TUBB4B[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 160862	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	LOC124210612, LOC124210613 +3786 more	Copy number gain	See cases	GPathogenic
Select item 150340	GRCh38/hg38 9p11.2-q34.3(chr9:193412-138159073)x3	LOC121331326, LOC121331327 +3785 more	Copy number gain	See cases	GPathogenic
Select item 150050	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138159073)x3	LOC126860737, LOC126860738 +3786 more	Copy number gain	See cases	GPathogenic
Select item 149828	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124524)x3	ABCA1, ABCA2 +3786 more	Copy number gain	See cases	GPathogenic
Select item 59875	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138114463)x3	LOC110121197, LOC110121234 +3786 more	Copy number gain	See cases	GPathogenic
Select item 33205	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	LOC121331342, LOC121331343 +3786 more	Copy number gain	See cases	GPathogenic
Select item 153518	GRCh38/hg38 9p24.3-q34.3(chr9:203861-138125937)x3	LOC113839542, LOC113839543 +3786 more	Copy number gain	See cases	GPathogenic
Select item 155409	GRCh38/hg38 9p24.3-q34.3(chr9:203862-138125937)x3	ABCA1, ABCA2 +3786 more	Copy number gain	See cases	GPathogenic
Select item 144309	GRCh38/hg38 9p24.3-q34.3(chr9:204193-138179445)	LOC130002189, LOC130002190 +3786 more	Copy number gain	See cases	GPathogenic
Select item 145579	GRCh38/hg38 9q33.2-34.3(chr9:121073102-138179445)x3	ABCA2, ABL1 +1272 more	Copy number gain	See cases	GPathogenic
Select item 57324	GRCh38/hg38 9q33.2-34.3(chr9:121112395-138075224)x3	ABCA2, ABL1 +1268 more	Copy number gain	See cases	GPathogenic
Select item 57353	GRCh38/hg38 9q33.2-34.3(chr9:122792658-138124532)x3	LOC130003132, LOC130003133 +1210 more	Copy number gain	See cases	GPathogenic
Select item 145575	GRCh38/hg38 9q34.11-34.3(chr9:129068560-138179445)x3	MED27, MIGA2 +789 more	Copy number gain	See cases	GPathogenic
Select item 144296	GRCh38/hg38 9q34.11-34.3(chr9:130513207-138124532)x3	LOC130003057, LOC130003058 +656 more	Copy number gain	See cases	GPathogenic
Select item 3238673	GRCh38/hg38 9q34.13-34.3(chr9:137552409-137879159)	LOC124375238, LOC124375239 +569 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 3238671	GRCh38/hg38 9q34.13-34.3(chr9:137552082-137728529)	GBGT1, GLT6D1 +552 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 3238668	GRCh38/hg38 9q34.13-34.3(chr9:137552409-138052113)	ABCA2, ABO +572 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 3238667	GRCh38/hg38 9q34.13-34.3(chr9:137552409-138059181)	LOC130002921, LOC130002922 +572 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 3238666	GRCh38/hg38 9q34.13-34.3(chr9:136926151-138059181)	LOC121366034, LOC121366035 +572 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 3238664	GRCh38/hg38 9q34.13-34.3(chr9:137590213-137817525)	SARDH, SEC16A +568 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 3238663	GRCh38/hg38 9q34.13-34.3(chr9:137590213-138052188)	ABCA2, ABO +572 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 154569	GRCh38/hg38 9q34.13-34.3(chr9:132386553-138059695)x3	LOC130003026, LOC130003027 +530 more	Copy number gain	See cases	GPathogenic
Select item 147626	GRCh38/hg38 9q34.13-34.3(chr9:132986903-138114463)x3	ABCA2, ABO +510 more	Copy number gain	See cases	GPathogenic
Select item 148759	GRCh38/hg38 9q34.2-34.3(chr9:133504071-138159073)x3	LOC129390118, LOC130002920 +439 more	Copy number gain	See cases	GPathogenic
Select item 154888	GRCh38/hg38 9q34.2-34.3(chr9:133918071-138159073)x3	INPP5E, KCNT1 +417 more	Copy number gain	See cases	GPathogenic
Select item 151031	GRCh38/hg38 9q34.2-34.3(chr9:133996227-138124524)x3	LOC130003077, LOC130003078 +405 more	Copy number gain	See cases	GPathogenic
Select item 59943	GRCh38/hg38 9q34.2-34.3(chr9:134174698-138138735)x3	ABCA2, AGPAT2 +392 more	Copy number gain	See cases	GPathogenic
Select item 3238701	GRCh38/hg38 9q34.2-34.3(chr9:134288333-138155727)	ABCA2, AGPAT2 +388 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 59136	GRCh38/hg38 9q34.2-34.3(chr9:134428674-138154922)x1	UAP1L1, UBAC1 +371 more	Copy number loss	See cases	GPathogenic
