HOXB13[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 148363	GRCh38/hg38 17q23.1-25.1(chr17:36449220-75053130)x3	LOC112533659, LOC112533660 +2032 more	Copy number gain	See cases	GPathogenic
Select item 57282	GRCh38/hg38 17q21.33-24.2(chr17:36449220-68170214)x3	AARSD1, AATF +1753 more	Copy number gain	See cases	GPathogenic
Select item 154833	GRCh38/hg38 17q21.32-21.33(chr17:47986886-49329397)x1	ABI3, ATP5MC1 +99 more	Copy number loss	See cases	GPathogenic
Select item 155384	GRCh38/hg38 17q21.32-21.33(chr17:48450628-49552921)x3	ABI3, ATP5MC1 +92 more	Copy number gain	See cases	GUncertain significance
Select item 59588	GRCh38/hg38 17q21.32-21.33(chr17:48520885-49511208)x1	ABI3, ATP5MC1 +87 more	Copy number loss	See cases	GPathogenic
Select item 691033	NM_006361.6(HOXB13):c.*160dup	HOXB13	Duplication (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691031	NM_006361.6(HOXB13):c.*155dup	HOXB13	Duplication (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691030	NM_006361.6(HOXB13):c.*153G>A	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691029	NM_006361.6(HOXB13):c.*153del	HOXB13	Deletion (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691028	NM_006361.6(HOXB13):c.*152G>C	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691027	NM_006361.6(HOXB13):c.151_152insC	HOXB13	Insertion (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691025	NM_006361.6(HOXB13):c.149_150insG	HOXB13	Insertion (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691026	NM_006361.6(HOXB13):c.*149del	HOXB13	Deletion (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691024	NM_006361.6(HOXB13):c.*148C>A	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691023	NM_006361.6(HOXB13):c.*146T>G	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691022	NM_006361.6(HOXB13):c.*146T>C	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691021	NM_006361.6(HOXB13):c.*146del	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 691020	NM_006361.6(HOXB13):c.*142C>A	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691019	NM_006361.6(HOXB13):c.*140G>T	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691018	NM_006361.6(HOXB13):c.*140G>C	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691017	NM_006361.6(HOXB13):c.*138T>G	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691016	NM_006361.6(HOXB13):c.*138del	HOXB13	Deletion (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691015	NM_006361.6(HOXB13):c.*137C>T	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691014	NM_006361.6(HOXB13):c.*137C>A	HOXB13	Single nucleotide variant (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 691013	NM_006361.6(HOXB13):c.*135T>G	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691012	NM_006361.6(HOXB13):c.*132G>C	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691011	NM_006361.6(HOXB13):c.*132G>A	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691010	NM_006361.6(HOXB13):c.*131T>C	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691009	NM_006361.6(HOXB13):c.*131T>A	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691008	NM_006361.6(HOXB13):c.*131del	HOXB13	Deletion (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691007	NM_006361.6(HOXB13):c.*130C>A	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691006	NM_006361.6(HOXB13):c.*129dup	HOXB13	Duplication (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691005	NM_006361.6(HOXB13):c.*126dup	HOXB13	Duplication (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691004	NM_006361.6(HOXB13):c.121_122insG	HOXB13	Insertion (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691003	NM_006361.6(HOXB13):c.120_121insG	HOXB13	Insertion (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691002	NM_006361.6(HOXB13):c.*119T>A	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691001	NM_006361.6(HOXB13):c.*118dup	HOXB13	Duplication (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691000	NM_006361.6(HOXB13):c.*115dup	HOXB13	Duplication (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 690999	NM_006361.6(HOXB13):c.*114C>A	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 690998	NM_006361.6(HOXB13):c.*110A>T	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 690997	NM_006361.6(HOXB13):c.*110A>G	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 690995	NM_006361.6(HOXB13):c.*108A>G	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 690994	NM_006361.6(HOXB13):c.105_108del	HOXB13	Deletion (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 690993	NM_006361.6(HOXB13):c.103_104del	HOXB13	Deletion (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691054	NM_006361.6(HOXB13):c.*95G>T	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691053	NM_006361.6(HOXB13):c.*93del	HOXB13	Deletion (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691052	NM_006361.6(HOXB13):c.*90C>T	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691051	NM_006361.6(HOXB13):c.*90C>G	HOXB13	Single nucleotide variant (3 prime UTR 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 691050	NM_006361.6(HOXB13):c.*86G>A	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691049	NM_006361.6(HOXB13):c.*80G>C	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691048	NM_006361.6(HOXB13):c.*78G>C	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1196252	NM_006361.6(HOXB13):c.*57G>A	HOXB13	Single nucleotide variant (3 prime UTR variant)	not provided	GLikely benign
Select item 691047	NM_006361.6(HOXB13):c.*45T>G	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691046	NM_006361.6(HOXB13):c.*45T>C	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691045	NM_006361.6(HOXB13):c.35_36insAAGG	HOXB13	Insertion (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691044	NM_006361.6(HOXB13):c.*33G>A	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691043	NM_006361.6(HOXB13):c.*29G>C	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691042	NM_006361.6(HOXB13):c.*28dup	HOXB13	Duplication (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 2647885	NM_006361.6(HOXB13):c.*28C>A	HOXB13	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 691041	NM_006361.6(HOXB13):c.*27G>C	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691040	NM_006361.6(HOXB13):c.*27G>A	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691039	NM_006361.6(HOXB13):c.*25dup	HOXB13	Duplication (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691037	NM_006361.6(HOXB13):c.*22dup	HOXB13	Duplication (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691038	NM_006361.6(HOXB13):c.*22G>T	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691034	NM_006361.6(HOXB13):c.*19dup	HOXB13	Duplication (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691032	NM_006361.6(HOXB13):c.*15T>C	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 690996	NM_006361.6(HOXB13):c.*10T>C	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691036	NM_006361.6(HOXB13):c.*1G>T	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 691035	NM_006361.6(HOXB13):c.*1G>A	HOXB13	Single nucleotide variant (3 prime UTR variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1578605	NM_006361.6(HOXB13):c.855A>G (p.Ter285=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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 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)	not provided +3 more	GConflicting classifications of pathogenicity; association
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 691227	NM_006361.6(HOXB13):c.851dup (p.Ter285LeuextTer?)	HOXB13	Duplication (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
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 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 2107164	NM_006361.6(HOXB13):c.849C>G (p.Thr283=)	HOXB13	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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 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)	not provided +1 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 691226	NM_006361.6(HOXB13):c.846del (p.Thr283fs)	HOXB13 (T283fs)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1801654	NM_006361.6(HOXB13):c.844_845del (p.Ala282fs)	HOXB13 (A282fs)	Microsatellite (frameshift variant)	Gastric cancer	GPathogenic
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)	not provided +1 more	GLikely benign
Select item 1330134	NM_006361.6(HOXB13):c.843del (p.Ser281fs)	HOXB13 (S281fs)	Deletion (frameshift variant)	not provided	GUncertain significance
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

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