_006361.6(HOXB13):c.776A>C (p.Gln259Pro)	HOXB13 (Q259P)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691198	NM_006361.6(HOXB13):c.774C>G (p.Arg258=)	HOXB13	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691197	NM_006361.6(HOXB13):c.772del (p.Arg258fs)	HOXB13 (R258fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691196	NM_006361.6(HOXB13):c.771G>A (p.Glu257=)	HOXB13	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691195	NM_006361.6(HOXB13):c.770A>G (p.Glu257Gly)	HOXB13 (E257G)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691194	NM_006361.6(HOXB13):c.769dup (p.Glu257fs)	HOXB13 (E257fs)	Duplication (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691193	NM_006361.6(HOXB13):c.767C>G (p.Ser256Trp)	HOXB13 (S256W)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691191	NM_006361.6(HOXB13):c.763dup (p.Leu255fs)	HOXB13 (L255fs)	Duplication (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691189	NM_006361.6(HOXB13):c.760delinsCC (p.Ser254fs)	HOXB13 (S254fs)	Indel (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691188	NM_006361.6(HOXB13):c.760del (p.Ser254fs)	HOXB13 (S254fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691187	NM_006361.6(HOXB13):c.760A>C (p.Ser254Arg)	HOXB13 (S254R)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691186	NM_006361.6(HOXB13):c.757del (p.Thr253fs)	HOXB13 (T253fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691185	NM_006361.6(HOXB13):c.757A>T (p.Thr253Ser)	HOXB13 (T253S)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691184	NM_006361.6(HOXB13):c.757_758del (p.Thr253fs)	HOXB13 (T253fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691183	NM_006361.6(HOXB13):c.753del (p.Ala252fs)	HOXB13 (A252fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691182	NM_006361.6(HOXB13):c.753A>C (p.Ala251=)	HOXB13	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691179	NM_006361.6(HOXB13):c.749C>G (p.Ser250Trp)	HOXB13 (S250W)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691177	NM_006361.6(HOXB13):c.746T>A (p.Ile249Asn)	HOXB13 (I249N)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691176	NM_006361.6(HOXB13):c.744G>T (p.Lys248Asn)	HOXB13 (K248N)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691175	NM_006361.6(HOXB13):c.743A>T (p.Lys248Met)	HOXB13 (K248M)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691174	NM_006361.6(HOXB13):c.742A>C (p.Lys248Gln)	HOXB13 (K248Q)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691173	NM_006361.6(HOXB13):c.740G>C (p.Arg247Pro)	HOXB13 (R247P)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691172	NM_006361.6(HOXB13):c.740del (p.Arg247fs)	HOXB13 (R247fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691171	NM_006361.6(HOXB13):c.736dup (p.Arg246fs)	HOXB13 (R246fs)	Duplication (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691170	NM_006361.6(HOXB13):c.734del (p.Lys245fs)	HOXB13 (K245fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691169	NM_006361.6(HOXB13):c.730dup (p.Asp244fs)	HOXB13 (D244fs)	Duplication (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691168	NM_006361.6(HOXB13):c.729_735del (p.Asp244fs)	HOXB13 (D244fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691167	NM_006361.6(HOXB13):c.727A>T (p.Lys243Ter)	HOXB13 (K243*)	Single nucleotide variant (nonsense)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691165	NM_006361.6(HOXB13):c.726C>T (p.Thr242=)	HOXB13	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691164	NM_006361.6(HOXB13):c.725C>A (p.Thr242Asn)	HOXB13 (T242N)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691163	NM_006361.6(HOXB13):c.724A>C (p.Thr242Pro)	HOXB13 (T242P)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691161	NM_006361.6(HOXB13):c.717del (p.Lys239fs)	HOXB13 (K239fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691160	NM_006361.6(HOXB13):c.716del (p.Lys239fs)	HOXB13 (K239fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691159	NM_006361.6(HOXB13):c.712A>T (p.Asn238Tyr)	HOXB13 (N238Y)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691158	NM_006361.6(HOXB13):c.711dup (p.Asn238Ter)	HOXB13 (N238*)	Duplication (nonsense)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691157	NM_006361.6(HOXB13):c.710C>T (p.Ala237Val)	HOXB13 (A237V)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691156	NM_006361.6(HOXB13):c.708G>C (p.Ala236=)	HOXB13	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691154	NM_006361.6(HOXB13):c.706del (p.Ala236fs)	HOXB13 (A236fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691153	NM_006361.6(HOXB13):c.705del (p.Glu234_Tyr235insTer)	HOXB13	Deletion (nonsense)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691152	NM_006361.6(HOXB13):c.701dup (p.Tyr235fs)	HOXB13 (Y235fs)	Duplication (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691151	NM_006361.6(HOXB13):c.696G>C (p.Glu232Asp)	HOXB13 (E232D)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691150	NM_006361.6(HOXB13):c.696del (p.Glu232fs)	HOXB13 (E232fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691147	NM_006361.6(HOXB13):c.678del (p.Gln227fs)	HOXB13 (Q227fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691146	NM_006361.6(HOXB13):c.671G>C (p.Ser224Thr)	HOXB13 (S224T)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691145	NM_006361.6(HOXB13):c.667T>G (p.Tyr223Asp)	HOXB13 (Y223D)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691144	NM_006361.6(HOXB13):c.666dup (p.Tyr223fs)	HOXB13 (Y223fs)	Duplication (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691143	NM_006361.6(HOXB13):c.665del (p.Pro222fs)	HOXB13 (P222fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691142	NM_006361.6(HOXB13):c.660dup (p.Ile221fs)	HOXB13 (I221fs)	Duplication (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691141	NM_006361.6(HOXB13):c.658del (p.Arg220fs)	HOXB13 (R220fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691140	NM_006361.6(HOXB13):c.657A>C (p.Lys219Asn)	HOXB13 (K219N)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691139	NM_006361.6(HOXB13):c.657dup (p.Arg220fs)	HOXB13 (R220fs)	Duplication (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691137	NM_006361.6(HOXB13):c.654del (p.Lys219fs)	HOXB13 (K219fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691136	NM_006361.6(HOXB13):c.651C>A (p.Arg217=)	HOXB13	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691134	NM_006361.6(HOXB13):c.647dup (p.Arg217fs)	HOXB13 (R217fs)	Duplication (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691133	NM_006361.6(HOXB13):c.646G>C (p.Gly216Arg)	HOXB13 (G216R)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691132	NM_006361.6(HOXB13):c.643del (p.Arg215fs)	HOXB13 (R215fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance

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