Select item 3238689	GRCh38/hg38 9q34.3(chr9:134642187-138121999)	ABCA2, AGPAT2 +367 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 2203758	GRCh38/hg38 9q34.3(chr9:134962336-137240181)x1	LOC124375251, LOC126860788 +265 more	Copy number loss	See cases	GPathogenic
Select item 3238697	GRCh38/hg38 9q34.3(chr9:135008333-138199729)	ABCA2, AGPAT2 +347 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 3238659	GRCh38/hg38 9q34.3(chr9:135182209-138129711)	UBAC1, ZMYND19 +346 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 3238707	GRCh38/hg38 9q34.3(chr9:135203306-138100471)	LOC130003123, LOC130003124 +345 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 3238694	GRCh38/hg38 9q34.3(chr9:135204722-138394717)	EHMT1, ENTPD2 +347 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 3238725	GRCh38/hg38 9q34.3(chr9:135338745-138124196)	ABCA2, AGPAT2 +344 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 59137	GRCh38/hg38 9q34.3(chr9:135452016-137613738)x1	ABCA2, AGPAT2 +311 more	Copy number loss	See cases	GPathogenic
Select item 155327	GRCh38/hg38 9q34.3(chr9:135704780-138125937)x4	QSOX2, RABL6 +324 more	Copy number gain	See cases	GLikely pathogenic
Select item 3238708	GRCh38/hg38 9q34.3(chr9:135791488-138262981)	ABCA2, AGPAT2 +325 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 3238669	GRCh38/hg38 9q34.3(chr9:135954288-138125938)	LOC130003073, LOC130003074 +310 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 3238658	GRCh38/hg38 9q34.3(chr9:135969078-138104469)	LOC126860801, LOC129390118 +309 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 3238700	GRCh38/hg38 9q34.3(chr9:136032451-138125938)	LOC130003044, LOC130003045 +309 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 161082	GRCh38/hg38 9q34.3(chr9:136323974-138014606)x1	LOC130003070, LOC130003071 +283 more	Copy number loss	See cases	GPathogenic
Select item 57416	GRCh38/hg38 9q34.3(chr9:136323974-138124532)x1	ABCA2, AGPAT2 +284 more	Copy number loss	See cases	GPathogenic
Select item 34625	GRCh38/hg38 9q34.3(chr9:136323974-138014606)x1	ABCA2, AGPAT2 +283 more	Copy number loss	See cases	GPathogenic
Select item 3238709	GRCh38/hg38 9q34.3(chr9:136684941-138124673)	ABCA2, AGPAT2 +227 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 3238683	GRCh38/hg38 9q34.3(chr9:136806104-138394717)	LOC130003043, LOC130003044 +199 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 3238682	GRCh38/hg38 9q34.3(chr9:137569711-138129711)	ABCA2, AJM1 +193 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 3238690	GRCh38/hg38 9q34.3(chr9:136817307-138133487)	ABCA2, AJM1 +193 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 3238672	GRCh38/hg38 9q34.3(chr9:137529711-138129711)	ABCA2, AJM1 +193 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 3238702	GRCh38/hg38 9q34.3(chr9:136869696-138172039)	ABCA2, ANAPC2 +176 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 154911	GRCh38/hg38 9q34.3(chr9:136877772-138124524)x1	ABCA2, ANAPC2 +176 more	Copy number loss	See cases	GPathogenic
Select item 3238681	GRCh38/hg38 9q34.3(chr9:137552082-138394717)	ABCA2, ANAPC2 +168 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 59140	GRCh38/hg38 9q34.3(chr9:136926575-138114463)x1	ABCA2, ANAPC2 +166 more	Copy number loss	See cases	GPathogenic
Select item 3238719	GRCh38/hg38 9q34.3(chr9:136993278-138200863)	LOC130003071, LOC130003072 +154 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 3238695	GRCh38/hg38 9q34.3(chr9:137059436-137902321)	ANAPC2, ARRDC1 +136 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 154677	GRCh38/hg38 9q34.3(chr9:137092629-137270028)x3	ANAPC2, CIMIP2A +43 more	Copy number gain	See cases	GBenign
Select item 59090	GRCh38/hg38 9q34.3(chr9:137092629-137375788)x1	ANAPC2, CIMIP2A +60 more	Copy number loss	See cases	GUncertain significance
Select item 3238688	GRCh38/hg38 9q34.3(chr9:137106653-138394717)	ANAPC2, ARRDC1 +128 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 3238717	GRCh38/hg38 9q34.3(chr9:137170000-138360000)	ANAPC2, ARRDC1 +114 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 59151	GRCh38/hg38 9q34.3(chr9:137215877-137830604)x1	ARRDC1, ARRDC1-AS1 +92 more	Copy number loss	See cases	GPathogenic
Select item 59141	GRCh38/hg38 9q34.3(chr9:137215877-138138735)x1	LOC130003144, LOC130003145 +101 more	Copy number loss	See cases	GPathogenic
Select item 3238676	GRCh38/hg38 9q34.3(chr9:137272928-137711050)	ARRDC1, ARRDC1-AS1 +71 more	Copy number loss	Kleefstra syndrome 1	GPathogenic
Select item 1245035	NM_006088.6(TUBB4B):c.-62G>T	TUBB4B	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 1182505	NM_006088.6(TUBB4B):c.-29C>A	TUBB4B	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 3045573	NM_006088.6(TUBB4B):c.-18GCC[7]	TUBB4B	Microsatellite (5 prime UTR variant)	TUBB4B-related disorder	GLikely benign
Select item 3041694	NM_006088.6(TUBB4B):c.-18GCC[4]	TUBB4B	Microsatellite (5 prime UTR variant)	TUBB4B-related disorder	GBenign
Select item 3030687	NM_006088.6(TUBB4B):c.-18GCC[2]	TUBB4B	Microsatellite (5 prime UTR variant)	TUBB4B-related disorder	GLikely benign
Select item 1608124	NM_006088.6(TUBB4B):c.12C>T (p.Ile4=)	TUBB4B	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2911761	NM_006088.6(TUBB4B):c.18C>T (p.His6=)	TUBB4B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1685193	NM_006088.6(TUBB4B):c.19T>G (p.Leu7Val)	TUBB4B (L7V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2786096	NM_006088.6(TUBB4B):c.27C>T (p.Ala9=)	TUBB4B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2888545	NM_006088.6(TUBB4B):c.48C>A (p.Ile16=)	TUBB4B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1552996	NM_006088.6(TUBB4B):c.57+10C>T	TUBB4B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1956711	NM_006088.6(TUBB4B):c.57+15C>T	TUBB4B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1897684	NM_006088.6(TUBB4B):c.58-16C>T	TUBB4B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2414321	NM_006088.6(TUBB4B):c.58-7C>T	TUBB4B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2970929	NM_006088.6(TUBB4B):c.58-4dup	TUBB4B	Duplication (intron variant)	not provided	GLikely benign
Select item 2763330	NM_006088.6(TUBB4B):c.58-3T>C	TUBB4B	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2900383	NM_006088.6(TUBB4B):c.60T>C (p.Phe20=)	TUBB4B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1488406	NM_006088.6(TUBB4B):c.76G>C (p.Asp26His)	TUBB4B (D26H)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 2894275	NM_006088.6(TUBB4B):c.84C>T (p.His28=)	TUBB4B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1939228	NM_006088.6(TUBB4B):c.108C>T (p.Tyr36=)	TUBB4B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3017654	NM_006088.6(TUBB4B):c.111C>T (p.His37=)	TUBB4B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1542596	NM_006088.6(TUBB4B):c.117C>T (p.Asp39=)	TUBB4B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2766086	NM_006088.6(TUBB4B):c.120C>T (p.Ser40=)	TUBB4B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1613507	NM_006088.6(TUBB4B):c.123C>T (p.Asp41=)	TUBB4B	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2720498	NM_006088.6(TUBB4B):c.138C>T (p.Arg46=)	TUBB4B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1541662	NM_006088.6(TUBB4B):c.144C>T (p.Asn48=)	TUBB4B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1635470	NM_006088.6(TUBB4B):c.162C>T (p.Ala54=)	TUBB4B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2181572	NM_006088.6(TUBB4B):c.166+7C>T	TUBB4B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1648284	NM_006088.6(TUBB4B):c.166+10C>T	TUBB4B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1229835	NM_006088.6(TUBB4B):c.166+13C>T	TUBB4B	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1644163	NM_006088.6(TUBB4B):c.167-12C>T	TUBB4B	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2919559	NM_006088.6(TUBB4B):c.169G>A (p.Gly57Ser)	TUBB4B (G57S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 741446	NM_006088.6(TUBB4B):c.189C>G (p.Ala63=)	TUBB4B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2083785	NM_006088.6(TUBB4B):c.207G>A (p.Glu69=)	TUBB4B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1655181	NM_006088.6(TUBB4B):c.240C>T (p.Pro80=)	TUBB4B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1608062	NM_006088.6(TUBB4B):c.243C>T (p.Phe81=)	TUBB4B	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3055036	NM_006088.6(TUBB4B):c.252C>A (p.Ile84=)	TUBB4B	Single nucleotide variant (synonymous variant)	TUBB4B-related disorder	GLikely benign

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